Item | Value |
---|---|
geneid | 9972 |
ensemblid | ENSG00000124789.12 |
hgncid | 8062 |
symbol | NUP153 |
name | nucleoporin 153 |
refseq_nuc | NM_005124.4 |
refseq_prot | NP_005115.2 |
ensembl_nuc | ENST00000262077.3 |
ensembl_prot | ENSP00000262077.3 |
mane_status | MANE Select |
chr | chr6 |
start | 17615037 |
end | 17706925 |
strand | - |
ver | v1.2 |
region | chr6:17615037-17706925 |
region5000 | chr6:17610037-17711925 |
regionname0 | NUP153_chr6_17615037_17706925 |
regionname5000 | NUP153_chr6_17610037_17711925 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1475 | 131 | 31 | 20 | 69 | 1 | 10 | 52 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0002 | 0/0 | 1475 | 59 | 15 | 2 | 40 | 0 | 2 | 32 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0003 | 1/0 | 1475 | 36 | 20 | 6 | 4 | 2 | 3 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0004 | 0/0 | 1475 | 29 | 2 | 10 | 11 | 4 | 2 | 8 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0005 | 0/1 | 1475 | 20 | 1 | 5 | 10 | 1 | 2 | 8 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0006 | 0/0 | 1475 | 19 | 5 | 7 | 1 | 4 | 2 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0007 | 0/0 | 1475 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0008 | 0/0 | 1475 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0009 | 0/0 | 1475 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0010 | 0/0 | 1475 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0011 | 0/0 | 1475 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0012 | 0/0 | 1475 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0013 | 0/0 | 1475 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0014 | 0/0 | 1475 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0015 | 0/0 | 1475 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0016 | 0/0 | 1475 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0017 | 0/0 | 1475 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0018 | 0/0 | 1475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
a0019 | 0/0 | 1475 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | MASGA others(1470): Show |
chr6 | 17610037 | 17711925 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4425 | 67 | 17 | 10 | 35 | 1 | 4 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0001c0003 | 0/0 | 4425 | 43 | 0 | 7 | 30 | 0 | 6 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0001c0009 | 0/0 | 4425 | 7 | 7 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0001c0011 | 0/0 | 4425 | 5 | 5 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0001c0013 | 0/0 | 4425 | 3 | 0 | 0 | 3 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0001c0014 | 0/0 | 4425 | 2 | 2 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0001c0016 | 0/0 | 4425 | 2 | 0 | 2 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0001c0021 | 0/0 | 4425 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0001c0032 | 0/0 | 4425 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0002c0002 | 0/0 | 4425 | 52 | 10 | 1 | 39 | 0 | 2 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0002c0010 | 0/0 | 4425 | 7 | 5 | 1 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0003c0004 | 0/0 | 4425 | 30 | 19 | 3 | 4 | 2 | 2 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0003c0012 | 0/0 | 4425 | 4 | 1 | 2 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0003c0023 | 1/0 | 4425 | 1 | 0 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0003c0025 | 0/0 | 4425 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0004c0005 | 0/0 | 4425 | 29 | 2 | 10 | 11 | 4 | 2 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0005c0006 | 0/1 | 4425 | 19 | 1 | 4 | 10 | 1 | 2 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0005c0017 | 0/0 | 4425 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0006c0007 | 0/0 | 4425 | 18 | 4 | 7 | 1 | 4 | 2 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0006c0022 | 0/0 | 4425 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0007c0008 | 0/0 | 4425 | 9 | 9 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0008c0015 | 0/0 | 4425 | 2 | 1 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0009c0027 | 0/0 | 4425 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0010c0026 | 0/0 | 4425 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0011c0033 | 0/0 | 4425 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0012c0019 | 0/0 | 4425 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0013c0020 | 0/0 | 4425 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0014c0018 | 0/0 | 4425 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0015c0031 | 0/0 | 4425 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0016c0024 | 0/0 | 4425 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0017c0030 | 0/0 | 4425 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0018c0028 | 0/0 | 4425 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 | ||
a0019c0029 | 0/0 | 4425 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATGGC others(4420): Show |
chr6 | 17610037 | 17711925 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6026 | 54 | 11 | 10 | 29 | 1 | 3 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0001t0003 | 0/0 | 6027 | 6 | 2 | 0 | 3 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0001c0001t0007 | 0/0 | 6026 | 2 | 0 | 0 | 2 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0001t0009 | 0/0 | 6026 | 2 | 2 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0001t0013 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6010): Show |
chr6 | 17610037 | 17711925 |
a0001c0001t0017 | 0/0 | 6026 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0001t0018 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0003t0001 | 0/0 | 6026 | 34 | 0 | 7 | 21 | 0 | 6 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0003t0003 | 0/0 | 6027 | 5 | 0 | 0 | 5 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0001c0003t0008 | 0/0 | 6026 | 2 | 0 | 0 | 2 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0003t0019 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0003t0021 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0009t0001 | 0/0 | 6026 | 4 | 4 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0009t0003 | 0/0 | 6027 | 2 | 2 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0001c0009t0011 | 0/0 | 6026 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0011t0001 | 0/0 | 6026 | 4 | 4 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0011t0003 | 0/0 | 6027 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0001c0013t0001 | 0/0 | 6026 | 2 | 0 | 0 | 2 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0013t0003 | 0/0 | 6027 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0001c0014t0001 | 0/0 | 6026 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0014t0003 | 0/0 | 6027 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0001c0016t0001 | 0/0 | 6026 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0016t0003 | 0/0 | 6027 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0001c0021t0001 | 0/0 | 6026 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0001c0032t0001 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0002c0002t0001 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0002c0002t0002 | 0/0 | 6026 | 40 | 7 | 1 | 30 | 0 | 2 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0002c0002t0004 | 0/0 | 6027 | 6 | 3 | 0 | 3 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0002c0002t0005 | 0/0 | 6009 | 3 | 0 | 0 | 3 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6004): Show |
chr6 | 17610037 | 17711925 |
a0002c0002t0014 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0002c0002t0020 | 0/0 | 6009 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6004): Show |
chr6 | 17610037 | 17711925 |
a0002c0010t0001 | 0/0 | 6026 | 2 | 2 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0002c0010t0002 | 0/0 | 6026 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0002c0010t0003 | 0/0 | 6027 | 2 | 1 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0002c0010t0012 | 0/0 | 6027 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0002c0010t0015 | 0/0 | 6026 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0003c0004t0001 | 0/0 | 6026 | 27 | 19 | 2 | 2 | 2 | 2 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0003c0004t0003 | 0/0 | 6027 | 3 | 0 | 1 | 2 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0003c0012t0001 | 0/0 | 6026 | 4 | 1 | 2 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0003c0023t0001 | 1/0 | 6026 | 1 | 0 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0003c0025t0001 | 0/0 | 6026 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0004c0005t0001 | 0/0 | 6026 | 26 | 2 | 8 | 10 | 4 | 2 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0004c0005t0003 | 0/0 | 6027 | 2 | 0 | 2 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0004c0005t0016 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0005c0006t0001 | 0/1 | 6026 | 13 | 1 | 4 | 4 | 1 | 2 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0005c0006t0003 | 0/0 | 6027 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0005c0006t0006 | 0/0 | 6026 | 3 | 0 | 0 | 3 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0005c0006t0010 | 0/0 | 6027 | 2 | 0 | 0 | 2 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0005c0017t0003 | 0/0 | 6027 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0006c0007t0001 | 0/0 | 6026 | 18 | 4 | 7 | 1 | 4 | 2 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0006c0022t0001 | 0/0 | 6026 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0007c0008t0001 | 0/0 | 6026 | 8 | 8 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0007c0008t0003 | 0/0 | 6027 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0008c0015t0001 | 0/0 | 6026 | 2 | 1 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0009c0027t0001 | 0/0 | 6026 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0010c0026t0003 | 0/0 | 6027 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0011c0033t0001 | 0/0 | 6026 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0012c0019t0003 | 0/0 | 6027 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6022): Show |
