Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 921 |
| ensemblid | ENSG00000110448.11 |
| hgncid | 1685 |
| symbol | CD5 |
| name | CD5 molecule |
| refseq_nuc | NM_014207.4 |
| refseq_prot | NP_055022.2 |
| ensembl_nuc | ENST00000347785.8 |
| ensembl_prot | ENSP00000342681.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 61102489 |
| end | 61127852 |
| strand | + |
| ver | v1.2 |
| region | chr11:61102489-61127852 |
| region5000 | chr11:61097489-61132852 |
| regionname0 | CD5_chr11_61102489_61127852 |
| regionname5000 | CD5_chr11_61097489_61132852 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 495 | 105 | 22 | 27 | 32 | 8 | 15 | 24 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| a0002 | 0/0 | 495 | 67 | 36 | 24 | 1 | 4 | 2 | 0 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| a0003 | 0/0 | 495 | 40 | 21 | 5 | 7 | 3 | 4 | 5 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| a0004 | 1/0 | 495 | 10 | 0 | 3 | 0 | 3 | 3 | 0 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| a0005 | 0/0 | 495 | 7 | 2 | 4 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| a0006 | 0/0 | 495 | 7 | 3 | 1 | 0 | 0 | 3 | 0 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| a0007 | 0/0 | 495 | 3 | 2 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| a0008 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| a0009 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| a0010 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| a0011 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| a0012 | 0/0 | 495 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | MPMGS others(490): Show |
chr11 | 61097489 | 61132852 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1485 | 105 | 22 | 27 | 32 | 8 | 15 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0002c0003 | 0/0 | 1485 | 32 | 6 | 20 | 0 | 4 | 2 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0002c0004 | 0/0 | 1485 | 19 | 17 | 2 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0002c0006 | 0/0 | 1485 | 9 | 6 | 2 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0002c0009 | 0/0 | 1485 | 4 | 4 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0002c0011 | 0/0 | 1485 | 3 | 3 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0003c0002 | 0/0 | 1485 | 40 | 21 | 5 | 7 | 3 | 4 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0004c0005 | 1/0 | 1485 | 10 | 0 | 3 | 0 | 3 | 3 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0005c0008 | 0/0 | 1485 | 7 | 2 | 4 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0006c0007 | 0/0 | 1485 | 7 | 3 | 1 | 0 | 0 | 3 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0007c0010 | 0/0 | 1485 | 3 | 2 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0008c0015 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0009c0014 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0010c0012 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0011c0013 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 | ||
| a0012c0016 | 0/0 | 1485 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | ATGCC others(1480): Show |
chr11 | 61097489 | 61132852 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3135 | 103 | 22 | 26 | 31 | 8 | 15 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3130): Show |
chr11 | 61097489 | 61132852 |
| a0001c0001t0008 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3130): Show |
chr11 | 61097489 | 61132852 |
| a0001c0001t0010 | 0/0 | 3135 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3130): Show |
chr11 | 61097489 | 61132852 |
| a0002c0003t0002 | 0/0 | 3127 | 20 | 0 | 17 | 0 | 2 | 1 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3122): Show |
chr11 | 61097489 | 61132852 |
| a0002c0003t0003 | 0/0 | 3128 | 9 | 4 | 2 | 0 | 2 | 1 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3123): Show |
chr11 | 61097489 | 61132852 |
| a0002c0003t0007 | 0/0 | 3128 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3123): Show |
chr11 | 61097489 | 61132852 |
| a0002c0003t0011 | 0/0 | 3123 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3118): Show |
chr11 | 61097489 | 61132852 |
| a0002c0004t0001 | 0/0 | 3135 | 4 | 3 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3130): Show |
chr11 | 61097489 | 61132852 |
| a0002c0004t0004 | 0/0 | 3127 | 15 | 14 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3122): Show |
chr11 | 61097489 | 61132852 |
| a0002c0006t0003 | 0/0 | 3128 | 9 | 6 | 2 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3123): Show |
chr11 | 61097489 | 61132852 |
| a0002c0009t0004 | 0/0 | 3127 | 4 | 4 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3122): Show |
chr11 | 61097489 | 61132852 |
| a0002c0011t0004 | 0/0 | 3127 | 3 | 3 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3122): Show |
chr11 | 61097489 | 61132852 |
| a0003c0002t0001 | 0/0 | 3135 | 33 | 15 | 4 | 7 | 3 | 4 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3130): Show |
chr11 | 61097489 | 61132852 |
| a0003c0002t0005 | 0/0 | 3131 | 3 | 3 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3126): Show |
chr11 | 61097489 | 61132852 |
| a0003c0002t0006 | 0/0 | 3135 | 4 | 3 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3130): Show |
chr11 | 61097489 | 61132852 |
| a0004c0005t0002 | 1/0 | 3127 | 9 | 0 | 3 | 0 | 3 | 2 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3122): Show |
chr11 | 61097489 | 61132852 |
| a0004c0005t0009 | 0/0 | 3127 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3122): Show |
chr11 | 61097489 | 61132852 |
| a0005c0008t0002 | 0/0 | 3127 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3122): Show |
chr11 | 61097489 | 61132852 |
| a0005c0008t0003 | 0/0 | 3128 | 5 | 1 | 3 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3123): Show |
chr11 | 61097489 | 61132852 |
| a0005c0008t0012 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3123): Show |
chr11 | 61097489 | 61132852 |
| a0006c0007t0001 | 0/0 | 3135 | 7 | 3 | 1 | 0 | 0 | 3 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3130): Show |
chr11 | 61097489 | 61132852 |
| a0007c0010t0001 | 0/0 | 3135 | 3 | 2 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3130): Show |
chr11 | 61097489 | 61132852 |
| a0008c0015t0005 | 0/0 | 3131 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3126): Show |
chr11 | 61097489 | 61132852 |
| a0009c0014t0001 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3130): Show |
chr11 | 61097489 | 61132852 |
| a0010c0012t0003 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3123): Show |
chr11 | 61097489 | 61132852 |
| a0011c0013t0001 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3130): Show |
chr11 | 61097489 | 61132852 |
| a0012c0016t0001 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | GAGAT others(3130): Show |
chr11 | 61097489 | 61132852 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 10 | 4 | 0 | 1 | 2 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0002 | 0/0 | 19 | 0 | 5 | 8 | 0 | 6 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0007 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0016 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0060 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0001c0001t0010g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0002g0003 | 0/0 | 13 | 0 | 11 | 0 | 1 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0003g0008 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0007g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0003t0011g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0004t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0004t0004g0004 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0004t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0004t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0004t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0004t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0004t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0004t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0004t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0006t0003g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0006t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0006t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0006t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0006t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0006t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0009t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0009t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0009t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0011t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0002c0011t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0006 | 0/0 | 8 | 3 | 1 | 0 | 2 | 2 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0003c0002t0006g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0004c0005t0002g0005 | 0/0 | 8 | 0 | 3 | 0 | 3 | 2 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0004c0005t0002g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0004c0005t0009g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0005c0008t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0005c0008t0003g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0005c0008t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0005c0008t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0005c0008t0012g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0006c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0006c0007t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0006c0007t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0006c0007t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0006c0007t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0006c0007t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0006c0007t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0007c0010t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0007c0010t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0007c0010t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0008c0015t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0009c0014t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0010c0012t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0011c0013t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| a0012c0016t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0002 | t0001 | g0006 | EUR | GBR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00140 | hp2 | a0002 | c0003 | t0002 | g0003 | EUR | GBR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00280 | hp1 | a0004 | c0005 | t0002 | g0005 | EUR | FIN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | FIN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00323 | hp2 | a0002 | c0003 | t0002 | g0055 | EUR | FIN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00609 | hp1 | a0003 | c0002 | t0001 | g0108 | EAS | CHS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00639 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00639 | hp2 | a0003 | c0002 | t0001 | g0112 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00642 | hp1 | a0002 | c0006 | t0003 | g0045 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00642 | hp2 | a0002 | c0003 | t0002 | g0113 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00738 | hp1 | a0002 | c0003 | t0002 | g0054 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00738 | hp2 | a0004 | c0005 | t0002 | g0005 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00741 | hp1 | a0005 | c0008 | t0003 | g0008 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01069 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01071 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01074 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01109 | hp1 | a0002 | c0004 | t0001 | g0012 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01109 | hp2 | a0003 | c0002 | t0001 | g0122 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01167 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01169 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01243 | hp1 | a0003 | c0002 | t0006 | g0010 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01255 | hp2 | a0002 | c0003 | t0003 | g0008 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01256 | hp1 | a0002 | c0003 | t0002 | g0048 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01256 | hp2 | a0001 | c0001 | t0010 | g0114 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01257 | hp1 | a0005 | c0008 | t0003 | g0018 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01257 | hp2 | a0006 | c0007 | t0001 | g0103 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01258 | hp1 | a0005 | c0008 | t0003 | g0018 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01258 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01261 | hp1 | a0002 | c0006 | t0003 | g0014 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01261 | hp2 | a0002 | c0003 | t0011 | g0003 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01346 | hp1 | a0003 | c0002 | t0001 | g0031 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01346 | hp2 | a0004 | c0005 | t0002 | g0005 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01358 | hp1 | a0005 | c0008 | t0002 | g0018 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01358 | hp2 | a0004 | c0005 | t0002 | g0005 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01433 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01433 | hp2 | a0003 | c0002 | t0001 | g0006 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01496 | hp1 | a0002 | c0004 | t0004 | g0004 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01496 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01515 | hp1 | a0002 | c0003 | t0003 | g0097 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01516 | hp2 | a0004 | c0005 | t0002 | g0005 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01517 | hp2 | a0002 | c0003 | t0003 | g0008 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01884 | hp1 | a0007 | c0010 | t0001 | g0075 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01884 | hp2 | a0002 | c0003 | t0003 | g0065 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01891 | hp1 | a0003 | c0002 | t0006 | g0010 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01891 | hp2 | a0003 | c0002 | t0001 | g0006 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01943 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01943 | hp2 | a0002 | c0003 | t0003 | g0008 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01978 | hp2 | a0002 | c0003 | t0002 | g0047 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01993 | hp1 | a0002 | c0003 | t0002 | g0052 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02055 | hp2 | a0002 | c0004 | t0004 | g0035 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02071 | hp2 | a0007 | c0010 | t0001 | g0100 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02132 | hp2 | a0003 | c0002 | t0001 | g0013 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02145 | hp1 | a0008 | c0015 | t0005 | g0046 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02165 | hp2 | a0002 | c0006 | t0003 | g0040 | EAS | CDX | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02257 | hp1 | a0003 | c0002 | t0001 | g0093 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02257 | hp2 | a0003 | c0002 | t0001 | g0006 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02258 | hp1 | a0002 | c0004 | t0004 | g0004 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02258 | hp2 | a0003 | c0002 | t0005 | g0116 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02280 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02300 | hp2 | a0002 | c0003 | t0002 | g0053 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02451 | hp1 | a0002 | c0006 | t0003 | g0019 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02451 | hp2 | a0003 | c0002 | t0001 | g0011 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02572 | hp2 | a0002 | c0003 | t0007 | g0021 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02602 | hp1 | a0004 | c0005 | t0002 | g0005 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02615 | hp1 | a0002 | c0009 | t0004 | g0020 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02615 | hp2 | a0002 | c0011 | t0004 | g0030 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02622 | hp1 | a0002 | c0004 | t0004 | g0078 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02622 | hp2 | a0009 | c0014 | t0001 | g0025 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02630 | hp2 | a0002 | c0009 | t0004 | g0020 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02647 | hp1 | a0010 | c0012 | t0003 | g0099 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02647 | hp2 | a0002 | c0006 | t0003 | g0098 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02717 | hp2 | a0002 | c0003 | t0007 | g0021 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02723 | hp2 | a0002 | c0006 | t0003 | g0014 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02735 | hp1 | a0002 | c0003 | t0003 | g0096 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02735 | hp2 | a0002 | c0003 | t0002 | g0003 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02809 | hp1 | a0002 | c0009 | t0004 | g0043 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02809 | hp2 | a0003 | c0002 | t0006 | g0010 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02818 | hp1 | a0002 | c0004 | t0004 | g0121 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02818 | hp2 | a0002 | c0006 | t0003 | g0039 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02886 | hp2 | a0003 | c0002 | t0001 | g0011 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02897 | hp1 | a0002 | c0009 | t0004 | g0070 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02897 | hp2 | a0006 | c0007 | t0001 | g0107 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02922 | hp1 | a0003 | c0002 | t0001 | g0123 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02965 | hp1 | a0002 | c0011 | t0004 | g0030 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02965 | hp2 | a0002 | c0006 | t0003 | g0019 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02976 | hp1 | a0002 | c0004 | t0004 | g0004 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02976 | hp2 | a0002 | c0006 | t0003 | g0014 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03130 | hp1 | a0006 | c0007 | t0001 | g0105 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03139 | hp1 | a0003 | c0002 | t0001 | g0011 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03139 | hp2 | a0002 | c0004 | t0004 | g0033 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03209 | hp1 | a0003 | c0002 | t0001 | g0088 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03209 | hp2 | a0002 | c0003 | t0003 | g0064 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03225 | hp2 | a0003 | c0002 | t0001 | g0006 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03239 | hp1 | a0005 | c0008 | t0003 | g0008 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03239 | hp2 | a0004 | c0005 | t0009 | g0049 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03453 | hp2 | a0002 | c0011 | t0004 | g0089 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03486 | hp1 | a0002 | c0003 | t0003 | g0041 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03486 | hp2 | a0011 | c0013 | t0001 | g0125 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03492 | hp2 | a0004 | c0005 | t0002 | g0005 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03540 | hp1 | a0003 | c0002 | t0001 | g0124 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03540 | hp2 | a0005 | c0008 | t0012 | g0094 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03579 | hp1 | a0003 | c0002 | t0001 | g0011 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03579 | hp2 | a0003 | c0002 | t0005 | g0111 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03654 | hp1 | a0003 | c0002 | t0001 | g0118 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03669 | hp1 | a0003 | c0002 | t0001 | g0006 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03669 | hp2 | a0006 | c0007 | t0001 | g0104 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03688 | hp2 | a0006 | c0007 | t0001 | g0101 | SAS | STU | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03927 | hp2 | a0006 | c0007 | t0001 | g0102 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG04204 | hp1 | a0003 | c0002 | t0001 | g0006 | SAS | STU | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18522 | hp1 | a0003 | c0002 | t0001 | g0038 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18522 | hp2 | a0002 | c0004 | t0004 | g0004 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18941 | hp2 | a0003 | c0002 | t0001 | g0115 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18947 | hp1 | a0003 | c0002 | t0001 | g0109 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18949 | hp1 | a0003 | c0002 | t0001 | g0013 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18951 | hp2 | a0012 | c0016 | t0001 | g0066 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18980 | hp2 | a0003 | c0002 | t0001 | g0013 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18998 | hp1 | a0003 | c0002 | t0001 | g0013 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19030 | hp2 | a0003 | c0002 | t0001 | g0120 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19043 | hp2 | a0002 | c0004 | t0004 | g0004 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19240 | hp1 | a0007 | c0010 | t0001 | g0001 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA19240 | hp2 | a0002 | c0004 | t0004 | g0004 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ASW | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA20129 | hp2 | a0002 | c0004 | t0004 | g0034 | AFR | ASW | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA20752 | hp2 | a0003 | c0002 | t0001 | g0031 | EUR | TSI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA20805 | hp1 | a0004 | c0005 | t0002 | g0005 | EUR | TSI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA20805 | hp2 | a0003 | c0002 | t0001 | g0006 | EUR | TSI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA20905 | hp1 | a0003 | c0002 | t0001 | g0079 | SAS | GIH | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG01123 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02486 | hp1 | a0006 | c0007 | t0001 | g0106 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02486 | hp2 | a0003 | c0002 | t0005 | g0110 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02559 | hp1 | a0003 | c0002 | t0001 | g0126 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG02559 | hp2 | a0003 | c0002 | t0001 | g0117 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03471 | hp1 | a0002 | c0004 | t0004 | g0036 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG03471 | hp2 | a0002 | c0004 | t0001 | g0012 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG06807 | hp1 | a0002 | c0004 | t0004 | g0004 | AFR | USA | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| HG06807 | hp2 | a0002 | c0003 | t0003 | g0042 | AFR | USA | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA20300 | hp1 | a0003 | c0002 | t0006 | g0010 | AFR | USA | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA20300 | hp2 | a0002 | c0004 | t0004 | g0004 | AFR | USA | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA21309 | hp1 | a0002 | c0004 | t0004 | g0092 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| NA21309 | hp2 | a0005 | c0008 | t0003 | g0095 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0060 | REF | REF | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| homoSapiens | grch38p0 | a0004 | c0005 | t0002 | g0051 | REF | REF | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61102594 | T | G | 3 | a0006 a0007 a0010 |
11 | HG01257.hp2 HG01884.hp1 HG02071.hp2 others(8): Show |
missense_variant | MODERATE | c.34T>G | p.Leu12Val | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/11 | 106/3127 | 34/1488 | 12/495 | chr11 | 61102594 | |||
| chr11:61115074 | G | A | 1 | a0011 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.74G>A | p.Arg25Gln | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/11 | 146/3127 | 74/1488 | 25/495 | chr11 | 61115074 | |||
| chr11:61119378 | A | G | 1 | a0012 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.608A>G | p.Asn203Ser | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/11 | 680/3127 | 608/1488 | 203/495 | chr11 | 61119378 | |||
| chr11:61119441 | C | T | 6 | a0003 a0005 a0006 others(3): Show |
57 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(54): Show |
missense_variant | MODERATE | c.671C>T | p.Pro224Leu | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/11 | 743/3127 | 671/1488 | 224/495 | chr11 | 61119441 | |||
| chr11:61123886 | C | T | 1 | a0008 | 1 | HG02145.hp1 | missense_variant&splice_region_variant | MODERATE | c.1228C>T | p.Arg410Cys | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/11 | 1300/3127 | 1228/1488 | 410/495 | chr11 | 61123886 | |||
| chr11:61123901 | C | T | 1 | a0009 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1243C>T | p.Arg415Cys | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/11 | 1315/3127 | 1243/1488 | 415/495 | chr11 | 61123901 | |||
| chr11:61125133 | C | T | 1 | a0002 | 9 | HG00642.hp1 HG01261.hp1 HG02165.hp2 others(6): Show |
missense_variant | MODERATE | c.1381C>T | p.His461Tyr | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/11 | 1453/3127 | 1381/1488 | 461/495 | chr11 | 61125133 | |||
| chr11:61125134 | A | G | 11 | a0001 a0002 a0003 others(8): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
missense_variant | MODERATE | c.1382A>G | p.His461Arg | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/11 | 1454/3127 | 1382/1488 | 461/495 | chr11 | 61125134 | |||
| chr11:61125763 | C | T | 8 | a0001 a0003 a0006 others(5): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
missense_variant | MODERATE | c.1412C>T | p.Ala471Val | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/11 | 1484/3127 | 1412/1488 | 471/495 | chr11 | 61125763 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61121687 | G | A | 1 | a0002c0004 | 19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
synonymous_variant | LOW | c.882G>A | p.Gly294Gly | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/11 | 954/3127 | 882/1488 | 294/495 | chr11 | 61121687 | |||
| chr11:61121774 | C | T | 1 | a0002c0009 | 4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.969C>T | p.Ser323Ser | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/11 | 1041/3127 | 969/1488 | 323/495 | chr11 | 61121774 | |||
| chr11:61122992 | C | T | 1 | a0002c0011 | 3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.1185C>T | p.Val395Val | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/11 | 1257/3127 | 1185/1488 | 395/495 | chr11 | 61122992 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61126545 | C | T | 1 | a0002c0003t0007 | 2 | HG02572.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*260C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 706 | chr11 | 61126545 | ||||||
| chr11:61126592 | C | T | 1 | a0005c0008t0012 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 753 | chr11 | 61126592 | ||||||
| chr11:61126732 | C | T | 1 | a0003c0002t0006 | 4 | HG01243.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*447C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 893 | chr11 | 61126732 | ||||||
| chr11:61126921 | CCTCT | C | 3 | a0002c0003t0011 a0003c0002t0005 a0008c0015t0005 |
5 | HG01261.hp2 HG02145.hp1 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*637_*640delCTCT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1083 | chr11 | 61126921 | ||||||
| chr11:61126957 | C | A | 1 | a0001c0001t0008 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1118 | chr11 | 61126957 | ||||||
| chr11:61127020 | G | T | 22 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(19): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*735G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1181 | chr11 | 61127020 | ||||||
| chr11:61127081 | A | G | 1 | a0004c0005t0009 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*796A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1242 | chr11 | 61127081 | ||||||
| chr11:61127122 | C | CT | 6 | a0002c0003t0003 a0002c0003t0007 a0002c0006t0003 others(3): Show |
27 | HG00642.hp1 HG00741.hp1 HG01255.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*839dupT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1286 | INFO_REALIGN_3_PRIME | chr11 | 61127122 | |||||
| chr11:61127333 | CGGCT | C | 13 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(10): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*1049_*1052delGGCT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1495 | chr11 | 61127333 | ||||||
| chr11:61127339 | C | T | 13 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(10): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*1054C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1500 | chr11 | 61127339 | ||||||
| chr11:61127363 | A | AACACATC others(5): Show |
13 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(10): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*1082_*1093dupCATC others(8): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1540 | INFO_REALIGN_3_PRIME | chr11 | 61127363 | |||||
| chr11:61127778 | C | T | 1 | a0001c0001t0010 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1493C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1939 | chr11 | 61127778 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61102641 | C | T | 1 | a0001c0001t0001g0009 | 5 | HG00735.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+26C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61102641 | |||||||
| chr11:61102783 | C | T | 2 | a0003c0002t0001g0126 a0011c0013t0001g0125 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.55+168C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61102783 | |||||||
| chr11:61102951 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.55+336G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61102951 | |||||||
| chr11:61103036 | C | A | 1 | a0002c0004t0004g0033 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.55+421C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103036 | |||||||
| chr11:61103039 | C | T | 1 | a0003c0002t0001g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.55+424C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103039 | |||||||
| chr11:61103078 | G | A | 6 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(3): Show |
13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+463G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103078 | |||||||
| chr11:61103108 | T | C | 6 | a0001c0001t0001g0015 a0002c0006t0003g0014 a0002c0006t0003g0019 others(3): Show |
11 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.55+493T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103108 | |||||||
| chr11:61103136 | C | A | 2 | a0002c0003t0003g0041 a0002c0003t0003g0042 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.55+521C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103136 | |||||||
| chr11:61103203 | G | A | 3 | a0003c0002t0001g0011 a0003c0002t0001g0124 a0003c0002t0006g0010 |
9 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.55+588G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103203 | |||||||
| chr11:61103640 | CTG | C | 48 | a0001c0001t0001g0015 a0001c0001t0001g0119 a0001c0001t0010g0114 others(45): Show |
77 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.55+1029_55+1030del others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61103640 | ||||||
| chr11:61103642 | G | GTGTGTGG others(56): Show |
6 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(3): Show |
13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+1030_55+1031ins others(63): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61103642 | ||||||
| chr11:61103663 | C | CTCTGTGT others(62): Show |
1 | a0002c0004t0004g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55+1099_55+1167dup others(69): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61103663 | ||||||
| chr11:61103663 | CTCTGTGT others(5): Show |
C | 2 | a0002c0006t0003g0014 a0003c0002t0001g0038 |
4 | HG01261.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+1064_55+1075del others(12): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61103663 | ||||||
| chr11:61103805 | G | T | 2 | a0003c0002t0001g0122 a0003c0002t0001g0123 |
