Item | Value |
---|---|
geneid | 51586 |
ensemblid | ENSG00000099917.17 |
hgncid | 14248 |
symbol | MED15 |
name | mediator complex subunit 15 |
refseq_nuc | NM_001003891.3 |
refseq_prot | NP_001003891.1 |
ensembl_nuc | ENST00000263205.11 |
ensembl_prot | ENSP00000263205.7 |
mane_status | MANE Select |
chr | chr22 |
start | 20507610 |
end | 20587619 |
strand | + |
ver | v1.2 |
region | chr22:20507610-20587619 |
region5000 | chr22:20502610-20592619 |
regionname0 | MED15_chr22_20507610_20587619 |
regionname5000 | MED15_chr22_20502610_20592619 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 788 | 264 | 65 | 51 | 111 | 11 | 25 | 78 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(783): Show |
chr22 | 20502610 | 20592619 |
a0002 | 0/0 | 789 | 51 | 9 | 8 | 21 | 4 | 9 | 16 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(784): Show |
chr22 | 20502610 | 20592619 |
a0003 | 0/0 | 787 | 8 | 4 | 1 | 1 | 0 | 2 | 1 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(782): Show |
chr22 | 20502610 | 20592619 |
a0004 | 0/0 | 785 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(780): Show |
chr22 | 20502610 | 20592619 |
a0005 | 0/0 | 788 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(783): Show |
chr22 | 20502610 | 20592619 |
a0006 | 0/0 | 784 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(779): Show |
chr22 | 20502610 | 20592619 |
a0007 | 0/0 | 787 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(782): Show |
chr22 | 20502610 | 20592619 |
a0008 | 0/0 | 788 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(783): Show |
chr22 | 20502610 | 20592619 |
a0009 | 0/0 | 792 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(787): Show |
chr22 | 20502610 | 20592619 |
a0010 | 0/0 | 788 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(783): Show |
chr22 | 20502610 | 20592619 |
a0011 | 0/0 | 788 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(783): Show |
chr22 | 20502610 | 20592619 |
a0012 | 0/0 | 788 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(783): Show |
chr22 | 20502610 | 20592619 |
a0013 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(781): Show |
chr22 | 20502610 | 20592619 |
a0014 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(783): Show |
chr22 | 20502610 | 20592619 |
a0015 | 0/0 | 778 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | MDVSG others(773): Show |
chr22 | 20502610 | 20592619 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2364 | 190 | 57 | 40 | 61 | 9 | 22 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0001c0002 | 0/0 | 2364 | 61 | 0 | 7 | 49 | 2 | 3 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0001c0004 | 0/0 | 2364 | 8 | 7 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0001c0006 | 0/0 | 2364 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0001c0017 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0001c0023 | 0/0 | 2364 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0001c0025 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0002c0003 | 0/0 | 2367 | 50 | 9 | 8 | 20 | 4 | 9 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2362): Show |
chr22 | 20502610 | 20592619 | ||
a0002c0014 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2362): Show |
chr22 | 20502610 | 20592619 | ||
a0003c0005 | 0/0 | 2361 | 6 | 3 | 1 | 1 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2356): Show |
chr22 | 20502610 | 20592619 | ||
a0003c0012 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2356): Show |
chr22 | 20502610 | 20592619 | ||
a0003c0020 | 0/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2356): Show |
chr22 | 20502610 | 20592619 | ||
a0004c0009 | 0/0 | 2355 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2350): Show |
chr22 | 20502610 | 20592619 | ||
a0004c0021 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2350): Show |
chr22 | 20502610 | 20592619 | ||
a0005c0007 | 0/0 | 2364 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0006c0010 | 0/0 | 2352 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2347): Show |
chr22 | 20502610 | 20592619 | ||
a0007c0011 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2356): Show |
chr22 | 20502610 | 20592619 | ||
a0008c0008 | 0/0 | 2364 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0009c0013 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2371): Show |
chr22 | 20502610 | 20592619 | ||
a0010c0022 | 0/0 | 2364 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0011c0019 | 0/0 | 2364 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0012c0018 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0013c0024 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2353): Show |
chr22 | 20502610 | 20592619 | ||
a0014c0016 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2359): Show |
chr22 | 20502610 | 20592619 | ||
a0015c0015 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | ATGGA others(2362): Show |
chr22 | 20502610 | 20592619 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3351 | 170 | 53 | 34 | 58 | 6 | 18 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0001t0002 | 0/0 | 3351 | 3 | 0 | 0 | 3 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0001t0003 | 0/0 | 3351 | 10 | 1 | 4 | 0 | 1 | 4 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0001t0005 | 0/0 | 3351 | 2 | 1 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0001t0006 | 0/0 | 3351 | 2 | 0 | 0 | 0 | 2 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0001t0007 | 0/0 | 3351 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0001t0009 | 0/0 | 3351 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0001t0013 | 0/0 | 3351 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0002t0002 | 0/0 | 3351 | 56 | 0 | 7 | 44 | 2 | 3 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0002t0004 | 0/0 | 3351 | 4 | 0 | 0 | 4 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0002t0008 | 0/0 | 3351 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0004t0001 | 0/0 | 3351 | 8 | 7 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0006t0001 | 0/0 | 3351 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0017t0001 | 0/0 | 3351 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0023t0001 | 0/0 | 3351 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0001c0025t0001 | 0/0 | 3351 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0002c0003t0001 | 0/0 | 3354 | 49 | 9 | 8 | 19 | 4 | 9 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3349): Show |
chr22 | 20502610 | 20592619 |
a0002c0003t0012 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3349): Show |
chr22 | 20502610 | 20592619 |
a0002c0014t0001 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3349): Show |
chr22 | 20502610 | 20592619 |
a0003c0005t0001 | 0/0 | 3348 | 4 | 2 | 1 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3343): Show |
chr22 | 20502610 | 20592619 |
a0003c0005t0002 | 0/0 | 3348 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3343): Show |
chr22 | 20502610 | 20592619 |
a0003c0005t0010 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3343): Show |
chr22 | 20502610 | 20592619 |
a0003c0012t0001 | 0/0 | 3348 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3343): Show |
chr22 | 20502610 | 20592619 |
a0003c0020t0002 | 0/0 | 3348 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3343): Show |
chr22 | 20502610 | 20592619 |
a0004c0009t0001 | 0/0 | 3342 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3337): Show |
chr22 | 20502610 | 20592619 |
a0004c0021t0002 | 0/0 | 3342 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3337): Show |
chr22 | 20502610 | 20592619 |
a0005c0007t0001 | 0/0 | 3351 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0006c0010t0001 | 0/0 | 3339 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3334): Show |
chr22 | 20502610 | 20592619 |
a0007c0011t0001 | 0/0 | 3348 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3343): Show |
chr22 | 20502610 | 20592619 |
a0008c0008t0002 | 0/0 | 3351 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0009c0013t0001 | 0/0 | 3363 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3358): Show |
chr22 | 20502610 | 20592619 |
a0010c0022t0003 | 0/0 | 3351 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0011c0019t0001 | 0/0 | 3351 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0012c0018t0001 | 0/0 | 3351 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0013c0024t0001 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3340): Show |
chr22 | 20502610 | 20592619 |
a0014c0016t0001 | 0/0 | 3351 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3346): Show |
chr22 | 20502610 | 20592619 |
a0015c0015t0011 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | GGCTC others(3349): Show |
chr22 | 20502610 | 20592619 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0001 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0001t0013g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0002t0008g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0006t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0006t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0017t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0023t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0001c0025t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0003t0012g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0002c0014t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0005t0010g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0012t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0003c0020t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0004c0009t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0004c0009t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0004c0021t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0005c0007t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0005c0007t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0006c0010t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0006c0010t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0007c0011t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0007c0011t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0008c0008t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0008c0008t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0009c0013t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0010c0022t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0011c0019t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0012c0018t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0013c0024t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0014c0016t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
a0015c0015t0011g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | GBR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0315 | EUR | GBR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00140 | hp2 | a0002 | c0003 | t0001 | g0157 | EUR | GBR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00280 | hp2 | a0002 | c0003 | t0001 | g0178 | EUR | FIN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00438 | hp1 | a0002 | c0003 | t0001 | g0106 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00438 | hp2 | a0002 | c0014 | t0001 | g0189 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | CHS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00733 | hp2 | a0002 | c0003 | t0001 | g0171 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00735 | hp2 | a0002 | c0003 | t0001 | g0162 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00741 | hp1 | a0009 | c0013 | t0001 | g0187 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01069 | hp1 | a0002 | c0003 | t0001 | g0169 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01070 | hp1 | a0005 | c0007 | t0001 | g0277 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0170 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01071 | hp2 | a0005 | c0007 | t0001 | g0279 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0237 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0172 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01109 | hp1 | a0002 | c0003 | t0001 | g0159 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01167 | hp2 | a0001 | c0006 | t0001 | g0136 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01168 | hp2 | a0001 | c0023 | t0001 | g0181 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01169 | hp2 | a0001 | c0006 | t0001 | g0133 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01192 | hp2 | a0002 | c0003 | t0001 | g0160 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01243 | hp2 | a0010 | c0022 | t0003 | g0062 | AMR | PUR | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01261 | hp2 | a0001 | c0004 | t0001 | g0140 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01346 | hp1 | a0001 | c0001 | t0005 | g0289 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0253 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01433 | hp2 | a0002 | c0003 | t0001 | g0148 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0282 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01515 | hp2 | a0002 | c0003 | t0001 | g0163 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01516 | hp1 | a0011 | c0019 | t0001 | g0089 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0235 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0278 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0236 | EUR | IBS | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01952 | hp1 | a0001 | c0001 | t0013 | g0284 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01978 | hp1 | a0003 | c0005 | t0001 | g0015 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02055 | hp2 | a0003 | c0005 | t0010 | g0299 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02071 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0258 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02132 | hp2 | a0001 | c0002 | t0004 | g0021 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02135 | hp1 | a0002 | c0003 | t0001 | g0175 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | CDX | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CDX | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | CDX | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02258 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0247 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02451 | hp1 | a0004 | c0009 | t0001 | g0211 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | KHV | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02572 | hp1 | a0003 | c0005 | t0001 | g0261 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02572 | hp2 | a0006 | c0010 | t0001 | g0275 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02602 | hp1 | a0003 | c0005 | t0002 | g0272 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02615 | hp1 | a0001 | c0004 | t0001 | g0143 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02630 | hp2 | a0002 | c0003 | t0001 | g0297 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0293 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02683 | hp2 | a0002 | c0003 | t0001 | g0180 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02698 | hp2 | a0002 | c0003 | t0001 | g0161 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02723 | hp1 | a0001 | c0004 | t0001 | g0146 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0087 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02809 | hp2 | a0006 | c0010 | t0001 | g0273 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0294 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02886 | hp2 | a0012 | c0018 | t0001 | g0030 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0142 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02970 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02976 | hp1 | a0002 | c0003 | t0001 | g0296 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03017 | hp1 | a0002 | c0003 | t0001 | g0131 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03017 | hp2 | a0002 | c0003 | t0001 | g0168 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03098 | hp2 | a0002 | c0003 | t0001 | g0298 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03139 | hp1 | a0003 | c0005 | t0001 | g0309 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03139 | hp2 | a0002 | c0003 | t0001 | g0295 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0144 | AFR | ESN | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03225 | hp2 | a0003 | c0012 | t0001 | g0310 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0185 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03579 | hp1 | a0013 | c0024 | t0001 | g0307 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03669 | hp1 | a0002 | c0003 | t0001 | g0182 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0270 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0076 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03704 | hp2 | a0002 | c0003 | t0001 | g0167 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0250 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03831 | hp2 | a0002 | c0003 | t0001 | g0132 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04184 | hp1 | a0002 | c0003 | t0001 | g0165 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0221 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18522 | hp1 | a0007 | c0011 | t0001 | g0137 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18747 | hp2 | a0002 | c0003 | t0001 | g0155 | EAS | CHB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18906 | hp1 | a0001 | c0004 | t0001 | g0139 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18939 | hp2 | a0002 | c0003 | t0001 | g0158 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18944 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18945 | hp2 | a0008 | c0008 | t0002 | g0216 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18952 | hp1 | a0002 | c0003 | t0001 | g0176 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18956 | hp2 | a0002 | c0003 | t0001 | g0150 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18962 | hp1 | a0002 | c0003 | t0001 | g0153 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18963 | hp2 | a0002 | c0003 | t0001 | g0179 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0184 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18977 | hp1 | a0014 | c0016 | t0001 | g0128 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18980 | hp1 | a0008 | c0008 | t0002 | g0215 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18993 | hp1 | a0002 | c0003 | t0001 | g0186 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18995 | hp1 | a0004 | c0021 | t0002 | g0255 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19000 | hp1 | a0002 | c0003 | t0001 | g0183 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19003 | hp1 | a0002 | c0003 | t0001 | g0164 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19009 | hp1 | a0002 | c0003 | t0012 | g0173 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19009 | hp2 | a0003 | c0005 | t0001 | g0151 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0156 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19043 | hp1 | a0004 | c0009 | t0001 | g0212 | AFR | LWK | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19057 | hp1 | a0002 | c0003 | t0001 | g0154 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19068 | hp2 | a0002 | c0003 | t0001 | g0149 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19070 | hp1 | a0001 | c0017 | t0001 | g0064 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19070 | hp2 | a0002 | c0003 | t0001 | g0174 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19085 | hp1 | a0001 | c0002 | t0008 | g0220 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19085 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19086 | hp2 | a0015 | c0015 | t0011 | g0177 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0152 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19240 | hp1 | a0001 | c0025 | t0001 | g0085 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20129 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | ASW | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ASW | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20805 | hp2 | a0002 | c0003 | t0001 | g0147 | EUR | TSI | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | GIH | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20905 | hp2 | a0003 | c0020 | t0002 | g0238 | SAS | GIH | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03471 | hp1 | a0002 | c0003 | t0001 | g0314 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0145 | AFR | MSL | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | USA | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18955 | hp1 | a0001 | c0002 | t0004 | g0022 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | USA | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | USA | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA21309 | hp1 | a0007 | c0011 | t0001 | g0138 | AFR | LWK | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | LWK | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0188 | REF | REF | MED15_chr22_20502610_20592619 | MED15 | chr22 | 20502610 | 20592619 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20564628 | CCAG | C | 2 | a0007 a0013 |
3 | HG03579.hp1 NA18522.hp1 NA21309.hp1 |
disruptive_inframe_deletion | MODERATE | c.654_656delGCA | p.Gln218del | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/18 | 723/3351 | 654/2367 | 218/788 | INFO_REALIGN_3_PRIME | chr22 | 20564628 | ||
chr22:20566526 | A | ACAG | 2 | a0002 a0015 |
52 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(49): Show |
conservative_inframe_insertion | MODERATE | c.784_786dupCAG | p.Gln262dup | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 856/3351 | 787/2367 | 263/788 | INFO_REALIGN_3_PRIME | chr22 | 20566526 | ||
chr22:20566526 | A | ACAGCAGC others(5): Show |
1 | a0009 | 1 | HG00741.hp1 | conservative_inframe_insertion | MODERATE | c.775_786dupCAGCAGCA others(4): Show |
p.Gln259_Gln262dup | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 856/3351 | 787/2367 | 263/788 | INFO_REALIGN_3_PRIME | chr22 | 20566526 | ||
chr22:20566526 | ACAG | A | 2 | a0003 a0013 |
9 | HG01978.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
conservative_inframe_deletion | MODERATE | c.784_786delCAG | p.Gln262del | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 853/3351 | 784/2367 | 262/788 | INFO_REALIGN_3_PRIME | chr22 | 20566526 | ||
chr22:20566526 | ACAGCAGC others(2): Show |
A | 1 | a0004 | 3 | HG02451.hp1 NA18995.hp1 NA19043.hp1 |
conservative_inframe_deletion | MODERATE | c.778_786delCAGCAGCA others(1): Show |
p.Gln260_Gln262del | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 847/3351 | 778/2367 | 260/788 | INFO_REALIGN_3_PRIME | chr22 | 20566526 | ||
chr22:20566526 | ACAGCAGC others(5): Show |
A | 1 | a0006 | 2 | HG02572.hp2 HG02809.hp2 |
conservative_inframe_deletion | MODERATE | c.775_786delCAGCAGCA others(4): Show |
p.Gln259_Gln262del | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 844/3351 | 775/2367 | 259/788 | INFO_REALIGN_3_PRIME | chr22 | 20566526 | ||
chr22:20566537 | A | G | 1 | a0010 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.761A>G | p.Gln254Arg | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 830/3351 | 761/2367 | 254/788 | chr22 | 20566537 | |||
chr22:20568611 | A | C | 1 | a0008 | 2 | NA18945.hp2 NA18980.hp1 |
missense_variant | MODERATE | c.1132A>C | p.Met378Leu | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/18 | 1201/3351 | 1132/2367 | 378/788 | chr22 | 20568611 | |||
chr22:20582641 | T | C | 1 | a0014 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.1303T>C | p.Ser435Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 10/18 | 1372/3351 | 1303/2367 | 435/788 | chr22 | 20582641 | |||
chr22:20582695 | C | G | 1 | a0011 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.1357C>G | p.Gln453Glu | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 10/18 | 1426/3351 | 1357/2367 | 453/788 | chr22 | 20582695 | |||
chr22:20584874 | C | T | 1 | a0005 | 2 | HG01070.hp1 HG01071.hp2 |
missense_variant | MODERATE | c.1823C>T | p.Pro608Leu | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 15/18 | 1892/3351 | 1823/2367 | 608/788 | chr22 | 20584874 | |||
chr22:20586669 | C | T | 1 | a0015 | 1 | NA19086.hp2 | stop_gained | HIGH | c.2332C>T | p.Gln778* | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 2401/3351 | 2332/2367 | 778/788 | chr22 | 20586669 | |||
chr22:20586675 | G | A | 1 | a0012 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.2338G>A | p.Val780Ile | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 2407/3351 | 2338/2367 | 780/788 | chr22 | 20586675 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20537195 | C | T | 1 | a0001c0025 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.147C>T | p.Ala49Ala | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/18 | 216/3351 | 147/2367 | 49/788 | chr22 | 20537195 | |||
chr22:20555084 | G | A | 1 | a0003c0012 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.387G>A | p.Pro129Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/18 | 456/3351 | 387/2367 | 129/788 | chr22 | 20555084 | |||
chr22:20566526 | A | G | 1 | a0001c0023 | 1 | HG01168.hp2 | synonymous_variant | LOW | c.750A>G | p.Gln250Gln | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/18 | 819/3351 | 750/2367 | 250/788 | chr22 | 20566526 | |||
chr22:20582646 | G | A | 1 | a0001c0006 | 2 | HG01167.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.1308G>A | p.Pro436Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 10/18 | 1377/3351 | 1308/2367 | 436/788 | chr22 | 20582646 | |||
chr22:20582688 | T | C | 1 | a0014c0016 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.1350T>C | p.Pro450Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 10/18 | 1419/3351 | 1350/2367 | 450/788 | chr22 | 20582688 | |||
chr22:20582888 | G | A | 1 | a0002c0014 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.1458G>A | p.Pro486Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 11/18 | 1527/3351 | 1458/2367 | 486/788 | chr22 | 20582888 | |||
chr22:20585113 | G | A | 2 | a0001c0004 a0007c0011 |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
synonymous_variant | LOW | c.1977G>A | p.Val659Val | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/18 | 2046/3351 | 1977/2367 | 659/788 | chr22 | 20585113 | |||
chr22:20585798 | G | A | 4 | a0001c0002 a0003c0020 a0004c0021 others(1): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
synonymous_variant | LOW | c.2202G>A | p.Pro734Pro | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/18 | 2271/3351 | 2202/2367 | 734/788 | chr22 | 20585798 | |||
chr22:20586590 | G | A | 1 | a0001c0017 | 1 | NA19070.hp1 | synonymous_variant | LOW | c.2253G>A | p.Ser751Ser | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 2322/3351 | 2253/2367 | 751/788 | chr22 | 20586590 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20507647 | G | A | 1 | a0001c0001t0007 | 1 | HG03195.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/18 | 32 | chr22 | 20507647 | ||||||
chr22:20586725 | C | T | 1 | a0001c0001t0013 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 21 | chr22 | 20586725 | ||||||
chr22:20586752 | C | T | 1 | a0001c0001t0006 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*48C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 48 | chr22 | 20586752 | ||||||
chr22:20586755 | C | T | 1 | a0002c0003t0012 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 51 | chr22 | 20586755 | ||||||
chr22:20586785 | C | T | 1 | a0015c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*81C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 81 | chr22 | 20586785 | ||||||
chr22:20586908 | G | A | 1 | a0001c0001t0005 | 2 | HG01346.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*204G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 204 | chr22 | 20586908 | ||||||
chr22:20587139 | G | A | 1 | a0015c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*435G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 435 | chr22 | 20587139 | ||||||
