Item | Value |
---|---|
geneid | 9969 |
ensemblid | ENSG00000108510.10 |
hgncid | 22474 |
symbol | MED13 |
name | mediator complex subunit 13 |
refseq_nuc | NM_005121.3 |
refseq_prot | NP_005112.2 |
ensembl_nuc | ENST00000397786.7 |
ensembl_prot | ENSP00000380888.2 |
mane_status | MANE Select |
chr | chr17 |
start | 61942605 |
end | 62065278 |
strand | - |
ver | v1.2 |
region | chr17:61942605-62065278 |
region5000 | chr17:61937605-62070278 |
regionname0 | MED13_chr17_61942605_62065278 |
regionname5000 | MED13_chr17_61937605_62070278 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2174 | 310 | 71 | 43 | 152 | 6 | 36 | 120 | MED13_chr17_61937605_62070278 | MED13 | MSASF others(2169): Show |
chr17 | 61937605 | 62070278 |
a0002 | 0/0 | 2174 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | MSASF others(2169): Show |
chr17 | 61937605 | 62070278 |
a0003 | 0/0 | 2174 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | MSASF others(2169): Show |
chr17 | 61937605 | 62070278 |
a0004 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | MSASF others(2169): Show |
chr17 | 61937605 | 62070278 |
a0005 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | MSASF others(2169): Show |
chr17 | 61937605 | 62070278 |
a0006 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | MSASF others(2169): Show |
chr17 | 61937605 | 62070278 |
a0007 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | MSASF others(2169): Show |
chr17 | 61937605 | 62070278 |
a0008 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | MSASF others(2169): Show |
chr17 | 61937605 | 62070278 |
a0009 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | MSASF others(2169): Show |
chr17 | 61937605 | 62070278 |
a0010 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | MSASF others(2169): Show |
chr17 | 61937605 | 62070278 |
a0011 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | MSASF others(2169): Show |
chr17 | 61937605 | 62070278 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 6522 | 182 | 28 | 31 | 91 | 5 | 26 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0002 | 0/0 | 6522 | 62 | 0 | 1 | 59 | 0 | 2 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0003 | 0/0 | 6522 | 40 | 24 | 8 | 2 | 1 | 5 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0004 | 0/0 | 6522 | 8 | 8 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0006 | 0/0 | 6522 | 5 | 4 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0007 | 0/0 | 6522 | 3 | 3 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0008 | 0/0 | 6522 | 2 | 0 | 0 | 0 | 0 | 2 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0009 | 0/0 | 6522 | 2 | 2 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0012 | 0/0 | 6522 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0015 | 0/0 | 6522 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0016 | 0/0 | 6522 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0017 | 0/1 | 6522 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0018 | 0/0 | 6522 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0001c0021 | 0/0 | 6522 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0002c0005 | 0/0 | 6522 | 7 | 7 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0003c0014 | 0/0 | 6522 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0004c0011 | 0/0 | 6522 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0005c0022 | 0/0 | 6522 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0006c0024 | 0/0 | 6522 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0007c0010 | 0/0 | 6522 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0008c0020 | 0/0 | 6522 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0009c0019 | 0/0 | 6522 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0010c0013 | 0/0 | 6522 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 | ||
a0011c0023 | 0/0 | 6522 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | ATGAG others(6517): Show |
chr17 | 61937605 | 62070278 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 10461 | 103 | 26 | 19 | 47 | 1 | 9 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0002 | 0/0 | 10459 | 45 | 1 | 6 | 26 | 0 | 12 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10454): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0003 | 0/0 | 10462 | 7 | 0 | 3 | 0 | 2 | 2 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10457): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0004 | 0/0 | 10461 | 6 | 0 | 0 | 6 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0007 | 0/0 | 10461 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0008 | 0/0 | 10460 | 2 | 0 | 0 | 1 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10455): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0010 | 0/0 | 10459 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10454): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0011 | 0/0 | 10462 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10457): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0012 | 0/0 | 10459 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10454): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0013 | 0/0 | 10458 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10453): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0014 | 0/0 | 10461 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0015 | 0/0 | 10461 | 2 | 1 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0016 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0018 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0019 | 0/0 | 10459 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10454): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0020 | 0/0 | 10459 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10454): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0021 | 0/0 | 10446 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10441): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0022 | 0/0 | 10460 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10455): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0025 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0001t0027 | 0/0 | 10461 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0002t0001 | 0/0 | 10461 | 56 | 0 | 1 | 53 | 0 | 2 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0002t0009 | 0/0 | 10461 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0002t0011 | 0/0 | 10462 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10457): Show |
chr17 | 61937605 | 62070278 |
a0001c0002t0023 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0002t0024 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0002t0026 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0003t0001 | 0/0 | 10461 | 34 | 20 | 8 | 0 | 1 | 5 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0003t0005 | 0/0 | 10461 | 4 | 4 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0003t0007 | 0/0 | 10461 | 2 | 0 | 0 | 2 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0004t0001 | 0/0 | 10461 | 8 | 8 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0006t0001 | 0/0 | 10461 | 4 | 3 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0006t0028 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0007t0006 | 0/0 | 10459 | 3 | 3 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10454): Show |
chr17 | 61937605 | 62070278 |
a0001c0008t0001 | 0/0 | 10461 | 2 | 0 | 0 | 0 | 0 | 2 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0009t0001 | 0/0 | 10461 | 2 | 2 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0012t0001 | 0/0 | 10461 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0015t0001 | 0/0 | 10461 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0016t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0017t0001 | 0/1 | 10461 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0018t0001 | 0/0 | 10461 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0001c0021t0017 | 0/0 | 10459 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10454): Show |
chr17 | 61937605 | 62070278 |
a0002c0005t0001 | 0/0 | 10461 | 7 | 7 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0003c0014t0014 | 0/0 | 10461 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0004c0011t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0005c0022t0006 | 0/0 | 10459 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10454): Show |
chr17 | 61937605 | 62070278 |
a0006c0024t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0007c0010t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0008c0020t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0009c0019t0008 | 0/0 | 10460 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10455): Show |
chr17 | 61937605 | 62070278 |
a0010c0013t0001 | 0/0 | 10461 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
a0011c0023t0001 | 0/0 | 10461 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | CTCTC others(10456): Show |
chr17 | 61937605 | 62070278 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0008g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0010g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0010g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0011g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0012g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0012g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0013g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0013g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0014g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0015g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0015g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0016g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0018g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0019g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0020g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0021g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0022g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0025g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0001t0027g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0009g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0011g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0023g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0024g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0002t0026g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0007g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0003t0007g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0006t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0006t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0006t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0006t0028g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0007t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0007t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0007t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0008t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0008t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0009t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0009t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0012t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0015t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0016t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0017t0001g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0018t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0001c0021t0017g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0002c0005t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0003c0014t0014g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0004c0011t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0005c0022t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0006c0024t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0007c0010t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0008c0020t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0009c0019t0008g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0010c0013t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
a0011c0023t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0027 | g0167 | EUR | GBR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0292 | EUR | GBR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00438 | hp2 | a0001 | c0003 | t0007 | g0298 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00558 | hp2 | a0001 | c0002 | t0009 | g0049 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00597 | hp2 | a0001 | c0003 | t0007 | g0325 | EAS | CHS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00639 | hp1 | a0001 | c0006 | t0001 | g0115 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0309 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0301 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0299 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0099 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01168 | hp2 | a0001 | c0001 | t0014 | g0286 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0304 | AMR | PUR | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01358 | hp2 | a0003 | c0014 | t0014 | g0287 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0297 | AMR | CLM | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0295 | EUR | IBS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | IBS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01517 | hp1 | a0001 | c0001 | t0022 | g0165 | EUR | IBS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0294 | EUR | IBS | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01884 | hp1 | a0001 | c0003 | t0005 | g0029 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0326 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01891 | hp1 | a0001 | c0004 | t0001 | g0011 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0114 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0052 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0089 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01952 | hp1 | a0001 | c0015 | t0001 | g0096 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01978 | hp1 | a0001 | c0003 | t0001 | g0308 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02027 | hp2 | a0001 | c0001 | t0025 | g0008 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02055 | hp1 | a0001 | c0006 | t0001 | g0116 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02055 | hp2 | a0001 | c0004 | t0001 | g0022 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02056 | hp2 | a0001 | c0001 | t0012 | g0256 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02080 | hp1 | a0001 | c0001 | t0019 | g0243 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02083 | hp1 | a0001 | c0002 | t0024 | g0057 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02145 | hp1 | a0004 | c0011 | t0001 | g0095 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02148 | hp1 | a0001 | c0018 | t0001 | g0076 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0293 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | CDX | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02257 | hp1 | a0005 | c0022 | t0006 | g0281 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02257 | hp2 | a0002 | c0005 | t0001 | g0006 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02280 | hp2 | a0001 | c0001 | t0015 | g0194 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02300 | hp2 | a0001 | c0001 | t0011 | g0016 | AMR | PEL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0109 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02451 | hp2 | a0002 | c0005 | t0001 | g0003 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | KHV | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02572 | hp2 | a0001 | c0009 | t0001 | g0103 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02630 | hp1 | a0001 | c0006 | t0028 | g0102 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02630 | hp2 | a0001 | c0016 | t0001 | g0322 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0105 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0323 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0291 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02717 | hp1 | a0001 | c0003 | t0005 | g0027 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0110 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02723 | hp2 | a0001 | c0004 | t0001 | g0010 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02735 | hp2 | a0001 | c0001 | t0008 | g0318 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0108 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02809 | hp2 | a0002 | c0005 | t0001 | g0230 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02818 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02895 | hp1 | a0001 | c0006 | t0001 | g0100 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02896 | hp2 | a0001 | c0009 | t0001 | g0097 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0098 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02970 | hp1 | a0006 | c0024 | t0001 | g0320 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0113 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02976 | hp1 | a0002 | c0005 | t0001 | g0231 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03017 | hp1 | a0001 | c0008 | t0001 | g0128 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03017 | hp2 | a0001 | c0001 | t0021 | g0254 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03130 | hp2 | a0007 | c0010 | t0001 | g0007 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0302 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03139 | hp2 | a0001 | c0006 | t0001 | g0101 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03209 | hp1 | a0001 | c0003 | t0005 | g0028 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03209 | hp2 | a0002 | c0005 | t0001 | g0004 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03486 | hp1 | a0001 | c0003 | t0005 | g0026 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03486 | hp2 | a0002 | c0005 | t0001 | g0289 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0259 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03491 | hp1 | a0001 | c0003 | t0001 | g0306 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03491 | hp2 | a0001 | c0001 | t0015 | g0156 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03492 | hp2 | a0001 | c0003 | t0001 | g0307 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | ESN | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03540 | hp2 | a0001 | c0007 | t0006 | g0280 | AFR | GWD | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03579 | hp1 | a0001 | c0021 | t0017 | g0283 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03579 | hp2 | a0002 | c0005 | t0001 | g0005 | AFR | MSL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03654 | hp2 | a0001 | c0012 | t0001 | g0305 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0296 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0300 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG03834 | hp2 | a0001 | c0008 | t0001 | g0122 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | BEB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0042 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0266 | SAS | STU | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0104 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | CHB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | CHB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | CHB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18906 | hp2 | a0008 | c0020 | t0001 | g0106 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18942 | hp1 | a0009 | c0019 | t0008 | g0310 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18946 | hp1 | a0001 | c0002 | t0026 | g0053 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18949 | hp2 | a0001 | c0002 | t0023 | g0059 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18956 | hp1 | a0001 | c0001 | t0008 | g0162 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18968 | hp2 | a0001 | c0001 | t0020 | g0247 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18973 | hp2 | a0001 | c0001 | t0018 | g0127 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18982 | hp2 | a0001 | c0001 | t0013 | g0316 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18983 | hp2 | a0001 | c0001 | t0016 | g0177 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18994 | hp1 | a0001 | c0002 | t0011 | g0063 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19005 | hp1 | a0001 | c0002 | t0009 | g0090 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0117 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19030 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19043 | hp2 | a0010 | c0013 | t0001 | g0215 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19058 | hp2 | a0011 | c0023 | t0001 | g0131 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19079 | hp2 | a0001 | c0001 | t0010 | g0265 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19081 | hp1 | a0001 | c0001 | t0013 | g0229 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19084 | hp1 | a0001 | c0001 | t0012 | g0258 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19091 | hp2 | a0001 | c0001 | t0010 | g0264 | EAS | JPT | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19240 | hp1 | a0001 | c0007 | t0006 | g0282 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0303 | AFR | ASW | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ASW | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0111 | AFR | ACB | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | USA | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | USA | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0112 | AFR | USA | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | USA | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA21309 | hp1 | a0001 | c0007 | t0006 | g0279 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | LWK | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
homoSapiens | chm13v2 | a0001 | c0017 | t0001 | g0009 | REF | REF | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0143 | REF | REF | MED13_chr17_61937605_62070278 | MED13 | chr17 | 61937605 | 62070278 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:61952972 | G | A | 1 | a0002 | 7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
missense_variant | MODERATE | c.6110C>T | p.Ala2037Val | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/30 | 6183/10461 | 6110/6525 | 2037/2174 | chr17 | 61952972 | |||
chr17:61956452 | T | A | 1 | a0010 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.5510A>T | p.Lys1837Ile | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 24/30 | 5583/10461 | 5510/6525 | 1837/2174 | chr17 | 61956452 | |||
chr17:61962895 | C | T | 1 | a0010 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.4921G>A | p.Val1641Ile | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/30 | 4994/10461 | 4921/6525 | 1641/2174 | chr17 | 61962895 | |||
chr17:61965027 | G | A | 1 | a0003 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.4823C>T | p.Pro1608Leu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/30 | 4896/10461 | 4823/6525 | 1608/2174 | chr17 | 61965027 | |||
chr17:61984758 | T | C | 1 | a0009 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.2584A>G | p.Thr862Ala | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 14/30 | 2657/10461 | 2584/6525 | 862/2174 | chr17 | 61984758 | |||
chr17:62010647 | T | C | 1 | a0005 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1870A>G | p.Lys624Glu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/30 | 1943/10461 | 1870/6525 | 624/2174 | chr17 | 62010647 | |||
chr17:62010859 | G | A | 1 | a0008 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1658C>T | p.Ser553Leu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/30 | 1731/10461 | 1658/6525 | 553/2174 | chr17 | 62010859 | |||
chr17:62033864 | A | C | 1 | a0004 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.737T>G | p.Leu246Trp | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/30 | 810/10461 | 737/6525 | 246/2174 | chr17 | 62033864 | |||
chr17:62033887 | C | A | 1 | a0011 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.714G>T | p.Gln238His | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/30 | 787/10461 | 714/6525 | 238/2174 | chr17 | 62033887 | |||
chr17:62063085 | T | C | 1 | a0006 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.283A>G | p.Ile95Val | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/30 | 356/10461 | 283/6525 | 95/2174 | chr17 | 62063085 | |||
chr17:62063099 | C | T | 1 | a0007 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.269G>A | p.Ser90Asn | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/30 | 342/10461 | 269/6525 | 90/2174 | chr17 | 62063099 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:61953049 | G | A | 1 | a0001c0012 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.6033C>T | p.Ile2011Ile | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/30 | 6106/10461 | 6033/6525 | 2011/2174 | chr17 | 61953049 | |||
chr17:61955422 | A | G | 1 | a0007c0010 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.5928T>C | p.Tyr1976Tyr | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/30 | 6001/10461 | 5928/6525 | 1976/2174 | chr17 | 61955422 | |||
chr17:61955530 | C | T | 2 | a0001c0007 a0005c0022 |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
synonymous_variant | LOW | c.5820G>A | p.Thr1940Thr | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/30 | 5893/10461 | 5820/6525 | 1940/2174 | chr17 | 61955530 | |||
chr17:61961088 | T | C | 1 | a0001c0016 | 1 | HG02630.hp2 | splice_region_variant&synonymous_variant | LOW | c.5259A>G | p.Arg1753Arg | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/30 | 5332/10461 | 5259/6525 | 1753/2174 | chr17 | 61961088 | |||
chr17:61962857 | G | A | 1 | a0001c0018 | 1 | HG02148.hp1 | synonymous_variant | LOW | c.4959C>T | p.Asp1653Asp | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/30 | 5032/10461 | 4959/6525 | 1653/2174 | chr17 | 61962857 | |||
chr17:61962968 | C | T | 8 | a0001c0002 a0001c0003 a0001c0006 others(5): Show |
113 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
synonymous_variant | LOW | c.4848G>A | p.Thr1616Thr | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/30 | 4921/10461 | 4848/6525 | 1616/2174 | chr17 | 61962968 | |||
chr17:61965074 | T | C | 1 | a0001c0004 | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.4776A>G | p.Leu1592Leu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/30 | 4849/10461 | 4776/6525 | 1592/2174 | chr17 | 61965074 | |||
chr17:61965329 | T | C | 1 | a0001c0015 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.4521A>G | p.Ala1507Ala | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/30 | 4594/10461 | 4521/6525 | 1507/2174 | chr17 | 61965329 | |||
chr17:61965407 | G | A | 1 | a0001c0016 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.4443C>T | p.Ala1481Ala | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/30 | 4516/10461 | 4443/6525 | 1481/2174 | chr17 | 61965407 | |||
chr17:61966568 | T | C | 2 | a0001c0002 a0001c0018 |
63 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
synonymous_variant | LOW | c.4275A>G | p.Lys1425Lys | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/30 | 4348/10461 | 4275/6525 | 1425/2174 | chr17 | 61966568 | |||
chr17:62011188 | T | C | 1 | a0001c0006 | 5 | HG00639.hp1 HG02055.hp1 HG02630.hp1 others(2): Show |
synonymous_variant | LOW | c.1329A>G | p.Ala443Ala | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/30 | 1402/10461 | 1329/6525 | 443/2174 | chr17 | 62011188 | |||
chr17:62029621 | T | C | 3 | a0001c0007 a0001c0021 a0005c0022 |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
synonymous_variant | LOW | c.1203A>G | p.Leu401Leu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/30 | 1276/10461 | 1203/6525 | 401/2174 | chr17 | 62029621 | |||
chr17:62031619 | G | A | 1 | a0001c0009 | 2 | HG02572.hp2 HG02896.hp2 |
synonymous_variant | LOW | c.834C>T | p.Tyr278Tyr | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/30 | 907/10461 | 834/6525 | 278/2174 | chr17 | 62031619 | |||
chr17:62052653 | C | G | 1 | a0001c0008 | 2 | HG03017.hp1 HG03834.hp2 |
synonymous_variant | LOW | c.354G>C | p.Leu118Leu | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/30 | 427/10461 | 354/6525 | 118/2174 | chr17 | 62052653 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:61942656 | GT | G | 5 | a0001c0001t0013 a0001c0001t0022 a0001c0007t0006 others(2): Show |
8 | HG01517.hp1 HG02257.hp1 HG03540.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3811delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3811 | chr17 | 61942656 | ||||||
chr17:61942662 | T | G | 2 | a0001c0001t0007 a0001c0003t0007 |
3 | HG00438.hp2 HG00597.hp2 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3806A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3806 | chr17 | 61942662 | ||||||
chr17:61942669 | T | A | 2 | a0001c0001t0020 a0001c0002t0023 |
2 | NA18949.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3799A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3799 | chr17 | 61942669 | ||||||
chr17:61942670 | A | T | 2 | a0001c0001t0014 a0003c0014t0014 |
2 | HG01168.hp2 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3798T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3798 | chr17 | 61942670 | ||||||
chr17:61942732 | G | A | 1 | a0001c0002t0024 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3736C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3736 | chr17 | 61942732 | ||||||
chr17:61942776 | AAAG | A | 7 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(4): Show |
54 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3689_*3691delCTT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3689 | chr17 | 61942776 | ||||||
chr17:61943057 | A | G | 2 | a0001c0001t0010 a0001c0001t0012 |
4 | HG02056.hp2 NA19079.hp2 NA19084.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3411T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 3411 | chr17 | 61943057 | ||||||
chr17:61943631 | A | G | 1 | a0001c0003t0005 | 4 | HG01884.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2837T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2837 | chr17 | 61943631 | ||||||
chr17:61944017 | G | A | 1 | a0001c0001t0015 | 2 | HG02280.hp2 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2451C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2451 | chr17 | 61944017 | ||||||
chr17:61944233 | G | A | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0012 others(4): Show |
59 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2235C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2235 | chr17 | 61944233 | ||||||
chr17:61944234 | T | C | 3 | a0001c0007t0006 a0001c0021t0017 a0005c0022t0006 |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2234A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2234 | chr17 | 61944234 | ||||||
chr17:61944288 | GTAAAGTC others(6): Show |
G | 1 | a0001c0001t0021 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2167_*2179delAATA others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2167 | chr17 | 61944288 | ||||||
chr17:61944372 | G | GT | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(7): Show |
63 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2095dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2095 | chr17 | 61944372 | ||||||
chr17:61944372 | GT | G | 5 | a0001c0001t0008 a0001c0007t0006 a0001c0021t0017 others(2): Show |
8 | HG02257.hp1 HG02735.hp2 HG03540.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2095delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2095 | chr17 | 61944372 | ||||||
chr17:61944392 | G | T | 1 | a0001c0002t0009 | 2 | HG00558.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2076C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2076 | chr17 | 61944392 | ||||||
chr17:61944454 | T | C | 3 | a0001c0007t0006 a0001c0021t0017 a0005c0022t0006 |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2014A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2014 | chr17 | 61944454 | ||||||
chr17:61944530 | T | C | 1 | a0001c0001t0025 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1938A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 1938 | chr17 | 61944530 | ||||||
chr17:61944587 | G | A | 3 | a0001c0007t0006 a0001c0021t0017 a0005c0022t0006 |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1881C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 1881 | chr17 | 61944587 | ||||||
chr17:61944680 | A | G | 1 | a0001c0001t0019 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1788T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 1788 | chr17 | 61944680 | ||||||
chr17:61944780 | G | T | 1 | a0001c0001t0018 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1688C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 1688 | chr17 | 61944780 | ||||||
chr17:61944955 | G | A | 1 | a0001c0002t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1513C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 1513 | chr17 | 61944955 | ||||||
chr17:61945522 | G | A | 3 | a0001c0007t0006 a0001c0021t0017 a0005c0022t0006 |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*946C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 946 | chr17 | 61945522 | ||||||
chr17:61945557 | C | G | 1 | a0001c0001t0004 | 6 | NA18949.hp1 NA18952.hp2 NA18959.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*911G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 911 | chr17 | 61945557 | ||||||
chr17:61945654 | T | C | 1 | a0001c0001t0027 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*814A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 814 | chr17 | 61945654 | ||||||
chr17:61946282 | A | G | 1 | a0001c0021t0017 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 186 | chr17 | 61946282 | ||||||
chr17:61946390 | A | C | 1 | a0001c0001t0016 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 78 | chr17 | 61946390 | ||||||
chr17:61946416 | G | A | 1 | a0001c0006t0028 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*52C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 52 | chr17 | 61946416 | ||||||
chr17:61946435 | G | A | 1 | a0001c0003t0005 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*33C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 33 | chr17 | 61946435 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:61946608 | G | C | 1 | a0001c0001t0007g0002 | 1 | HG01099.hp1 | splice_region_variant&intron_variant | LOW | c.6393-8C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 29/29 | chr17 | 61946608 | |||||||
chr17:61947030 | C | G | 30 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(27): Show |
30 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.6292-13G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947030 | |||||||
chr17:61947194 | G | GT | 8 | a0001c0001t0001g0182 a0001c0001t0001g0210 a0001c0001t0007g0002 others(5): Show |
8 | HG01099.hp1 HG01109.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.6292-178dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947194 | |||||||
chr17:61947199 | T | G | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6292-182A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947199 | |||||||
chr17:61947200 | T | G | 1 | a0001c0002t0001g0083 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.6292-183A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947200 | |||||||
chr17:61947244 | G | T | 1 | a0001c0001t0002g0272 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.6292-227C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947244 | |||||||
chr17:61947341 | T | C | 1 | a0001c0003t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6292-324A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947341 | |||||||
chr17:61947408 | C | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6292-391G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947408 | |||||||
chr17:61947497 | G | T | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.6292-480C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947497 | |||||||
chr17:61947553 | G | A | 1 | a0002c0005t0001g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6292-536C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947553 | |||||||
chr17:61947650 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6292-633C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61947650 | |||||||
chr17:61948006 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.6292-989A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948006 | |||||||
chr17:61948059 | C | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6292-1042G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948059 | |||||||
chr17:61948203 | A | G | 1 | a0001c0003t0007g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6292-1186T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948203 | |||||||
chr17:61948384 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6292-1367A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948384 | |||||||
chr17:61948761 | AAC | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.6292-1746_6292-174 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948761 | |||||||
chr17:61948776 | G | A | 3 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 |
3 | HG03669.hp1 NA18975.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.6292-1759C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948776 | |||||||
chr17:61948808 | C | G | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.6292-1791G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948808 | |||||||
chr17:61948816 | G | C | 1 | a0001c0001t0002g0245 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.6292-1799C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948816 | |||||||
chr17:61948861 | C | A | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6292-1844G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61948861 | |||||||
chr17:61949328 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.6291+1497G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949328 | |||||||
chr17:61949329 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6291+1496C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949329 | |||||||
chr17:61949474 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.6291+1351C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949474 | |||||||
chr17:61949562 | G | A | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6291+1263C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949562 | |||||||
chr17:61949597 | T | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6291+1228A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949597 | |||||||
chr17:61949632 | T | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.6291+1193A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949632 | |||||||
chr17:61949708 | G | A | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.6291+1117C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949708 | |||||||
chr17:61949732 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.6291+1093C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949732 | |||||||
chr17:61949744 | G | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(13): Show |
16 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.6291+1081C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949744 | |||||||
chr17:61949751 | G | A | 5 | a0001c0001t0001g0195 a0001c0001t0001g0199 a0001c0001t0001g0200 others(2): Show |
5 | NA18612.hp2 NA18946.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.6291+1074C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949751 | |||||||
chr17:61949780 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.6291+1045G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949780 | |||||||
