Item | Value |
---|---|
geneid | 729 |
ensemblid | ENSG00000039537.16 |
hgncid | 1339 |
symbol | C6 |
name | complement C6 |
refseq_nuc | NM_000065.5 |
refseq_prot | NP_000056.2 |
ensembl_nuc | ENST00000337836.10 |
ensembl_prot | ENSP00000338861.5 |
mane_status | MANE Select |
chr | chr5 |
start | 41142116 |
end | 41213532 |
strand | - |
ver | v1.2 |
region | chr5:41142116-41213532 |
region5000 | chr5:41137116-41218532 |
regionname0 | C6_chr5_41142116_41213532 |
regionname5000 | C6_chr5_41137116_41218532 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 934 | 187 | 38 | 37 | 80 | 6 | 26 | 55 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0002 | 1/1 | 934 | 177 | 37 | 25 | 91 | 10 | 12 | 72 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0003 | 0/0 | 934 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0004 | 0/0 | 934 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | MARLS others(929): Show |
chr5 | 41137116 | 41218532 |
a0005 | 0/0 | 934 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0006 | 0/0 | 934 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0007 | 0/0 | 934 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0008 | 0/0 | 934 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0009 | 0/0 | 934 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0010 | 0/0 | 934 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0011 | 0/0 | 934 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0012 | 0/0 | 934 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0013 | 0/0 | 934 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0014 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0015 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0016 | 0/0 | 934 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0017 | 0/0 | 934 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0018 | 0/0 | 934 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0019 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0020 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
a0021 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | MARRS others(929): Show |
chr5 | 41137116 | 41218532 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2802 | 170 | 31 | 31 | 80 | 5 | 23 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0001c0003 | 0/0 | 2802 | 11 | 7 | 2 | 0 | 1 | 1 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0001c0006 | 0/0 | 2802 | 3 | 0 | 2 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0001c0011 | 0/0 | 2802 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0001c0022 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0002c0002 | 0/1 | 2802 | 170 | 34 | 25 | 89 | 10 | 11 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0002c0014 | 0/0 | 2802 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0002c0015 | 1/0 | 2802 | 2 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0002c0027 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0002c0028 | 0/0 | 2802 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0002c0029 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0003c0004 | 0/0 | 2802 | 8 | 0 | 0 | 8 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0004c0008 | 0/0 | 2802 | 3 | 2 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0005c0005 | 0/0 | 2802 | 3 | 3 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0006c0007 | 0/0 | 2802 | 3 | 3 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0007c0016 | 0/0 | 2802 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0008c0017 | 0/0 | 2802 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0009c0009 | 0/0 | 2802 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0010c0010 | 0/0 | 2802 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0011c0012 | 0/0 | 2802 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0012c0013 | 0/0 | 2802 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0013c0024 | 0/0 | 2802 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0014c0020 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0015c0030 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0016c0023 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0017c0026 | 0/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0018c0019 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0019c0018 | 0/0 | 2802 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0020c0025 | 0/0 | 2802 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 | ||
a0021c0021 | 0/0 | 2802 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | ATGGC others(2797): Show |
chr5 | 41137116 | 41218532 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3691 | 106 | 17 | 20 | 57 | 0 | 12 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0001c0001t0002 | 0/0 | 3691 | 52 | 4 | 10 | 23 | 4 | 11 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0001c0001t0004 | 0/0 | 3691 | 7 | 7 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0001c0001t0007 | 0/0 | 3691 | 3 | 2 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCC others(3686): Show |
chr5 | 41137116 | 41218532 |
a0001c0001t0012 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0001c0001t0013 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0001c0003t0001 | 0/0 | 3691 | 11 | 7 | 2 | 0 | 1 | 1 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0001c0006t0002 | 0/0 | 3691 | 3 | 0 | 2 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0001c0011t0002 | 0/0 | 3691 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0001c0022t0001 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0002t0001 | 0/1 | 3691 | 82 | 22 | 11 | 36 | 6 | 6 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0002t0002 | 0/0 | 3691 | 39 | 4 | 4 | 27 | 2 | 2 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0002t0003 | 0/0 | 3691 | 39 | 7 | 7 | 21 | 2 | 2 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0002t0005 | 0/0 | 3691 | 6 | 0 | 1 | 5 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0002t0008 | 0/0 | 3691 | 3 | 0 | 2 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0002t0010 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0014t0009 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0014t0011 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0015t0002 | 1/0 | 3691 | 2 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0027t0002 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0028t0001 | 0/0 | 3691 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0002c0029t0005 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0003c0004t0001 | 0/0 | 3691 | 8 | 0 | 0 | 8 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0004c0008t0001 | 0/0 | 3691 | 3 | 2 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0005c0005t0006 | 0/0 | 3691 | 3 | 3 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0006c0007t0003 | 0/0 | 3691 | 3 | 3 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0007c0016t0003 | 0/0 | 3691 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0008c0017t0004 | 0/0 | 3691 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0009c0009t0001 | 0/0 | 3691 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0010c0010t0001 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0010c0010t0006 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0011c0012t0004 | 0/0 | 3691 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0012c0013t0001 | 0/0 | 3691 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0013c0024t0001 | 0/0 | 3691 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0014c0020t0001 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0015c0030t0002 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0016c0023t0001 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0017c0026t0001 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0018c0019t0002 | 0/0 | 3691 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0019c0018t0001 | 0/0 | 3691 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0020c0025t0001 | 0/0 | 3691 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
a0021c0021t0001 | 0/0 | 3691 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | AGGCT others(3686): Show |
chr5 | 41137116 | 41218532 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0017 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0007g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0012g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0001t0013g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0006t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0006t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0006t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0011t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0001c0022t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0003 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0009 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0005g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0008g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0008g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0008g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0002t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0014t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0014t0011g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0015t0002g0036 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0027t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0028t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0002c0029t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0003c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0004c0008t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0004c0008t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0004c0008t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0005c0005t0006g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0005c0005t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0006c0007t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0006c0007t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0006c0007t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0007c0016t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0007c0016t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0008c0017t0004g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0009c0009t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0009c0009t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0010c0010t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0010c0010t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0011c0012t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0011c0012t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0012c0013t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0012c0013t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0013c0024t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0014c0020t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0015c0030t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0016c0023t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0017c0026t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0018c0019t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0019c0018t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0020c0025t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
a0021c0021t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0003 | t0001 | g0119 | EUR | GBR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0062 | EUR | GBR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00280 | hp1 | a0002 | c0002 | t0003 | g0101 | EUR | FIN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0034 | EUR | FIN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0206 | EUR | FIN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0056 | EUR | FIN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0234 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00609 | hp1 | a0007 | c0016 | t0003 | g0095 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00609 | hp2 | a0003 | c0004 | t0001 | g0153 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | CHS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0177 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01070 | hp2 | a0002 | c0002 | t0003 | g0092 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01071 | hp2 | a0002 | c0002 | t0003 | g0094 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01074 | hp1 | a0001 | c0006 | t0002 | g0143 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01081 | hp1 | a0001 | c0006 | t0002 | g0141 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01109 | hp2 | a0002 | c0002 | t0003 | g0008 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01167 | hp2 | a0008 | c0017 | t0004 | g0028 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0204 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01168 | hp2 | a0001 | c0011 | t0002 | g0019 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01169 | hp1 | a0008 | c0017 | t0004 | g0028 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01169 | hp2 | a0001 | c0011 | t0002 | g0019 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0203 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0043 | AMR | PUR | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01257 | hp2 | a0013 | c0024 | t0001 | g0301 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0320 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01361 | hp2 | a0004 | c0008 | t0001 | g0151 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01496 | hp2 | a0002 | c0002 | t0003 | g0116 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0158 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0033 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0159 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0168 | EUR | IBS | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01884 | hp1 | a0002 | c0014 | t0009 | g0048 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0042 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01934 | hp2 | a0002 | c0002 | t0003 | g0098 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01981 | hp1 | a0002 | c0002 | t0003 | g0091 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02004 | hp1 | a0002 | c0002 | t0008 | g0316 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02004 | hp2 | a0002 | c0002 | t0003 | g0114 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02055 | hp1 | a0002 | c0002 | t0003 | g0008 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02074 | hp2 | a0002 | c0002 | t0003 | g0009 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02129 | hp1 | a0002 | c0015 | t0002 | g0036 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0123 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | CDX | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | CDX | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02257 | hp2 | a0009 | c0009 | t0001 | g0083 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02258 | hp1 | a0010 | c0010 | t0006 | g0045 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02258 | hp2 | a0014 | c0020 | t0001 | g0322 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02273 | hp2 | a0002 | c0002 | t0008 | g0317 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0121 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PEL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0008 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02451 | hp2 | a0002 | c0014 | t0011 | g0085 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02572 | hp2 | a0002 | c0002 | t0003 | g0023 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0145 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02615 | hp2 | a0015 | c0030 | t0002 | g0235 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02630 | hp1 | a0005 | c0005 | t0006 | g0046 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02630 | hp2 | a0009 | c0009 | t0001 | g0130 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0185 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02698 | hp2 | a0001 | c0022 | t0001 | g0290 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02717 | hp1 | a0010 | c0010 | t0001 | g0263 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02723 | hp2 | a0006 | c0007 | t0003 | g0105 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02735 | hp1 | a0002 | c0002 | t0008 | g0318 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02738 | hp1 | a0016 | c0023 | t0001 | g0291 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0162 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0044 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0129 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02895 | hp2 | a0005 | c0005 | t0006 | g0018 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0126 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0164 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0165 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02897 | hp2 | a0005 | c0005 | t0006 | g0018 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0125 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02922 | hp2 | a0011 | c0012 | t0004 | g0138 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03041 | hp1 | a0002 | c0029 | t0005 | g0319 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0124 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03195 | hp1 | a0004 | c0008 | t0001 | g0323 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03195 | hp2 | a0002 | c0002 | t0003 | g0023 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03209 | hp1 | a0011 | c0012 | t0004 | g0136 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03209 | hp2 | a0006 | c0007 | t0003 | g0104 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0127 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0213 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03516 | hp1 | a0006 | c0007 | t0003 | g0106 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | ESN | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03579 | hp2 | a0002 | c0002 | t0010 | g0047 | AFR | MSL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03688 | hp1 | a0002 | c0027 | t0002 | g0223 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0167 | SAS | PJL | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0110 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03834 | hp1 | a0001 | c0003 | t0001 | g0122 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0086 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03942 | hp1 | a0017 | c0026 | t0001 | g0183 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0166 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0184 | SAS | STU | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0237 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18522 | hp2 | a0004 | c0008 | t0001 | g0150 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | CHB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18939 | hp1 | a0002 | c0002 | t0003 | g0096 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18941 | hp1 | a0002 | c0028 | t0001 | g0186 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18943 | hp2 | a0002 | c0002 | t0003 | g0009 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18947 | hp2 | a0012 | c0013 | t0001 | g0280 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18948 | hp1 | a0002 | c0002 | t0003 | g0087 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18949 | hp2 | a0003 | c0004 | t0001 | g0011 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18953 | hp2 | a0012 | c0013 | t0001 | g0279 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18959 | hp2 | a0002 | c0002 | t0005 | g0178 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18965 | hp1 | a0003 | c0004 | t0001 | g0011 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18969 | hp1 | a0003 | c0004 | t0001 | g0156 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18971 | hp2 | a0002 | c0002 | t0003 | g0113 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18974 | hp2 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18978 | hp1 | a0002 | c0002 | t0003 | g0115 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18983 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18984 | hp1 | a0003 | c0004 | t0001 | g0154 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18985 | hp1 | a0003 | c0004 | t0001 | g0157 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18986 | hp1 | a0002 | c0002 | t0003 | g0024 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18988 | hp1 | a0002 | c0002 | t0003 | g0088 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18989 | hp2 | a0019 | c0018 | t0001 | g0285 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18994 | hp1 | a0002 | c0002 | t0003 | g0103 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18995 | hp1 | a0002 | c0002 | t0005 | g0030 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18997 | hp1 | a0002 | c0002 | t0005 | g0176 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18997 | hp2 | a0003 | c0004 | t0001 | g0011 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19000 | hp2 | a0002 | c0002 | t0003 | g0112 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19003 | hp2 | a0003 | c0004 | t0001 | g0155 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19004 | hp1 | a0020 | c0025 | t0001 | g0152 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | LWK | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | LWK | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | LWK | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0128 | AFR | LWK | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19054 | hp2 | a0002 | c0002 | t0003 | g0108 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19056 | hp1 | a0007 | c0016 | t0003 | g0099 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19065 | hp2 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19066 | hp2 | a0021 | c0021 | t0001 | g0281 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19077 | hp2 | a0002 | c0002 | t0003 | g0093 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19079 | hp2 | a0002 | c0002 | t0003 | g0024 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19080 | hp1 | a0002 | c0002 | t0005 | g0175 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19081 | hp2 | a0002 | c0002 | t0005 | g0030 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19082 | hp2 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19084 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19086 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19088 | hp2 | a0002 | c0002 | t0003 | g0100 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19089 | hp2 | a0002 | c0002 | t0003 | g0102 | EAS | JPT | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19240 | hp1 | a0002 | c0002 | t0003 | g0089 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | YRI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | ASW | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20129 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | ASW | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20752 | hp1 | a0001 | c0001 | t0013 | g0257 | EUR | TSI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20752 | hp2 | a0002 | c0002 | t0003 | g0097 | EUR | TSI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0202 | EUR | TSI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | TSI | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | GIH | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20905 | hp2 | a0001 | c0006 | t0002 | g0324 | SAS | GIH | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0118 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG01123 | hp2 | a0002 | c0002 | t0005 | g0174 | AMR | CLM | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02109 | hp1 | a0002 | c0002 | t0003 | g0090 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0208 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0207 | AFR | ACB | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0212 | AFR | USA | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
HG06807 | hp2 | a0018 | c0019 | t0002 | g0059 | AFR | USA | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0120 | AFR | USA | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0200 | REF | REF | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
homoSapiens | grch38p0 | a0002 | c0015 | t0002 | g0036 | REF | REF | C6_chr5_41137116_41218532 | C6 | chr5 | 41137116 | 41218532 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:41142830 | C | T | 2 | a0003 a0020 |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
missense_variant | MODERATE | c.2800G>A | p.Ala934Thr | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 2977/3691 | 2800/2805 | 934/934 | chr5 | 41142830 | |||
chr5:41149429 | G | A | 2 | a0005 a0014 |
4 | HG02258.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
missense_variant | MODERATE | c.2435C>T | p.Thr812Ile | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/18 | 2612/3691 | 2435/2805 | 812/934 | chr5 | 41149429 | |||
chr5:41149460 | C | G | 1 | a0021 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.2404G>C | p.Val802Leu | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/18 | 2581/3691 | 2404/2805 | 802/934 | chr5 | 41149460 | |||
chr5:41153812 | T | C | 1 | a0008 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant&splice_region_variant | MODERATE | c.2288A>G | p.Lys763Arg | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/18 | 2465/3691 | 2288/2805 | 763/934 | chr5 | 41153812 | |||
chr5:41153915 | C | T | 1 | a0017 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.2185G>A | p.Glu729Lys | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/18 | 2362/3691 | 2185/2805 | 729/934 | chr5 | 41153915 | |||
chr5:41154987 | C | T | 1 | a0010 | 2 | HG02258.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.2086G>A | p.Asp696Asn | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/18 | 2263/3691 | 2086/2805 | 696/934 | chr5 | 41154987 | |||
chr5:41159090 | C | T | 2 | a0003 a0020 |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
missense_variant | MODERATE | c.1848G>A | p.Met616Ile | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/18 | 2025/3691 | 1848/2805 | 616/934 | chr5 | 41159090 | |||
chr5:41159237 | C | G | 2 | a0003 a0020 |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
missense_variant | MODERATE | c.1701G>C | p.Gln567His | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/18 | 1878/3691 | 1701/2805 | 567/934 | chr5 | 41159237 | |||
chr5:41160271 | C | T | 3 | a0005 a0009 a0014 |
6 | HG02257.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
missense_variant | MODERATE | c.1555G>A | p.Asp519Asn | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/18 | 1732/3691 | 1555/2805 | 519/934 | chr5 | 41160271 | |||
chr5:41161764 | C | G | 1 | a0014 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1387G>C | p.Gly463Arg | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/18 | 1564/3691 | 1387/2805 | 463/934 | chr5 | 41161764 | |||
chr5:41161796 | C | T | 1 | a0018 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1355G>A | p.Gly452Glu | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/18 | 1532/3691 | 1355/2805 | 452/934 | chr5 | 41161796 | |||
chr5:41161817 | C | T | 1 | a0020 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.1334G>A | p.Arg445Gln | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/18 | 1511/3691 | 1334/2805 | 445/934 | chr5 | 41161817 | |||
chr5:41161850 | A | T | 1 | a0019 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.1301T>A | p.Ile434Lys | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/18 | 1478/3691 | 1301/2805 | 434/934 | chr5 | 41161850 | |||
chr5:41161851 | T | C | 1 | a0007 | 2 | HG00609.hp1 NA19056.hp1 |
missense_variant | MODERATE | c.1300A>G | p.Ile434Val | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/18 | 1477/3691 | 1300/2805 | 434/934 | chr5 | 41161851 | |||
chr5:41172327 | T | C | 1 | a0011 | 2 | HG02922.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.1189A>G | p.Lys397Glu | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/18 | 1366/3691 | 1189/2805 | 397/934 | chr5 | 41172327 | |||
chr5:41176663 | G | A | 2 | a0012 a0021 |
3 | NA18947.hp2 NA18953.hp2 NA19066.hp2 |
missense_variant | MODERATE | c.980C>T | p.Thr327Met | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/18 | 1157/3691 | 980/2805 | 327/934 | chr5 | 41176663 | |||
chr5:41181379 | T | C | 1 | a0016 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.907A>G | p.Ile303Val | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/18 | 1084/3691 | 907/2805 | 303/934 | chr5 | 41181379 | |||
chr5:41181438 | A | C | 1 | a0006 | 3 | HG02723.hp2 HG03209.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.848T>G | p.Ile283Ser | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/18 | 1025/3691 | 848/2805 | 283/934 | chr5 | 41181438 | |||
