Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5781 |
| ensemblid | ENSG00000179295.19 |
| hgncid | 9644 |
| symbol | PTPN11 |
| name | protein tyrosine phosphatase non-receptor type 11 |
| refseq_nuc | NM_002834.5 |
| refseq_prot | NP_002825.3 |
| ensembl_nuc | ENST00000351677.7 |
| ensembl_prot | ENSP00000340944.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 112418947 |
| end | 112509918 |
| strand | + |
| ver | v1.2 |
| region | chr12:112418947-112509918 |
| region5000 | chr12:112413947-112514918 |
| regionname0 | PTPN11_chr12_112418947_112509918 |
| regionname5000 | PTPN11_chr12_112413947_112514918 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 593 | 298 | 84 | 46 | 133 | 6 | 27 | 110 | PTPN11_chr12_112413947_112514918 | PTPN11 | MTSRR others(588): Show |
chr12 | 112413947 | 112514918 |
| a0002 | 0/0 | 593 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | MTSRR others(588): Show |
chr12 | 112413947 | 112514918 |
| a0003 | 0/0 | 593 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | MTSRR others(588): Show |
chr12 | 112413947 | 112514918 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1779 | 287 | 73 | 46 | 133 | 6 | 27 | PTPN11_chr12_112413947_112514918 | PTPN11 | ATGAC others(1774): Show |
chr12 | 112413947 | 112514918 | ||
| a0001c0002 | 0/0 | 1779 | 11 | 11 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | ATGAC others(1774): Show |
chr12 | 112413947 | 112514918 | ||
| a0002c0004 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | ATGAC others(1774): Show |
chr12 | 112413947 | 112514918 | ||
| a0003c0003 | 0/0 | 1779 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | ATGAC others(1774): Show |
chr12 | 112413947 | 112514918 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6070 | 114 | 41 | 12 | 52 | 1 | 8 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6065): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0002 | 0/0 | 6064 | 78 | 7 | 13 | 54 | 1 | 3 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6059): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0003 | 1/1 | 6073 | 59 | 6 | 18 | 17 | 3 | 13 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6068): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0004 | 0/0 | 6067 | 7 | 5 | 1 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6062): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0005 | 0/0 | 6067 | 6 | 6 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6062): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0006 | 0/0 | 6069 | 5 | 2 | 2 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6064): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0007 | 0/0 | 6070 | 3 | 3 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6065): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0008 | 0/0 | 6049 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6044): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0009 | 0/0 | 6067 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6062): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0010 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6065): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0011 | 0/0 | 6073 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6068): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0012 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6065): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0013 | 0/0 | 6073 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6068): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0014 | 0/0 | 6073 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6068): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0015 | 0/0 | 6073 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6068): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0016 | 0/0 | 6073 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6068): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0017 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6065): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0018 | 0/0 | 6067 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6062): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0019 | 0/0 | 6064 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6059): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0020 | 0/0 | 6049 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6044): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0021 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6065): Show |
chr12 | 112413947 | 112514918 |
| a0001c0001t0022 | 0/0 | 6070 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6065): Show |
chr12 | 112413947 | 112514918 |
| a0001c0002t0001 | 0/0 | 6070 | 11 | 11 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6065): Show |
chr12 | 112413947 | 112514918 |
| a0002c0004t0003 | 0/0 | 6073 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6068): Show |
chr12 | 112413947 | 112514918 |
| a0003c0003t0003 | 0/0 | 6073 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | AGTCT others(6068): Show |
chr12 | 112413947 | 112514918 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0011g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0012g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0013g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0014g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0015g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0016g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0017g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0018g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0019g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0020g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0021g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0001t0022g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0002c0004t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| a0003c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0097 | EUR | GBR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0261 | EUR | GBR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0142 | EUR | GBR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0118 | EUR | GBR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | CHS | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0264 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0145 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02056 | hp2 | a0002 | c0004 | t0003 | g0189 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CDX | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | CDX | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02280 | hp2 | a0001 | c0001 | t0021 | g0154 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02523 | hp2 | a0001 | c0001 | t0010 | g0169 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0133 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0188 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0014 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03017 | hp1 | a0003 | c0003 | t0003 | g0127 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0258 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03195 | hp2 | a0001 | c0001 | t0018 | g0050 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0252 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0111 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03704 | hp1 | a0001 | c0001 | t0016 | g0153 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0134 | SAS | BEB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03831 | hp2 | a0001 | c0001 | t0022 | g0283 | SAS | BEB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0285 | SAS | BEB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0143 | SAS | BEB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0183 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18994 | hp2 | a0001 | c0001 | t0015 | g0102 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19002 | hp2 | a0001 | c0001 | t0019 | g0202 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19004 | hp1 | a0001 | c0001 | t0014 | g0151 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0122 | AFR | LWK | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19057 | hp2 | a0001 | c0001 | t0008 | g0228 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19070 | hp1 | a0001 | c0001 | t0017 | g0072 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19076 | hp2 | a0001 | c0001 | t0012 | g0213 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19079 | hp1 | a0001 | c0001 | t0013 | g0191 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19083 | hp2 | a0001 | c0001 | t0011 | g0157 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19086 | hp1 | a0001 | c0001 | t0020 | g0232 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ASW | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ASW | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0126 | EUR | TSI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0152 | SAS | GIH | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | GIH | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | USA | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | USA | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | LWK | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0128 | REF | REF | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0159 | REF | REF | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112477951 | G | A | 1 | a0003 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1028G>A | p.Arg343Gln | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/16 | 1193/6073 | 1028/1782 | 343/593 | chr12 | 112477951 | |||
| chr12:112504711 | G | A | 1 | a0002 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.1729G>A | p.Ala577Thr | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/16 | 1894/6073 | 1729/1782 | 577/593 | chr12 | 112504711 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112450435 | C | T | 1 | a0001c0002 | 11 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(8): Show |
synonymous_variant | LOW | c.255C>T | p.His85His | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/16 | 420/6073 | 255/1782 | 85/593 | chr12 | 112450435 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112418991 | G | T | 1 | a0001c0001t0022 | 1 | HG03831.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-121G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/16 | chr12 | 112418991 | |||||||
| chr12:112505898 | ATTTGGAA others(11): Show |
A | 1 | a0001c0001t0008 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*108_*125delTTGGAA others(12): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1136 | INFO_REALIGN_3_PRIME | chr12 | 112505898 | |||||
| chr12:112505967 | G | T | 1 | a0001c0001t0021 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*175G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1203 | chr12 | 112505967 | ||||||
| chr12:112506097 | G | A | 1 | a0001c0001t0009 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*305G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1333 | chr12 | 112506097 | ||||||
| chr12:112506121 | T | C | 1 | a0001c0001t0010 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*329T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1357 | chr12 | 112506121 | ||||||
| chr12:112506462 | G | A | 1 | a0001c0001t0007 | 3 | HG03516.hp1 HG03540.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*670G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1698 | chr12 | 112506462 | ||||||
| chr12:112506630 | G | A | 1 | a0001c0001t0011 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*838G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1866 | chr12 | 112506630 | ||||||
| chr12:112506797 | CG | C | 1 | a0001c0001t0006 | 5 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1006delG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2034 | chr12 | 112506797 | ||||||
| chr12:112506927 | T | G | 1 | a0001c0001t0012 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1135T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2163 | chr12 | 112506927 | ||||||
| chr12:112506946 | TTGA | T | 9 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(6): Show |
138 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1199_*1201delATG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2227 | INFO_REALIGN_3_PRIME | chr12 | 112506946 | |||||
| chr12:112506946 | TTGATGA | T | 5 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(2): Show |
16 | HG01109.hp1 HG01891.hp2 HG02559.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1196_*1201delATGA others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2224 | INFO_REALIGN_3_PRIME | chr12 | 112506946 | |||||
| chr12:112506946 | TTGATGAT others(2): Show |
T | 2 | a0001c0001t0002 a0001c0001t0019 |
79 | HG00140.hp1 HG00544.hp2 HG00735.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1193_*1201delATGA others(5): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2221 | INFO_REALIGN_3_PRIME | chr12 | 112506946 | |||||
| chr12:112506946 | TTGATGAT others(17): Show |
T | 1 | a0001c0001t0020 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1178_*1201delATGA others(20): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2206 | INFO_REALIGN_3_PRIME | chr12 | 112506946 | |||||
| chr12:112507166 | G | C | 1 | a0001c0001t0005 | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1374G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2402 | chr12 | 112507166 | ||||||
| chr12:112507921 | A | G | 1 | a0001c0001t0019 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2129A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 3157 | chr12 | 112507921 | ||||||
| chr12:112508244 | G | A | 1 | a0001c0001t0013 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2452G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 3480 | chr12 | 112508244 | ||||||
| chr12:112508514 | T | C | 1 | a0001c0001t0014 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2722T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 3750 | chr12 | 112508514 | ||||||
| chr12:112508719 | T | A | 1 | a0001c0001t0018 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2927T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 3955 | chr12 | 112508719 | ||||||
| chr12:112509173 | A | G | 1 | a0001c0001t0016 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3381A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 4409 | chr12 | 112509173 | ||||||
| chr12:112509294 | A | G | 1 | a0001c0001t0017 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3502A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 4530 | chr12 | 112509294 | ||||||
| chr12:112509330 | T | C | 1 | a0001c0001t0015 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3538T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 4566 | chr12 | 112509330 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112419150 | G | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(16): Show |
21 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.14+25G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112419150 | |||||||
| chr12:112419179 | C | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+54C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112419179 | |||||||
| chr12:112419232 | C | G | 1 | a0001c0001t0002g0289 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.14+107C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112419232 | |||||||
| chr12:112419571 | G | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.14+446G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112419571 | |||||||
| chr12:112419858 | C | T | 1 | a0001c0001t0002g0286 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.14+733C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112419858 | |||||||
| chr12:112420727 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+1602G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112420727 | |||||||
| chr12:112420954 | A | AG | 3 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 |
3 | HG02622.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.14+1831dupG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112420954 | ||||||
| chr12:112421093 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.14+1968T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112421093 | |||||||
| chr12:112422061 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.14+2936G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112422061 | |||||||
| chr12:112422078 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.14+2953T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112422078 | |||||||
| chr12:112422309 | T | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+3184T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112422309 | |||||||
| chr12:112422625 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 |
3 | NA18992.hp1 NA19065.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.14+3500G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112422625 | |||||||
| chr12:112423112 | A | G | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+3987A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112423112 | |||||||
| chr12:112423726 | C | T | 1 | a0001c0001t0004g0285 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.14+4601C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112423726 | |||||||
| chr12:112423740 | C | CT | 21 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(18): Show |
23 | HG01109.hp2 HG01934.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.14+4637dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112423740 | ||||||
| chr12:112423740 | CT | C | 10 | a0001c0001t0001g0031 a0001c0001t0002g0039 a0001c0001t0002g0040 others(7): Show |
10 | HG01109.hp1 HG01256.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.14+4637delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112423740 | ||||||
| chr12:112423805 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0004g0032 |
3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.14+4680G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112423805 | |||||||
| chr12:112424098 | C | T | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14+4973C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424098 | |||||||