2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.55+1190G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103805 | |||||||
| chr11:61103841 | T | G | 1 | a0002c0004t0001g0012 | 4 | HG01109.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+1226T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103841 | |||||||
| chr11:61103909 | GT | G | 8 | a0002c0003t0003g0008 a0002c0003t0003g0096 a0002c0003t0003g0097 others(5): Show |
14 | HG00741.hp1 HG01109.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.55+1295delT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103909 | |||||||
| chr11:61103910 | T | G | 1 | a0005c0008t0002g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.55+1295T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103910 | |||||||
| chr11:61103911 | GT | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0002c0003t0007g0021 others(12): Show |
29 | HG01261.hp1 HG01496.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.55+1297delT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103911 | |||||||
| chr11:61103912 | T | G | 43 | a0001c0001t0001g0119 a0001c0001t0010g0114 a0002c0003t0002g0113 others(40): Show |
67 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.55+1297T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103912 | |||||||
| chr11:61103918 | G | A | 9 | a0006c0007t0001g0101 a0006c0007t0001g0102 a0006c0007t0001g0103 others(6): Show |
9 | HG01257.hp2 HG02071.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.55+1303G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103918 | |||||||
| chr11:61104072 | CTG | C | 46 | a0001c0001t0001g0037 a0001c0001t0001g0119 a0001c0001t0010g0114 others(43): Show |
77 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.55+1464_55+1465del others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61104072 | ||||||
| chr11:61104104 | ACTGTGTG others(16): Show |
A | 2 | a0002c0003t0003g0041 a0002c0003t0003g0042 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.55+1497_55+1519del others(23): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61104104 | ||||||
| chr11:61104218 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.55+1603G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104218 | |||||||
| chr11:61104236 | T | C | 1 | a0002c0006t0003g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.55+1621T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104236 | |||||||
| chr11:61104334 | A | G | 6 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(3): Show |
13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+1719A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104334 | |||||||
| chr11:61104430 | C | T | 1 | a0006c0007t0001g0107 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.55+1815C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104430 | |||||||
| chr11:61104601 | C | A | 41 | a0001c0001t0001g0119 a0001c0001t0010g0114 a0002c0003t0002g0113 others(38): Show |
65 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.55+1986C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104601 | |||||||
| chr11:61104636 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.55+2021C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104636 | |||||||
| chr11:61104750 | A | G | 1 | a0002c0006t0003g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.55+2135A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104750 | |||||||
| chr11:61104801 | C | T | 7 | a0001c0001t0001g0015 a0002c0006t0003g0014 a0002c0006t0003g0019 others(4): Show |
12 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.55+2186C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104801 | |||||||
| chr11:61104821 | C | T | 7 | a0001c0001t0001g0015 a0002c0006t0003g0014 a0002c0006t0003g0019 others(4): Show |
12 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.55+2206C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104821 | |||||||
| chr11:61105000 | A | G | 41 | a0001c0001t0001g0119 a0001c0001t0010g0114 a0002c0003t0002g0113 others(38): Show |
65 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.55+2385A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105000 | |||||||
| chr11:61105079 | TG | T | 6 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(3): Show |
13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+2468delG | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61105079 | ||||||
| chr11:61105108 | C | G | 9 | a0006c0007t0001g0101 a0006c0007t0001g0102 a0006c0007t0001g0103 others(6): Show |
9 | HG01257.hp2 HG02071.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.55+2493C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105108 | |||||||
| chr11:61105151 | C | T | 2 | a0002c0011t0004g0030 a0002c0011t0004g0089 |
3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.55+2536C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105151 | |||||||
| chr11:61105156 | G | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(114): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.55+2541G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105156 | |||||||
| chr11:61105200 | C | T | 2 | a0002c0003t0003g0041 a0002c0003t0003g0042 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.55+2585C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105200 | |||||||
| chr11:61105246 | G | C | 32 | a0001c0001t0001g0119 a0001c0001t0010g0114 a0002c0003t0002g0113 others(29): Show |
56 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.55+2631G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105246 | |||||||
| chr11:61105306 | C | T | 1 | a0002c0006t0003g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.55+2691C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105306 | |||||||
| chr11:61105372 | G | C | 5 | a0002c0003t0007g0021 a0002c0009t0004g0020 a0002c0009t0004g0043 others(2): Show |
7 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2757G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105372 | |||||||
| chr11:61105372 | G | T | 1 | a0003c0002t0001g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.55+2757G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105372 | |||||||
| chr11:61105415 | G | A | 7 | a0001c0001t0001g0015 a0002c0006t0003g0014 a0002c0006t0003g0019 others(4): Show |
12 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.55+2800G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105415 | |||||||
| chr11:61105631 | C | G | 1 | a0001c0001t0001g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.55+3016C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105631 | |||||||
| chr11:61105706 | A | G | 41 | a0001c0001t0001g0119 a0001c0001t0010g0114 a0002c0003t0002g0113 others(38): Show |
65 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.55+3091A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105706 | |||||||
| chr11:61106080 | G | A | 7 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(4): Show |
14 | HG00642.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.55+3465G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61106080 | |||||||
| chr11:61106081 | C | T | 1 | a0003c0002t0001g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.55+3466C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61106081 | |||||||
| chr11:61106124 | C | CA | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(47): Show |
108 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.55+3529dupA | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61106124 | ||||||
| chr11:61106124 | C | CAA | 18 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0056 others(15): Show |
25 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.55+3528_55+3529dup others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61106124 | ||||||
| chr11:61106124 | C | CAAA | 27 | a0001c0001t0010g0114 a0002c0003t0002g0113 a0002c0003t0003g0008 others(24): Show |
47 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.55+3527_55+3529dup others(3): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61106124 | ||||||
| chr11:61106124 | CAAAAA | C | 7 | a0002c0003t0007g0021 a0002c0009t0004g0020 a0003c0002t0001g0120 others(4): Show |
9 | HG01109.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.55+3525_55+3529del others(5): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61106124 | ||||||
| chr11:61106650 | C | T | 1 | a0006c0007t0001g0104 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.55+4035C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61106650 | |||||||
| chr11:61107243 | C | T | 1 | a0002c0006t0003g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.55+4628C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107243 | |||||||
| chr11:61107287 | G | A | 6 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(3): Show |
13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+4672G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107287 | |||||||
| chr11:61107557 | T | G | 55 | a0001c0001t0001g0037 a0001c0001t0001g0119 a0001c0001t0010g0114 others(52): Show |
89 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.55+4942T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107557 | |||||||
| chr11:61107729 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0083 others(1): Show |
5 | HG00280.hp2 HG01123.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+5114C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107729 | |||||||
| chr11:61107748 | C | T | 1 | a0002c0004t0001g0012 | 4 | HG01109.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+5133C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107748 | |||||||
| chr11:61107816 | G | A | 9 | a0006c0007t0001g0101 a0006c0007t0001g0102 a0006c0007t0001g0103 others(6): Show |
9 | HG01257.hp2 HG02071.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.55+5201G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107816 | |||||||
| chr11:61107847 | C | T | 11 | a0001c0001t0001g0119 a0001c0001t0010g0114 a0002c0003t0002g0113 others(8): Show |
25 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.55+5232C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107847 | |||||||
| chr11:61108134 | G | A | 2 | a0003c0002t0001g0126 a0011c0013t0001g0125 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.55+5519G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108134 | |||||||
| chr11:61108434 | T | C | 14 | a0002c0003t0003g0008 a0002c0003t0003g0096 a0002c0003t0003g0097 others(11): Show |
24 | HG00609.hp1 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.55+5819T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108434 | |||||||
| chr11:61108520 | C | T | 3 | a0002c0003t0007g0021 a0002c0009t0004g0020 a0002c0009t0004g0043 |
5 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+5905C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108520 | |||||||