chr17:61949824 | T | C | 1 | a0007c0010t0001g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6291+1001A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949824 | |||||||
chr17:61949878 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0007g0002 |
2 | HG01099.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6291+947A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949878 | |||||||
chr17:61949967 | G | A | 1 | a0001c0002t0001g0080 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.6291+858C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61949967 | |||||||
chr17:61950285 | A | C | 1 | a0001c0002t0001g0074 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.6291+540T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950285 | |||||||
chr17:61950385 | G | GT | 10 | a0001c0001t0001g0222 a0001c0003t0001g0023 a0001c0003t0001g0025 others(7): Show |
10 | HG01358.hp1 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.6291+439dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950385 | |||||||
chr17:61950386 | T | G | 1 | a0001c0002t0001g0031 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6291+439A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950386 | |||||||
chr17:61950388 | T | G | 1 | a0001c0012t0001g0305 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.6291+437A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950388 | |||||||
chr17:61950418 | T | C | 1 | a0001c0001t0015g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6291+407A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950418 | |||||||
chr17:61950509 | G | A | 2 | a0001c0001t0003g0290 a0001c0001t0003g0297 |
2 | HG01106.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.6291+316C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950509 | |||||||
chr17:61950516 | T | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6291+309A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950516 | |||||||
chr17:61950532 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6291+293G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950532 | |||||||
chr17:61950703 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.6291+122G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 28/29 | chr17 | 61950703 | |||||||
chr17:61951257 | A | C | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.6118-259T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951257 | |||||||
chr17:61951444 | C | T | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.6118-446G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951444 | |||||||
chr17:61951484 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.6118-486T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951484 | |||||||
chr17:61951515 | T | C | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.6118-517A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951515 | |||||||
chr17:61951665 | T | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6118-667A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951665 | |||||||
chr17:61951975 | G | A | 1 | a0001c0001t0018g0127 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.6118-977C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61951975 | |||||||
chr17:61952168 | C | T | 2 | a0001c0004t0001g0010 a0001c0004t0001g0011 |
2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.6117+797G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952168 | |||||||
chr17:61952172 | C | T | 2 | a0001c0002t0009g0049 a0001c0002t0009g0090 |
2 | HG00558.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.6117+793G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952172 | |||||||
chr17:61952330 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6117+635C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952330 | |||||||
chr17:61952571 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.6117+394G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952571 | |||||||
chr17:61952616 | C | G | 35 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(32): Show |
35 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.6117+349G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952616 | |||||||
chr17:61952753 | C | T | 8 | a0001c0002t0001g0001 a0001c0002t0001g0056 a0001c0002t0001g0080 others(5): Show |
8 | HG02027.hp1 NA18960.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.6117+212G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952753 | |||||||
chr17:61952835 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6117+130G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952835 | |||||||
chr17:61952930 | C | T | 1 | a0001c0003t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6117+35G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 27/29 | chr17 | 61952930 | |||||||
chr17:61953513 | A | G | 2 | a0001c0001t0002g0250 a0001c0001t0002g0263 |
2 | HG01109.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.5969-400T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61953513 | |||||||
chr17:61953795 | A | G | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5969-682T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61953795 | |||||||
chr17:61953929 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | NA19066.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.5969-816G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61953929 | |||||||
chr17:61954083 | G | A | 1 | a0001c0001t0016g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5969-970C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954083 | |||||||
chr17:61954118 | C | T | 1 | a0007c0010t0001g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5969-1005G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954118 | |||||||
chr17:61954132 | G | C | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.5969-1019C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954132 | |||||||
chr17:61954250 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.5968+1132C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954250 | |||||||
chr17:61954413 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.5968+969A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954413 | |||||||
chr17:61954528 | G | A | 7 | a0001c0001t0002g0246 a0001c0001t0002g0261 a0001c0001t0002g0269 others(4): Show |
7 | HG00438.hp1 NA18963.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.5968+854C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954528 | |||||||
chr17:61954670 | G | A | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.5968+712C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954670 | |||||||
chr17:61954714 | C | T | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.5968+668G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954714 | |||||||
chr17:61954770 | G | A | 1 | a0001c0001t0008g0162 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.5968+612C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954770 | |||||||
chr17:61954840 | A | G | 1 | a0007c0010t0001g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5968+542T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954840 | |||||||
chr17:61954903 | T | C | 1 | a0001c0006t0028g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5968+479A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954903 | |||||||
chr17:61954969 | G | A | 1 | a0001c0001t0002g0257 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5968+413C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61954969 | |||||||
chr17:61955003 | A | G | 1 | a0001c0003t0001g0291 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5968+379T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955003 | |||||||
chr17:61955020 | T | G | 60 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(57): Show |
60 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.5968+362A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955020 | |||||||
chr17:61955120 | C | T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5968+262G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955120 | |||||||
chr17:61955147 | CTCT | C | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.5968+232_5968+234d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955147 | |||||||
chr17:61955280 | T | C | 1 | a0001c0002t0001g0031 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5968+102A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955280 | |||||||
chr17:61955289 | A | T | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.5968+93T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955289 | |||||||
chr17:61955304 | TCA | T | 5 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0150 others(2): Show |
5 | HG02155.hp2 HG02523.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.5968+76_5968+77del others(2): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 26/29 | chr17 | 61955304 | |||||||
chr17:61955646 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5782+34C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 25/29 | chr17 | 61955646 | |||||||
chr17:61955855 | T | TA | 34 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0138 others(31): Show |
34 | HG00639.hp1 HG01346.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.5624-18dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 24/29 | chr17 | 61955855 | |||||||
chr17:61955855 | T | TAA | 10 | a0001c0001t0001g0160 a0001c0001t0001g0189 a0001c0001t0001g0315 others(7): Show |
10 | HG00642.hp1 HG01109.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.5624-19_5624-18dup others(2): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 24/29 | chr17 | 61955855 | |||||||
chr17:61955855 | TA | T | 13 | a0001c0001t0001g0150 a0001c0001t0002g0244 a0001c0001t0002g0263 others(10): Show |
13 | HG01109.hp1 HG02451.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.5624-18delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 24/29 | chr17 | 61955855 | |||||||
chr17:61956292 | A | T | 1 | a0001c0001t0016g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5623+47T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 24/29 | chr17 | 61956292 | |||||||
chr17:61956679 | A | G | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.5481-198T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956679 | |||||||
chr17:61956854 | T | A | 1 | a0001c0002t0001g0086 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.5481-373A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956854 | |||||||
chr17:61956872 | G | C | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.5481-391C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956872 | |||||||
chr17:61956877 | C | T | 1 | a0001c0001t0002g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5481-396G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956877 | |||||||
chr17:61956889 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.5481-408A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956889 | |||||||
chr17:61956995 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5481-514T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61956995 | |||||||
chr17:61957002 | T | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(3): Show |
6 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.5481-521A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957002 | |||||||
chr17:61957139 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5481-658G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957139 | |||||||
chr17:61957165 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5481-684C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957165 | |||||||
chr17:61957195 | C | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0216 |
2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5481-714G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957195 | |||||||
chr17:61957255 | C | T | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.5481-774G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957255 | |||||||
chr17:61957280 | A | C | 1 | a0001c0012t0001g0305 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5481-799T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957280 | |||||||
chr17:61957334 | C | T | 3 | a0001c0001t0002g0267 a0001c0001t0002g0274 a0001c0001t0013g0316 |
3 | HG00423.hp1 NA18943.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.5481-853G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957334 | |||||||
chr17:61957344 | A | G | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5481-863T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957344 | |||||||
chr17:61957356 | A | AT | 15 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
15 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.5481-876dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957356 | |||||||
chr17:61957419 | T | C | 3 | a0001c0003t0001g0098 a0001c0003t0001g0104 a0001c0003t0001g0110 |
3 | HG02717.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5481-938A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957419 | |||||||
chr17:61957485 | G | A | 30 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(27): Show |
30 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.5481-1004C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957485 | |||||||
chr17:61957590 | C | T | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.5481-1109G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957590 | |||||||
chr17:61957833 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5481-1352G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957833 | |||||||
chr17:61957834 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0206 |
2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.5481-1353T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957834 | |||||||
chr17:61957884 | A | C | 1 | a0001c0001t0003g0136 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.5481-1403T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957884 | |||||||
chr17:61957951 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.5481-1470C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957951 | |||||||
chr17:61957989 | C | T | 1 | a0001c0002t0001g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5481-1508G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61957989 | |||||||
chr17:61958075 | A | G | 2 | a0001c0003t0001g0030 a0001c0003t0001g0323 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.5481-1594T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958075 | |||||||
chr17:61958143 | C | T | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.5481-1662G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958143 | |||||||
chr17:61958188 | C | G | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5481-1707G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958188 | |||||||
chr17:61958208 | C | T | 8 | a0001c0003t0001g0023 a0001c0003t0001g0025 a0001c0003t0001g0030 others(5): Show |
8 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.5481-1727G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958208 | |||||||
chr17:61958348 | G | T | 2 | a0001c0001t0002g0232 a0001c0001t0002g0234 |
2 | NA18967.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.5481-1867C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958348 | |||||||
chr17:61958417 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5481-1936G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958417 | |||||||
chr17:61958488 | A | G | 102 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(99): Show |
102 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.5481-2007T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958488 | |||||||
chr17:61958577 | C | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5481-2096G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958577 | |||||||
chr17:61958901 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5480+1966T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61958901 | |||||||
chr17:61959349 | A | C | 1 | a0001c0003t0001g0300 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5480+1518T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959349 | |||||||
chr17:61959496 | T | C | 1 | a0001c0001t0002g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5480+1371A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959496 | |||||||
chr17:61959630 | C | T | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(13): Show |
16 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.5480+1237G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959630 | |||||||
chr17:61959726 | C | CT | 10 | a0001c0001t0001g0118 a0001c0001t0001g0130 a0001c0001t0001g0132 others(7): Show |
10 | HG01978.hp2 HG02109.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.5480+1140dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959726 | |||||||
chr17:61959726 | CT | C | 183 | a0001c0001t0001g0144 a0001c0001t0001g0149 a0001c0001t0001g0173 others(180): Show |
183 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.5480+1140delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959726 | |||||||
chr17:61959726 | CTT | C | 9 | a0001c0001t0002g0250 a0001c0002t0001g0044 a0001c0002t0001g0080 others(6): Show |
9 | HG01175.hp1 HG01993.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.5480+1139_5480+114 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959726 | |||||||
chr17:61959746 | T | G | 6 | a0001c0001t0001g0196 a0001c0001t0001g0284 a0001c0001t0001g0285 others(3): Show |
6 | HG00642.hp2 HG01167.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.5480+1121A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959746 | |||||||
chr17:61959768 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG02559.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.5480+1099C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959768 | |||||||
chr17:61959789 | T | C | 202 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(199): Show |
202 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.5480+1078A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959789 | |||||||
chr17:61959946 | G | A | 1 | a0002c0005t0001g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5480+921C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61959946 | |||||||
chr17:61960239 | T | C | 4 | a0001c0003t0005g0026 a0001c0003t0005g0027 a0001c0003t0005g0028 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5480+628A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960239 | |||||||
chr17:61960256 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0206 |
2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.5480+611A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960256 | |||||||
chr17:61960296 | C | G | 1 | a0001c0001t0013g0316 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.5480+571G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960296 | |||||||
chr17:61960330 | G | A | 9 | a0001c0003t0001g0023 a0001c0003t0001g0024 a0001c0003t0001g0025 others(6): Show |
9 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.5480+537C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960330 | |||||||
chr17:61960502 | G | A | 1 | a0001c0002t0001g0065 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.5480+365C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960502 | |||||||
chr17:61960721 | C | T | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5480+146G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960721 | |||||||
chr17:61960817 | C | T | 2 | a0001c0001t0002g0236 a0001c0001t0002g0249 |
2 | NA18962.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.5480+50G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960817 | |||||||
chr17:61960849 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.5480+18A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 23/29 | chr17 | 61960849 | |||||||
chr17:61961194 | T | C | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5257-104A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961194 | |||||||
chr17:61961253 | G | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5257-163C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961253 | |||||||
chr17:61961481 | C | T | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.5256+107G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961481 | |||||||
chr17:61961519 | CA | C | 158 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(155): Show |
158 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.5256+68delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961519 | |||||||
chr17:61961519 | CAA | C | 26 | a0001c0001t0010g0264 a0001c0002t0001g0001 a0001c0002t0001g0038 others(23): Show |
26 | HG00558.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.5256+67_5256+68del others(2): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961519 | |||||||
chr17:61961519 | CAAA | C | 11 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(8): Show |
11 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5256+66_5256+68del others(3): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 22/29 | chr17 | 61961519 | |||||||
chr17:61961790 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5065-11A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61961790 | |||||||
chr17:61961872 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5065-93T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61961872 | |||||||
chr17:61961899 | A | T | 60 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(57): Show |
60 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.5065-120T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61961899 | |||||||
chr17:61961911 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5065-132A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61961911 | |||||||
chr17:61962054 | G | A | 2 | a0001c0003t0001g0099 a0001c0015t0001g0096 |
2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.5065-275C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962054 | |||||||
chr17:61962076 | A | G | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.5065-297T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962076 | |||||||
chr17:61962141 | C | G | 1 | a0001c0002t0001g0047 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5065-362G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962141 | |||||||
chr17:61962178 | C | G | 91 | a0001c0002t0001g0001 a0001c0002t0001g0031 a0001c0002t0001g0032 others(88): Show |
91 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.5065-399G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962178 | |||||||
chr17:61962243 | G | A | 6 | a0001c0001t0001g0134 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG00558.hp1 NA18948.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.5065-464C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962243 | |||||||
chr17:61962248 | T | C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5065-469A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962248 | |||||||
chr17:61962307 | A | T | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.5064+445T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962307 | |||||||
chr17:61962343 | T | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.5064+409A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962343 | |||||||
chr17:61962363 | G | A | 60 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(57): Show |
60 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.5064+389C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962363 | |||||||
chr17:61962478 | C | T | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.5064+274G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962478 | |||||||
chr17:61962634 | A | G | 31 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0130 others(28): Show |
31 | HG00140.hp1 HG01106.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.5064+118T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962634 | |||||||
chr17:61962745 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01261.hp2 | splice_region_variant&intron_variant | LOW | c.5064+7G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 21/29 | chr17 | 61962745 | |||||||
chr17:61963046 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4845-75A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963046 | |||||||
chr17:61963166 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4845-195T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963166 | |||||||
chr17:61963202 | CA | C | 151 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(148): Show |
151 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.4845-232delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | |||||||
chr17:61963202 | CAA | C | 107 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0147 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.4845-233_4845-232d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | |||||||
chr17:61963202 | CAAA | C | 6 | a0001c0002t0001g0034 a0001c0002t0001g0062 a0001c0002t0001g0069 others(3): Show |
6 | HG02027.hp1 HG02132.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.4845-234_4845-232d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | |||||||
chr17:61963202 | CAAAAA | C | 6 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4845-236_4845-232d others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | |||||||
chr17:61963202 | CAAAAAAA | C | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4845-238_4845-232d others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | |||||||
chr17:61963202 | CAAAAAAA others(5): Show |
C | 1 | a0001c0004t0001g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4845-243_4845-232d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963202 | |||||||
chr17:61963227 | A | G | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4845-256T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963227 | |||||||
chr17:61963229 | A | AGAAAGAA others(3): Show |
4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.4845-259_4845-258i others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963229 | |||||||
chr17:61963231 | G | A | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.4845-260C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963231 | |||||||
chr17:61963235 | G | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.4845-264C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963235 | |||||||
chr17:61963261 | TAGGGTA | T | 209 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(206): Show |
209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.4845-296_4845-291d others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963261 | |||||||
chr17:61963436 | T | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4845-465A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963436 | |||||||
chr17:61963458 | C | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0223 a0001c0001t0002g0092 others(1): Show |
4 | HG02896.hp1 HG04184.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.4845-487G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963458 | |||||||
chr17:61963591 | C | T | 1 | a0001c0002t0001g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4845-620G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61963591 | |||||||
chr17:61964000 | A | G | 2 | a0001c0002t0001g0035 a0001c0002t0001g0317 |
2 | NA18965.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.4844+1006T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964000 | |||||||
chr17:61964232 | A | G | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4844+774T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964232 | |||||||
chr17:61964302 | A | G | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4844+704T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964302 | |||||||
chr17:61964408 | C | T | 1 | a0001c0003t0001g0291 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4844+598G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964408 | |||||||
chr17:61964486 | G | T | 5 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0001c0001t0002g0248 others(2): Show |
5 | HG00642.hp1 HG01433.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.4844+520C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964486 | |||||||
chr17:61964554 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | NA19066.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.4844+452C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964554 | |||||||
chr17:61964688 | C | T | 1 | a0001c0002t0001g0081 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4844+318G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964688 | |||||||
chr17:61964836 | T | G | 1 | a0001c0001t0012g0256 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4844+170A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964836 | |||||||
chr17:61964893 | A | G | 203 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(200): Show |
203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.4844+113T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964893 | |||||||
chr17:61964912 | C | T | 1 | a0001c0003t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4844+94G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964912 | |||||||
chr17:61964953 | A | C | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4844+53T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 20/29 | chr17 | 61964953 | |||||||
chr17:61965591 | T | C | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4382-123A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61965591 | |||||||
chr17:61965752 | T | C | 1 | a0001c0002t0023g0059 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.4382-284A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61965752 | |||||||
chr17:61965951 | T | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4382-483A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61965951 | |||||||
chr17:61965990 | A | G | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.4381+472T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61965990 | |||||||
chr17:61966029 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4381+433G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61966029 | |||||||
chr17:61966121 | T | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.4381+341A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61966121 | |||||||
chr17:61966210 | C | T | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4381+252G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61966210 | |||||||
chr17:61966245 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG02559.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.4381+217C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 19/29 | chr17 | 61966245 | |||||||
chr17:61966898 | A | C | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.4192-247T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61966898 | |||||||
chr17:61967447 | T | C | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4191+588A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967447 | |||||||
chr17:61967581 | A | G | 1 | a0001c0002t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4191+454T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967581 | |||||||
chr17:61967805 | C | T | 1 | a0001c0003t0001g0099 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4191+230G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967805 | |||||||
chr17:61967809 | C | G | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.4191+226G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967809 | |||||||
chr17:61967898 | C | A | 1 | a0001c0001t0001g0220 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4191+137G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967898 | |||||||
chr17:61967934 | C | T | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.4191+101G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 18/29 | chr17 | 61967934 | |||||||
chr17:61968313 | T | TTTTATTT others(1): Show |
62 | a0001c0002t0001g0001 a0001c0002t0001g0031 a0001c0002t0001g0034 others(59): Show |
62 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.3968-63_3968-56dup others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968313 | |||||||
chr17:61968313 | T | TTTTATTT others(5): Show |
3 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0070 |
3 | NA18612.hp1 NA18975.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.3968-67_3968-56dup others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968313 | |||||||
chr17:61968316 | T | C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3968-58A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968316 | |||||||
chr17:61968412 | G | GCC | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.3968-156_3968-155d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968412 | |||||||
chr17:61968472 | C | T | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3968-214G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968472 | |||||||
chr17:61968516 | C | T | 1 | a0001c0007t0006g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3968-258G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968516 | |||||||
chr17:61968528 | G | A | 1 | a0001c0004t0001g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3968-270C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968528 | |||||||
chr17:61968748 | C | T | 1 | a0001c0002t0001g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3968-490G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968748 | |||||||
chr17:61968915 | C | G | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.3968-657G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61968915 | |||||||
chr17:61969279 | G | A | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.3968-1021C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969279 | |||||||
chr17:61969365 | AC | A | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.3968-1108delG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969365 | |||||||
chr17:61969366 | C | A | 269 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(266): Show |
269 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(266): Show |
intron_variant | MODIFIER | c.3968-1108G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969366 | |||||||
chr17:61969416 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3968-1158G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969416 | |||||||
chr17:61969576 | C | T | 1 | a0001c0018t0001g0076 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3968-1318G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969576 | |||||||
chr17:61969653 | G | A | 2 | a0001c0002t0001g0081 a0001c0002t0001g0083 |
2 | NA19074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3968-1395C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969653 | |||||||
chr17:61969761 | C | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.3968-1503G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61969761 | |||||||
chr17:61970281 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3968-2023T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970281 | |||||||
chr17:61970679 | C | CA | 35 | a0001c0001t0001g0094 a0001c0001t0001g0118 a0001c0001t0001g0120 others(32): Show |
35 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.3967+2047dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970679 | |||||||
chr17:61970679 | CA | C | 91 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(88): Show |
91 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.3967+2047delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970679 | |||||||
chr17:61970679 | CAA | C | 77 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0237 others(74): Show |
77 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.3967+2046_3967+204 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970679 | |||||||
chr17:61970726 | G | GT | 207 | a0001c0001t0001g0094 a0001c0001t0001g0120 a0001c0001t0001g0121 others(204): Show |
207 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.3967+2000dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970726 | |||||||
chr17:61970726 | G | GTT | 22 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(19): Show |
22 | HG01175.hp1 HG01346.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.3967+1999_3967+200 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970726 | |||||||
chr17:61970960 | G | T | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3967+1767C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61970960 | |||||||
chr17:61971113 | T | A | 203 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(200): Show |
203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.3967+1614A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971113 | |||||||
chr17:61971221 | T | A | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.3967+1506A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971221 | |||||||
chr17:61971275 | CT | C | 6 | a0001c0001t0001g0315 a0001c0001t0002g0268 a0001c0002t0001g0069 others(3): Show |
6 | HG01346.hp2 HG02145.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.3967+1451delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971275 | |||||||
chr17:61971278 | T | G | 7 | a0001c0001t0001g0140 a0001c0001t0004g0139 a0001c0001t0004g0141 others(4): Show |
7 | NA18949.hp1 NA18952.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.3967+1449A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971278 | |||||||
chr17:61971317 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3967+1410G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971317 | |||||||
chr17:61971592 | C | T | 7 | a0001c0002t0001g0039 a0001c0002t0001g0044 a0001c0002t0001g0046 others(4): Show |
7 | HG01928.hp2 HG01934.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.3967+1135G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971592 | |||||||
chr17:61971593 | G | A | 1 | a0001c0003t0001g0110 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3967+1134C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971593 | |||||||
chr17:61971596 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3967+1131C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971596 | |||||||
chr17:61971599 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0206 |
2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3967+1128A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971599 | |||||||
chr17:61971649 | T | G | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3967+1078A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971649 | |||||||
chr17:61971791 | G | A | 1 | a0001c0003t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3967+936C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971791 | |||||||
chr17:61971850 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.3967+877A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971850 | |||||||
chr17:61971856 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3967+871G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971856 | |||||||
chr17:61971875 | G | A | 31 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0130 others(28): Show |
31 | HG00140.hp1 HG01106.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.3967+852C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971875 | |||||||
chr17:61971906 | C | G | 1 | a0001c0001t0020g0247 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3967+821G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61971906 | |||||||
chr17:61972168 | A | G | 2 | a0001c0001t0001g0205 a0011c0023t0001g0131 |
2 | NA18972.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.3967+559T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61972168 | |||||||