chr5:41181465 | T | C | 1 | a0015 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.821A>G | p.Gln274Arg | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/18 | 998/3691 | 821/2805 | 274/934 | chr5 | 41181465 | |||
chr5:41181531 | G | A | 1 | a0013 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.755C>T | p.Thr252Ile | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/18 | 932/3691 | 755/2805 | 252/934 | chr5 | 41181531 | |||
chr5:41186119 | G | A | 1 | a0008 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.677C>T | p.Thr226Ile | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/18 | 854/3691 | 677/2805 | 226/934 | chr5 | 41186119 | |||
chr5:41199857 | G | T | 12 | a0001 a0005 a0009 others(9): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
missense_variant | MODERATE | c.356C>A | p.Ala119Glu | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/18 | 533/3691 | 356/2805 | 119/934 | chr5 | 41199857 | |||
chr5:41203220 | C | A | 1 | a0004 | 3 | HG01361.hp2 HG03195.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.11G>T | p.Arg4Leu | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/18 | 188/3691 | 11/2805 | 4/934 | chr5 | 41203220 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:41142837 | C | T | 1 | a0002c0027 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.2793G>A | p.Lys931Lys | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 2970/3691 | 2793/2805 | 931/934 | chr5 | 41142837 | |||
chr5:41153940 | T | C | 1 | a0002c0028 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.2160A>G | p.Arg720Arg | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/18 | 2337/3691 | 2160/2805 | 720/934 | chr5 | 41153940 | |||
chr5:41155006 | G | A | 1 | a0002c0029 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.2067C>T | p.Asp689Asp | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/18 | 2244/3691 | 2067/2805 | 689/934 | chr5 | 41155006 | |||
chr5:41155048 | G | A | 1 | a0001c0011 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.2025C>T | p.Gly675Gly | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/18 | 2202/3691 | 2025/2805 | 675/934 | chr5 | 41155048 | |||
chr5:41158761 | G | A | 29 | a0001c0001 a0001c0003 a0001c0006 others(26): Show |
399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
synonymous_variant | LOW | c.1881C>T | p.Asp627Asp | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/18 | 2058/3691 | 1881/2805 | 627/934 | chr5 | 41158761 | |||
chr5:41159243 | G | A | 2 | a0003c0004 a0020c0025 |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
synonymous_variant | LOW | c.1695C>T | p.Asp565Asp | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/18 | 1872/3691 | 1695/2805 | 565/934 | chr5 | 41159243 | |||
chr5:41160191 | A | G | 1 | a0001c0006 | 3 | HG01074.hp1 HG01081.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.1635T>C | p.Ser545Ser | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/18 | 1812/3691 | 1635/2805 | 545/934 | chr5 | 41160191 | |||
chr5:41160209 | A | G | 3 | a0002c0014 a0003c0004 a0020c0025 |
11 | HG00609.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
synonymous_variant | LOW | c.1617T>C | p.Cys539Cys | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/18 | 1794/3691 | 1617/2805 | 539/934 | chr5 | 41160209 | |||
chr5:41176593 | G | A | 1 | a0021c0021 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.1050C>T | p.Asn350Asn | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/18 | 1227/3691 | 1050/2805 | 350/934 | chr5 | 41176593 | |||
chr5:41176710 | A | G | 2 | a0003c0004 a0020c0025 |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
synonymous_variant | LOW | c.933T>C | p.Ser311Ser | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/18 | 1110/3691 | 933/2805 | 311/934 | chr5 | 41176710 | |||
chr5:41181476 | T | A | 2 | a0001c0022 a0016c0023 |
2 | HG02698.hp2 HG02738.hp1 |
synonymous_variant | LOW | c.810A>T | p.Ser270Ser | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/18 | 987/3691 | 810/2805 | 270/934 | chr5 | 41181476 | |||
chr5:41186118 | T | G | 1 | a0001c0003 | 11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
synonymous_variant | LOW | c.678A>C | p.Thr226Thr | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/18 | 855/3691 | 678/2805 | 226/934 | chr5 | 41186118 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:41142167 | A | C | 1 | a0002c0002t0008 | 3 | HG02004.hp1 HG02273.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*658T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 658 | chr5 | 41142167 | ||||||
chr5:41142188 | C | G | 6 | a0001c0001t0004 a0001c0001t0007 a0002c0014t0009 others(3): Show |
16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*637G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 637 | chr5 | 41142188 | ||||||
chr5:41142249 | T | C | 1 | a0001c0001t0012 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*576A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 576 | chr5 | 41142249 | ||||||
chr5:41142471 | G | T | 2 | a0002c0002t0005 a0002c0029t0005 |
7 | HG01123.hp2 HG03041.hp1 NA18959.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*354C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 354 | chr5 | 41142471 | ||||||
chr5:41142504 | C | T | 33 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(30): Show |
299 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*321G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 321 | chr5 | 41142504 | ||||||
chr5:41142530 | A | G | 6 | a0001c0001t0004 a0001c0001t0007 a0002c0014t0009 others(3): Show |
16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*295T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 295 | chr5 | 41142530 | ||||||
chr5:41142583 | C | T | 6 | a0001c0001t0004 a0001c0001t0007 a0002c0014t0009 others(3): Show |
16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*242G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 242 | chr5 | 41142583 | ||||||
chr5:41142626 | C | T | 1 | a0001c0001t0012 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*199G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 199 | chr5 | 41142626 | ||||||
chr5:41142744 | T | C | 1 | a0001c0001t0013 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 18/18 | 81 | chr5 | 41142744 | ||||||
chr5:41203242 | C | T | 4 | a0002c0002t0003 a0002c0014t0011 a0006c0007t0003 others(1): Show |
45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-12G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/18 | 12 | chr5 | 41203242 | ||||||
chr5:41213435 | G | T | 2 | a0002c0002t0010 a0002c0014t0009 |
2 | HG01884.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-80C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/18 | 10205 | chr5 | 41213435 | ||||||
chr5:41213497 | C | G | 2 | a0005c0005t0006 a0010c0010t0006 |
4 | HG02258.hp1 HG02630.hp1 HG02895.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-142G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/18 | 10267 | chr5 | 41213497 | ||||||
chr5:41213528 | A | G | 1 | a0001c0001t0007 | 3 | HG01243.hp2 HG01891.hp2 HG02818.hp2 |
5_prime_UTR_variant | MODIFIER | c.-173T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/18 | 10298 | chr5 | 41213528 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:41143214 | C | T | 1 | a0001c0001t0004g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2624-208G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143214 | |||||||
chr5:41143320 | C | T | 3 | a0002c0002t0002g0199 a0002c0002t0002g0216 a0002c0002t0002g0217 |
3 | NA18951.hp2 NA19077.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2624-314G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143320 | |||||||
chr5:41143321 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2624-315C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143321 | |||||||
chr5:41143477 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2624-471C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143477 | |||||||
chr5:41143545 | G | A | 7 | a0001c0001t0001g0140 a0002c0002t0001g0035 a0002c0002t0001g0146 others(4): Show |
8 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2624-539C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143545 | |||||||
chr5:41143654 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(119): Show |
154 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.2624-648C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143654 | |||||||
chr5:41143736 | C | T | 14 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(11): Show |
16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2624-730G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143736 | |||||||
chr5:41143835 | C | T | 6 | a0002c0002t0005g0030 a0002c0002t0005g0174 a0002c0002t0005g0175 others(3): Show |
7 | HG01123.hp2 HG03041.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.2624-829G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41143835 | |||||||
chr5:41144223 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2624-1217A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144223 | |||||||
chr5:41144237 | G | A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2624-1231C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144237 | |||||||
chr5:41144267 | G | A | 6 | a0002c0002t0005g0030 a0002c0002t0005g0174 a0002c0002t0005g0175 others(3): Show |
7 | HG01123.hp2 HG03041.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.2624-1261C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144267 | |||||||
chr5:41144294 | G | A | 6 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(3): Show |
6 | HG00140.hp1 HG01123.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.2624-1288C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144294 | |||||||
chr5:41144352 | C | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0302 |
2 | HG01928.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.2624-1346G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144352 | |||||||
chr5:41144353 | G | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(41): Show |
55 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.2624-1347C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144353 | |||||||
chr5:41144363 | G | C | 1 | a0002c0002t0001g0032 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2624-1357C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144363 | |||||||
chr5:41144387 | C | G | 1 | a0015c0030t0002g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2624-1381G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144387 | |||||||
chr5:41144513 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2624-1507A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144513 | |||||||
chr5:41144574 | C | A | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2624-1568G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144574 | |||||||
chr5:41144751 | T | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(106): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2624-1745A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144751 | |||||||
chr5:41144787 | C | T | 1 | a0002c0002t0002g0207 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2624-1781G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144787 | |||||||
chr5:41144792 | G | A | 5 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0125 others(2): Show |
5 | HG02145.hp2 HG02896.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2624-1786C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144792 | |||||||
chr5:41144875 | G | A | 14 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(11): Show |
16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2624-1869C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144875 | |||||||
chr5:41144889 | T | C | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2624-1883A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144889 | |||||||
chr5:41144901 | C | A | 14 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(11): Show |
16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2624-1895G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144901 | |||||||
chr5:41144940 | A | G | 5 | a0005c0005t0006g0018 a0005c0005t0006g0046 a0009c0009t0001g0083 others(2): Show |
6 | HG02257.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2624-1934T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144940 | |||||||
chr5:41144948 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(198): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.2624-1942C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144948 | |||||||
chr5:41144959 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2624-1953G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41144959 | |||||||
chr5:41145041 | A | C | 1 | a0004c0008t0001g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2624-2035T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145041 | |||||||
chr5:41145106 | G | A | 1 | a0002c0002t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2624-2100C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145106 | |||||||
chr5:41145182 | A | G | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2624-2176T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145182 | |||||||
chr5:41145411 | C | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG01167.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2624-2405G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145411 | |||||||
chr5:41145412 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0251 others(7): Show |
13 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.2624-2406C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145412 | |||||||
chr5:41145458 | G | T | 1 | a0002c0002t0002g0216 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2624-2452C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145458 | |||||||
chr5:41145523 | G | A | 1 | a0001c0001t0004g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2624-2517C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145523 | |||||||
chr5:41145620 | A | G | 9 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0057 others(6): Show |
16 | HG00438.hp2 HG00558.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.2624-2614T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145620 | |||||||
chr5:41145643 | G | A | 1 | a0001c0001t0007g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2624-2637C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145643 | |||||||
chr5:41145692 | C | T | 8 | a0002c0014t0009g0048 a0003c0004t0001g0011 a0003c0004t0001g0153 others(5): Show |
10 | HG00609.hp2 HG01884.hp1 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.2624-2686G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145692 | |||||||
chr5:41145701 | C | T | 2 | a0002c0002t0003g0008 a0002c0002t0003g0089 |
4 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2624-2695G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145701 | |||||||
chr5:41145816 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2624-2810C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145816 | |||||||
chr5:41145849 | T | A | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2624-2843A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145849 | |||||||
chr5:41145864 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2624-2858A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145864 | |||||||
chr5:41145921 | A | G | 2 | a0009c0009t0001g0083 a0009c0009t0001g0130 |
2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2624-2915T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41145921 | |||||||
chr5:41146152 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2623+3089C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146152 | |||||||
chr5:41146175 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(105): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2623+3066G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146175 | |||||||
chr5:41146176 | G | A | 14 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(11): Show |
16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2623+3065C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146176 | |||||||
chr5:41146178 | T | C | 1 | a0002c0002t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2623+3063A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146178 | |||||||
chr5:41146274 | TG | T | 59 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(56): Show |
73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2623+2966delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146274 | |||||||
chr5:41146322 | A | T | 14 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(11): Show |
16 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.2623+2919T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146322 | |||||||
chr5:41146357 | C | T | 2 | a0002c0002t0001g0158 a0002c0002t0001g0168 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2623+2884G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146357 | |||||||
chr5:41146529 | A | T | 4 | a0001c0001t0001g0135 a0004c0008t0001g0150 a0004c0008t0001g0151 others(1): Show |
4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2623+2712T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146529 | |||||||
chr5:41146531 | C | A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2623+2710G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146531 | |||||||
chr5:41146676 | T | A | 1 | a0001c0001t0001g0249 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2623+2565A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146676 | |||||||
chr5:41146748 | C | CT | 11 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(8): Show |
13 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2623+2492dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146748 | |||||||
chr5:41146888 | T | C | 13 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(10): Show |
14 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2623+2353A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146888 | |||||||
chr5:41146899 | A | T | 1 | a0002c0002t0005g0178 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2623+2342T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146899 | |||||||
chr5:41146921 | C | CA | 8 | a0002c0002t0002g0207 a0002c0002t0002g0208 a0002c0002t0005g0176 others(5): Show |
10 | HG00609.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2623+2319dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146921 | |||||||
chr5:41146921 | C | T | 1 | a0002c0014t0009g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2623+2320G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146921 | |||||||
chr5:41146921 | CA | C | 18 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(15): Show |
19 | HG00140.hp1 HG01123.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.2623+2319delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41146921 | |||||||
chr5:41147076 | C | T | 1 | a0015c0030t0002g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2623+2165G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147076 | |||||||
chr5:41147198 | G | A | 13 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(10): Show |
14 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2623+2043C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147198 | |||||||
chr5:41147232 | G | T | 10 | a0002c0002t0001g0029 a0002c0002t0001g0158 a0002c0002t0001g0161 others(7): Show |
11 | HG01515.hp1 HG01517.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2623+2009C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147232 | |||||||
chr5:41147426 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(105): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2623+1815C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147426 | |||||||
chr5:41147542 | C | T | 2 | a0002c0002t0002g0007 a0002c0002t0002g0215 |
5 | NA18945.hp1 NA18959.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.2623+1699G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147542 | |||||||
chr5:41147555 | A | G | 3 | a0002c0002t0005g0030 a0002c0002t0005g0175 a0002c0002t0005g0176 |
4 | NA18995.hp1 NA18997.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2623+1686T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147555 | |||||||
chr5:41147613 | T | C | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2623+1628A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147613 | |||||||
chr5:41147739 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2623+1502C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147739 | |||||||
chr5:41147778 | C | T | 1 | a0002c0002t0001g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2623+1463G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147778 | |||||||
chr5:41147869 | C | T | 5 | a0002c0002t0001g0013 a0002c0002t0001g0230 a0002c0002t0001g0231 others(2): Show |
7 | HG00408.hp1 HG00673.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.2623+1372G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41147869 | |||||||
chr5:41148023 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(84): Show |
110 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.2623+1218G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148023 | |||||||
chr5:41148097 | T | A | 1 | a0001c0001t0001g0321 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2623+1144A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148097 | |||||||
chr5:41148127 | T | G | 1 | a0001c0001t0001g0278 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2623+1114A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148127 | |||||||
chr5:41148395 | T | G | 13 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(10): Show |
14 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2623+846A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148395 | |||||||
chr5:41148400 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(275): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2623+841T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148400 | |||||||
chr5:41148401 | C | T | 2 | a0002c0002t0002g0222 a0002c0002t0002g0227 |
2 | NA18974.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2623+840G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148401 | |||||||
chr5:41148408 | A | C | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2623+833T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148408 | |||||||
chr5:41148441 | T | A | 1 | a0001c0001t0001g0242 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2623+800A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148441 | |||||||
chr5:41148477 | A | G | 1 | a0002c0002t0002g0234 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2623+764T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148477 | |||||||
chr5:41148757 | C | T | 13 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(10): Show |
14 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2623+484G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148757 | |||||||
chr5:41148793 | C | G | 1 | a0002c0002t0008g0316 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2623+448G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148793 | |||||||
chr5:41148802 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2623+439C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148802 | |||||||
chr5:41148851 | T | C | 4 | a0001c0001t0001g0135 a0004c0008t0001g0150 a0004c0008t0001g0151 others(1): Show |
4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2623+390A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148851 | |||||||
chr5:41148978 | C | T | 12 | a0002c0002t0001g0005 a0002c0002t0001g0029 a0002c0002t0001g0158 others(9): Show |
17 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2623+263G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41148978 | |||||||
chr5:41149040 | A | G | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2623+201T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41149040 | |||||||
chr5:41149045 | C | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(105): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2623+196G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41149045 | |||||||
chr5:41149133 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(105): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2623+108T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41149133 | |||||||
chr5:41149156 | G | C | 5 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0125 others(2): Show |
5 | HG02145.hp2 HG02896.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2623+85C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41149156 | |||||||
chr5:41149182 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(76): Show |
102 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.2623+59C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 17/17 | chr5 | 41149182 | |||||||
chr5:41149618 | T | A | 1 | a0006c0007t0003g0106 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2382-136A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149618 | |||||||
chr5:41149636 | A | C | 1 | a0002c0014t0009g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2382-154T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149636 | |||||||
chr5:41149701 | T | G | 1 | a0021c0021t0001g0281 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2382-219A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149701 | |||||||
chr5:41149808 | A | G | 13 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(10): Show |
14 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2381+127T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149808 | |||||||
chr5:41149818 | T | C | 1 | a0001c0003t0001g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2381+117A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149818 | |||||||
chr5:41149858 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2381+77G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 16/17 | chr5 | 41149858 | |||||||
chr5:41150080 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2291-55T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150080 | |||||||
chr5:41150324 | T | A | 7 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(4): Show |
7 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2291-299A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150324 | |||||||
chr5:41150684 | C | T | 1 | a0002c0002t0002g0218 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2291-659G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150684 | |||||||
chr5:41150687 | G | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(41): Show |
55 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.2291-662C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150687 | |||||||
chr5:41150812 | G | A | 1 | a0010c0010t0001g0263 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2291-787C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150812 | |||||||
chr5:41150844 | GC | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(84): Show |
110 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.2291-820delG | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150844 | |||||||
chr5:41150852 | A | AC | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(125): Show |
161 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.2291-828dupG | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150852 | |||||||
chr5:41150884 | T | TA | 31 | a0001c0001t0002g0073 a0001c0001t0004g0025 a0001c0001t0004g0082 others(28): Show |
33 | HG00140.hp1 HG01123.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.2291-860dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150884 | |||||||
chr5:41150884 | TA | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(105): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2291-860delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150884 | |||||||
chr5:41150913 | G | T | 1 | a0001c0001t0002g0072 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2291-888C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150913 | |||||||
chr5:41150974 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2291-949T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41150974 | |||||||
chr5:41151061 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2291-1036T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151061 | |||||||
chr5:41151177 | A | AT | 2 | a0002c0002t0001g0027 a0002c0002t0001g0147 |
3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2291-1153dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151177 | |||||||
chr5:41151178 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(84): Show |
110 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.2291-1153A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151178 | |||||||
chr5:41151200 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2291-1175C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151200 | |||||||