| chr11:61108690 | G | A | 2 | a0003c0002t0001g0126 a0011c0013t0001g0125 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.55+6075G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108690 | |||||||
| chr11:61108700 | G | C | 14 | a0001c0001t0001g0119 a0001c0001t0010g0114 a0002c0003t0002g0113 others(11): Show |
28 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.55+6085G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108700 | |||||||
| chr11:61108739 | T | G | 1 | a0003c0002t0001g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55+6124T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108739 | |||||||
| chr11:61108744 | G | C | 8 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(5): Show |
15 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.55+6129G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108744 | |||||||
| chr11:61108829 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(48): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.55+6214G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108829 | |||||||
| chr11:61108927 | C | T | 1 | a0006c0007t0001g0107 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.56-6129C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108927 | |||||||
| chr11:61109060 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(106): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.56-5996A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109060 | |||||||
| chr11:61109089 | C | G | 7 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(4): Show |
14 | HG00642.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.56-5967C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109089 | |||||||
| chr11:61109118 | C | T | 1 | a0002c0003t0002g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.56-5938C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109118 | |||||||
| chr11:61109255 | G | C | 7 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(4): Show |
14 | HG00642.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.56-5801G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109255 | |||||||
| chr11:61109343 | C | T | 1 | a0003c0002t0001g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.56-5713C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109343 | |||||||
| chr11:61109378 | G | A | 2 | a0003c0002t0001g0126 a0011c0013t0001g0125 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.56-5678G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109378 | |||||||
| chr11:61109518 | CT | C | 43 | a0001c0001t0001g0119 a0001c0001t0010g0114 a0002c0003t0002g0048 others(40): Show |
67 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.56-5527delT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61109518 | ||||||
| chr11:61109614 | C | A | 3 | a0002c0003t0007g0021 a0002c0009t0004g0020 a0002c0009t0004g0043 |
5 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-5442C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109614 | |||||||
| chr11:61109653 | G | A | 1 | a0002c0004t0004g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.56-5403G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109653 | |||||||
| chr11:61109739 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(114): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.56-5317A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109739 | |||||||
| chr11:61109935 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.56-5121G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109935 | |||||||
| chr11:61109964 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.56-5092G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109964 | |||||||
| chr11:61110112 | G | A | 7 | a0002c0003t0003g0041 a0002c0003t0003g0042 a0002c0003t0007g0021 others(4): Show |
9 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-4944G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110112 | |||||||
| chr11:61110152 | G | T | 5 | a0002c0003t0003g0041 a0002c0003t0003g0042 a0002c0003t0007g0021 others(2): Show |
7 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-4904G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110152 | |||||||
| chr11:61110300 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.56-4756T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110300 | |||||||
| chr11:61110313 | C | T | 4 | a0003c0002t0001g0011 a0003c0002t0001g0120 a0003c0002t0001g0124 others(1): Show |
10 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-4743C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110313 | |||||||
| chr11:61110354 | T | C | 1 | a0002c0004t0004g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.56-4702T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110354 | |||||||
| chr11:61110886 | T | G | 2 | a0002c0003t0003g0041 a0002c0003t0003g0042 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.56-4170T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110886 | |||||||
| chr11:61110898 | T | G | 5 | a0003c0002t0001g0088 a0003c0002t0005g0110 a0003c0002t0005g0111 others(2): Show |
5 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-4158T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110898 | |||||||
| chr11:61110941 | G | A | 1 | a0002c0004t0004g0121 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.56-4115G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110941 | |||||||
| chr11:61111139 | C | T | 1 | a0002c0003t0002g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.56-3917C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111139 | |||||||
| chr11:61111190 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(48): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.56-3866C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111190 | |||||||
| chr11:61111393 | G | A | 1 | a0010c0012t0003g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.56-3663G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111393 | |||||||
| chr11:61111423 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0082 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.56-3633A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111423 | |||||||
| chr11:61111443 | C | T | 11 | a0002c0003t0003g0064 a0002c0003t0003g0065 a0006c0007t0001g0101 others(8): Show |
11 | HG01257.hp2 HG01884.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-3613C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111443 | |||||||
| chr11:61111517 | G | A | 6 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(3): Show |
13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-3539G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111517 | |||||||
| chr11:61111578 | T | C | 1 | a0012c0016t0001g0066 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.56-3478T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111578 | |||||||
| chr11:61111676 | C | T | 1 | a0002c0003t0003g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-3380C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111676 | |||||||
| chr11:61111775 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG00140.hp1 HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.56-3281G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111775 | |||||||
| chr11:61112059 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.56-2997G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112059 | |||||||
| chr11:61112131 | G | A | 1 | a0002c0006t0003g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.56-2925G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112131 | |||||||
| chr11:61112193 | G | A | 11 | a0002c0003t0003g0064 a0002c0003t0003g0065 a0006c0007t0001g0101 others(8): Show |
11 | HG01257.hp2 HG01884.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-2863G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112193 | |||||||
| chr11:61112306 | C | CATCT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
10 | HG02015.hp1 HG02015.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.56-2749_56-2746dup others(4): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61112306 | ||||||
| chr11:61112503 | G | A | 2 | a0002c0011t0004g0030 a0002c0011t0004g0089 |
3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.56-2553G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112503 | |||||||
| chr11:61112536 | C | T | 2 | a0003c0002t0001g0088 a0003c0002t0001g0109 |
2 | HG03209.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.56-2520C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112536 | |||||||
| chr11:61112643 | C | CA | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(48): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.56-2403dupA | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61112643 | ||||||
| chr11:61112962 | C | T | 6 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(3): Show |
13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-2094C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112962 | |||||||
| chr11:61113194 | A | T | 11 | a0002c0003t0003g0008 a0002c0003t0003g0096 a0002c0003t0003g0097 others(8): Show |
18 | HG00741.hp1 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.56-1862A>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113194 | |||||||
| chr11:61113204 | G | C | 1 | a0007c0010t0001g0100 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.56-1852G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113204 | |||||||
| chr11:61113206 | T | C | 2 | a0002c0006t0003g0040 a0007c0010t0001g0100 |
2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.56-1850T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113206 | |||||||
| chr11:61113384 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(106): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.56-1672A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113384 | |||||||
| chr11:61113418 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.56-1638G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113418 | |||||||
| chr11:61113670 | CT | C | 3 | a0003c0002t0001g0013 a0003c0002t0001g0093 a0003c0002t0001g0109 |
6 | HG02132.hp2 HG02257.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-1376delT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61113670 | ||||||
| chr11:61113695 | A | G | 11 | a0002c0003t0003g0064 a0002c0003t0003g0065 a0006c0007t0001g0101 others(8): Show |
11 | HG01257.hp2 HG01884.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-1361A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113695 | |||||||
| chr11:61113747 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.56-1309C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113747 | |||||||
| chr11:61113960 | G | A | 3 | a0002c0003t0007g0021 a0002c0009t0004g0020 a0002c0009t0004g0043 |
5 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-1096G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113960 | |||||||
| chr11:61114289 | T | TC | 2 | a0001c0001t0001g0029 a0001c0001t0001g0062 |