chr17:61972663 | T | C | 1 | a0001c0003t0005g0028 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3967+64A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 17/29 | chr17 | 61972663 | |||||||
chr17:61972948 | T | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.3806-60A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61972948 | |||||||
chr17:61973073 | T | G | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.3806-185A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973073 | |||||||
chr17:61973181 | T | C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3806-293A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973181 | |||||||
chr17:61973289 | A | G | 2 | a0001c0002t0001g0056 a0001c0002t0001g0084 |
2 | NA18960.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.3806-401T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973289 | |||||||
chr17:61973731 | C | T | 1 | a0001c0003t0001g0302 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3806-843G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973731 | |||||||
chr17:61973859 | T | A | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3806-971A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973859 | |||||||
chr17:61973931 | C | G | 1 | a0001c0001t0002g0262 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3806-1043G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973931 | |||||||
chr17:61973959 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3806-1071C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61973959 | |||||||
chr17:61974309 | TGGGA | T | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-1425_3806-142 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974309 | |||||||
chr17:61974330 | T | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0216 |
2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3806-1442A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974330 | |||||||
chr17:61974392 | C | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3806-1504G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974392 | |||||||
chr17:61974397 | C | A | 1 | a0001c0001t0002g0269 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3806-1509G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974397 | |||||||
chr17:61974542 | T | G | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3806-1654A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974542 | |||||||
chr17:61974550 | T | TG | 203 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(200): Show |
203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.3806-1663_3806-166 others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974550 | |||||||
chr17:61974723 | C | T | 2 | a0001c0001t0015g0156 a0001c0001t0015g0194 |
2 | HG02280.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.3806-1835G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974723 | |||||||
chr17:61974782 | T | A | 1 | a0001c0001t0019g0243 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3806-1894A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974782 | |||||||
chr17:61974975 | A | C | 4 | a0001c0002t0001g0045 a0001c0002t0001g0048 a0001c0002t0001g0055 others(1): Show |
4 | NA18983.hp1 NA19009.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.3806-2087T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61974975 | |||||||
chr17:61975139 | T | TA | 19 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0130 others(16): Show |
19 | HG02155.hp2 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.3806-2252dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975139 | |||||||
chr17:61975154 | T | A | 1 | a0001c0001t0001g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3806-2266A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975154 | |||||||
chr17:61975154 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3806-2266A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975154 | |||||||
chr17:61975214 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3806-2326G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975214 | |||||||
chr17:61975505 | T | G | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-2617A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975505 | |||||||
chr17:61975630 | A | C | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3806-2742T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975630 | |||||||
chr17:61975676 | A | G | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-2788T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975676 | |||||||
chr17:61975762 | T | A | 1 | a0001c0004t0001g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3806-2874A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975762 | |||||||
chr17:61975842 | C | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-2954G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975842 | |||||||
chr17:61975885 | A | G | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-2997T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975885 | |||||||
chr17:61975934 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3806-3046A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61975934 | |||||||
chr17:61976011 | C | T | 1 | a0001c0003t0001g0300 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3806-3123G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976011 | |||||||
chr17:61976012 | G | A | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3806-3124C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976012 | |||||||
chr17:61976023 | A | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3806-3135T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976023 | |||||||
chr17:61976094 | T | C | 5 | a0001c0006t0001g0100 a0001c0006t0001g0101 a0001c0006t0001g0115 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3806-3206A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976094 | |||||||
chr17:61976197 | C | T | 1 | a0001c0002t0001g0040 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3806-3309G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976197 | |||||||
chr17:61976198 | G | A | 2 | a0001c0001t0002g0092 a0001c0001t0002g0093 |
2 | NA18952.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3806-3310C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976198 | |||||||
chr17:61976256 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0011g0016 |
2 | HG02300.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3806-3368A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976256 | |||||||
chr17:61976743 | G | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.3806-3855C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976743 | |||||||
chr17:61976896 | C | G | 83 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(80): Show |
83 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.3806-4008G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61976896 | |||||||
chr17:61977090 | C | A | 2 | a0001c0003t0001g0099 a0001c0015t0001g0096 |
2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.3806-4202G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977090 | |||||||
chr17:61977192 | T | G | 1 | a0001c0006t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3806-4304A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977192 | |||||||
chr17:61977298 | T | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3806-4410A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977298 | |||||||
chr17:61977475 | G | A | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3806-4587C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977475 | |||||||
chr17:61977540 | C | G | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3806-4652G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977540 | |||||||
chr17:61977744 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3805+4454C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977744 | |||||||
chr17:61977824 | C | G | 78 | a0001c0001t0001g0094 a0001c0001t0001g0119 a0001c0001t0001g0123 others(75): Show |
78 | HG00140.hp1 HG00558.hp1 HG01106.hp1 others(75): Show |
intron_variant | MODIFIER | c.3805+4374G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977824 | |||||||
chr17:61977880 | G | T | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3805+4318C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61977880 | |||||||
chr17:61978151 | C | CT | 61 | a0001c0001t0001g0205 a0001c0001t0002g0092 a0001c0001t0002g0093 others(58): Show |
61 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.3805+4046dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978151 | |||||||
chr17:61978250 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3805+3948T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978250 | |||||||
chr17:61978347 | G | C | 6 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(3): Show |
6 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3805+3851C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978347 | |||||||
chr17:61978453 | G | T | 11 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(8): Show |
11 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3805+3745C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978453 | |||||||
chr17:61978525 | TG | T | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.3805+3672delC | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978525 | |||||||
chr17:61978585 | A | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0205 others(1): Show |
4 | HG02155.hp2 HG02523.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.3805+3613T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978585 | |||||||
chr17:61978769 | CT | C | 6 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0001c0001t0001g0199 others(3): Show |
6 | NA18612.hp2 NA18946.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.3805+3428delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978769 | |||||||
chr17:61978902 | T | C | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.3805+3296A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61978902 | |||||||
chr17:61979068 | T | G | 1 | a0001c0002t0001g0031 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3805+3130A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61979068 | |||||||
chr17:61979386 | C | T | 6 | a0001c0001t0002g0237 a0001c0007t0006g0279 a0001c0007t0006g0280 others(3): Show |
6 | HG02257.hp1 HG02735.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.3805+2812G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61979386 | |||||||
chr17:61979547 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3805+2651C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61979547 | |||||||
chr17:61979749 | C | A | 1 | a0001c0003t0007g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3805+2449G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61979749 | |||||||
chr17:61979951 | G | A | 1 | a0001c0003t0007g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3805+2247C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61979951 | |||||||
chr17:61980144 | A | G | 103 | a0001c0002t0001g0001 a0001c0002t0001g0031 a0001c0002t0001g0032 others(100): Show |
103 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.3805+2054T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980144 | |||||||
chr17:61980194 | AAAAC | A | 8 | a0001c0001t0002g0257 a0001c0001t0002g0260 a0001c0001t0002g0262 others(5): Show |
8 | HG01081.hp1 HG01109.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.3805+2000_3805+200 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980194 | |||||||
chr17:61980277 | C | G | 1 | a0001c0003t0001g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3805+1921G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980277 | |||||||
chr17:61980310 | T | C | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.3805+1888A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980310 | |||||||
chr17:61980359 | T | G | 12 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(9): Show |
12 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.3805+1839A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980359 | |||||||
chr17:61980528 | C | A | 1 | a0001c0003t0001g0110 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3805+1670G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980528 | |||||||
chr17:61980655 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3805+1543T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980655 | |||||||
chr17:61980832 | C | T | 12 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(9): Show |
12 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.3805+1366G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980832 | |||||||
chr17:61980908 | A | G | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3805+1290T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980908 | |||||||
chr17:61980956 | C | A | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3805+1242G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61980956 | |||||||
chr17:61981024 | A | AT | 20 | a0001c0003t0001g0098 a0001c0003t0001g0104 a0001c0003t0001g0105 others(17): Show |
20 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.3805+1173dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981024 | |||||||
chr17:61981057 | C | T | 209 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(206): Show |
209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.3805+1141G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981057 | |||||||
chr17:61981441 | T | TCTAAATG others(20): Show |
2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3805+756_3805+757i others(29): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981441 | |||||||
chr17:61981548 | T | C | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3805+650A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981548 | |||||||
chr17:61981621 | A | G | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3805+577T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981621 | |||||||
chr17:61981808 | T | G | 1 | a0001c0001t0002g0277 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3805+390A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981808 | |||||||
chr17:61981828 | T | C | 7 | a0001c0001t0001g0124 a0001c0001t0001g0144 a0001c0001t0001g0145 others(4): Show |
7 | HG02622.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3805+370A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981828 | |||||||
chr17:61981897 | T | A | 2 | a0001c0002t0001g0050 a0001c0002t0001g0064 |
2 | NA18945.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.3805+301A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 16/29 | chr17 | 61981897 | |||||||
chr17:61983341 | A | T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2889-227T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983341 | |||||||
chr17:61983730 | C | A | 1 | a0001c0001t0001g0134 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2888+441G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983730 | |||||||
chr17:61983731 | C | CT | 68 | a0001c0001t0001g0094 a0001c0001t0001g0120 a0001c0001t0001g0133 others(65): Show |
68 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2888+439dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983731 | |||||||
chr17:61983731 | CT | C | 87 | a0001c0002t0001g0001 a0001c0002t0001g0031 a0001c0002t0001g0033 others(84): Show |
87 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2888+439delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983731 | |||||||
chr17:61983731 | CTT | C | 8 | a0001c0002t0001g0038 a0001c0002t0001g0058 a0001c0002t0001g0070 others(5): Show |
8 | HG02257.hp1 HG03540.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.2888+438_2888+439d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983731 | |||||||
chr17:61983798 | G | A | 2 | a0001c0003t0001g0099 a0001c0015t0001g0096 |
2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.2888+373C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61983798 | |||||||
chr17:61984132 | A | G | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2888+39T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 15/29 | chr17 | 61984132 | |||||||
chr17:61984584 | T | C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2691+67A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 14/29 | chr17 | 61984584 | |||||||
chr17:61984964 | G | A | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2476+36C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 13/29 | chr17 | 61984964 | |||||||
chr17:61985191 | A | C | 2 | a0001c0001t0010g0264 a0001c0001t0010g0265 |
2 | NA19079.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2386-101T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985191 | |||||||
chr17:61985231 | T | C | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2386-141A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985231 | |||||||
chr17:61985244 | T | C | 4 | a0001c0003t0001g0291 a0001c0003t0001g0292 a0001c0003t0001g0299 others(1): Show |
4 | HG00140.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2386-154A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985244 | |||||||
chr17:61985287 | G | A | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2386-197C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985287 | |||||||
chr17:61985348 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2386-258T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985348 | |||||||
chr17:61985581 | G | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2386-491C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985581 | |||||||
chr17:61985593 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2386-503G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985593 | |||||||
chr17:61985661 | A | G | 2 | a0001c0003t0001g0099 a0001c0015t0001g0096 |
2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.2386-571T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61985661 | |||||||
chr17:61986001 | C | G | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2386-911G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61986001 | |||||||
chr17:61986393 | G | A | 1 | a0001c0002t0001g0074 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2385+614C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61986393 | |||||||
chr17:61986407 | C | T | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2385+600G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 12/29 | chr17 | 61986407 | |||||||
chr17:61987308 | G | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(7): Show |
10 | HG00140.hp2 HG01346.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.2264-180C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987308 | |||||||
chr17:61987463 | C | T | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2264-335G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987463 | |||||||
chr17:61987547 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2264-419A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987547 | |||||||
chr17:61987603 | T | C | 1 | a0001c0001t0004g0211 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2264-475A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987603 | |||||||
chr17:61987781 | G | A | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2264-653C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987781 | |||||||
chr17:61987889 | C | T | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2264-761G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987889 | |||||||
chr17:61987918 | T | C | 9 | a0001c0002t0001g0034 a0001c0002t0001g0041 a0001c0002t0001g0045 others(6): Show |
9 | HG02132.hp1 NA18612.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.2264-790A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61987918 | |||||||
chr17:61988133 | A | G | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2264-1005T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988133 | |||||||
chr17:61988281 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2264-1153C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988281 | |||||||
chr17:61988282 | T | C | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2264-1154A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988282 | |||||||
chr17:61988423 | T | C | 5 | a0001c0002t0001g0038 a0001c0002t0001g0058 a0001c0002t0001g0091 others(2): Show |
5 | HG02148.hp1 NA18956.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.2264-1295A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988423 | |||||||
chr17:61988705 | A | G | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2264-1577T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988705 | |||||||
chr17:61988735 | GT | G | 7 | a0001c0001t0001g0020 a0001c0001t0011g0016 a0001c0007t0006g0279 others(4): Show |
7 | HG02257.hp1 HG02300.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2264-1608delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988735 | |||||||
chr17:61988765 | T | C | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2264-1637A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988765 | |||||||
chr17:61988965 | C | T | 1 | a0001c0001t0003g0301 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2264-1837G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61988965 | |||||||
chr17:61989014 | C | CT | 11 | a0001c0001t0001g0118 a0001c0001t0001g0179 a0001c0001t0001g0190 others(8): Show |
11 | HG01109.hp2 HG01346.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.2264-1887dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989014 | |||||||
chr17:61989014 | CT | C | 31 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0130 others(28): Show |
31 | HG00140.hp1 HG01106.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.2264-1887delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989014 | |||||||
chr17:61989043 | G | A | 1 | a0001c0001t0021g0254 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2264-1915C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989043 | |||||||
chr17:61989129 | A | G | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2264-2001T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989129 | |||||||
chr17:61989176 | G | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2264-2048C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989176 | |||||||
chr17:61989427 | C | T | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2264-2299G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989427 | |||||||
chr17:61989467 | T | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2264-2339A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989467 | |||||||
chr17:61989478 | A | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2264-2350T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989478 | |||||||
chr17:61989710 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2264-2582T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61989710 | |||||||
chr17:61990172 | T | C | 1 | a0001c0001t0027g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2263+2368A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990172 | |||||||
chr17:61990264 | T | C | 1 | a0001c0001t0002g0250 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2263+2276A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990264 | |||||||
chr17:61990337 | T | C | 1 | a0001c0004t0001g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2263+2203A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990337 | |||||||
chr17:61990589 | C | CTATA | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2263+1947_2263+195 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990589 | |||||||
chr17:61990602 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0314 |
2 | HG04199.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.2263+1938A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990602 | |||||||
chr17:61990604 | C | T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2263+1936G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990604 | |||||||
chr17:61990612 | C | T | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2263+1928G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990612 | |||||||
chr17:61990615 | T | A | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2263+1925A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990615 | |||||||
chr17:61990616 | T | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2263+1924A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990616 | |||||||
chr17:61990627 | G | GTA | 15 | a0001c0001t0001g0118 a0001c0001t0001g0137 a0001c0001t0001g0151 others(12): Show |
15 | HG00558.hp1 HG01516.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.2263+1911_2263+191 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | |||||||
chr17:61990627 | G | GTATA | 14 | a0001c0001t0001g0134 a0001c0001t0001g0152 a0001c0001t0001g0153 others(11): Show |
14 | HG01261.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2263+1909_2263+191 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | |||||||
chr17:61990627 | G | GTATATA | 5 | a0001c0001t0001g0315 a0001c0007t0006g0279 a0001c0007t0006g0280 others(2): Show |
5 | HG01346.hp2 HG02257.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2263+1907_2263+191 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | |||||||
chr17:61990627 | G | GTATATAT others(7): Show |
1 | a0001c0003t0001g0099 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2263+1899_2263+191 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | |||||||
chr17:61990627 | G | GTATATAT others(15): Show |
1 | a0001c0015t0001g0096 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2263+1891_2263+191 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | |||||||
chr17:61990627 | G | GTATGTGT others(15): Show |
1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2263+1912_2263+191 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | |||||||
chr17:61990627 | G | GTGTATA | 6 | a0002c0005t0001g0004 a0002c0005t0001g0005 a0002c0005t0001g0006 others(3): Show |
6 | HG02257.hp2 HG02809.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2263+1912_2263+191 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | |||||||
chr17:61990627 | G | GTGTATAT others(3): Show |
1 | a0001c0003t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2263+1912_2263+191 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | |||||||
chr17:61990627 | G | GTGTATAT others(9): Show |
1 | a0002c0005t0001g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2263+1912_2263+191 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | |||||||
chr17:61990627 | GTA | G | 69 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(66): Show |
69 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2263+1911_2263+191 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | |||||||
chr17:61990627 | GTATA | G | 3 | a0001c0001t0002g0235 a0001c0001t0003g0136 a0006c0024t0001g0320 |
3 | HG02970.hp1 HG03490.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.2263+1909_2263+191 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990627 | |||||||
chr17:61990629 | A | G | 9 | a0001c0001t0001g0140 a0001c0001t0001g0144 a0001c0001t0004g0139 others(6): Show |
9 | HG02148.hp2 HG03130.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.2263+1911T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990629 | |||||||
chr17:61990633 | A | G | 1 | a0001c0001t0002g0235 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2263+1907T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990633 | |||||||
chr17:61990650 | T | C | 2 | a0001c0001t0001g0212 a0001c0003t0001g0114 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2263+1890A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | |||||||
chr17:61990650 | T | TAC | 6 | a0001c0001t0002g0257 a0001c0001t0002g0260 a0001c0001t0002g0262 others(3): Show |
6 | HG01081.hp1 HG02258.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.2263+1888_2263+188 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | |||||||
chr17:61990650 | T | TATATATA others(3): Show |
13 | a0001c0003t0001g0105 a0001c0003t0001g0107 a0001c0003t0001g0109 others(10): Show |
13 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.2263+1889_2263+189 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | |||||||
chr17:61990650 | T | TATATATA others(5): Show |
2 | a0001c0003t0001g0108 a0001c0006t0001g0115 |
2 | HG00639.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2263+1889_2263+189 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | |||||||
chr17:61990650 | T | TATATATA others(7): Show |
1 | a0001c0006t0001g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2263+1889_2263+189 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | |||||||
chr17:61990650 | T | TATATATA others(9): Show |
2 | a0001c0003t0001g0098 a0001c0003t0001g0110 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2263+1889_2263+189 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | |||||||
chr17:61990650 | T | TATATATA others(15): Show |
1 | a0001c0003t0001g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2263+1889_2263+189 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990650 | |||||||
chr17:61990699 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2263+1841A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990699 | |||||||
chr17:61990879 | G | A | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2263+1661C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990879 | |||||||
chr17:61990931 | G | A | 3 | a0001c0001t0002g0267 a0001c0001t0002g0274 a0001c0001t0013g0316 |
3 | HG00423.hp1 NA18943.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.2263+1609C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61990931 | |||||||
chr17:61991055 | C | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2263+1485G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991055 | |||||||
chr17:61991200 | T | C | 209 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(206): Show |
209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.2263+1340A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991200 | |||||||
chr17:61991548 | C | T | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2263+992G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991548 | |||||||
chr17:61991648 | T | C | 2 | a0001c0001t0010g0264 a0001c0001t0010g0265 |
2 | NA19079.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2263+892A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991648 | |||||||
chr17:61991797 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0183 |
2 | NA18982.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2263+743A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991797 | |||||||
chr17:61991844 | C | T | 6 | a0001c0001t0001g0196 a0001c0001t0001g0284 a0001c0001t0001g0285 others(3): Show |
6 | HG00642.hp2 HG01167.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.2263+696G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991844 | |||||||
chr17:61991847 | T | C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2263+693A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991847 | |||||||
chr17:61991934 | C | T | 1 | a0001c0001t0003g0301 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2263+606G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991934 | |||||||
chr17:61991980 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2263+560C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61991980 | |||||||
chr17:61992160 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2263+380A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61992160 | |||||||
chr17:61992213 | T | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2263+327A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61992213 | |||||||
chr17:61992248 | C | T | 1 | a0002c0005t0001g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2263+292G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61992248 | |||||||
chr17:61992264 | G | A | 1 | a0001c0001t0016g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2263+276C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 11/29 | chr17 | 61992264 | |||||||
chr17:61992642 | T | G | 1 | a0001c0003t0001g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2182-21A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992642 | |||||||
chr17:61992788 | G | T | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2182-167C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992788 | |||||||
chr17:61992831 | C | T | 1 | a0001c0002t0001g0039 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2182-210G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992831 | |||||||
chr17:61992851 | C | T | 11 | a0001c0003t0001g0105 a0001c0003t0001g0107 a0001c0003t0001g0108 others(8): Show |
11 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2182-230G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992851 | |||||||
chr17:61992925 | C | T | 1 | a0001c0003t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2182-304G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61992925 | |||||||
chr17:61993000 | T | C | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2182-379A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993000 | |||||||
chr17:61993039 | A | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2182-418T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993039 | |||||||
chr17:61993105 | T | C | 1 | a0001c0001t0002g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2182-484A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993105 | |||||||
chr17:61993196 | C | CT | 57 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(54): Show |
57 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.2182-576dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993196 | |||||||
chr17:61993196 | C | CTT | 6 | a0001c0001t0001g0020 a0001c0002t0001g0078 a0001c0003t0001g0114 others(3): Show |
6 | HG00544.hp1 HG01891.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.2182-577_2182-576d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993196 | |||||||
chr17:61993199 | TC | T | 8 | a0001c0001t0002g0093 a0001c0001t0002g0233 a0001c0001t0002g0242 others(5): Show |
8 | NA18945.hp1 NA18968.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.2182-579delG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993199 | |||||||
chr17:61993200 | C | T | 195 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(192): Show |
195 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.2182-579G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993200 | |||||||
chr17:61993202 | T | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2182-581A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993202 | |||||||
chr17:61993667 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2182-1046G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993667 | |||||||
chr17:61993696 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2182-1075C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993696 | |||||||
chr17:61993709 | C | G | 11 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0001c0001t0001g0199 others(8): Show |
11 | HG00544.hp2 HG00597.hp1 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.2182-1088G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993709 | |||||||
chr17:61993793 | T | C | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2182-1172A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993793 | |||||||
chr17:61993804 | G | A | 1 | a0001c0001t0018g0127 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2182-1183C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993804 | |||||||
chr17:61993891 | T | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2181+1261A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993891 | |||||||
chr17:61993919 | G | A | 56 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(53): Show |
56 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2181+1233C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993919 | |||||||
chr17:61993937 | A | G | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+1215T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993937 | |||||||
chr17:61993948 | C | A | 1 | a0001c0003t0001g0030 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2181+1204G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993948 | |||||||
chr17:61993948 | CA | C | 92 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(89): Show |
92 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.2181+1203delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993948 | |||||||
chr17:61993948 | CAA | C | 54 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(51): Show |
54 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.2181+1202_2181+120 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993948 | |||||||
chr17:61993952 | A | C | 1 | a0001c0001t0025g0008 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2181+1200T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993952 | |||||||
chr17:61993980 | C | T | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2181+1172G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61993980 | |||||||
chr17:61994004 | A | AT | 7 | a0001c0001t0001g0214 a0001c0002t0001g0039 a0001c0004t0001g0013 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2181+1147dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994004 | |||||||
chr17:61994120 | T | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2181+1032A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994120 | |||||||
chr17:61994394 | A | G | 4 | a0001c0003t0001g0291 a0001c0003t0001g0292 a0001c0003t0001g0299 others(1): Show |
4 | HG00140.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+758T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994394 | |||||||
chr17:61994410 | C | T | 14 | a0001c0002t0001g0036 a0001c0002t0001g0037 a0001c0002t0001g0040 others(11): Show |
14 | HG00423.hp2 HG00558.hp2 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.2181+742G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994410 | |||||||
chr17:61994471 | A | C | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2181+681T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994471 | |||||||
chr17:61994591 | A | G | 1 | a0002c0005t0001g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2181+561T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994591 | |||||||
chr17:61994606 | C | T | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2181+546G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994606 | |||||||
chr17:61994856 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2181+296C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994856 | |||||||
chr17:61994922 | G | C | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+230C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61994922 | |||||||
chr17:61995000 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2181+152G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61995000 | |||||||
chr17:61995018 | A | G | 4 | a0001c0003t0001g0291 a0001c0003t0001g0292 a0001c0003t0001g0299 others(1): Show |
4 | HG00140.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+134T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61995018 | |||||||
chr17:61995030 | T | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2181+122A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61995030 | |||||||
chr17:61995070 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2181+82T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 10/29 | chr17 | 61995070 | |||||||
chr17:61995371 | T | TA | 4 | a0001c0003t0001g0296 a0001c0003t0001g0300 a0001c0003t0001g0306 others(1): Show |
4 | HG03491.hp1 HG03492.hp2 HG03710.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1968-7dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995371 | |||||||