chr6 | 17610037 | 17711925 |
a0013c0020t0001 | 0/0 | 6026 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0014c0018t0001 | 0/0 | 6026 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0015c0031t0001 | 0/0 | 6026 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0016c0024t0001 | 0/0 | 6026 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0017c0030t0001 | 0/0 | 6026 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0018c0028t0002 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
a0019c0029t0001 | 0/0 | 6026 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | ATTCT others(6021): Show |
chr6 | 17610037 | 17711925 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0009g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0009g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0013g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0017g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0001t0018g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0019g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0003t0021g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0009t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0009t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0009t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0009t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0009t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0009t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0009t0011g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0011t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0011t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0011t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0011t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0011t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0013t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0013t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0013t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0014t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0014t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0016t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0016t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0021t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0001c0032t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0014g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0002t0020g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0010t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0010t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0010t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0010t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0010t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0010t0012g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0002c0010t0015g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0004t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0012t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0012t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0012t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0012t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0023t0001g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0003c0025t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0004c0005t0016g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0293 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0006g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0006g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0006g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0010g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0006t0010g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0005c0017t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0007t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0006c0022t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0007c0008t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0007c0008t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0007c0008t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0007c0008t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0007c0008t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0007c0008t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0007c0008t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0007c0008t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0007c0008t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0008c0015t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0008c0015t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0009c0027t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0010c0026t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0011c0033t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0012c0019t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0013c0020t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0014c0018t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0015c0031t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0016c0024t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0017c0030t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0018c0028t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
a0019c0029t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0006 | c0007 | t0001 | g0259 | EUR | GBR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00099 | hp2 | a0005 | c0006 | t0001 | g0288 | EUR | GBR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00140 | hp1 | a0004 | c0005 | t0001 | g0064 | EUR | GBR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00140 | hp2 | a0006 | c0007 | t0001 | g0107 | EUR | GBR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00280 | hp1 | a0006 | c0007 | t0001 | g0120 | EUR | FIN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00280 | hp2 | a0004 | c0005 | t0001 | g0054 | EUR | FIN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00323 | hp1 | a0004 | c0005 | t0001 | g0073 | EUR | FIN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00323 | hp2 | a0003 | c0004 | t0001 | g0090 | EUR | FIN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00408 | hp1 | a0005 | c0006 | t0001 | g0281 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00408 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00438 | hp2 | a0002 | c0002 | t0004 | g0005 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00544 | hp1 | a0004 | c0005 | t0001 | g0066 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00609 | hp1 | a0001 | c0003 | t0001 | g0119 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00609 | hp2 | a0001 | c0003 | t0008 | g0129 | EAS | CHS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00639 | hp1 | a0005 | c0006 | t0001 | g0292 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0248 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00642 | hp2 | a0006 | c0007 | t0001 | g0108 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0137 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00735 | hp2 | a0008 | c0015 | t0001 | g0085 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0263 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00738 | hp2 | a0004 | c0005 | t0001 | g0065 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00741 | hp1 | a0006 | c0007 | t0001 | g0112 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG00741 | hp2 | a0004 | c0005 | t0003 | g0029 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01069 | hp1 | a0006 | c0007 | t0001 | g0110 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0142 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0150 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01074 | hp2 | a0004 | c0005 | t0001 | g0055 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0135 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01099 | hp2 | a0006 | c0007 | t0001 | g0109 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01109 | hp1 | a0003 | c0012 | t0001 | g0278 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01109 | hp2 | a0004 | c0005 | t0001 | g0061 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0131 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01175 | hp1 | a0004 | c0005 | t0003 | g0030 