3 | NA18941.hp1 NA19088.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.56-765dupC | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61114289 | ||||||
| chr11:61114303 | A | T | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.56-753A>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114303 | |||||||
| chr11:61114371 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.56-685C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114371 | |||||||
| chr11:61114378 | C | T | 6 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(3): Show |
13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-678C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114378 | |||||||
| chr11:61114454 | G | GCATACAT others(1): Show |
51 | a0001c0001t0001g0037 a0002c0003t0002g0113 a0002c0003t0003g0008 others(48): Show |
83 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.56-591_56-584dupTA others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61114454 | ||||||
| chr11:61114454 | G | GCATACAT others(5): Show |
2 | a0003c0002t0001g0126 a0011c0013t0001g0125 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.56-595_56-584dupTA others(10): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61114454 | ||||||
| chr11:61114513 | T | C | 33 | a0002c0003t0002g0113 a0002c0003t0003g0008 a0002c0003t0003g0096 others(30): Show |
57 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.56-543T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114513 | |||||||
| chr11:61114570 | G | A | 1 | a0002c0006t0003g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.56-486G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114570 | |||||||
| chr11:61114753 | A | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0067 |
3 | NA18977.hp2 NA19010.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.56-303A>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114753 | |||||||
| chr11:61114812 | G | A | 5 | a0002c0003t0003g0041 a0002c0003t0003g0042 a0002c0003t0007g0021 others(2): Show |
7 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-244G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114812 | |||||||
| chr11:61115176 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG02015.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.94+82G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115176 | |||||||
| chr11:61115250 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0069 |
7 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+156T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115250 | |||||||
| chr11:61115355 | T | C | 1 | a0001c0001t0010g0114 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.94+261T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115355 | |||||||
| chr11:61115454 | G | A | 1 | a0010c0012t0003g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.94+360G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115454 | |||||||
| chr11:61115496 | G | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0002c0006t0003g0014 others(5): Show |
13 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+402G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115496 | |||||||
| chr11:61115503 | G | A | 9 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0002c0006t0003g0014 others(6): Show |
14 | HG00642.hp1 HG01261.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+409G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115503 | |||||||
| chr11:61115622 | C | G | 36 | a0002c0003t0003g0008 a0002c0003t0003g0096 a0002c0003t0003g0097 others(33): Show |
49 | HG00609.hp1 HG00741.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.94+528C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115622 | |||||||
| chr11:61115864 | A | C | 6 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(3): Show |
13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+770A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115864 | |||||||
| chr11:61115972 | C | T | 1 | a0002c0003t0003g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+878C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115972 | |||||||
| chr11:61116090 | G | A | 6 | a0002c0003t0003g0041 a0002c0003t0003g0042 a0002c0003t0007g0021 others(3): Show |
8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+996G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116090 | |||||||
| chr11:61116134 | A | G | 7 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(4): Show |
14 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+1040A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116134 | |||||||
| chr11:61116251 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.94+1157G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116251 | |||||||
| chr11:61116297 | C | T | 1 | a0003c0002t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94+1203C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116297 | |||||||
| chr11:61116328 | G | T | 2 | a0002c0003t0003g0064 a0002c0003t0003g0065 |
2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.94+1234G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116328 | |||||||
| chr11:61116343 | G | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0002c0004t0001g0012 others(5): Show |
16 | HG01109.hp1 HG01261.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+1249G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116343 | |||||||
| chr11:61116377 | C | T | 1 | a0002c0004t0004g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.94+1283C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116377 | |||||||
| chr11:61116402 | A | C | 1 | a0002c0003t0003g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.94+1308A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116402 | |||||||
| chr11:61116419 | A | C | 1 | a0002c0003t0003g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.94+1325A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116419 | |||||||
| chr11:61116425 | A | C | 1 | a0002c0003t0003g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.94+1331A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116425 | |||||||
| chr11:61116469 | C | T | 22 | a0002c0003t0003g0008 a0002c0003t0003g0096 a0002c0003t0003g0097 others(19): Show |
29 | HG00609.hp1 HG00741.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.94+1375C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116469 | |||||||
| chr11:61116470 | G | A | 16 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0086 others(13): Show |
31 | HG00642.hp1 HG01109.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.94+1376G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116470 | |||||||
| chr11:61116488 | CCA | C | 6 | a0002c0003t0003g0041 a0002c0003t0003g0042 a0002c0003t0007g0021 others(3): Show |
8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+1402_94+1403del others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116488 | ||||||
| chr11:61116494 | ACAC | A | 10 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(7): Show |
20 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+1407_94+1409del others(3): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116494 | ||||||
| chr11:61116513 | ACAC | A | 4 | a0003c0002t0005g0110 a0003c0002t0005g0111 a0003c0002t0005g0116 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+1420_94+1422del others(3): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116513 | |||||||
| chr11:61116533 | C | A | 1 | a0002c0003t0003g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.94+1439C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116533 | |||||||
| chr11:61116539 | C | CCA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(55): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.94+1457_94+1458dup others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116539 | ||||||
| chr11:61116549 | AC | A | 6 | a0002c0003t0003g0041 a0002c0003t0003g0042 a0002c0003t0007g0021 others(3): Show |
8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+1456delC | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116549 | |||||||
| chr11:61116553 | C | A | 1 | a0002c0006t0003g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94+1459C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116553 | |||||||
| chr11:61116554 | A | C | 1 | a0002c0006t0003g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94+1460A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116554 | |||||||
| chr11:61116619 | ACACACAC others(2): Show |
A | 6 | a0002c0003t0003g0041 a0002c0003t0003g0042 a0002c0003t0007g0021 others(3): Show |
8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-1536_95-1528del others(9): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116619 | ||||||
| chr11:61116666 | CCA | C | 16 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0086 others(13): Show |
31 | HG00642.hp1 HG01109.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.95-1497_95-1496del others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116666 | ||||||
| chr11:61116691 | CATACACA others(22): Show |
C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(47): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.95-1466_95-1438del others(29): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116691 | ||||||
| chr11:61116705 | ACAC | A | 1 | a0003c0002t0006g0010 | 4 | HG01243.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1466_95-1464del others(3): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116705 | ||||||
| chr11:61116713 | T | C | 7 | a0001c0001t0001g0037 a0002c0004t0004g0004 a0002c0004t0004g0033 others(4): Show |
14 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.95-1462T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116713 | |||||||
| chr11:61116772 | GCAC | G | 16 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0086 others(13): Show |
31 | HG00642.hp1 HG01109.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.95-1396_95-1394del others(3): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116772 | ||||||
| chr11:61116806 | A | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(47): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.95-1369A>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116806 | |||||||
| chr11:61116814 | C | T | 6 | a0002c0003t0003g0041 a0002c0003t0003g0042 a0002c0003t0007g0021 others(3): Show |
8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-1361C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116814 | |||||||
| chr11:61116848 | C | T | 1 | a0005c0008t0003g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-1327C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116848 | |||||||
| chr11:61116866 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.95-1309A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116866 | |||||||