| chr12:112424402 | T | A | 1 | a0001c0001t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.14+5277T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424402 | |||||||
| chr12:112424855 | A | G | 9 | a0001c0001t0002g0040 a0001c0001t0002g0266 a0001c0001t0002g0267 others(6): Show |
9 | HG01071.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.14+5730A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424855 | |||||||
| chr12:112424867 | T | TTG | 22 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0248 others(19): Show |
23 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.14+5764_14+5765dup others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424867 | ||||||
| chr12:112424877 | GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0001g0284 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.14+5766_14+5779del others(14): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424877 | ||||||
| chr12:112424881 | GTGTGTGT others(3): Show |
G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0243 |
2 | NA18946.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.14+5766_14+5775del others(10): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424881 | ||||||
| chr12:112424883 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0003 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.14+5765_14+5766ins others(10): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424883 | ||||||
| chr12:112424885 | G | GTGTGTGT others(1): Show |
7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
8 | HG02145.hp2 HG02451.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.14+5765_14+5766ins others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424885 | ||||||
| chr12:112424885 | GTGTGTA | G | 41 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0005 others(38): Show |
48 | HG00544.hp2 HG00735.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.14+5766_14+5771del others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424885 | ||||||
| chr12:112424887 | GTGTA | G | 20 | a0001c0001t0001g0217 a0001c0001t0002g0039 a0001c0001t0002g0040 others(17): Show |
20 | HG01071.hp2 HG01256.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.14+5766_14+5769del others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424887 | ||||||
| chr12:112424889 | G | GTGTA | 3 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 |
3 | HG02622.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.14+5765_14+5766ins others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424889 | ||||||
| chr12:112424889 | GTA | G | 8 | a0001c0001t0001g0136 a0001c0001t0002g0208 a0001c0001t0002g0215 others(5): Show |
8 | HG01928.hp2 HG01952.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.14+5766_14+5767del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424889 | ||||||
| chr12:112424891 | A | ATG | 22 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0131 others(19): Show |
22 | HG00140.hp2 HG00738.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.14+5793_14+5794dup others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424891 | ||||||
| chr12:112424891 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(15): Show |
20 | HG00621.hp2 HG01258.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.14+5766A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424891 | |||||||
| chr12:112424893 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.14+5768G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424893 | |||||||
| chr12:112424916 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.14+5791T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424916 | |||||||
| chr12:112424942 | CCAT | C | 74 | a0001c0001t0001g0194 a0001c0001t0001g0217 a0001c0001t0002g0001 others(71): Show |
81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.14+5818_14+5820del others(3): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424942 | |||||||
| chr12:112424956 | T | TTG | 13 | a0001c0001t0001g0024 a0001c0001t0003g0180 a0001c0001t0003g0181 others(10): Show |
13 | HG02056.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.14+5883_14+5884dup others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112424956 | T | TTGTG | 7 | a0001c0001t0001g0042 a0001c0001t0001g0190 a0001c0001t0001g0288 others(4): Show |
7 | HG01099.hp2 HG01168.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+5881_14+5884dup others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112424956 | TTG | T | 48 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0031 others(45): Show |
48 | HG00140.hp1 HG00735.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.14+5883_14+5884del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112424956 | TTGTG | T | 73 | a0001c0001t0001g0006 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
81 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.14+5881_14+5884del others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112424956 | TTGTGTG | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0043 others(39): Show |
43 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.14+5879_14+5884del others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112424956 | TTGTGTGT others(1): Show |
T | 11 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
11 | HG02257.hp2 HG02922.hp1 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+5877_14+5884del others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112424956 | TTGTGTGT others(3): Show |
T | 9 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG02027.hp1 HG02055.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.14+5875_14+5884del others(10): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112424956 | TTGTGTGT others(5): Show |
T | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
13 | HG01993.hp2 HG02074.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+5873_14+5884del others(12): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112424956 | TTGTGTGT others(9): Show |
T | 2 | a0001c0001t0001g0052 a0001c0001t0003g0051 |
2 | HG01071.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.14+5869_14+5884del others(16): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112424956 | TTGTGTGT others(13): Show |
T | 2 | a0001c0001t0001g0049 a0001c0001t0018g0050 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.14+5865_14+5884del others(20): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112424956 | TTGTGTGT others(15): Show |
T | 1 | a0001c0001t0004g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.14+5863_14+5884del others(22): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112424956 | TTGTGTGT others(21): Show |
T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01943.hp2 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+5857_14+5884del others(28): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | ||||||
| chr12:112425000 | G | A | 2 | a0001c0001t0005g0015 a0001c0001t0005g0016 |
2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.14+5875G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425000 | |||||||
| chr12:112425002 | G | A | 6 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0005g0017 others(3): Show |
6 | HG02622.hp2 HG02976.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.14+5877G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425002 | |||||||
| chr12:112425004 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0003g0002 a0001c0001t0004g0023 others(1): Show |
5 | HG02451.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+5879G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425004 | |||||||
| chr12:112425004 | GTGTGTA | G | 6 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0005g0017 others(3): Show |
6 | HG02622.hp2 HG02976.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.14+5883_14+5888del others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112425004 | ||||||
| chr12:112425006 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+5881G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425006 | |||||||
| chr12:112425006 | GTGTA | G | 4 | a0001c0001t0001g0007 a0001c0001t0003g0002 a0001c0001t0004g0023 others(1): Show |
5 | HG02451.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+5886_14+5889del others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112425006 | ||||||
| chr12:112425008 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0009 |
2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.14+5883G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425008 | |||||||
| chr12:112425008 | GTA | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+5885_14+5886del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112425008 | ||||||
| chr12:112425010 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0009 |
2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.14+5885A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425010 | |||||||
| chr12:112425202 | T | C | 1 | a0001c0001t0003g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.14+6077T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425202 | |||||||
| chr12:112425318 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.14+6193G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425318 | |||||||
| chr12:112425347 | A | G | 2 | a0001c0002t0001g0178 a0001c0002t0001g0179 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.14+6222A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425347 | |||||||
| chr12:112425755 | G | A | 74 | a0001c0001t0001g0194 a0001c0001t0001g0217 a0001c0001t0002g0001 others(71): Show |
81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.14+6630G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425755 | |||||||
| chr12:112425793 | A | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.14+6668A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425793 | |||||||
| chr12:112425943 | C | T | 1 | a0001c0001t0004g0023 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.14+6818C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425943 | |||||||
| chr12:112426224 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+7099G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112426224 | |||||||
| chr12:112426298 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+7173G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112426298 | |||||||
| chr12:112426512 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0003g0147 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.14+7387C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112426512 | |||||||
| chr12:112426685 | T | A | 1 | a0001c0001t0002g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.14+7560T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112426685 | |||||||
| chr12:112427071 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.14+7946C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427071 | |||||||
| chr12:112427201 | G | A | 74 | a0001c0001t0001g0194 a0001c0001t0001g0217 a0001c0001t0002g0001 others(71): Show |
81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.14+8076G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427201 | |||||||
| chr12:112427294 | C | G | 1 | a0001c0001t0022g0283 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.14+8169C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427294 | |||||||
| chr12:112427494 | C | T | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14+8369C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427494 | |||||||
| chr12:112427545 | C | CA | 7 | a0001c0001t0001g0099 a0001c0001t0005g0015 a0001c0001t0005g0016 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+8432dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112427545 | ||||||
| chr12:112427759 | T | G | 1 | a0001c0001t0001g0053 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.14+8634T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427759 | |||||||
| chr12:112427774 | C | A | 74 | a0001c0001t0001g0194 a0001c0001t0001g0217 a0001c0001t0002g0001 others(71): Show |
81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.14+8649C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427774 | |||||||
| chr12:112427827 | T | C | 2 | a0001c0002t0001g0178 a0001c0002t0001g0179 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.14+8702T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427827 | |||||||
| chr12:112427888 | C | T | 16 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(13): Show |
16 | HG01993.hp2 HG02135.hp2 HG03710.hp2 others(13): Show |
intron_variant | MODIFIER | c.14+8763C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427888 | |||||||
| chr12:112427898 | G | A | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14+8773G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427898 | |||||||
| chr12:112427996 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(168): Show |
182 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(179): Show |
intron_variant | MODIFIER | c.14+8871T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427996 | |||||||
| chr12:112428029 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+8904G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112428029 | |||||||
| chr12:112428396 | CT | C | 177 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(174): Show |
186 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(183): Show |
intron_variant | MODIFIER | c.14+9292delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112428396 | ||||||
| chr12:112428526 | T | A | 3 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 |
3 | HG02622.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.14+9401T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112428526 | |||||||
| chr12:112428651 | GA | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0098 a0001c0001t0001g0174 others(4): Show |
7 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+9536delA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112428651 | ||||||
| chr12:112428652 | A | G | 5 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0093 others(2): Show |
5 | HG00621.hp1 NA18959.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+9527A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112428652 | |||||||
| chr12:112428872 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+9747C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112428872 | |||||||
| chr12:112429027 | G | A | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14+9902G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429027 | |||||||
| chr12:112429094 | A | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.14+9969A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429094 | |||||||
| chr12:112429125 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.14+10000A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429125 | |||||||
| chr12:112429481 | C | CT | 25 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0093 others(22): Show |
25 | HG00735.hp2 HG01071.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.14+10381dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112429481 | ||||||
| chr12:112429481 | C | CTT | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0018 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.14+10380_14+10381d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112429481 | ||||||
| chr12:112429481 | CT | C | 13 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): Show |
13 | HG01167.hp1 HG01943.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+10381delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112429481 | ||||||
| chr12:112429795 | T | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.14+10670T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429795 | |||||||
| chr12:112429865 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.14+10740G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429865 | |||||||
| chr12:112429951 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+10826G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429951 | |||||||
| chr12:112429972 | T | C | 1 | a0001c0001t0003g0080 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.14+10847T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429972 | |||||||
| chr12:112430163 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.14+11038G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112430163 | |||||||
| chr12:112430320 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.14+11195A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112430320 | |||||||
| chr12:112430330 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.14+11205C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112430330 | |||||||
| chr12:112430625 | A | G | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+11500A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112430625 | |||||||
| chr12:112430752 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.14+11627G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112430752 | |||||||
| chr12:112431022 | G | T | 3 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0036 |
3 | HG02109.hp2 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.14+11897G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431022 | |||||||
| chr12:112431075 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+11950G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431075 | |||||||
| chr12:112431265 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.14+12140G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431265 | |||||||
| chr12:112431288 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.14+12163C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431288 | |||||||
| chr12:112431572 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.14+12447C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431572 | |||||||
| chr12:112431761 | C | G | 1 | a0001c0001t0002g0227 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.14+12636C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431761 | |||||||
| chr12:112431892 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.14+12767C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431892 | |||||||
| chr12:112431926 | TAA | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG00621.hp2 NA18945.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.14+12805_14+12806d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112431926 | ||||||