chr22:20587163 | T | C | 8 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0004 others(5): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*459T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 459 | chr22 | 20587163 | ||||||
chr22:20587215 | A | C | 1 | a0015c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 511 | chr22 | 20587215 | ||||||
chr22:20587250 | G | C | 1 | a0001c0001t0009 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 546 | chr22 | 20587250 | ||||||
chr22:20587264 | C | T | 2 | a0001c0001t0003 a0010c0022t0003 |
11 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*560C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 560 | chr22 | 20587264 | ||||||
chr22:20587279 | C | T | 1 | a0003c0005t0010 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 575 | chr22 | 20587279 | ||||||
chr22:20587380 | C | T | 1 | a0015c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*676C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 676 | chr22 | 20587380 | ||||||
chr22:20587445 | A | T | 1 | a0001c0002t0004 | 4 | HG02071.hp2 HG02132.hp2 NA18944.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*741A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 741 | chr22 | 20587445 | ||||||
chr22:20587498 | G | A | 1 | a0001c0002t0008 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 794 | chr22 | 20587498 | ||||||
chr22:20587613 | C | T | 1 | a0015c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 909 | chr22 | 20587613 | ||||||
chr22:20587614 | T | C | 1 | a0015c0015t0011 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 18/18 | 910 | chr22 | 20587614 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:20507862 | G | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0316 a0001c0001t0001g0317 others(8): Show |
11 | HG00642.hp1 HG01081.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+116G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20507862 | |||||||
chr22:20507886 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.68+140C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20507886 | |||||||
chr22:20507896 | C | T | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+150C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20507896 | |||||||
chr22:20508261 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.68+515C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508261 | |||||||
chr22:20508286 | G | T | 1 | a0001c0001t0001g0312 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.68+540G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508286 | |||||||
chr22:20508359 | T | G | 133 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0015 others(130): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.68+613T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508359 | |||||||
chr22:20508433 | A | G | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+687A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508433 | |||||||
chr22:20508493 | C | G | 1 | a0001c0001t0001g0311 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68+747C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508493 | |||||||
chr22:20508600 | C | G | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68+854C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508600 | |||||||
chr22:20508915 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.68+1169G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20508915 | |||||||
chr22:20509092 | G | C | 2 | a0002c0003t0001g0131 a0002c0003t0001g0132 |
2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.68+1346G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509092 | |||||||
chr22:20509150 | C | T | 7 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
7 | HG00544.hp1 NA18971.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+1404C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509150 | |||||||
chr22:20509530 | G | A | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+1784G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509530 | |||||||
chr22:20509598 | G | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0006t0001g0133 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1852G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509598 | |||||||
chr22:20509624 | C | T | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68+1878C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509624 | |||||||
chr22:20509671 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+1925C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509671 | |||||||
chr22:20509757 | T | C | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+2011T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509757 | |||||||
chr22:20509998 | C | T | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.68+2252C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20509998 | |||||||
chr22:20510055 | C | G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(6): Show |
10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+2309C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510055 | |||||||
chr22:20510082 | G | A | 2 | a0002c0003t0001g0147 a0002c0003t0001g0148 |
2 | HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.68+2336G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510082 | |||||||
chr22:20510088 | T | G | 3 | a0002c0003t0001g0149 a0002c0003t0001g0150 a0003c0005t0001g0151 |
3 | NA18956.hp2 NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.68+2342T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510088 | |||||||
chr22:20510105 | A | G | 12 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(9): Show |
13 | HG02055.hp2 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.68+2359A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510105 | |||||||
chr22:20510134 | C | T | 5 | a0001c0004t0001g0142 a0001c0004t0001g0143 a0001c0004t0001g0144 others(2): Show |
5 | HG02615.hp1 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+2388C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510134 | |||||||
chr22:20510203 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.68+2457C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510203 | |||||||
chr22:20510254 | C | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.68+2508C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510254 | |||||||
chr22:20510314 | A | C | 5 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
5 | HG01952.hp1 HG03927.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+2568A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510314 | |||||||
chr22:20510380 | A | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(6): Show |
10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+2634A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510380 | |||||||
chr22:20510417 | A | T | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+2671A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510417 | |||||||
chr22:20510557 | C | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(6): Show |
10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+2811C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510557 | |||||||
chr22:20510653 | C | T | 16 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(13): Show |
16 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.68+2907C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510653 | |||||||
chr22:20510659 | C | T | 1 | a0003c0005t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.68+2913C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510659 | |||||||
chr22:20510790 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68+3044A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510790 | |||||||
chr22:20510858 | A | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0121 others(124): Show |
135 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.68+3112A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20510858 | |||||||
chr22:20511004 | A | C | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+3258A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20511004 | |||||||
chr22:20511465 | C | G | 1 | a0002c0014t0001g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.68+3719C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20511465 | |||||||
chr22:20511498 | G | GA | 123 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0122 others(120): Show |
131 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.68+3763dupA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511498 | ||||||
chr22:20511812 | C | A | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68+4066C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20511812 | |||||||
chr22:20511944 | G | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0014 others(132): Show |
144 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.68+4198G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20511944 | |||||||
chr22:20511982 | T | G | 1 | a0001c0001t0001g0276 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.68+4236T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20511982 | |||||||
chr22:20511988 | C | CT | 18 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(15): Show |
18 | HG00423.hp1 HG00544.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+4259dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | ||||||
chr22:20511988 | C | CTTTTTTT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0194 others(81): Show |
91 | HG00423.hp2 HG00558.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.68+4253_68+4259dup others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | ||||||
chr22:20511988 | C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(11): Show |
14 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.68+4252_68+4259dup others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | ||||||
chr22:20511988 | C | CTTTTTTT others(2): Show |
7 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(4): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.68+4251_68+4259dup others(9): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | ||||||
chr22:20511988 | C | CTTTTTTT others(3): Show |
12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+4250_68+4259dup others(10): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | ||||||
chr22:20511988 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0281 a0001c0001t0006g0282 a0001c0006t0001g0136 others(1): Show |
4 | HG01106.hp2 HG01167.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+4249_68+4259dup others(11): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | ||||||
chr22:20511988 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+4248_68+4259dup others(12): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20511988 | ||||||
chr22:20512006 | G | T | 279 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.68+4260G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512006 | |||||||
chr22:20512091 | C | T | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+4345C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512091 | |||||||
chr22:20512101 | A | G | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+4355A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512101 | |||||||
chr22:20512277 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.68+4531T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512277 | |||||||
chr22:20512371 | C | T | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+4625C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512371 | |||||||
chr22:20512389 | T | C | 1 | a0002c0003t0001g0152 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.68+4643T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512389 | |||||||
chr22:20512547 | G | A | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+4801G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512547 | |||||||
chr22:20512567 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.68+4821G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512567 | |||||||
chr22:20512587 | C | CT | 95 | a0001c0001t0001g0014 a0001c0001t0001g0104 a0001c0001t0001g0105 others(92): Show |
100 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.68+4863dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20512587 | ||||||
chr22:20512587 | C | CTT | 6 | a0001c0001t0001g0122 a0001c0001t0001g0135 a0001c0001t0001g0305 others(3): Show |
6 | HG00408.hp1 HG02486.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+4862_68+4863dup others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20512587 | ||||||
chr22:20512587 | CT | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0018 others(29): Show |
35 | HG01891.hp1 HG01952.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.68+4863delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20512587 | ||||||
chr22:20512626 | C | G | 1 | a0001c0004t0001g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68+4880C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512626 | |||||||
chr22:20512758 | A | AT | 12 | a0001c0001t0001g0103 a0001c0001t0001g0291 a0001c0001t0001g0292 others(9): Show |
13 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.68+5026dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20512758 | ||||||
chr22:20512786 | A | T | 60 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(57): Show |
64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.68+5040A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512786 | |||||||
chr22:20512795 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.68+5049T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512795 | |||||||
chr22:20512833 | C | T | 18 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+5087C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512833 | |||||||
chr22:20512930 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0112 a0011c0019t0001g0089 |
3 | HG01099.hp1 HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.68+5184C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512930 | |||||||
chr22:20512976 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.68+5230G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512976 | |||||||
chr22:20512978 | G | A | 198 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(195): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.68+5232G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20512978 | |||||||
chr22:20513040 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0112 a0011c0019t0001g0089 |
3 | HG01099.hp1 HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.68+5294G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513040 | |||||||
chr22:20513282 | CT | C | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0015 others(256): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.68+5551delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20513282 | ||||||
chr22:20513282 | CTT | C | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+5550_68+5551del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20513282 | ||||||
chr22:20513732 | C | T | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+5986C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513732 | |||||||
chr22:20513923 | G | C | 1 | a0001c0001t0001g0316 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.68+6177G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513923 | |||||||
chr22:20513936 | C | A | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+6190C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513936 | |||||||
chr22:20513965 | G | A | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+6219G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513965 | |||||||
chr22:20513966 | C | T | 1 | a0004c0009t0001g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.68+6220C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20513966 | |||||||
chr22:20514009 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.68+6263C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514009 | |||||||
chr22:20514239 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+6493C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514239 | |||||||
chr22:20514307 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+6561A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514307 | |||||||
chr22:20514342 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.68+6596A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514342 | |||||||
chr22:20514387 | T | C | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+6641T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514387 | |||||||
chr22:20514419 | T | G | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+6673T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514419 | |||||||
chr22:20514677 | C | T | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+6931C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514677 | |||||||
chr22:20514678 | G | A | 2 | a0007c0011t0001g0137 a0007c0011t0001g0138 |
2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.68+6932G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514678 | |||||||
chr22:20514730 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.68+6984C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514730 | |||||||
chr22:20514813 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.68+7067C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514813 | |||||||
chr22:20514849 | G | T | 18 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+7103G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514849 | |||||||
chr22:20514898 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.68+7152G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514898 | |||||||
chr22:20514910 | C | T | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+7164C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20514910 | |||||||
chr22:20515188 | C | T | 7 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(4): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.68+7442C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515188 | |||||||
chr22:20515191 | G | C | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.68+7445G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515191 | |||||||
chr22:20515222 | A | T | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+7476A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515222 | |||||||
chr22:20515280 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0190 others(30): Show |
36 | HG01891.hp1 HG01952.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.68+7534A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515280 | |||||||
chr22:20515463 | TA | T | 319 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(316): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.68+7729delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20515463 | ||||||
chr22:20515514 | G | C | 1 | a0003c0005t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.68+7768G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515514 | |||||||
chr22:20515674 | C | T | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+7928C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515674 | |||||||
chr22:20515678 | G | A | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+7932G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515678 | |||||||
chr22:20515701 | G | A | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+7955G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515701 | |||||||
chr22:20515741 | G | A | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+7995G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515741 | |||||||
chr22:20515867 | G | A | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+8121G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20515867 | |||||||
chr22:20516001 | A | AAAAC | 278 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.68+8263_68+8266dup others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20516001 | ||||||
chr22:20516045 | G | A | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.68+8299G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516045 | |||||||
chr22:20516091 | C | T | 1 | a0007c0011t0001g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68+8345C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516091 | |||||||
chr22:20516102 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.68+8356A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516102 | |||||||
chr22:20516141 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.68+8395C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516141 | |||||||
chr22:20516317 | A | AAAT | 7 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0025t0001g0085 others(4): Show |
7 | HG02055.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+8595_68+8597dup others(3): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20516317 | ||||||
chr22:20516381 | G | A | 1 | a0001c0002t0002g0009 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.68+8635G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516381 | |||||||
chr22:20516398 | C | T | 5 | a0001c0004t0001g0142 a0001c0004t0001g0143 a0001c0004t0001g0144 others(2): Show |
5 | HG02615.hp1 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+8652C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516398 | |||||||
chr22:20516683 | AT | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0190 others(30): Show |
36 | HG01891.hp1 HG01952.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.68+8939delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20516683 | ||||||
chr22:20516809 | A | T | 1 | a0001c0002t0002g0246 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.68+9063A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516809 | |||||||
chr22:20516853 | A | G | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+9107A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516853 | |||||||
chr22:20516884 | T | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0194 a0001c0001t0001g0197 |
3 | HG03710.hp2 HG04115.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.68+9138T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516884 | |||||||
chr22:20516905 | T | C | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+9159T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20516905 | |||||||
chr22:20517051 | T | C | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+9305T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517051 | |||||||
chr22:20517103 | A | AT | 70 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(67): Show |
75 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.68+9371dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20517103 | ||||||
chr22:20517106 | T | A | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+9360T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517106 | |||||||
chr22:20517383 | C | T | 1 | a0009c0013t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.68+9637C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517383 | |||||||
chr22:20517456 | C | T | 9 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(6): Show |
10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+9710C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517456 | |||||||
chr22:20517467 | A | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.68+9721A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517467 | |||||||
chr22:20517677 | A | G | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+9931A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517677 | |||||||
chr22:20517743 | A | G | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+9997A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517743 | |||||||
chr22:20517750 | T | C | 1 | a0003c0012t0001g0310 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.68+10004T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517750 | |||||||
chr22:20517823 | G | C | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+10077G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20517823 | |||||||
chr22:20517852 | A | ATTT | 33 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0190 others(30): Show |
36 | HG01891.hp1 HG01952.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.68+10112_68+10114d others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20517852 | ||||||
chr22:20518070 | T | TGACATTG others(25): Show |
106 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(103): Show |
113 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.68+10325_68+10356d others(34): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20518070 | ||||||
chr22:20518070 | T | TGACATTG others(25): Show |
1 | a0001c0002t0002g0258 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.68+10332_68+10333i others(34): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20518070 | ||||||
chr22:20518075 | T | TTGACGTG others(25): Show |
1 | a0006c0010t0001g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.68+10356_68+10357i others(34): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20518075 | ||||||
chr22:20518080 | G | GTGAGGGA others(25): Show |
5 | a0001c0002t0002g0214 a0001c0002t0002g0217 a0001c0002t0002g0218 others(2): Show |
5 | HG00544.hp2 NA18941.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+10356_68+10357i others(34): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20518080 | ||||||
chr22:20518220 | C | T | 10 | a0001c0001t0001g0196 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
10 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+10474C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518220 | |||||||
chr22:20518228 | C | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.68+10482C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518228 | |||||||
chr22:20518434 | T | G | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+10688T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518434 | |||||||
chr22:20518504 | A | G | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+10758A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518504 | |||||||
chr22:20518551 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.68+10805T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518551 | |||||||
chr22:20518551 | T | TTGAG | 3 | a0001c0002t0004g0003 a0001c0002t0004g0021 a0001c0002t0004g0022 |
4 | HG02071.hp2 HG02132.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+10808_68+10811d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20518551 | ||||||
chr22:20518568 | C | T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.68+10822C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20518568 | |||||||
chr22:20519106 | G | A | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+11360G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519106 | |||||||
chr22:20519271 | A | G | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+11525A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519271 | |||||||
chr22:20519325 | T | C | 322 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.68+11579T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519325 | |||||||
chr22:20519401 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.68+11655T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519401 | |||||||
chr22:20519437 | G | GT | 49 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0082 others(46): Show |
52 | HG01261.hp2 HG01891.hp1 HG01952.hp1 others(49): Show |
intron_variant | MODIFIER | c.68+11706dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20519437 | ||||||
chr22:20519588 | G | A | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+11842G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519588 | |||||||
chr22:20519605 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.68+11859C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20519605 | |||||||
chr22:20520161 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0304 a0001c0001t0001g0305 |
4 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+12415A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520161 | |||||||
chr22:20520209 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.68+12463A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520209 | |||||||
chr22:20520253 | G | A | 11 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(8): Show |