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01175 | hp2 | a0006 | c0007 | t0001 | g0261 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01192 | hp1 | a0004 | c0005 | t0001 | g0252 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01192 | hp2 | a0009 | c0027 | t0001 | g0306 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01243 | hp1 | a0005 | c0017 | t0003 | g0036 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01243 | hp2 | a0003 | c0012 | t0001 | g0279 | AMR | PUR | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01255 | hp1 | a0002 | c0010 | t0003 | g0008 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01255 | hp2 | a0001 | c0016 | t0001 | g0209 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01257 | hp2 | a0003 | c0025 | t0001 | g0301 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01358 | hp1 | a0010 | c0026 | t0003 | g0011 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01358 | hp2 | a0006 | c0007 | t0001 | g0189 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01361 | hp2 | a0001 | c0021 | t0001 | g0098 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0144 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01496 | hp1 | a0003 | c0004 | t0001 | g0295 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01496 | hp2 | a0001 | c0016 | t0003 | g0034 | AMR | CLM | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01517 | hp1 | a0004 | c0005 | t0001 | g0063 | EUR | IBS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01517 | hp2 | a0011 | c0033 | t0001 | g0140 | EUR | IBS | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01884 | hp1 | a0001 | c0009 | t0001 | g0139 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01884 | hp2 | a0003 | c0004 | t0001 | g0303 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01891 | hp1 | a0006 | c0007 | t0001 | g0105 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01928 | hp1 | a0004 | c0005 | t0001 | g0070 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01975 | hp1 | a0003 | c0004 | t0001 | g0092 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01975 | hp2 | a0004 | c0005 | t0001 | g0068 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01978 | hp1 | a0003 | c0004 | t0003 | g0009 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01978 | hp2 | a0012 | c0019 | t0003 | g0035 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01981 | hp1 | a0004 | c0005 | t0001 | g0072 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01993 | hp1 | a0005 | c0006 | t0001 | g0290 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG01993 | hp2 | a0006 | c0007 | t0001 | g0125 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02004 | hp1 | a0004 | c0005 | t0001 | g0071 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02004 | hp2 | a0005 | c0006 | t0001 | g0291 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02027 | hp1 | a0001 | c0001 | t0007 | g0178 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02027 | hp2 | a0003 | c0004 | t0003 | g0031 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02055 | hp1 | a0013 | c0020 | t0001 | g0191 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02055 | hp2 | a0001 | c0009 | t0001 | g0164 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02056 | hp2 | a0001 | c0001 | t0007 | g0266 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02071 | hp1 | a0006 | c0007 | t0001 | g0103 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02074 | hp2 | a0001 | c0003 | t0001 | g0104 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02080 | hp1 | a0001 | c0003 | t0001 | g0190 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02080 | hp2 | a0004 | c0005 | t0001 | g0057 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02135 | hp2 | a0003 | c0004 | t0003 | g0010 | EAS | KHV | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02145 | hp1 | a0007 | c0008 | t0003 | g0022 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02145 | hp2 | a0001 | c0009 | t0003 | g0016 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02165 | hp1 | a0002 | c0002 | t0005 | g0244 | EAS | CDX | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02257 | hp1 | a0006 | c0007 | t0001 | g0123 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02257 | hp2 | a0001 | c0001 | t0017 | g0116 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02258 | hp2 | a0007 | c0008 | t0001 | g0198 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02280 | hp1 | a0001 | c0011 | t0001 | g0042 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0308 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02293 | hp2 | a0005 | c0006 | t0001 | g0305 | AMR | PEL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0245 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02572 | hp1 | a0003 | c0004 | t0001 | g0079 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02572 | hp2 | a0003 | c0004 | t0001 | g0300 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02615 | hp1 | a0007 | c0008 | t0001 | g0202 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02615 | hp2 | a0001 | c0014 | t0003 | g0014 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02622 | hp1 | a0003 | c0004 | t0001 | g0083 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02622 | hp2 | a0006 | c0007 | t0001 | g0106 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02630 | hp1 | a0007 | c0008 | t0001 | g0201 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02630 | hp2 | a0002 | c0010 | t0001 | g0053 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02647 | hp1 | a0003 | c0004 | t0001 | g0256 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02647 | hp2 | a0003 | c0004 | t0001 | g0286 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02683 | hp1 | a0014 | c0018 | t0001 | g0282 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02683 | hp2 | a0006 | c0007 | t0001 | g0117 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0121 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02698 | hp2 | a0003 | c0004 | t0001 | g0094 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0249 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02735 | hp1 | a0015 | c0031 | t0001 | g0100 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02735 | hp2 | a0003 | c0012 | t0001 | g0275 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02738 | hp2 | a0004 | c0005 | t0001 | g0255 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02809 | hp1 | a0007 | c0008 | t0001 | g0204 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02809 | hp2 | a0002 | c0002 | t0002 | g0052 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02886 | hp1 | a0001 | c0011 | t0001 | g0089 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02886 | hp2 | a0003 | c0004 | t0001 | g0076 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02896 | hp2 | a0001 | c0009 | t0001 | g0161 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02897 | hp2 | a0007 | c0008 | t0001 | g0200 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02922 | hp1 | a0006 | c0007 | t0001 | g0113 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02922 | hp2 | a0003 | c0004 | t0001 | g0285 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02970 | hp1 | a0002 | c0002 | t0002 | g0250 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02970 | hp2 | a0002 | c0010 | t0003 | g0007 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02976 | hp1 | a0001 | c0011 | t0001 | g0088 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02976 | hp2 | a0001 | c0009 | t0001 | g0149 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0228 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03041 | hp1 | a0003 | c0004 | t0001 | g0075 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0251 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03139 | hp1 | a0006 | c0022 | t0001 | g0159 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03195 | hp1 | a0003 | c0004 | t0001 | g0257 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03195 | hp2 | a0003 | c0004 | t0001 | g0082 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0307 | AFR | MSL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03225 | hp2 | a0001 | c0011 | t0001 | g0041 | AFR | MSL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0134 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03239 | hp2 | a0005 | c0006 | t0001 | g0294 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03453 | hp1 | a0001 | c0014 | t0001 | g0118 | AFR | MSL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03453 | hp2 | a0001 | c0011 | t0003 | g0002 | AFR | MSL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0247 | AFR | MSL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03486 | hp2 | a0007 | c0008 | t0001 | g0203 | AFR | MSL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03516 | hp1 | a0016 | c0024 | t0001 | g0084 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03516 | hp2 | a0001 | c0009 | t0003 | g0017 | AFR | ESN | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03540 | hp1 | a0002 | c0010 | t0015 | g0274 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03540 | hp2 | a0003 | c0004 | t0001 | g0077 | AFR | GWD | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03579 | hp1 | a0003 | c0004 | t0001 | g0298 | AFR | MSL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03579 | hp2 | a0002 | c0002 | t0004 | g0026 | AFR | MSL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03654 | hp1 | a0017 | c0030 | t0001 | g0138 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0051 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0132 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03704 | hp1 | a0003 | c0004 | t0001 | g0302 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03704 | hp2 | a0006 | c0007 | t0001 | g0127 | SAS | PJL | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0143 | SAS | BEB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG04184 | hp1 | a0004 | c0005 | t0001 | g0039 | SAS | BEB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG04184 | hp2 | a0001 | c0003 | t0001 | g0262 | SAS | BEB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18522 | hp1 | a0003 | c0004 | t0001 | g0297 | AFR | YRI | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18612 | hp1 | a0004 | c0005 | t0001 | g0060 | EAS | CHB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18612 | hp2 | a0005 | c0006 | t0006 | g0313 | EAS | CHB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18747 | hp1 | a0003 | c0004 | t0001 | g0093 | EAS | CHB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18747 | hp2 | a0001 | c0003 | t0008 | g0128 | EAS | CHB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18906 | hp2 | a0007 | c0008 | t0001 | g0197 | AFR | YRI | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0192 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0133 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18946 | hp1 | a0004 | c0005 | t0001 | g0062 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18949 | hp1 | a0002 | c0010 | t0012 | g0004 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18949 | hp2 | a0001 | c0003 | t0003 | g0025 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18950 | hp2 | a0001 | c0013 | t0003 | g0023 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18951 | hp2 | a0003 | c0004 | t0001 | g0091 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18952 | hp2 | a0005 | c0006 | t0006 | g0314 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18953 | hp1 | a0005 | c0006 | t0003 | g0037 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18953 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18956 | hp2 | a0001 | c0003 | t0003 | g0024 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18957 | hp2 | a0002 | c0002 | t0014 | g0213 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18960 | hp1 | a0004 | c0005 | t0016 | g0212 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18960 | hp2 | a0001 | c0032 | t0001 | g0205 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18962 | hp1 | a0004 | c0005 | t0001 | g0056 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18962 | hp2 | a0001 | c0003 | t0021 | g0316 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18966 | hp1 | a0002 | c0002 | t0005 | g0237 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18968 | hp1 | a0005 | c0006 | t0006 | g0312 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18971 | hp2 | a0004 | c0005 | t0001 | g0253 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18978 | hp1 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18980 | hp2 | a0005 | c0006 | t0001 | g0289 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18982 | hp2 | a0005 | c0006 | t0001 | g0287 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18983 | hp2 | a0001 | c0013 | t0001 | g0206 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0126 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18984 | hp2 | a0002 | c0002 | t0005 | g0229 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0271 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18994 | hp2 | a0005 | c0006 | t0001 | g0304 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18998 | hp1 | a0004 | c0005 | t0001 | g0074 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18999 | hp1 | a0004 | c0005 | t0001 | g0058 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA18999 | hp2 | a0002 | c0002 | t0020 | g0315 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19000 | hp1 | a0001 | c0003 | t0001 | g0208 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19002 | hp1 | a0001 | c0003 | t0003 | g0032 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19005 | hp2 | a0004 | c0005 | t0001 | g0067 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19009 | hp1 | a0001 | c0003 | t0003 | g0015 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19009 | hp2 | a0001 | c0001 | t0018 | g0195 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19011 | hp1 | a0018 | c0028 | t0002 | g0239 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19030 | hp1 | a0002 | c0002 | t0004 | g0027 | AFR | LWK | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19030 | hp2 | a0001 | c0001 | t0013 | g0038 | AFR | LWK | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19043 | hp1 | a0007 | c0008 | t0001 | g0199 | AFR | LWK | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19043 | hp2 | a0003 | c0004 | t0001 | g0284 | AFR | LWK | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19054 | hp1 | a0001 | c0003 | t0019 | g0309 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19056 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19058 | hp2 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19062 | hp2 | a0005 | c0006 | t0010 | g0311 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19074 | hp1 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19078 | hp1 | a0005 | c0006 | t0010 | g0310 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19080 | hp1 | a0004 | c0005 | t0001 | g0059 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0124 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19085 | hp2 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19089 | hp1 | a0001 | c0003 | t0001 | g0272 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19091 | hp2 | a0001 | c0013 | t0001 | g0273 | EAS | JPT | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19240 | hp1 | a0003 | c0004 | t0001 | g0081 | AFR | YRI | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA19240 | hp2 | a0001 | c0009 | t0011 | g0001 | AFR | YRI | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ASW | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA20129 | hp2 | a0004 | c0005 | t0001 | g0069 | AFR | ASW | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA20752 | hp1 | a0006 | c0007 | t0001 | g0115 | EUR | TSI | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA20752 | hp2 | a0019 | c0029 | t0001 | g0276 | EUR | TSI | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA20805 | hp2 | a0003 | c0004 | t0001 | g0211 | EUR | TSI | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA20905 | hp1 | a0001 | c0003 | t0001 | g0122 | SAS | GIH | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA20905 | hp2 | a0005 | c0006 | t0001 | g0283 | SAS | GIH | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02109 | hp1 | a0002 | c0002 | t0004 | g0028 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02486 | hp1 | a0002 | c0010 | t0001 | g0254 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02486 | hp2 | a0003 | c0004 | t0001 | g0080 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02559 | hp1 | a0003 | c0004 | t0001 | g0296 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG02559 | hp2 | a0002 | c0010 | t0002 | g0220 | AFR | ACB | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG06807 | hp1 | a0005 | c0006 | t0001 | g0280 | AFR | USA | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
HG06807 | hp2 | a0003 | c0012 | t0001 | g0277 | AFR | USA | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA20300 | hp1 | a0004 | c0005 | t0001 | g0087 | AFR | USA | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA20300 | hp2 | a0008 | c0015 | t0001 | g0086 | AFR | USA | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0246 | AFR | LWK | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
NA21309 | hp2 | a0003 | c0004 | t0001 | g0299 | AFR | LWK | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
homoSapiens | chm13v2 | a0005 | c0006 | t0001 | g0293 | REF | REF | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
homoSapiens | grch38p0 | a0003 | c0023 | t0001 | g0078 | REF | REF | NUP153_chr6_17610037_17711925 | NUP153 | chr6 | 17610037 | 17711925 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:17624573 | T | C | 1 | a0007 | 9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
missense_variant | MODERATE | c.4162A>G | p.Thr1388Ala | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/22 | 4700/6026 | 4162/4428 | 1388/1475 | chr6 | 17624573 | |||
chr6:17625841 | C | T | 1 | a0013 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.3868G>A | p.Gly1290Ser | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 19/22 | 4406/6026 | 3868/4428 | 1290/1475 | chr6 | 17625841 | |||