| chr12:112431931 | AG | A | 5 | a0001c0001t0001g0100 a0001c0001t0002g0197 a0001c0001t0002g0198 others(2): Show |
5 | NA18947.hp1 NA18960.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+12812delG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112431931 | ||||||
| chr12:112431976 | A | G | 4 | a0001c0001t0001g0092 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+12851A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431976 | |||||||
| chr12:112432051 | A | G | 6 | a0001c0001t0001g0098 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
6 | HG02055.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+12926A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432051 | |||||||
| chr12:112432098 | T | C | 3 | a0001c0001t0003g0075 a0001c0001t0003g0129 a0001c0001t0003g0130 |
3 | NA18984.hp2 NA18986.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.14+12973T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432098 | |||||||
| chr12:112432204 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0113 a0001c0001t0001g0149 |
3 | NA18971.hp1 NA18980.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.14+13079A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432204 | |||||||
| chr12:112432537 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.14+13412C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432537 | |||||||
| chr12:112432593 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.14+13468C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432593 | |||||||
| chr12:112432668 | C | CA | 17 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0055 others(14): Show |
17 | HG01993.hp2 HG02135.hp2 HG02738.hp1 others(14): Show |
intron_variant | MODIFIER | c.14+13561dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112432668 | ||||||
| chr12:112432668 | CA | C | 7 | a0001c0001t0003g0075 a0001c0001t0003g0117 a0001c0001t0004g0023 others(4): Show |
7 | HG02897.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+13561delA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112432668 | ||||||
| chr12:112432813 | C | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
5 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-13463C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432813 | |||||||
| chr12:112432866 | T | C | 6 | a0001c0001t0001g0156 a0001c0001t0006g0145 a0001c0001t0006g0258 others(3): Show |
6 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-13410T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432866 | |||||||
| chr12:112432941 | A | G | 3 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 |
3 | HG02622.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.15-13335A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432941 | |||||||
| chr12:112433094 | C | T | 1 | a0001c0001t0002g0281 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.15-13182C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433094 | |||||||
| chr12:112433108 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.15-13168G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433108 | |||||||
| chr12:112433372 | C | G | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.15-12904C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433372 | |||||||
| chr12:112433538 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0091 |
4 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-12738A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433538 | |||||||
| chr12:112433568 | A | G | 16 | a0001c0001t0002g0142 a0001c0001t0003g0037 a0001c0001t0003g0097 others(13): Show |
16 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.15-12708A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433568 | |||||||
| chr12:112433780 | A | G | 1 | a0001c0001t0004g0047 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.15-12496A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433780 | |||||||
| chr12:112433831 | T | C | 1 | a0001c0001t0005g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15-12445T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433831 | |||||||
| chr12:112434236 | C | T | 1 | a0001c0001t0003g0130 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.15-12040C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112434236 | |||||||
| chr12:112434606 | C | CA | 8 | a0001c0001t0001g0083 a0001c0001t0001g0093 a0001c0001t0002g0196 others(5): Show |
8 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-11656dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112434606 | ||||||
| chr12:112434606 | CA | C | 6 | a0001c0001t0001g0190 a0001c0001t0003g0037 a0001c0001t0003g0170 others(3): Show |
6 | HG01256.hp2 HG02622.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.15-11656delA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112434606 | ||||||
| chr12:112434717 | C | T | 1 | a0001c0001t0005g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15-11559C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112434717 | |||||||
| chr12:112434955 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.15-11321T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112434955 | |||||||
| chr12:112435183 | C | T | 5 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 others(2): Show |
5 | NA18946.hp1 NA18950.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-11093C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112435183 | |||||||
| chr12:112435287 | T | C | 1 | a0001c0001t0005g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.15-10989T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112435287 | |||||||
| chr12:112435419 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.15-10857C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112435419 | |||||||
| chr12:112435422 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.15-10854T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112435422 | |||||||
| chr12:112435647 | G | GT | 97 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
99 | HG00621.hp1 HG00621.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.15-10610dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112435647 | ||||||
| chr12:112435647 | G | GTT | 15 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(12): Show |
16 | HG01167.hp1 HG01361.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.15-10611_15-10610d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112435647 | ||||||
| chr12:112435647 | GT | G | 13 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0052 others(10): Show |
13 | HG01978.hp2 HG02257.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.15-10610delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112435647 | ||||||
| chr12:112436214 | T | G | 28 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(25): Show |
28 | HG00140.hp2 HG00738.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.15-10062T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436214 | |||||||
| chr12:112436375 | A | G | 6 | a0001c0001t0001g0156 a0001c0001t0006g0145 a0001c0001t0006g0258 others(3): Show |
6 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-9901A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436375 | |||||||
| chr12:112436407 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.15-9869C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436407 | |||||||
| chr12:112436501 | T | A | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15-9775T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436501 | |||||||
| chr12:112436781 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.15-9495C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436781 | |||||||
| chr12:112436937 | G | A | 1 | a0001c0002t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.15-9339G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436937 | |||||||
| chr12:112437085 | T | G | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-9191T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437085 | |||||||
| chr12:112437089 | C | T | 2 | a0001c0001t0003g0184 a0001c0001t0013g0191 |
2 | NA19056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.15-9187C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437089 | |||||||
| chr12:112437313 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15-8963G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437313 | |||||||
| chr12:112437381 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0003g0147 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.15-8895G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437381 | |||||||
| chr12:112437779 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.15-8497T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437779 | |||||||
| chr12:112437888 | A | G | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15-8388A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437888 | |||||||
| chr12:112437959 | C | T | 2 | a0001c0002t0001g0033 a0001c0002t0001g0192 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.15-8317C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437959 | |||||||
| chr12:112438287 | G | A | 1 | a0001c0001t0005g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.15-7989G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112438287 | |||||||
| chr12:112438615 | G | C | 4 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0104 others(1): Show |
4 | HG02027.hp2 NA18949.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-7661G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112438615 | |||||||
| chr12:112438850 | C | A | 3 | a0001c0001t0001g0276 a0001c0001t0007g0122 a0001c0001t0007g0252 |
3 | HG03098.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.15-7426C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112438850 | |||||||
| chr12:112438932 | G | GT | 67 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(64): Show |
69 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.15-7339dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112438932 | ||||||
| chr12:112438950 | T | C | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.15-7326T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112438950 | |||||||
| chr12:112439215 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-7061C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439215 | |||||||
| chr12:112439243 | C | A | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-7033C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439243 | |||||||
| chr12:112439280 | T | A | 1 | a0001c0002t0001g0178 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15-6996T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439280 | |||||||
| chr12:112439500 | G | A | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-6776G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439500 | |||||||
| chr12:112439784 | T | A | 7 | a0001c0001t0001g0026 a0001c0001t0002g0208 a0001c0001t0002g0210 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-6492T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439784 | |||||||
| chr12:112439785 | A | T | 8 | a0001c0001t0001g0156 a0001c0001t0003g0137 a0001c0001t0006g0145 others(5): Show |
8 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-6491A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439785 | |||||||
| chr12:112439790 | A | C | 6 | a0001c0001t0001g0136 a0001c0001t0001g0259 a0001c0001t0001g0262 others(3): Show |
6 | HG01258.hp1 HG01496.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-6486A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439790 | |||||||
| chr12:112439792 | A | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-6484A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439792 | |||||||
| chr12:112439795 | AC | A | 6 | a0001c0001t0001g0100 a0001c0001t0001g0112 a0001c0001t0002g0233 others(3): Show |
6 | HG03516.hp1 NA18960.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.15-6480delC | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439795 | |||||||
| chr12:112439796 | C | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(220): Show |
234 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(231): Show |
intron_variant | MODIFIER | c.15-6480C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439796 | |||||||
| chr12:112439797 | A | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-6479A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439797 | |||||||
| chr12:112440464 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.15-5812C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440464 | |||||||
| chr12:112440563 | C | CT | 68 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(65): Show |
68 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.15-5685dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112440563 | ||||||
| chr12:112440563 | C | CTT | 7 | a0001c0001t0001g0082 a0001c0001t0001g0287 a0001c0001t0001g0288 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.15-5686_15-5685dup others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112440563 | ||||||
| chr12:112440563 | CT | C | 10 | a0001c0001t0002g0040 a0001c0001t0002g0266 a0001c0001t0002g0267 others(7): Show |
10 | HG01071.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.15-5685delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112440563 | ||||||
| chr12:112440622 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-5654G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440622 | |||||||
| chr12:112440626 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.15-5650C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440626 | |||||||
| chr12:112440698 | C | G | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15-5578C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440698 | |||||||
| chr12:112440920 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15-5356T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440920 | |||||||
| chr12:112440965 | C | CT | 8 | a0001c0001t0002g0205 a0001c0001t0002g0222 a0001c0001t0002g0223 others(5): Show |
8 | HG00735.hp1 HG02622.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-5295dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112440965 | ||||||
| chr12:112440965 | CT | C | 12 | a0001c0001t0001g0049 a0001c0001t0001g0288 a0001c0001t0002g0201 others(9): Show |
12 | HG01168.hp1 HG01256.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.15-5295delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112440965 | ||||||
| chr12:112440969 | T | TC | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-5307_15-5306ins others(1): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440969 | |||||||
| chr12:112441007 | A | G | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-5269A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441007 | |||||||
| chr12:112441019 | A | G | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-5257A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441019 | |||||||
| chr12:112441042 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.15-5234G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441042 | |||||||
| chr12:112441113 | C | G | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-5163C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441113 | |||||||
| chr12:112441143 | T | C | 1 | a0001c0001t0004g0023 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.15-5133T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441143 | |||||||
| chr12:112441550 | A | C | 1 | a0001c0001t0002g0280 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.15-4726A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441550 | |||||||
| chr12:112442068 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0013 |
2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.15-4208C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442068 | |||||||
| chr12:112442151 | A | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(16): Show |
21 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.15-4125A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442151 | |||||||
| chr12:112442315 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.15-3961T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442315 | |||||||
| chr12:112442704 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-3572C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442704 | |||||||
| chr12:112442742 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.15-3534G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442742 | |||||||
| chr12:112442775 | T | C | 11 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(8): Show |
11 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-3501T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442775 | |||||||
| chr12:112442830 | T | TTA | 11 | a0001c0001t0001g0030 a0001c0001t0001g0052 a0001c0001t0003g0126 others(8): Show |
11 | HG00544.hp1 HG01978.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.15-3399_15-3398dup others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | T | TTATA | 12 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0042 others(9): Show |
12 | HG00140.hp2 HG01167.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.15-3401_15-3398dup others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | T | TTATATA | 5 | a0001c0001t0001g0121 a0001c0001t0003g0133 a0001c0001t0014g0151 others(2): Show |
5 | HG02683.hp2 HG03017.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-3403_15-3398dup others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0003g0144 others(1): Show |
4 | HG00738.hp1 HG01361.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-3405_15-3398dup others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | T | TTATATAT others(3): Show |
1 | a0001c0001t0003g0134 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.15-3407_15-3398dup others(10): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | T | TTATATAT others(5): Show |
3 | a0001c0001t0003g0037 a0001c0001t0003g0120 a0001c0001t0003g0193 |
3 | HG01256.hp2 HG01433.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.15-3409_15-3398dup others(12): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | T | TTATATAT others(13): Show |
1 | a0001c0001t0003g0168 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.15-3417_15-3398dup others(20): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTA | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0057 others(14): Show |