12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.68+12507G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520253 | |||||||
chr22:20520268 | T | C | 2 | a0007c0011t0001g0137 a0007c0011t0001g0138 |
2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.68+12522T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520268 | |||||||
chr22:20520346 | T | C | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+12600T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520346 | |||||||
chr22:20520417 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(3): Show |
6 | HG02083.hp2 NA18978.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+12671G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520417 | |||||||
chr22:20520689 | T | C | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+12943T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520689 | |||||||
chr22:20520695 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+12949C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520695 | |||||||
chr22:20520866 | A | G | 3 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 |
3 | HG01261.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.68+13120A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520866 | |||||||
chr22:20520892 | A | C | 1 | a0001c0001t0001g0081 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.68+13146A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20520892 | |||||||
chr22:20521025 | T | C | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+13279T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521025 | |||||||
chr22:20521088 | A | AT | 26 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(23): Show |
26 | HG00735.hp1 HG01981.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.68+13368dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | ||||||
chr22:20521088 | A | ATT | 29 | a0001c0001t0001g0008 a0001c0001t0001g0080 a0001c0001t0001g0190 others(26): Show |
31 | HG00558.hp1 HG01255.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.68+13367_68+13368d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | ||||||
chr22:20521088 | A | ATTT | 53 | a0001c0001t0001g0002 a0001c0001t0001g0194 a0001c0001t0001g0204 others(50): Show |
58 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.68+13366_68+13368d others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | ||||||
chr22:20521088 | A | ATTTT | 10 | a0001c0002t0002g0214 a0001c0002t0002g0218 a0001c0002t0002g0251 others(7): Show |
10 | HG01358.hp1 HG02135.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.68+13365_68+13368d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | ||||||
chr22:20521088 | AT | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(14): Show |
18 | HG00099.hp2 HG00408.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.68+13368delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | ||||||
chr22:20521088 | ATTTT | A | 7 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0293 others(4): Show |
7 | HG02647.hp2 HG02818.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+13365_68+13368d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521088 | ||||||
chr22:20521096 | T | TTTTTTTT others(289): Show |
12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+13365_68+13366i others(298): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521096 | ||||||
chr22:20521097 | T | TTTTTTTT others(288): Show |
3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.68+13365_68+13366i others(297): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521097 | ||||||
chr22:20521097 | T | TTTTTTTT others(293): Show |
1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68+13368_68+13369i others(302): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521097 | ||||||
chr22:20521117 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.68+13371G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521117 | |||||||
chr22:20521119 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(122): Show |
133 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.68+13373T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521119 | |||||||
chr22:20521198 | G | T | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.68+13452G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521198 | |||||||
chr22:20521231 | G | C | 2 | a0002c0003t0001g0155 a0002c0003t0001g0156 |
2 | NA18747.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.68+13485G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521231 | |||||||
chr22:20521242 | A | G | 1 | a0001c0001t0001g0311 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68+13496A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521242 | |||||||
chr22:20521283 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | NA18943.hp1 NA18950.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+13537G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521283 | |||||||
chr22:20521391 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.68+13645C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521391 | |||||||
chr22:20521400 | G | GT | 7 | a0001c0001t0001g0194 a0001c0001t0005g0288 a0001c0001t0005g0289 others(4): Show |
7 | HG01346.hp1 HG02451.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+13659dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521400 | ||||||
chr22:20521406 | G | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(123): Show |
134 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.68+13660G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521406 | |||||||
chr22:20521427 | C | T | 11 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(8): Show |
12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.68+13681C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521427 | |||||||
chr22:20521490 | G | A | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.68+13744G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521490 | |||||||
chr22:20521550 | AT | A | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.68+13820delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521550 | ||||||
chr22:20521656 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.68+13910A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521656 | |||||||
chr22:20521666 | G | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
6 | HG00423.hp1 HG02040.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+13920G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521666 | |||||||
chr22:20521675 | C | T | 2 | a0001c0001t0003g0005 a0001c0001t0003g0070 |
3 | HG01168.hp1 HG01169.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.68+13929C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521675 | |||||||
chr22:20521676 | G | A | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68+13930G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521676 | |||||||
chr22:20521691 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0025t0001g0085 |
3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.68+13945T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521691 | |||||||
chr22:20521695 | C | CTTAT | 64 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(61): Show |
66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.68+13986_68+13989d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | ||||||
chr22:20521695 | C | CTTATTTA others(1): Show |
6 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0003g0068 others(3): Show |
6 | HG00438.hp2 HG00741.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+13982_68+13989d others(10): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | ||||||
chr22:20521695 | CTTAT | C | 36 | a0001c0001t0001g0008 a0001c0001t0001g0088 a0001c0001t0001g0190 others(33): Show |
37 | HG01952.hp1 HG02145.hp2 HG02257.hp1 others(34): Show |
intron_variant | MODIFIER | c.68+13986_68+13989d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | ||||||
chr22:20521695 | CTTATTTA others(1): Show |
C | 5 | a0001c0001t0001g0308 a0001c0001t0005g0288 a0001c0001t0005g0289 others(2): Show |
5 | HG01346.hp1 HG02055.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+13982_68+13989d others(10): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | ||||||
chr22:20521695 | CTTATTTA others(5): Show |
C | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+13978_68+13989d others(14): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | ||||||
chr22:20521695 | CTTATTTA others(13): Show |
C | 76 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0226 others(73): Show |
80 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.68+13970_68+13989d others(22): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20521695 | ||||||
chr22:20521713 | T | G | 3 | a0001c0002t0004g0003 a0001c0002t0004g0021 a0001c0002t0004g0022 |
4 | HG02071.hp2 HG02132.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+13967T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521713 | |||||||
chr22:20521923 | G | A | 1 | a0002c0003t0001g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.68+14177G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521923 | |||||||
chr22:20521988 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.68+14242C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20521988 | |||||||
chr22:20522222 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(123): Show |
134 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.68+14476A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522222 | |||||||
chr22:20522284 | C | T | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68+14538C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522284 | |||||||
chr22:20522309 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.68+14563T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522309 | |||||||
chr22:20522317 | A | G | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68+14571A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522317 | |||||||
chr22:20522339 | T | C | 2 | a0002c0003t0001g0183 a0002c0003t0001g0184 |
2 | NA18967.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.68+14593T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522339 | |||||||
chr22:20522412 | T | G | 1 | a0001c0002t0002g0223 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.68+14666T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522412 | |||||||
chr22:20522554 | G | A | 11 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(8): Show |
12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.69-14563G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522554 | |||||||
chr22:20522675 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-14442G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522675 | |||||||
chr22:20522722 | G | A | 1 | a0001c0002t0002g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.69-14395G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522722 | |||||||
chr22:20522938 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.69-14179C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20522938 | |||||||
chr22:20523016 | A | T | 1 | a0001c0001t0001g0315 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.69-14101A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523016 | |||||||
chr22:20523065 | G | C | 1 | a0001c0001t0001g0302 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.69-14052G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523065 | |||||||
chr22:20523155 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
5 | HG02145.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.69-13962A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523155 | |||||||
chr22:20523297 | G | A | 7 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(4): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.69-13820G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523297 | |||||||
chr22:20523314 | A | G | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.69-13803A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523314 | |||||||
chr22:20523358 | T | A | 9 | a0001c0001t0001g0292 a0001c0001t0003g0068 a0001c0001t0005g0288 others(6): Show |
9 | HG01346.hp1 HG01934.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.69-13759T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523358 | |||||||
chr22:20523359 | A | T | 2 | a0001c0002t0002g0249 a0001c0002t0002g0269 |
2 | HG00621.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.69-13758A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523359 | |||||||
chr22:20523480 | C | G | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-13637C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523480 | |||||||
chr22:20523626 | C | G | 5 | a0001c0002t0002g0192 a0001c0002t0002g0223 a0001c0002t0002g0257 others(2): Show |
5 | NA18948.hp2 NA18955.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-13491C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523626 | |||||||
chr22:20523702 | C | T | 1 | a0001c0002t0002g0256 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.69-13415C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523702 | |||||||
chr22:20523769 | T | C | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69-13348T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523769 | |||||||
chr22:20523888 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.69-13229G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20523888 | |||||||
chr22:20524072 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.69-13045C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20524072 | |||||||
chr22:20524084 | T | C | 1 | a0003c0005t0001g0309 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.69-13033T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20524084 | |||||||
chr22:20524473 | C | G | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-12644C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20524473 | |||||||
chr22:20524550 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.69-12567C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20524550 | |||||||
chr22:20524613 | T | TTTTTG | 12 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0308 others(9): Show |
13 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.69-12489_69-12485d others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20524613 | ||||||
chr22:20524798 | TTTTAGTA others(9): Show |
T | 1 | a0001c0001t0001g0115 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.69-12299_69-12284d others(18): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20524798 | ||||||
chr22:20524840 | C | T | 11 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(8): Show |
12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.69-12277C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20524840 | |||||||
chr22:20525080 | G | A | 1 | a0002c0003t0001g0152 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.69-12037G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525080 | |||||||
chr22:20525320 | G | GT | 41 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0190 others(38): Show |
44 | HG01346.hp1 HG01891.hp1 HG01952.hp1 others(41): Show |
intron_variant | MODIFIER | c.69-11787dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20525320 | ||||||
chr22:20525501 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-11616C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525501 | |||||||
chr22:20525530 | C | CT | 7 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0103 others(4): Show |
7 | HG02135.hp1 HG02257.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-11564dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20525530 | ||||||
chr22:20525530 | CT | C | 13 | a0001c0001t0001g0026 a0001c0001t0001g0262 a0001c0001t0001g0285 others(10): Show |
13 | HG00544.hp2 HG01346.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.69-11564delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20525530 | ||||||
chr22:20525530 | CTT | C | 87 | a0001c0001t0001g0008 a0001c0001t0001g0190 a0001c0001t0001g0191 others(84): Show |
91 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.69-11565_69-11564d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20525530 | ||||||
chr22:20525530 | CTTTTTTT | C | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(11): Show |
14 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.69-11570_69-11564d others(9): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20525530 | ||||||
chr22:20525578 | C | T | 3 | a0001c0002t0002g0244 a0001c0002t0002g0245 a0001c0002t0002g0267 |
3 | NA18943.hp2 NA18966.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.69-11539C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525578 | |||||||
chr22:20525602 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-11515T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525602 | |||||||
chr22:20525694 | G | A | 1 | a0002c0003t0001g0185 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.69-11423G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525694 | |||||||
chr22:20525717 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.69-11400G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525717 | |||||||
chr22:20525725 | G | A | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-11392G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525725 | |||||||
chr22:20525746 | G | C | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69-11371G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525746 | |||||||
chr22:20525816 | G | T | 1 | a0001c0001t0001g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.69-11301G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525816 | |||||||
chr22:20525824 | C | T | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69-11293C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525824 | |||||||
chr22:20525832 | G | A | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-11285G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525832 | |||||||
chr22:20525864 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-11253G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20525864 | |||||||
chr22:20526147 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-10970T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526147 | |||||||
chr22:20526423 | C | T | 3 | a0001c0002t0002g0243 a0008c0008t0002g0215 a0008c0008t0002g0216 |
3 | HG02155.hp2 NA18945.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.69-10694C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526423 | |||||||
chr22:20526458 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69-10659A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526458 | |||||||
chr22:20526611 | A | T | 9 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(6): Show |
10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-10506A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526611 | |||||||
chr22:20526632 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-10485A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526632 | |||||||
chr22:20526824 | G | A | 60 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(57): Show |
64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.69-10293G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20526824 | |||||||
chr22:20527098 | T | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0037 others(22): Show |
26 | HG00408.hp2 HG00423.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.69-10019T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527098 | |||||||
chr22:20527142 | G | C | 1 | a0001c0001t0001g0318 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.69-9975G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527142 | |||||||
chr22:20527391 | C | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0190 others(30): Show |
36 | HG01891.hp1 HG01952.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.69-9726C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527391 | |||||||
chr22:20527453 | G | A | 4 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 others(1): Show |
4 | HG01255.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-9664G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527453 | |||||||
chr22:20527453 | G | GT | 16 | a0001c0001t0001g0053 a0001c0001t0001g0105 a0001c0001t0001g0134 others(13): Show |
16 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.69-9656dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20527453 | ||||||
chr22:20527675 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.69-9442C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527675 | |||||||
chr22:20527734 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.69-9383C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527734 | |||||||
chr22:20527951 | C | T | 1 | a0008c0008t0002g0216 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69-9166C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20527951 | |||||||
chr22:20527956 | CA | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0066 others(108): Show |
118 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.69-9141delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20527956 | ||||||
chr22:20527956 | CAA | C | 13 | a0001c0001t0001g0191 a0001c0001t0001g0208 a0001c0001t0001g0291 others(10): Show |
14 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.69-9142_69-9141del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20527956 | ||||||
chr22:20528040 | C | T | 4 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0003c0005t0001g0309 others(1): Show |
4 | HG01346.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.69-9077C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528040 | |||||||
chr22:20528041 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.69-9076G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528041 | |||||||
chr22:20528102 | C | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(6): Show |
10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-9015C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528102 | |||||||
chr22:20528136 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-8981G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528136 | |||||||
chr22:20528160 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.69-8957C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528160 | |||||||
chr22:20528254 | T | C | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69-8863T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528254 | |||||||
chr22:20528322 | C | G | 9 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(6): Show |
10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-8795C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528322 | |||||||
chr22:20528353 | C | T | 1 | a0002c0003t0001g0182 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.69-8764C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528353 | |||||||
chr22:20528357 | A | C | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69-8760A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528357 | |||||||
chr22:20528448 | GCA | G | 3 | a0001c0001t0001g0276 a0001c0001t0001g0280 a0003c0005t0010g0299 |
3 | HG00741.hp2 HG02055.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.69-8666_69-8665del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20528448 | ||||||
chr22:20528542 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.69-8575C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528542 | |||||||
chr22:20528634 | C | T | 1 | a0004c0021t0002g0255 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.69-8483C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528634 | |||||||
chr22:20528665 | A | T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0134 a0001c0001t0001g0135 others(15): Show |
19 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.69-8452A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528665 | |||||||
chr22:20528739 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0198 |
2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.69-8378C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528739 | |||||||
chr22:20528742 | C | T | 1 | a0002c0003t0001g0106 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.69-8375C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20528742 | |||||||
chr22:20529032 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.69-8085C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529032 | |||||||
chr22:20529035 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.69-8082C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529035 | |||||||
chr22:20529090 | C | T | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-8027C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529090 | |||||||
chr22:20529162 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
277 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.69-7955T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529162 | |||||||
chr22:20529351 | G | A | 240 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(237): Show |
253 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.69-7766G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529351 | |||||||
chr22:20529367 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0210 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.69-7750C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529367 | |||||||
chr22:20529453 | T | G | 5 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(2): Show |
5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-7664T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529453 | |||||||
chr22:20529603 | T | C | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69-7514T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529603 | |||||||
chr22:20529724 | C | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.69-7393C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529724 | |||||||
chr22:20529774 | TAGGG | T | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7341_69-7338del others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20529774 | ||||||
chr22:20529779 | A | C | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7338A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529779 | |||||||
chr22:20529783 | G | T | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7334G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529783 | |||||||
chr22:20529784 | G | A | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7333G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529784 | |||||||
chr22:20529787 | TCAC | T | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7327_69-7325del others(3): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20529787 | ||||||
chr22:20529791 | C | T | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7326C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529791 | |||||||
chr22:20529792 | A | G | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7325A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529792 | |||||||
chr22:20529794 | G | A | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.69-7323G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529794 | |||||||
chr22:20529915 | C | T | 1 | a0002c0003t0001g0174 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.69-7202C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529915 | |||||||
chr22:20529950 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-7167C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20529950 | |||||||
chr22:20530006 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.69-7111G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530006 | |||||||
chr22:20530013 | C | T | 13 | a0001c0002t0002g0010 a0001c0002t0002g0222 a0001c0002t0002g0240 others(10): Show |
14 | HG00558.hp1 HG02056.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.69-7104C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530013 | |||||||
chr22:20530301 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.69-6816C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530301 | |||||||
chr22:20530546 | T | C | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69-6571T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530546 | |||||||