| chr11:61117025 | G | C | 1 | a0002c0004t0004g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.95-1150G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117025 | |||||||
| chr11:61117160 | T | C | 3 | a0006c0007t0001g0101 a0006c0007t0001g0102 a0006c0007t0001g0104 |
3 | HG03669.hp2 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.95-1015T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117160 | |||||||
| chr11:61117551 | C | T | 1 | a0002c0006t0003g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.95-624C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117551 | |||||||
| chr11:61117701 | G | T | 6 | a0002c0003t0003g0041 a0002c0003t0003g0042 a0002c0003t0007g0021 others(3): Show |
8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-474G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117701 | |||||||
| chr11:61117817 | A | T | 1 | a0002c0004t0004g0033 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.95-358A>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117817 | |||||||
| chr11:61117901 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.95-274G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117901 | |||||||
| chr11:61118502 | C | A | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.400+22C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 3/10 | chr11 | 61118502 | |||||||
| chr11:61118514 | G | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0002c0006t0003g0014 others(4): Show |
12 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+34G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 3/10 | chr11 | 61118514 | |||||||
| chr11:61118543 | C | T | 1 | a0003c0002t0001g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.400+63C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 3/10 | chr11 | 61118543 | |||||||
| chr11:61119047 | T | C | 22 | a0002c0003t0003g0008 a0002c0003t0003g0096 a0002c0003t0003g0097 others(19): Show |
29 | HG00609.hp1 HG00741.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.463+70T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 4/10 | chr11 | 61119047 | |||||||
| chr11:61119211 | C | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0002c0006t0003g0014 others(4): Show |
12 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.464-23C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 4/10 | chr11 | 61119211 | |||||||
| chr11:61119857 | A | G | 16 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0002c0003t0003g0064 others(13): Show |
28 | HG00642.hp1 HG01261.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.805+282A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61119857 | |||||||
| chr11:61119960 | GC | G | 5 | a0001c0001t0001g0082 a0002c0003t0007g0021 a0002c0009t0004g0020 others(2): Show |
7 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.805+386delC | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61119960 | |||||||
| chr11:61120241 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.805+666A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61120241 | |||||||
| chr11:61120467 | C | T | 8 | a0002c0004t0004g0004 a0002c0004t0004g0033 a0002c0004t0004g0034 others(5): Show |
15 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.805+892C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61120467 | |||||||
| chr11:61120529 | C | T | 37 | a0001c0001t0001g0082 a0002c0003t0002g0003 a0002c0003t0002g0047 others(34): Show |
66 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.805+954C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61120529 | |||||||
| chr11:61120809 | G | T | 2 | a0002c0011t0004g0030 a0002c0011t0004g0089 |
3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.806-802G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61120809 | |||||||
| chr11:61121029 | G | C | 9 | a0002c0004t0001g0012 a0002c0004t0004g0004 a0002c0004t0004g0033 others(6): Show |
19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.806-582G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121029 | |||||||
| chr11:61121047 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(116): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.806-564T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121047 | |||||||
| chr11:61121062 | C | T | 1 | a0005c0008t0012g0094 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.806-549C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121062 | |||||||
| chr11:61121116 | G | A | 1 | a0002c0011t0004g0089 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.806-495G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121116 | |||||||
| chr11:61121253 | AGTGGACC others(3): Show |
A | 1 | a0002c0004t0001g0012 | 4 | HG01109.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-352_806-343del others(10): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 61121253 | ||||||
| chr11:61121319 | C | T | 1 | a0008c0015t0005g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.806-292C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121319 | |||||||
| chr11:61121451 | G | A | 2 | a0002c0011t0004g0030 a0002c0011t0004g0089 |
3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.806-160G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121451 | |||||||
| chr11:61121570 | T | G | 9 | a0002c0004t0001g0012 a0002c0004t0004g0004 a0002c0004t0004g0033 others(6): Show |
19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.806-41T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121570 | |||||||
| chr11:61121926 | G | A | 9 | a0002c0004t0001g0012 a0002c0004t0004g0004 a0002c0004t0004g0033 others(6): Show |
19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1099+22G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61121926 | |||||||
| chr11:61122002 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG01975.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1099+98T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122002 | |||||||
| chr11:61122158 | TCTC | T | 1 | a0002c0004t0001g0012 | 4 | HG01109.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099+257_1099+259d others(5): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122158 | ||||||
| chr11:61122168 | C | T | 1 | a0002c0003t0002g0053 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1099+264C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122168 | |||||||
| chr11:61122263 | A | AATGG | 6 | a0002c0003t0002g0052 a0002c0011t0004g0030 a0002c0011t0004g0089 others(3): Show |
7 | HG01109.hp2 HG01993.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099+382_1099+385d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122263 | ||||||
| chr11:61122290 | T | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG01975.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1099+386T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122290 | |||||||
| chr11:61122290 | TGGTG | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(35): Show |
74 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1099+408_1099+411d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122290 | ||||||
| chr11:61122292 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG01975.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1099+388G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122292 | |||||||
| chr11:61122294 | G | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG01975.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1099+390G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122294 | |||||||
| chr11:61122308 | G | GTGGA | 5 | a0001c0001t0001g0026 a0001c0001t0001g0074 a0001c0001t0001g0090 others(2): Show |
6 | HG00323.hp1 HG02055.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099+407_1099+408i others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122308 | ||||||
| chr11:61122308 | GTGGGTGG others(1): Show |
G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0001c0001t0001g0073 others(6): Show |
10 | HG02145.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099+408_1099+415d others(10): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122308 | ||||||
| chr11:61122308 | GTGGGTGG others(9): Show |
G | 2 | a0002c0011t0004g0030 a0002c0011t0004g0089 |
3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1099+408_1099+423d others(18): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122308 | ||||||
| chr11:61122312 | G | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(53): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1099+408G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122312 | |||||||
| chr11:61122312 | G | GTGGA | 1 | a0004c0005t0002g0005 | 5 | HG00738.hp2 HG01346.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099+446_1099+449d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122312 | ||||||
| chr11:61122312 | G | GTGGATGG others(1): Show |
2 | a0004c0005t0002g0005 a0004c0005t0009g0049 |
4 | HG00280.hp1 HG01516.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099+442_1099+449d others(10): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122312 | ||||||
| chr11:61122312 | GTGGA | G | 5 | a0002c0003t0002g0003 a0002c0003t0002g0055 a0002c0004t0001g0012 others(2): Show |
8 | HG00323.hp2 HG01109.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099+446_1099+449d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122312 | ||||||
| chr11:61122354 | C | G | 4 | a0002c0006t0003g0014 a0006c0007t0001g0105 a0007c0010t0001g0075 others(1): Show |
6 | HG01261.hp1 HG01884.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099+450C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122354 | |||||||
| chr11:61122354 | C | T | 12 | a0001c0001t0001g0037 a0003c0002t0001g0006 a0003c0002t0001g0011 others(9): Show |
26 | HG00099.hp1 HG00639.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1099+450C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122354 | |||||||
| chr11:61122356 | G | A | 4 | a0002c0006t0003g0014 a0006c0007t0001g0105 a0007c0010t0001g0075 others(1): Show |
6 | HG01261.hp1 HG01884.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099+452G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122356 | |||||||
| chr11:61122358 | G | C | 3 | a0002c0006t0003g0014 a0007c0010t0001g0075 a0010c0012t0003g0099 |
5 | HG01261.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099+454G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122358 | |||||||
| chr11:61122360 | G | A | 1 | a0006c0007t0001g0105 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1099+456G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122360 | |||||||
| chr11:61122362 | G | C | 1 | a0006c0007t0001g0105 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1099+458G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122362 | |||||||
| chr11:61122368 | A | G | 2 | a0002c0006t0003g0014 a0006c0007t0001g0105 |
4 | HG01261.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099+464A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122368 | |||||||