17 | HG00140.hp1 HG01928.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.15-3399_15-3398del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATA | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0059 others(14): Show |
17 | HG00099.hp2 HG00741.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.15-3401_15-3398del others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATA | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0058 others(7): Show |
10 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.15-3403_15-3398del others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATAT others(1): Show |
T | 18 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0029 others(15): Show |
18 | HG01099.hp2 HG01109.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.15-3405_15-3398del others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATAT others(3): Show |
T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0276 a0001c0001t0004g0285 others(2): Show |
5 | HG02559.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.15-3407_15-3398del others(10): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATAT others(5): Show |
T | 1 | a0001c0001t0018g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.15-3409_15-3398del others(12): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATAT others(9): Show |
T | 1 | a0001c0001t0003g0163 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.15-3413_15-3398del others(16): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATAT others(11): Show |
T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0099 a0001c0001t0001g0103 others(3): Show |
6 | HG02738.hp1 HG02922.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-3415_15-3398del others(18): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATAT others(13): Show |
T | 69 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(66): Show |
71 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.15-3417_15-3398del others(20): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATAT others(19): Show |
T | 2 | a0001c0001t0002g0237 a0001c0001t0003g0137 |
2 | HG02165.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.15-3423_15-3398del others(26): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATAT others(21): Show |
T | 72 | a0001c0001t0001g0194 a0001c0001t0001g0217 a0001c0001t0002g0001 others(69): Show |
79 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.15-3425_15-3398del others(28): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATAT others(23): Show |
T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0287 a0001c0001t0001g0288 |
3 | HG01168.hp1 HG01169.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.15-3427_15-3398del others(30): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATAT others(25): Show |
T | 1 | a0001c0001t0003g0260 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.15-3429_15-3398del others(32): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442830 | TTATATAT others(29): Show |
T | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15-3433_15-3398del others(36): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | ||||||
| chr12:112442859 | T | TATATATA others(18): Show |
1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.15-3408_15-3407ins others(25): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442859 | ||||||
| chr12:112442859 | T | TATATATA others(22): Show |
1 | a0001c0001t0001g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.15-3402_15-3401ins others(29): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442859 | ||||||
| chr12:112442877 | T | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(71): Show |
76 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.15-3399T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442877 | |||||||
| chr12:112442877 | T | TATAA | 2 | a0001c0001t0003g0002 a0001c0001t0005g0018 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.15-3398_15-3397ins others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442877 | ||||||
| chr12:112442902 | A | ATGTATGT others(2): Show |
166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(163): Show |
177 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(174): Show |
intron_variant | MODIFIER | c.15-3373_15-3365dup others(9): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442902 | ||||||
| chr12:112443026 | A | G | 3 | a0001c0001t0006g0145 a0001c0001t0006g0258 a0001c0001t0006g0263 |
3 | HG01361.hp2 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.15-3250A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443026 | |||||||
| chr12:112443505 | T | C | 74 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(71): Show |
76 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.15-2771T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443505 | |||||||
| chr12:112443538 | G | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(167): Show |
181 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(178): Show |
intron_variant | MODIFIER | c.15-2738G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443538 | |||||||
| chr12:112443653 | C | CT | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(23): Show |
29 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.15-2606dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112443653 | ||||||
| chr12:112443715 | T | C | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.15-2561T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443715 | |||||||
| chr12:112443733 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.15-2543A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443733 | |||||||
| chr12:112443845 | G | C | 1 | a0001c0001t0003g0150 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.15-2431G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443845 | |||||||
| chr12:112444069 | G | C | 11 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(8): Show |
11 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-2207G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444069 | |||||||
| chr12:112444071 | G | A | 1 | a0001c0001t0011g0157 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.15-2205G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444071 | |||||||
| chr12:112444107 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.15-2169C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444107 | |||||||
| chr12:112444119 | G | A | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-2157G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444119 | |||||||
| chr12:112444128 | A | G | 1 | a0001c0001t0003g0075 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.15-2148A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444128 | |||||||
| chr12:112444140 | T | C | 4 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0104 others(1): Show |
4 | HG02027.hp2 NA18949.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-2136T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444140 | |||||||
| chr12:112444192 | A | G | 69 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(66): Show |
71 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.15-2084A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444192 | |||||||
| chr12:112444490 | C | T | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-1786C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444490 | |||||||
| chr12:112444491 | G | A | 1 | a0001c0001t0002g0224 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.15-1785G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444491 | |||||||
| chr12:112444591 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.15-1685C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444591 | |||||||
| chr12:112444679 | A | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0004g0032 |
3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.15-1597A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444679 | |||||||
| chr12:112445041 | ATG | A | 6 | a0001c0001t0002g0208 a0001c0001t0002g0210 a0001c0001t0002g0234 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-1221_15-1220del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112445041 | ||||||
| chr12:112445055 | G | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(9): Show |
14 | HG02132.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.15-1221G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445055 | |||||||
| chr12:112445262 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0004g0032 |
3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.15-1014G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445262 | |||||||
| chr12:112445336 | T | G | 1 | a0001c0001t0002g0242 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.15-940T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445336 | |||||||
| chr12:112445339 | C | G | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15-937C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445339 | |||||||
| chr12:112445636 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.15-640A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445636 | |||||||
| chr12:112445639 | C | CT | 7 | a0001c0001t0001g0013 a0001c0001t0001g0083 a0001c0001t0001g0089 others(4): Show |
7 | HG00621.hp1 HG01993.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-620dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112445639 | ||||||
| chr12:112445672 | G | A | 13 | a0001c0001t0003g0037 a0001c0001t0003g0097 a0001c0001t0003g0120 others(10): Show |
13 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.15-604G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445672 | |||||||
| chr12:112445719 | G | A | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-557G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445719 | |||||||
| chr12:112445871 | C | T | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.15-405C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445871 | |||||||
| chr12:112445978 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.15-298C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445978 | |||||||
| chr12:112446074 | A | G | 1 | a0001c0001t0003g0096 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.15-202A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112446074 | |||||||
| chr12:112446081 | C | A | 3 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 |
3 | HG02622.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.15-195C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112446081 | |||||||
| chr12:112446740 | AT | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0106 others(6): Show |
9 | HG01167.hp1 HG02027.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+357delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 112446740 | ||||||
| chr12:112447192 | A | G | 6 | a0001c0001t0002g0208 a0001c0001t0002g0210 a0001c0001t0002g0234 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+794A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112447192 | |||||||
| chr12:112447349 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0002g0241 |
2 | NA18973.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.137+951C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112447349 | |||||||
| chr12:112447463 | A | G | 6 | a0001c0001t0002g0208 a0001c0001t0002g0210 a0001c0001t0002g0234 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+1065A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112447463 | |||||||
| chr12:112447705 | G | A | 74 | a0001c0001t0001g0066 a0001c0001t0001g0194 a0001c0001t0001g0217 others(71): Show |
81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.137+1307G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112447705 | |||||||
| chr12:112447799 | C | CT | 16 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(13): Show |
16 | HG01952.hp2 HG02027.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.137+1420dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 112447799 | ||||||
| chr12:112447835 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137+1437C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112447835 | |||||||
| chr12:112448175 | C | G | 1 | a0002c0004t0003g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.137+1777C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112448175 | |||||||
| chr12:112449046 | C | T | 5 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0093 others(2): Show |
5 | HG00621.hp1 NA18959.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-1272C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449046 | |||||||
| chr12:112449204 | C | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(283): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.138-1114C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449204 | |||||||
| chr12:112449211 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138-1107G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449211 | |||||||
| chr12:112449240 | C | T | 4 | a0001c0001t0001g0276 a0001c0001t0007g0111 a0001c0001t0007g0122 others(1): Show |
4 | HG03098.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-1078C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449240 | |||||||
| chr12:112449333 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG00621.hp2 NA18945.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.138-985G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449333 | |||||||
| chr12:112449371 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0255 |
4 | HG01099.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-947G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449371 | |||||||
| chr12:112449497 | ACT | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-818_138-817del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 112449497 | ||||||
| chr12:112449756 | T | A | 1 | a0001c0001t0003g0170 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.138-562T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449756 | |||||||
| chr12:112449925 | C | T | 4 | a0001c0001t0001g0276 a0001c0001t0007g0111 a0001c0001t0007g0122 others(1): Show |
4 | HG03098.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-393C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449925 | |||||||
| chr12:112449928 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.138-390G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449928 | |||||||
| chr12:112449990 | G | A | 2 | a0001c0001t0003g0138 a0001c0001t0003g0171 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.138-328G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449990 | |||||||
| chr12:112450086 | C | CA | 7 | a0001c0001t0001g0277 a0001c0001t0005g0015 a0001c0001t0005g0016 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-216dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 112450086 | ||||||
| chr12:112450137 | G | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-181G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112450137 | |||||||
| chr12:112450238 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138-80G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112450238 | |||||||
| chr12:112450241 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.138-77G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112450241 | |||||||
| chr12:112450888 | C | A | 10 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0118 others(7): Show |
10 | HG00140.hp2 HG00738.hp1 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+376C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112450888 | |||||||
| chr12:112451242 | T | C | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.332+730T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451242 | |||||||
| chr12:112451320 | T | A | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.332+808T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451320 | |||||||
| chr12:112451511 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0046 |
2 | HG01943.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.332+999C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451511 | |||||||
| chr12:112451851 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.332+1339C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451851 | |||||||
| chr12:112451880 | T | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.333-1315T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451880 | |||||||
| chr12:112451936 | C | T | 1 | a0001c0001t0005g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.333-1259C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451936 | |||||||
| chr12:112452118 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0002g0195 a0001c0001t0002g0203 others(1): Show |
4 | HG02027.hp1 HG02135.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-1077C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112452118 | |||||||
| chr12:112452178 | A | G | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-1017A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112452178 | |||||||
| chr12:112452263 | G | A | 1 | a0001c0001t0013g0191 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.333-932G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112452263 | |||||||
| chr12:112452601 | C | T | 4 | a0001c0002t0001g0038 a0001c0002t0001g0185 a0001c0002t0001g0186 others(1): Show |
4 | HG02965.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-594C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112452601 | |||||||
| chr12:112452972 | A | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(165): Show |
179 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(176): Show |
intron_variant | MODIFIER | c.333-223A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112452972 | |||||||
| chr12:112453465 | A | G | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+78A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453465 | |||||||
| chr12:112453488 | T | TTTTA | 17 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(14): Show |
19 | HG01496.hp1 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.525+129_525+132dup others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 112453488 | ||||||
| chr12:112453532 | T | A | 1 | a0001c0001t0002g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.525+145T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453532 | |||||||