chr22:20530623 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0014 others(130): Show |
142 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.69-6494C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530623 | |||||||
chr22:20530714 | G | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | NA18971.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.69-6403G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530714 | |||||||
chr22:20530750 | A | AG | 10 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0281 others(7): Show |
10 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-6366dupG | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20530750 | ||||||
chr22:20530768 | G | A | 1 | a0004c0009t0001g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69-6349G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530768 | |||||||
chr22:20530813 | A | G | 2 | a0001c0001t0001g0308 a0001c0002t0002g0247 |
2 | HG02165.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.69-6304A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530813 | |||||||
chr22:20530934 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.69-6183T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530934 | |||||||
chr22:20530971 | A | C | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69-6146A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20530971 | |||||||
chr22:20531020 | C | T | 60 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(57): Show |
64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.69-6097C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20531020 | |||||||
chr22:20531131 | C | T | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-5986C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20531131 | |||||||
chr22:20531187 | CTCAGTTT others(1): Show |
C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(159): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.69-5929_69-5922del others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20531187 | |||||||
chr22:20531402 | G | A | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-5715G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20531402 | |||||||
chr22:20531991 | G | A | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.69-5126G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20531991 | |||||||
chr22:20532465 | G | A | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.69-4652G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20532465 | |||||||
chr22:20532793 | A | G | 36 | a0001c0001t0001g0014 a0001c0001t0001g0134 a0001c0001t0001g0135 others(33): Show |
38 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.69-4324A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20532793 | |||||||
chr22:20532879 | G | T | 5 | a0001c0002t0002g0192 a0001c0002t0002g0223 a0001c0002t0002g0257 others(2): Show |
5 | NA18948.hp2 NA18955.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-4238G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20532879 | |||||||
chr22:20532905 | G | A | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-4212G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20532905 | |||||||
chr22:20532963 | T | G | 1 | a0001c0001t0002g0319 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.69-4154T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20532963 | |||||||
chr22:20533067 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.69-4050A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533067 | |||||||
chr22:20533246 | C | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.69-3871C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533246 | |||||||
chr22:20533317 | C | G | 8 | a0001c0002t0002g0012 a0001c0002t0002g0235 a0001c0002t0002g0236 others(5): Show |
9 | HG00423.hp2 HG00738.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.69-3800C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533317 | |||||||
chr22:20533327 | G | A | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-3790G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533327 | |||||||
chr22:20533336 | A | G | 2 | a0001c0002t0002g0234 a0001c0002t0002g0246 |
2 | NA18983.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.69-3781A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533336 | |||||||
chr22:20533685 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0304 a0001c0001t0001g0305 |
4 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-3432C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533685 | |||||||
chr22:20533795 | C | T | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69-3322C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533795 | |||||||
chr22:20533880 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0050 others(2): Show |
5 | HG01891.hp2 HG01978.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-3237C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20533880 | |||||||
chr22:20534082 | A | G | 1 | a0001c0025t0001g0085 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.69-3035A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534082 | |||||||
chr22:20534127 | T | C | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69-2990T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534127 | |||||||
chr22:20534154 | C | T | 2 | a0001c0002t0002g0265 a0001c0002t0002g0271 |
2 | HG00544.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.69-2963C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534154 | |||||||
chr22:20534439 | A | G | 2 | a0001c0001t0001g0286 a0001c0001t0002g0287 |
2 | NA18956.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.69-2678A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534439 | |||||||
chr22:20534451 | G | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-2666G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534451 | |||||||
chr22:20534488 | C | G | 9 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(6): Show |
10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-2629C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534488 | |||||||
chr22:20534541 | G | A | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.69-2576G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534541 | |||||||
chr22:20534639 | C | T | 10 | a0001c0001t0001g0196 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
10 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-2478C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534639 | |||||||
chr22:20534640 | A | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
277 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.69-2477A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534640 | |||||||
chr22:20534641 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-2476C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534641 | |||||||
chr22:20534646 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.69-2471A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534646 | |||||||
chr22:20534797 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.69-2320G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534797 | |||||||
chr22:20534815 | A | G | 27 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(24): Show |
28 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.69-2302A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534815 | |||||||
chr22:20534817 | T | C | 29 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(26): Show |
30 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.69-2300T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534817 | |||||||
chr22:20534984 | G | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.69-2133G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20534984 | |||||||
chr22:20535082 | C | G | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-2035C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535082 | |||||||
chr22:20535319 | A | G | 1 | a0001c0023t0001g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.69-1798A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535319 | |||||||
chr22:20535352 | A | T | 1 | a0001c0001t0001g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.69-1765A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535352 | |||||||
chr22:20535383 | A | G | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69-1734A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535383 | |||||||
chr22:20535399 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0086 others(2): Show |
6 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.69-1718C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535399 | |||||||
chr22:20535563 | CT | C | 13 | a0001c0001t0001g0226 a0001c0001t0001g0291 a0001c0001t0001g0292 others(10): Show |
14 | HG01169.hp2 HG02258.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.69-1540delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535563 | ||||||
chr22:20535621 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-1496G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535621 | |||||||
chr22:20535639 | C | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(258): Show |
276 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.69-1478C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535639 | |||||||
chr22:20535646 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(8): Show |
12 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.69-1471G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535646 | |||||||
chr22:20535660 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.69-1457T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535660 | |||||||
chr22:20535708 | T | C | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.69-1409T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535708 | |||||||
chr22:20535716 | T | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0190 a0001c0001t0001g0197 others(10): Show |
13 | HG00642.hp1 HG01081.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.69-1401T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535716 | |||||||
chr22:20535721 | A | G | 16 | a0001c0001t0001g0015 a0001c0001t0001g0208 a0001c0001t0001g0263 others(13): Show |
16 | HG00642.hp1 HG01081.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.69-1396A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535721 | |||||||
chr22:20535740 | T | A | 38 | a0001c0001t0001g0014 a0001c0001t0001g0083 a0001c0001t0001g0084 others(35): Show |
39 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.69-1377T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535740 | |||||||
chr22:20535750 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0074 others(1): Show |
4 | HG02735.hp1 HG03669.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.69-1367A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535750 | |||||||
chr22:20535758 | A | G | 7 | a0001c0001t0001g0048 a0002c0003t0001g0131 a0002c0003t0001g0132 others(4): Show |
7 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-1359A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535758 | |||||||
chr22:20535772 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.69-1345G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535772 | |||||||
chr22:20535831 | C | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.69-1286C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535831 | |||||||
chr22:20535839 | G | A | 1 | a0003c0012t0001g0310 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.69-1278G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535839 | |||||||
chr22:20535872 | C | CT | 7 | a0001c0001t0001g0040 a0001c0001t0001g0105 a0001c0001t0001g0108 others(4): Show |
7 | HG01433.hp2 HG03831.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.69-1222dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | ||||||
chr22:20535872 | CT | C | 59 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0111 others(56): Show |
63 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.69-1222delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | ||||||
chr22:20535872 | CTT | C | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.69-1223_69-1222del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | ||||||
chr22:20535872 | CTTT | C | 11 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0308 others(8): Show |
12 | HG01169.hp2 HG02165.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.69-1224_69-1222del others(3): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | ||||||
chr22:20535872 | CTTTTT | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0063 others(5): Show |
8 | HG01346.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.69-1226_69-1222del others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | ||||||
chr22:20535872 | CTTTTTT | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.69-1227_69-1222del others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr22 | 20535872 | ||||||
chr22:20535882 | T | C | 12 | a0001c0001t0001g0042 a0001c0001t0001g0075 a0001c0001t0001g0196 others(9): Show |
12 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.69-1235T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535882 | |||||||
chr22:20535980 | G | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(151): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.69-1137G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535980 | |||||||
chr22:20535998 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-1119T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20535998 | |||||||
chr22:20536026 | G | A | 1 | a0002c0003t0001g0165 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.69-1091G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536026 | |||||||
chr22:20536242 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-875A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536242 | |||||||
chr22:20536272 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.69-845T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536272 | |||||||
chr22:20536284 | A | T | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69-833A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536284 | |||||||
chr22:20536359 | G | T | 1 | a0001c0001t0001g0322 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.69-758G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536359 | |||||||
chr22:20536370 | G | A | 3 | a0001c0004t0001g0143 a0001c0004t0001g0144 a0001c0004t0001g0146 |
3 | HG02615.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.69-747G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536370 | |||||||
chr22:20536390 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0108 a0001c0001t0001g0199 |
3 | HG03540.hp1 HG03834.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.69-727G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536390 | |||||||
chr22:20536511 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.69-606A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536511 | |||||||
chr22:20536792 | G | A | 1 | a0004c0009t0001g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.69-325G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536792 | |||||||
chr22:20536853 | G | A | 9 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(6): Show |
10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.69-264G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536853 | |||||||
chr22:20536972 | C | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(146): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.69-145C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20536972 | |||||||
chr22:20537079 | T | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.69-38T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20537079 | |||||||
chr22:20537093 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.69-24G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 1/17 | chr22 | 20537093 | |||||||
chr22:20537211 | C | CCCTA | 64 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0111 others(61): Show |
68 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.156+8_156+11dupCCT others(1): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20537211 | ||||||
chr22:20537258 | A | G | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.156+54A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537258 | |||||||
chr22:20537281 | G | A | 167 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(164): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.156+77G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537281 | |||||||
chr22:20537393 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0210 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.156+189G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537393 | |||||||
chr22:20537438 | C | T | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+234C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537438 | |||||||
chr22:20537555 | C | T | 64 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0111 others(61): Show |
68 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.156+351C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537555 | |||||||
chr22:20537641 | G | T | 65 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0111 others(62): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.156+437G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537641 | |||||||
chr22:20537763 | T | G | 1 | a0003c0005t0001g0151 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.156+559T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537763 | |||||||
chr22:20537786 | G | A | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.156+582G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537786 | |||||||
chr22:20537803 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.156+599C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537803 | |||||||
chr22:20537930 | C | A | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.156+726C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537930 | |||||||
chr22:20537936 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | NA18943.hp1 NA18950.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+732T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20537936 | |||||||
chr22:20538026 | C | T | 1 | a0002c0003t0001g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.156+822C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538026 | |||||||
chr22:20538085 | GC | G | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | HG02129.hp2 NA18950.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+883delC | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20538085 | ||||||
chr22:20538143 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0102 |
2 | HG01496.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.156+939C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538143 | |||||||
chr22:20538304 | C | T | 4 | a0001c0001t0003g0020 a0001c0001t0003g0055 a0001c0001t0003g0068 others(1): Show |
4 | HG01243.hp2 HG01934.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+1100C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538304 | |||||||
chr22:20538310 | C | T | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.156+1106C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538310 | |||||||
chr22:20538451 | T | G | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.156+1247T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538451 | |||||||
chr22:20538545 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0304 a0001c0001t0001g0305 |
4 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+1341C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538545 | |||||||
chr22:20538626 | T | C | 1 | a0001c0002t0002g0266 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.156+1422T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538626 | |||||||
chr22:20538693 | G | A | 1 | a0002c0003t0001g0162 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.156+1489G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538693 | |||||||
chr22:20538709 | C | CGT | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.156+1517_156+1518d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20538709 | ||||||
chr22:20538762 | C | T | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.156+1558C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538762 | |||||||
chr22:20538819 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.156+1615C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538819 | |||||||
chr22:20538853 | C | G | 1 | a0001c0001t0001g0002 | 3 | HG02280.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.156+1649C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538853 | |||||||
chr22:20538907 | G | T | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.156+1703G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538907 | |||||||
chr22:20538981 | A | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0050 others(2): Show |
5 | HG01891.hp2 HG01978.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+1777A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20538981 | |||||||
chr22:20539287 | T | TG | 11 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0308 others(8): Show |
12 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+2086dupG | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20539287 | ||||||
chr22:20539326 | G | A | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.156+2122G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539326 | |||||||
chr22:20539480 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.156+2276G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539480 | |||||||
chr22:20539482 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(156): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.156+2278T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539482 | |||||||
chr22:20539627 | C | G | 1 | a0001c0002t0002g0250 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.156+2423C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539627 | |||||||
chr22:20539884 | C | T | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+2680C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539884 | |||||||
chr22:20539915 | G | C | 1 | a0002c0003t0001g0178 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.156+2711G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20539915 | |||||||
chr22:20540135 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.156+2931G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20540135 | |||||||
chr22:20540508 | A | G | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.156+3304A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20540508 | |||||||
chr22:20540737 | C | A | 9 | a0001c0001t0001g0130 a0001c0001t0003g0001 a0001c0001t0003g0005 others(6): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+3533C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20540737 | |||||||
chr22:20540871 | T | C | 60 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(57): Show |
64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.156+3667T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20540871 | |||||||
chr22:20540892 | T | TCAA | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.156+3713_156+3715d others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20540892 | ||||||
chr22:20540976 | C | T | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0025t0001g0085 |
3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.156+3772C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20540976 | |||||||
chr22:20541085 | A | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0104 a0012c0018t0001g0030 |
3 | HG01891.hp2 HG02280.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.156+3881A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541085 | |||||||
chr22:20541239 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.156+4035A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541239 | |||||||
chr22:20541342 | A | G | 2 | a0002c0003t0001g0152 a0015c0015t0011g0177 |
2 | NA19086.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.156+4138A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541342 | |||||||
chr22:20541353 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.156+4149A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541353 | |||||||
chr22:20541486 | G | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0198 |
2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.156+4282G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541486 | |||||||
chr22:20541584 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.156+4380G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541584 | |||||||
chr22:20541640 | C | T | 9 | a0002c0003t0001g0131 a0002c0003t0001g0132 a0002c0003t0001g0147 others(6): Show |
9 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.156+4436C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541640 | |||||||
chr22:20541650 | A | AT | 15 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0002t0002g0250 others(12): Show |
16 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.156+4464dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20541650 | ||||||
chr22:20541650 | AT | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(183): Show |
196 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.156+4464delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20541650 | ||||||
chr22:20541751 | ACAATTAC others(14): Show |
A | 1 | a0002c0014t0001g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.156+4549_156+4569d others(23): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20541751 | ||||||
chr22:20541870 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.156+4666G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541870 | |||||||
chr22:20541884 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0025t0001g0085 |
3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.156+4680G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541884 | |||||||
chr22:20541934 | C | T | 16 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0194 others(13): Show |
16 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.156+4730C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20541934 | |||||||
chr22:20542275 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.156+5071A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542275 | |||||||
chr22:20542406 | G | A | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.156+5202G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542406 | |||||||
chr22:20542613 | T | C | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.156+5409T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542613 | |||||||
chr22:20542639 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.156+5435G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542639 | |||||||
chr22:20542694 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.156+5490T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542694 | |||||||
chr22:20542739 | C | G | 2 | a0001c0002t0002g0234 a0001c0002t0002g0246 |
2 | NA18983.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.156+5535C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542739 | |||||||
chr22:20542780 | C | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.156+5576C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542780 | |||||||
chr22:20542945 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(8): Show |
12 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+5741T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20542945 | |||||||
chr22:20543035 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.156+5831G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543035 | |||||||
chr22:20543110 | TTTGTGTG others(12): Show |
T | 1 | a0001c0001t0001g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.156+5908_156+5926d others(21): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543110 | ||||||
chr22:20543111 | T | TTG | 9 | a0001c0001t0001g0166 a0001c0001t0001g0292 a0001c0001t0001g0308 others(6): Show |
9 | HG00280.hp2 HG02165.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+5947_156+5948d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | T | TTGTG | 23 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0111 others(20): Show |