chr17:61995619 | T | G | 2 | a0001c0003t0001g0303 a0001c0003t0001g0304 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1968-254A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995619 | |||||||
chr17:61995659 | A | C | 1 | a0001c0006t0001g0101 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1968-294T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995659 | |||||||
chr17:61995958 | T | C | 2 | a0001c0001t0002g0266 a0001c0001t0021g0254 |
2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1968-593A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995958 | |||||||
chr17:61995967 | C | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(5): Show |
8 | HG01346.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1968-602G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995967 | |||||||
chr17:61995971 | T | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1968-606A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995971 | |||||||
chr17:61995972 | C | T | 2 | a0002c0005t0001g0004 a0002c0005t0001g0006 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1968-607G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61995972 | |||||||
chr17:61996316 | C | A | 1 | a0007c0010t0001g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1968-951G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61996316 | |||||||
chr17:61996421 | G | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1968-1056C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61996421 | |||||||
chr17:61996506 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1968-1141G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61996506 | |||||||
chr17:61996826 | C | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968-1461G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61996826 | |||||||
chr17:61996873 | T | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1968-1508A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61996873 | |||||||
chr17:61997014 | C | T | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968-1649G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997014 | |||||||
chr17:61997065 | T | C | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1968-1700A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997065 | |||||||
chr17:61997393 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1968-2028T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997393 | |||||||
chr17:61997410 | T | C | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968-2045A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997410 | |||||||
chr17:61997787 | C | T | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1968-2422G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997787 | |||||||
chr17:61997894 | T | C | 2 | a0001c0003t0001g0303 a0001c0003t0001g0304 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1968-2529A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61997894 | |||||||
chr17:61998253 | T | C | 2 | a0001c0001t0002g0262 a0001c0001t0002g0276 |
2 | HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1968-2888A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998253 | |||||||
chr17:61998560 | CAAAT | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968-3199_1968-319 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998560 | |||||||
chr17:61998592 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1968-3227G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998592 | |||||||
chr17:61998596 | C | CT | 54 | a0001c0001t0001g0094 a0001c0001t0001g0118 a0001c0001t0001g0149 others(51): Show |
54 | HG00438.hp1 HG00597.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1968-3232dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998596 | |||||||
chr17:61998596 | C | CTT | 19 | a0001c0001t0001g0186 a0001c0003t0001g0098 a0001c0003t0001g0104 others(16): Show |
19 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1968-3233_1968-323 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998596 | |||||||
chr17:61998678 | C | T | 1 | a0001c0002t0001g0086 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1968-3313G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998678 | |||||||
chr17:61998706 | C | T | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1968-3341G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998706 | |||||||
chr17:61998717 | G | A | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968-3352C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998717 | |||||||
chr17:61998839 | TCCTCCCA others(6): Show |
T | 1 | a0001c0004t0001g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1968-3487_1968-347 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998839 | |||||||
chr17:61998887 | C | T | 1 | a0001c0002t0001g0321 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1968-3522G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998887 | |||||||
chr17:61998925 | CT | C | 92 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0126 others(89): Show |
92 | HG00140.hp1 HG00558.hp1 HG01106.hp1 others(89): Show |
intron_variant | MODIFIER | c.1968-3561delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998925 | |||||||
chr17:61998925 | CTT | C | 216 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(213): Show |
216 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.1968-3562_1968-356 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998925 | |||||||
chr17:61998925 | CTTT | C | 13 | a0001c0001t0002g0093 a0001c0001t0002g0237 a0001c0001t0002g0242 others(10): Show |
13 | HG00642.hp1 HG02132.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.1968-3563_1968-356 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998925 | |||||||
chr17:61998931 | T | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0178 a0001c0001t0001g0179 |
3 | NA18985.hp1 NA19005.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1968-3566A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998931 | |||||||
chr17:61998953 | G | A | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1968-3588C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61998953 | |||||||
chr17:61999158 | T | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968-3793A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999158 | |||||||
chr17:61999171 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG02559.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1968-3806A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999171 | |||||||
chr17:61999180 | A | C | 1 | a0001c0002t0001g0321 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1968-3815T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999180 | |||||||
chr17:61999356 | A | C | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1968-3991T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999356 | |||||||
chr17:61999536 | G | A | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1968-4171C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999536 | |||||||
chr17:61999726 | A | G | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(13): Show |
16 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1968-4361T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999726 | |||||||
chr17:61999807 | A | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1968-4442T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999807 | |||||||
chr17:61999878 | G | A | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1968-4513C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 61999878 | |||||||
chr17:62000060 | A | T | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1968-4695T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000060 | |||||||
chr17:62000101 | A | G | 1 | a0001c0003t0007g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1968-4736T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000101 | |||||||
chr17:62000491 | A | G | 101 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(98): Show |
101 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1968-5126T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000491 | |||||||
chr17:62000492 | A | G | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1968-5127T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000492 | |||||||
chr17:62000539 | G | A | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1968-5174C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000539 | |||||||
chr17:62000677 | T | A | 1 | a0001c0001t0002g0235 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1968-5312A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62000677 | |||||||
chr17:62001353 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1968-5988C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001353 | |||||||
chr17:62001382 | C | CACATCAC others(3): Show |
2 | a0001c0001t0001g0214 a0001c0001t0001g0220 |
2 | NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1968-6018_1968-601 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001382 | |||||||
chr17:62001384 | A | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0220 |
2 | NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1968-6019T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001384 | |||||||
chr17:62001386 | A | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0220 |
2 | NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1968-6021T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001386 | |||||||
chr17:62001387 | C | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0220 |
2 | NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1968-6022G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001387 | |||||||
chr17:62001597 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1968-6232G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001597 | |||||||
chr17:62001620 | A | C | 4 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1968-6255T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001620 | |||||||
chr17:62001674 | T | C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1968-6309A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001674 | |||||||
chr17:62001678 | G | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968-6313C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001678 | |||||||
chr17:62001749 | A | G | 2 | a0001c0002t0001g0039 a0001c0002t0001g0046 |
2 | NA18961.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1968-6384T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001749 | |||||||
chr17:62001822 | C | T | 1 | a0001c0003t0001g0303 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1968-6457G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001822 | |||||||
chr17:62001931 | C | A | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1968-6566G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62001931 | |||||||
chr17:62002298 | T | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1968-6933A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002298 | |||||||
chr17:62002400 | A | C | 4 | a0001c0002t0001g0054 a0001c0002t0001g0056 a0001c0002t0001g0072 others(1): Show |
4 | NA18946.hp1 NA18951.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1968-7035T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002400 | |||||||
chr17:62002489 | C | CA | 104 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0120 others(101): Show |
104 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.1968-7125dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002489 | |||||||
chr17:62002489 | C | CAA | 10 | a0001c0001t0001g0020 a0001c0001t0001g0149 a0001c0001t0001g0212 others(7): Show |
10 | HG01109.hp2 HG01175.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1968-7126_1968-712 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002489 | |||||||
chr17:62002489 | CAAAA | C | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1968-7128_1968-712 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002489 | |||||||
chr17:62002528 | C | G | 1 | a0001c0002t0001g0091 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1968-7163G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002528 | |||||||
chr17:62002563 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1968-7198G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002563 | |||||||
chr17:62002701 | C | T | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1968-7336G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002701 | |||||||
chr17:62002707 | G | GA | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968-7343dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002707 | |||||||
chr17:62002781 | T | C | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1968-7416A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002781 | |||||||
chr17:62002886 | A | G | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1968-7521T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002886 | |||||||
chr17:62002944 | T | C | 2 | a0001c0003t0001g0099 a0001c0015t0001g0096 |
2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1968-7579A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62002944 | |||||||
chr17:62003109 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1967+7441C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003109 | |||||||
chr17:62003148 | A | AT | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG02559.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1967+7401dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003148 | |||||||
chr17:62003149 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1967+7401A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003149 | |||||||
chr17:62003191 | AT | A | 203 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(200): Show |
203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.1967+7358delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003191 | |||||||
chr17:62003364 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1967+7186C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003364 | |||||||
chr17:62003417 | C | T | 1 | a0001c0012t0001g0305 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1967+7133G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003417 | |||||||
chr17:62003599 | C | CA | 14 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
14 | HG01175.hp2 HG02040.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1967+6950dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | |||||||
chr17:62003599 | C | CAAA | 29 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(26): Show |
29 | HG00639.hp1 HG01952.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1967+6948_1967+695 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | |||||||
chr17:62003599 | C | CAAAA | 18 | a0001c0001t0001g0019 a0001c0001t0001g0118 a0001c0001t0001g0212 others(15): Show |
18 | HG01109.hp2 HG01346.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1967+6947_1967+695 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | |||||||
chr17:62003599 | C | CAAAAA | 8 | a0001c0001t0002g0228 a0001c0001t0002g0244 a0001c0001t0002g0257 others(5): Show |
8 | HG01081.hp1 HG01099.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1967+6946_1967+695 others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | |||||||
chr17:62003599 | C | CAAAAAA | 107 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0232 others(104): Show |
107 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1967+6945_1967+695 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | |||||||
chr17:62003599 | C | CAAAAAAA | 27 | a0001c0001t0002g0233 a0001c0001t0002g0239 a0001c0001t0002g0240 others(24): Show |
27 | HG01175.hp1 HG01433.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1967+6944_1967+695 others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | |||||||
chr17:62003599 | C | CAAAAAAA others(1): Show |
9 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0253 others(6): Show |
9 | HG02027.hp1 HG02257.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.1967+6943_1967+695 others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | |||||||
chr17:62003599 | CA | C | 24 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0160 others(21): Show |
24 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1967+6950delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62003599 | |||||||
chr17:62004054 | T | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1967+6496A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004054 | |||||||
chr17:62004246 | T | C | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1967+6304A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004246 | |||||||
chr17:62004262 | A | C | 1 | a0001c0001t0001g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1967+6288T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004262 | |||||||
chr17:62004280 | A | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+6270T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004280 | |||||||
chr17:62004321 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1967+6229T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004321 | |||||||
chr17:62004611 | G | C | 1 | a0001c0002t0001g0091 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1967+5939C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004611 | |||||||
chr17:62004832 | C | T | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1967+5718G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004832 | |||||||
chr17:62004845 | T | C | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1967+5705A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004845 | |||||||
chr17:62004847 | G | A | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1967+5703C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004847 | |||||||
chr17:62004897 | CT | C | 7 | a0001c0001t0001g0135 a0001c0001t0001g0284 a0001c0006t0001g0100 others(4): Show |
7 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+5652delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004897 | |||||||
chr17:62004897 | CTT | C | 67 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(64): Show |
67 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1967+5651_1967+565 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004897 | |||||||
chr17:62004897 | CTTT | C | 171 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(168): Show |
171 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.1967+5650_1967+565 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004897 | |||||||
chr17:62004908 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1967+5642A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004908 | |||||||
chr17:62004931 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1967+5619C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004931 | |||||||
chr17:62004987 | G | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0278 |
3 | NA18965.hp2 NA19012.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1967+5563C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62004987 | |||||||
chr17:62005385 | C | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0201 |
2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1967+5165G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005385 | |||||||
chr17:62005523 | G | T | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1967+5027C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005523 | |||||||
chr17:62005538 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1967+5012C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005538 | |||||||
chr17:62005555 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1967+4995C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005555 | |||||||
chr17:62005566 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1967+4984T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005566 | |||||||
chr17:62005587 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1967+4963G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005587 | |||||||
chr17:62005610 | TAA | T | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1967+4938_1967+493 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005610 | |||||||
chr17:62005815 | A | T | 4 | a0001c0003t0001g0296 a0001c0003t0001g0300 a0001c0003t0001g0306 others(1): Show |
4 | HG03491.hp1 HG03492.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967+4735T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005815 | |||||||
chr17:62005847 | G | T | 95 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(92): Show |
95 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1967+4703C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005847 | |||||||
chr17:62005934 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1967+4616C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005934 | |||||||
chr17:62005980 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1967+4570C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62005980 | |||||||
chr17:62006023 | A | C | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1967+4527T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006023 | |||||||
chr17:62006198 | G | GGACTTAA others(7): Show |
5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+4351_1967+435 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006198 | |||||||
chr17:62006213 | G | A | 209 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(206): Show |
209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.1967+4337C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006213 | |||||||
chr17:62006270 | T | TA | 16 | a0001c0001t0001g0178 a0001c0001t0001g0212 a0001c0001t0002g0239 others(13): Show |
16 | HG01891.hp1 HG02080.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1967+4279dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006270 | |||||||
chr17:62006270 | TA | T | 9 | a0001c0001t0001g0146 a0001c0001t0001g0214 a0001c0002t0001g0058 others(6): Show |
9 | HG01884.hp2 HG02040.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1967+4279delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006270 | |||||||
chr17:62006284 | A | AG | 17 | a0001c0001t0001g0151 a0001c0001t0001g0163 a0001c0001t0001g0180 others(14): Show |
17 | HG00558.hp1 HG00597.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1967+4265dupC | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006284 | |||||||
chr17:62006285 | G | A | 80 | a0001c0001t0001g0315 a0001c0001t0002g0092 a0001c0001t0002g0093 others(77): Show |
80 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1967+4265C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006285 | |||||||
chr17:62006353 | A | T | 2 | a0001c0002t0001g0081 a0001c0002t0001g0083 |
2 | NA19074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1967+4197T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006353 | |||||||
chr17:62006374 | C | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+4176G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006374 | |||||||
chr17:62006613 | TTC | T | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1967+3935_1967+393 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006613 | |||||||
chr17:62006692 | C | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+3858G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006692 | |||||||
chr17:62006904 | G | A | 3 | a0001c0003t0001g0111 a0001c0003t0001g0113 a0001c0003t0001g0117 |
3 | HG02559.hp2 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1967+3646C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62006904 | |||||||
chr17:62007112 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1967+3438C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007112 | |||||||
chr17:62007112 | G | C | 2 | a0001c0004t0001g0010 a0001c0004t0001g0011 |
2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1967+3438C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007112 | |||||||
chr17:62007120 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1967+3430T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007120 | |||||||
chr17:62007273 | C | T | 5 | a0001c0004t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 others(2): Show |
5 | HG02055.hp2 HG02818.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1967+3277G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007273 | |||||||
chr17:62007368 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1967+3182T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007368 | |||||||
chr17:62007436 | A | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0201 |
2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1967+3114T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007436 | |||||||
chr17:62007461 | C | G | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1967+3089G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007461 | |||||||
chr17:62007575 | G | A | 1 | a0001c0007t0006g0279 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1967+2975C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007575 | |||||||
chr17:62007582 | T | C | 65 | a0001c0002t0001g0001 a0001c0002t0001g0031 a0001c0002t0001g0032 others(62): Show |
65 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1967+2968A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007582 | |||||||
chr17:62007585 | A | T | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1967+2965T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007585 | |||||||
chr17:62007634 | G | C | 1 | a0001c0001t0002g0240 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1967+2916C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007634 | |||||||
chr17:62007729 | C | T | 2 | a0001c0001t0002g0250 a0001c0001t0002g0263 |
2 | HG01109.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1967+2821G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007729 | |||||||
chr17:62007797 | A | G | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1967+2753T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62007797 | |||||||
chr17:62008016 | C | CA | 10 | a0001c0001t0001g0130 a0001c0001t0001g0150 a0001c0001t0001g0157 others(7): Show |
10 | HG01175.hp2 HG02523.hp1 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.1967+2533dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAA | 6 | a0001c0003t0001g0023 a0001c0003t0001g0024 a0001c0003t0001g0030 others(3): Show |
6 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1967+2529_1967+253 others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAA | 52 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(49): Show |
52 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1967+2528_1967+253 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA | 41 | a0001c0001t0001g0019 a0001c0001t0001g0213 a0001c0001t0003g0290 others(38): Show |
41 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1967+2527_1967+253 others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(3): Show |
19 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(16): Show |
19 | HG00438.hp1 HG02071.hp1 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.1967+2524_1967+253 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(4): Show |
26 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 others(23): Show |
26 | HG00423.hp1 HG00642.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1967+2523_1967+253 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(5): Show |
6 | a0001c0001t0002g0237 a0001c0001t0002g0257 a0001c0001t0002g0260 others(3): Show |
6 | HG01081.hp1 HG01109.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1967+2522_1967+253 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0118 a0001c0001t0002g0238 a0001c0001t0002g0251 others(1): Show |
4 | HG02976.hp2 NA18948.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1967+2521_1967+253 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(7): Show |
1 | a0002c0005t0001g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1967+2520_1967+253 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0120 a0001c0003t0001g0099 a0001c0015t0001g0096 others(1): Show |
4 | HG01109.hp2 HG01952.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967+2518_1967+253 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0121 a0001c0001t0001g0216 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1967+2517_1967+253 others(21): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(11): Show |
3 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0002c0005t0001g0005 |
3 | HG01891.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1967+2516_1967+253 others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(13): Show |
2 | a0001c0004t0001g0014 a0002c0005t0001g0289 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1967+2514_1967+253 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(14): Show |
3 | a0001c0004t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0015 |
3 | HG03516.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1967+2533_1967+253 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(15): Show |
1 | a0001c0004t0001g0022 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(16): Show |
1 | a0002c0005t0001g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(27): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(17): Show |
1 | a0002c0005t0001g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(28): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(19): Show |
1 | a0001c0004t0001g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(30): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(25): Show |
1 | a0001c0003t0001g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(36): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(28): Show |
1 | a0002c0005t0001g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(39): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | C | CAAAAAAA others(29): Show |
1 | a0002c0005t0001g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1967+2533_1967+253 others(40): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008016 | CAA | C | 17 | a0001c0001t0001g0214 a0001c0003t0001g0107 a0001c0003t0001g0108 others(14): Show |
17 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1967+2532_1967+253 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008016 | |||||||
chr17:62008039 | T | C | 101 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(98): Show |
101 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1967+2511A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008039 | |||||||
chr17:62008043 | C | A | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1967+2507G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008043 | |||||||
chr17:62008058 | C | G | 1 | a0001c0002t0001g0071 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1967+2492G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008058 | |||||||
chr17:62008074 | T | G | 2 | a0001c0003t0001g0099 a0001c0015t0001g0096 |
2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1967+2476A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008074 | |||||||
chr17:62008125 | G | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+2425C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008125 | |||||||
chr17:62008266 | A | C | 203 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(200): Show |
203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.1967+2284T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008266 | |||||||
chr17:62008295 | G | T | 1 | a0001c0001t0012g0256 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1967+2255C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008295 | |||||||
chr17:62008304 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1967+2246G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008304 | |||||||
chr17:62008305 | G | A | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+2245C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008305 | |||||||
chr17:62008317 | C | CA | 13 | a0001c0001t0001g0149 a0001c0001t0001g0155 a0001c0001t0001g0182 others(10): Show |
13 | HG00597.hp1 HG03195.hp1 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.1967+2232dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | C | CAAAAAAA others(2): Show |
54 | a0001c0001t0002g0093 a0001c0001t0002g0228 a0001c0001t0002g0233 others(51): Show |
54 | HG00423.hp2 HG00642.hp1 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.1967+2224_1967+223 others(13): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | C | CAAAAAAA others(3): Show |
69 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 others(66): Show |
69 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1967+2223_1967+223 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | C | CAAAAAAA others(4): Show |
36 | a0001c0001t0002g0234 a0001c0001t0002g0241 a0001c0001t0002g0242 others(33): Show |
36 | HG00438.hp1 HG00639.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1967+2222_1967+223 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | C | CAAAAAAA others(5): Show |
12 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0002g0266 others(9): Show |
12 | HG00438.hp2 HG00544.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.1967+2221_1967+223 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | C | CAAAAAAA others(6): Show |
7 | a0001c0001t0001g0020 a0001c0001t0002g0311 a0001c0001t0011g0016 others(4): Show |
7 | HG01978.hp1 HG02293.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+2220_1967+223 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | C | CAAAAAAA others(7): Show |
2 | a0001c0002t0001g0074 a0001c0003t0001g0304 |
2 | HG01243.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1967+2219_1967+223 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1967+2216_1967+223 others(21): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | C | CAAAAAAA others(13): Show |
1 | a0001c0007t0006g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1967+2213_1967+223 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | C | CAAAAAAA others(14): Show |
1 | a0001c0007t0006g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1967+2212_1967+223 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | C | CAAAAAAA others(16): Show |
1 | a0005c0022t0006g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1967+2210_1967+223 others(27): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | C | CAAAAAAA others(21): Show |
1 | a0001c0007t0006g0279 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1967+2232_1967+223 others(32): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | CA | C | 8 | a0001c0001t0001g0159 a0001c0001t0001g0189 a0001c0001t0001g0195 others(5): Show |
8 | HG01168.hp1 HG01168.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1967+2232delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008317 | CAAAA | C | 7 | a0001c0001t0001g0315 a0001c0004t0001g0012 a0001c0004t0001g0013 others(4): Show |
7 | HG01346.hp2 HG02055.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1967+2229_1967+223 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008317 | |||||||
chr17:62008449 | G | A | 2 | a0001c0008t0001g0122 a0001c0008t0001g0128 |
2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1967+2101C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008449 | |||||||
chr17:62008611 | G | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+1939C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008611 | |||||||
chr17:62008699 | C | G | 1 | a0001c0006t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1967+1851G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008699 | |||||||
chr17:62008861 | A | G | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+1689T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62008861 | |||||||
chr17:62009025 | C | A | 208 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(205): Show |
208 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.1967+1525G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009025 | |||||||
chr17:62009147 | G | C | 37 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(34): Show |
37 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1967+1403C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009147 | |||||||
chr17:62009226 | T | C | 3 | a0001c0003t0001g0303 a0001c0003t0001g0304 a0001c0012t0001g0305 |
3 | HG01243.hp2 HG03654.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1967+1324A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009226 | |||||||
chr17:62009324 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1967+1226C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009324 | |||||||
chr17:62009328 | G | A | 1 | a0001c0004t0001g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1967+1222C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009328 | |||||||
chr17:62009565 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1967+985C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009565 | |||||||
chr17:62009624 | A | G | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+926T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009624 | |||||||
chr17:62009653 | G | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+897C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009653 | |||||||
chr17:62009721 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1967+829A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009721 | |||||||
chr17:62009834 | T | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(13): Show |
16 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1967+716A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009834 | |||||||
chr17:62009837 | G | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1967+713C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009837 | |||||||
chr17:62009847 | T | C | 1 | a0001c0002t0001g0065 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1967+703A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009847 | |||||||
chr17:62009859 | G | A | 1 | a0001c0008t0001g0122 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1967+691C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009859 | |||||||
chr17:62009894 | G | A | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1967+656C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009894 | |||||||
chr17:62009988 | G | A | 65 | a0001c0002t0001g0001 a0001c0002t0001g0031 a0001c0002t0001g0032 others(62): Show |
65 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1967+562C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62009988 | |||||||
chr17:62010107 | A | T | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1967+443T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010107 | |||||||
chr17:62010121 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1967+429G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010121 | |||||||
chr17:62010149 | A | G | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1967+401T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010149 | |||||||
chr17:62010153 | G | A | 5 | a0001c0001t0002g0268 a0001c0007t0006g0279 a0001c0007t0006g0280 others(2): Show |
5 | HG02257.hp1 HG02698.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1967+397C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010153 | |||||||
chr17:62010168 | C | T | 8 | a0001c0003t0001g0023 a0001c0003t0001g0025 a0001c0003t0001g0030 others(5): Show |
8 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1967+382G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010168 | |||||||
chr17:62010216 | C | CA | 7 | a0001c0001t0002g0272 a0001c0004t0001g0012 a0001c0004t0001g0013 others(4): Show |
7 | HG02055.hp2 HG02071.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1967+333dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010216 | |||||||
chr17:62010279 | T | C | 1 | a0001c0001t0027g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1967+271A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | 62010279 | |||||||