chr5:41151307 | C | T | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2291-1282G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151307 | |||||||
chr5:41151459 | G | C | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2291-1434C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151459 | |||||||
chr5:41151507 | C | A | 1 | a0004c0008t0001g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2291-1482G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151507 | |||||||
chr5:41151859 | G | GA | 11 | a0002c0002t0001g0013 a0002c0002t0001g0230 a0002c0002t0001g0231 others(8): Show |
15 | HG00408.hp1 HG00609.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.2291-1835dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151859 | |||||||
chr5:41151859 | GA | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(96): Show |
125 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.2291-1835delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151859 | |||||||
chr5:41151863 | A | G | 1 | a0002c0002t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2291-1838T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41151863 | |||||||
chr5:41152005 | G | C | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2290+1805C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152005 | |||||||
chr5:41152097 | A | C | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2290+1713T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152097 | |||||||
chr5:41152159 | A | C | 2 | a0002c0002t0001g0027 a0002c0002t0001g0147 |
3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2290+1651T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152159 | |||||||
chr5:41152197 | A | G | 1 | a0001c0001t0002g0073 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2290+1613T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152197 | |||||||
chr5:41152243 | A | T | 11 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(8): Show |
13 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2290+1567T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152243 | |||||||
chr5:41152267 | C | A | 1 | a0002c0002t0003g0096 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2290+1543G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152267 | |||||||
chr5:41152319 | G | A | 2 | a0002c0002t0003g0024 a0002c0002t0003g0096 |
3 | NA18939.hp1 NA18986.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2290+1491C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152319 | |||||||
chr5:41152465 | C | T | 1 | a0002c0002t0002g0177 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2290+1345G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152465 | |||||||
chr5:41152493 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2290+1317G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152493 | |||||||
chr5:41152555 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0315 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2290+1255C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152555 | |||||||
chr5:41152563 | C | T | 4 | a0001c0001t0001g0135 a0004c0008t0001g0150 a0004c0008t0001g0151 others(1): Show |
4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2290+1247G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152563 | |||||||
chr5:41152587 | A | G | 104 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0134 others(101): Show |
126 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2290+1223T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152587 | |||||||
chr5:41152658 | CT | C | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2290+1151delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152658 | |||||||
chr5:41152661 | G | C | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2290+1149C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152661 | |||||||
chr5:41152717 | A | G | 32 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(29): Show |
35 | HG00140.hp1 HG01123.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.2290+1093T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152717 | |||||||
chr5:41152727 | A | T | 78 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(75): Show |
92 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2290+1083T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152727 | |||||||
chr5:41152846 | G | C | 46 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(43): Show |
57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.2290+964C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152846 | |||||||
chr5:41152937 | A | G | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2290+873T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152937 | |||||||
chr5:41152973 | C | T | 1 | a0002c0002t0001g0225 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2290+837G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152973 | |||||||
chr5:41152983 | T | C | 5 | a0005c0005t0006g0018 a0005c0005t0006g0046 a0009c0009t0001g0083 others(2): Show |
6 | HG02257.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2290+827A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41152983 | |||||||
chr5:41153183 | T | C | 1 | a0002c0002t0001g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2290+627A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153183 | |||||||
chr5:41153259 | T | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(41): Show |
55 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.2290+551A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153259 | |||||||
chr5:41153341 | G | T | 1 | a0001c0001t0012g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2290+469C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153341 | |||||||
chr5:41153344 | T | C | 1 | a0002c0002t0001g0171 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2290+466A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153344 | |||||||
chr5:41153357 | A | G | 1 | a0012c0013t0001g0279 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2290+453T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153357 | |||||||
chr5:41153435 | CACTT | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG01167.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2290+371_2290+374d others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153435 | |||||||
chr5:41153579 | C | G | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2290+231G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153579 | |||||||
chr5:41153593 | C | T | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2290+217G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153593 | |||||||
chr5:41153626 | A | C | 2 | a0001c0001t0001g0140 a0002c0002t0001g0146 |
2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2290+184T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153626 | |||||||
chr5:41153685 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0238 |
3 | HG02976.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2290+125T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153685 | |||||||
chr5:41153696 | T | C | 2 | a0002c0014t0009g0048 a0002c0014t0011g0085 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2290+114A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153696 | |||||||
chr5:41153756 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2290+54G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 15/17 | chr5 | 41153756 | |||||||
chr5:41154048 | A | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(272): Show |
341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.2102-50T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154048 | |||||||
chr5:41154113 | C | T | 1 | a0002c0002t0001g0149 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2102-115G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154113 | |||||||
chr5:41154282 | A | G | 1 | a0002c0002t0003g0091 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2102-284T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154282 | |||||||
chr5:41154334 | A | G | 74 | a0001c0001t0001g0016 a0001c0001t0001g0134 a0001c0001t0001g0278 others(71): Show |
94 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.2102-336T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154334 | |||||||
chr5:41154342 | A | G | 7 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2102-344T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154342 | |||||||
chr5:41154401 | TC | T | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2102-404delG | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154401 | |||||||
chr5:41154426 | T | C | 91 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(88): Show |
108 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.2102-428A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154426 | |||||||
chr5:41154648 | G | A | 2 | a0002c0002t0001g0027 a0002c0002t0001g0147 |
3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2101+324C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154648 | |||||||
chr5:41154925 | A | G | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2101+47T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 14/17 | chr5 | 41154925 | |||||||
chr5:41155147 | A | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-43T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155147 | |||||||
chr5:41155220 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1969-116G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155220 | |||||||
chr5:41155331 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-227G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155331 | |||||||
chr5:41155563 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-459G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155563 | |||||||
chr5:41155612 | C | G | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1969-508G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155612 | |||||||
chr5:41155641 | A | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-537T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155641 | |||||||
chr5:41155744 | A | C | 2 | a0002c0014t0009g0048 a0002c0014t0011g0085 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1969-640T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155744 | |||||||
chr5:41155772 | C | CA | 10 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(7): Show |
11 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1969-669dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155772 | |||||||
chr5:41155791 | A | C | 1 | a0001c0001t0002g0055 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1969-687T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155791 | |||||||
chr5:41155806 | A | G | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-702T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155806 | |||||||
chr5:41155810 | G | C | 1 | a0001c0003t0001g0122 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1969-706C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155810 | |||||||
chr5:41155875 | AATAAT | A | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-776_1969-772d others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155875 | |||||||
chr5:41155906 | T | C | 55 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(52): Show |
68 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1969-802A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41155906 | |||||||
chr5:41156063 | T | C | 1 | a0002c0002t0001g0320 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1969-959A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156063 | |||||||
chr5:41156111 | C | T | 2 | a0010c0010t0001g0263 a0010c0010t0006g0045 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1969-1007G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156111 | |||||||
chr5:41156129 | T | C | 1 | a0003c0004t0001g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1969-1025A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156129 | |||||||
chr5:41156173 | A | G | 12 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(9): Show |
12 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1969-1069T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156173 | |||||||
chr5:41156285 | T | A | 1 | a0002c0002t0001g0320 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1969-1181A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156285 | |||||||
chr5:41156457 | A | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0251 others(8): Show |
14 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.1969-1353T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156457 | |||||||
chr5:41156498 | C | T | 1 | a0002c0002t0001g0225 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1969-1394G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156498 | |||||||
chr5:41156569 | A | G | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1969-1465T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156569 | |||||||
chr5:41156611 | C | T | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1969-1507G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156611 | |||||||
chr5:41156688 | T | C | 1 | a0002c0002t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1969-1584A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156688 | |||||||
chr5:41156787 | C | A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1969-1683G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156787 | |||||||
chr5:41156821 | T | A | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-1717A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41156821 | |||||||
chr5:41157122 | T | G | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1968+1552A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157122 | |||||||
chr5:41157165 | G | A | 1 | a0002c0002t0001g0190 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1968+1509C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157165 | |||||||
chr5:41157238 | C | T | 82 | a0001c0001t0001g0016 a0001c0001t0001g0134 a0001c0001t0001g0278 others(79): Show |
104 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1968+1436G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157238 | |||||||
chr5:41157298 | G | C | 10 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(7): Show |
12 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1968+1376C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157298 | |||||||
chr5:41157398 | G | A | 1 | a0002c0002t0001g0181 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1968+1276C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157398 | |||||||
chr5:41157410 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1968+1264C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157410 | |||||||
chr5:41157412 | G | A | 1 | a0002c0002t0003g0097 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1968+1262C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157412 | |||||||
chr5:41157975 | G | C | 2 | a0002c0002t0003g0088 a0002c0002t0003g0109 |
2 | NA18988.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1968+699C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157975 | |||||||
chr5:41157983 | T | C | 1 | a0002c0002t0002g0236 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1968+691A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41157983 | |||||||
chr5:41158009 | A | G | 1 | a0002c0002t0001g0231 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1968+665T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158009 | |||||||
chr5:41158067 | G | C | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1968+607C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158067 | |||||||
chr5:41158069 | A | G | 9 | a0002c0014t0009g0048 a0002c0014t0011g0085 a0003c0004t0001g0011 others(6): Show |
11 | HG00609.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1968+605T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158069 | |||||||
chr5:41158076 | A | T | 5 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(2): Show |
5 | HG01346.hp1 HG02055.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968+598T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158076 | |||||||
chr5:41158165 | TA | T | 3 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0002c0002t0001g0320 |
4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1968+508delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158165 | |||||||
chr5:41158197 | T | TA | 12 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0251 others(9): Show |
15 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1968+476dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158197 | |||||||
chr5:41158197 | TA | T | 8 | a0001c0001t0001g0140 a0002c0002t0001g0035 a0002c0002t0001g0146 others(5): Show |
9 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1968+476delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158197 | |||||||
chr5:41158250 | G | C | 1 | a0011c0012t0004g0136 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1968+424C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158250 | |||||||
chr5:41158347 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0013g0257 |
2 | HG01243.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1968+327T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158347 | |||||||
chr5:41158387 | A | G | 76 | a0001c0001t0001g0016 a0001c0001t0001g0134 a0001c0001t0001g0278 others(73): Show |
96 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1968+287T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158387 | |||||||
chr5:41158404 | A | G | 1 | a0002c0002t0002g0220 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1968+270T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158404 | |||||||
chr5:41158465 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1968+209C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158465 | |||||||
chr5:41158470 | A | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(271): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1968+204T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158470 | |||||||
chr5:41158473 | T | A | 3 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0020c0025t0001g0152 |
5 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1968+201A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158473 | |||||||
chr5:41158515 | A | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1968+159T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158515 | |||||||
chr5:41158569 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(271): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1968+105A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158569 | |||||||
chr5:41158640 | A | C | 2 | a0002c0002t0001g0027 a0002c0002t0001g0147 |
3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1968+34T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158640 | |||||||
chr5:41158650 | A | G | 2 | a0002c0014t0009g0048 a0002c0014t0011g0085 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1968+24T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 13/17 | chr5 | 41158650 | |||||||
chr5:41158807 | G | A | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1857-22C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/17 | chr5 | 41158807 | |||||||
chr5:41158865 | A | G | 4 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(1): Show |
4 | HG00741.hp2 HG01256.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857-80T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/17 | chr5 | 41158865 | |||||||
chr5:41158884 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0068 |
3 | HG01256.hp1 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1857-99T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/17 | chr5 | 41158884 | |||||||
chr5:41159014 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0238 |
3 | HG02976.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1856+68T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 12/17 | chr5 | 41159014 | |||||||
chr5:41159407 | C | T | 74 | a0001c0001t0001g0016 a0001c0001t0001g0134 a0001c0001t0001g0278 others(71): Show |
94 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1685-154G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159407 | |||||||
chr5:41159427 | C | T | 4 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(1): Show |
4 | HG00741.hp2 HG01256.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685-174G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159427 | |||||||
chr5:41159551 | T | C | 75 | a0001c0001t0001g0016 a0001c0001t0001g0134 a0001c0001t0001g0278 others(72): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1685-298A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159551 | |||||||
chr5:41159573 | T | C | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1685-320A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159573 | |||||||
chr5:41159620 | G | T | 75 | a0001c0001t0001g0016 a0001c0001t0001g0134 a0001c0001t0001g0278 others(72): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1685-367C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159620 | |||||||
chr5:41159643 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1685-390G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159643 | |||||||
chr5:41159646 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1685-393C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159646 | |||||||
chr5:41159647 | C | A | 1 | a0001c0001t0001g0299 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1685-394G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159647 | |||||||
chr5:41159648 | C | CTAACTAT others(13): Show |
1 | a0001c0001t0001g0299 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1685-396_1685-395i others(22): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159648 | |||||||
chr5:41159868 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1684+274T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159868 | |||||||
chr5:41159963 | A | G | 75 | a0001c0001t0001g0016 a0001c0001t0001g0134 a0001c0001t0001g0278 others(72): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1684+179T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41159963 | |||||||
chr5:41160006 | G | A | 1 | a0001c0001t0007g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1684+136C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41160006 | |||||||
chr5:41160016 | C | T | 3 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0002c0002t0001g0320 |
4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1684+126G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 11/17 | chr5 | 41160016 | |||||||
chr5:41160463 | A | C | 1 | a0002c0002t0001g0148 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1459-96T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41160463 | |||||||
chr5:41160604 | G | A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1459-237C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41160604 | |||||||
chr5:41160714 | G | A | 9 | a0002c0014t0009g0048 a0002c0014t0011g0085 a0003c0004t0001g0011 others(6): Show |
11 | HG00609.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1459-347C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41160714 | |||||||
chr5:41160963 | G | T | 1 | a0002c0002t0010g0047 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1459-596C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41160963 | |||||||
chr5:41160970 | A | G | 9 | a0002c0014t0009g0048 a0002c0014t0011g0085 a0003c0004t0001g0011 others(6): Show |
11 | HG00609.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1459-603T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41160970 | |||||||
chr5:41161120 | C | T | 1 | a0002c0002t0001g0230 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1458+573G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161120 | |||||||
chr5:41161150 | A | G | 1 | a0001c0001t0004g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1458+543T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161150 | |||||||
chr5:41161178 | G | A | 1 | a0002c0014t0009g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1458+515C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161178 | |||||||
chr5:41161387 | A | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(58): Show |
80 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1458+306T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161387 | |||||||
chr5:41161419 | A | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(271): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1458+274T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161419 | |||||||
chr5:41161422 | G | A | 2 | a0001c0001t0007g0043 a0001c0001t0007g0044 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1458+271C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 10/17 | chr5 | 41161422 | |||||||
chr5:41162144 | G | T | 1 | a0001c0001t0001g0264 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1292-285C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162144 | |||||||
chr5:41162170 | C | T | 1 | a0002c0002t0001g0210 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1292-311G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162170 | |||||||
chr5:41162268 | T | A | 1 | a0003c0004t0001g0154 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1292-409A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162268 | |||||||
chr5:41162382 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1292-523G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162382 | |||||||
chr5:41162461 | G | A | 9 | a0002c0014t0009g0048 a0002c0014t0011g0085 a0003c0004t0001g0011 others(6): Show |
11 | HG00609.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-602C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162461 | |||||||
chr5:41162574 | TCTAA | T | 3 | a0005c0005t0006g0018 a0005c0005t0006g0046 a0014c0020t0001g0322 |
4 | HG02258.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-719_1292-716d others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162574 | |||||||
chr5:41162577 | A | G | 74 | a0001c0001t0001g0016 a0001c0001t0001g0134 a0001c0001t0001g0278 others(71): Show |
94 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1292-718T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162577 | |||||||
chr5:41162662 | G | C | 8 | a0001c0001t0001g0140 a0002c0002t0001g0035 a0002c0002t0001g0146 others(5): Show |
9 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-803C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162662 | |||||||
chr5:41162813 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1292-954G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162813 | |||||||
chr5:41162828 | G | A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-969C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41162828 | |||||||
chr5:41163163 | GA | G | 34 | a0001c0001t0001g0038 a0001c0001t0001g0133 a0001c0001t0001g0238 others(31): Show |
37 | HG00140.hp1 HG01123.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.1292-1305delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163163 | |||||||
chr5:41163163 | GAA | G | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-1306_1292-130 others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163163 | |||||||
chr5:41163219 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0275 a0001c0001t0001g0277 |
5 | NA18960.hp2 NA18973.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-1360T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163219 | |||||||
chr5:41163310 | C | CT | 8 | a0001c0001t0004g0117 a0001c0001t0007g0042 a0001c0001t0007g0043 others(5): Show |
10 | HG01071.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1292-1452dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163310 | |||||||
chr5:41163310 | C | CTTT | 17 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0251 others(14): Show |
20 | HG00323.hp1 HG00597.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1292-1454_1292-145 others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163310 | |||||||
chr5:41163310 | C | CTTTT | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(53): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.1292-1455_1292-145 others(8): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163310 | |||||||
chr5:41163310 | CT | C | 18 | a0001c0001t0002g0076 a0001c0001t0004g0025 a0001c0001t0004g0137 others(15): Show |
20 | HG01192.hp2 HG01257.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1292-1452delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163310 | |||||||
chr5:41163310 | CTTT | C | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-1454_1292-145 others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163310 | |||||||
chr5:41163340 | T | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-1481A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163340 | |||||||