chr6:17626068 | C | T | 1 | a0008 | 2 | HG00735.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.3641G>A | p.Ser1214Asn | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 19/22 | 4179/6026 | 3641/4428 | 1214/1475 | chr6 | 17626068 | |||
chr6:17626105 | T | C | 1 | a0008 | 2 | HG00735.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.3604A>G | p.Thr1202Ala | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 19/22 | 4142/6026 | 3604/4428 | 1202/1475 | chr6 | 17626105 | |||
chr6:17628786 | G | A | 1 | a0018 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.3413C>T | p.Ser1138Leu | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/22 | 3951/6026 | 3413/4428 | 1138/1475 | chr6 | 17628786 | |||
chr6:17629053 | T | C | 1 | a0015 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.3146A>G | p.Asn1049Ser | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/22 | 3684/6026 | 3146/4428 | 1049/1475 | chr6 | 17629053 | |||
chr6:17629218 | G | C | 1 | a0011 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.2981C>G | p.Ser994Cys | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/22 | 3519/6026 | 2981/4428 | 994/1475 | chr6 | 17629218 | |||
chr6:17629398 | A | G | 1 | a0014 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.2801T>C | p.Ile934Thr | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/22 | 3339/6026 | 2801/4428 | 934/1475 | chr6 | 17629398 | |||
chr6:17632802 | G | C | 1 | a0006 | 19 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(16): Show |
missense_variant | MODERATE | c.2507C>G | p.Ser836Cys | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/22 | 3045/6026 | 2507/4428 | 836/1475 | chr6 | 17632802 | |||
chr6:17632830 | C | T | 12 | a0001 a0002 a0004 others(9): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
missense_variant | MODERATE | c.2479G>A | p.Ala827Thr | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/22 | 3017/6026 | 2479/4428 | 827/1475 | chr6 | 17632830 | |||
chr6:17637155 | G | A | 1 | a0008 | 2 | HG00735.hp2 NA20300.hp2 |
missense_variant&splice_region_variant | MODERATE | c.2462C>T | p.Pro821Leu | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/22 | 3000/6026 | 2462/4428 | 821/1475 | chr6 | 17637155 | |||
chr6:17637335 | G | C | 1 | a0019 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.2282C>G | p.Thr761Arg | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/22 | 2820/6026 | 2282/4428 | 761/1475 | chr6 | 17637335 | |||
chr6:17637419 | A | G | 1 | a0017 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.2198T>C | p.Val733Ala | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/22 | 2736/6026 | 2198/4428 | 733/1475 | chr6 | 17637419 | |||
chr6:17639956 | T | G | 1 | a0016 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.1829A>C | p.Asp610Ala | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/22 | 2367/6026 | 1829/4428 | 610/1475 | chr6 | 17639956 | |||
chr6:17649242 | G | A | 1 | a0010 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1454C>T | p.Pro485Leu | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/22 | 1992/6026 | 1454/4428 | 485/1475 | chr6 | 17649242 | |||
chr6:17662030 | T | G | 1 | a0009 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.1256A>C | p.Glu419Ala | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 10/22 | 1794/6026 | 1256/4428 | 419/1475 | chr6 | 17662030 | |||
chr6:17665248 | G | C | 4 | a0002 a0004 a0007 others(1): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
missense_variant | MODERATE | c.1206C>G | p.Asn402Lys | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/22 | 1744/6026 | 1206/4428 | 402/1475 | chr6 | 17665248 | |||
chr6:17675015 | T | C | 3 | a0004 a0012 a0014 |
31 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(28): Show |
missense_variant | MODERATE | c.742A>G | p.Ile248Val | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/22 | 1280/6026 | 742/4428 | 248/1475 | chr6 | 17675015 | |||
chr6:17688462 | C | T | 3 | a0005 a0012 a0014 |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
missense_variant | MODERATE | c.268G>A | p.Asp90Asn | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/22 | 806/6026 | 268/4428 | 90/1475 | chr6 | 17688462 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:17624715 | G | A | 1 | a0001c0021 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.4020C>T | p.Gly1340Gly | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/22 | 4558/6026 | 4020/4428 | 1340/1475 | chr6 | 17624715 | |||
chr6:17625842 | G | A | 2 | a0001c0013 a0001c0032 |
4 | NA18950.hp2 NA18960.hp2 NA18983.hp2 others(1): Show |
synonymous_variant | LOW | c.3867C>T | p.Phe1289Phe | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 19/22 | 4405/6026 | 3867/4428 | 1289/1475 | chr6 | 17625842 | |||
chr6:17626022 | T | G | 1 | a0001c0014 | 2 | HG02615.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.3687A>C | p.Gly1229Gly | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 19/22 | 4225/6026 | 3687/4428 | 1229/1475 | chr6 | 17626022 | |||
chr6:17628860 | A | G | 1 | a0011c0033 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.3339T>C | p.Ser1113Ser | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/22 | 3877/6026 | 3339/4428 | 1113/1475 | chr6 | 17628860 | |||
chr6:17628941 | G | A | 1 | a0007c0008 | 9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
synonymous_variant | LOW | c.3258C>T | p.Asn1086Asn | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/22 | 3796/6026 | 3258/4428 | 1086/1475 | chr6 | 17628941 | |||
chr6:17629082 | T | A | 1 | a0001c0032 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.3117A>T | p.Ile1039Ile | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/22 | 3655/6026 | 3117/4428 | 1039/1475 | chr6 | 17629082 | |||
chr6:17629385 | G | A | 29 | a0001c0001 a0001c0003 a0001c0009 others(26): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
synonymous_variant | LOW | c.2814C>T | p.Ser938Ser | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/22 | 3352/6026 | 2814/4428 | 938/1475 | chr6 | 17629385 | |||
chr6:17637727 | G | A | 1 | a0001c0009 | 7 | HG01884.hp1 HG02055.hp2 HG02145.hp2 others(4): Show |
synonymous_variant | LOW | c.1890C>T | p.Thr630Thr | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/22 | 2428/6026 | 1890/4428 | 630/1475 | chr6 | 17637727 | |||
chr6:17639985 | T | G | 1 | a0003c0025 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.1800A>C | p.Ala600Ala | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/22 | 2338/6026 | 1800/4428 | 600/1475 | chr6 | 17639985 | |||
chr6:17669502 | T | C | 1 | a0005c0017 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.897A>G | p.Gln299Gln | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 6/22 | 1435/6026 | 897/4428 | 299/1475 | chr6 | 17669502 | |||
chr6:17675322 | T | C | 2 | a0003c0012 a0019c0029 |
5 | HG01109.hp1 HG01243.hp2 HG02735.hp2 others(2): Show |
synonymous_variant | LOW | c.630A>G | p.Pro210Pro | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 4/22 | 1168/6026 | 630/4428 | 210/1475 | chr6 | 17675322 | |||
chr6:17688463 | G | A | 1 | a0001c0016 | 2 | HG01255.hp2 HG01496.hp2 |
synonymous_variant | LOW | c.267C>T | p.Ala89Ala | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/22 | 805/6026 | 267/4428 | 89/1475 | chr6 | 17688463 | |||
chr6:17688567 | G | A | 8 | a0001c0003 a0001c0013 a0001c0016 others(5): Show |
70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
synonymous_variant | LOW | c.163C>T | p.Leu55Leu | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/22 | 701/6026 | 163/4428 | 55/1475 | chr6 | 17688567 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:17615272 | A | T | 1 | a0001c0003t0008 | 2 | HG00609.hp2 NA18747.hp2 |
3_prime_UTR_variant | MODIFIER | c.*825T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 22/22 | 825 | chr6 | 17615272 | ||||||
chr6:17615558 | A | G | 1 | a0004c0005t0016 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*539T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 22/22 | 539 | chr6 | 17615558 | ||||||
chr6:17615572 | C | A | 1 | a0001c0001t0017 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*525G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 22/22 | 525 | chr6 | 17615572 | ||||||
chr6:17615599 | C | T | 1 | a0001c0001t0007 | 2 | HG02027.hp1 HG02056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*498G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 22/22 | 498 | chr6 | 17615599 | ||||||
chr6:17615630 | C | T | 1 | a0002c0010t0015 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 22/22 | 467 | chr6 | 17615630 | ||||||
chr6:17615671 | T | C | 2 | a0002c0002t0014 a0002c0010t0012 |
2 | NA18949.hp1 NA18957.hp2 |
3_prime_UTR_variant | MODIFIER | c.*426A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 22/22 | 426 | chr6 | 17615671 | ||||||
chr6:17615672 | CTCTAATC others(10): Show |
C | 2 | a0002c0002t0005 a0002c0002t0020 |
4 | HG02165.hp1 NA18966.hp1 NA18984.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*408_*424delATTCTG others(11): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 22/22 | 408 | chr6 | 17615672 | ||||||
chr6:17616025 | C | T | 8 | a0002c0002t0002 a0002c0002t0004 a0002c0002t0005 others(5): Show |