| chr12:112453646 | G | GT | 6 | a0001c0001t0001g0251 a0001c0001t0001g0276 a0001c0001t0002g0124 others(3): Show |
6 | HG03098.hp2 HG03516.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+275dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 112453646 | ||||||
| chr12:112453647 | T | G | 1 | a0001c0001t0002g0242 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.525+260T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453647 | |||||||
| chr12:112453657 | T | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0052 |
2 | HG01978.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.525+270T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453657 | |||||||
| chr12:112453658 | T | G | 3 | a0001c0001t0006g0145 a0001c0001t0006g0258 a0001c0001t0006g0263 |
3 | HG01361.hp2 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.525+271T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453658 | |||||||
| chr12:112453659 | T | G | 7 | a0001c0001t0001g0049 a0001c0001t0004g0021 a0001c0001t0004g0022 others(4): Show |
7 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+272T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453659 | |||||||
| chr12:112453723 | G | A | 1 | a0001c0001t0004g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.525+336G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453723 | |||||||
| chr12:112453764 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.525+377C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453764 | |||||||
| chr12:112453778 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0165 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.525+391T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453778 | |||||||
| chr12:112453925 | G | A | 1 | a0001c0001t0002g0206 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.525+538G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453925 | |||||||
| chr12:112454203 | T | C | 1 | a0001c0001t0007g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-361T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112454203 | |||||||
| chr12:112454424 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.526-140A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112454424 | |||||||
| chr12:112454528 | TAAC | T | 3 | a0001c0001t0005g0017 a0001c0001t0005g0019 a0001c0001t0005g0020 |
3 | HG03453.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.526-33_526-31delCA others(1): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 112454528 | ||||||
| chr12:112454818 | C | CT | 10 | a0001c0001t0001g0099 a0001c0001t0001g0277 a0001c0001t0002g0225 others(7): Show |
10 | HG02148.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.642+159dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 112454818 | ||||||
| chr12:112454818 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.642+138C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112454818 | |||||||
| chr12:112454818 | CT | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0069 others(14): Show |
17 | HG01099.hp1 HG02273.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.642+159delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 112454818 | ||||||
| chr12:112454922 | C | T | 1 | a0001c0001t0003g0167 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.642+242C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112454922 | |||||||
| chr12:112455154 | C | G | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.642+474C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112455154 | |||||||
| chr12:112455162 | A | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.642+482A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112455162 | |||||||
| chr12:112455232 | C | CT | 10 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0083 others(7): Show |
10 | HG00621.hp1 HG00621.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.642+573dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 112455232 | ||||||
| chr12:112455352 | C | T | 1 | a0001c0001t0004g0285 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.643-598C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112455352 | |||||||
| chr12:112455688 | C | G | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.643-262C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112455688 | |||||||
| chr12:112455792 | C | T | 1 | a0001c0001t0002g0281 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.643-158C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112455792 | |||||||
| chr12:112455871 | G | GT | 17 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0083 others(14): Show |
17 | HG00621.hp1 HG00621.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.643-62dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 112455871 | ||||||
| chr12:112455871 | GT | G | 11 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0001g0049 others(8): Show |
11 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-62delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 112455871 | ||||||
| chr12:112456458 | CT | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(156): Show |
170 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(167): Show |
intron_variant | MODIFIER | c.756+413delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112456458 | ||||||
| chr12:112456458 | CTT | C | 6 | a0001c0001t0001g0025 a0001c0001t0002g0219 a0001c0001t0004g0021 others(3): Show |
6 | HG01167.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.756+412_756+413del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112456458 | ||||||
| chr12:112456899 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.756+836G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112456899 | |||||||
| chr12:112457163 | C | G | 1 | a0001c0001t0002g0218 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.756+1100C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457163 | |||||||
| chr12:112457337 | G | A | 74 | a0001c0001t0001g0194 a0001c0001t0001g0217 a0001c0001t0002g0001 others(71): Show |
81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.756+1274G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457337 | |||||||
| chr12:112457407 | C | T | 1 | a0001c0001t0011g0157 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756+1344C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457407 | |||||||
| chr12:112457493 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.756+1430T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457493 | |||||||
| chr12:112457878 | A | G | 3 | a0001c0001t0002g0226 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02080.hp1 NA18961.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.756+1815A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457878 | |||||||
| chr12:112457908 | G | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0091 |
4 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+1845G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457908 | |||||||
| chr12:112459036 | A | AG | 275 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(272): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.756+2973_756+2974i others(3): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459036 | |||||||
| chr12:112459144 | GCAGT | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0287 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.756+3084_756+3087d others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459144 | ||||||
| chr12:112459326 | T | C | 3 | a0001c0001t0006g0145 a0001c0001t0006g0258 a0001c0001t0006g0263 |
3 | HG01361.hp2 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.756+3263T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459326 | |||||||
| chr12:112459365 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.756+3302A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459365 | |||||||
| chr12:112459433 | CT | C | 6 | a0001c0001t0001g0112 a0001c0001t0002g0198 a0001c0001t0002g0222 others(3): Show |
6 | HG02976.hp1 NA18951.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.756+3385delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459433 | ||||||
| chr12:112459435 | T | G | 1 | a0001c0001t0003g0132 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.756+3372T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459435 | |||||||
| chr12:112459793 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0003g0147 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.756+3730T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459793 | |||||||
| chr12:112459868 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.756+3805C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459868 | |||||||
| chr12:112459908 | T | TAC | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
41 | HG01258.hp1 HG01361.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.756+3878_756+3879d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459908 | ||||||
| chr12:112459908 | T | TACAC | 7 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(4): Show |
7 | HG00099.hp1 HG01099.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.756+3876_756+3879d others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459908 | ||||||
| chr12:112459908 | TAC | T | 15 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0058 others(12): Show |
15 | HG00621.hp2 HG02165.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.756+3878_756+3879d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459908 | ||||||
| chr12:112459908 | TACAC | T | 45 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0067 others(42): Show |
45 | HG00140.hp1 HG00621.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.756+3876_756+3879d others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459908 | ||||||
| chr12:112460087 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.756+4024A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460087 | |||||||
| chr12:112460175 | C | T | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.756+4112C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460175 | |||||||
| chr12:112460316 | C | A | 3 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0036 |
3 | HG02109.hp2 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.756+4253C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460316 | |||||||
| chr12:112460482 | T | G | 2 | a0001c0001t0003g0133 a0001c0001t0003g0134 |
2 | HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.756+4419T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460482 | |||||||
| chr12:112460570 | G | C | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.756+4507G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460570 | |||||||
| chr12:112460660 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG01943.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+4597G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460660 | |||||||
| chr12:112460710 | T | C | 1 | a0001c0001t0011g0157 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756+4647T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460710 | |||||||
| chr12:112460874 | T | G | 1 | a0001c0001t0002g0199 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.756+4811T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460874 | |||||||
| chr12:112461292 | G | A | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.756+5229G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112461292 | |||||||
| chr12:112461338 | CT | C | 7 | a0001c0001t0002g0243 a0001c0001t0005g0015 a0001c0001t0005g0016 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.756+5289delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112461338 | ||||||
| chr12:112461433 | C | T | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.756+5370C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112461433 | |||||||
| chr12:112461655 | A | G | 1 | a0001c0002t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.756+5592A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112461655 | |||||||
| chr12:112461676 | C | T | 2 | a0001c0002t0001g0178 a0001c0002t0001g0179 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.756+5613C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112461676 | |||||||
| chr12:112462528 | T | C | 2 | a0001c0001t0003g0143 a0001c0001t0016g0153 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.756+6465T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112462528 | |||||||
| chr12:112462906 | T | C | 3 | a0001c0001t0001g0049 a0001c0001t0004g0048 a0001c0001t0018g0050 |
3 | HG02976.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.756+6843T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112462906 | |||||||
| chr12:112462978 | C | G | 4 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0238 others(1): Show |
4 | HG00735.hp1 HG01081.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+6915C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112462978 | |||||||
| chr12:112463656 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.756+7593T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112463656 | |||||||
| chr12:112463787 | A | G | 1 | a0001c0001t0002g0199 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.756+7724A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112463787 | |||||||
| chr12:112463877 | G | C | 2 | a0001c0001t0005g0016 a0001c0001t0005g0018 |
2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.756+7814G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112463877 | |||||||
| chr12:112463911 | C | T | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.756+7848C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112463911 | |||||||
| chr12:112464236 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0165 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.756+8173C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112464236 | |||||||
| chr12:112464281 | G | A | 2 | a0001c0002t0001g0033 a0001c0002t0001g0192 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.756+8218G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112464281 | |||||||
| chr12:112464520 | C | T | 24 | a0001c0001t0001g0217 a0001c0001t0002g0001 a0001c0001t0002g0005 others(21): Show |
31 | HG00544.hp2 HG02071.hp1 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.757-8424C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112464520 | |||||||
| chr12:112465004 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0275 |
3 | HG01109.hp2 HG02145.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.757-7940C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465004 | |||||||
| chr12:112465129 | G | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0254 others(3): Show |
7 | HG01081.hp2 HG01099.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.757-7815G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465129 | |||||||
| chr12:112465169 | C | T | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-7775C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465169 | |||||||
| chr12:112465193 | A | G | 1 | a0001c0001t0018g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.757-7751A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465193 | |||||||
| chr12:112465238 | C | T | 1 | a0001c0001t0002g0224 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.757-7706C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465238 | |||||||
| chr12:112465420 | C | CA | 12 | a0001c0001t0001g0115 a0001c0001t0001g0276 a0001c0001t0002g0280 others(9): Show |
12 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.757-7508dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112465420 | ||||||
| chr12:112465473 | T | A | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.757-7471T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465473 | |||||||
| chr12:112465546 | C | T | 1 | a0001c0001t0005g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.757-7398C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465546 | |||||||
| chr12:112465595 | A | G | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.757-7349A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465595 | |||||||
| chr12:112465989 | G | A | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-6955G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465989 | |||||||
| chr12:112466010 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.757-6934C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466010 | |||||||
| chr12:112466068 | A | G | 1 | a0001c0001t0002g0216 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.757-6876A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466068 | |||||||
| chr12:112466346 | T | C | 1 | a0001c0001t0003g0193 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.757-6598T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466346 | |||||||
| chr12:112466427 | A | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(70): Show |
75 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.757-6517A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466427 | |||||||
| chr12:112466596 | C | T | 2 | a0001c0001t0003g0135 a0001c0001t0003g0168 |
2 | HG02080.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.757-6348C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466596 | |||||||
| chr12:112466605 | G | A | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-6339G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466605 | |||||||
| chr12:112466666 | A | G | 1 | a0001c0001t0002g0201 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.757-6278A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466666 | |||||||
| chr12:112466685 | G | T | 1 | a0001c0001t0002g0218 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.757-6259G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466685 | |||||||
| chr12:112466773 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.757-6171A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466773 | |||||||
| chr12:112466904 | C | G | 6 | a0001c0001t0001g0060 a0001c0001t0001g0089 a0001c0001t0001g0094 others(3): Show |
6 | HG02056.hp1 HG02071.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.757-6040C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466904 | |||||||
| chr12:112466909 | T | TGGTCCTT others(6): Show |
6 | a0001c0001t0001g0060 a0001c0001t0001g0089 a0001c0001t0001g0094 others(3): Show |