23 | HG00621.hp1 HG02074.hp1 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.156+5945_156+5948d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | T | TTGTGTG | 37 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(34): Show |
39 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.156+5943_156+5948d others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | T | TTGTGTGT others(1): Show |
9 | a0001c0002t0002g0009 a0001c0002t0002g0193 a0001c0002t0002g0235 others(6): Show |
10 | HG00408.hp1 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+5941_156+5948d others(10): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | T | TTGTGTGT others(3): Show |
1 | a0001c0002t0002g0011 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.156+5939_156+5948d others(12): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | TTGTG | T | 10 | a0001c0001t0001g0065 a0001c0004t0001g0139 a0001c0004t0001g0140 others(7): Show |
11 | HG01261.hp2 HG02258.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.156+5945_156+5948d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | TTGTGTG | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0105 a0001c0001t0001g0108 |
3 | HG03834.hp1 HG04184.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.156+5943_156+5948d others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | TTGTGTGT others(5): Show |
T | 1 | a0002c0003t0001g0148 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.156+5937_156+5948d others(14): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | TTGTGTGT others(7): Show |
T | 10 | a0001c0001t0001g0274 a0001c0001t0006g0278 a0001c0001t0006g0282 others(7): Show |
10 | HG01255.hp1 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+5935_156+5948d others(16): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | TTGTGTGT others(9): Show |
T | 10 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(7): Show |
10 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+5933_156+5948d others(18): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | TTGTGTGT others(11): Show |
T | 6 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0204 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+5931_156+5948d others(20): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | TTGTGTGT others(13): Show |
T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(160): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.156+5929_156+5948d others(22): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | TTGTGTGT others(15): Show |
T | 1 | a0001c0001t0001g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.156+5927_156+5948d others(24): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543111 | TTGTGTGT others(19): Show |
T | 1 | a0001c0001t0001g0097 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.156+5923_156+5948d others(28): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543111 | ||||||
chr22:20543142 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.156+5938T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543142 | |||||||
chr22:20543202 | C | CT | 6 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0303 others(3): Show |
7 | HG01109.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+6024dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | ||||||
chr22:20543202 | CT | C | 12 | a0001c0001t0001g0105 a0001c0001t0001g0291 a0001c0001t0001g0292 others(9): Show |
13 | HG00741.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.156+6024delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | ||||||
chr22:20543202 | CTT | C | 18 | a0001c0001t0001g0315 a0001c0004t0001g0139 a0001c0004t0001g0140 others(15): Show |
18 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.156+6023_156+6024d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | ||||||
chr22:20543202 | CTTT | C | 39 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(36): Show |
40 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.156+6022_156+6024d others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | ||||||
chr22:20543202 | CTTTT | C | 14 | a0001c0001t0001g0035 a0001c0001t0001g0045 a0001c0001t0001g0061 others(11): Show |
14 | HG00558.hp2 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.156+6021_156+6024d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | ||||||
chr22:20543202 | CTTTTT | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(145): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.156+6020_156+6024d others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | ||||||
chr22:20543202 | CTTTTTT | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0092 others(3): Show |
6 | HG01256.hp2 HG01346.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+6019_156+6024d others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | ||||||
chr22:20543202 | CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0281 others(7): Show |
10 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.156+6017_156+6024d others(10): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | ||||||
chr22:20543202 | CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0001g0274 a0001c0002t0002g0214 a0001c0002t0002g0218 others(3): Show |
6 | HG01255.hp1 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+6015_156+6024d others(12): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | ||||||
chr22:20543202 | CTTTTTTT others(4): Show |
C | 58 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(55): Show |
62 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.156+6014_156+6024d others(13): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20543202 | ||||||
chr22:20543272 | C | T | 7 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(4): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.156+6068C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543272 | |||||||
chr22:20543359 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.156+6155C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543359 | |||||||
chr22:20543559 | C | T | 273 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(270): Show |
288 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.156+6355C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543559 | |||||||
chr22:20543561 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.156+6357T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543561 | |||||||
chr22:20543596 | C | T | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+6392C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543596 | |||||||
chr22:20543597 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.156+6393G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543597 | |||||||
chr22:20543627 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.156+6423G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543627 | |||||||
chr22:20543718 | C | T | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.156+6514C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543718 | |||||||
chr22:20543833 | T | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(158): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.156+6629T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543833 | |||||||
chr22:20543853 | C | T | 11 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0308 others(8): Show |
12 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+6649C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543853 | |||||||
chr22:20543870 | T | G | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.156+6666T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20543870 | |||||||
chr22:20544036 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.156+6832T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544036 | |||||||
chr22:20544115 | G | A | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.156+6911G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544115 | |||||||
chr22:20544120 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(8): Show |
12 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+6916T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544120 | |||||||
chr22:20544221 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0198 |
2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.156+7017C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544221 | |||||||
chr22:20544388 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.157-7048G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544388 | |||||||
chr22:20544394 | G | A | 1 | a0001c0001t0001g0002 | 3 | HG02280.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.157-7042G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544394 | |||||||
chr22:20544403 | C | T | 5 | a0001c0002t0002g0214 a0001c0002t0002g0217 a0001c0002t0002g0218 others(2): Show |
5 | HG00544.hp2 NA18941.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.157-7033C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544403 | |||||||
chr22:20544470 | C | A | 1 | a0003c0012t0001g0310 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.157-6966C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544470 | |||||||
chr22:20544528 | G | A | 11 | a0001c0001t0001g0292 a0001c0004t0001g0139 a0001c0004t0001g0140 others(8): Show |
11 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-6908G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544528 | |||||||
chr22:20544632 | C | T | 1 | a0001c0002t0002g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.157-6804C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544632 | |||||||
chr22:20544669 | A | C | 59 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0002t0002g0009 others(56): Show |
63 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.157-6767A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544669 | |||||||
chr22:20544729 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.157-6707T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544729 | |||||||
chr22:20544870 | TA | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-6563delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20544870 | ||||||
chr22:20544899 | G | A | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.157-6537G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544899 | |||||||
chr22:20544967 | G | A | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.157-6469G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20544967 | |||||||
chr22:20545029 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(187): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.157-6407G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545029 | |||||||
chr22:20545076 | A | G | 12 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0308 others(9): Show |
13 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157-6360A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545076 | |||||||
chr22:20545347 | C | T | 62 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(59): Show |
66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.157-6089C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545347 | |||||||
chr22:20545418 | G | A | 60 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(57): Show |
64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.157-6018G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545418 | |||||||
chr22:20545473 | C | CA | 12 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(9): Show |
13 | HG02135.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157-5943dupA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20545473 | ||||||
chr22:20545473 | C | CAAAAA | 46 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(43): Show |
50 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.157-5947_157-5943d others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20545473 | ||||||
chr22:20545473 | C | CAAAAAA | 11 | a0001c0002t0002g0192 a0001c0002t0002g0223 a0001c0002t0002g0227 others(8): Show |
11 | HG00621.hp1 HG00621.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-5948_157-5943d others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20545473 | ||||||
chr22:20545473 | CA | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(191): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.157-5943delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20545473 | ||||||
chr22:20545568 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.157-5868C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545568 | |||||||
chr22:20545674 | T | A | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.157-5762T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545674 | |||||||
chr22:20545684 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.157-5752G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545684 | |||||||
chr22:20545689 | T | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.157-5747T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545689 | |||||||
chr22:20545704 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.157-5732G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545704 | |||||||
chr22:20545787 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(187): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.157-5649T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20545787 | |||||||
chr22:20546044 | G | A | 1 | a0002c0003t0001g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157-5392G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546044 | |||||||
chr22:20546189 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.157-5247T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546189 | |||||||
chr22:20546290 | G | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(160): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.157-5146G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546290 | |||||||
chr22:20546322 | A | C | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.157-5114A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546322 | |||||||
chr22:20546379 | G | A | 1 | a0003c0012t0001g0310 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.157-5057G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546379 | |||||||
chr22:20546493 | T | G | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.157-4943T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546493 | |||||||
chr22:20546502 | G | GT | 88 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0023 others(85): Show |
94 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.157-4926dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20546502 | ||||||
chr22:20546502 | G | GTT | 22 | a0001c0001t0001g0038 a0001c0001t0001g0134 a0001c0001t0001g0135 others(19): Show |
22 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.157-4927_157-4926d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20546502 | ||||||
chr22:20546511 | G | T | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(274): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.157-4925G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546511 | |||||||
chr22:20546642 | G | A | 1 | a0001c0004t0001g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.157-4794G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546642 | |||||||
chr22:20546657 | C | T | 11 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(8): Show |
12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.157-4779C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546657 | |||||||
chr22:20546714 | C | T | 1 | a0001c0002t0002g0012 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.157-4722C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546714 | |||||||
chr22:20546757 | C | CA | 3 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 |
3 | HG01261.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.157-4678dupA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20546757 | ||||||
chr22:20546789 | C | T | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-4647C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20546789 | |||||||
chr22:20547063 | CAT | C | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.157-4372_157-4371d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547063 | |||||||
chr22:20547133 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.157-4303A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547133 | |||||||
chr22:20547228 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.157-4208T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547228 | |||||||
chr22:20547235 | C | T | 1 | a0001c0002t0002g0012 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.157-4201C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547235 | |||||||
chr22:20547333 | G | A | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-4103G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547333 | |||||||
chr22:20547363 | T | C | 11 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(8): Show |
12 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.157-4073T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547363 | |||||||
chr22:20547409 | G | C | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.157-4027G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547409 | |||||||
chr22:20547410 | A | G | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-4026A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547410 | |||||||
chr22:20547500 | A | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0082 |
2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.157-3936A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547500 | |||||||
chr22:20547511 | G | A | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-3925G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547511 | |||||||
chr22:20547519 | C | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.157-3917C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547519 | |||||||
chr22:20547628 | G | GCTAACAC others(13): Show |
1 | a0001c0001t0001g0311 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.157-3805_157-3786d others(22): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20547628 | ||||||
chr22:20547692 | C | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.157-3744C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547692 | |||||||
chr22:20547748 | G | A | 1 | a0001c0004t0001g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.157-3688G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547748 | |||||||
chr22:20547754 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | NA18971.hp2 NA19066.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.157-3682C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547754 | |||||||
chr22:20547830 | A | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0191 a0001c0001t0001g0199 others(5): Show |
9 | HG02145.hp2 HG02258.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.157-3606A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547830 | |||||||
chr22:20547978 | C | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.157-3458C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20547978 | |||||||
chr22:20548152 | TTTTTTTG | T | 60 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(57): Show |
64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.157-3265_157-3259d others(9): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr22 | 20548152 | ||||||
chr22:20548231 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0069 |
3 | HG02040.hp1 NA18747.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.157-3205G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20548231 | |||||||
chr22:20548585 | C | T | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-2851C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20548585 | |||||||
chr22:20548693 | T | C | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.157-2743T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20548693 | |||||||
chr22:20549123 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(187): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.157-2313C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549123 | |||||||
chr22:20549152 | T | C | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.157-2284T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549152 | |||||||
chr22:20549154 | G | A | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.157-2282G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549154 | |||||||
chr22:20549230 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.157-2206T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549230 | |||||||
chr22:20549231 | G | A | 3 | a0001c0001t0001g0290 a0004c0009t0001g0211 a0004c0009t0001g0212 |
3 | HG01258.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.157-2205G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549231 | |||||||
chr22:20549409 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-2027G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549409 | |||||||
chr22:20549495 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.157-1941T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549495 | |||||||
chr22:20549576 | C | G | 73 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(70): Show |
78 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.157-1860C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549576 | |||||||
chr22:20549744 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0050 others(2): Show |
5 | HG01891.hp2 HG01978.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-1692C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549744 | |||||||
chr22:20549768 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.157-1668G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549768 | |||||||
chr22:20549786 | G | C | 73 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(70): Show |
78 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.157-1650G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549786 | |||||||
chr22:20549977 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0104 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.157-1459A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20549977 | |||||||
chr22:20550389 | G | A | 1 | a0003c0005t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.157-1047G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550389 | |||||||
chr22:20550584 | C | T | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.157-852C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550584 | |||||||
chr22:20550742 | G | A | 1 | a0002c0003t0001g0182 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.157-694G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550742 | |||||||
chr22:20550775 | T | G | 12 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0308 others(9): Show |
13 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.157-661T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550775 | |||||||
chr22:20550795 | A | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.157-641A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550795 | |||||||
chr22:20550801 | T | C | 321 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(318): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.157-635T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550801 | |||||||
chr22:20550918 | T | C | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-518T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550918 | |||||||
chr22:20550922 | G | A | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.157-514G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550922 | |||||||
chr22:20550945 | C | T | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.157-491C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20550945 | |||||||
chr22:20551280 | C | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0191 a0001c0001t0001g0200 others(4): Show |
8 | HG02145.hp2 HG02258.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.157-156C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20551280 | |||||||
chr22:20551288 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.157-148G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20551288 | |||||||
chr22:20551333 | A | G | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-103A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20551333 | |||||||
chr22:20551335 | G | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0037 others(8): Show |
12 | HG00408.hp2 HG00423.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.157-101G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20551335 | |||||||
chr22:20551359 | C | T | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-77C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2/17 | chr22 | 20551359 | |||||||
chr22:20551623 | A | C | 1 | a0009c0013t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.208+136A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20551623 | |||||||
chr22:20551664 | C | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.208+177C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20551664 | |||||||
chr22:20551732 | A | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0112 a0011c0019t0001g0089 |
3 | HG01099.hp1 HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.208+245A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20551732 | |||||||
chr22:20551765 | C | G | 1 | a0001c0001t0001g0025 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.208+278C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20551765 | |||||||
chr22:20552055 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.208+568A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552055 | |||||||
chr22:20552079 | C | T | 1 | a0001c0002t0002g0242 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.208+592C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552079 | |||||||
chr22:20552080 | G | A | 9 | a0001c0001t0001g0130 a0001c0001t0003g0001 a0001c0001t0003g0005 others(6): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.208+593G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552080 | |||||||
chr22:20552096 | C | G | 1 | a0001c0002t0002g0269 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.208+609C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552096 | |||||||
chr22:20552167 | C | T | 11 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0308 others(8): Show |
12 | HG02165.hp1 HG02258.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.208+680C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552167 | |||||||
chr22:20552185 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.208+698C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552185 | |||||||
chr22:20552190 | G | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.208+703G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552190 | |||||||
chr22:20552509 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.209-636G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552509 | |||||||
chr22:20552661 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.209-484C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552661 | |||||||
chr22:20552713 | A | G | 2 | a0005c0007t0001g0277 a0005c0007t0001g0279 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.209-432A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552713 | |||||||
chr22:20552838 | T | C | 2 | a0001c0002t0002g0235 a0001c0002t0002g0236 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.209-307T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552838 | |||||||
chr22:20552933 | A | G | 1 | a0001c0002t0002g0259 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.209-212A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20552933 | |||||||
chr22:20553016 | T | C | 134 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(131): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.209-129T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20553016 | |||||||
chr22:20553119 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209-26G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 3/17 | chr22 | 20553119 | |||||||