chr17:62011317 | C | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1284-84G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011317 | |||||||
chr17:62011318 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1284-85C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011318 | |||||||
chr17:62011346 | C | A | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284-113G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011346 | |||||||
chr17:62011401 | T | C | 9 | a0001c0003t0001g0023 a0001c0003t0001g0024 a0001c0003t0001g0025 others(6): Show |
9 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1284-168A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011401 | |||||||
chr17:62011454 | C | G | 1 | a0001c0003t0001g0293 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1284-221G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011454 | |||||||
chr17:62011457 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1284-224T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011457 | |||||||
chr17:62011550 | T | A | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284-317A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011550 | |||||||
chr17:62011877 | G | A | 14 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 others(11): Show |
14 | HG02027.hp1 HG02293.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.1284-644C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011877 | |||||||
chr17:62011911 | A | G | 17 | a0001c0003t0001g0105 a0001c0003t0001g0107 a0001c0003t0001g0108 others(14): Show |
17 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1284-678T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011911 | |||||||
chr17:62011975 | G | A | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1284-742C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62011975 | |||||||
chr17:62012088 | C | T | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1284-855G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012088 | |||||||
chr17:62012215 | C | CA | 7 | a0001c0001t0002g0246 a0001c0001t0002g0261 a0001c0001t0002g0269 others(4): Show |
7 | HG00438.hp1 NA18963.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284-983dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012215 | |||||||
chr17:62012327 | C | CT | 14 | a0001c0001t0001g0126 a0001c0001t0001g0179 a0001c0001t0001g0192 others(11): Show |
14 | HG01243.hp1 HG01243.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.1284-1095dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012327 | |||||||
chr17:62012327 | C | CTT | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284-1096_1284-109 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012327 | |||||||
chr17:62012327 | CT | C | 63 | a0001c0001t0001g0123 a0001c0001t0001g0174 a0001c0001t0001g0175 others(60): Show |
63 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1284-1095delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012327 | |||||||
chr17:62012327 | CTT | C | 31 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0003t0001g0098 others(28): Show |
31 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1284-1096_1284-109 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012327 | |||||||
chr17:62012359 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284-1126G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012359 | |||||||
chr17:62012422 | G | A | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1284-1189C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012422 | |||||||
chr17:62012542 | C | T | 4 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284-1309G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012542 | |||||||
chr17:62012552 | A | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | HG02559.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1284-1319T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012552 | |||||||
chr17:62012619 | C | T | 1 | a0001c0003t0001g0300 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1284-1386G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012619 | |||||||
chr17:62012620 | G | A | 1 | a0001c0008t0001g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1284-1387C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012620 | |||||||
chr17:62012621 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1284-1388A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012621 | |||||||
chr17:62012696 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1284-1463A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012696 | |||||||
chr17:62012705 | C | CT | 5 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0150 others(2): Show |
5 | HG02155.hp2 HG02523.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-1473dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012705 | |||||||
chr17:62012724 | C | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-1491G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012724 | |||||||
chr17:62012760 | C | T | 1 | a0001c0001t0021g0254 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1284-1527G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012760 | |||||||
chr17:62012800 | T | A | 1 | a0001c0003t0001g0024 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1284-1567A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012800 | |||||||
chr17:62012838 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1284-1605C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012838 | |||||||
chr17:62012888 | G | T | 2 | a0001c0002t0001g0084 a0001c0002t0001g0087 |
2 | NA18960.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1284-1655C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62012888 | |||||||
chr17:62013166 | A | C | 2 | a0001c0001t0002g0260 a0001c0001t0003g0259 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1284-1933T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62013166 | |||||||
chr17:62013338 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-2105G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62013338 | |||||||
chr17:62013637 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1284-2404G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62013637 | |||||||
chr17:62013780 | C | T | 1 | a0001c0001t0002g0311 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1284-2547G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62013780 | |||||||
chr17:62013854 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1284-2621G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62013854 | |||||||
chr17:62014040 | C | T | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1284-2807G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014040 | |||||||
chr17:62014042 | C | T | 6 | a0001c0004t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 others(3): Show |
6 | HG02055.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284-2809G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014042 | |||||||
chr17:62014130 | T | C | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1284-2897A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014130 | |||||||
chr17:62014169 | T | C | 5 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0150 others(2): Show |
5 | HG02155.hp2 HG02523.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-2936A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014169 | |||||||
chr17:62014308 | T | TTATATAT others(3): Show |
1 | a0001c0006t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1284-3076_1284-307 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014308 | |||||||
chr17:62014308 | T | TTATATAT others(5): Show |
5 | a0001c0003t0001g0114 a0001c0006t0001g0100 a0001c0006t0001g0101 others(2): Show |
5 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284-3076_1284-307 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014308 | |||||||
chr17:62014308 | T | TTATATAT others(7): Show |
2 | a0001c0003t0001g0105 a0001c0003t0001g0109 |
2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1284-3076_1284-307 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014308 | |||||||
chr17:62014308 | T | TTATATAT others(9): Show |
8 | a0001c0003t0001g0104 a0001c0003t0001g0107 a0001c0003t0001g0110 others(5): Show |
8 | HG02559.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-3076_1284-307 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014308 | |||||||
chr17:62014308 | T | TTATATAT others(11): Show |
3 | a0001c0003t0001g0108 a0001c0003t0001g0112 a0001c0003t0001g0117 |
3 | HG02809.hp1 NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1284-3076_1284-307 others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014308 | |||||||
chr17:62014310 | T | A | 21 | a0001c0001t0001g0315 a0001c0003t0001g0104 a0001c0003t0001g0105 others(18): Show |
21 | HG00639.hp1 HG01346.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1284-3077A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | |||||||
chr17:62014310 | T | TTA | 89 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 others(86): Show |
89 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1284-3079_1284-307 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | |||||||
chr17:62014310 | T | TTATA | 73 | a0001c0001t0002g0246 a0001c0001t0002g0261 a0001c0001t0002g0269 others(70): Show |
73 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1284-3081_1284-307 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | |||||||
chr17:62014310 | T | TTATATA | 5 | a0001c0001t0001g0202 a0001c0002t0001g0073 a0001c0002t0001g0074 others(2): Show |
5 | HG01109.hp2 HG02056.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284-3083_1284-307 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | |||||||
chr17:62014310 | T | TTATATAT others(5): Show |
4 | a0001c0004t0001g0014 a0001c0004t0001g0015 a0001c0004t0001g0021 others(1): Show |
4 | HG02055.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-3089_1284-307 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | |||||||
chr17:62014310 | T | TTATATAT others(7): Show |
2 | a0001c0004t0001g0012 a0001c0004t0001g0013 |
2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1284-3091_1284-307 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | |||||||
chr17:62014310 | T | TTATATAT others(31): Show |
1 | a0001c0004t0001g0011 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1284-3078_1284-307 others(42): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | |||||||
chr17:62014310 | T | TTATATAT others(57): Show |
1 | a0001c0004t0001g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1284-3078_1284-307 others(68): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014310 | |||||||
chr17:62014379 | C | T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1284-3146G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014379 | |||||||
chr17:62014520 | T | C | 31 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0130 others(28): Show |
31 | HG00140.hp1 HG01106.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1284-3287A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014520 | |||||||
chr17:62014545 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1284-3312C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014545 | |||||||
chr17:62014596 | C | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1284-3363G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014596 | |||||||
chr17:62014658 | T | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-3425A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014658 | |||||||
chr17:62014672 | T | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-3439A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014672 | |||||||
chr17:62014996 | G | A | 23 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0160 others(20): Show |
23 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1284-3763C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62014996 | |||||||
chr17:62015215 | G | A | 5 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0001c0001t0002g0248 others(2): Show |
5 | HG00642.hp1 HG01433.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-3982C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015215 | |||||||
chr17:62015397 | G | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1284-4164C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015397 | |||||||
chr17:62015504 | G | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-4271C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015504 | |||||||
chr17:62015708 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1284-4475C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015708 | |||||||
chr17:62015786 | T | C | 57 | a0001c0001t0001g0221 a0001c0001t0002g0092 a0001c0001t0002g0093 others(54): Show |
57 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.1284-4553A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015786 | |||||||
chr17:62015819 | T | TAC | 3 | a0001c0002t0009g0049 a0001c0002t0024g0057 a0001c0021t0017g0283 |
3 | HG00558.hp2 HG02083.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1284-4588_1284-458 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015819 | |||||||
chr17:62015825 | C | CACTA | 98 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(95): Show |
98 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1284-4593_1284-459 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015825 | |||||||
chr17:62015833 | A | T | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284-4600T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015833 | |||||||
chr17:62015834 | T | C | 94 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(91): Show |
94 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1284-4601A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015834 | |||||||
chr17:62015836 | C | T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1284-4603G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015836 | |||||||
chr17:62015865 | GTA | G | 7 | a0001c0003t0001g0299 a0002c0005t0001g0003 a0002c0005t0001g0004 others(4): Show |
7 | HG01099.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284-4634_1284-463 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015865 | |||||||
chr17:62015867 | A | ATG | 112 | a0001c0001t0001g0213 a0001c0001t0003g0290 a0001c0001t0003g0294 others(109): Show |
112 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1284-4636_1284-463 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015867 | |||||||
chr17:62015879 | A | G | 8 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0047 others(5): Show |
8 | HG02132.hp1 NA18612.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-4646T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015879 | |||||||
chr17:62015888 | C | T | 109 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(106): Show |
109 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1284-4655G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015888 | |||||||
chr17:62015890 | C | T | 8 | a0001c0002t0001g0034 a0001c0002t0001g0045 a0001c0002t0001g0047 others(5): Show |
8 | HG02132.hp1 NA18612.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-4657G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015890 | |||||||
chr17:62015902 | T | C | 10 | a0001c0002t0001g0034 a0001c0002t0001g0041 a0001c0002t0001g0045 others(7): Show |
10 | HG02132.hp1 NA18612.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.1284-4669A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015902 | |||||||
chr17:62015915 | C | CACACACA others(9): Show |
1 | a0001c0001t0002g0270 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1284-4683_1284-468 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | C | CACATACA others(3): Show |
1 | a0001c0001t0002g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1284-4683_1284-468 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | C | CAT | 7 | a0001c0001t0001g0137 a0001c0001t0001g0154 a0001c0001t0001g0166 others(4): Show |
7 | HG01358.hp1 HG01516.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1284-4684_1284-468 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | C | CATAT | 6 | a0001c0001t0001g0151 a0001c0001t0001g0161 a0001c0001t0001g0185 others(3): Show |
6 | HG00558.hp1 HG01346.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1284-4686_1284-468 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | C | CATATAT | 7 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0164 others(4): Show |
7 | HG01934.hp1 HG01993.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1284-4688_1284-468 others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | C | CATATATA others(1): Show |
3 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0197 |
3 | NA18948.hp1 NA18980.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1284-4690_1284-468 others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0214 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1284-4692_1284-468 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | C | CATATATA others(5): Show |
2 | a0001c0001t0004g0139 a0001c0001t0004g0211 |
2 | NA18952.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1284-4694_1284-468 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | C | CATATATA others(7): Show |
1 | a0001c0001t0001g0218 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1284-4696_1284-468 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | C | CATATATA others(9): Show |
1 | a0001c0002t0001g0062 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1284-4698_1284-468 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | C | CATATATA others(15): Show |
1 | a0001c0001t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1284-4704_1284-468 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | CATATATA others(3): Show |
C | 1 | a0001c0001t0001g0220 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1284-4692_1284-468 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015915 | CATATATA others(7): Show |
C | 1 | a0001c0001t0001g0119 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1284-4696_1284-468 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015915 | |||||||
chr17:62015917 | T | C | 88 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(85): Show |
88 | HG00438.hp1 HG00639.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.1284-4684A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015917 | |||||||
chr17:62015917 | T | TATATATA others(28): Show |
1 | a0001c0007t0006g0279 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1284-4685_1284-468 others(39): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015917 | |||||||
chr17:62015919 | T | C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(12): Show |
15 | HG00438.hp1 HG00639.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1284-4686A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015919 | |||||||
chr17:62015921 | T | C | 2 | a0001c0001t0002g0228 a0001c0001t0002g0250 |
2 | HG01175.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1284-4688A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015921 | |||||||
chr17:62015923 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1284-4690A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015923 | |||||||
chr17:62015925 | T | TACACACA others(20): Show |
3 | a0001c0007t0006g0280 a0001c0007t0006g0282 a0005c0022t0006g0281 |
3 | HG02257.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1284-4693_1284-469 others(31): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015925 | |||||||
chr17:62015930 | ATATATAT others(19): Show |
A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0155 |
3 | NA18950.hp2 NA18970.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1284-4723_1284-469 others(30): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015930 | |||||||
chr17:62015932 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0008g0162 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1284-4724_1284-470 others(29): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015932 | |||||||
chr17:62015932 | ATATATAT others(33): Show |
A | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1284-4739_1284-470 others(44): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015932 | |||||||
chr17:62015934 | A | T | 2 | a0001c0002t0001g0051 a0001c0003t0001g0309 |
2 | HG00639.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1284-4701T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015934 | |||||||
chr17:62015934 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1284-4722_1284-470 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015934 | |||||||
chr17:62015936 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0201 |
2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1284-4726_1284-470 others(27): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015936 | |||||||
chr17:62015936 | ATATATAT others(17): Show |
A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1284-4727_1284-470 others(28): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015936 | |||||||
chr17:62015936 | ATATATAT others(24): Show |
A | 2 | a0001c0001t0002g0092 a0001c0001t0002g0093 |
2 | NA18952.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1284-4734_1284-470 others(35): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015936 | |||||||
chr17:62015938 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0015g0156 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1284-4727_1284-470 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015938 | |||||||
chr17:62015938 | ATATATAT others(19): Show |
A | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1284-4731_1284-470 others(30): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015938 | |||||||
chr17:62015940 | ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0206 |
2 | HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1284-4727_1284-470 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015940 | |||||||
chr17:62015940 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1284-4728_1284-470 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015940 | |||||||
chr17:62015942 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1284-4726_1284-471 others(21): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015942 | |||||||
chr17:62015942 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0022g0165 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1284-4727_1284-471 others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015942 | |||||||
chr17:62015942 | ATATATAT others(15): Show |
A | 3 | a0001c0001t0001g0121 a0001c0001t0002g0248 a0001c0001t0002g0255 |
3 | HG00642.hp1 HG01433.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1284-4731_1284-471 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015942 | |||||||
chr17:62015944 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1284-4722_1284-471 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015944 | |||||||
chr17:62015944 | ATATATAT others(13): Show |
A | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1284-4731_1284-471 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015944 | |||||||
chr17:62015944 | ATATATAT others(15): Show |
A | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1284-4733_1284-471 others(26): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015944 | |||||||
chr17:62015946 | ATATATAT others(10): Show |
A | 1 | a0001c0015t0001g0096 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1284-4730_1284-471 others(21): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015946 | |||||||
chr17:62015946 | ATATATAT others(11): Show |
A | 2 | a0002c0005t0001g0003 a0002c0005t0001g0005 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1284-4731_1284-471 others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015946 | |||||||
chr17:62015946 | ATATATAT others(12): Show |
A | 4 | a0001c0001t0002g0237 a0001c0003t0001g0098 a0001c0003t0001g0104 others(1): Show |
4 | HG02717.hp2 HG02735.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284-4732_1284-471 others(23): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015946 | |||||||
chr17:62015948 | A | T | 5 | a0001c0001t0003g0294 a0001c0001t0003g0295 a0001c0003t0001g0293 others(2): Show |
5 | HG01516.hp1 HG01517.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284-4715T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | |||||||
chr17:62015948 | ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0196 |
2 | HG00642.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1284-4725_1284-471 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | |||||||
chr17:62015948 | ATATATAT others(8): Show |
A | 1 | a0001c0003t0001g0099 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1284-4730_1284-471 others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | |||||||
chr17:62015948 | ATATATAT others(9): Show |
A | 2 | a0002c0005t0001g0004 a0002c0005t0001g0006 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1284-4731_1284-471 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | |||||||
chr17:62015948 | ATATATAT others(13): Show |
A | 1 | a0001c0003t0001g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1284-4735_1284-471 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | |||||||
chr17:62015948 | ATATATAT others(14): Show |
A | 1 | a0001c0002t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1284-4736_1284-471 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015948 | |||||||
chr17:62015950 | A | T | 3 | a0001c0002t0001g0040 a0001c0002t0001g0088 a0001c0003t0001g0304 |
3 | HG01243.hp2 NA18954.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1284-4717T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | |||||||
chr17:62015950 | ATATATTT others(3): Show |
A | 2 | a0001c0001t0001g0205 a0003c0014t0014g0287 |
2 | HG01358.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1284-4727_1284-471 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | |||||||
chr17:62015950 | ATATATTT others(5): Show |
A | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1284-4729_1284-471 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | |||||||
chr17:62015950 | ATATATTT others(8): Show |
A | 1 | a0001c0006t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1284-4732_1284-471 others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | |||||||
chr17:62015950 | ATATATTT others(9): Show |
A | 1 | a0007c0010t0001g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1284-4733_1284-471 others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | |||||||
chr17:62015950 | ATATATTT others(10): Show |
A | 1 | a0001c0003t0001g0111 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1284-4734_1284-471 others(21): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | |||||||
chr17:62015950 | ATATATTT others(14): Show |
A | 1 | a0001c0002t0024g0057 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1284-4738_1284-471 others(25): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015950 | |||||||
chr17:62015951 | TATA | T | 13 | a0001c0001t0003g0290 a0001c0001t0003g0297 a0001c0001t0003g0301 others(10): Show |
13 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1284-4721_1284-471 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015951 | |||||||
chr17:62015952 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1284-4719T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015952 | |||||||
chr17:62015952 | ATATTTTT others(5): Show |
A | 1 | a0002c0005t0001g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1284-4731_1284-472 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015952 | |||||||
chr17:62015952 | ATATTTTT others(6): Show |
A | 5 | a0001c0001t0002g0239 a0001c0001t0010g0265 a0001c0003t0001g0114 others(2): Show |
5 | HG01891.hp2 HG02602.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284-4732_1284-472 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015952 | |||||||
chr17:62015952 | ATATTTTT others(8): Show |
A | 1 | a0001c0003t0001g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1284-4734_1284-472 others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015952 | |||||||
chr17:62015953 | TA | T | 22 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0002t0001g0001 others(19): Show |
22 | HG00597.hp2 HG02027.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.1284-4721delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015953 | |||||||
chr17:62015954 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0184 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1284-4722_1284-472 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | A | ATATATAT others(8): Show |
1 | a0001c0002t0026g0053 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1284-4722_1284-472 others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | A | ATATATAT others(12): Show |
1 | a0001c0002t0001g0061 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1284-4722_1284-472 others(23): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0208 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1284-4722_1284-472 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | A | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0220 a0001c0002t0001g0044 others(1): Show |
4 | HG01934.hp2 HG01993.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-4721T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | AT | A | 10 | a0001c0001t0001g0179 a0001c0001t0001g0188 a0001c0001t0001g0212 others(7): Show |
10 | HG00438.hp1 HG02071.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284-4722delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATT | A | 10 | a0001c0001t0001g0129 a0001c0001t0001g0159 a0001c0001t0001g0171 others(7): Show |
10 | HG00140.hp1 HG00597.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATTT | A | 15 | a0001c0001t0001g0173 a0001c0001t0001g0198 a0001c0001t0001g0209 others(12): Show |
15 | HG01099.hp1 HG01175.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1284-4724_1284-472 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATTTT | A | 10 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0123 others(7): Show |
10 | HG01168.hp1 HG02922.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.1284-4725_1284-472 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATTTTT | A | 19 | a0001c0001t0001g0124 a0001c0001t0001g0186 a0001c0001t0001g0199 others(16): Show |
19 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1284-4726_1284-472 others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATTTTTTT | A | 9 | a0001c0001t0001g0157 a0001c0001t0001g0192 a0001c0001t0002g0269 others(6): Show |
9 | HG01243.hp1 HG01516.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1284-4728_1284-472 others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATTTTTTT others(2): Show |
A | 8 | a0001c0001t0001g0017 a0001c0003t0001g0025 a0001c0003t0001g0030 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-4730_1284-472 others(13): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(4): Show |
7 | HG02055.hp2 HG02300.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1284-4731_1284-472 others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0010g0264 a0001c0006t0001g0100 a0001c0006t0001g0101 others(1): Show |
4 | HG02055.hp1 HG02895.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284-4732_1284-472 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATTTTTTT others(5): Show |
A | 1 | a0001c0004t0001g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1284-4733_1284-472 others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATTTTTTT others(6): Show |
A | 1 | a0001c0003t0001g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1284-4734_1284-472 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0213 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1284-4735_1284-472 others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015954 | ATTTTTTT others(8): Show |
A | 1 | a0001c0003t0001g0323 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1284-4736_1284-472 others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015954 | |||||||
chr17:62015955 | T | TA | 9 | a0001c0001t0001g0146 a0001c0001t0002g0228 a0001c0001t0002g0235 others(6): Show |
9 | HG02622.hp1 HG03540.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015955 | |||||||
chr17:62015955 | T | TATA | 12 | a0001c0001t0001g0172 a0001c0001t0001g0203 a0001c0001t0001g0219 others(9): Show |
12 | HG02056.hp2 HG02083.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015955 | |||||||
chr17:62015955 | T | TATATA | 3 | a0001c0001t0001g0169 a0001c0001t0002g0240 a0001c0001t0002g0252 |
3 | HG01928.hp1 NA18948.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(9): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015955 | |||||||
chr17:62015955 | T | TATATATA | 5 | a0001c0001t0002g0253 a0001c0001t0012g0258 a0001c0001t0021g0254 others(2): Show |
5 | HG02572.hp1 HG02970.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015955 | |||||||
chr17:62015955 | T | TATATATA others(4): Show |
3 | a0001c0001t0001g0202 a0001c0001t0003g0136 a0001c0001t0025g0008 |
3 | HG02027.hp2 HG02895.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1284-4723_1284-472 others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015955 | |||||||
chr17:62015956 | T | A | 44 | a0001c0001t0001g0094 a0001c0001t0001g0134 a0001c0001t0001g0137 others(41): Show |
44 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1284-4723A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015956 | |||||||
chr17:62015957 | T | A | 77 | a0001c0001t0001g0146 a0001c0001t0001g0169 a0001c0001t0001g0172 others(74): Show |
77 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1284-4724A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015957 | |||||||
chr17:62015957 | T | TA | 16 | a0001c0002t0001g0036 a0001c0002t0001g0038 a0001c0002t0001g0041 others(13): Show |
16 | HG00423.hp2 HG00558.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1284-4725_1284-472 others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015957 | |||||||
chr17:62015958 | T | A | 41 | a0001c0001t0001g0094 a0001c0001t0001g0129 a0001c0001t0001g0159 others(38): Show |
41 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1284-4725A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015958 | |||||||
chr17:62015959 | T | A | 104 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0173 others(101): Show |
104 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1284-4726A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015959 | |||||||
chr17:62015959 | T | TATA | 10 | a0001c0002t0001g0031 a0001c0002t0001g0033 a0001c0002t0001g0035 others(7): Show |
10 | HG00544.hp1 HG02080.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1284-4727_1284-472 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015959 | |||||||
chr17:62015960 | T | A | 45 | a0001c0001t0001g0094 a0001c0001t0001g0118 a0001c0001t0001g0120 others(42): Show |
45 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1284-4727A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015960 | |||||||
chr17:62015961 | T | A | 120 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0199 others(117): Show |
120 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1284-4728A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015961 | |||||||
chr17:62015962 | T | A | 32 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0133 others(29): Show |
32 | HG00423.hp1 HG00438.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1284-4729A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015962 | |||||||
chr17:62015963 | T | A | 123 | a0001c0001t0001g0216 a0001c0001t0001g0225 a0001c0001t0002g0228 others(120): Show |
123 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1284-4730A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015963 | |||||||
chr17:62015964 | T | A | 25 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0002g0238 others(22): Show |
25 | HG00423.hp1 HG00438.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1284-4731A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015964 | |||||||
chr17:62015965 | T | A | 118 | a0001c0001t0001g0017 a0001c0001t0002g0228 a0001c0001t0002g0235 others(115): Show |
118 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1284-4732A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015965 | |||||||
chr17:62015966 | T | A | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
20 | HG00438.hp2 HG01928.hp2 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.1284-4733A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015966 | |||||||
chr17:62015967 | T | A | 100 | a0001c0001t0001g0017 a0001c0001t0002g0246 a0001c0001t0002g0257 others(97): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1284-4734A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015967 | |||||||
chr17:62015968 | T | A | 13 | a0001c0001t0001g0020 a0001c0001t0002g0278 a0001c0001t0011g0016 others(10): Show |
13 | HG00438.hp2 HG01928.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.1284-4735A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015968 | |||||||
chr17:62015969 | T | A | 72 | a0001c0001t0002g0257 a0001c0002t0001g0001 a0001c0002t0001g0031 others(69): Show |
72 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1284-4736A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015969 | |||||||
chr17:62015969 | T | TATATATA others(6): Show |
1 | a0001c0002t0001g0032 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1284-4737_1284-473 others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015969 | |||||||
chr17:62015970 | T | A | 9 | a0001c0002t0001g0039 a0001c0002t0001g0044 a0001c0002t0001g0046 others(6): Show |
9 | HG00438.hp2 HG01928.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1284-4737A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015970 | |||||||
chr17:62015971 | T | A | 16 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0041 others(13): Show |
16 | HG02132.hp1 HG02622.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.1284-4738A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015971 | |||||||
chr17:62015993 | C | T | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1284-4760G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62015993 | |||||||
chr17:62016061 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(1): Show |
4 | HG03130.hp1 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-4828G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016061 | |||||||
chr17:62016165 | C | A | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-4932G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016165 | |||||||
chr17:62016172 | C | CA | 22 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 others(19): Show |
22 | HG01952.hp1 HG02071.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1284-4940dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016172 | |||||||
chr17:62016174 | AC | A | 3 | a0001c0001t0001g0315 a0001c0003t0001g0107 a0004c0011t0001g0095 |
3 | HG01346.hp2 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1284-4942delG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016174 | |||||||
chr17:62016175 | C | A | 104 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(101): Show |
104 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.1284-4942G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016175 | |||||||
chr17:62016177 | A | C | 2 | a0001c0001t0002g0236 a0001c0001t0002g0249 |
2 | NA18962.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1284-4944T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016177 | |||||||
chr17:62016178 | C | A | 107 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(104): Show |
107 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.1284-4945G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016178 | |||||||
chr17:62016178 | C | CA | 6 | a0001c0001t0001g0220 a0001c0001t0004g0227 a0001c0007t0006g0279 others(3): Show |