54 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*72G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 22/22 | 72 | chr6 | 17616025 | ||||||
chr6:17616060 | G | C | 1 | a0001c0001t0018 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*37C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 22/22 | 37 | chr6 | 17616060 | ||||||
chr6:17706424 | AAGGGGGC others(5): Show |
A | 1 | a0001c0001t0013 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-49_-38delCTCCCGCC others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/22 | 38 | chr6 | 17706424 | ||||||
chr6:17706431 | C | G | 1 | a0001c0001t0001 | 1 | HG01928.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/22 | 44 | chr6 | 17706431 | ||||||
chr6:17706432 | G | C | 1 | a0001c0001t0001 | 1 | HG01928.hp2 | 5_prime_UTR_variant | MODIFIER | c.-45C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/22 | 45 | chr6 | 17706432 | ||||||
chr6:17706545 | T | G | 1 | a0001c0001t0009 | 2 | HG02280.hp2 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-158A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/22 | 158 | chr6 | 17706545 | ||||||
chr6:17706587 | A | AG | 19 | a0001c0001t0003 a0001c0001t0013 a0001c0003t0003 others(16): Show |
39 | HG00438.hp2 HG00597.hp2 HG00741.hp2 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-201dupC | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/22 | 201 | chr6 | 17706587 | ||||||
chr6:17706610 | G | C | 1 | a0001c0003t0019 | 1 | NA19054.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-223C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/22 | chr6 | 17706610 | |||||||
chr6:17706648 | C | T | 1 | a0001c0009t0011 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-261G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/22 | 261 | chr6 | 17706648 | ||||||
chr6:17706682 | C | A | 2 | a0005c0006t0006 a0005c0006t0010 |
5 | NA18612.hp2 NA18952.hp2 NA18968.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-295G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/22 | chr6 | 17706682 | |||||||
chr6:17706869 | G | A | 1 | a0002c0002t0020 | 1 | NA18999.hp2 | 5_prime_UTR_variant | MODIFIER | c.-482C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/22 | 482 | chr6 | 17706869 | ||||||
chr6:17706894 | C | A | 1 | a0001c0003t0021 | 1 | NA18962.hp2 | 5_prime_UTR_variant | MODIFIER | c.-507G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/22 | 507 | chr6 | 17706894 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:17616262 | C | G | 312 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(309): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.4344-81G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 21/21 | chr6 | 17616262 | |||||||
chr6:17616282 | T | TG | 148 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0102 others(145): Show |
148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.4344-102dupC | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 21/21 | chr6 | 17616282 | |||||||
chr6:17616283 | G | T | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4344-102C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 21/21 | chr6 | 17616283 | |||||||
chr6:17616284 | G | GC | 3 | a0003c0004t0001g0079 a0006c0007t0001g0113 a0006c0022t0001g0159 |
3 | HG02572.hp1 HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4344-104_4344-103i others(3): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 21/21 | chr6 | 17616284 | |||||||
chr6:17616325 | C | T | 190 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(187): Show |
190 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.4344-144G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 21/21 | chr6 | 17616325 | |||||||
chr6:17616438 | G | A | 1 | a0012c0019t0003g0035 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4343+89C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 21/21 | chr6 | 17616438 | |||||||
chr6:17616702 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
splice_region_variant&intron_variant | LOW | c.4175-7A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17616702 | |||||||
chr6:17616745 | TTTTG | T | 4 | a0001c0001t0009g0307 a0001c0001t0009g0308 a0004c0005t0001g0069 others(1): Show |
4 | HG02280.hp2 HG03209.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.4175-54_4175-51del others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17616745 | |||||||
chr6:17616781 | G | A | 55 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(52): Show |
55 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4175-86C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17616781 | |||||||
chr6:17616979 | T | G | 1 | a0002c0010t0015g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4175-284A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17616979 | |||||||
chr6:17617029 | G | A | 1 | a0003c0012t0001g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4175-334C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17617029 | |||||||
chr6:17617044 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4175-349G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17617044 | |||||||
chr6:17617384 | C | G | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.4175-689G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17617384 | |||||||
chr6:17617465 | T | TA | 141 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(138): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.4175-771dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17617465 | |||||||
chr6:17617465 | T | TAA | 11 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0153 others(8): Show |
11 | HG01167.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.4175-772_4175-771d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17617465 | |||||||
chr6:17617465 | TA | T | 19 | a0002c0002t0002g0046 a0002c0002t0002g0051 a0002c0002t0002g0215 others(16): Show |
19 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.4175-771delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17617465 | |||||||
chr6:17617549 | G | C | 1 | a0006c0022t0001g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4175-854C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17617549 | |||||||
chr6:17617572 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.4175-877C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17617572 | |||||||
chr6:17617621 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4175-926G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17617621 | |||||||
chr6:17617716 | G | A | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4175-1021C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17617716 | |||||||
chr6:17617784 | G | A | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.4175-1089C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17617784 | |||||||
chr6:17618011 | G | A | 54 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(51): Show |
54 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.4175-1316C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618011 | |||||||
chr6:17618022 | A | G | 6 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(3): Show |
6 | HG01496.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.4175-1327T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618022 | |||||||
chr6:17618089 | T | C | 1 | a0002c0010t0001g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4175-1394A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618089 | |||||||
chr6:17618274 | C | T | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.4175-1579G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618274 | |||||||
chr6:17618275 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4175-1580C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618275 | |||||||
chr6:17618292 | C | A | 253 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(250): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.4175-1597G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618292 | |||||||
chr6:17618393 | C | T | 1 | a0002c0010t0001g0254 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4175-1698G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618393 | |||||||
chr6:17618459 | G | T | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4175-1764C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618459 | |||||||
chr6:17618527 | T | C | 1 | a0001c0003t0001g0131 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4175-1832A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618527 | |||||||
chr6:17618560 | CTCTTTT | C | 28 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0056 others(25): Show |
28 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.4175-1871_4175-186 others(10): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618560 | |||||||
chr6:17618562 | CT | C | 64 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(61): Show |
64 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.4175-1868delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618562 | |||||||
chr6:17618562 | CTT | C | 152 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(149): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.4175-1869_4175-186 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618562 | |||||||