| chr11:61122370 | GGAT | G | 2 | a0002c0006t0003g0014 a0006c0007t0001g0105 |
4 | HG01261.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099+471_1099+473d others(5): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122370 | ||||||
| chr11:61122373 | T | TGATG | 3 | a0002c0003t0002g0003 a0002c0004t0004g0004 a0002c0004t0004g0121 |
3 | HG02735.hp2 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1100-490_1100-487d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122373 | ||||||
| chr11:61122373 | TGATG | T | 5 | a0002c0003t0002g0003 a0002c0003t0002g0053 a0002c0004t0004g0034 others(2): Show |
8 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1100-490_1100-487d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122373 | ||||||
| chr11:61122373 | TGATGGAT others(1): Show |
T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0022 others(11): Show |
20 | HG00642.hp1 HG01109.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1100-494_1100-487d others(10): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122373 | ||||||
| chr11:61122373 | TGATGGAT others(5): Show |
T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(87): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1100-498_1100-487d others(14): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122373 | ||||||
| chr11:61122373 | TGATGGAT others(9): Show |
T | 3 | a0001c0001t0001g0028 a0002c0004t0001g0012 a0002c0004t0004g0092 |
4 | HG01516.hp1 HG01517.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099+501_1100-487d others(18): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122373 | ||||||
| chr11:61122375 | A | G | 3 | a0006c0007t0001g0105 a0007c0010t0001g0075 a0010c0012t0003g0099 |
3 | HG01884.hp1 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1099+471A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122375 | |||||||
| chr11:61122380 | TG | T | 1 | a0002c0006t0003g0014 | 3 | HG01261.hp1 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1099+478delG | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122380 | ||||||
| chr11:61122384 | TG | T | 3 | a0006c0007t0001g0105 a0007c0010t0001g0075 a0010c0012t0003g0099 |
3 | HG01884.hp1 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1099+482delG | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122384 | ||||||
| chr11:61122409 | G | C | 3 | a0002c0009t0004g0020 a0002c0009t0004g0043 a0002c0009t0004g0070 |
4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-498G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122409 | |||||||
| chr11:61122410 | G | A | 3 | a0002c0009t0004g0020 a0002c0009t0004g0043 a0002c0009t0004g0070 |
4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-497G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122410 | |||||||
| chr11:61122411 | A | G | 3 | a0002c0009t0004g0020 a0002c0009t0004g0043 a0002c0009t0004g0070 |
4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-496A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122411 | |||||||
| chr11:61122415 | A | G | 3 | a0002c0009t0004g0020 a0002c0009t0004g0043 a0002c0009t0004g0070 |
4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-492A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122415 | |||||||
| chr11:61122418 | GATCA | G | 3 | a0002c0009t0004g0020 a0002c0009t0004g0043 a0002c0009t0004g0070 |
4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-488_1100-485d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122418 | |||||||
| chr11:61122434 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(82): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1100-473G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122434 | |||||||
| chr11:61122557 | C | T | 2 | a0002c0003t0003g0041 a0002c0003t0003g0042 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1100-350C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122557 | |||||||
| chr11:61122586 | AT | A | 12 | a0002c0003t0003g0008 a0002c0003t0003g0064 a0002c0003t0003g0065 others(9): Show |
17 | HG00741.hp1 HG01255.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1100-319delT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122586 | ||||||
| chr11:61122695 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1100-212G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122695 | |||||||
| chr11:61123091 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(71): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1225+59C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123091 | |||||||
| chr11:61123136 | C | T | 9 | a0002c0004t0001g0012 a0002c0004t0004g0004 a0002c0004t0004g0033 others(6): Show |
19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1225+104C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123136 | |||||||
| chr11:61123175 | C | G | 1 | a0003c0002t0005g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1225+143C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123175 | |||||||
| chr11:61123397 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(116): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1225+365A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123397 | |||||||
| chr11:61123675 | C | T | 20 | a0002c0003t0003g0008 a0002c0003t0003g0041 a0002c0003t0003g0042 others(17): Show |
28 | HG00642.hp1 HG00741.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1226-209C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123675 | |||||||
| chr11:61123676 | G | T | 9 | a0002c0004t0001g0012 a0002c0004t0004g0004 a0002c0004t0004g0033 others(6): Show |
19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1226-208G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123676 | |||||||
| chr11:61123690 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1226-194G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123690 | |||||||
| chr11:61123811 | A | G | 32 | a0002c0003t0003g0008 a0002c0003t0003g0041 a0002c0003t0003g0042 others(29): Show |
51 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1226-73A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123811 | |||||||
| chr11:61123838 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(116): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1226-46T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123838 | |||||||
| chr11:61123949 | C | T | 21 | a0001c0001t0001g0071 a0002c0003t0003g0008 a0002c0003t0003g0041 others(18): Show |
29 | HG00642.hp1 HG00741.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.1279+12C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61123949 | |||||||
| chr11:61123980 | A | G | 2 | a0002c0003t0003g0041 a0002c0003t0003g0042 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1279+43A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61123980 | |||||||
| chr11:61124058 | C | T | 3 | a0001c0001t0001g0037 a0003c0002t0001g0011 a0003c0002t0001g0124 |
6 | HG02451.hp2 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+121C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124058 | |||||||
| chr11:61124154 | G | A | 1 | a0003c0002t0006g0010 | 4 | HG01243.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+217G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124154 | |||||||
| chr11:61124163 | T | G | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1279+226T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124163 | |||||||
| chr11:61124513 | GTC | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0009c0014t0001g0025 |
3 | HG02622.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1280-517_1280-516d others(4): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 61124513 | ||||||
| chr11:61124605 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0085 others(1): Show |
5 | HG01081.hp1 HG01169.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1280-427C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124605 | |||||||
| chr11:61124629 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1280-403C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124629 | |||||||
| chr11:61124685 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1280-347T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124685 | |||||||
| chr11:61124732 | C | T | 2 | a0002c0004t0004g0078 a0002c0004t0004g0092 |
2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1280-300C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124732 | |||||||
| chr11:61125201 | C | T | 2 | a0002c0011t0004g0030 a0002c0011t0004g0089 |
3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1399+50C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/10 | chr11 | 61125201 | |||||||
| chr11:61125202 | G | A | 6 | a0002c0006t0003g0014 a0002c0006t0003g0019 a0002c0006t0003g0039 others(3): Show |
9 | HG00642.hp1 HG01261.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.1399+51G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/10 | chr11 | 61125202 | |||||||
| chr11:61125275 | A | G | 3 | a0002c0004t0001g0012 a0002c0004t0004g0078 a0002c0004t0004g0092 |
6 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1399+124A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/10 | chr11 | 61125275 | |||||||
| chr11:61125639 | C | T | 1 | a0006c0007t0001g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1400-112C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/10 | chr11 | 61125639 | |||||||
| chr11:61125850 | G | C | 2 | a0004c0005t0002g0005 a0004c0005t0009g0049 |
9 | HG00280.hp1 HG00738.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.*2+9G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61125850 | |||||||
| chr11:61125934 | C | T | 3 | a0002c0004t0001g0012 a0002c0004t0004g0078 a0002c0004t0004g0092 |
6 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.*2+93C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61125934 | |||||||
| chr11:61126115 | G | A | 2 | a0002c0004t0004g0078 a0002c0004t0004g0092 |
2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*3-173G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61126115 | |||||||
| chr11:61126159 | C | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(116): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.*3-129C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61126159 | |||||||
| chr11:61126162 | A | G | 1 | a0003c0002t0001g0117 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*3-126A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61126162 | |||||||
| chr11:61126227 | C | T | 6 | a0002c0006t0003g0014 a0002c0006t0003g0019 a0002c0006t0003g0039 others(3): Show |
9 | HG00642.hp1 HG01261.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.*3-61C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61126227 | |||||||
| chr11:61126279 | AC | A | 3 | a0002c0009t0004g0020 a0002c0009t0004g0043 a0002c0009t0004g0070 |
4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.*3-5delC | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 61126279 |