chr5:41163356 | A | C | 1 | a0002c0002t0002g0237 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1292-1497T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163356 | |||||||
chr5:41163395 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1292-1536G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163395 | |||||||
chr5:41163459 | T | A | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-1600A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163459 | |||||||
chr5:41163463 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(271): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1292-1604A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163463 | |||||||
chr5:41163473 | T | C | 31 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(28): Show |
34 | HG00140.hp1 HG00609.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.1292-1614A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163473 | |||||||
chr5:41163649 | G | A | 2 | a0010c0010t0001g0263 a0010c0010t0006g0045 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1292-1790C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163649 | |||||||
chr5:41163773 | T | C | 1 | a0003c0004t0001g0153 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1292-1914A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163773 | |||||||
chr5:41163994 | T | C | 1 | a0001c0003t0001g0122 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1292-2135A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41163994 | |||||||
chr5:41164021 | C | T | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-2162G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164021 | |||||||
chr5:41164025 | A | G | 15 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(12): Show |
18 | HG00609.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1292-2166T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164025 | |||||||
chr5:41164114 | A | G | 1 | a0002c0002t0001g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1292-2255T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164114 | |||||||
chr5:41164144 | A | G | 2 | a0010c0010t0001g0263 a0010c0010t0006g0045 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1292-2285T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164144 | |||||||
chr5:41164165 | TA | T | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-2307delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164165 | |||||||
chr5:41164168 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1292-2309T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164168 | |||||||
chr5:41164176 | A | G | 3 | a0001c0001t0001g0134 a0002c0002t0003g0023 a0002c0002t0003g0090 |
4 | HG02109.hp1 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-2317T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164176 | |||||||
chr5:41164179 | A | C | 62 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(59): Show |
76 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1292-2320T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164179 | |||||||
chr5:41164193 | T | G | 15 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(12): Show |
18 | HG00609.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1292-2334A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164193 | |||||||
chr5:41164232 | G | A | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1292-2373C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164232 | |||||||
chr5:41164282 | G | T | 2 | a0010c0010t0001g0263 a0010c0010t0006g0045 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1292-2423C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164282 | |||||||
chr5:41164294 | G | A | 1 | a0002c0002t0002g0033 | 2 | HG01516.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1292-2435C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164294 | |||||||
chr5:41164413 | C | T | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-2554G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164413 | |||||||
chr5:41164423 | T | C | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-2564A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164423 | |||||||
chr5:41164547 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0068 |
3 | HG01256.hp1 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1292-2688C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164547 | |||||||
chr5:41164692 | A | C | 1 | a0002c0002t0001g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1292-2833T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164692 | |||||||
chr5:41164721 | G | C | 2 | a0002c0014t0009g0048 a0002c0014t0011g0085 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1292-2862C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164721 | |||||||
chr5:41164839 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1292-2980A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41164839 | |||||||
chr5:41165082 | T | A | 19 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(16): Show |
20 | HG00140.hp1 HG01123.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1292-3223A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165082 | |||||||
chr5:41165172 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1292-3313T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165172 | |||||||
chr5:41165222 | AT | A | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-3364delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165222 | |||||||
chr5:41165228 | G | A | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-3369C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165228 | |||||||
chr5:41165282 | G | A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-3423C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165282 | |||||||
chr5:41165287 | T | C | 8 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(5): Show |
9 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1292-3428A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165287 | |||||||
chr5:41165319 | T | G | 1 | a0002c0002t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1292-3460A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165319 | |||||||
chr5:41165324 | G | A | 1 | a0001c0001t0002g0020 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1292-3465C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165324 | |||||||
chr5:41165402 | A | G | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1292-3543T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165402 | |||||||
chr5:41165642 | C | T | 46 | a0001c0001t0001g0016 a0001c0001t0001g0278 a0002c0002t0001g0006 others(43): Show |
58 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1292-3783G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165642 | |||||||
chr5:41165652 | A | G | 1 | a0001c0003t0001g0119 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1292-3793T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165652 | |||||||
chr5:41165669 | G | A | 2 | a0010c0010t0001g0263 a0010c0010t0006g0045 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1292-3810C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165669 | |||||||
chr5:41165832 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1292-3973G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165832 | |||||||
chr5:41165884 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1292-4025A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41165884 | |||||||
chr5:41166067 | A | T | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-4208T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166067 | |||||||
chr5:41166075 | A | G | 2 | a0002c0002t0001g0031 a0002c0002t0001g0170 |
3 | HG02293.hp2 NA18948.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1292-4216T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166075 | |||||||
chr5:41166080 | G | A | 5 | a0005c0005t0006g0018 a0005c0005t0006g0046 a0009c0009t0001g0083 others(2): Show |
6 | HG02257.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-4221C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166080 | |||||||
chr5:41166153 | G | T | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-4294C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166153 | |||||||
chr5:41166255 | A | C | 4 | a0002c0002t0001g0185 a0002c0002t0008g0316 a0002c0002t0008g0317 others(1): Show |
4 | HG02004.hp1 HG02273.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-4396T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166255 | |||||||
chr5:41166377 | C | CT | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG01167.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1292-4519dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166377 | |||||||
chr5:41166382 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1292-4523A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166382 | |||||||
chr5:41166571 | A | AT | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-4713dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166571 | |||||||
chr5:41166591 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(236): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.1292-4732A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166591 | |||||||
chr5:41166598 | C | T | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1292-4739G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166598 | |||||||
chr5:41166672 | TG | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0251 others(10): Show |
16 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1292-4814delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166672 | |||||||
chr5:41166751 | C | A | 2 | a0002c0014t0009g0048 a0002c0014t0011g0085 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1292-4892G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166751 | |||||||
chr5:41166798 | ATTTCAAT others(9): Show |
A | 4 | a0001c0001t0001g0135 a0004c0008t0001g0150 a0004c0008t0001g0151 others(1): Show |
4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-4955_1292-494 others(20): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166798 | |||||||
chr5:41166923 | C | T | 1 | a0002c0002t0002g0228 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1292-5064G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166923 | |||||||
chr5:41166954 | A | G | 9 | a0002c0002t0001g0005 a0002c0002t0001g0029 a0002c0002t0001g0159 others(6): Show |
14 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1292-5095T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166954 | |||||||
chr5:41166988 | C | A | 1 | a0015c0030t0002g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1292-5129G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41166988 | |||||||
chr5:41167100 | G | A | 1 | a0001c0001t0012g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1291+5125C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167100 | |||||||
chr5:41167143 | G | A | 1 | a0017c0026t0001g0183 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1291+5082C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167143 | |||||||
chr5:41167143 | G | C | 2 | a0003c0004t0001g0156 a0003c0004t0001g0157 |
2 | NA18969.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1291+5082C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167143 | |||||||
chr5:41167157 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0251 others(8): Show |
14 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.1291+5068T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167157 | |||||||
chr5:41167274 | G | T | 5 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(2): Show |
5 | HG01346.hp1 HG02055.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+4951C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167274 | |||||||
chr5:41167302 | A | G | 5 | a0001c0001t0002g0026 a0001c0001t0002g0142 a0001c0006t0002g0141 others(2): Show |
6 | HG01074.hp1 HG01081.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+4923T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167302 | |||||||
chr5:41167364 | A | T | 1 | a0001c0001t0002g0056 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1291+4861T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167364 | |||||||
chr5:41167450 | C | T | 1 | a0015c0030t0002g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1291+4775G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167450 | |||||||
chr5:41167472 | C | T | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+4753G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167472 | |||||||
chr5:41167476 | A | T | 1 | a0001c0001t0007g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1291+4749T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41167476 | |||||||
chr5:41168124 | G | C | 1 | a0001c0001t0002g0058 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1291+4101C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168124 | |||||||
chr5:41168210 | G | T | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+4015C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168210 | |||||||
chr5:41168389 | G | T | 90 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(87): Show |
106 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1291+3836C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168389 | |||||||
chr5:41168499 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1291+3726G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168499 | |||||||
chr5:41168655 | A | G | 10 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(7): Show |
12 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1291+3570T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168655 | |||||||
chr5:41168673 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1291+3552A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168673 | |||||||
chr5:41168710 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1291+3515G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168710 | |||||||
chr5:41168820 | C | T | 2 | a0002c0002t0001g0031 a0002c0002t0001g0170 |
3 | HG02293.hp2 NA18948.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1291+3405G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41168820 | |||||||
chr5:41169002 | C | T | 47 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(44): Show |
58 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1291+3223G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169002 | |||||||
chr5:41169065 | G | A | 1 | a0002c0002t0003g0100 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1291+3160C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169065 | |||||||
chr5:41169121 | C | T | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1291+3104G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169121 | |||||||
chr5:41169183 | G | A | 1 | a0001c0001t0002g0026 | 2 | HG03927.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1291+3042C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169183 | |||||||
chr5:41169220 | G | A | 2 | a0001c0003t0001g0123 a0001c0003t0001g0124 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1291+3005C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169220 | |||||||
chr5:41169300 | T | C | 16 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(13): Show |
19 | HG00609.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1291+2925A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169300 | |||||||
chr5:41169317 | G | A | 2 | a0001c0001t0002g0247 a0001c0001t0002g0248 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1291+2908C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169317 | |||||||
chr5:41169328 | C | T | 3 | a0002c0002t0010g0047 a0002c0014t0009g0048 a0002c0014t0011g0085 |
3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+2897G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169328 | |||||||
chr5:41169427 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(57): Show |
79 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.1291+2798G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169427 | |||||||
chr5:41169433 | C | T | 1 | a0009c0009t0001g0130 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1291+2792G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169433 | |||||||
chr5:41169466 | T | A | 1 | a0002c0002t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1291+2759A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169466 | |||||||
chr5:41169486 | T | C | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1291+2739A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169486 | |||||||
chr5:41169756 | C | T | 3 | a0002c0002t0001g0005 a0002c0002t0001g0159 a0002c0002t0001g0167 |
7 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1291+2469G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169756 | |||||||
chr5:41169757 | G | A | 1 | a0002c0002t0003g0008 | 3 | HG01109.hp2 HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1291+2468C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169757 | |||||||
chr5:41169785 | A | G | 1 | a0002c0002t0001g0185 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1291+2440T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169785 | |||||||
chr5:41169951 | C | T | 2 | a0002c0014t0009g0048 a0002c0014t0011g0085 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1291+2274G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169951 | |||||||
chr5:41169985 | GT | G | 9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1291+2239delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41169985 | |||||||
chr5:41170025 | T | G | 1 | a0008c0017t0004g0028 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1291+2200A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170025 | |||||||
chr5:41170060 | G | A | 1 | a0002c0002t0003g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1291+2165C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170060 | |||||||
chr5:41170113 | A | G | 59 | a0001c0001t0001g0134 a0001c0001t0004g0025 a0001c0001t0004g0084 others(56): Show |
69 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1291+2112T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170113 | |||||||
chr5:41170121 | T | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+2104A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170121 | |||||||
chr5:41170166 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1291+2059G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170166 | |||||||
chr5:41170205 | C | T | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+2020G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170205 | |||||||
chr5:41170249 | A | T | 1 | a0003c0004t0001g0154 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1291+1976T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170249 | |||||||
chr5:41170261 | C | T | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+1964G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170261 | |||||||
chr5:41170508 | C | T | 47 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(44): Show |
58 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1291+1717G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170508 | |||||||
chr5:41170645 | A | T | 3 | a0002c0002t0010g0047 a0002c0014t0009g0048 a0002c0014t0011g0085 |
3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+1580T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170645 | |||||||
chr5:41170709 | A | G | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+1516T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170709 | |||||||
chr5:41170977 | A | C | 1 | a0002c0002t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1291+1248T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41170977 | |||||||
chr5:41171323 | A | G | 1 | a0006c0007t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1291+902T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171323 | |||||||
chr5:41171386 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1291+839G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171386 | |||||||
chr5:41171400 | C | A | 1 | a0002c0002t0002g0237 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1291+825G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171400 | |||||||
chr5:41171410 | G | T | 2 | a0002c0002t0001g0027 a0002c0002t0001g0147 |
3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1291+815C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171410 | |||||||
chr5:41171450 | T | C | 3 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0002c0002t0001g0320 |
4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291+775A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171450 | |||||||
chr5:41171464 | C | T | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+761G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171464 | |||||||
chr5:41171492 | T | C | 1 | a0002c0002t0001g0187 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1291+733A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171492 | |||||||
chr5:41171512 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+713C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171512 | |||||||
chr5:41171735 | T | C | 1 | a0002c0002t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1291+490A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171735 | |||||||
chr5:41171772 | A | G | 1 | a0001c0003t0001g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1291+453T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171772 | |||||||
chr5:41171787 | C | T | 1 | a0002c0002t0002g0198 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1291+438G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171787 | |||||||
chr5:41171852 | A | G | 1 | a0002c0002t0002g0204 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1291+373T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171852 | |||||||
chr5:41171971 | T | A | 3 | a0002c0002t0010g0047 a0002c0014t0009g0048 a0002c0014t0011g0085 |
3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291+254A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 9/17 | chr5 | 41171971 | |||||||
chr5:41172351 | G | A | 2 | a0002c0002t0001g0189 a0002c0002t0001g0190 |
2 | HG00597.hp1 HG02040.hp1 |
splice_region_variant&intron_variant | LOW | c.1169-4C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172351 | |||||||
chr5:41172416 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1169-69G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172416 | |||||||
chr5:41172531 | C | A | 1 | a0009c0009t0001g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1169-184G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172531 | |||||||
chr5:41172563 | T | G | 3 | a0002c0002t0010g0047 a0002c0014t0009g0048 a0002c0014t0011g0085 |
3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1169-216A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172563 | |||||||
chr5:41172698 | C | T | 1 | a0008c0017t0004g0028 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1169-351G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172698 | |||||||
chr5:41172868 | G | T | 1 | a0009c0009t0001g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1169-521C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172868 | |||||||
chr5:41172889 | A | G | 1 | a0001c0001t0004g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1169-542T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172889 | |||||||
chr5:41172900 | T | C | 1 | a0005c0005t0006g0018 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1169-553A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41172900 | |||||||
chr5:41173071 | T | G | 3 | a0002c0002t0010g0047 a0002c0014t0009g0048 a0002c0014t0011g0085 |
3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1169-724A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173071 | |||||||
chr5:41173151 | T | C | 1 | a0002c0002t0002g0229 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1169-804A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173151 | |||||||
chr5:41173188 | T | C | 3 | a0002c0002t0010g0047 a0002c0014t0009g0048 a0002c0014t0011g0085 |
3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1169-841A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173188 | |||||||
chr5:41173192 | C | T | 1 | a0008c0017t0004g0028 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1169-845G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173192 | |||||||
chr5:41173203 | C | T | 7 | a0002c0002t0001g0029 a0002c0002t0001g0160 a0002c0002t0001g0161 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1169-856G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173203 | |||||||
chr5:41173263 | T | C | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1169-916A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173263 | |||||||
chr5:41173509 | A | G | 1 | a0001c0001t0002g0022 | 2 | HG01515.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1169-1162T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173509 | |||||||
chr5:41173585 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1169-1238A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173585 | |||||||
chr5:41173728 | C | T | 1 | a0001c0001t0002g0022 | 2 | HG01515.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1169-1381G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173728 | |||||||
chr5:41173729 | G | A | 1 | a0002c0002t0002g0202 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1169-1382C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173729 | |||||||
chr5:41173740 | AG | A | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1169-1394delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173740 | |||||||
chr5:41173785 | A | G | 3 | a0002c0002t0010g0047 a0002c0014t0009g0048 a0002c0014t0011g0085 |
3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1169-1438T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41173785 | |||||||
chr5:41174055 | G | A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1169-1708C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174055 | |||||||
chr5:41174176 | T | C | 4 | a0002c0002t0003g0024 a0002c0002t0003g0096 a0002c0002t0003g0102 others(1): Show |
5 | NA18939.hp1 NA18986.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1169-1829A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174176 | |||||||
chr5:41174258 | G | T | 1 | a0001c0001t0007g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1169-1911C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174258 | |||||||
chr5:41174323 | C | G | 22 | a0001c0001t0004g0025 a0001c0001t0004g0082 a0001c0001t0004g0084 others(19): Show |
23 | HG00140.hp1 HG01123.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1169-1976G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174323 | |||||||
chr5:41174388 | G | A | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1169-2041C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174388 | |||||||
chr5:41174420 | C | T | 1 | a0002c0002t0002g0219 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1168+2055G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174420 | |||||||
chr5:41174465 | G | A | 1 | a0001c0001t0007g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1168+2010C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174465 | |||||||
chr5:41174570 | T | G | 3 | a0002c0002t0010g0047 a0002c0014t0009g0048 a0002c0014t0011g0085 |
3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1168+1905A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174570 | |||||||
chr5:41174636 | G | A | 1 | a0002c0002t0002g0228 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1168+1839C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174636 | |||||||
chr5:41174834 | T | C | 1 | a0001c0003t0001g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1168+1641A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174834 | |||||||
chr5:41174985 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1168+1490T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174985 | |||||||
chr5:41174995 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1168+1480G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41174995 | |||||||
chr5:41175137 | C | T | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168+1338G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175137 | |||||||
chr5:41175156 | G | A | 1 | a0002c0002t0001g0170 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1168+1319C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175156 | |||||||
chr5:41175171 | T | C | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168+1304A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175171 | |||||||
chr5:41175223 | C | A | 2 | a0002c0002t0002g0207 a0002c0002t0002g0208 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1168+1252G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175223 | |||||||
chr5:41175257 | T | C | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168+1218A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175257 | |||||||