chr6:17618562 | CTTT | C | 57 | a0001c0001t0001g0169 a0001c0001t0001g0179 a0001c0003t0001g0121 others(54): Show |
57 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.4175-1870_4175-186 others(7): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618562 | |||||||
chr6:17618564 | T | C | 4 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0089 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4175-1869A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618564 | |||||||
chr6:17618565 | T | C | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(12): Show |
15 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.4175-1870A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618565 | |||||||
chr6:17618566 | T | C | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4175-1871A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618566 | |||||||
chr6:17618667 | G | A | 29 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0055 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.4175-1972C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618667 | |||||||
chr6:17618670 | A | G | 10 | a0002c0002t0002g0216 a0002c0002t0002g0217 a0002c0002t0002g0218 others(7): Show |
10 | HG00558.hp1 HG02135.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.4175-1975T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618670 | |||||||
chr6:17618756 | T | C | 3 | a0003c0004t0001g0080 a0005c0006t0006g0314 a0005c0006t0010g0310 |
3 | HG02486.hp2 NA18952.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.4175-2061A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618756 | |||||||
chr6:17618761 | T | C | 1 | a0007c0008t0001g0202 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4175-2066A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618761 | |||||||
chr6:17618773 | A | C | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4175-2078T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618773 | |||||||
chr6:17618777 | A | G | 2 | a0002c0002t0002g0221 a0002c0002t0002g0224 |
2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4175-2082T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618777 | |||||||
chr6:17618781 | T | C | 1 | a0002c0002t0002g0227 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4175-2086A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618781 | |||||||
chr6:17618791 | A | C | 2 | a0002c0002t0005g0237 a0002c0010t0001g0053 |
2 | HG02630.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.4175-2096T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618791 | |||||||
chr6:17618791 | A | G | 1 | a0006c0007t0001g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4175-2096T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618791 | |||||||
chr6:17618808 | T | C | 3 | a0004c0005t0001g0063 a0004c0005t0001g0064 a0004c0005t0001g0065 |
3 | HG00140.hp1 HG00738.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4175-2113A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618808 | |||||||
chr6:17618812 | C | T | 1 | a0003c0012t0001g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4175-2117G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618812 | |||||||
chr6:17618855 | T | C | 3 | a0002c0010t0001g0053 a0002c0010t0003g0007 a0002c0010t0003g0008 |
3 | HG01255.hp1 HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.4175-2160A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618855 | |||||||
chr6:17618954 | A | G | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.4175-2259T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17618954 | |||||||
chr6:17619041 | G | A | 1 | a0006c0007t0001g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4175-2346C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17619041 | |||||||
chr6:17619088 | T | C | 55 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(52): Show |
55 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4175-2393A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17619088 | |||||||
chr6:17619153 | G | T | 8 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4175-2458C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17619153 | |||||||
chr6:17619510 | A | T | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.4175-2815T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17619510 | |||||||
chr6:17619513 | C | T | 4 | a0003c0004t0001g0081 a0003c0004t0001g0082 a0003c0004t0001g0083 others(1): Show |
4 | HG02622.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4175-2818G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17619513 | |||||||
chr6:17619533 | G | C | 2 | a0003c0004t0001g0093 a0003c0004t0003g0010 |
2 | HG02135.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.4175-2838C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17619533 | |||||||
chr6:17619627 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4175-2932T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17619627 | |||||||
chr6:17619959 | G | T | 1 | a0002c0002t0004g0005 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4175-3264C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17619959 | |||||||
chr6:17620071 | C | T | 3 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0003g0002 |
3 | HG02280.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4175-3376G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620071 | |||||||
chr6:17620095 | C | CA | 59 | a0001c0001t0001g0096 a0001c0001t0001g0152 a0001c0001t0001g0154 others(56): Show |
59 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.4175-3401dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620095 | |||||||
chr6:17620095 | C | CAA | 17 | a0001c0001t0003g0021 a0001c0001t0009g0307 a0001c0001t0009g0308 others(14): Show |
17 | HG00140.hp2 HG00280.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.4175-3402_4175-340 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620095 | |||||||
chr6:17620095 | CA | C | 53 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0003t0001g0132 others(50): Show |
53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.4175-3401delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620095 | |||||||
chr6:17620095 | CAA | C | 53 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(50): Show |
53 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.4175-3402_4175-340 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620095 | |||||||
chr6:17620095 | CAAA | C | 7 | a0002c0002t0002g0048 a0002c0002t0002g0052 a0002c0002t0002g0215 others(4): Show |
7 | HG02559.hp2 HG02809.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.4175-3403_4175-340 others(7): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620095 | |||||||
chr6:17620095 | CAAAAAAA others(3): Show |
C | 56 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0101 others(53): Show |
56 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.4175-3410_4175-340 others(14): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620095 | |||||||
chr6:17620095 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0102 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4175-3411_4175-340 others(15): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620095 | |||||||
chr6:17620124 | A | G | 2 | a0003c0012t0001g0277 a0003c0012t0001g0279 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4175-3429T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620124 | |||||||
chr6:17620230 | C | T | 1 | a0001c0003t0021g0316 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.4175-3535G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620230 | |||||||
chr6:17620231 | T | C | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.4175-3536A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620231 | |||||||
chr6:17620713 | T | C | 17 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(14): Show |
17 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.4174+3848A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620713 | |||||||
chr6:17620740 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4174+3821C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620740 | |||||||
chr6:17620777 | A | C | 4 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(1): Show |
4 | HG02145.hp1 HG02258.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.4174+3784T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620777 | |||||||
chr6:17620797 | C | T | 1 | a0003c0012t0001g0275 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4174+3764G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17620797 | |||||||
chr6:17621008 | C | G | 1 | a0003c0004t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4174+3553G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17621008 | |||||||
chr6:17621014 | CAAAACA | C | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.4174+3541_4174+354 others(10): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17621014 | |||||||
chr6:17621131 | T | C | 1 | a0002c0002t0002g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4174+3430A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17621131 | |||||||
chr6:17621467 | C | T | 1 | a0002c0002t0002g0230 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4174+3094G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17621467 | |||||||