6 | HG02257.hp1 HG03540.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284-4946dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016178 | |||||||
chr17:62016181 | A | C | 102 | a0001c0001t0001g0134 a0001c0001t0001g0189 a0001c0001t0001g0191 others(99): Show |
102 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1284-4948T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016181 | |||||||
chr17:62016183 | A | C | 1 | a0001c0001t0002g0313 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1284-4950T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016183 | |||||||
chr17:62016371 | G | C | 1 | a0001c0003t0001g0291 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1284-5138C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016371 | |||||||
chr17:62016521 | T | C | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1284-5288A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016521 | |||||||
chr17:62016522 | C | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-5289G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016522 | |||||||
chr17:62016666 | A | C | 1 | a0001c0001t0001g0207 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1284-5433T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016666 | |||||||
chr17:62016785 | G | C | 1 | a0001c0007t0006g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1284-5552C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62016785 | |||||||
chr17:62017033 | T | A | 31 | a0001c0002t0001g0034 a0001c0002t0001g0041 a0001c0002t0001g0045 others(28): Show |
31 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1284-5800A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017033 | |||||||
chr17:62017179 | T | C | 1 | a0001c0003t0001g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1284-5946A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017179 | |||||||
chr17:62017219 | T | TA | 88 | a0001c0001t0001g0193 a0001c0001t0001g0204 a0001c0001t0001g0324 others(85): Show |
88 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1284-5987dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017219 | |||||||
chr17:62017219 | T | TAA | 16 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(13): Show |
16 | HG00544.hp1 HG00639.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1284-5988_1284-598 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017219 | |||||||
chr17:62017219 | TA | T | 72 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(69): Show |
72 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1284-5987delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017219 | |||||||
chr17:62017243 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(3): Show |
6 | HG02258.hp1 HG02300.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284-6010T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017243 | |||||||
chr17:62017303 | G | A | 1 | a0001c0003t0007g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1284-6070C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017303 | |||||||
chr17:62017352 | A | G | 1 | a0001c0001t0002g0255 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1284-6119T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017352 | |||||||
chr17:62017378 | G | C | 4 | a0001c0001t0010g0264 a0001c0001t0010g0265 a0001c0001t0012g0256 others(1): Show |
4 | HG02056.hp2 NA19079.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-6145C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017378 | |||||||
chr17:62017446 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1284-6213A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017446 | |||||||
chr17:62017546 | T | C | 4 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1284-6313A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017546 | |||||||
chr17:62017813 | T | C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1284-6580A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017813 | |||||||
chr17:62017870 | T | C | 2 | a0001c0003t0007g0298 a0001c0003t0007g0325 |
2 | HG00438.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.1284-6637A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017870 | |||||||
chr17:62017941 | T | C | 1 | a0001c0002t0023g0059 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1284-6708A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017941 | |||||||
chr17:62017954 | G | A | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1284-6721C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62017954 | |||||||
chr17:62018136 | G | A | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-6903C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018136 | |||||||
chr17:62018224 | T | C | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1284-6991A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018224 | |||||||
chr17:62018355 | A | G | 1 | a0001c0001t0002g0253 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1284-7122T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018355 | |||||||
chr17:62018359 | C | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(3): Show |
6 | HG02258.hp1 HG02300.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284-7126G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018359 | |||||||
chr17:62018438 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1284-7205G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018438 | |||||||
chr17:62018446 | T | A | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-7213A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018446 | |||||||
chr17:62018561 | A | G | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284-7328T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018561 | |||||||
chr17:62018575 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1284-7342C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018575 | |||||||
chr17:62018715 | C | CA | 122 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0192 others(119): Show |
122 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1284-7483dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018715 | |||||||
chr17:62018715 | CA | C | 8 | a0001c0001t0002g0241 a0002c0005t0001g0003 a0002c0005t0001g0004 others(5): Show |
8 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-7483delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018715 | |||||||
chr17:62018888 | A | C | 38 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(35): Show |
38 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1284-7655T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018888 | |||||||
chr17:62018954 | GATCC | G | 4 | a0001c0003t0001g0291 a0001c0003t0001g0292 a0001c0003t0001g0299 others(1): Show |
4 | HG00140.hp2 HG01099.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284-7725_1284-772 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62018954 | |||||||
chr17:62019201 | T | C | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1284-7968A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019201 | |||||||
chr17:62019384 | TATAA | T | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1284-8155_1284-815 others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019384 | |||||||
chr17:62019390 | T | C | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1284-8157A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019390 | |||||||
chr17:62019428 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1284-8195A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019428 | |||||||
chr17:62019441 | A | G | 1 | a0001c0002t0023g0059 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1284-8208T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019441 | |||||||
chr17:62019720 | G | A | 85 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(82): Show |
85 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1284-8487C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019720 | |||||||
chr17:62019746 | C | CT | 11 | a0001c0001t0001g0207 a0001c0001t0002g0250 a0001c0001t0002g0311 others(8): Show |
11 | HG01175.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1284-8514dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019746 | |||||||
chr17:62019845 | G | A | 1 | a0001c0003t0001g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1284-8612C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019845 | |||||||
chr17:62019947 | C | A | 8 | a0001c0003t0001g0023 a0001c0003t0001g0025 a0001c0003t0001g0030 others(5): Show |
8 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1284-8714G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019947 | |||||||
chr17:62019948 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1284-8715C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62019948 | |||||||
chr17:62020035 | C | T | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1284-8802G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020035 | |||||||
chr17:62020231 | CT | C | 105 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(102): Show |
105 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1284-8999delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020231 | |||||||
chr17:62020256 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1284-9023T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020256 | |||||||
chr17:62020296 | C | A | 97 | a0001c0001t0001g0204 a0001c0001t0003g0290 a0001c0001t0003g0294 others(94): Show |
97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1284-9063G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020296 | |||||||
chr17:62020438 | A | G | 209 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(206): Show |
209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.1283+9103T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020438 | |||||||
chr17:62020533 | C | T | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1283+9008G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020533 | |||||||
chr17:62020560 | T | C | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1283+8981A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020560 | |||||||
chr17:62020580 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1283+8961G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020580 | |||||||
chr17:62020600 | C | T | 2 | a0001c0002t0001g0081 a0001c0002t0001g0083 |
2 | NA19074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1283+8941G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020600 | |||||||
chr17:62020601 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1283+8940C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020601 | |||||||
chr17:62020633 | C | G | 1 | a0001c0001t0002g0277 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1283+8908G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020633 | |||||||
chr17:62020658 | C | T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1283+8883G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020658 | |||||||
chr17:62020685 | C | CT | 11 | a0001c0001t0001g0183 a0001c0001t0001g0196 a0001c0001t0001g0220 others(8): Show |
11 | HG00423.hp1 HG00642.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1283+8855dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020685 | |||||||
chr17:62020685 | CT | C | 9 | a0001c0001t0001g0134 a0001c0001t0001g0186 a0001c0001t0001g0189 others(6): Show |
9 | HG01168.hp1 HG01168.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1283+8855delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020685 | |||||||
chr17:62020687 | T | C | 1 | a0001c0018t0001g0076 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1283+8854A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020687 | |||||||
chr17:62020703 | T | C | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1283+8838A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020703 | |||||||
chr17:62020706 | TA | T | 9 | a0001c0001t0002g0092 a0001c0001t0002g0240 a0001c0001t0002g0257 others(6): Show |
9 | HG01081.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1283+8834delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020706 | |||||||
chr17:62020707 | A | T | 185 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(182): Show |
185 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.1283+8834T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020707 | |||||||
chr17:62020726 | T | C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1283+8815A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020726 | |||||||
chr17:62020733 | C | G | 2 | a0001c0003t0001g0030 a0001c0003t0001g0323 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1283+8808G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020733 | |||||||
chr17:62020741 | T | G | 2 | a0001c0003t0001g0030 a0001c0003t0001g0323 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1283+8800A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020741 | |||||||
chr17:62020849 | T | C | 2 | a0001c0002t0001g0036 a0001c0002t0001g0037 |
2 | HG00423.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1283+8692A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020849 | |||||||
chr17:62020872 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1283+8669A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020872 | |||||||
chr17:62020895 | T | G | 29 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(26): Show |
29 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1283+8646A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62020895 | |||||||
chr17:62021066 | G | A | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1283+8475C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021066 | |||||||
chr17:62021255 | G | A | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1283+8286C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021255 | |||||||
chr17:62021278 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1283+8263G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021278 | |||||||
chr17:62021284 | ACCTCCCG others(93): Show |
A | 2 | a0001c0002t0001g0051 a0001c0002t0001g0321 |
2 | HG02523.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1283+8157_1283+825 others(104): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021284 | |||||||
chr17:62021344 | A | G | 322 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(319): Show |
322 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(319): Show |
intron_variant | MODIFIER | c.1283+8197T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021344 | |||||||
chr17:62021356 | C | T | 202 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(199): Show |
202 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.1283+8185G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021356 | |||||||
chr17:62021360 | C | T | 1 | a0001c0001t0012g0258 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1283+8181G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021360 | |||||||
chr17:62021375 | TCCCCACC others(42): Show |
T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1283+8117_1283+816 others(53): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021375 | |||||||
chr17:62021391 | G | A | 100 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(97): Show |
100 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1283+8150C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021391 | |||||||
chr17:62021408 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0003g0136 |
2 | HG01358.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1283+8133C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021408 | |||||||
chr17:62021428 | C | A | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1283+8113G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021428 | |||||||
chr17:62021503 | C | T | 24 | a0001c0002t0024g0057 a0001c0003t0001g0098 a0001c0003t0001g0099 others(21): Show |
24 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1283+8038G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021503 | |||||||
chr17:62021504 | G | A | 11 | a0001c0003t0001g0105 a0001c0003t0001g0107 a0001c0003t0001g0108 others(8): Show |
11 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1283+8037C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021504 | |||||||
chr17:62021521 | C | T | 2 | a0001c0001t0002g0248 a0001c0001t0002g0255 |
2 | HG00642.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1283+8020G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021521 | |||||||
chr17:62021628 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1283+7913G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021628 | |||||||
chr17:62021777 | C | T | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+7764G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021777 | |||||||
chr17:62021797 | G | A | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1283+7744C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021797 | |||||||
chr17:62021939 | C | T | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1283+7602G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021939 | |||||||
chr17:62021982 | C | A | 1 | a0002c0005t0001g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1283+7559G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62021982 | |||||||
chr17:62022152 | A | C | 1 | a0001c0001t0001g0208 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1283+7389T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022152 | |||||||
chr17:62022165 | C | CA | 9 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0172 others(6): Show |
9 | HG01106.hp1 HG01346.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1283+7375dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022165 | |||||||
chr17:62022172 | A | T | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1283+7369T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022172 | |||||||
chr17:62022173 | AAAT | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02300.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+7365_1283+736 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022173 | |||||||
chr17:62022174 | A | AAT | 59 | a0001c0001t0001g0094 a0001c0001t0001g0125 a0001c0001t0001g0126 others(56): Show |
59 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1283+7365_1283+736 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022174 | |||||||
chr17:62022174 | A | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0193 others(2): Show |
5 | HG02109.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1283+7367T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022174 | |||||||
chr17:62022174 | AAT | A | 90 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(87): Show |
90 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.1283+7365_1283+736 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022174 | |||||||
chr17:62022175 | AT | A | 90 | a0001c0001t0001g0204 a0001c0001t0003g0290 a0001c0001t0003g0294 others(87): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1283+7365delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022175 | |||||||
chr17:62022175 | ATAT | A | 3 | a0001c0001t0001g0213 a0001c0001t0002g0273 a0001c0001t0020g0247 |
3 | HG02258.hp1 NA18968.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1283+7363_1283+736 others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022175 | |||||||
chr17:62022176 | T | A | 46 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(43): Show |
46 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1283+7365A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022176 | |||||||
chr17:62022178 | T | A | 182 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0172 others(179): Show |
182 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.1283+7363A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022178 | |||||||
chr17:62022180 | T | A | 99 | a0001c0001t0001g0204 a0001c0001t0002g0232 a0001c0001t0002g0233 others(96): Show |
99 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1283+7361A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022180 | |||||||
chr17:62022182 | T | A | 3 | a0001c0003t0001g0111 a0001c0003t0001g0113 a0001c0003t0001g0117 |
3 | HG02559.hp2 HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1283+7359A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022182 | |||||||
chr17:62022216 | G | A | 97 | a0001c0001t0001g0204 a0001c0001t0003g0290 a0001c0001t0003g0294 others(94): Show |
97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1283+7325C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022216 | |||||||
chr17:62022447 | C | A | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1283+7094G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022447 | |||||||
chr17:62022588 | A | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+6953T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022588 | |||||||
chr17:62022675 | A | G | 14 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0130 others(11): Show |
14 | HG02155.hp2 HG02280.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1283+6866T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022675 | |||||||
chr17:62022751 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1283+6790A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022751 | |||||||
chr17:62022875 | A | T | 323 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(320): Show |
323 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(320): Show |
intron_variant | MODIFIER | c.1283+6666T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62022875 | |||||||
chr17:62023017 | A | T | 1 | a0001c0002t0001g0091 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1283+6524T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023017 | |||||||
chr17:62023112 | G | A | 1 | a0001c0002t0001g0034 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1283+6429C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023112 | |||||||
chr17:62023317 | T | C | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1283+6224A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023317 | |||||||
chr17:62023604 | C | T | 4 | a0001c0003t0005g0026 a0001c0003t0005g0027 a0001c0003t0005g0028 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+5937G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023604 | |||||||
chr17:62023698 | C | T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1283+5843G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023698 | |||||||
chr17:62023735 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1283+5806C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023735 | |||||||
chr17:62023739 | GCC | G | 209 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(206): Show |
209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.1283+5800_1283+580 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023739 | |||||||
chr17:62023745 | C | T | 1 | a0001c0002t0001g0074 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1283+5796G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023745 | |||||||
chr17:62023800 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0216 |
2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1283+5741T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023800 | |||||||
chr17:62023864 | A | T | 1 | a0001c0012t0001g0305 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1283+5677T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023864 | |||||||
chr17:62023944 | C | T | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1283+5597G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023944 | |||||||
chr17:62023958 | A | G | 3 | a0001c0001t0002g0267 a0001c0001t0002g0274 a0001c0001t0013g0316 |
3 | HG00423.hp1 NA18943.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1283+5583T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023958 | |||||||
chr17:62023985 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1283+5556A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62023985 | |||||||
chr17:62024020 | T | C | 10 | a0001c0001t0001g0134 a0001c0001t0001g0151 a0001c0001t0001g0152 others(7): Show |
10 | HG00558.hp1 HG02083.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.1283+5521A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024020 | |||||||
chr17:62024021 | G | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1283+5520C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024021 | |||||||
chr17:62024023 | C | CT | 102 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(99): Show |
102 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1283+5517dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024023 | |||||||
chr17:62024023 | C | CTT | 97 | a0001c0001t0001g0204 a0001c0001t0002g0273 a0001c0001t0003g0290 others(94): Show |
97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1283+5516_1283+551 others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024023 | |||||||
chr17:62024078 | C | T | 29 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(26): Show |
29 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1283+5463G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024078 | |||||||
chr17:62024091 | C | G | 1 | a0001c0004t0001g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1283+5450G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024091 | |||||||
chr17:62024181 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0183 |
2 | NA18982.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1283+5360G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024181 | |||||||
chr17:62024210 | A | T | 2 | a0001c0002t0001g0051 a0001c0002t0001g0321 |
2 | HG02523.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1283+5331T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024210 | |||||||
chr17:62024211 | T | G | 58 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1283+5330A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024211 | |||||||
chr17:62024382 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1283+5159G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024382 | |||||||
chr17:62024487 | G | A | 97 | a0001c0001t0001g0204 a0001c0001t0003g0290 a0001c0001t0003g0294 others(94): Show |
97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1283+5054C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024487 | |||||||
chr17:62024534 | A | T | 1 | a0001c0001t0001g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1283+5007T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024534 | |||||||
chr17:62024655 | T | C | 29 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(26): Show |
29 | HG01928.hp2 HG01934.hp2 HG01993.hp2 others(26): Show |
intron_variant | MODIFIER | c.1283+4886A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024655 | |||||||
chr17:62024661 | A | G | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+4880T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024661 | |||||||
chr17:62024714 | T | C | 2 | a0001c0001t0002g0250 a0001c0001t0002g0263 |
2 | HG01109.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1283+4827A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62024714 | |||||||
chr17:62025127 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1283+4414C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025127 | |||||||
chr17:62025336 | C | T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1283+4205G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025336 | |||||||
chr17:62025416 | C | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1283+4125G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025416 | |||||||
chr17:62025606 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1283+3935C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025606 | |||||||
chr17:62025618 | C | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+3923G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025618 | |||||||
chr17:62025641 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1283+3900C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025641 | |||||||
chr17:62025668 | T | A | 209 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(206): Show |
209 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.1283+3873A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025668 | |||||||
chr17:62025695 | C | T | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1283+3846G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025695 | |||||||
chr17:62025753 | A | G | 1 | a0001c0001t0002g0261 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1283+3788T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025753 | |||||||
chr17:62025820 | C | T | 1 | a0002c0005t0001g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1283+3721G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62025820 | |||||||
chr17:62026272 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0013g0229 |
2 | NA19058.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1283+3269C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026272 | |||||||
chr17:62026478 | T | TA | 9 | a0001c0001t0001g0175 a0001c0002t0001g0073 a0001c0003t0001g0323 others(6): Show |
9 | HG02056.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1283+3062dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026478 | |||||||
chr17:62026545 | C | T | 1 | a0001c0012t0001g0305 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1283+2996G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026545 | |||||||
chr17:62026791 | C | T | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1283+2750G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026791 | |||||||
chr17:62026901 | A | G | 1 | a0001c0004t0001g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1283+2640T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026901 | |||||||
chr17:62026970 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1283+2571G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62026970 | |||||||
chr17:62027108 | A | G | 1 | a0001c0003t0007g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1283+2433T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027108 | |||||||
chr17:62027264 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1283+2277C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027264 | |||||||
chr17:62027311 | G | A | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1283+2230C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027311 | |||||||
chr17:62027312 | C | T | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1283+2229G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027312 | |||||||
chr17:62027399 | C | G | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+2142G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027399 | |||||||
chr17:62027531 | C | A | 1 | a0001c0008t0001g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1283+2010G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027531 | |||||||
chr17:62027536 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1283+2005G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027536 | |||||||
chr17:62027606 | T | C | 1 | a0011c0023t0001g0131 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1283+1935A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027606 | |||||||
chr17:62027623 | T | C | 1 | a0001c0002t0001g0067 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1283+1918A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027623 | |||||||
chr17:62027713 | A | T | 15 | a0001c0002t0001g0036 a0001c0002t0001g0037 a0001c0002t0001g0040 others(12): Show |
15 | HG00423.hp2 HG00558.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.1283+1828T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027713 | |||||||
chr17:62027770 | T | C | 2 | a0001c0003t0001g0099 a0001c0015t0001g0096 |
2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1283+1771A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027770 | |||||||
chr17:62027865 | A | AT | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+1675dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027865 | |||||||
chr17:62027869 | C | A | 7 | a0001c0001t0001g0134 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG00558.hp1 NA18948.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1283+1672G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62027869 | |||||||
chr17:62028099 | G | A | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1283+1442C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028099 | |||||||
chr17:62028110 | C | G | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1283+1431G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028110 | |||||||
chr17:62028112 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1283+1429C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028112 | |||||||
chr17:62028283 | A | G | 1 | a0001c0001t0015g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1283+1258T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028283 | |||||||
chr17:62028323 | A | G | 1 | a0001c0004t0001g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1283+1218T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028323 | |||||||
chr17:62028489 | T | C | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1283+1052A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028489 | |||||||
chr17:62028553 | T | TA | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+987dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028553 | |||||||
chr17:62028560 | A | C | 1 | a0001c0001t0001g0150 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1283+981T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028560 | |||||||
chr17:62028623 | T | C | 3 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
3 | NA18945.hp1 NA18967.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1283+918A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028623 | |||||||
chr17:62028679 | T | TA | 8 | a0001c0001t0001g0193 a0001c0001t0001g0212 a0001c0001t0001g0213 others(5): Show |
8 | HG01106.hp2 HG01175.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1283+861dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028679 | |||||||
chr17:62028679 | TA | T | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0005t0001g0003 others(3): Show |
6 | HG00558.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1283+861delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028679 | |||||||
chr17:62028804 | C | G | 58 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1283+737G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028804 | |||||||
chr17:62028863 | A | G | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1283+678T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028863 | |||||||
chr17:62028907 | T | C | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1283+634A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62028907 | |||||||
chr17:62029038 | A | G | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+503T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029038 | |||||||
chr17:62029041 | A | G | 1 | a0001c0001t0003g0136 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1283+500T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029041 | |||||||
chr17:62029105 | G | C | 1 | a0001c0003t0001g0300 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1283+436C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029105 | |||||||
chr17:62029315 | A | G | 1 | a0001c0001t0014g0286 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1283+226T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029315 | |||||||
chr17:62029420 | TC | T | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1283+120delG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029420 | |||||||
chr17:62029474 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1283+67C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029474 | |||||||
chr17:62029484 | T | C | 1 | a0001c0002t0001g0082 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1283+57A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029484 | |||||||
chr17:62029493 | G | A | 27 | a0001c0001t0001g0118 a0001c0003t0001g0098 a0001c0003t0001g0099 others(24): Show |
27 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1283+48C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029493 | |||||||
chr17:62029511 | T | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1283+30A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | 62029511 | |||||||
chr17:62030194 | T | C | 2 | a0001c0001t0002g0260 a0001c0001t0003g0259 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1010-181A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/29 | chr17 | 62030194 | |||||||
chr17:62030309 | G | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1010-296C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/29 | chr17 | 62030309 | |||||||
chr17:62030522 | A | T | 1 | a0001c0001t0003g0301 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1010-509T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/29 | chr17 | 62030522 | |||||||
chr17:62031151 | G | C | 1 | a0001c0002t0001g0031 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1009+293C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/29 | chr17 | 62031151 | |||||||
chr17:62031197 | G | A | 1 | a0001c0002t0001g0051 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1009+247C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 6/29 | chr17 | 62031197 | |||||||
chr17:62031675 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.815-37G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62031675 | |||||||
chr17:62031680 | T | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(13): Show |
16 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.815-42A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62031680 | |||||||
chr17:62031796 | CT | C | 55 | a0001c0001t0001g0118 a0001c0001t0001g0173 a0001c0001t0002g0092 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.815-159delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62031796 | |||||||
chr17:62032167 | C | A | 2 | a0001c0002t0001g0060 a0001c0002t0001g0288 |
2 | NA18980.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.815-529G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62032167 | |||||||
chr17:62032479 | G | GA | 12 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0133 others(9): Show |
12 | HG00140.hp1 HG01109.hp1 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.815-842dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62032479 | |||||||
chr17:62032479 | GA | G | 29 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0039 others(26): Show |
29 | HG01928.hp2 HG01934.hp2 HG01993.hp2 others(26): Show |
intron_variant | MODIFIER | c.815-842delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62032479 | |||||||
chr17:62032516 | C | T | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.815-878G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62032516 | |||||||
chr17:62032583 | C | G | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.815-945G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62032583 | |||||||
chr17:62033045 | A | C | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.814+742T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033045 | |||||||
chr17:62033068 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.814+719A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033068 | |||||||
chr17:62033076 | G | T | 1 | a0001c0002t0001g0321 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.814+711C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033076 | |||||||
chr17:62033090 | T | G | 3 | a0001c0001t0002g0267 a0001c0001t0002g0274 a0001c0001t0013g0316 |
3 | HG00423.hp1 NA18943.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.814+697A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033090 | |||||||