chr22:20553294 | G | A | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.238+120G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553294 | |||||||
chr22:20553363 | CTG | C | 10 | a0001c0001t0001g0196 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
10 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+192_238+193del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr22 | 20553363 | ||||||
chr22:20553432 | C | G | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.238+258C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553432 | |||||||
chr22:20553729 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.238+555G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553729 | |||||||
chr22:20553778 | T | C | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.238+604T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553778 | |||||||
chr22:20553825 | C | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0001g0099 |
3 | HG01081.hp1 HG01256.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.238+651C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553825 | |||||||
chr22:20553828 | G | A | 163 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(160): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.238+654G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553828 | |||||||
chr22:20553959 | C | G | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.238+785C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553959 | |||||||
chr22:20553965 | T | C | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.238+791T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20553965 | |||||||
chr22:20554066 | C | G | 1 | a0001c0001t0001g0276 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.239-870C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554066 | |||||||
chr22:20554228 | C | T | 60 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(57): Show |
64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.239-708C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554228 | |||||||
chr22:20554276 | T | G | 1 | a0001c0001t0001g0194 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.239-660T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554276 | |||||||
chr22:20554415 | A | C | 163 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(160): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.239-521A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554415 | |||||||
chr22:20554445 | A | C | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.239-491A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554445 | |||||||
chr22:20554449 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.239-487G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554449 | |||||||
chr22:20554526 | C | T | 1 | a0001c0002t0002g0232 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.239-410C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554526 | |||||||
chr22:20554581 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0308 |
2 | HG02165.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.239-355G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554581 | |||||||
chr22:20554640 | G | A | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.239-296G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554640 | |||||||
chr22:20554700 | T | A | 2 | a0002c0003t0001g0152 a0015c0015t0011g0177 |
2 | NA19086.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.239-236T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554700 | |||||||
chr22:20554706 | T | C | 134 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(131): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.239-230T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554706 | |||||||
chr22:20554844 | C | T | 1 | a0001c0002t0002g0222 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.239-92C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554844 | |||||||
chr22:20554864 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.239-72C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554864 | |||||||
chr22:20554919 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0316 a0001c0001t0001g0317 others(8): Show |
11 | HG00642.hp1 HG01081.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.239-17C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 4/17 | chr22 | 20554919 | |||||||
chr22:20555161 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0077 a0001c0001t0001g0082 others(2): Show |
5 | HG02074.hp2 HG02155.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+13C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555161 | |||||||
chr22:20555202 | A | G | 1 | a0008c0008t0002g0215 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.451+54A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555202 | |||||||
chr22:20555239 | A | G | 1 | a0002c0003t0001g0172 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.451+91A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555239 | |||||||
chr22:20555257 | G | A | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.451+109G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555257 | |||||||
chr22:20555354 | C | T | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.451+206C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555354 | |||||||
chr22:20555387 | G | C | 45 | a0001c0001t0001g0166 a0001c0023t0001g0181 a0002c0003t0001g0007 others(42): Show |
46 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.451+239G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555387 | |||||||
chr22:20555744 | C | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG01081.hp1 HG01256.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+596C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555744 | |||||||
chr22:20555746 | G | T | 46 | a0001c0001t0001g0166 a0001c0001t0001g0315 a0001c0023t0001g0181 others(43): Show |
47 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.451+598G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555746 | |||||||
chr22:20555753 | G | T | 10 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(7): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+605G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555753 | |||||||
chr22:20555790 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0303 |
2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.451+642C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555790 | |||||||
chr22:20555804 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.451+656C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555804 | |||||||
chr22:20555878 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.451+730C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555878 | |||||||
chr22:20555906 | A | G | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.451+758A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555906 | |||||||
chr22:20555933 | G | C | 2 | a0002c0003t0001g0157 a0002c0003t0001g0178 |
2 | HG00140.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.451+785G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555933 | |||||||
chr22:20555934 | G | A | 60 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.451+786G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555934 | |||||||
chr22:20555960 | C | T | 1 | a0001c0002t0002g0253 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.451+812C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555960 | |||||||
chr22:20555977 | C | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.451+829C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20555977 | |||||||
chr22:20556012 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.451+864C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556012 | |||||||
chr22:20556034 | C | T | 1 | a0003c0005t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.451+886C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556034 | |||||||
chr22:20556195 | C | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(2): Show |
5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+1047C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556195 | |||||||
chr22:20556302 | G | GT | 53 | a0001c0001t0001g0019 a0001c0001t0001g0088 a0001c0001t0001g0226 others(50): Show |
57 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.451+1170dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20556302 | ||||||
chr22:20556302 | G | GTT | 11 | a0001c0001t0001g0231 a0001c0002t0002g0192 a0001c0002t0002g0217 others(8): Show |
11 | HG00423.hp2 HG02135.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+1169_451+1170d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20556302 | ||||||
chr22:20556302 | GT | G | 86 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0040 others(83): Show |
89 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.451+1170delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20556302 | ||||||
chr22:20556396 | A | G | 163 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(160): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.451+1248A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556396 | |||||||
chr22:20556466 | A | G | 1 | a0003c0005t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.451+1318A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556466 | |||||||
chr22:20556478 | T | G | 1 | a0002c0003t0001g0153 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.451+1330T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556478 | |||||||
chr22:20556546 | C | T | 60 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(57): Show |
64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.451+1398C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556546 | |||||||
chr22:20556579 | C | T | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.451+1431C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556579 | |||||||
chr22:20556596 | A | G | 133 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(130): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.451+1448A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556596 | |||||||
chr22:20556673 | C | G | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.451+1525C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556673 | |||||||
chr22:20556793 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.451+1645A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556793 | |||||||
chr22:20556962 | T | C | 1 | a0001c0002t0002g0259 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.451+1814T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20556962 | |||||||
chr22:20557094 | A | C | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.451+1946A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557094 | |||||||
chr22:20557270 | G | A | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.451+2122G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557270 | |||||||
chr22:20557386 | T | G | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.451+2238T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557386 | |||||||
chr22:20557390 | C | G | 1 | a0001c0001t0001g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451+2242C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557390 | |||||||
chr22:20557469 | A | C | 72 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(69): Show |
77 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.451+2321A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557469 | |||||||
chr22:20557742 | G | A | 1 | a0001c0002t0002g0270 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.451+2594G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557742 | |||||||
chr22:20557881 | C | T | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.451+2733C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557881 | |||||||
chr22:20557888 | C | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.451+2740C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557888 | |||||||
chr22:20557922 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01070.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.451+2774C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557922 | |||||||
chr22:20557966 | C | T | 61 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.451+2818C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557966 | |||||||
chr22:20557967 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+2819G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557967 | |||||||
chr22:20557996 | C | T | 1 | a0003c0012t0001g0310 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.451+2848C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20557996 | |||||||
chr22:20558116 | GAA | G | 5 | a0001c0004t0001g0142 a0001c0004t0001g0143 a0001c0004t0001g0144 others(2): Show |
5 | HG02615.hp1 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+2972_451+2973d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20558116 | ||||||
chr22:20558341 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.451+3193G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558341 | |||||||
chr22:20558506 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0191 a0001c0001t0001g0200 others(4): Show |
8 | HG02145.hp2 HG02258.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.451+3358A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558506 | |||||||
chr22:20558555 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0086 others(2): Show |
6 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.451+3407A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558555 | |||||||
chr22:20558592 | T | C | 5 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(2): Show |
5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+3444T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558592 | |||||||
chr22:20558683 | A | G | 163 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(160): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.451+3535A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558683 | |||||||
chr22:20558708 | G | A | 9 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(6): Show |
10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+3560G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558708 | |||||||
chr22:20558725 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.451+3577T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558725 | |||||||
chr22:20558799 | G | A | 1 | a0001c0002t0002g0237 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.451+3651G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558799 | |||||||
chr22:20558920 | A | G | 1 | a0003c0005t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.451+3772A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20558920 | |||||||
chr22:20559048 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.451+3900C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559048 | |||||||
chr22:20559064 | G | A | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.451+3916G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559064 | |||||||
chr22:20559223 | A | G | 163 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(160): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.451+4075A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559223 | |||||||
chr22:20559241 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.451+4093C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559241 | |||||||
chr22:20559262 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.451+4114G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559262 | |||||||
chr22:20559345 | TAGAAGCT others(8): Show |
T | 2 | a0001c0002t0002g0234 a0001c0002t0002g0246 |
2 | NA18983.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.451+4202_451+4216d others(17): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20559345 | ||||||
chr22:20559470 | G | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0014 others(190): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.451+4322G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559470 | |||||||
chr22:20559558 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.451+4410A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559558 | |||||||
chr22:20559591 | G | A | 46 | a0001c0001t0001g0166 a0001c0001t0001g0315 a0001c0023t0001g0181 others(43): Show |
47 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.451+4443G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559591 | |||||||
chr22:20559659 | C | T | 1 | a0002c0003t0001g0171 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.451+4511C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559659 | |||||||
chr22:20559785 | C | G | 1 | a0001c0001t0001g0291 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.451+4637C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559785 | |||||||
chr22:20559929 | G | A | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.452-4521G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20559929 | |||||||
chr22:20560261 | C | CTATTAT | 59 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0002t0002g0009 others(56): Show |
63 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.452-4171_452-4166d others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20560261 | ||||||
chr22:20560340 | C | T | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.452-4110C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560340 | |||||||
chr22:20560372 | C | G | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.452-4078C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560372 | |||||||
chr22:20560402 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0006t0001g0133 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-4048C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560402 | |||||||
chr22:20560411 | C | T | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.452-4039C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560411 | |||||||
chr22:20560412 | G | A | 58 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0002t0002g0009 others(55): Show |
62 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.452-4038G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560412 | |||||||
chr22:20560421 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.452-4029C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560421 | |||||||
chr22:20560453 | C | T | 1 | a0001c0002t0002g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.452-3997C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560453 | |||||||
chr22:20560454 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0025t0001g0085 |
3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.452-3996G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560454 | |||||||
chr22:20560470 | G | A | 60 | a0001c0001t0001g0040 a0001c0001t0001g0065 a0001c0001t0001g0105 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.452-3980G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560470 | |||||||
chr22:20560474 | A | G | 25 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0061 others(22): Show |
25 | HG00558.hp2 HG01261.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.452-3976A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560474 | |||||||
chr22:20560484 | C | T | 2 | a0002c0003t0001g0149 a0002c0003t0001g0150 |
2 | NA18956.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.452-3966C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560484 | |||||||
chr22:20560509 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.452-3941C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560509 | |||||||
chr22:20560528 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.452-3922G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560528 | |||||||
chr22:20560558 | T | C | 1 | a0001c0002t0002g0269 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.452-3892T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560558 | |||||||
chr22:20560671 | C | T | 60 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.452-3779C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560671 | |||||||
chr22:20560776 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.452-3674G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20560776 | |||||||
chr22:20561101 | A | G | 1 | a0002c0003t0001g0156 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.452-3349A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561101 | |||||||
chr22:20561241 | C | T | 2 | a0001c0001t0001g0306 a0001c0001t0001g0311 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.452-3209C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561241 | |||||||
chr22:20561248 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(4): Show |
8 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-3202C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561248 | |||||||
chr22:20561330 | C | G | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.452-3120C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561330 | |||||||
chr22:20561344 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.452-3106C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561344 | |||||||
chr22:20561345 | G | A | 1 | a0002c0003t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.452-3105G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561345 | |||||||
chr22:20561388 | C | T | 56 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(53): Show |
59 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.452-3062C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561388 | |||||||
chr22:20561435 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.452-3015G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561435 | |||||||
chr22:20561452 | G | A | 3 | a0001c0001t0001g0086 a0001c0001t0001g0120 a0001c0001t0009g0087 |
3 | HG02809.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.452-2998G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561452 | |||||||
chr22:20561505 | T | C | 3 | a0001c0004t0001g0143 a0001c0004t0001g0144 a0001c0004t0001g0146 |
3 | HG02615.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.452-2945T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561505 | |||||||
chr22:20561549 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.452-2901T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561549 | |||||||
chr22:20561572 | A | G | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.452-2878A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561572 | |||||||
chr22:20561702 | C | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-2748C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561702 | |||||||
chr22:20561703 | G | A | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.452-2747G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561703 | |||||||
chr22:20561941 | T | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
5 | NA18943.hp1 NA18950.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-2509T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561941 | |||||||
chr22:20561944 | T | C | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.452-2506T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561944 | |||||||
chr22:20561986 | CTCAA | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0025t0001g0085 |
3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.452-2456_452-2453d others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20561986 | ||||||
chr22:20561996 | C | T | 1 | a0001c0002t0002g0248 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.452-2454C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20561996 | |||||||
chr22:20562046 | A | T | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.452-2404A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562046 | |||||||
chr22:20562230 | G | C | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.452-2220G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562230 | |||||||
chr22:20562333 | A | G | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.452-2117A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562333 | |||||||
chr22:20562380 | A | T | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.452-2070A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562380 | |||||||
chr22:20562407 | CAG | C | 61 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.452-2040_452-2039d others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20562407 | ||||||
chr22:20562465 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.452-1985A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562465 | |||||||
chr22:20562545 | C | T | 9 | a0001c0001t0001g0130 a0001c0001t0003g0001 a0001c0001t0003g0005 others(6): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-1905C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562545 | |||||||
chr22:20562586 | G | C | 1 | a0001c0002t0002g0240 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.452-1864G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562586 | |||||||
chr22:20562641 | C | G | 1 | a0001c0002t0002g0240 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.452-1809C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562641 | |||||||
chr22:20562682 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.452-1768G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562682 | |||||||
chr22:20562780 | A | G | 122 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(119): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.452-1670A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562780 | |||||||
chr22:20562863 | C | T | 1 | a0002c0003t0001g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.452-1587C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20562863 | |||||||
chr22:20563017 | C | T | 61 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.452-1433C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563017 | |||||||
chr22:20563035 | C | CA | 6 | a0001c0001t0001g0100 a0001c0001t0001g0274 a0001c0001t0005g0288 others(3): Show |
6 | HG01255.hp1 HG01346.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.452-1403dupA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20563035 | ||||||
chr22:20563035 | CA | C | 70 | a0001c0001t0001g0102 a0001c0001t0001g0120 a0001c0001t0001g0226 others(67): Show |
75 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.452-1403delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr22 | 20563035 | ||||||
chr22:20563118 | A | T | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.452-1332A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563118 | |||||||
chr22:20563143 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.452-1307A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563143 | |||||||
chr22:20563240 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(8): Show |
12 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-1210A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563240 | |||||||
chr22:20563241 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0005g0288 a0001c0001t0005g0289 |
3 | HG01346.hp1 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.452-1209T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563241 | |||||||
chr22:20563397 | A | G | 9 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(6): Show |
10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-1053A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563397 | |||||||
chr22:20563544 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.452-906C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563544 | |||||||
chr22:20563544 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0090 a0001c0001t0001g0112 others(1): Show |
4 | HG01099.hp1 HG01516.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-906C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563544 | |||||||
chr22:20563775 | C | T | 2 | a0004c0009t0001g0211 a0004c0009t0001g0212 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.452-675C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563775 | |||||||
chr22:20563965 | C | T | 1 | a0002c0003t0001g0182 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.452-485C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20563965 | |||||||