chr5:41175322 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(274): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1168+1153C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175322 | |||||||
chr5:41175361 | T | TATGTATG others(10): Show |
1 | a0001c0001t0001g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1168+1097_1168+111 others(21): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175361 | |||||||
chr5:41175377 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1168+1098C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175377 | |||||||
chr5:41175383 | A | G | 1 | a0002c0002t0003g0107 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1168+1092T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175383 | |||||||
chr5:41175454 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168+1021G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175454 | |||||||
chr5:41175517 | G | A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168+958C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175517 | |||||||
chr5:41175978 | T | G | 1 | a0001c0001t0002g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1168+497A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175978 | |||||||
chr5:41175998 | T | C | 2 | a0002c0002t0003g0092 a0002c0002t0003g0094 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1168+477A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41175998 | |||||||
chr5:41176088 | T | C | 2 | a0002c0002t0001g0232 a0002c0002t0001g0233 |
2 | HG00408.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1168+387A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41176088 | |||||||
chr5:41176218 | T | TAGGAAAT others(1215): Show |
1 | a0001c0001t0001g0309 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1168+256_1168+257i others(1224): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41176218 | |||||||
chr5:41176233 | C | A | 2 | a0002c0002t0001g0027 a0002c0002t0001g0147 |
3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1168+242G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41176233 | |||||||
chr5:41176247 | A | C | 1 | a0001c0001t0001g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1168+228T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 8/17 | chr5 | 41176247 | |||||||
chr5:41176914 | AG | A | 45 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(42): Show |
56 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.928-200delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41176914 | |||||||
chr5:41177158 | T | C | 2 | a0006c0007t0003g0104 a0006c0007t0003g0106 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.928-443A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177158 | |||||||
chr5:41177197 | T | C | 1 | a0003c0004t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.928-482A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177197 | |||||||
chr5:41177215 | G | T | 1 | a0001c0001t0001g0250 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.928-500C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177215 | |||||||
chr5:41177323 | C | A | 1 | a0002c0002t0001g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.928-608G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177323 | |||||||
chr5:41177595 | ATAACTGT others(7): Show |
A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-894_928-881del others(14): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177595 | |||||||
chr5:41177925 | A | G | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-1210T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177925 | |||||||
chr5:41177959 | A | G | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.928-1244T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41177959 | |||||||
chr5:41178267 | A | G | 1 | a0002c0002t0003g0096 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.928-1552T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178267 | |||||||
chr5:41178300 | C | A | 1 | a0002c0002t0005g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928-1585G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178300 | |||||||
chr5:41178301 | T | A | 1 | a0002c0002t0005g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928-1586A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178301 | |||||||
chr5:41178302 | G | A | 1 | a0002c0002t0005g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928-1587C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178302 | |||||||
chr5:41178339 | C | T | 1 | a0002c0002t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.928-1624G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178339 | |||||||
chr5:41178433 | T | G | 1 | a0001c0022t0001g0290 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.928-1718A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178433 | |||||||
chr5:41178442 | ATTTTC | A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-1732_928-1728d others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178442 | |||||||
chr5:41178466 | C | CT | 15 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(12): Show |
16 | HG01346.hp1 HG01361.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.928-1752dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178466 | |||||||
chr5:41178466 | CT | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(149): Show |
191 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.928-1752delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178466 | |||||||
chr5:41178472 | T | C | 1 | a0008c0017t0004g0028 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.928-1757A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178472 | |||||||
chr5:41178495 | G | A | 39 | a0001c0001t0001g0134 a0002c0002t0001g0196 a0002c0002t0003g0008 others(36): Show |
48 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.928-1780C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178495 | |||||||
chr5:41178497 | G | A | 39 | a0001c0001t0001g0134 a0002c0002t0001g0196 a0002c0002t0003g0008 others(36): Show |
48 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.928-1782C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178497 | |||||||
chr5:41178497 | GACAGA | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(221): Show |
281 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.928-1787_928-1783d others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178497 | |||||||
chr5:41178503 | G | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(221): Show |
281 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.928-1788C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178503 | |||||||
chr5:41178549 | C | T | 2 | a0001c0001t0001g0294 a0001c0001t0001g0304 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.928-1834G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178549 | |||||||
chr5:41178578 | T | C | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-1863A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178578 | |||||||
chr5:41178596 | C | T | 1 | a0002c0002t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.928-1881G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178596 | |||||||
chr5:41178632 | C | T | 1 | a0002c0002t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-1917G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178632 | |||||||
chr5:41178766 | G | A | 1 | a0002c0002t0001g0320 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.928-2051C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178766 | |||||||
chr5:41178767 | C | T | 43 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0002c0002t0001g0196 others(40): Show |
52 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.928-2052G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178767 | |||||||
chr5:41178768 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.928-2053C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178768 | |||||||
chr5:41178917 | G | A | 7 | a0001c0001t0001g0140 a0002c0002t0001g0035 a0002c0002t0001g0146 others(4): Show |
8 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-2202C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178917 | |||||||
chr5:41178923 | C | T | 14 | a0001c0001t0001g0286 a0002c0002t0001g0005 a0002c0002t0001g0029 others(11): Show |
19 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.928-2208G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178923 | |||||||
chr5:41178998 | C | T | 2 | a0001c0001t0007g0043 a0001c0001t0007g0044 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.928-2283G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41178998 | |||||||
chr5:41179015 | G | A | 1 | a0002c0002t0003g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.928-2300C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179015 | |||||||
chr5:41179054 | G | A | 2 | a0002c0002t0001g0201 a0002c0002t0002g0033 |
3 | HG01516.hp1 HG01952.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.927+2305C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179054 | |||||||
chr5:41179117 | G | A | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.927+2242C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179117 | |||||||
chr5:41179300 | T | G | 4 | a0001c0001t0001g0135 a0004c0008t0001g0150 a0004c0008t0001g0151 others(1): Show |
4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+2059A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179300 | |||||||
chr5:41179418 | A | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0254 a0001c0001t0001g0296 others(4): Show |
9 | HG01081.hp2 HG01257.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.927+1941T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179418 | |||||||
chr5:41179447 | C | T | 1 | a0017c0026t0001g0183 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.927+1912G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179447 | |||||||
chr5:41179537 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.927+1822C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179537 | |||||||
chr5:41179583 | C | T | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+1776G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179583 | |||||||
chr5:41179735 | T | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+1624A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179735 | |||||||
chr5:41179760 | T | C | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+1599A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179760 | |||||||
chr5:41179823 | TAAAG | T | 3 | a0002c0002t0010g0047 a0002c0014t0009g0048 a0002c0014t0011g0085 |
3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.927+1532_927+1535d others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179823 | |||||||
chr5:41179960 | G | A | 3 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 |
3 | HG01891.hp2 HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.927+1399C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41179960 | |||||||
chr5:41180015 | G | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(275): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.927+1344C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180015 | |||||||
chr5:41180085 | G | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(275): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.927+1274C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180085 | |||||||
chr5:41180149 | A | G | 1 | a0002c0002t0001g0170 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.927+1210T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180149 | |||||||
chr5:41180269 | T | C | 72 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(69): Show |
85 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.927+1090A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180269 | |||||||
chr5:41180307 | C | T | 55 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(52): Show |
67 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.927+1052G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180307 | |||||||
chr5:41180407 | T | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(61): Show |
86 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.927+952A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180407 | |||||||
chr5:41180490 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.927+869C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180490 | |||||||
chr5:41180498 | T | TGAAGAAT others(11): Show |
6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+860_927+861ins others(18): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180498 | |||||||
chr5:41180595 | A | G | 1 | a0002c0002t0001g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.927+764T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180595 | |||||||
chr5:41180699 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.927+660G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180699 | |||||||
chr5:41180832 | T | TA | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(77): Show |
105 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.927+526dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180832 | |||||||
chr5:41180832 | TA | T | 12 | a0001c0001t0001g0133 a0001c0001t0004g0082 a0001c0001t0004g0117 others(9): Show |
12 | HG01167.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.927+526delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41180832 | |||||||
chr5:41181049 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.927+310G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41181049 | |||||||
chr5:41181078 | G | A | 9 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(6): Show |
10 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.927+281C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41181078 | |||||||
chr5:41181080 | A | G | 1 | a0002c0002t0001g0221 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.927+279T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41181080 | |||||||
chr5:41181236 | C | T | 4 | a0001c0001t0001g0135 a0004c0008t0001g0150 a0004c0008t0001g0151 others(1): Show |
4 | HG01361.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+123G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 7/17 | chr5 | 41181236 | |||||||
chr5:41181610 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.727-51C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181610 | |||||||
chr5:41181657 | A | G | 1 | a0002c0002t0002g0202 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.727-98T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181657 | |||||||
chr5:41181797 | C | T | 1 | a0002c0002t0003g0107 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.727-238G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181797 | |||||||
chr5:41181877 | G | T | 1 | a0002c0002t0002g0199 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.727-318C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181877 | |||||||
chr5:41181915 | G | A | 1 | a0002c0002t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.727-356C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181915 | |||||||
chr5:41181940 | C | A | 1 | a0002c0014t0009g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.727-381G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41181940 | |||||||
chr5:41182031 | C | T | 1 | a0001c0001t0007g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.727-472G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182031 | |||||||
chr5:41182241 | G | A | 3 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0002c0002t0001g0320 |
4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-682C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182241 | |||||||
chr5:41182262 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(79): Show |
107 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.727-703G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182262 | |||||||
chr5:41182266 | T | C | 1 | a0001c0003t0001g0122 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.727-707A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182266 | |||||||
chr5:41182302 | G | T | 1 | a0002c0002t0001g0191 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.727-743C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182302 | |||||||
chr5:41182318 | G | A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-759C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182318 | |||||||
chr5:41182344 | G | C | 1 | a0001c0001t0002g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.727-785C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182344 | |||||||
chr5:41182546 | T | C | 2 | a0001c0001t0001g0293 a0001c0001t0001g0315 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.727-987A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182546 | |||||||
chr5:41182630 | T | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0018c0019t0002g0059 |
3 | HG00140.hp2 HG01074.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.727-1071A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182630 | |||||||
chr5:41182849 | CAG | C | 3 | a0002c0002t0010g0047 a0002c0014t0009g0048 a0002c0014t0011g0085 |
3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.727-1292_727-1291d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182849 | |||||||
chr5:41182942 | T | G | 1 | a0002c0002t0003g0088 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.727-1383A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182942 | |||||||
chr5:41182963 | T | C | 1 | a0002c0002t0001g0192 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.727-1404A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182963 | |||||||
chr5:41182995 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0068 |
3 | HG01256.hp1 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.727-1436G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41182995 | |||||||
chr5:41183066 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG02083.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.727-1507G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183066 | |||||||
chr5:41183156 | T | C | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-1597A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183156 | |||||||
chr5:41183394 | A | G | 1 | a0019c0018t0001g0285 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.727-1835T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183394 | |||||||
chr5:41183517 | A | C | 8 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(5): Show |
8 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.727-1958T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183517 | |||||||
chr5:41183539 | A | G | 4 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 others(1): Show |
4 | HG02015.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-1980T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183539 | |||||||
chr5:41183661 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.727-2102G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183661 | |||||||
chr5:41183677 | A | G | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-2118T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183677 | |||||||
chr5:41183976 | TA | T | 12 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(9): Show |
14 | HG00609.hp2 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.726+2093delT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183976 | |||||||
chr5:41183977 | AG | A | 14 | a0002c0002t0001g0005 a0002c0002t0001g0029 a0002c0002t0001g0158 others(11): Show |
19 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.726+2092delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183977 | |||||||
chr5:41183978 | G | C | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+2092C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183978 | |||||||
chr5:41183979 | G | A | 6 | a0001c0001t0004g0025 a0001c0001t0004g0084 a0001c0001t0004g0137 others(3): Show |
7 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.726+2091C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41183979 | |||||||
chr5:41184140 | G | GA | 63 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0238 others(60): Show |
76 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.726+1929dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184140 | |||||||
chr5:41184274 | T | G | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+1796A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184274 | |||||||
chr5:41184296 | T | A | 1 | a0002c0002t0003g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.726+1774A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184296 | |||||||
chr5:41184342 | T | C | 46 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(43): Show |
57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.726+1728A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184342 | |||||||
chr5:41184376 | G | T | 2 | a0002c0002t0002g0219 a0002c0002t0002g0220 |
2 | HG02040.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.726+1694C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184376 | |||||||
chr5:41184462 | ATTTTCTT others(3): Show |
A | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.726+1598_726+1607d others(12): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184462 | |||||||
chr5:41184482 | C | CT | 70 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0238 others(67): Show |
83 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.726+1587dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184482 | |||||||
chr5:41184533 | G | A | 4 | a0002c0002t0003g0008 a0002c0002t0003g0023 a0002c0002t0003g0089 others(1): Show |
7 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.726+1537C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184533 | |||||||
chr5:41184537 | T | C | 1 | a0002c0002t0002g0203 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.726+1533A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184537 | |||||||
chr5:41184726 | G | A | 68 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0238 others(65): Show |
82 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.726+1344C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184726 | |||||||
chr5:41184752 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.726+1318T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184752 | |||||||
chr5:41184953 | T | A | 2 | a0001c0001t0002g0247 a0001c0001t0002g0248 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.726+1117A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41184953 | |||||||
chr5:41185049 | G | T | 1 | a0002c0002t0003g0110 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.726+1021C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185049 | |||||||
chr5:41185070 | C | A | 85 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(82): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.726+1000G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185070 | |||||||
chr5:41185143 | A | G | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.726+927T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185143 | |||||||
chr5:41185195 | G | A | 6 | a0002c0002t0001g0035 a0002c0002t0001g0146 a0002c0002t0001g0197 others(3): Show |
7 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.726+875C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185195 | |||||||
chr5:41185259 | T | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(262): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.726+811A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185259 | |||||||
chr5:41185274 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.726+796G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185274 | |||||||
chr5:41185406 | A | G | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.726+664T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185406 | |||||||
chr5:41185416 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.726+654C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185416 | |||||||
chr5:41185418 | C | T | 1 | a0002c0002t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.726+652G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185418 | |||||||
chr5:41185505 | G | A | 8 | a0001c0001t0002g0026 a0001c0001t0012g0129 a0001c0006t0002g0141 others(5): Show |
9 | HG01074.hp1 HG01081.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.726+565C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185505 | |||||||
chr5:41185544 | C | T | 38 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(35): Show |
48 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.726+526G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185544 | |||||||
chr5:41185575 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0261 |
3 | HG02602.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.726+495A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185575 | |||||||
chr5:41185629 | G | C | 1 | a0002c0002t0001g0233 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.726+441C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185629 | |||||||
chr5:41185697 | C | G | 7 | a0002c0002t0003g0009 a0002c0002t0003g0010 a0002c0002t0003g0112 others(4): Show |
11 | HG01496.hp2 HG02004.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.726+373G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185697 | |||||||
chr5:41185744 | G | A | 3 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0002c0002t0001g0320 |
4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+326C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185744 | |||||||
chr5:41185767 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.726+303T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185767 | |||||||
chr5:41185792 | C | T | 1 | a0007c0016t0003g0095 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.726+278G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185792 | |||||||
chr5:41185796 | G | T | 1 | a0002c0002t0001g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.726+274C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185796 | |||||||
chr5:41185810 | A | C | 39 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(36): Show |
47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.726+260T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185810 | |||||||
chr5:41185818 | C | A | 2 | a0002c0002t0001g0027 a0002c0002t0001g0147 |
3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.726+252G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 6/17 | chr5 | 41185818 | |||||||
chr5:41186270 | A | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.588-62T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186270 | |||||||
chr5:41186347 | C | CT | 84 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(81): Show |
97 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.588-140dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186347 | |||||||
chr5:41186412 | G | T | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-204C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186412 | |||||||
chr5:41186470 | A | G | 1 | a0006c0007t0003g0105 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.588-262T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186470 | |||||||
chr5:41186664 | A | G | 85 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(82): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.588-456T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186664 | |||||||
chr5:41186692 | T | C | 85 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(82): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.588-484A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186692 | |||||||
chr5:41186772 | A | G | 85 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(82): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.588-564T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186772 | |||||||
chr5:41186907 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.588-699A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186907 | |||||||
chr5:41186918 | T | TA | 9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.588-711dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186918 | |||||||
chr5:41186940 | T | C | 2 | a0001c0001t0002g0247 a0001c0001t0002g0248 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.588-732A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186940 | |||||||
chr5:41186942 | A | T | 1 | a0018c0019t0002g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.588-734T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41186942 | |||||||
chr5:41187002 | T | C | 2 | a0002c0002t0001g0172 a0002c0002t0001g0173 |
2 | NA18961.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.588-794A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187002 | |||||||
chr5:41187094 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.588-886G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187094 | |||||||
chr5:41187137 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.588-929T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187137 | |||||||