6 | HG02056.hp1 HG02071.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.757-6034_757-6022d others(15): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112466909 | ||||||
| chr12:112467118 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.757-5826A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467118 | |||||||
| chr12:112467151 | A | G | 5 | a0001c0001t0001g0136 a0001c0001t0001g0259 a0001c0001t0001g0262 others(2): Show |
5 | HG01071.hp1 HG01258.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.757-5793A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467151 | |||||||
| chr12:112467167 | C | A | 2 | a0001c0001t0001g0121 a0001c0001t0003g0147 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.757-5777C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467167 | |||||||
| chr12:112467467 | A | G | 2 | a0001c0001t0003g0143 a0001c0001t0016g0153 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.757-5477A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467467 | |||||||
| chr12:112467486 | G | A | 1 | a0001c0001t0002g0219 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.757-5458G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467486 | |||||||
| chr12:112467737 | C | T | 26 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(23): Show |
26 | HG00140.hp2 HG00738.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.757-5207C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467737 | |||||||
| chr12:112467962 | C | T | 3 | a0001c0001t0002g0226 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG02080.hp1 NA18961.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.757-4982C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467962 | |||||||
| chr12:112468045 | C | A | 5 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0112 others(2): Show |
5 | NA18942.hp1 NA18960.hp2 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.757-4899C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468045 | |||||||
| chr12:112468218 | G | A | 2 | a0001c0001t0005g0016 a0001c0001t0005g0018 |
2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.757-4726G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468218 | |||||||
| chr12:112468310 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.757-4634T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468310 | |||||||
| chr12:112468611 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(267): Show |
281 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(278): Show |
intron_variant | MODIFIER | c.757-4333A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468611 | |||||||
| chr12:112468648 | G | T | 1 | a0001c0001t0002g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.757-4296G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468648 | |||||||
| chr12:112468728 | C | A | 1 | a0001c0001t0002g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.757-4216C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468728 | |||||||
| chr12:112468835 | C | G | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.757-4109C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468835 | |||||||
| chr12:112468843 | G | A | 4 | a0001c0001t0001g0276 a0001c0001t0007g0111 a0001c0001t0007g0122 others(1): Show |
4 | HG03098.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-4101G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468843 | |||||||
| chr12:112469069 | C | CA | 18 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0206 others(15): Show |
25 | HG00544.hp2 HG02132.hp2 NA18941.hp1 others(22): Show |
intron_variant | MODIFIER | c.757-3866dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112469069 | ||||||
| chr12:112469178 | A | C | 1 | a0001c0001t0002g0289 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.757-3766A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112469178 | |||||||
| chr12:112469258 | G | C | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.757-3686G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112469258 | |||||||
| chr12:112469572 | T | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.757-3372T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112469572 | |||||||
| chr12:112469579 | A | G | 1 | a0001c0001t0002g0289 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.757-3365A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112469579 | |||||||
| chr12:112470147 | C | T | 1 | a0003c0003t0003g0127 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.757-2797C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112470147 | |||||||
| chr12:112470330 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.757-2614T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112470330 | |||||||
| chr12:112470899 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.757-2045C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112470899 | |||||||
| chr12:112471125 | G | A | 5 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0093 others(2): Show |
5 | HG00621.hp1 NA18959.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.757-1819G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471125 | |||||||
| chr12:112471451 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.757-1493A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471451 | |||||||
| chr12:112471452 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.757-1492G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471452 | |||||||
| chr12:112471454 | A | AAG | 65 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(62): Show |
67 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.757-1454_757-1453d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | ||||||
| chr12:112471454 | A | AAGAG | 37 | a0001c0001t0001g0027 a0001c0001t0001g0049 a0001c0001t0001g0108 others(34): Show |
43 | HG00544.hp2 HG01099.hp1 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.757-1456_757-1453d others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | ||||||
| chr12:112471454 | A | AAGAGAG | 6 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0001g0065 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.757-1458_757-1453d others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | ||||||
| chr12:112471454 | A | AAGAGAGA others(3): Show |
4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-1462_757-1453d others(12): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | ||||||
| chr12:112471454 | A | AAGAGAGA others(5): Show |
1 | a0001c0001t0003g0163 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.757-1464_757-1453d others(14): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | ||||||
| chr12:112471454 | A | AGAGAGAG others(4): Show |
1 | a0001c0001t0001g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.757-1490_757-1489i others(13): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471454 | |||||||
| chr12:112471454 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0013g0191 |
2 | HG02572.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.757-1490A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471454 | |||||||
| chr12:112471454 | AAG | A | 14 | a0001c0001t0001g0110 a0001c0001t0001g0254 a0001c0001t0002g0218 others(11): Show |
14 | HG01081.hp2 HG01934.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.757-1454_757-1453d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | ||||||
| chr12:112471454 | AAGAG | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
10 | HG01168.hp1 HG01169.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.757-1456_757-1453d others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | ||||||
| chr12:112471454 | AAGAGAG | A | 5 | a0001c0001t0002g0196 a0001c0001t0003g0133 a0001c0002t0001g0034 others(2): Show |
5 | HG02109.hp2 HG02683.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.757-1458_757-1453d others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | ||||||
| chr12:112471526 | A | G | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-1418A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471526 | |||||||
| chr12:112471536 | T | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(66): Show |
71 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.757-1408T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471536 | |||||||
| chr12:112471566 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.757-1378G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471566 | |||||||
| chr12:112471592 | T | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.757-1352T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471592 | |||||||
| chr12:112471643 | G | T | 1 | a0001c0001t0003g0163 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.757-1301G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471643 | |||||||
| chr12:112471713 | G | T | 3 | a0001c0001t0001g0276 a0001c0001t0007g0122 a0001c0001t0007g0252 |
3 | HG03098.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.757-1231G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471713 | |||||||
| chr12:112471918 | A | G | 3 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0036 |
3 | HG02109.hp2 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.757-1026A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471918 | |||||||
| chr12:112472306 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.757-638A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472306 | |||||||
| chr12:112472415 | G | A | 2 | a0001c0001t0006g0261 a0001c0001t0006g0264 |
2 | HG00099.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.757-529G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472415 | |||||||
| chr12:112472463 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.757-481G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472463 | |||||||
| chr12:112472565 | G | A | 5 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0093 others(2): Show |
5 | HG00621.hp1 NA18959.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.757-379G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472565 | |||||||
| chr12:112472576 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.757-368C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472576 | |||||||
| chr12:112472720 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.757-224C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472720 | |||||||
| chr12:112472875 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0091 |
4 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.757-69T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472875 | |||||||
| chr12:112473356 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.853+316T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473356 | |||||||
| chr12:112473419 | C | T | 1 | a0001c0001t0006g0263 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.853+379C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473419 | |||||||
| chr12:112473509 | G | C | 2 | a0001c0002t0001g0033 a0001c0002t0001g0192 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.853+469G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473509 | |||||||
| chr12:112473635 | T | TC | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.853+596dupC | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 112473635 | ||||||
| chr12:112473720 | G | A | 1 | a0001c0001t0002g0203 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.853+680G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473720 | |||||||
| chr12:112473821 | G | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0254 others(3): Show |
7 | HG01081.hp2 HG01099.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.853+781G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473821 | |||||||
| chr12:112473845 | C | CA | 20 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(17): Show |
22 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.853+817dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 112473845 | ||||||
| chr12:112473978 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.853+938G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473978 | |||||||
| chr12:112474287 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.853+1247C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112474287 | |||||||
| chr12:112474389 | T | A | 1 | a0001c0001t0012g0213 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.853+1349T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112474389 | |||||||
| chr12:112474393 | A | T | 1 | a0001c0001t0012g0213 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.853+1353A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112474393 | |||||||
| chr12:112474728 | A | G | 2 | a0001c0001t0007g0122 a0001c0001t0007g0252 |
2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.853+1688A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112474728 | |||||||
| chr12:112475063 | C | T | 2 | a0001c0001t0003g0143 a0001c0001t0016g0153 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.853+2023C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112475063 | |||||||
| chr12:112475246 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.853+2206C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112475246 | |||||||
| chr12:112475441 | T | TG | 11 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(8): Show |
13 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.854-2204dupG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 112475441 | ||||||
| chr12:112475528 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0003g0147 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.854-2123T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112475528 | |||||||
| chr12:112475988 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0013 |
2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.854-1663T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112475988 | |||||||
| chr12:112476030 | C | T | 1 | a0001c0001t0005g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.854-1621C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476030 | |||||||
| chr12:112476038 | C | A | 1 | a0001c0001t0012g0213 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.854-1613C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476038 | |||||||
| chr12:112476248 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.854-1403A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476248 | |||||||
| chr12:112476397 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0013 |
2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.854-1254G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476397 | |||||||
| chr12:112476419 | A | T | 1 | a0001c0001t0012g0213 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.854-1232A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476419 | |||||||
| chr12:112476527 | G | A | 74 | a0001c0001t0001g0194 a0001c0001t0001g0217 a0001c0001t0002g0001 others(71): Show |
81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.854-1124G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476527 | |||||||
| chr12:112476541 | G | T | 1 | a0001c0001t0012g0213 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.854-1110G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476541 | |||||||
| chr12:112476864 | T | A | 1 | a0001c0001t0001g0194 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.854-787T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476864 | |||||||
| chr12:112477047 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.854-604G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477047 | |||||||
| chr12:112477103 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.854-548G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477103 | |||||||
| chr12:112477120 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.854-531G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477120 | |||||||
| chr12:112477172 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.854-479A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477172 | |||||||
| chr12:112477362 | T | C | 1 | a0001c0001t0002g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.854-289T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477362 | |||||||
| chr12:112477428 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.854-223C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477428 | |||||||
| chr12:112477494 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.854-157C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477494 | |||||||
| chr12:112477619 | A | C | 7 | a0001c0001t0002g0040 a0001c0001t0002g0266 a0001c0001t0002g0267 others(4): Show |
7 | HG01256.hp1 HG01258.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.854-32A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477619 | |||||||
| chr12:112477621 | T | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0259 a0001c0001t0001g0262 |
3 | HG01496.hp1 HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.854-30T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477621 | |||||||
| chr12:112477630 | C | T | 6 | a0001c0001t0001g0156 a0001c0001t0006g0145 a0001c0001t0006g0258 others(3): Show |
6 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-21C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477630 | |||||||
| chr12:112478400 | C | G | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092+385C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478400 | |||||||
| chr12:112478444 | A | G | 2 | a0001c0001t0003g0096 a0001c0001t0003g0163 |
2 | NA19058.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1092+429A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478444 | |||||||
| chr12:112478532 | G | A | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1092+517G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478532 | |||||||
| chr12:112478716 | G | A | 1 | a0001c0001t0003g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1092+701G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478716 | |||||||
| chr12:112478879 | C | T | 6 | a0001c0001t0001g0156 a0001c0001t0006g0145 a0001c0001t0006g0258 others(3): Show |
6 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092+864C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478879 | |||||||
| chr12:112478981 | T | G | 21 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(18): Show |
23 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.1092+966T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478981 | |||||||