chr17:62033140 | G | A | 1 | a0001c0008t0001g0122 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.814+647C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033140 | |||||||
chr17:62033401 | T | C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.814+386A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033401 | |||||||
chr17:62033416 | A | G | 2 | a0001c0003t0001g0306 a0001c0003t0001g0307 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.814+371T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033416 | |||||||
chr17:62033565 | T | C | 2 | a0001c0001t0010g0264 a0001c0001t0010g0265 |
2 | NA19079.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.814+222A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033565 | |||||||
chr17:62033751 | C | T | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.814+36G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 5/29 | chr17 | 62033751 | |||||||
chr17:62034107 | A | C | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.617-123T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034107 | |||||||
chr17:62034486 | CA | C | 232 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(229): Show |
232 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.617-503delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034486 | |||||||
chr17:62034496 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.617-512T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034496 | |||||||
chr17:62034666 | T | C | 1 | a0001c0002t0001g0067 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.617-682A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034666 | |||||||
chr17:62034680 | A | G | 1 | a0011c0023t0001g0131 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.617-696T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034680 | |||||||
chr17:62034731 | G | T | 1 | a0001c0002t0001g0001 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.616+732C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62034731 | |||||||
chr17:62035104 | G | C | 1 | a0001c0018t0001g0076 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.616+359C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62035104 | |||||||
chr17:62035116 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.616+347C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4/29 | chr17 | 62035116 | |||||||
chr17:62035722 | C | A | 2 | a0001c0001t0001g0188 a0001c0001t0007g0002 |
2 | HG01099.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.471-114G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62035722 | |||||||
chr17:62035881 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.471-273T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62035881 | |||||||
chr17:62036090 | C | CT | 93 | a0001c0001t0003g0290 a0001c0001t0003g0297 a0001c0001t0003g0301 others(90): Show |
93 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.471-483dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036090 | |||||||
chr17:62036105 | A | T | 3 | a0001c0001t0002g0238 a0001c0001t0002g0251 a0001c0001t0002g0252 |
3 | NA18948.hp2 NA18966.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.471-497T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036105 | |||||||
chr17:62036373 | G | A | 20 | a0001c0003t0001g0098 a0001c0003t0001g0104 a0001c0003t0001g0105 others(17): Show |
20 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.471-765C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036373 | |||||||
chr17:62036424 | T | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-816A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036424 | |||||||
chr17:62036460 | G | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-852C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036460 | |||||||
chr17:62036466 | T | G | 58 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.471-858A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036466 | |||||||
chr17:62036481 | A | AGAAAATA others(352): Show |
1 | a0001c0003t0001g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.471-874_471-873ins others(359): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036481 | |||||||
chr17:62036862 | G | A | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.471-1254C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036862 | |||||||
chr17:62036869 | G | C | 2 | a0002c0005t0001g0230 a0002c0005t0001g0231 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.471-1261C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62036869 | |||||||
chr17:62037065 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.471-1457T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037065 | |||||||
chr17:62037162 | C | T | 4 | a0001c0003t0005g0026 a0001c0003t0005g0027 a0001c0003t0005g0028 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.471-1554G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037162 | |||||||
chr17:62037419 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.471-1811G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037419 | |||||||
chr17:62037495 | T | C | 1 | a0001c0002t0001g0041 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.471-1887A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037495 | |||||||
chr17:62037522 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.471-1914C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037522 | |||||||
chr17:62037528 | G | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-1920C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037528 | |||||||
chr17:62037666 | C | CA | 8 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(5): Show |
8 | HG01346.hp2 HG02280.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.471-2059dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037666 | |||||||
chr17:62037666 | CA | C | 6 | a0001c0001t0001g0158 a0001c0001t0001g0186 a0001c0007t0006g0279 others(3): Show |
6 | HG01993.hp1 HG02257.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.471-2059delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037666 | |||||||
chr17:62037673 | A | T | 1 | a0001c0004t0001g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.471-2065T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037673 | |||||||
chr17:62037955 | C | CA | 7 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0154 others(4): Show |
7 | HG03195.hp1 NA18946.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.471-2348dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | |||||||
chr17:62037955 | C | CAA | 42 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0034 others(39): Show |
42 | HG00558.hp2 HG00639.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.471-2349_471-2348d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | |||||||
chr17:62037955 | C | CAAA | 22 | a0001c0002t0001g0001 a0001c0002t0001g0033 a0001c0002t0001g0041 others(19): Show |
22 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.471-2350_471-2348d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | |||||||
chr17:62037955 | C | CAAAA | 18 | a0001c0001t0003g0294 a0001c0001t0003g0295 a0001c0001t0003g0297 others(15): Show |
18 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.471-2351_471-2348d others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | |||||||
chr17:62037955 | C | CAAAAA | 7 | a0001c0002t0001g0078 a0001c0002t0001g0085 a0001c0002t0001g0317 others(4): Show |
7 | HG00544.hp1 HG01884.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.471-2352_471-2348d others(7): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | |||||||
chr17:62037955 | CA | C | 69 | a0001c0001t0001g0094 a0001c0001t0001g0119 a0001c0001t0001g0123 others(66): Show |
69 | HG00140.hp1 HG00544.hp2 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.471-2348delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | |||||||
chr17:62037955 | CAA | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0118 others(15): Show |
18 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.471-2349_471-2348d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | |||||||
chr17:62037955 | CAAA | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0212 others(4): Show |
7 | HG01346.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.471-2350_471-2348d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | |||||||
chr17:62037955 | CAAAAAAA others(5): Show |
C | 2 | a0001c0003t0001g0104 a0001c0003t0001g0110 |
2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.471-2359_471-2348d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | |||||||
chr17:62037955 | CAAAAAAA others(6): Show |
C | 83 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(80): Show |
83 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.471-2360_471-2348d others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62037955 | |||||||
chr17:62038421 | G | GCATTTTA others(27): Show |
4 | a0001c0003t0001g0296 a0001c0003t0001g0300 a0001c0003t0001g0306 others(1): Show |
4 | HG03491.hp1 HG03492.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.471-2847_471-2814d others(36): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038421 | |||||||
chr17:62038431 | AT | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-2824delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038431 | |||||||
chr17:62038433 | A | G | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-2825T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038433 | |||||||
chr17:62038746 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.471-3138G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038746 | |||||||
chr17:62038830 | AT | A | 25 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0003t0001g0098 others(22): Show |
25 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.471-3223delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038830 | |||||||
chr17:62038887 | CTGGCCTC others(7): Show |
C | 1 | a0001c0003t0001g0323 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.471-3293_471-3280d others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62038887 | |||||||
chr17:62039026 | G | C | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.471-3418C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039026 | |||||||
chr17:62039084 | T | C | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.471-3476A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039084 | |||||||
chr17:62039226 | A | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.471-3618T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039226 | |||||||
chr17:62039239 | G | A | 208 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(205): Show |
208 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.471-3631C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039239 | |||||||
chr17:62039346 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471-3738C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039346 | |||||||
chr17:62039383 | A | T | 1 | a0001c0001t0002g0093 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.471-3775T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039383 | |||||||
chr17:62039388 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02145.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.471-3780A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039388 | |||||||
chr17:62039552 | TA | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-3945delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039552 | |||||||
chr17:62039586 | GA | G | 6 | a0001c0001t0001g0189 a0001c0001t0001g0196 a0001c0001t0001g0285 others(3): Show |
6 | HG00642.hp2 HG01168.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.471-3979delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039586 | |||||||
chr17:62039587 | A | AT | 12 | a0001c0001t0001g0094 a0001c0001t0001g0126 a0001c0001t0001g0133 others(9): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.471-3980dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039587 | |||||||
chr17:62039587 | AT | A | 67 | a0001c0001t0001g0121 a0001c0001t0001g0216 a0001c0001t0001g0315 others(64): Show |
67 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.471-3980delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039587 | |||||||
chr17:62039587 | ATT | A | 97 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(94): Show |
97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.471-3981_471-3980d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039587 | |||||||
chr17:62039653 | G | A | 2 | a0001c0002t0001g0051 a0001c0002t0001g0321 |
2 | HG02523.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.471-4045C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039653 | |||||||
chr17:62039737 | G | A | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.471-4129C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039737 | |||||||
chr17:62039842 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.471-4234C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039842 | |||||||
chr17:62039881 | G | T | 1 | a0001c0003t0005g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.471-4273C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039881 | |||||||
chr17:62039930 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.471-4322T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62039930 | |||||||
chr17:62040317 | C | T | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.471-4709G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62040317 | |||||||
chr17:62040417 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.471-4809G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62040417 | |||||||
chr17:62040594 | T | C | 1 | a0001c0003t0001g0299 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.471-4986A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62040594 | |||||||
chr17:62040602 | G | A | 1 | a0001c0001t0016g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.471-4994C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62040602 | |||||||
chr17:62040758 | A | C | 203 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(200): Show |
203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.471-5150T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62040758 | |||||||
chr17:62041174 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.471-5566A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041174 | |||||||
chr17:62041235 | A | G | 2 | a0001c0003t0001g0099 a0001c0015t0001g0096 |
2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.471-5627T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041235 | |||||||
chr17:62041244 | TG | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.471-5637delC | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041244 | |||||||
chr17:62041333 | T | C | 1 | a0001c0003t0001g0089 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.471-5725A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041333 | |||||||
chr17:62041349 | G | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.471-5741C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041349 | |||||||
chr17:62041743 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.471-6135T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041743 | |||||||
chr17:62041885 | C | T | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.471-6277G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041885 | |||||||
chr17:62041964 | T | C | 1 | a0001c0002t0024g0057 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.471-6356A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62041964 | |||||||
chr17:62042176 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.471-6568T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042176 | |||||||
chr17:62042318 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.471-6710G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042318 | |||||||
chr17:62042432 | C | T | 1 | a0001c0003t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.471-6824G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042432 | |||||||
chr17:62042433 | A | C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471-6825T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042433 | |||||||
chr17:62042444 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0182 a0001c0001t0001g0223 |
3 | HG01167.hp2 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.471-6836G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042444 | |||||||
chr17:62042474 | A | G | 2 | a0001c0001t0002g0228 a0001c0001t0002g0271 |
2 | HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.471-6866T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042474 | |||||||
chr17:62042554 | T | C | 103 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(100): Show |
103 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.471-6946A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042554 | |||||||
chr17:62042560 | C | CA | 112 | a0001c0001t0001g0019 a0001c0001t0001g0129 a0001c0001t0001g0154 others(109): Show |
112 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.471-6953dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042560 | |||||||
chr17:62042560 | C | CAA | 26 | a0001c0001t0002g0228 a0001c0001t0003g0297 a0001c0002t0001g0031 others(23): Show |
26 | HG00639.hp1 HG01243.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.471-6954_471-6953d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042560 | |||||||
chr17:62042560 | C | CAAA | 11 | a0001c0003t0001g0104 a0001c0003t0001g0107 a0001c0003t0001g0108 others(8): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.471-6955_471-6953d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042560 | |||||||
chr17:62042582 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.471-6974G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042582 | |||||||
chr17:62042590 | C | A | 1 | a0001c0002t0001g0086 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.471-6982G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042590 | |||||||
chr17:62042839 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.471-7231C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62042839 | |||||||
chr17:62043156 | C | CA | 28 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(25): Show |
28 | HG00140.hp2 HG00544.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.471-7549dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | |||||||
chr17:62043156 | C | CAA | 43 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0001g0193 others(40): Show |
43 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.471-7550_471-7549d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | |||||||
chr17:62043156 | C | CAAA | 27 | a0001c0001t0003g0290 a0001c0001t0003g0295 a0001c0001t0003g0297 others(24): Show |
27 | HG00423.hp2 HG01106.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.471-7551_471-7549d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | |||||||
chr17:62043156 | C | CAAAA | 6 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 others(3): Show |
6 | HG01099.hp2 HG02080.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.471-7552_471-7549d others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | |||||||
chr17:62043156 | C | CAAAAAAA others(4): Show |
1 | a0001c0007t0006g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.471-7559_471-7549d others(13): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | |||||||
chr17:62043156 | C | CAAAAAAA others(5): Show |
1 | a0001c0007t0006g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.471-7560_471-7549d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | |||||||
chr17:62043156 | C | CAAAAAAA others(7): Show |
1 | a0005c0022t0006g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.471-7562_471-7549d others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | |||||||
chr17:62043156 | C | CAAAAAAA others(11): Show |
1 | a0001c0007t0006g0279 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471-7566_471-7549d others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | |||||||
chr17:62043156 | CA | C | 82 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0129 others(79): Show |
82 | HG00140.hp1 HG00558.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.471-7549delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | |||||||
chr17:62043156 | CAAAAAAA others(5): Show |
C | 2 | a0001c0002t0001g0061 a0001c0002t0001g0073 |
2 | HG02056.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.471-7560_471-7549d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | |||||||
chr17:62043156 | CAAAAAAA others(8): Show |
C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.471-7563_471-7549d others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043156 | |||||||
chr17:62043168 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0002g0272 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.471-7577_471-7561d others(19): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043168 | |||||||
chr17:62043179 | A | G | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471-7571T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043179 | |||||||
chr17:62043181 | A | AG | 12 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.471-7574_471-7573i others(3): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043181 | |||||||
chr17:62043181 | A | G | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0315 |
3 | HG01346.hp2 HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.471-7573T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043181 | |||||||
chr17:62043181 | AAAAG | A | 50 | a0001c0001t0001g0184 a0001c0001t0001g0221 a0001c0001t0002g0092 others(47): Show |
50 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.471-7577_471-7574d others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043181 | |||||||
chr17:62043182 | AAAG | A | 7 | a0001c0001t0002g0251 a0001c0001t0002g0260 a0001c0001t0002g0263 others(4): Show |
7 | HG01109.hp1 HG02056.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.471-7577_471-7575d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043182 | |||||||
chr17:62043193 | G | A | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.471-7585C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043193 | |||||||
chr17:62043224 | C | A | 1 | a0001c0002t0001g0061 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.471-7616G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043224 | |||||||
chr17:62043271 | G | A | 1 | a0001c0003t0001g0303 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.471-7663C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62043271 | |||||||
chr17:62044232 | TA | T | 26 | a0001c0001t0001g0020 a0001c0001t0001g0130 a0001c0001t0001g0132 others(23): Show |
26 | HG00558.hp1 HG00597.hp1 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.470+8304delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044232 | |||||||
chr17:62044462 | T | C | 1 | a0001c0002t0001g0087 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.470+8075A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044462 | |||||||
chr17:62044468 | C | T | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+8069G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044468 | |||||||
chr17:62044594 | T | C | 2 | a0001c0004t0001g0010 a0001c0004t0001g0011 |
2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.470+7943A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044594 | |||||||
chr17:62044697 | T | C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+7840A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044697 | |||||||
chr17:62044739 | T | G | 1 | a0001c0003t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.470+7798A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044739 | |||||||
chr17:62044783 | T | A | 58 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.470+7754A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62044783 | |||||||
chr17:62045019 | CAAA | C | 7 | a0001c0001t0001g0124 a0001c0001t0001g0144 a0001c0001t0001g0145 others(4): Show |
7 | HG02622.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.470+7515_470+7517d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045019 | |||||||
chr17:62045039 | AT | A | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.470+7497delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045039 | |||||||
chr17:62045097 | G | A | 203 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(200): Show |
203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.470+7440C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045097 | |||||||
chr17:62045112 | A | G | 1 | a0001c0018t0001g0076 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.470+7425T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045112 | |||||||
chr17:62045174 | T | A | 3 | a0001c0003t0001g0098 a0001c0003t0001g0104 a0001c0003t0001g0110 |
3 | HG02717.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.470+7363A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045174 | |||||||
chr17:62045445 | C | T | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.470+7092G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045445 | |||||||
chr17:62045472 | A | T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+7065T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62045472 | |||||||
chr17:62046097 | A | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+6440T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046097 | |||||||
chr17:62046219 | G | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.470+6318C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046219 | |||||||
chr17:62046248 | T | A | 3 | a0001c0003t0001g0098 a0001c0003t0001g0104 a0001c0003t0001g0110 |
3 | HG02717.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.470+6289A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046248 | |||||||
chr17:62046280 | GA | G | 7 | a0001c0001t0001g0140 a0001c0001t0004g0139 a0001c0001t0004g0141 others(4): Show |
7 | NA18949.hp1 NA18952.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.470+6256delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046280 | |||||||
chr17:62046755 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.470+5782A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046755 | |||||||
chr17:62046950 | A | G | 102 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(99): Show |
102 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.470+5587T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62046950 | |||||||
chr17:62047033 | CT | C | 201 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(198): Show |
201 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.470+5503delA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047033 | |||||||
chr17:62047140 | A | G | 203 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(200): Show |
203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.470+5397T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047140 | |||||||
chr17:62047188 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.470+5349A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047188 | |||||||
chr17:62047208 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.470+5329A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047208 | |||||||
chr17:62047221 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.470+5316T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047221 | |||||||
chr17:62047228 | G | A | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.470+5309C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047228 | |||||||
chr17:62047470 | T | C | 323 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(320): Show |
323 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(320): Show |
intron_variant | MODIFIER | c.470+5067A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047470 | |||||||
chr17:62047582 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.470+4955T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047582 | |||||||
chr17:62047655 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.470+4882C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047655 | |||||||
chr17:62047685 | C | T | 4 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.470+4852G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047685 | |||||||
chr17:62047694 | C | A | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.470+4843G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047694 | |||||||
chr17:62047793 | A | G | 1 | a0001c0003t0001g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.470+4744T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047793 | |||||||
chr17:62047849 | C | T | 1 | a0001c0001t0003g0301 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.470+4688G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62047849 | |||||||
chr17:62048019 | T | TATATAC | 47 | a0001c0001t0001g0118 a0001c0001t0001g0284 a0001c0001t0003g0290 others(44): Show |
47 | HG00597.hp2 HG00639.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.470+4512_470+4517d others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048019 | |||||||
chr17:62048019 | T | TATATACA others(5): Show |
5 | a0001c0001t0001g0020 a0001c0001t0021g0254 a0001c0002t0001g0062 others(2): Show |
5 | HG02818.hp2 HG03017.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.470+4506_470+4517d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048019 | |||||||
chr17:62048037 | CATATACA others(5): Show |
C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+4488_470+4499d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048037 | |||||||
chr17:62048039 | T | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+4498A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048039 | |||||||
chr17:62048043 | C | CAT | 15 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0125 others(12): Show |
15 | HG01261.hp2 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.470+4492_470+4493d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATAT | 5 | a0001c0004t0001g0015 a0002c0005t0001g0003 a0002c0005t0001g0004 others(2): Show |
5 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.470+4490_470+4493d others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATATACA others(1): Show |
19 | a0001c0002t0001g0001 a0001c0002t0001g0036 a0001c0002t0001g0042 others(16): Show |
19 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.470+4493_470+4494i others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATATACA others(3): Show |
11 | a0001c0001t0001g0017 a0001c0001t0003g0294 a0001c0001t0003g0295 others(8): Show |
11 | HG01516.hp1 HG01517.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.470+4493_470+4494i others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATATACA others(7): Show |
1 | a0001c0001t0011g0016 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.470+4493_470+4494i others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATATACA others(9): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0003t0001g0292 |
3 | HG00140.hp2 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.470+4493_470+4494i others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATATACA others(13): Show |
1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.470+4493_470+4494i others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATATACA others(5): Show |
3 | a0001c0002t0001g0035 a0001c0002t0001g0075 a0001c0003t0001g0023 |
3 | HG02965.hp2 NA18965.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.470+4493_470+4494i others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATATACA others(7): Show |
17 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0002t0001g0034 others(14): Show |
17 | HG01934.hp2 HG01993.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.470+4493_470+4494i others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATATACA others(9): Show |
7 | a0001c0002t0001g0047 a0001c0002t0001g0064 a0001c0002t0001g0070 others(4): Show |
7 | HG01928.hp2 HG02080.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.470+4493_470+4494i others(18): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATATACA others(11): Show |
1 | a0001c0002t0001g0055 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.470+4493_470+4494i others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATATATA others(1): Show |
4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+4486_470+4493d others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | C | CATATATA others(7): Show |
1 | a0001c0002t0001g0048 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.470+4480_470+4493d others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048043 | CAT | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(1): Show |
4 | HG03130.hp1 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+4492_470+4493d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048043 | |||||||
chr17:62048045 | T | TATAC | 7 | a0001c0001t0002g0237 a0001c0001t0002g0266 a0001c0002t0001g0040 others(4): Show |
7 | HG02572.hp2 HG02735.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.470+4491_470+4492i others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048045 | |||||||
chr17:62048045 | T | TATACATA others(3): Show |
58 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.470+4491_470+4492i others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048045 | |||||||
chr17:62048045 | T | TATACATA others(15): Show |
1 | a0001c0003t0001g0024 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.470+4491_470+4492i others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048045 | |||||||
chr17:62048047 | T | TAC | 4 | a0001c0003t0001g0293 a0001c0003t0001g0303 a0001c0003t0001g0304 others(1): Show |
4 | HG00639.hp2 HG01243.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.470+4489_470+4490i others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048047 | |||||||
chr17:62048049 | T | C | 4 | a0001c0001t0001g0138 a0001c0001t0025g0008 a0001c0002t0001g0067 others(1): Show |
4 | HG02027.hp2 HG02056.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.470+4488A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048049 | |||||||
chr17:62048051 | T | C | 2 | a0001c0001t0002g0237 a0001c0002t0001g0043 |
2 | HG02735.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.470+4486A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048051 | |||||||
chr17:62048056 | A | G | 5 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0008g0318 others(2): Show |
5 | HG01167.hp1 HG01168.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.470+4481T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048056 | |||||||
chr17:62048057 | T | C | 1 | a0001c0003t0005g0029 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.470+4480A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048057 | |||||||
chr17:62048058 | A | G | 10 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0001g0203 others(7): Show |
10 | HG03669.hp2 HG06807.hp2 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.470+4479T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048058 | |||||||
chr17:62048064 | G | A | 101 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(98): Show |
101 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.470+4473C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048064 | |||||||
chr17:62048077 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.470+4460A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048077 | |||||||
chr17:62048166 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.470+4371C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048166 | |||||||
chr17:62048221 | C | T | 21 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(18): Show |
21 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.470+4316G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048221 | |||||||
chr17:62048242 | T | C | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.470+4295A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048242 | |||||||
chr17:62048265 | C | T | 1 | a0001c0001t0008g0318 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.470+4272G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048265 | |||||||
chr17:62048266 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+4271C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048266 | |||||||
chr17:62048302 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+4235C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048302 | |||||||
chr17:62048394 | G | C | 7 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(4): Show |
7 | HG02257.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.470+4143C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048394 | |||||||
chr17:62048398 | C | CA | 25 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0126 others(22): Show |
25 | HG00642.hp2 HG01099.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.470+4138dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048398 | |||||||
chr17:62048398 | CA | C | 40 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(37): Show |
40 | HG01167.hp2 HG01433.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.470+4138delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048398 | |||||||
chr17:62048398 | CAA | C | 160 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0092 others(157): Show |
160 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.470+4137_470+4138d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048398 | |||||||
chr17:62048398 | CAAA | C | 6 | a0001c0001t0002g0236 a0001c0001t0002g0237 a0001c0002t0001g0001 others(3): Show |
6 | HG01109.hp2 HG01952.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.470+4136_470+4138d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048398 | |||||||
chr17:62048398 | CAAAAAAA others(6): Show |
C | 6 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.470+4126_470+4138d others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048398 | |||||||
chr17:62048445 | G | C | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+4092C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048445 | |||||||
chr17:62048463 | A | G | 1 | a0001c0002t0001g0043 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.470+4074T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048463 | |||||||
chr17:62048536 | A | G | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.470+4001T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048536 | |||||||
chr17:62048543 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0205 others(1): Show |
4 | HG02155.hp2 HG02523.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+3994G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048543 | |||||||
chr17:62048680 | T | C | 6 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.470+3857A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048680 | |||||||
chr17:62048903 | A | G | 5 | a0001c0004t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 others(2): Show |
5 | HG02055.hp2 HG02818.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.470+3634T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62048903 | |||||||
chr17:62049078 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.470+3451_470+3458d others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049078 | C | CAAAAAAA others(2): Show |
7 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(4): Show |
7 | HG02257.hp1 HG02257.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.470+3450_470+3458d others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049078 | C | CAAAAAAA others(3): Show |
4 | a0001c0002t0001g0071 a0001c0003t0001g0099 a0001c0015t0001g0096 others(1): Show |
4 | HG01109.hp2 HG01952.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.470+3449_470+3458d others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049078 | C | CAAAAAAA others(4): Show |