chr22:20564117 | C | T | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.452-333C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564117 | |||||||
chr22:20564175 | C | T | 1 | a0001c0001t0013g0284 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.452-275C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564175 | |||||||
chr22:20564198 | C | G | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.452-252C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564198 | |||||||
chr22:20564228 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.452-222T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564228 | |||||||
chr22:20564231 | T | G | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.452-219T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564231 | |||||||
chr22:20564240 | A | G | 2 | a0007c0011t0001g0137 a0007c0011t0001g0138 |
2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.452-210A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564240 | |||||||
chr22:20564343 | C | T | 1 | a0001c0002t0002g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.452-107C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 5/17 | chr22 | 20564343 | |||||||
chr22:20564778 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.690+90G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20564778 | |||||||
chr22:20564880 | C | T | 1 | a0009c0013t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.690+192C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20564880 | |||||||
chr22:20565019 | A | G | 163 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(160): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.690+331A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565019 | |||||||
chr22:20565085 | G | A | 1 | a0002c0003t0001g0154 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.690+397G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565085 | |||||||
chr22:20565089 | C | T | 1 | a0003c0005t0010g0299 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.690+401C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565089 | |||||||
chr22:20565090 | G | A | 61 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.690+402G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565090 | |||||||
chr22:20565109 | T | C | 167 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(164): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.690+421T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565109 | |||||||
chr22:20565117 | C | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.690+429C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565117 | |||||||
chr22:20565148 | A | G | 1 | a0001c0001t0005g0288 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.690+460A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565148 | |||||||
chr22:20565159 | G | A | 10 | a0001c0001t0001g0233 a0001c0002t0002g0011 a0001c0002t0002g0224 others(7): Show |
11 | HG00621.hp2 HG02056.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.690+471G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565159 | |||||||
chr22:20565430 | T | G | 2 | a0001c0002t0002g0214 a0001c0002t0002g0218 |
2 | NA19002.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.690+742T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565430 | |||||||
chr22:20565468 | C | T | 46 | a0001c0001t0001g0166 a0001c0001t0001g0315 a0001c0023t0001g0181 others(43): Show |
47 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.690+780C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565468 | |||||||
chr22:20565709 | C | A | 1 | a0001c0001t0001g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.691-758C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565709 | |||||||
chr22:20565709 | C | T | 1 | a0001c0001t0005g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.691-758C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565709 | |||||||
chr22:20565757 | C | T | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.691-710C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565757 | |||||||
chr22:20565896 | C | CCCAGGCA others(11): Show |
2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.691-568_691-551dup others(18): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr22 | 20565896 | ||||||
chr22:20565912 | G | C | 51 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(48): Show |
52 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.691-555G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565912 | |||||||
chr22:20565922 | G | A | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.691-545G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20565922 | |||||||
chr22:20566030 | C | CT | 78 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0031 others(75): Show |
81 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.691-417dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr22 | 20566030 | ||||||
chr22:20566030 | CT | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0014 others(16): Show |
22 | HG02083.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.691-417delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr22 | 20566030 | ||||||
chr22:20566030 | CTT | C | 11 | a0001c0001t0001g0308 a0001c0001t0005g0288 a0001c0001t0005g0289 others(8): Show |
12 | HG01346.hp1 HG02165.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.691-418_691-417del others(2): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr22 | 20566030 | ||||||
chr22:20566030 | CTTTT | C | 60 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.691-420_691-417del others(4): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr22 | 20566030 | ||||||
chr22:20566101 | G | A | 2 | a0001c0001t0001g0204 a0003c0005t0001g0261 |
2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.691-366G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566101 | |||||||
chr22:20566149 | C | A | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.691-318C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566149 | |||||||
chr22:20566284 | C | T | 1 | a0003c0005t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.691-183C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566284 | |||||||
chr22:20566339 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.691-128C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566339 | |||||||
chr22:20566407 | A | G | 2 | a0001c0002t0002g0234 a0001c0002t0002g0246 |
2 | NA18983.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.691-60A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566407 | |||||||
chr22:20566415 | G | A | 7 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(4): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-52G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 6/17 | chr22 | 20566415 | |||||||
chr22:20566969 | C | T | 1 | a0002c0003t0001g0294 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1041+152C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20566969 | |||||||
chr22:20567035 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1041+218A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567035 | |||||||
chr22:20567052 | A | G | 163 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(160): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1041+235A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567052 | |||||||
chr22:20567068 | G | T | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1041+251G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567068 | |||||||
chr22:20567168 | G | A | 8 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(5): Show |
9 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1041+351G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567168 | |||||||
chr22:20567436 | C | G | 9 | a0001c0002t0002g0009 a0001c0002t0002g0012 a0001c0002t0002g0235 others(6): Show |
11 | HG00423.hp2 HG00738.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1041+619C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567436 | |||||||
chr22:20567499 | G | C | 1 | a0001c0001t0001g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1041+682G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567499 | |||||||
chr22:20567585 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1041+768G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567585 | |||||||
chr22:20567606 | G | T | 122 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(119): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1041+789G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567606 | |||||||
chr22:20567672 | A | C | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1042-849A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567672 | |||||||
chr22:20567869 | T | G | 9 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0002c0003t0001g0013 others(6): Show |
10 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042-652T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567869 | |||||||
chr22:20567943 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1042-578G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20567943 | |||||||
chr22:20568029 | T | C | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1042-492T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568029 | |||||||
chr22:20568183 | C | T | 2 | a0001c0001t0001g0285 a0001c0001t0013g0284 |
2 | HG01952.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1042-338C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568183 | |||||||
chr22:20568231 | G | A | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1042-290G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568231 | |||||||
chr22:20568289 | G | C | 1 | a0001c0002t0002g0256 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1042-232G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568289 | |||||||
chr22:20568409 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1042-112G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568409 | |||||||
chr22:20568438 | A | G | 2 | a0001c0001t0001g0306 a0001c0001t0001g0311 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1042-83A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 7/17 | chr22 | 20568438 | |||||||
chr22:20568923 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1152+292T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20568923 | |||||||
chr22:20568932 | G | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0231 |
2 | NA18939.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1152+301G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20568932 | |||||||
chr22:20568960 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1152+329C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20568960 | |||||||
chr22:20569074 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1152+443C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569074 | |||||||
chr22:20569419 | G | A | 1 | a0002c0003t0001g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1152+788G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569419 | |||||||
chr22:20569459 | C | T | 1 | a0001c0002t0002g0256 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1152+828C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569459 | |||||||
chr22:20569460 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1152+829G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569460 | |||||||
chr22:20569583 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1152+952G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569583 | |||||||
chr22:20569635 | TGAG | T | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(11): Show |
14 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1152+1009_1152+101 others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20569635 | ||||||
chr22:20569741 | A | G | 163 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(160): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1152+1110A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569741 | |||||||
chr22:20569872 | G | T | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1152+1241G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20569872 | |||||||
chr22:20570066 | C | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0203 a0001c0001t0001g0262 |
4 | HG02145.hp2 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+1435C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570066 | |||||||
chr22:20570087 | C | T | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1152+1456C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570087 | |||||||
chr22:20570088 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0002g0043 |
2 | HG02300.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1152+1457G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570088 | |||||||
chr22:20570192 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1152+1561T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570192 | |||||||
chr22:20570224 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1152+1593C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570224 | |||||||
chr22:20570269 | G | A | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0303 |
3 | HG02818.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1152+1638G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570269 | |||||||
chr22:20570304 | T | G | 61 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1152+1673T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570304 | |||||||
chr22:20570315 | G | A | 1 | a0001c0002t0004g0021 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1152+1684G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570315 | |||||||
chr22:20570318 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1152+1687C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570318 | |||||||
chr22:20570333 | G | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0203 a0001c0001t0001g0262 |
4 | HG02145.hp2 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+1702G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570333 | |||||||
chr22:20570393 | CT | C | 84 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(81): Show |
85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1152+1778delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570393 | ||||||
chr22:20570414 | C | T | 2 | a0001c0002t0002g0192 a0001c0002t0002g0260 |
2 | NA18948.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1152+1783C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570414 | |||||||
chr22:20570494 | C | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0280 |
2 | HG00741.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1152+1863C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570494 | |||||||
chr22:20570526 | G | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0006t0001g0133 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+1895G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570526 | |||||||
chr22:20570614 | C | A | 1 | a0003c0005t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1152+1983C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570614 | |||||||
chr22:20570652 | A | C | 1 | a0001c0002t0002g0012 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1152+2021A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570652 | |||||||
chr22:20570726 | T | TTTTC | 14 | a0001c0002t0002g0193 a0001c0002t0002g0214 a0001c0002t0002g0217 others(11): Show |
14 | HG00408.hp1 HG01069.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1152+2115_1152+211 others(8): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570726 | ||||||
chr22:20570726 | T | TTTTCTTT others(1): Show |
15 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(12): Show |
15 | HG00140.hp2 HG00621.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1152+2111_1152+211 others(12): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570726 | ||||||
chr22:20570746 | C | CTT | 6 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0302 others(3): Show |
7 | HG01109.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152+2144_1152+214 others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | ||||||
chr22:20570746 | C | CTTTTTTT others(5): Show |
1 | a0002c0003t0001g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1152+2134_1152+214 others(16): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | ||||||
chr22:20570746 | CT | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(112): Show |
120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1152+2145delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | ||||||
chr22:20570746 | CTT | C | 12 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0054 others(9): Show |
12 | HG00733.hp1 HG01070.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1152+2144_1152+214 others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | ||||||
chr22:20570746 | CTTT | C | 7 | a0001c0001t0001g0135 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG00741.hp2 HG01071.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152+2143_1152+214 others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | ||||||
chr22:20570746 | CTTTTTTT others(3): Show |
C | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1152+2136_1152+214 others(14): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | ||||||
chr22:20570746 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0005g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1152+2135_1152+214 others(15): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | ||||||
chr22:20570746 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0063 a0001c0001t0005g0288 |
2 | HG02698.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1152+2134_1152+214 others(16): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | ||||||
chr22:20570746 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1152+2133_1152+214 others(17): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | ||||||
chr22:20570746 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1152+2130_1152+214 others(20): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570746 | ||||||
chr22:20570747 | T | TTTC | 50 | a0001c0001t0001g0198 a0001c0001t0001g0231 a0001c0001t0001g0233 others(47): Show |
53 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1152+2118_1152+211 others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570747 | ||||||
chr22:20570747 | T | TTTCTTTC | 27 | a0001c0001t0001g0166 a0002c0003t0001g0007 a0002c0003t0001g0149 others(24): Show |
28 | HG00438.hp2 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1152+2118_1152+211 others(11): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570747 | ||||||
chr22:20570747 | T | TTTCTTTC others(4): Show |
1 | a0001c0023t0001g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1152+2118_1152+211 others(15): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570747 | ||||||
chr22:20570748 | T | TTCTTTCT others(3): Show |
1 | a0002c0003t0001g0132 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1152+2118_1152+211 others(14): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570748 | ||||||
chr22:20570749 | T | TCTTTCTT others(2): Show |
4 | a0001c0001t0001g0105 a0002c0003t0001g0162 a0002c0003t0001g0164 others(1): Show |
4 | HG00280.hp2 HG00735.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+2118_1152+211 others(13): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570749 | |||||||
chr22:20570750 | T | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(13): Show |
16 | HG00140.hp2 HG01069.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1152+2119T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570750 | |||||||
chr22:20570751 | T | C | 38 | a0001c0001t0001g0166 a0001c0004t0001g0142 a0001c0004t0001g0143 others(35): Show |
39 | HG00438.hp2 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1152+2120T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570751 | |||||||
chr22:20570753 | T | C | 2 | a0001c0001t0001g0315 a0002c0003t0001g0164 |
2 | HG00099.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1152+2122T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570753 | |||||||
chr22:20570754 | T | C | 1 | a0002c0003t0001g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1152+2123T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570754 | |||||||
chr22:20570755 | T | C | 2 | a0002c0003t0001g0170 a0002c0003t0001g0171 |
2 | HG00733.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1152+2124T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570755 | |||||||
chr22:20570757 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1152+2126T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570757 | |||||||
chr22:20570773 | T | TTTTTTTT others(3): Show |
1 | a0001c0001t0001g0311 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1152+2145_1152+214 others(14): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20570773 | ||||||
chr22:20570814 | G | A | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1152+2183G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570814 | |||||||
chr22:20570830 | A | G | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1152+2199A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570830 | |||||||
chr22:20570850 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1152+2219C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570850 | |||||||
chr22:20570917 | A | G | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1152+2286A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20570917 | |||||||
chr22:20571060 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1152+2429G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571060 | |||||||
chr22:20571067 | C | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(2): Show |
5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152+2436C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571067 | |||||||
chr22:20571102 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1152+2471A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571102 | |||||||
chr22:20571275 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1152+2644A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571275 | |||||||
chr22:20571337 | C | G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(6): Show |
10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1152+2706C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571337 | |||||||
chr22:20571347 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1152+2716G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571347 | |||||||
chr22:20571373 | C | T | 1 | a0003c0005t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1152+2742C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571373 | |||||||
chr22:20571428 | C | T | 1 | a0003c0005t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1152+2797C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571428 | |||||||
chr22:20571473 | G | T | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1152+2842G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571473 | |||||||
chr22:20571658 | C | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1152+3027C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20571658 | |||||||
chr22:20572008 | G | C | 315 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(312): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1153-3105G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572008 | |||||||
chr22:20572214 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1153-2899A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572214 | |||||||
chr22:20572272 | G | A | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0274 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1153-2841G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572272 | |||||||
chr22:20572338 | G | A | 61 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1153-2775G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572338 | |||||||
chr22:20572517 | T | G | 2 | a0004c0009t0001g0211 a0004c0009t0001g0212 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1153-2596T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572517 | |||||||
chr22:20572526 | C | T | 61 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(58): Show |
65 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1153-2587C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572526 | |||||||
chr22:20572601 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1153-2512C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572601 | |||||||
chr22:20572637 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1153-2476A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572637 | |||||||
chr22:20572639 | G | GC | 163 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(160): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1153-2473dupC | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20572639 | ||||||
chr22:20572739 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1153-2374C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572739 | |||||||
chr22:20572786 | G | A | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1153-2327G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572786 | |||||||
chr22:20572812 | C | T | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1153-2301C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572812 | |||||||
chr22:20572839 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1153-2274C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572839 | |||||||
chr22:20572966 | C | CT | 73 | a0001c0001t0001g0123 a0001c0001t0001g0134 a0001c0001t0001g0135 others(70): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1153-2130dupT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | 20572966 | ||||||
chr22:20572971 | T | TC | 5 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(2): Show |
5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-2142_1153-214 others(5): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20572971 | |||||||
chr22:20573046 | G | T | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-2067G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573046 | |||||||
chr22:20573092 | C | T | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-2021C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573092 | |||||||
chr22:20573247 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1153-1866C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573247 | |||||||
chr22:20573256 | C | T | 61 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1153-1857C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573256 | |||||||
chr22:20573326 | G | A | 9 | a0001c0001t0001g0196 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
9 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1153-1787G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573326 | |||||||
chr22:20573388 | G | A | 58 | a0001c0001t0001g0233 a0001c0002t0002g0009 a0001c0002t0002g0010 others(55): Show |
62 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1153-1725G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573388 | |||||||
chr22:20573429 | T | C | 62 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(59): Show |
66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1153-1684T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573429 | |||||||
chr22:20573515 | G | A | 61 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1153-1598G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573515 | |||||||
chr22:20573711 | C | T | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-1402C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573711 | |||||||
chr22:20573717 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1153-1396T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573717 | |||||||
chr22:20573753 | T | G | 1 | a0002c0003t0001g0296 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1153-1360T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573753 | |||||||
chr22:20573830 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1153-1283C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573830 | |||||||
chr22:20573843 | C | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1153-1270C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573843 | |||||||