chr5:41187155 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.588-947T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187155 | |||||||
chr5:41187234 | T | C | 1 | a0002c0002t0003g0110 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.588-1026A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187234 | |||||||
chr5:41187392 | G | A | 1 | a0002c0002t0001g0201 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.588-1184C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187392 | |||||||
chr5:41187466 | A | G | 1 | a0002c0002t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.588-1258T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187466 | |||||||
chr5:41187526 | C | T | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.588-1318G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187526 | |||||||
chr5:41187547 | G | C | 1 | a0002c0002t0003g0101 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.588-1339C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187547 | |||||||
chr5:41187560 | T | G | 2 | a0002c0002t0001g0027 a0002c0002t0001g0147 |
3 | HG01192.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.588-1352A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187560 | |||||||
chr5:41187581 | T | A | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.588-1373A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187581 | |||||||
chr5:41187699 | T | TAC | 16 | a0001c0001t0001g0140 a0001c0001t0001g0269 a0001c0001t0001g0297 others(13): Show |
18 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-1493_588-1492d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | |||||||
chr5:41187699 | T | TACAC | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(74): Show |
100 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.588-1495_588-1492d others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | |||||||
chr5:41187699 | T | TACACAC | 64 | a0001c0001t0001g0321 a0002c0002t0001g0005 a0002c0002t0001g0006 others(61): Show |
81 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.588-1497_588-1492d others(8): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | |||||||
chr5:41187699 | T | TACACACA others(1): Show |
18 | a0002c0002t0001g0158 a0002c0002t0001g0159 a0002c0002t0001g0166 others(15): Show |
22 | HG01496.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.588-1499_588-1492d others(10): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | |||||||
chr5:41187699 | TAC | T | 5 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0003c0004t0001g0011 others(2): Show |
8 | HG00609.hp2 HG01192.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.588-1493_588-1492d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | |||||||
chr5:41187699 | TACACAC | T | 6 | a0002c0002t0001g0035 a0002c0002t0001g0146 a0002c0002t0001g0197 others(3): Show |
7 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-1497_588-1492d others(8): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187699 | |||||||
chr5:41187708 | AC | A | 84 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(81): Show |
97 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.588-1501delG | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187708 | |||||||
chr5:41187728 | C | T | 2 | a0009c0009t0001g0083 a0009c0009t0001g0130 |
2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.588-1520G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187728 | |||||||
chr5:41187855 | T | A | 132 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(129): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.588-1647A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41187855 | |||||||
chr5:41188189 | G | A | 124 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(121): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.588-1981C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188189 | |||||||
chr5:41188392 | G | C | 7 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.588-2184C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188392 | |||||||
chr5:41188413 | T | A | 6 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0258 others(3): Show |
6 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.588-2205A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188413 | |||||||
chr5:41188465 | AC | A | 37 | a0002c0002t0001g0006 a0002c0002t0001g0012 a0002c0002t0001g0031 others(34): Show |
46 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.588-2258delG | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188465 | |||||||
chr5:41188546 | C | T | 6 | a0002c0002t0001g0035 a0002c0002t0001g0146 a0002c0002t0001g0197 others(3): Show |
7 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-2338G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188546 | |||||||
chr5:41188602 | T | A | 4 | a0001c0001t0002g0002 a0001c0001t0002g0063 a0001c0001t0002g0073 others(1): Show |
10 | HG00438.hp2 HG00558.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.588-2394A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188602 | |||||||
chr5:41188653 | G | GA | 4 | a0002c0002t0003g0008 a0002c0002t0003g0023 a0002c0002t0003g0089 others(1): Show |
7 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-2446dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188653 | |||||||
chr5:41188734 | T | C | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.588-2526A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41188734 | |||||||
chr5:41189069 | C | T | 1 | a0002c0002t0001g0148 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.588-2861G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189069 | |||||||
chr5:41189187 | A | G | 3 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0002c0002t0001g0320 |
4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-2979T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189187 | |||||||
chr5:41189336 | G | A | 2 | a0002c0002t0010g0047 a0002c0014t0009g0048 |
2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.588-3128C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189336 | |||||||
chr5:41189357 | A | C | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.588-3149T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189357 | |||||||
chr5:41189367 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.588-3159G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189367 | |||||||
chr5:41189466 | T | A | 18 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.588-3258A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189466 | |||||||
chr5:41189567 | A | G | 1 | a0002c0002t0003g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.588-3359T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189567 | |||||||
chr5:41189603 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.588-3395G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189603 | |||||||
chr5:41189774 | C | G | 1 | a0002c0002t0001g0201 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.588-3566G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189774 | |||||||
chr5:41189809 | A | C | 132 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(129): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.588-3601T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189809 | |||||||
chr5:41189843 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.588-3635C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189843 | |||||||
chr5:41189984 | A | C | 124 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(121): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.588-3776T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41189984 | |||||||
chr5:41190038 | G | C | 85 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(82): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.588-3830C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190038 | |||||||
chr5:41190099 | C | T | 1 | a0002c0002t0002g0218 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.588-3891G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190099 | |||||||
chr5:41190184 | C | G | 7 | a0002c0002t0001g0029 a0002c0002t0001g0160 a0002c0002t0001g0161 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.588-3976G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190184 | |||||||
chr5:41190275 | A | G | 3 | a0002c0002t0002g0199 a0002c0002t0002g0216 a0002c0002t0002g0217 |
3 | NA18951.hp2 NA19077.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.588-4067T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190275 | |||||||
chr5:41190297 | A | C | 85 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(82): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.588-4089T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190297 | |||||||
chr5:41190352 | C | A | 55 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(52): Show |
67 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.588-4144G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190352 | |||||||
chr5:41190493 | C | T | 9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.588-4285G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190493 | |||||||
chr5:41190597 | A | C | 18 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.588-4389T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190597 | |||||||
chr5:41190681 | A | T | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG02698.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.588-4473T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190681 | |||||||
chr5:41190778 | A | G | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.588-4570T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190778 | |||||||
chr5:41190836 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.588-4628G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41190836 | |||||||
chr5:41191011 | A | AACATGTA others(2): Show |
8 | a0001c0001t0002g0020 a0001c0001t0002g0022 a0001c0001t0002g0055 others(5): Show |
10 | HG00323.hp2 HG01192.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+4772_587+4780d others(11): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191011 | |||||||
chr5:41191067 | C | CTTT | 39 | a0001c0001t0001g0038 a0001c0001t0001g0241 a0001c0001t0001g0242 others(36): Show |
51 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.587+4722_587+4724d others(5): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | |||||||
chr5:41191067 | C | CTTTT | 30 | a0001c0001t0001g0135 a0001c0001t0001g0238 a0001c0001t0001g0239 others(27): Show |
31 | HG00140.hp1 HG00735.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.587+4721_587+4724d others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | |||||||
chr5:41191067 | C | CTTTTT | 10 | a0001c0001t0001g0133 a0001c0001t0002g0049 a0001c0001t0002g0052 others(7): Show |
10 | HG00621.hp1 HG01167.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.587+4720_587+4724d others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | |||||||
chr5:41191067 | CT | C | 41 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0040 others(38): Show |
48 | HG00323.hp2 HG00597.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.587+4724delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | |||||||
chr5:41191067 | CTT | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(140): Show |
187 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.587+4723_587+4724d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | |||||||
chr5:41191067 | CTTT | C | 6 | a0001c0001t0001g0282 a0002c0002t0001g0188 a0002c0002t0003g0101 others(3): Show |
6 | HG00280.hp1 HG01361.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.587+4722_587+4724d others(5): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191067 | |||||||
chr5:41191159 | C | T | 39 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(36): Show |
47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.587+4633G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191159 | |||||||
chr5:41191221 | C | T | 1 | a0001c0006t0002g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.587+4571G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191221 | |||||||
chr5:41191316 | C | T | 3 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0002c0002t0001g0320 |
4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+4476G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191316 | |||||||
chr5:41191335 | C | A | 1 | a0001c0001t0001g0306 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.587+4457G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191335 | |||||||
chr5:41191451 | A | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(270): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.587+4341T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191451 | |||||||
chr5:41191511 | C | T | 3 | a0002c0002t0010g0047 a0002c0014t0009g0048 a0002c0014t0011g0085 |
3 | HG01884.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.587+4281G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191511 | |||||||
chr5:41191678 | G | T | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.587+4114C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191678 | |||||||
chr5:41191793 | C | CT | 15 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0082 others(12): Show |
16 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.587+3998dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191793 | |||||||
chr5:41191793 | C | CTT | 16 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(13): Show |
16 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.587+3997_587+3998d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191793 | |||||||
chr5:41191793 | CT | C | 10 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(7): Show |
11 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.587+3998delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191793 | |||||||
chr5:41191799 | T | A | 9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+3993A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191799 | |||||||
chr5:41191826 | G | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(276): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.587+3966C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191826 | |||||||
chr5:41191887 | A | T | 1 | a0001c0001t0004g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.587+3905T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41191887 | |||||||
chr5:41192052 | C | T | 3 | a0004c0008t0001g0150 a0004c0008t0001g0151 a0004c0008t0001g0323 |
3 | HG01361.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.587+3740G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192052 | |||||||
chr5:41192079 | A | G | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587+3713T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192079 | |||||||
chr5:41192214 | C | A | 19 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0040 others(16): Show |
24 | HG00597.hp2 HG01081.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.587+3578G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192214 | |||||||
chr5:41192217 | T | A | 18 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.587+3575A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192217 | |||||||
chr5:41192258 | T | C | 5 | a0002c0002t0001g0013 a0002c0002t0001g0230 a0002c0002t0001g0231 others(2): Show |
7 | HG00408.hp1 HG00673.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.587+3534A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192258 | |||||||
chr5:41192313 | A | G | 1 | a0002c0002t0001g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.587+3479T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192313 | |||||||
chr5:41192332 | A | G | 1 | a0001c0001t0007g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.587+3460T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192332 | |||||||
chr5:41192399 | A | G | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.587+3393T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192399 | |||||||
chr5:41192406 | G | A | 1 | a0002c0002t0002g0236 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.587+3386C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192406 | |||||||
chr5:41192463 | T | A | 1 | a0002c0002t0001g0032 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.587+3329A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192463 | |||||||
chr5:41192511 | C | T | 3 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0002c0002t0001g0320 |
4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+3281G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192511 | |||||||
chr5:41192603 | G | GT | 13 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(10): Show |
14 | HG01243.hp2 HG01891.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.587+3188dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192603 | |||||||
chr5:41192623 | A | C | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG01167.hp1 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+3169T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192623 | |||||||
chr5:41192828 | G | T | 46 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(43): Show |
57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.587+2964C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192828 | |||||||
chr5:41192897 | A | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(79): Show |
106 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.587+2895T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192897 | |||||||
chr5:41192905 | T | C | 7 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+2887A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192905 | |||||||
chr5:41192986 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.587+2806G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41192986 | |||||||
chr5:41193189 | A | G | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | NA19011.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.587+2603T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193189 | |||||||
chr5:41193204 | C | G | 1 | a0002c0029t0005g0319 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.587+2588G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193204 | |||||||
chr5:41193311 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+2481C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193311 | |||||||
chr5:41193422 | G | A | 2 | a0001c0003t0001g0125 a0001c0003t0001g0126 |
2 | HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.587+2370C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193422 | |||||||
chr5:41193590 | A | G | 3 | a0004c0008t0001g0150 a0004c0008t0001g0151 a0004c0008t0001g0323 |
3 | HG01361.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.587+2202T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193590 | |||||||
chr5:41193591 | T | G | 3 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0002c0002t0001g0320 |
4 | HG01192.hp2 HG01261.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+2201A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193591 | |||||||
chr5:41193795 | A | AT | 28 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(25): Show |
39 | HG00140.hp1 HG00408.hp2 HG01981.hp2 others(36): Show |
intron_variant | MODIFIER | c.587+1996dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193795 | |||||||
chr5:41193795 | A | ATT | 108 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0238 others(105): Show |
131 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.587+1995_587+1996d others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193795 | |||||||
chr5:41193795 | A | ATTT | 6 | a0001c0001t0002g0063 a0001c0001t0004g0082 a0001c0001t0007g0043 others(3): Show |
6 | HG01243.hp2 HG01981.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.587+1994_587+1996d others(5): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193795 | |||||||
chr5:41193795 | AT | A | 48 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0012 others(45): Show |
63 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.587+1996delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193795 | |||||||
chr5:41193816 | G | A | 36 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(33): Show |
44 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.587+1976C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193816 | |||||||
chr5:41193882 | G | T | 1 | a0002c0002t0002g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.587+1910C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193882 | |||||||
chr5:41193984 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.587+1808C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41193984 | |||||||
chr5:41194208 | C | T | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+1584G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194208 | |||||||
chr5:41194213 | A | T | 2 | a0009c0009t0001g0083 a0009c0009t0001g0130 |
2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.587+1579T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194213 | |||||||
chr5:41194243 | G | A | 46 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0012 others(43): Show |
60 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.587+1549C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194243 | |||||||
chr5:41194418 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(266): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.587+1374A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194418 | |||||||
chr5:41194431 | C | T | 1 | a0001c0001t0004g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.587+1361G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194431 | |||||||
chr5:41194554 | G | T | 1 | a0001c0001t0002g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.587+1238C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194554 | |||||||
chr5:41194717 | T | C | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.587+1075A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194717 | |||||||
chr5:41194722 | A | AT | 62 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0238 others(59): Show |
75 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.587+1069dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194722 | |||||||
chr5:41194780 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.587+1012A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41194780 | |||||||
chr5:41195111 | T | G | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.587+681A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195111 | |||||||
chr5:41195207 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.587+585G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195207 | |||||||
chr5:41195278 | A | G | 2 | a0002c0002t0002g0144 a0002c0002t0002g0214 |
2 | NA18960.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.587+514T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195278 | |||||||
chr5:41195311 | A | G | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG01167.hp1 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+481T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195311 | |||||||
chr5:41195382 | C | T | 7 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+410G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195382 | |||||||
chr5:41195598 | C | T | 39 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(36): Show |
47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.587+194G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 5/17 | chr5 | 41195598 | |||||||
chr5:41195977 | T | C | 1 | a0001c0001t0002g0022 | 2 | HG01515.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.446-44A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41195977 | |||||||
chr5:41196011 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.446-78G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196011 | |||||||
chr5:41196088 | C | T | 4 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(1): Show |
4 | HG00140.hp2 HG01074.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-155G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196088 | |||||||
chr5:41196110 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.446-177A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196110 | |||||||
chr5:41196128 | C | T | 39 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(36): Show |
47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.446-195G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196128 | |||||||
chr5:41196171 | A | G | 18 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.446-238T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196171 | |||||||
chr5:41196209 | A | G | 55 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0012 others(52): Show |
71 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.446-276T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196209 | |||||||
chr5:41196273 | G | A | 3 | a0004c0008t0001g0150 a0004c0008t0001g0151 a0004c0008t0001g0323 |
3 | HG01361.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.446-340C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196273 | |||||||
chr5:41196433 | T | C | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-500A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196433 | |||||||
chr5:41196508 | A | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.446-575T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196508 | |||||||
chr5:41196549 | G | A | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.446-616C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196549 | |||||||
chr5:41196658 | A | G | 1 | a0001c0001t0004g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.446-725T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196658 | |||||||
chr5:41196680 | A | G | 7 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.446-747T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196680 | |||||||
chr5:41196967 | T | C | 2 | a0001c0001t0004g0025 a0001c0001t0004g0137 |
3 | HG01884.hp2 HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.446-1034A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196967 | |||||||
chr5:41196973 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(141): Show |
181 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.446-1040T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41196973 | |||||||
chr5:41197278 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.446-1345G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41197278 | |||||||
chr5:41197282 | A | G | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG01167.hp1 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-1349T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41197282 | |||||||
chr5:41197370 | A | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(141): Show |
181 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.446-1437T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41197370 | |||||||
chr5:41197467 | C | A | 7 | a0002c0002t0001g0035 a0002c0002t0001g0146 a0002c0002t0001g0197 others(4): Show |
8 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-1534G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41197467 | |||||||
chr5:41197639 | A | G | 1 | a0002c0002t0002g0213 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.446-1706T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41197639 | |||||||
chr5:41198015 | A | G | 14 | a0002c0002t0001g0005 a0002c0002t0001g0029 a0002c0002t0001g0158 others(11): Show |
19 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.445+1753T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198015 | |||||||
chr5:41198045 | C | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+1723G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198045 | |||||||
chr5:41198060 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.445+1708G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198060 | |||||||
chr5:41198099 | A | G | 52 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0012 others(49): Show |
67 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.445+1669T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198099 | |||||||
chr5:41198122 | C | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(276): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.445+1646G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198122 | |||||||
chr5:41198136 | C | T | 9 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(6): Show |
10 | HG01884.hp2 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.445+1632G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198136 | |||||||
chr5:41198137 | G | A | 2 | a0002c0002t0003g0102 a0002c0002t0003g0103 |
2 | NA18994.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.445+1631C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198137 | |||||||
chr5:41198402 | A | T | 4 | a0002c0002t0003g0008 a0002c0002t0003g0023 a0002c0002t0003g0089 others(1): Show |