12 | a0001c0001t0002g0271 a0001c0001t0002g0273 a0001c0002t0001g0001 others(9): Show |
12 | HG01891.hp1 HG02723.hp2 HG03710.hp2 others(9): Show |
intron_variant | MODIFIER | c.470+3448_470+3458d others(13): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049078 | C | CAAAAAAA others(5): Show |
104 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(101): Show |
104 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.470+3447_470+3458d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049078 | C | CAAAAAAA others(6): Show |
30 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 others(27): Show |
30 | HG00423.hp1 HG00438.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.470+3446_470+3458d others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049078 | C | CAAAAAAA others(7): Show |
18 | a0001c0001t0002g0234 a0001c0001t0002g0266 a0001c0001t0010g0264 others(15): Show |
18 | HG00544.hp1 HG01891.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.470+3445_470+3458d others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049078 | C | CAAAAAAA others(8): Show |
5 | a0001c0002t0001g0074 a0001c0003t0001g0111 a0001c0003t0001g0112 others(2): Show |
5 | HG02559.hp2 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.470+3444_470+3458d others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049078 | C | CAAAAAAA others(11): Show |
1 | a0001c0004t0001g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.470+3458_470+3459i others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049078 | C | CAAAAAAA others(13): Show |
1 | a0001c0004t0001g0021 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.470+3458_470+3459i others(22): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049078 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.470+3458_470+3459i others(23): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049078 | C | CAAAAAAA others(20): Show |
2 | a0007c0010t0001g0007 a0010c0013t0001g0215 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.470+3458_470+3459i others(29): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049078 | |||||||
chr17:62049261 | C | A | 203 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(200): Show |
203 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.470+3276G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049261 | |||||||
chr17:62049342 | G | A | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0195 others(19): Show |
22 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.470+3195C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049342 | |||||||
chr17:62049411 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.470+3126C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049411 | |||||||
chr17:62049539 | C | G | 2 | a0001c0001t0002g0311 a0001c0001t0002g0312 |
2 | HG02293.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.470+2998G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049539 | |||||||
chr17:62049586 | GA | G | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+2950delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049586 | |||||||
chr17:62049626 | G | A | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+2911C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049626 | |||||||
chr17:62049635 | G | C | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.470+2902C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049635 | |||||||
chr17:62049669 | C | T | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.470+2868G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049669 | |||||||
chr17:62049683 | G | A | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.470+2854C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049683 | |||||||
chr17:62049801 | G | A | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+2736C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049801 | |||||||
chr17:62049822 | C | T | 1 | a0001c0003t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.470+2715G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049822 | |||||||
chr17:62049892 | T | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+2645A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049892 | |||||||
chr17:62049930 | C | CAAAAAAA others(3): Show |
9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(6): Show |
9 | HG02109.hp1 HG02258.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.470+2597_470+2606d others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | |||||||
chr17:62049930 | C | CAAAAAAA others(4): Show |
107 | a0001c0001t0001g0315 a0001c0001t0003g0290 a0001c0001t0003g0294 others(104): Show |
107 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.470+2596_470+2606d others(13): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | |||||||
chr17:62049930 | C | CAAAAAAA others(5): Show |
17 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0036 others(14): Show |
17 | HG00423.hp2 HG00597.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.470+2595_470+2606d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | |||||||
chr17:62049930 | C | CAAAAAAA others(6): Show |
8 | a0001c0003t0001g0308 a0001c0004t0001g0010 a0001c0004t0001g0011 others(5): Show |
8 | HG01891.hp1 HG01978.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.470+2594_470+2606d others(15): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | |||||||
chr17:62049930 | C | CAAAAAAA others(7): Show |
2 | a0001c0004t0001g0015 a0001c0004t0001g0021 |
2 | HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.470+2606_470+2607i others(16): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | |||||||
chr17:62049930 | C | CAAAAAAA others(8): Show |
1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470+2606_470+2607i others(17): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049930 | |||||||
chr17:62049943 | A | AAAAAAAA others(3): Show |
1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.470+2593_470+2594i others(12): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62049943 | |||||||
chr17:62050232 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.470+2305G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62050232 | |||||||
chr17:62050471 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.470+2066A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62050471 | |||||||
chr17:62050645 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0011g0016 |
2 | HG02300.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.470+1892C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62050645 | |||||||
chr17:62050789 | A | G | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.470+1748T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62050789 | |||||||
chr17:62051072 | T | A | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+1465A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62051072 | |||||||
chr17:62051304 | G | A | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.470+1233C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62051304 | |||||||
chr17:62051635 | A | AAAAC | 101 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(98): Show |
101 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.470+898_470+901dup others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62051635 | |||||||
chr17:62051853 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.470+684C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62051853 | |||||||
chr17:62051896 | T | C | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.470+641A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62051896 | |||||||
chr17:62052066 | T | C | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.470+471A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052066 | |||||||
chr17:62052194 | T | G | 1 | a0001c0002t0001g0069 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.470+343A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052194 | |||||||
chr17:62052248 | G | A | 1 | a0001c0002t0001g0070 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.470+289C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052248 | |||||||
chr17:62052382 | T | TA | 12 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0324 others(9): Show |
12 | HG01978.hp2 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.470+154dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052382 | |||||||
chr17:62052427 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.470+110T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052427 | |||||||
chr17:62052514 | C | T | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.470+23G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | 62052514 | |||||||
chr17:62052710 | A | G | 1 | a0007c0010t0001g0007 | 1 | HG03130.hp2 | splice_region_variant&intron_variant | LOW | c.302-5T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62052710 | |||||||
chr17:62053041 | C | T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.302-336G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053041 | |||||||
chr17:62053127 | G | C | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.302-422C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053127 | |||||||
chr17:62053218 | T | G | 1 | a0001c0007t0006g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.302-513A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053218 | |||||||
chr17:62053286 | A | G | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.302-581T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053286 | |||||||
chr17:62053683 | T | C | 58 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.302-978A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053683 | |||||||
chr17:62053873 | A | C | 2 | a0001c0002t0001g0036 a0001c0002t0001g0037 |
2 | HG00423.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.302-1168T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053873 | |||||||
chr17:62053958 | C | T | 1 | a0001c0001t0003g0290 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.302-1253G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053958 | |||||||
chr17:62053988 | C | T | 4 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-1283G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62053988 | |||||||
chr17:62054200 | G | A | 22 | a0001c0003t0001g0098 a0001c0003t0001g0099 a0001c0003t0001g0104 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.302-1495C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054200 | |||||||
chr17:62054319 | A | C | 1 | a0001c0001t0011g0016 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.302-1614T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054319 | |||||||
chr17:62054689 | A | C | 1 | a0001c0001t0018g0127 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.302-1984T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054689 | |||||||
chr17:62054745 | C | A | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.302-2040G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054745 | |||||||
chr17:62054765 | G | C | 19 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0107 others(16): Show |
19 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.302-2060C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054765 | |||||||
chr17:62054863 | G | C | 1 | a0001c0001t0002g0277 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.302-2158C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62054863 | |||||||
chr17:62055142 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.302-2437G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055142 | |||||||
chr17:62055369 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.302-2664C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055369 | |||||||
chr17:62055397 | C | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0278 |
3 | NA18965.hp2 NA19012.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.302-2692G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055397 | |||||||
chr17:62055408 | A | C | 1 | a0001c0001t0001g0218 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.302-2703T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055408 | |||||||
chr17:62055446 | T | C | 1 | a0001c0003t0001g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.302-2741A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055446 | |||||||
chr17:62055716 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.302-3011C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055716 | |||||||
chr17:62055740 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.302-3035A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055740 | |||||||
chr17:62055770 | C | T | 5 | a0001c0004t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 others(2): Show |
5 | HG02055.hp2 HG02818.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.302-3065G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055770 | |||||||
chr17:62055837 | T | C | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.302-3132A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055837 | |||||||
chr17:62055943 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.302-3238T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62055943 | |||||||
chr17:62056048 | A | G | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.302-3343T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056048 | |||||||
chr17:62056164 | G | A | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.302-3459C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056164 | |||||||
chr17:62056179 | G | C | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.302-3474C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056179 | |||||||
chr17:62056253 | CGTT | C | 53 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(50): Show |
53 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.302-3551_302-3549d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056253 | |||||||
chr17:62056393 | T | C | 97 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(94): Show |
97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.302-3688A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056393 | |||||||
chr17:62056603 | C | CT | 199 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.302-3899dupA | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056603 | |||||||
chr17:62056610 | T | TC | 4 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0001g0075 others(1): Show |
4 | HG00544.hp1 HG02056.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-3906_302-3905i others(3): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056610 | |||||||
chr17:62056926 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.302-4221G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62056926 | |||||||
chr17:62057174 | A | G | 9 | a0001c0003t0001g0023 a0001c0003t0001g0024 a0001c0003t0001g0025 others(6): Show |
9 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-4469T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057174 | |||||||
chr17:62057179 | T | C | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.302-4474A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057179 | |||||||
chr17:62057234 | TTA | T | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-4531_302-4530d others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057234 | |||||||
chr17:62057536 | T | C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-4831A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057536 | |||||||
chr17:62057550 | CAAT | C | 55 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.302-4848_302-4846d others(5): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057550 | |||||||
chr17:62057822 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.302-5117C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057822 | |||||||
chr17:62057916 | C | T | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.301+5151G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62057916 | |||||||
chr17:62058221 | T | A | 1 | a0001c0001t0002g0272 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.301+4846A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058221 | |||||||
chr17:62058437 | C | G | 4 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(1): Show |
4 | HG02257.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+4630G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058437 | |||||||
chr17:62058437 | C | T | 1 | a0001c0003t0001g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.301+4630G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058437 | |||||||
chr17:62058508 | G | A | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.301+4559C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058508 | |||||||
chr17:62058520 | C | CA | 22 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(19): Show |
22 | HG00544.hp1 HG01243.hp2 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.301+4546dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058520 | |||||||
chr17:62058520 | CA | C | 6 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0002t0001g0034 others(3): Show |
6 | HG02132.hp1 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+4546delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058520 | |||||||
chr17:62058537 | A | G | 3 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 |
3 | HG03669.hp1 NA18975.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.301+4530T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058537 | |||||||
chr17:62058539 | A | AG | 56 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(53): Show |
56 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.301+4527_301+4528i others(3): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058539 | |||||||
chr17:62058539 | A | G | 2 | a0001c0001t0013g0229 a0001c0008t0001g0122 |
2 | HG03834.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.301+4528T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058539 | |||||||
chr17:62058807 | G | A | 94 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(91): Show |
94 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.301+4260C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62058807 | |||||||
chr17:62059139 | C | T | 1 | a0001c0001t0004g0217 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.301+3928G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059139 | |||||||
chr17:62059206 | A | G | 1 | a0001c0001t0002g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.301+3861T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059206 | |||||||
chr17:62059286 | C | T | 94 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(91): Show |
94 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.301+3781G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059286 | |||||||
chr17:62059398 | T | C | 1 | a0001c0002t0001g0079 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.301+3669A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059398 | |||||||
chr17:62059427 | T | C | 1 | a0001c0001t0004g0211 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.301+3640A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059427 | |||||||
chr17:62059430 | C | G | 1 | a0001c0001t0004g0217 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.301+3637G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059430 | |||||||
chr17:62059482 | G | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.301+3585C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059482 | |||||||
chr17:62059630 | G | C | 1 | a0001c0021t0017g0283 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.301+3437C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059630 | |||||||
chr17:62059724 | T | C | 207 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(204): Show |
207 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.301+3343A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059724 | |||||||
chr17:62059782 | C | T | 1 | a0001c0001t0013g0316 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.301+3285G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059782 | |||||||
chr17:62059822 | A | C | 1 | a0001c0015t0001g0096 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.301+3245T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059822 | |||||||
chr17:62059854 | G | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+3213C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059854 | |||||||
chr17:62059925 | A | C | 2 | a0001c0004t0001g0010 a0001c0004t0001g0011 |
2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.301+3142T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059925 | |||||||
chr17:62059925 | A | G | 1 | a0004c0011t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.301+3142T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62059925 | |||||||
chr17:62060058 | G | A | 58 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.301+3009C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060058 | |||||||
chr17:62060104 | G | A | 5 | a0001c0002t0001g0001 a0001c0002t0001g0084 a0001c0002t0001g0085 others(2): Show |
5 | HG02027.hp1 NA18960.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+2963C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060104 | |||||||
chr17:62060282 | G | A | 58 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.301+2785C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060282 | |||||||
chr17:62060286 | C | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.301+2781G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060286 | |||||||
chr17:62060448 | G | A | 1 | a0001c0012t0001g0305 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.301+2619C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060448 | |||||||
chr17:62060462 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.301+2605A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060462 | |||||||
chr17:62060475 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0216 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.301+2592G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060475 | |||||||
chr17:62060486 | G | A | 58 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.301+2581C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060486 | |||||||
chr17:62060508 | T | C | 9 | a0001c0002t0001g0001 a0001c0002t0001g0080 a0001c0002t0001g0081 others(6): Show |
9 | HG02027.hp1 HG02040.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+2559A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060508 | |||||||
chr17:62060600 | A | G | 100 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(97): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.301+2467T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060600 | |||||||
chr17:62060620 | G | A | 84 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(81): Show |
84 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.301+2447C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060620 | |||||||
chr17:62060620 | G | C | 1 | a0010c0013t0001g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.301+2447C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060620 | |||||||
chr17:62060621 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.301+2446G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060621 | |||||||
chr17:62060632 | G | A | 1 | a0001c0006t0001g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.301+2435C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060632 | |||||||
chr17:62060644 | C | CA | 22 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0219 others(19): Show |
22 | HG00544.hp2 HG00597.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.301+2422dupT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060644 | |||||||
chr17:62060644 | CA | C | 89 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(86): Show |
89 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.301+2422delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060644 | |||||||
chr17:62060930 | C | T | 4 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+2137G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060930 | |||||||
chr17:62060968 | G | A | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2099C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060968 | |||||||
chr17:62060972 | T | G | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2095A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060972 | |||||||
chr17:62060973 | ACAGGCGT others(29): Show |
A | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2058_301+2093d others(38): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62060973 | |||||||
chr17:62061011 | T | G | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2056A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061011 | |||||||
chr17:62061016 | A | C | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2051T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061016 | |||||||
chr17:62061018 | G | T | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2049C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061018 | |||||||
chr17:62061020 | T | G | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2047A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061020 | |||||||
chr17:62061024 | A | G | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+2043T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061024 | |||||||
chr17:62061130 | AACCTAGA others(29): Show |
A | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1901_301+1936d others(38): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061130 | |||||||
chr17:62061168 | A | T | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1899T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061168 | |||||||
chr17:62061171 | G | A | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1896C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061171 | |||||||
chr17:62061172 | C | G | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1895G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061172 | |||||||
chr17:62061177 | C | A | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1890G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061177 | |||||||
chr17:62061211 | A | G | 2 | a0001c0001t0001g0118 a0007c0010t0001g0007 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.301+1856T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061211 | |||||||
chr17:62061371 | GA | G | 85 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(82): Show |
85 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.301+1695delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061371 | |||||||
chr17:62061443 | T | A | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1624A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061443 | |||||||
chr17:62061448 | A | G | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1619T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061448 | |||||||
chr17:62061450 | A | G | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1617T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061450 | |||||||
chr17:62061451 | G | T | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1616C>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061451 | |||||||
chr17:62061497 | C | G | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1570G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061497 | |||||||
chr17:62061499 | A | C | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1568T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061499 | |||||||
chr17:62061505 | C | A | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1562G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061505 | |||||||
chr17:62061539 | G | A | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1528C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061539 | |||||||
chr17:62061552 | A | G | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1515T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061552 | |||||||
chr17:62061553 | T | C | 58 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0228 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.301+1514A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061553 | |||||||
chr17:62061554 | A | T | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1513T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061554 | |||||||
chr17:62061557 | T | G | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1510A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061557 | |||||||
chr17:62061570 | T | A | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1497A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061570 | |||||||
chr17:62061579 | TTCAACAA others(5): Show |
T | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1476_301+1487d others(14): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061579 | |||||||
chr17:62061592 | T | A | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1475A>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061592 | |||||||
chr17:62061594 | C | A | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.301+1473G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061594 | |||||||
chr17:62061620 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.301+1447T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62061620 | |||||||
chr17:62062027 | C | G | 2 | a0001c0001t0002g0092 a0001c0001t0002g0093 |
2 | NA18952.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.301+1040G>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062027 | |||||||
chr17:62062139 | A | T | 96 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(93): Show |
96 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.301+928T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062139 | |||||||
chr17:62062164 | G | A | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+903C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062164 | |||||||
chr17:62062209 | T | C | 1 | a0001c0001t0002g0312 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.301+858A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062209 | |||||||
chr17:62062289 | C | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
14 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.301+778G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062289 | |||||||
chr17:62062460 | CTCT | C | 5 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0008g0318 others(2): Show |
5 | HG01167.hp1 HG01168.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+604_301+606del others(3): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062460 | |||||||
chr17:62062578 | AACACACA others(20): Show |
A | 1 | a0001c0003t0001g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.301+462_301+488del others(27): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062578 | |||||||
chr17:62062578 | AACACACA others(26): Show |
A | 1 | a0001c0002t0001g0288 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.301+456_301+488del others(33): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062578 | |||||||
chr17:62062589 | ACACACAC others(4): Show |
A | 4 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+467_301+477del others(11): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062589 | |||||||
chr17:62062590 | CACACACA others(13): Show |
C | 5 | a0001c0007t0006g0279 a0001c0007t0006g0280 a0001c0007t0006g0282 others(2): Show |
5 | HG02257.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+457_301+476del others(20): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062590 | |||||||
chr17:62062598 | CACCACA | C | 5 | a0001c0003t0001g0098 a0001c0003t0001g0104 a0001c0003t0001g0110 others(2): Show |
5 | HG02572.hp2 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+463_301+468del others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062598 | |||||||
chr17:62062598 | CACCACAC others(1): Show |
C | 29 | a0001c0002t0001g0038 a0001c0002t0001g0058 a0001c0002t0001g0065 others(26): Show |
29 | HG00639.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.301+461_301+468del others(8): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062598 | |||||||
chr17:62062598 | CACCACAC others(3): Show |
C | 80 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(77): Show |
80 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.301+459_301+468del others(10): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062598 | |||||||
chr17:62062599 | A | C | 2 | a0001c0003t0001g0099 a0001c0015t0001g0096 |
2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.301+468T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062599 | |||||||
chr17:62062599 | AC | A | 3 | a0001c0001t0001g0205 a0001c0001t0001g0212 a0001c0016t0001g0322 |
3 | HG02109.hp1 HG02630.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.301+467delG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062599 | |||||||
chr17:62062600 | C | A | 2 | a0001c0003t0001g0099 a0001c0015t0001g0096 |
2 | HG01109.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.301+467G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | |||||||
chr17:62062600 | C | CA | 56 | a0001c0001t0001g0213 a0001c0001t0002g0092 a0001c0001t0002g0093 others(53): Show |
56 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.301+466_301+467ins others(1): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | |||||||
chr17:62062600 | C | CCA | 8 | a0001c0001t0001g0094 a0001c0001t0001g0137 a0001c0001t0001g0160 others(5): Show |
8 | HG01261.hp1 HG01346.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.301+465_301+466dup others(2): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | |||||||
chr17:62062600 | C | CCACA | 25 | a0001c0001t0001g0119 a0001c0001t0001g0134 a0001c0001t0001g0138 others(22): Show |
25 | HG00558.hp1 HG01516.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.301+463_301+466dup others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | |||||||
chr17:62062600 | C | CCACACA | 4 | a0001c0001t0001g0135 a0001c0001t0001g0170 a0001c0001t0001g0182 others(1): Show |
4 | HG01167.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+461_301+466dup others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | |||||||
chr17:62062600 | CCA | C | 31 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0129 others(28): Show |
31 | HG00140.hp1 HG01168.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.301+465_301+466del others(2): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | |||||||
chr17:62062600 | CCACA | C | 41 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(38): Show |
41 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.301+463_301+466del others(4): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | |||||||
chr17:62062600 | CCACACA | C | 19 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(16): Show |
19 | HG01243.hp1 HG01934.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.301+461_301+466del others(6): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062600 | |||||||
chr17:62062602 | A | AC | 7 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0253 others(4): Show |
7 | HG02293.hp1 HG03486.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+464dupG | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062602 | |||||||
chr17:62062603 | CA | C | 50 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0092 others(47): Show |
50 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.301+463delT | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062603 | |||||||
chr17:62062616 | A | C | 4 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+451T>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062616 | |||||||
chr17:62062759 | C | T | 1 | a0001c0001t0025g0008 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.301+308G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062759 | |||||||
chr17:62062790 | G | A | 1 | a0002c0005t0001g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.301+277C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 2/29 | chr17 | 62062790 | |||||||
chr17:62063564 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.67-263C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62063564 | |||||||
chr17:62063601 | G | C | 21 | a0001c0001t0003g0290 a0001c0001t0003g0294 a0001c0001t0003g0295 others(18): Show |
21 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.67-300C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62063601 | |||||||
chr17:62063717 | A | T | 4 | a0002c0005t0001g0003 a0002c0005t0001g0004 a0002c0005t0001g0005 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-416T>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62063717 | |||||||
chr17:62064002 | T | C | 1 | a0009c0019t0008g0310 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.67-701A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064002 | |||||||
chr17:62064034 | G | A | 2 | a0001c0001t0002g0311 a0001c0001t0002g0312 |
2 | HG02293.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.67-733C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064034 | |||||||
chr17:62064194 | G | A | 1 | a0001c0001t0002g0313 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.67-893C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064194 | |||||||
chr17:62064201 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.67-900A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064201 | |||||||
chr17:62064255 | C | T | 1 | a0001c0001t0007g0002 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.66+885G>A | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064255 | |||||||
chr17:62064342 | G | C | 1 | a0001c0001t0001g0315 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.66+798C>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064342 | |||||||
chr17:62064608 | A | G | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.66+532T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064608 | |||||||
chr17:62064726 | G | A | 1 | a0001c0001t0013g0316 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.66+414C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064726 | |||||||
chr17:62064740 | A | G | 1 | a0001c0002t0001g0001 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.66+400T>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064740 | |||||||
chr17:62064760 | T | C | 1 | a0001c0002t0001g0317 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.66+380A>G | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064760 | |||||||
chr17:62064813 | G | A | 1 | a0001c0001t0008g0318 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.66+327C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064813 | |||||||
chr17:62064833 | C | A | 1 | a0001c0001t0001g0319 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.66+307G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064833 | |||||||
chr17:62064849 | G | A | 1 | a0006c0024t0001g0320 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.66+291C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064849 | |||||||
chr17:62064880 | T | G | 1 | a0001c0002t0001g0321 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.66+260A>C | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064880 | |||||||
chr17:62064904 | G | A | 1 | a0001c0016t0001g0322 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.66+236C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62064904 | |||||||
chr17:62065011 | G | A | 2 | a0001c0001t0001g0324 a0001c0003t0001g0323 |
2 | HG01978.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.66+129C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62065011 | |||||||
chr17:62065019 | G | A | 1 | a0001c0003t0007g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.66+121C>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62065019 | |||||||
chr17:62065110 | C | A | 1 | a0001c0003t0001g0326 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.66+30G>T | MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 1/29 | chr17 | 62065110 |