| chr12:112479009 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(18): Show |
23 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.1092+994T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112479009 | |||||||
| chr12:112479345 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1092+1330A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112479345 | |||||||
| chr12:112479559 | T | C | 2 | a0001c0002t0001g0178 a0001c0002t0001g0179 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1092+1544T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112479559 | |||||||
| chr12:112479863 | T | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0190 |
2 | HG04115.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1092+1848T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112479863 | |||||||
| chr12:112480084 | C | T | 1 | a0001c0001t0004g0047 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1093-1990C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480084 | |||||||
| chr12:112480107 | G | A | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1093-1967G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480107 | |||||||
| chr12:112480366 | C | CT | 76 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(73): Show |
78 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.1093-1690dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 112480366 | ||||||
| chr12:112480366 | CT | C | 19 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0156 others(16): Show |
19 | HG00099.hp2 HG01099.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1093-1690delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 112480366 | ||||||
| chr12:112480422 | A | G | 1 | a0001c0001t0002g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1093-1652A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480422 | |||||||
| chr12:112480448 | G | T | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
183 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(180): Show |
intron_variant | MODIFIER | c.1093-1626G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480448 | |||||||
| chr12:112480460 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1093-1614G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480460 | |||||||
| chr12:112480486 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
183 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(180): Show |
intron_variant | MODIFIER | c.1093-1588T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480486 | |||||||
| chr12:112480555 | A | AG | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(240): Show |
254 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(251): Show |
intron_variant | MODIFIER | c.1093-1517dupG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 112480555 | ||||||
| chr12:112480611 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1093-1463C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480611 | |||||||
| chr12:112480652 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0013 |
2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1093-1422G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480652 | |||||||
| chr12:112480687 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1093-1387C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480687 | |||||||
| chr12:112480847 | G | T | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1093-1227G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480847 | |||||||
| chr12:112480915 | A | C | 1 | a0001c0001t0002g0229 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1093-1159A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480915 | |||||||
| chr12:112481744 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1093-330G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112481744 | |||||||
| chr12:112482065 | C | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1093-9C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112482065 | |||||||
| chr12:112482463 | C | T | 9 | a0001c0001t0002g0040 a0001c0001t0002g0266 a0001c0001t0002g0267 others(6): Show |
9 | HG01071.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1224+258C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112482463 | |||||||
| chr12:112482602 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1224+397C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112482602 | |||||||
| chr12:112482797 | A | G | 1 | a0001c0001t0002g0273 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1224+592A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112482797 | |||||||
| chr12:112483042 | A | G | 1 | a0001c0001t0010g0169 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1224+837A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483042 | |||||||
| chr12:112483098 | T | C | 1 | a0001c0001t0002g0243 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1224+893T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483098 | |||||||
| chr12:112483687 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1224+1482C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483687 | |||||||
| chr12:112483831 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1224+1626C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483831 | |||||||
| chr12:112483857 | T | C | 1 | a0001c0001t0003g0163 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1224+1652T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483857 | |||||||
| chr12:112483893 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1224+1688G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483893 | |||||||
| chr12:112483931 | T | C | 1 | a0001c0001t0003g0132 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1224+1726T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483931 | |||||||
| chr12:112483933 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1224+1728C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483933 | |||||||
| chr12:112484096 | C | T | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1224+1891C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484096 | |||||||
| chr12:112484235 | A | G | 1 | a0001c0001t0003g0096 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1224+2030A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484235 | |||||||
| chr12:112484286 | G | A | 2 | a0001c0002t0001g0178 a0001c0002t0001g0179 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1224+2081G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484286 | |||||||
| chr12:112484533 | C | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(71): Show |
76 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.1225-1942C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484533 | |||||||
| chr12:112484725 | G | A | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(197): Show |
211 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(208): Show |
intron_variant | MODIFIER | c.1225-1750G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484725 | |||||||
| chr12:112484775 | A | C | 1 | a0001c0001t0002g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1225-1700A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484775 | |||||||
| chr12:112484923 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1225-1552G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484923 | |||||||
| chr12:112485032 | G | T | 1 | a0001c0001t0014g0151 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1225-1443G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485032 | |||||||
| chr12:112485177 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1225-1298C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485177 | |||||||
| chr12:112485334 | C | T | 1 | a0001c0001t0022g0283 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1225-1141C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485334 | |||||||
| chr12:112485557 | G | A | 28 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0042 others(25): Show |
28 | HG00099.hp2 HG01099.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1225-918G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485557 | |||||||
| chr12:112485588 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1225-887C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485588 | |||||||
| chr12:112485589 | G | A | 42 | a0001c0001t0001g0217 a0001c0001t0002g0001 a0001c0001t0002g0005 others(39): Show |
49 | HG00544.hp2 HG02027.hp1 HG02071.hp1 others(46): Show |
intron_variant | MODIFIER | c.1225-886G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485589 | |||||||
| chr12:112485887 | A | C | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225-588A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485887 | |||||||
| chr12:112485982 | GA | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(8): Show |
13 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1225-477delA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 112485982 | ||||||
| chr12:112486010 | T | TAATAAA | 204 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(201): Show |
215 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(212): Show |
intron_variant | MODIFIER | c.1225-464_1225-463i others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 112486010 | ||||||
| chr12:112486412 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1225-63G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112486412 | |||||||
| chr12:112486425 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1225-50A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112486425 | |||||||
| chr12:112486649 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0274 |
2 | NA18954.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1379+20C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112486649 | |||||||
| chr12:112486902 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1379+273G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112486902 | |||||||
| chr12:112486937 | C | T | 2 | a0001c0002t0001g0178 a0001c0002t0001g0179 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1379+308C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112486937 | |||||||
| chr12:112486999 | G | T | 1 | a0001c0001t0005g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1379+370G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112486999 | |||||||
| chr12:112487023 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0113 a0001c0001t0001g0149 |
3 | NA18971.hp1 NA18980.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1379+394T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112487023 | |||||||
| chr12:112487115 | TTCTCTC | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1379+500_1379+505d others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 112487115 | ||||||
| chr12:112487116 | TC | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0123 |
3 | HG02132.hp1 HG02523.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1379+488delC | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112487116 | |||||||
| chr12:112487135 | T | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0254 others(3): Show |
7 | HG01081.hp2 HG01099.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1379+506T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112487135 | |||||||
| chr12:112487718 | A | G | 2 | a0001c0001t0004g0048 a0001c0001t0018g0050 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1380-725A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112487718 | |||||||
| chr12:112488661 | C | T | 1 | a0001c0001t0003g0075 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1447+151C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 12/15 | chr12 | 112488661 | |||||||
| chr12:112488968 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1448-56C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 12/15 | chr12 | 112488968 | |||||||
| chr12:112489407 | C | T | 2 | a0001c0001t0003g0137 a0001c0001t0010g0169 |
2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1599+232C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489407 | |||||||
| chr12:112489468 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1599+293C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489468 | |||||||
| chr12:112489549 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1599+374C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489549 | |||||||
| chr12:112489560 | C | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(4): Show |
9 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1599+385C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489560 | |||||||
| chr12:112489605 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1599+430G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489605 | |||||||
| chr12:112489668 | C | T | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+493C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489668 | |||||||
| chr12:112490241 | C | T | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+1066C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490241 | |||||||
| chr12:112490297 | G | C | 4 | a0001c0002t0001g0038 a0001c0002t0001g0185 a0001c0002t0001g0186 others(1): Show |
4 | HG02965.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+1122G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490297 | |||||||
| chr12:112490304 | C | CT | 82 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0082 others(79): Show |
89 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.1599+1148dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112490304 | ||||||
| chr12:112490393 | A | G | 4 | a0001c0001t0003g0161 a0001c0001t0003g0167 a0001c0001t0003g0173 others(1): Show |
4 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+1218A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490393 | |||||||
| chr12:112490503 | C | T | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1599+1328C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490503 | |||||||
| chr12:112490594 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1599+1419C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490594 | |||||||
| chr12:112490601 | C | T | 2 | a0001c0001t0004g0048 a0001c0001t0018g0050 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1599+1426C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490601 | |||||||
| chr12:112490603 | C | T | 2 | a0001c0001t0004g0285 a0001c0001t0022g0283 |
2 | HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1599+1428C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490603 | |||||||
| chr12:112490647 | G | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): Show |
213 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(210): Show |
intron_variant | MODIFIER | c.1599+1472G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490647 | |||||||
| chr12:112490792 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1599+1617A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490792 | |||||||
| chr12:112491272 | G | GA | 74 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0174 others(71): Show |
81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.1599+2112dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112491272 | ||||||
| chr12:112491903 | C | T | 3 | a0001c0001t0003g0075 a0001c0001t0003g0129 a0001c0001t0003g0130 |
3 | NA18984.hp2 NA18986.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1599+2728C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112491903 | |||||||
| chr12:112492068 | A | G | 1 | a0001c0001t0002g0267 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1599+2893A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492068 | |||||||
| chr12:112492476 | G | T | 18 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0001t0001g0098 others(15): Show |
18 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1599+3301G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492476 | |||||||
| chr12:112492539 | A | T | 1 | a0001c0001t0005g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1599+3364A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492539 | |||||||
| chr12:112492604 | A | G | 1 | a0001c0002t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1599+3429A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492604 | |||||||
| chr12:112492610 | C | T | 1 | a0001c0001t0005g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1599+3435C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492610 | |||||||
| chr12:112492611 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1599+3436G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492611 | |||||||
| chr12:112492616 | G | C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
5 | HG01943.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1599+3441G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492616 | |||||||
| chr12:112492671 | T | C | 17 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0124 others(14): Show |
24 | HG00544.hp2 HG02132.hp2 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.1599+3496T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492671 | |||||||
| chr12:112492713 | C | T | 10 | a0001c0001t0002g0208 a0001c0001t0002g0210 a0001c0001t0002g0234 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1599+3538C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492713 | |||||||
| chr12:112492724 | A | G | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+3549A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492724 | |||||||
| chr12:112492737 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
24 | HG01081.hp2 HG01099.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.1599+3562T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492737 | |||||||
| chr12:112492752 | T | C | 1 | a0001c0001t0004g0285 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1599+3577T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492752 | |||||||
| chr12:112492812 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1599+3637C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492812 | |||||||
| chr12:112492856 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0274 |
2 | NA18954.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1599+3681T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492856 | |||||||
| chr12:112492975 | A | G | 2 | a0001c0001t0002g0201 a0001c0001t0019g0202 |