7 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.445+1366T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198402 | |||||||
chr5:41198665 | A | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(78): Show |
105 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.445+1103T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198665 | |||||||
chr5:41198667 | A | G | 3 | a0001c0001t0001g0265 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG00408.hp2 NA18968.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.445+1101T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198667 | |||||||
chr5:41198720 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.445+1048G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198720 | |||||||
chr5:41198749 | T | C | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.445+1019A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198749 | |||||||
chr5:41198855 | C | T | 2 | a0002c0002t0001g0172 a0002c0002t0001g0173 |
2 | NA18961.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.445+913G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198855 | |||||||
chr5:41198891 | C | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0251 others(7): Show |
13 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.445+877G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198891 | |||||||
chr5:41198910 | G | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(164): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.445+858C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198910 | |||||||
chr5:41198966 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(163): Show |
203 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.445+802T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41198966 | |||||||
chr5:41199020 | G | C | 1 | a0001c0001t0001g0303 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.445+748C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199020 | |||||||
chr5:41199038 | C | T | 1 | a0006c0007t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.445+730G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199038 | |||||||
chr5:41199056 | A | G | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+712T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199056 | |||||||
chr5:41199093 | C | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+675G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199093 | |||||||
chr5:41199136 | A | G | 39 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(36): Show |
47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.445+632T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199136 | |||||||
chr5:41199303 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.445+465G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199303 | |||||||
chr5:41199314 | C | T | 2 | a0002c0002t0001g0034 a0002c0002t0001g0206 |
3 | HG00280.hp2 HG00323.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.445+454G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199314 | |||||||
chr5:41199379 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.445+389T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199379 | |||||||
chr5:41199474 | T | C | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.445+294A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199474 | |||||||
chr5:41199514 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(141): Show |
181 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.445+254A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199514 | |||||||
chr5:41199527 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(164): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.445+241A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199527 | |||||||
chr5:41199747 | C | T | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.445+21G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 4/17 | chr5 | 41199747 | |||||||
chr5:41200024 | C | T | 1 | a0002c0002t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301-112G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200024 | |||||||
chr5:41200180 | C | T | 5 | a0005c0005t0006g0018 a0005c0005t0006g0046 a0010c0010t0001g0263 others(2): Show |
6 | HG02258.hp1 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-268G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200180 | |||||||
chr5:41200211 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.301-299A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200211 | |||||||
chr5:41200251 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(164): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.301-339G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200251 | |||||||
chr5:41200256 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(164): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.301-344C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200256 | |||||||
chr5:41200281 | T | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.301-369A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200281 | |||||||
chr5:41200307 | G | A | 3 | a0006c0007t0003g0104 a0006c0007t0003g0105 a0006c0007t0003g0106 |
3 | HG02723.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.301-395C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200307 | |||||||
chr5:41200360 | C | T | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.301-448G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200360 | |||||||
chr5:41200446 | T | C | 46 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(43): Show |
57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.301-534A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200446 | |||||||
chr5:41200624 | T | C | 2 | a0002c0002t0001g0164 a0002c0002t0001g0165 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.301-712A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200624 | |||||||
chr5:41200658 | G | T | 1 | a0001c0001t0007g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.301-746C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200658 | |||||||
chr5:41200693 | T | C | 7 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(4): Show |
7 | HG00140.hp1 HG01123.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.301-781A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200693 | |||||||
chr5:41200724 | G | T | 46 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(43): Show |
57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.301-812C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200724 | |||||||
chr5:41200863 | C | A | 1 | a0002c0002t0008g0318 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.300+695G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200863 | |||||||
chr5:41200870 | TTTGTTG | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0134 |
3 | HG02809.hp1 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.300+682_300+687del others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200870 | |||||||
chr5:41200888 | GTTGTT | G | 6 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0123 others(3): Show |
6 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.300+665_300+669del others(5): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200888 | |||||||
chr5:41200888 | GTTGTTT | G | 11 | a0001c0001t0012g0129 a0001c0003t0001g0120 a0001c0003t0001g0124 others(8): Show |
11 | HG02055.hp1 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.300+664_300+669del others(6): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200888 | |||||||
chr5:41200888 | GTTGTTTT | G | 20 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0082 others(17): Show |
22 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.300+663_300+669del others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200888 | |||||||
chr5:41200888 | GTTGTTTT others(1): Show |
G | 27 | a0002c0002t0003g0009 a0002c0002t0003g0010 a0002c0002t0003g0024 others(24): Show |
32 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.300+662_300+669del others(8): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200888 | |||||||
chr5:41200891 | G | GT | 32 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0034 others(29): Show |
41 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.300+666dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200891 | G | GTT | 38 | a0002c0002t0001g0006 a0002c0002t0001g0012 a0002c0002t0001g0013 others(35): Show |
46 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.300+665_300+666dup others(2): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200891 | G | GTTT | 16 | a0002c0002t0001g0180 a0002c0002t0001g0189 a0002c0002t0001g0209 others(13): Show |
19 | HG00597.hp1 HG00738.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.300+664_300+666dup others(3): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200891 | G | GTTTTGTT others(3): Show |
1 | a0002c0002t0001g0005 | 2 | HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.300+666_300+667ins others(10): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200891 | G | GTTTTTTT | 7 | a0002c0002t0001g0005 a0002c0002t0001g0029 a0002c0002t0001g0159 others(4): Show |
8 | HG00738.hp1 HG01517.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.300+660_300+666dup others(7): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200891 | G | GTTTTTTT others(3): Show |
2 | a0002c0002t0001g0005 a0002c0002t0001g0168 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.300+657_300+666dup others(10): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200891 | G | GTTTTTTT others(4): Show |
2 | a0002c0002t0001g0005 a0002c0002t0001g0167 |
2 | HG00741.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.300+656_300+666dup others(11): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200891 | G | T | 1 | a0002c0002t0005g0178 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.300+667C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200891 | GTT | G | 9 | a0001c0001t0001g0004 a0001c0001t0002g0002 a0001c0001t0002g0051 others(6): Show |
9 | HG00621.hp1 HG02135.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+665_300+666del others(2): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200891 | GTTT | G | 36 | a0001c0001t0001g0041 a0001c0001t0001g0249 a0001c0001t0001g0258 others(33): Show |
44 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.300+664_300+666del others(3): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200891 | GTTTT | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(68): Show |
90 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.300+663_300+666del others(4): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200891 | GTTTTT | G | 26 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0038 others(23): Show |
28 | HG00323.hp2 HG00423.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.300+662_300+666del others(5): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200891 | |||||||
chr5:41200895 | T | G | 1 | a0001c0001t0001g0307 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.300+663A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200895 | |||||||
chr5:41200915 | T | A | 1 | a0011c0012t0004g0138 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.300+643A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200915 | |||||||
chr5:41200924 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.300+634C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41200924 | |||||||
chr5:41201013 | T | A | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.300+545A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201013 | |||||||
chr5:41201017 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(134): Show |
173 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.300+541C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201017 | |||||||
chr5:41201055 | A | G | 39 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(36): Show |
47 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.300+503T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201055 | |||||||
chr5:41201084 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG01358.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.300+474G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201084 | |||||||
chr5:41201097 | G | A | 1 | a0002c0002t0001g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.300+461C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201097 | |||||||
chr5:41201104 | G | A | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.300+454C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201104 | |||||||
chr5:41201237 | G | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+321C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201237 | |||||||
chr5:41201269 | C | T | 2 | a0002c0002t0001g0172 a0002c0002t0001g0173 |
2 | NA18961.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.300+289G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201269 | |||||||
chr5:41201324 | T | C | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.300+234A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201324 | |||||||
chr5:41201463 | G | A | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.300+95C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201463 | |||||||
chr5:41201526 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.300+32G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201526 | |||||||
chr5:41201530 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.300+28A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 3/17 | chr5 | 41201530 | |||||||
chr5:41201744 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.144-30T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201744 | |||||||
chr5:41201769 | C | T | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-55G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201769 | |||||||
chr5:41201785 | T | G | 1 | a0001c0001t0001g0305 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.144-71A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201785 | |||||||
chr5:41201831 | T | C | 4 | a0002c0002t0003g0010 a0002c0002t0003g0112 a0002c0002t0003g0113 others(1): Show |
6 | NA18971.hp2 NA18974.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-117A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201831 | |||||||
chr5:41201845 | A | G | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-131T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201845 | |||||||
chr5:41201850 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-136C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41201850 | |||||||
chr5:41202211 | A | G | 5 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0002c0002t0001g0320 others(2): Show |
6 | HG01192.hp2 HG01261.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-497T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202211 | |||||||
chr5:41202237 | C | T | 1 | a0001c0006t0002g0324 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.144-523G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202237 | |||||||
chr5:41202292 | AG | A | 7 | a0002c0002t0001g0201 a0002c0002t0002g0033 a0002c0002t0002g0145 others(4): Show |
8 | HG01168.hp1 HG01175.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.144-579delC | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202292 | |||||||
chr5:41202366 | T | G | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-652A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202366 | |||||||
chr5:41202595 | T | G | 1 | a0002c0002t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143+493A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202595 | |||||||
chr5:41202656 | C | G | 1 | a0001c0001t0002g0057 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.143+432G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202656 | |||||||
chr5:41202768 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.143+320G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202768 | |||||||
chr5:41202809 | A | AAAGCTTG others(1): Show |
9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.143+271_143+278dup others(8): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202809 | |||||||
chr5:41202869 | T | C | 1 | a0002c0002t0001g0166 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.143+219A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202869 | |||||||
chr5:41202894 | C | T | 1 | a0005c0005t0006g0018 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.143+194G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202894 | |||||||
chr5:41202904 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.143+184C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 2/17 | chr5 | 41202904 | |||||||
chr5:41203445 | A | G | 15 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(12): Show |
15 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20-195T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41203445 | |||||||
chr5:41203855 | G | T | 1 | a0001c0001t0012g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-20-605C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41203855 | |||||||
chr5:41203902 | G | A | 37 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(34): Show |
45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-20-652C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41203902 | |||||||
chr5:41203994 | C | T | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-744G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41203994 | |||||||
chr5:41203995 | G | A | 5 | a0002c0002t0003g0088 a0002c0002t0003g0107 a0002c0002t0003g0108 others(2): Show |
5 | NA18988.hp1 NA19054.hp2 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-745C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41203995 | |||||||
chr5:41204071 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-20-821C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204071 | |||||||
chr5:41204199 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-949C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204199 | |||||||
chr5:41204201 | C | T | 57 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0012 others(54): Show |
73 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-20-951G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204201 | |||||||
chr5:41204230 | A | T | 1 | a0001c0001t0001g0264 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-20-980T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204230 | |||||||
chr5:41204241 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-991C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204241 | |||||||
chr5:41204446 | G | T | 1 | a0002c0002t0001g0171 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-20-1196C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204446 | |||||||
chr5:41204459 | C | T | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1209G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204459 | |||||||
chr5:41204559 | G | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(73): Show |
99 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-20-1309C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204559 | |||||||
chr5:41204659 | C | CT | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(123): Show |
161 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.-20-1410dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204659 | |||||||
chr5:41204664 | T | C | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-20-1414A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204664 | |||||||
chr5:41204670 | C | T | 5 | a0001c0001t0001g0244 a0001c0001t0001g0307 a0001c0001t0001g0315 others(2): Show |
5 | HG01433.hp2 HG02055.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1420G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204670 | |||||||
chr5:41204670 | CT | C | 31 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(28): Show |
32 | HG00140.hp1 HG00323.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.-20-1421delA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204670 | |||||||
chr5:41204671 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-20-1421A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204671 | |||||||
chr5:41204675 | T | C | 4 | a0002c0002t0001g0005 a0002c0002t0001g0027 a0002c0002t0001g0167 others(1): Show |
9 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20-1425A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204675 | |||||||
chr5:41204677 | T | C | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02056.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-20-1427A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204677 | |||||||
chr5:41204737 | T | A | 1 | a0002c0002t0002g0204 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-20-1487A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204737 | |||||||
chr5:41204739 | G | A | 46 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(43): Show |
57 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-20-1489C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204739 | |||||||
chr5:41204806 | A | T | 15 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(12): Show |
15 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20-1556T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204806 | |||||||
chr5:41204872 | C | T | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1622G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41204872 | |||||||
chr5:41205016 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1766C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205016 | |||||||
chr5:41205030 | G | A | 2 | a0002c0002t0001g0189 a0002c0002t0001g0190 |
2 | HG00597.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.-20-1780C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205030 | |||||||
chr5:41205060 | A | G | 1 | a0002c0002t0002g0205 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-20-1810T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205060 | |||||||
chr5:41205126 | T | C | 37 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(34): Show |
45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-20-1876A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205126 | |||||||
chr5:41205174 | C | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20-1924G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205174 | |||||||
chr5:41205190 | A | G | 1 | a0001c0003t0001g0118 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-20-1940T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205190 | |||||||
chr5:41205242 | G | A | 7 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-1992C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205242 | |||||||
chr5:41205297 | C | T | 1 | a0010c0010t0001g0263 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20-2047G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205297 | |||||||
chr5:41205376 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2126C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205376 | |||||||
chr5:41205386 | C | T | 9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-2136G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205386 | |||||||
chr5:41205387 | G | T | 9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-2137C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205387 | |||||||
chr5:41205418 | G | A | 7 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-2168C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205418 | |||||||
chr5:41205446 | G | A | 1 | a0002c0002t0001g0191 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-20-2196C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205446 | |||||||
chr5:41205506 | C | T | 57 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0012 others(54): Show |
73 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.-20-2256G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205506 | |||||||
chr5:41205508 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2258C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205508 | |||||||
chr5:41205577 | C | T | 1 | a0002c0002t0002g0237 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-20-2327G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205577 | |||||||
chr5:41205582 | C | A | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-20-2332G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205582 | |||||||
chr5:41205589 | G | A | 5 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0125 others(2): Show |
5 | HG00544.hp1 HG02145.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-2339C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205589 | |||||||
chr5:41205680 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-20-2430G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205680 | |||||||
chr5:41205681 | C | A | 3 | a0002c0002t0001g0320 a0002c0002t0010g0047 a0002c0014t0009g0048 |
3 | HG01261.hp1 HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-20-2431G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205681 | |||||||
chr5:41205682 | G | A | 9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-2432C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205682 | |||||||
chr5:41205706 | A | T | 1 | a0001c0001t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-20-2456T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205706 | |||||||
chr5:41205713 | G | C | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2463C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205713 | |||||||
chr5:41205760 | G | A | 1 | a0015c0030t0002g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20-2510C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205760 | |||||||
chr5:41205787 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-20-2537G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205787 | |||||||
chr5:41205818 | C | G | 7 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-2568G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205818 | |||||||
chr5:41205884 | C | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG00323.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-20-2634G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205884 | |||||||
chr5:41205905 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2655C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205905 | |||||||
chr5:41205958 | A | G | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2708T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205958 | |||||||
chr5:41205963 | C | T | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0011t0002g0019 |
4 | HG00735.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2713G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205963 | |||||||
chr5:41205972 | C | T | 1 | a0002c0002t0002g0237 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-20-2722G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41205972 | |||||||
chr5:41206000 | G | C | 2 | a0002c0002t0003g0086 a0002c0002t0003g0110 |
2 | HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-20-2750C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206000 | |||||||
chr5:41206059 | C | A | 3 | a0005c0005t0006g0018 a0005c0005t0006g0046 a0010c0010t0006g0045 |
4 | HG02258.hp1 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2809G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206059 | |||||||
chr5:41206083 | C | T | 1 | a0001c0003t0001g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-20-2833G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206083 | |||||||
chr5:41206277 | C | T | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-20-3027G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206277 | |||||||
chr5:41206329 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-3079G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206329 | |||||||
chr5:41206330 | G | A | 2 | a0001c0003t0001g0118 a0001c0003t0001g0119 |
2 | HG00140.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-20-3080C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206330 | |||||||
chr5:41206404 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0261 |
3 | HG02602.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-20-3154G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206404 | |||||||
chr5:41206420 | A | G | 2 | a0002c0002t0003g0112 a0002c0002t0003g0113 |
2 | NA18971.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-20-3170T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206420 | |||||||
chr5:41206575 | G | A | 2 | a0002c0002t0010g0047 a0002c0014t0009g0048 |
2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-20-3325C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206575 | |||||||
chr5:41206630 | T | C | 18 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-20-3380A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206630 | |||||||
chr5:41206699 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20-3449C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206699 | |||||||