chr22:20573878 | C | T | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-1235C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573878 | |||||||
chr22:20573947 | C | T | 12 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(9): Show |
13 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1153-1166C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573947 | |||||||
chr22:20573979 | G | A | 61 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1153-1134G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20573979 | |||||||
chr22:20574271 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1153-842A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574271 | |||||||
chr22:20574278 | A | G | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-835A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574278 | |||||||
chr22:20574284 | G | A | 1 | a0001c0002t0002g0234 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1153-829G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574284 | |||||||
chr22:20574330 | G | A | 2 | a0007c0011t0001g0137 a0007c0011t0001g0138 |
2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1153-783G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574330 | |||||||
chr22:20574401 | T | G | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1153-712T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574401 | |||||||
chr22:20574497 | T | C | 3 | a0001c0001t0001g0274 a0006c0010t0001g0273 a0006c0010t0001g0275 |
3 | HG01255.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1153-616T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574497 | |||||||
chr22:20574522 | C | T | 125 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(122): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1153-591C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574522 | |||||||
chr22:20574604 | G | T | 3 | a0001c0002t0002g0223 a0001c0002t0002g0257 a0001c0002t0002g0259 |
3 | NA18955.hp2 NA18957.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1153-509G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574604 | |||||||
chr22:20574661 | C | T | 5 | a0001c0002t0002g0224 a0001c0002t0002g0225 a0001c0002t0002g0249 others(2): Show |
5 | HG00621.hp2 HG02071.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153-452C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574661 | |||||||
chr22:20574690 | T | G | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1153-423T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574690 | |||||||
chr22:20574787 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1153-326C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574787 | |||||||
chr22:20574797 | T | C | 64 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(61): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1153-316T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574797 | |||||||
chr22:20574808 | T | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0190 others(11): Show |
17 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1153-305T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574808 | |||||||
chr22:20574999 | C | G | 161 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0105 others(158): Show |
169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1153-114C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20574999 | |||||||
chr22:20575055 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1153-58C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | chr22 | 20575055 | |||||||
chr22:20575368 | CT | C | 17 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0191 others(14): Show |
17 | HG00735.hp2 HG00738.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1272+151delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20575368 | ||||||
chr22:20575469 | G | A | 1 | a0009c0013t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1272+237G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575469 | |||||||
chr22:20575495 | C | A | 149 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(146): Show |
156 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1272+263C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575495 | |||||||
chr22:20575593 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1272+361C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575593 | |||||||
chr22:20575627 | C | T | 61 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1272+395C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575627 | |||||||
chr22:20575637 | C | T | 51 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(48): Show |
52 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.1272+405C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575637 | |||||||
chr22:20575688 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1272+456A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575688 | |||||||
chr22:20575692 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1272+460C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575692 | |||||||
chr22:20575705 | C | T | 1 | a0001c0002t0002g0250 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1272+473C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575705 | |||||||
chr22:20575721 | AT | A | 7 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(4): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+495delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20575721 | ||||||
chr22:20575768 | CA | C | 123 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(120): Show |
129 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1272+546delA | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20575768 | ||||||
chr22:20575778 | A | C | 64 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(61): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1272+546A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575778 | |||||||
chr22:20575788 | C | T | 7 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(4): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+556C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20575788 | |||||||
chr22:20576055 | CT | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
9 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272+827delT | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20576055 | ||||||
chr22:20576253 | T | C | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1272+1021T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576253 | |||||||
chr22:20576329 | G | A | 2 | a0003c0005t0001g0309 a0003c0012t0001g0310 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1272+1097G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576329 | |||||||
chr22:20576433 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1272+1201C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576433 | |||||||
chr22:20576691 | TGGG | T | 61 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1272+1462_1272+146 others(7): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20576691 | ||||||
chr22:20576704 | T | G | 64 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(61): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1272+1472T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576704 | |||||||
chr22:20576807 | T | C | 64 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(61): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1272+1575T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576807 | |||||||
chr22:20576836 | G | C | 64 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(61): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1272+1604G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576836 | |||||||
chr22:20576891 | G | T | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1272+1659G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576891 | |||||||
chr22:20576929 | G | T | 1 | a0001c0001t0007g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1272+1697G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20576929 | |||||||
chr22:20577015 | T | C | 2 | a0004c0009t0001g0211 a0004c0009t0001g0212 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1272+1783T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577015 | |||||||
chr22:20577111 | C | T | 1 | a0001c0002t0002g0192 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1272+1879C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577111 | |||||||
chr22:20577170 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1272+1938G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577170 | |||||||
chr22:20577203 | T | G | 7 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(4): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+1971T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577203 | |||||||
chr22:20577257 | G | A | 11 | a0001c0002t0002g0009 a0001c0002t0002g0012 a0001c0002t0002g0221 others(8): Show |
13 | HG00423.hp2 HG00738.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+2025G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577257 | |||||||
chr22:20577456 | C | T | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1272+2224C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577456 | |||||||
chr22:20577726 | C | G | 1 | a0002c0003t0001g0176 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1272+2494C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577726 | |||||||
chr22:20577823 | G | A | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1272+2591G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577823 | |||||||
chr22:20577876 | T | A | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1272+2644T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577876 | |||||||
chr22:20577880 | G | A | 1 | a0001c0001t0005g0288 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1272+2648G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577880 | |||||||
chr22:20577936 | T | A | 1 | a0001c0002t0002g0222 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1272+2704T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577936 | |||||||
chr22:20577951 | T | G | 8 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(5): Show |
9 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272+2719T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577951 | |||||||
chr22:20577955 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1272+2723G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577955 | |||||||
chr22:20577992 | C | T | 165 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(162): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1272+2760C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20577992 | |||||||
chr22:20578028 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1272+2796G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578028 | |||||||
chr22:20578053 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1272+2821T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578053 | |||||||
chr22:20578167 | C | T | 1 | a0001c0001t0005g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1272+2935C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578167 | |||||||
chr22:20578171 | C | T | 7 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(4): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+2939C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578171 | |||||||
chr22:20578176 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1272+2944C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578176 | |||||||
chr22:20578271 | A | G | 1 | a0013c0024t0001g0307 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1272+3039A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578271 | |||||||
chr22:20578354 | C | A | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1272+3122C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578354 | |||||||
chr22:20578393 | C | A | 7 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(4): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+3161C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578393 | |||||||
chr22:20578425 | C | T | 64 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(61): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1272+3193C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578425 | |||||||
chr22:20578426 | C | G | 126 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(123): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1272+3194C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578426 | |||||||
chr22:20578606 | G | A | 1 | a0001c0002t0002g0222 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1272+3374G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578606 | |||||||
chr22:20578676 | CAG | C | 9 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(6): Show |
10 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272+3445_1272+344 others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578676 | |||||||
chr22:20578825 | A | G | 2 | a0007c0011t0001g0137 a0007c0011t0001g0138 |
2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1272+3593A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578825 | |||||||
chr22:20578910 | CCT | C | 55 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(52): Show |
58 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1272+3681_1272+368 others(6): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20578910 | ||||||
chr22:20578922 | C | T | 1 | a0001c0002t0002g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1273-3689C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578922 | |||||||
chr22:20578949 | G | A | 1 | a0003c0005t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1273-3662G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20578949 | |||||||
chr22:20579149 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1273-3462C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579149 | |||||||
chr22:20579381 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1273-3230C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579381 | |||||||
chr22:20579448 | C | T | 2 | a0001c0001t0001g0285 a0001c0001t0013g0284 |
2 | HG01952.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1273-3163C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579448 | |||||||
chr22:20579497 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0302 a0001c0001t0001g0304 others(1): Show |
5 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273-3114C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579497 | |||||||
chr22:20579536 | C | T | 1 | a0001c0001t0002g0287 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1273-3075C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579536 | |||||||
chr22:20579614 | T | C | 65 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(62): Show |
70 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1273-2997T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579614 | |||||||
chr22:20579753 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1273-2858C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579753 | |||||||
chr22:20579757 | C | G | 1 | a0001c0001t0002g0287 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1273-2854C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579757 | |||||||
chr22:20579952 | T | A | 65 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(62): Show |
70 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1273-2659T>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20579952 | |||||||
chr22:20580124 | C | T | 7 | a0002c0003t0001g0013 a0002c0003t0001g0293 a0002c0003t0001g0294 others(4): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1273-2487C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580124 | |||||||
chr22:20580221 | C | T | 10 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 others(7): Show |
10 | HG01261.hp2 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1273-2390C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580221 | |||||||
chr22:20580338 | C | G | 1 | a0001c0001t0001g0202 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1273-2273C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580338 | |||||||
chr22:20580476 | AG | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0050 others(2): Show |
5 | HG01891.hp2 HG01978.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273-2133delG | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr22 | 20580476 | ||||||
chr22:20580685 | T | G | 62 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0233 others(59): Show |
67 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1273-1926T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580685 | |||||||
chr22:20580722 | C | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1273-1889C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580722 | |||||||
chr22:20580897 | G | A | 1 | a0001c0001t0001g0002 | 3 | HG02280.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1273-1714G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580897 | |||||||
chr22:20580942 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1273-1669G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580942 | |||||||
chr22:20580986 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1273-1625G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20580986 | |||||||
chr22:20581089 | A | G | 285 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(282): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1273-1522A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581089 | |||||||
chr22:20581105 | G | A | 6 | a0002c0003t0001g0293 a0002c0003t0001g0294 a0002c0003t0001g0295 others(3): Show |
6 | HG02451.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1273-1506G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581105 | |||||||
chr22:20581159 | C | T | 1 | a0002c0003t0001g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1273-1452C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581159 | |||||||
chr22:20581253 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0025t0001g0085 |
3 | HG02630.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1273-1358G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581253 | |||||||
chr22:20581386 | A | C | 48 | a0001c0001t0001g0118 a0001c0001t0001g0166 a0001c0001t0001g0285 others(45): Show |
49 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.1273-1225A>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581386 | |||||||
chr22:20581398 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1273-1213G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581398 | |||||||
chr22:20581430 | G | A | 2 | a0001c0001t0005g0288 a0001c0001t0005g0289 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1273-1181G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581430 | |||||||
chr22:20581444 | G | A | 124 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(121): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1273-1167G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581444 | |||||||
chr22:20581659 | G | A | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0276 others(9): Show |
12 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1273-952G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581659 | |||||||
chr22:20581805 | G | C | 1 | a0001c0001t0001g0283 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1273-806G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581805 | |||||||
chr22:20581840 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1273-771C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581840 | |||||||
chr22:20581920 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1273-691C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20581920 | |||||||
chr22:20582047 | C | T | 29 | a0001c0001t0001g0014 a0001c0001t0001g0274 a0001c0001t0001g0276 others(26): Show |
30 | HG00741.hp2 HG01109.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.1273-564C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582047 | |||||||
chr22:20582228 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1273-383G>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582228 | |||||||
chr22:20582411 | G | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | HG02257.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1273-200G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582411 | |||||||
chr22:20582533 | T | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
11 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1273-78T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582533 | |||||||
chr22:20582534 | G | A | 3 | a0001c0004t0001g0139 a0001c0004t0001g0140 a0001c0004t0001g0141 |
3 | HG01261.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1273-77G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582534 | |||||||
chr22:20582565 | C | T | 1 | a0001c0002t0002g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1273-46C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582565 | |||||||
chr22:20582586 | G | A | 6 | a0001c0004t0001g0142 a0001c0004t0001g0144 a0001c0004t0001g0145 others(3): Show |
6 | HG02723.hp1 HG02895.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1273-25G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 9/17 | chr22 | 20582586 | |||||||
chr22:20582764 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1409+17G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 10/17 | chr22 | 20582764 | |||||||
chr22:20583314 | C | T | 60 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1673-16C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 12/17 | chr22 | 20583314 | |||||||
chr22:20583406 | CACAGCCC others(8): Show |
C | 1 | a0015c0015t0011g0177 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1736+14_1736+28del others(15): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 13/17 | chr22 | 20583406 | |||||||
chr22:20583893 | G | A | 61 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(58): Show |
66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1737-466G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 13/17 | chr22 | 20583893 | |||||||
chr22:20583940 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1737-419A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 13/17 | chr22 | 20583940 | |||||||
chr22:20584090 | A | G | 64 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(61): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1737-269A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 13/17 | chr22 | 20584090 | |||||||
chr22:20584175 | G | C | 1 | a0002c0003t0001g0314 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1737-184G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 13/17 | chr22 | 20584175 | |||||||
chr22:20584485 | T | C | 64 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0312 others(61): Show |
69 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1803+60T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 14/17 | chr22 | 20584485 | |||||||
chr22:20584488 | T | C | 197 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(194): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1803+63T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 14/17 | chr22 | 20584488 | |||||||
chr22:20584836 | G | A | 64 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(61): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1804-19G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 14/17 | chr22 | 20584836 | |||||||
chr22:20585321 | C | A | 61 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(58): Show |
66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.2131+54C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585321 | |||||||
chr22:20585330 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2131+63C>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585330 | |||||||
chr22:20585344 | A | G | 1 | a0001c0002t0002g0221 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2131+77A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585344 | |||||||
chr22:20585345 | G | C | 1 | a0002c0003t0001g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2131+78G>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585345 | |||||||
chr22:20585422 | C | T | 1 | a0001c0004t0001g0140 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2131+155C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585422 | |||||||
chr22:20585468 | A | T | 2 | a0001c0001t0001g0058 a0001c0001t0002g0043 |
2 | HG02300.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2131+201A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585468 | |||||||
chr22:20585524 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2132-204T>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585524 | |||||||
chr22:20585562 | CCAGGCTT others(19): Show |
C | 1 | a0015c0015t0011g0177 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2132-165_2132-140d others(28): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 16/17 | chr22 | 20585562 | |||||||
chr22:20585921 | T | C | 162 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0051 others(159): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.2230+95T>C | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20585921 | |||||||
chr22:20585923 | C | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(2): Show |
5 | HG02615.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.2230+97C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20585923 | |||||||
chr22:20585979 | A | G | 64 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(61): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.2230+153A>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20585979 | |||||||
chr22:20585985 | C | G | 125 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(122): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2230+159C>G | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20585985 | |||||||
chr22:20586004 | C | T | 61 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(58): Show |
66 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.2230+178C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586004 | |||||||
chr22:20586044 | C | T | 2 | a0001c0004t0001g0142 a0001c0004t0001g0145 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2230+218C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586044 | |||||||
chr22:20586190 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
9 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2230+364G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586190 | |||||||
chr22:20586223 | A | T | 1 | a0015c0015t0011g0177 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2231-345A>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586223 | |||||||
chr22:20586278 | C | CCAGAGCT others(9): Show |
1 | a0001c0001t0001g0048 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2231-257_2231-242d others(18): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr22 | 20586278 | ||||||
chr22:20586278 | CCAGAGCT others(9): Show |
C | 9 | a0001c0001t0001g0274 a0001c0001t0009g0087 a0001c0002t0002g0252 others(6): Show |
9 | HG01192.hp2 HG01255.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2231-257_2231-242d others(18): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr22 | 20586278 | ||||||
chr22:20586430 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2231-138C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586430 | |||||||
chr22:20586474 | G | A | 1 | a0001c0002t0002g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2231-94G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586474 | |||||||
chr22:20586507 | G | A | 63 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0065 others(60): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.2231-61G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586507 | |||||||
chr22:20586529 | G | A | 1 | a0011c0019t0001g0089 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2231-39G>A | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586529 | |||||||
chr22:20586535 | C | T | 9 | a0001c0001t0001g0130 a0001c0001t0003g0001 a0001c0001t0003g0005 others(6): Show |
12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.2231-33C>T | MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 17/17 | chr22 | 20586535 |