2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1599+3800A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492975 | |||||||
| chr12:112492986 | T | C | 4 | a0001c0002t0001g0038 a0001c0002t0001g0185 a0001c0002t0001g0186 others(1): Show |
4 | HG02965.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+3811T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492986 | |||||||
| chr12:112493074 | T | C | 1 | a0001c0001t0002g0286 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1599+3899T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112493074 | |||||||
| chr12:112493220 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1599+4045G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112493220 | |||||||
| chr12:112493383 | AT | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(12): Show |
17 | HG01256.hp1 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1599+4227delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112493383 | ||||||
| chr12:112493479 | G | A | 1 | a0001c0001t0003g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1599+4304G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112493479 | |||||||
| chr12:112493559 | T | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0001t0001g0098 others(4): Show |
7 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+4384T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112493559 | |||||||
| chr12:112493871 | T | A | 1 | a0001c0001t0002g0199 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1599+4696T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112493871 | |||||||
| chr12:112494030 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1599+4855A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112494030 | |||||||
| chr12:112494444 | A | G | 1 | a0001c0001t0002g0240 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1599+5269A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112494444 | |||||||
| chr12:112494476 | GTTA | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1599+5304_1599+530 others(7): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112494476 | ||||||
| chr12:112494867 | C | T | 2 | a0001c0001t0008g0228 a0001c0001t0020g0232 |
2 | NA19057.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1599+5692C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112494867 | |||||||
| chr12:112495023 | T | G | 16 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(13): Show |
16 | HG01993.hp2 HG02135.hp2 HG03710.hp2 others(13): Show |
intron_variant | MODIFIER | c.1599+5848T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495023 | |||||||
| chr12:112495029 | A | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG02055.hp1 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1599+5854A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495029 | |||||||
| chr12:112495242 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG02055.hp1 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1599+6067A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495242 | |||||||
| chr12:112495573 | A | G | 1 | a0001c0001t0003g0260 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1599+6398A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495573 | |||||||
| chr12:112495731 | G | A | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(165): Show |
179 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(176): Show |
intron_variant | MODIFIER | c.1600-6413G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495731 | |||||||
| chr12:112495898 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1600-6246A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495898 | |||||||
| chr12:112495988 | C | A | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-6156C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495988 | |||||||
| chr12:112496116 | A | G | 3 | a0001c0001t0007g0111 a0001c0001t0007g0122 a0001c0001t0007g0252 |
3 | HG03516.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1600-6028A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112496116 | |||||||
| chr12:112496526 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG00621.hp2 NA18945.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1600-5618T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112496526 | |||||||
| chr12:112496810 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1600-5334C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112496810 | |||||||
| chr12:112496905 | G | C | 1 | a0001c0001t0014g0151 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1600-5239G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112496905 | |||||||
| chr12:112497159 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0004g0032 |
3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1600-4985G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497159 | |||||||
| chr12:112497171 | C | CA | 13 | a0001c0001t0001g0063 a0001c0001t0001g0077 a0001c0001t0001g0078 others(10): Show |
13 | HG01361.hp2 HG02109.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1600-4952dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112497171 | ||||||
| chr12:112497171 | CA | C | 110 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(107): Show |
119 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1600-4952delA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112497171 | ||||||
| chr12:112497171 | CAA | C | 8 | a0001c0001t0002g0196 a0001c0001t0005g0015 a0001c0001t0005g0016 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1600-4953_1600-495 others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112497171 | ||||||
| chr12:112497260 | G | A | 6 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0017 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600-4884G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497260 | |||||||
| chr12:112497414 | T | A | 1 | a0001c0001t0002g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1600-4730T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497414 | |||||||
| chr12:112497540 | C | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(71): Show |
76 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.1600-4604C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497540 | |||||||
| chr12:112497568 | A | G | 1 | a0001c0001t0012g0213 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1600-4576A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497568 | |||||||
| chr12:112497696 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1600-4448G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497696 | |||||||
| chr12:112497749 | C | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(168): Show |
182 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(179): Show |
intron_variant | MODIFIER | c.1600-4395C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497749 | |||||||
| chr12:112497793 | G | A | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-4351G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497793 | |||||||
| chr12:112497793 | G | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600-4351G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497793 | |||||||
| chr12:112497962 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1600-4182G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497962 | |||||||
| chr12:112498152 | C | CA | 74 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0005 others(71): Show |
81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.1600-3982dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112498152 | ||||||
| chr12:112498161 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1600-3983A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112498161 | |||||||
| chr12:112498270 | C | T | 1 | a0001c0001t0014g0151 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1600-3874C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112498270 | |||||||
| chr12:112498326 | C | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(3): Show |
6 | NA18952.hp2 NA18973.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1600-3818C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112498326 | |||||||
| chr12:112498463 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1600-3681C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112498463 | |||||||
| chr12:112499114 | ATCT | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600-3026_1600-302 others(7): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112499114 | ||||||
| chr12:112499327 | T | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1600-2817T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112499327 | |||||||
| chr12:112499430 | C | T | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-2714C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112499430 | |||||||
| chr12:112499496 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1600-2648C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112499496 | |||||||
| chr12:112499623 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1600-2521G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112499623 | |||||||
| chr12:112499943 | T | TA | 8 | a0001c0001t0001g0082 a0001c0001t0002g0199 a0001c0001t0002g0247 others(5): Show |
8 | HG01891.hp2 HG02074.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1600-2183dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112499943 | ||||||
| chr12:112500182 | A | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600-1962A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500182 | |||||||
| chr12:112500338 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1600-1806T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500338 | |||||||
| chr12:112500402 | A | G | 2 | a0001c0002t0001g0033 a0001c0002t0001g0192 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1600-1742A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500402 | |||||||
| chr12:112500484 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1600-1660C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500484 | |||||||
| chr12:112500565 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-1579G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500565 | |||||||
| chr12:112500657 | T | G | 12 | a0001c0001t0001g0024 a0001c0001t0001g0156 a0001c0001t0001g0287 others(9): Show |
12 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600-1487T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500657 | |||||||
| chr12:112500920 | C | T | 1 | a0001c0001t0002g0243 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1600-1224C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500920 | |||||||
| chr12:112500951 | CCAGAGTG | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0025 others(67): Show |
72 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.1600-1189_1600-118 others(11): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112500951 | ||||||
| chr12:112500999 | G | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0098 a0001c0001t0001g0174 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600-1145G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500999 | |||||||
| chr12:112501286 | G | A | 1 | a0001c0001t0004g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1600-858G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501286 | |||||||
| chr12:112501557 | G | A | 2 | a0001c0001t0004g0048 a0001c0001t0018g0050 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1600-587G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501557 | |||||||
| chr12:112501573 | C | T | 2 | a0001c0001t0004g0048 a0001c0001t0018g0050 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1600-571C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501573 | |||||||
| chr12:112501727 | T | C | 2 | a0001c0001t0003g0133 a0001c0001t0003g0134 |
2 | HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1600-417T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501727 | |||||||
| chr12:112501759 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1600-385C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501759 | |||||||
| chr12:112501814 | A | T | 1 | a0001c0001t0003g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1600-330A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501814 | |||||||
| chr12:112501992 | C | G | 1 | a0001c0001t0009g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1600-152C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501992 | |||||||
| chr12:112502049 | C | T | 204 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(201): Show |
215 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(212): Show |
intron_variant | MODIFIER | c.1600-95C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112502049 | |||||||
| chr12:112502303 | A | G | 1 | a0001c0001t0014g0151 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1712+47A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112502303 | |||||||
| chr12:112502345 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1712+89G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112502345 | |||||||
| chr12:112502545 | G | C | 2 | a0001c0001t0004g0048 a0001c0001t0018g0050 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1712+289G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112502545 | |||||||
| chr12:112502655 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1712+399G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112502655 | |||||||
| chr12:112502891 | G | T | 3 | a0001c0001t0002g0210 a0001c0001t0002g0234 a0001c0001t0002g0236 |
3 | HG02109.hp1 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1712+635G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112502891 | |||||||
| chr12:112503027 | C | T | 1 | a0001c0001t0021g0154 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1712+771C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503027 | |||||||
| chr12:112503243 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1712+987G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503243 | |||||||
| chr12:112503322 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1712+1066A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503322 | |||||||
| chr12:112503351 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(4): Show |
9 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1712+1095C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503351 | |||||||
| chr12:112503368 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1712+1112T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503368 | |||||||
| chr12:112503464 | G | A | 1 | a0001c0001t0018g0050 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1712+1208G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503464 | |||||||
| chr12:112503550 | C | A | 73 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0039 others(70): Show |
80 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(77): Show |
intron_variant | MODIFIER | c.1713-1145C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503550 | |||||||
| chr12:112503572 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1713-1123C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503572 | |||||||
| chr12:112503627 | A | G | 1 | a0001c0002t0001g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1713-1068A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503627 | |||||||
| chr12:112503767 | G | A | 231 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(228): Show |
242 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(239): Show |
intron_variant | MODIFIER | c.1713-928G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503767 | |||||||
| chr12:112503946 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1713-749T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503946 | |||||||
| chr12:112504325 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1713-370A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112504325 | |||||||
| chr12:112504368 | G | T | 1 | a0001c0001t0002g0234 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1713-327G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112504368 | |||||||
| chr12:112504549 | G | A | 73 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0039 others(70): Show |
80 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(77): Show |
intron_variant | MODIFIER | c.1713-146G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112504549 | |||||||
| chr12:112504942 | T | C | 1 | a0001c0001t0003g0129 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.*32+146T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112504942 | |||||||
| chr12:112505063 | C | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0190 a0001c0001t0003g0080 |
3 | HG03654.hp1 HG04115.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.*32+267C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505063 | |||||||
| chr12:112505393 | A | G | 231 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(228): Show |
242 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(239): Show |
intron_variant | MODIFIER | c.*33-432A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505393 | |||||||
| chr12:112505464 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0098 a0001c0001t0001g0174 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.*33-361C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505464 | |||||||
| chr12:112505536 | T | C | 5 | a0001c0001t0006g0145 a0001c0001t0006g0258 a0001c0001t0006g0261 others(2): Show |
5 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.*33-289T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505536 | |||||||
| chr12:112505656 | C | CA | 40 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0042 others(37): Show |
40 | HG00735.hp2 HG00738.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.*33-144dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 112505656 | ||||||
| chr12:112505673 | A | C | 8 | a0001c0001t0001g0121 a0001c0001t0003g0147 a0001c0001t0005g0015 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.*33-152A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505673 | |||||||
| chr12:112505674 | A | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0039 others(68): Show |
78 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.*33-151A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505674 |