chr5:41206759 | C | A | 18 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-20-3509G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206759 | |||||||
chr5:41206770 | A | G | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3520T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206770 | |||||||
chr5:41206774 | C | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3524G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206774 | |||||||
chr5:41206774 | C | T | 1 | a0001c0003t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20-3524G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206774 | |||||||
chr5:41206777 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3527C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206777 | |||||||
chr5:41206783 | C | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3533G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206783 | |||||||
chr5:41206785 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3535C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206785 | |||||||
chr5:41206787 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-20-3537C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206787 | |||||||
chr5:41206787 | G | T | 14 | a0002c0002t0001g0005 a0002c0002t0001g0029 a0002c0002t0001g0158 others(11): Show |
19 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20-3537C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206787 | |||||||
chr5:41206909 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(209): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-20-3659A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206909 | |||||||
chr5:41206930 | A | T | 6 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0258 others(3): Show |
6 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-3680T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206930 | |||||||
chr5:41206933 | C | T | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-20-3683G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206933 | |||||||
chr5:41206940 | T | C | 37 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(34): Show |
45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-20-3690A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206940 | |||||||
chr5:41206945 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-20-3695A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41206945 | |||||||
chr5:41207027 | C | T | 7 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-3777G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207027 | |||||||
chr5:41207062 | G | A | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | HG01167.hp1 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-3812C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207062 | |||||||
chr5:41207063 | G | T | 3 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
3 | HG02015.hp1 HG02074.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-20-3813C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207063 | |||||||
chr5:41207064 | C | T | 1 | a0002c0002t0001g0170 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-20-3814G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207064 | |||||||
chr5:41207071 | A | G | 1 | a0002c0002t0003g0088 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-20-3821T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207071 | |||||||
chr5:41207101 | C | A | 1 | a0001c0001t0004g0139 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-20-3851G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207101 | |||||||
chr5:41207111 | G | A | 4 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(1): Show |
4 | HG00741.hp2 HG01256.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-3861C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207111 | |||||||
chr5:41207254 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-20-4004A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207254 | |||||||
chr5:41207297 | T | G | 52 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0012 others(49): Show |
67 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.-20-4047A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207297 | |||||||
chr5:41207302 | G | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-4052C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207302 | |||||||
chr5:41207358 | T | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(266): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.-20-4108A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207358 | |||||||
chr5:41207574 | G | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(266): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.-20-4324C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207574 | |||||||
chr5:41207660 | T | C | 38 | a0002c0002t0001g0006 a0002c0002t0001g0012 a0002c0002t0001g0031 others(35): Show |
48 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-20-4410A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207660 | |||||||
chr5:41207695 | G | T | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20-4445C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207695 | |||||||
chr5:41207834 | A | G | 1 | a0002c0002t0001g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-20-4584T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207834 | |||||||
chr5:41207882 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-20-4632A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41207882 | |||||||
chr5:41208040 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-4790C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208040 | |||||||
chr5:41208072 | C | T | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-20-4822G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208072 | |||||||
chr5:41208157 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-4907C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208157 | |||||||
chr5:41208190 | A | C | 2 | a0002c0002t0001g0158 a0002c0002t0001g0159 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-20-4940T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208190 | |||||||
chr5:41208259 | G | C | 1 | a0001c0001t0007g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-20-5009C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208259 | |||||||
chr5:41208260 | A | G | 44 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(41): Show |
53 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.-20-5010T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208260 | |||||||
chr5:41208272 | A | G | 1 | a0002c0002t0003g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-20-5022T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208272 | |||||||
chr5:41208333 | A | G | 6 | a0002c0002t0001g0201 a0002c0002t0002g0033 a0002c0002t0002g0145 others(3): Show |
7 | HG01168.hp1 HG01175.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+5043T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208333 | |||||||
chr5:41208348 | G | T | 1 | a0001c0001t0012g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-21+5028C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208348 | |||||||
chr5:41208391 | A | G | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+4985T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208391 | |||||||
chr5:41208418 | A | G | 18 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21+4958T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208418 | |||||||
chr5:41208449 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-21+4927T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208449 | |||||||
chr5:41208470 | C | T | 1 | a0002c0002t0003g0086 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-21+4906G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208470 | |||||||
chr5:41208584 | T | C | 44 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(41): Show |
53 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.-21+4792A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208584 | |||||||
chr5:41208598 | C | T | 38 | a0002c0002t0001g0006 a0002c0002t0001g0012 a0002c0002t0001g0031 others(35): Show |
48 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+4778G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208598 | |||||||
chr5:41208648 | A | G | 7 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+4728T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208648 | |||||||
chr5:41208718 | G | A | 3 | a0002c0002t0001g0320 a0002c0002t0010g0047 a0002c0014t0009g0048 |
3 | HG01261.hp1 HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-21+4658C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208718 | |||||||
chr5:41208742 | C | CA | 7 | a0003c0004t0001g0011 a0003c0004t0001g0153 a0003c0004t0001g0154 others(4): Show |
9 | HG00609.hp2 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21+4633dupT | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208742 | |||||||
chr5:41208751 | T | C | 1 | a0002c0002t0001g0193 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-21+4625A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208751 | |||||||
chr5:41208798 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0238 |
3 | HG02976.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-21+4578T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208798 | |||||||
chr5:41208915 | C | T | 37 | a0002c0002t0001g0006 a0002c0002t0001g0012 a0002c0002t0001g0031 others(34): Show |
46 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.-21+4461G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208915 | |||||||
chr5:41208916 | G | A | 67 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(64): Show |
76 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.-21+4460C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208916 | |||||||
chr5:41208955 | C | T | 52 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0012 others(49): Show |
67 | HG00544.hp2 HG00597.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.-21+4421G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41208955 | |||||||
chr5:41209183 | A | C | 37 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(34): Show |
45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-21+4193T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209183 | |||||||
chr5:41209193 | A | G | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+4183T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209193 | |||||||
chr5:41209283 | T | A | 13 | a0002c0002t0001g0005 a0002c0002t0001g0029 a0002c0002t0001g0158 others(10): Show |
18 | HG00738.hp1 HG00741.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21+4093A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209283 | |||||||
chr5:41209344 | C | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+4032G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209344 | |||||||
chr5:41209444 | G | C | 37 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(34): Show |
45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-21+3932C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209444 | |||||||
chr5:41209481 | C | G | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+3895G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209481 | |||||||
chr5:41209484 | T | C | 67 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(64): Show |
76 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.-21+3892A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209484 | |||||||
chr5:41209494 | C | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(269): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-21+3882G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209494 | |||||||
chr5:41209512 | C | A | 37 | a0002c0002t0001g0006 a0002c0002t0001g0012 a0002c0002t0001g0031 others(34): Show |
46 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.-21+3864G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209512 | |||||||
chr5:41209533 | C | A | 1 | a0002c0002t0003g0116 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-21+3843G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209533 | |||||||
chr5:41209573 | C | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(266): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.-21+3803G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209573 | |||||||
chr5:41209734 | A | T | 1 | a0002c0002t0001g0149 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-21+3642T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209734 | |||||||
chr5:41209771 | C | T | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+3605G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209771 | |||||||
chr5:41209772 | G | A | 2 | a0002c0002t0001g0194 a0002c0002t0001g0195 |
2 | HG03579.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-21+3604C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209772 | |||||||
chr5:41209833 | A | C | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+3543T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209833 | |||||||
chr5:41209946 | T | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(269): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-21+3430A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41209946 | |||||||
chr5:41210004 | G | T | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+3372C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210004 | |||||||
chr5:41210096 | G | A | 1 | a0002c0002t0003g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-21+3280C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210096 | |||||||
chr5:41210111 | T | C | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+3265A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210111 | |||||||
chr5:41210114 | G | A | 18 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21+3262C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210114 | |||||||
chr5:41210147 | G | T | 3 | a0002c0002t0001g0320 a0002c0002t0010g0047 a0002c0014t0009g0048 |
3 | HG01261.hp1 HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-21+3229C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210147 | |||||||
chr5:41210156 | C | G | 1 | a0002c0002t0002g0199 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-21+3220G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210156 | |||||||
chr5:41210180 | C | G | 1 | a0001c0001t0007g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-21+3196G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210180 | |||||||
chr5:41210182 | G | C | 1 | a0002c0002t0002g0198 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-21+3194C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210182 | |||||||
chr5:41210183 | G | T | 1 | a0002c0002t0002g0198 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-21+3193C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210183 | |||||||
chr5:41210281 | C | A | 1 | a0002c0002t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-21+3095G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210281 | |||||||
chr5:41210295 | A | C | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+3081T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210295 | |||||||
chr5:41210349 | A | T | 1 | a0001c0001t0004g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-21+3027T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210349 | |||||||
chr5:41210378 | A | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0238 a0001c0001t0001g0239 others(6): Show |
10 | HG01346.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21+2998T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210378 | |||||||
chr5:41210400 | C | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(121): Show |
157 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-21+2976G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210400 | |||||||
chr5:41210470 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | NA19000.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-21+2906G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210470 | |||||||
chr5:41210508 | A | G | 1 | a0002c0002t0001g0148 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-21+2868T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210508 | |||||||
chr5:41210571 | C | A | 23 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(20): Show |
23 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.-21+2805G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210571 | |||||||
chr5:41210611 | A | T | 2 | a0001c0003t0001g0118 a0001c0003t0001g0119 |
2 | HG00140.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-21+2765T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210611 | |||||||
chr5:41210616 | G | A | 1 | a0001c0003t0001g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-21+2760C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210616 | |||||||
chr5:41210649 | G | A | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+2727C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210649 | |||||||
chr5:41210714 | C | T | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+2662G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210714 | |||||||
chr5:41210765 | T | C | 18 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21+2611A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210765 | |||||||
chr5:41210820 | G | T | 1 | a0001c0001t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21+2556C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210820 | |||||||
chr5:41210891 | C | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(269): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-21+2485G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210891 | |||||||
chr5:41210937 | C | A | 1 | a0002c0002t0001g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-21+2439G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41210937 | |||||||
chr5:41211034 | A | G | 5 | a0002c0002t0001g0027 a0002c0002t0001g0147 a0002c0002t0001g0320 others(2): Show |
6 | HG01192.hp2 HG01261.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+2342T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211034 | |||||||
chr5:41211047 | C | T | 1 | a0002c0002t0001g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-21+2329G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211047 | |||||||
chr5:41211101 | G | A | 5 | a0001c0001t0004g0082 a0001c0001t0004g0117 a0001c0001t0007g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+2275C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211101 | |||||||
chr5:41211131 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-21+2245T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211131 | |||||||
chr5:41211170 | A | G | 36 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(33): Show |
44 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-21+2206T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211170 | |||||||
chr5:41211202 | A | G | 1 | a0002c0002t0001g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-21+2174T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211202 | |||||||
chr5:41211217 | T | C | 1 | a0002c0002t0002g0236 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-21+2159A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211217 | |||||||
chr5:41211263 | G | T | 1 | a0001c0001t0004g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-21+2113C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211263 | |||||||
chr5:41211268 | A | C | 11 | a0001c0003t0001g0118 a0001c0003t0001g0119 a0001c0003t0001g0120 others(8): Show |
11 | HG00140.hp1 HG01123.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+2108T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211268 | |||||||
chr5:41211269 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-21+2107C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211269 | |||||||
chr5:41211272 | C | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(269): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-21+2104G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211272 | |||||||
chr5:41211293 | C | G | 1 | a0002c0014t0011g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-21+2083G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211293 | |||||||
chr5:41211294 | G | A | 1 | a0001c0003t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-21+2082C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211294 | |||||||
chr5:41211310 | T | C | 3 | a0001c0001t0012g0129 a0009c0009t0001g0083 a0009c0009t0001g0130 |
3 | HG02257.hp2 HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-21+2066A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211310 | |||||||
chr5:41211318 | C | CATGGCAT | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(134): Show |
173 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.-21+2051_-21+2057d others(9): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211318 | |||||||
chr5:41211353 | G | A | 7 | a0002c0002t0003g0009 a0002c0002t0003g0010 a0002c0002t0003g0112 others(4): Show |
11 | HG01496.hp2 HG02004.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+2023C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211353 | |||||||
chr5:41211459 | C | G | 1 | a0001c0001t0004g0025 | 2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-21+1917G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211459 | |||||||
chr5:41211504 | C | A | 1 | a0009c0009t0001g0083 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-21+1872G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211504 | |||||||
chr5:41211547 | T | G | 1 | a0002c0002t0002g0237 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-21+1829A>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211547 | |||||||
chr5:41211687 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(78): Show |
105 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.-21+1689C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211687 | |||||||
chr5:41211732 | T | A | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG01167.hp1 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+1644A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211732 | |||||||
chr5:41211751 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(134): Show |
173 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.-21+1625A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211751 | |||||||
chr5:41211782 | C | CT | 67 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(64): Show |
76 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.-21+1593_-21+1594i others(3): Show |
C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211782 | |||||||
chr5:41211795 | G | A | 18 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(15): Show |
18 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21+1581C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211795 | |||||||
chr5:41211847 | A | G | 1 | a0002c0002t0001g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-21+1529T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211847 | |||||||
chr5:41211932 | T | A | 1 | a0001c0001t0002g0081 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-21+1444A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211932 | |||||||
chr5:41211978 | A | C | 7 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+1398T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41211978 | |||||||
chr5:41212025 | G | A | 20 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(17): Show |
20 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-21+1351C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212025 | |||||||
chr5:41212114 | T | A | 3 | a0002c0002t0008g0316 a0002c0002t0008g0317 a0002c0002t0008g0318 |
3 | HG02004.hp1 HG02273.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-21+1262A>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212114 | |||||||
chr5:41212169 | T | C | 1 | a0002c0029t0005g0319 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-21+1207A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212169 | |||||||
chr5:41212260 | C | T | 1 | a0002c0002t0002g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-21+1116G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212260 | |||||||
chr5:41212263 | G | A | 38 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(35): Show |
48 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+1113C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212263 | |||||||
chr5:41212285 | C | T | 1 | a0002c0002t0002g0144 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-21+1091G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212285 | |||||||
chr5:41212291 | G | A | 3 | a0002c0002t0001g0320 a0002c0002t0010g0047 a0002c0014t0009g0048 |
3 | HG01261.hp1 HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-21+1085C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212291 | |||||||
chr5:41212333 | G | C | 1 | a0001c0001t0001g0321 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-21+1043C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212333 | |||||||
chr5:41212349 | C | T | 11 | a0001c0001t0001g0135 a0001c0001t0002g0026 a0001c0001t0002g0142 others(8): Show |
13 | HG01074.hp1 HG01081.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-21+1027G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212349 | |||||||
chr5:41212350 | G | T | 3 | a0001c0001t0007g0042 a0001c0001t0007g0043 a0001c0001t0007g0044 |
3 | HG01243.hp2 HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-21+1026C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212350 | |||||||
chr5:41212361 | A | T | 3 | a0001c0001t0007g0042 a0001c0001t0007g0043 a0001c0001t0007g0044 |
3 | HG01243.hp2 HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-21+1015T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212361 | |||||||
chr5:41212410 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-21+966G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212410 | |||||||
chr5:41212439 | G | A | 1 | a0014c0020t0001g0322 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21+937C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212439 | |||||||
chr5:41212509 | G | C | 20 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(17): Show |
20 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-21+867C>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212509 | |||||||
chr5:41212560 | C | G | 4 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 others(1): Show |
4 | HG02015.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+816G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212560 | |||||||
chr5:41212628 | C | A | 1 | a0004c0008t0001g0323 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-21+748G>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212628 | |||||||
chr5:41212634 | T | C | 7 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+742A>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212634 | |||||||
chr5:41212669 | A | G | 44 | a0001c0001t0001g0135 a0001c0001t0004g0025 a0001c0001t0004g0084 others(41): Show |
53 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.-21+707T>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212669 | |||||||
chr5:41212699 | G | A | 3 | a0001c0001t0007g0042 a0001c0001t0007g0043 a0001c0001t0007g0044 |
3 | HG01243.hp2 HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-21+677C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212699 | |||||||
chr5:41212931 | G | T | 2 | a0001c0001t0004g0082 a0009c0009t0001g0083 |
2 | HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-21+445C>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212931 | |||||||
chr5:41212970 | C | T | 20 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(17): Show |
20 | HG00140.hp1 HG01123.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-21+406G>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41212970 | |||||||
chr5:41213006 | A | AT | 37 | a0002c0002t0003g0008 a0002c0002t0003g0009 a0002c0002t0003g0010 others(34): Show |
45 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-21+369dupA | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41213006 | |||||||
chr5:41213006 | A | T | 1 | a0001c0001t0004g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-21+370T>A | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41213006 | |||||||
chr5:41213071 | G | A | 1 | a0001c0006t0002g0324 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-21+305C>T | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41213071 | |||||||
chr5:41213144 | A | C | 2 | a0001c0001t0004g0082 a0009c0009t0001g0083 |
2 | HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-21+232T>G | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41213144 | |||||||
chr5:41213233 | C | G | 38 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(35): Show |
48 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+143G>C | C6 | ENSG00000039537.16 | transcript | ENST00000337836.10 | protein_coding | 1/17 | chr5 | 41213233 |