chr6:17621474 | A | G | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.4174+3087T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17621474 | |||||||
chr6:17621584 | T | G | 2 | a0001c0014t0001g0118 a0001c0014t0003g0014 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4174+2977A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17621584 | |||||||
chr6:17621612 | T | C | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.4174+2949A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17621612 | |||||||
chr6:17621748 | G | T | 4 | a0002c0002t0002g0052 a0002c0002t0002g0247 a0002c0002t0002g0248 others(1): Show |
4 | HG00642.hp1 HG02809.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4174+2813C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17621748 | |||||||
chr6:17621785 | AGAGTT | A | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.4174+2771_4174+277 others(9): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17621785 | |||||||
chr6:17622141 | C | A | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.4174+2420G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17622141 | |||||||
chr6:17622240 | G | A | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4174+2321C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17622240 | |||||||
chr6:17622289 | A | C | 1 | a0006c0007t0001g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4174+2272T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17622289 | |||||||
chr6:17622403 | A | G | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4174+2158T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17622403 | |||||||
chr6:17622443 | C | T | 1 | a0001c0032t0001g0205 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.4174+2118G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17622443 | |||||||
chr6:17622486 | T | G | 1 | a0002c0002t0002g0235 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.4174+2075A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17622486 | |||||||
chr6:17622614 | A | C | 1 | a0005c0017t0003g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4174+1947T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17622614 | |||||||
chr6:17622691 | A | AT | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.4174+1869dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17622691 | |||||||
chr6:17623022 | T | C | 2 | a0003c0004t0001g0080 a0003c0004t0001g0257 |
2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4174+1539A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623022 | |||||||
chr6:17623042 | A | C | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4174+1519T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623042 | |||||||
chr6:17623062 | G | A | 57 | a0001c0009t0003g0017 a0002c0002t0001g0222 a0002c0002t0002g0046 others(54): Show |
57 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.4174+1499C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623062 | |||||||
chr6:17623129 | C | CA | 29 | a0001c0001t0001g0163 a0001c0001t0009g0307 a0001c0001t0009g0308 others(26): Show |
29 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.4174+1431dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623129 | |||||||
chr6:17623309 | T | A | 5 | a0005c0006t0006g0312 a0005c0006t0006g0313 a0005c0006t0006g0314 others(2): Show |
5 | NA18612.hp2 NA18952.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.4174+1252A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623309 | |||||||
chr6:17623332 | C | T | 2 | a0003c0004t0001g0080 a0003c0004t0001g0257 |
2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4174+1229G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623332 | |||||||
chr6:17623357 | C | CA | 16 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(13): Show |
16 | HG01109.hp1 HG01891.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.4174+1203dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623357 | |||||||
chr6:17623357 | CA | C | 166 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(163): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.4174+1203delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623357 | |||||||
chr6:17623357 | CAA | C | 8 | a0001c0003t0001g0119 a0001c0003t0001g0131 a0001c0003t0008g0128 others(5): Show |
8 | HG00609.hp1 HG00609.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.4174+1202_4174+120 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623357 | |||||||
chr6:17623793 | T | A | 1 | a0005c0006t0001g0292 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4174+768A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623793 | |||||||
chr6:17623802 | G | A | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.4174+759C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623802 | |||||||
chr6:17623829 | C | A | 289 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.4174+732G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17623829 | |||||||
chr6:17624169 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4174+392T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17624169 | |||||||
chr6:17624204 | C | G | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.4174+357G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17624204 | |||||||
chr6:17624399 | G | T | 2 | a0002c0002t0002g0221 a0002c0002t0002g0224 |
2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4174+162C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17624399 | |||||||
chr6:17624420 | C | A | 2 | a0001c0011t0001g0088 a0001c0011t0001g0089 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4174+141G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 20/21 | chr6 | 17624420 | |||||||
chr6:17624945 | T | C | 1 | a0002c0002t0002g0218 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.3902-112A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 19/21 | chr6 | 17624945 | |||||||
chr6:17624986 | T | C | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.3902-153A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 19/21 | chr6 | 17624986 | |||||||
chr6:17625434 | G | A | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3901+374C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 19/21 | chr6 | 17625434 | |||||||
chr6:17625566 | A | G | 1 | a0001c0003t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3901+242T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 19/21 | chr6 | 17625566 | |||||||
chr6:17625705 | C | T | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.3901+103G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 19/21 | chr6 | 17625705 | |||||||
chr6:17625708 | C | T | 16 | a0001c0001t0001g0099 a0001c0001t0001g0168 a0001c0001t0001g0171 others(13): Show |
16 | HG00544.hp2 HG01257.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.3901+100G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 19/21 | chr6 | 17625708 | |||||||
chr6:17626250 | T | C | 1 | a0002c0010t0015g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3545-86A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17626250 | |||||||
chr6:17626330 | T | C | 1 | a0007c0008t0001g0202 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3545-166A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17626330 | |||||||
chr6:17626365 | C | G | 3 | a0003c0012t0001g0275 a0003c0012t0001g0279 a0019c0029t0001g0276 |
3 | HG01243.hp2 HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3545-201G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17626365 | |||||||
chr6:17626820 | C | T | 1 | a0004c0005t0001g0068 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3545-656G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17626820 | |||||||
chr6:17626822 | A | G | 1 | a0001c0003t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3545-658T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17626822 | |||||||
chr6:17627186 | A | G | 2 | a0003c0004t0001g0080 a0003c0004t0001g0257 |
2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3545-1022T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17627186 | |||||||
chr6:17627203 | G | A | 6 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(3): Show |
6 | HG01167.hp2 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3545-1039C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17627203 | |||||||
chr6:17627257 | T | C | 1 | a0004c0005t0001g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3545-1093A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17627257 | |||||||
chr6:17627258 | G | A | 1 | a0001c0003t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3545-1094C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17627258 | |||||||
chr6:17627263 | T | C | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.3545-1099A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17627263 | |||||||
chr6:17627359 | T | C | 148 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(145): Show |
148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.3545-1195A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17627359 | |||||||
chr6:17627485 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3544+1170C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17627485 | |||||||
chr6:17627544 | G | A | 1 | a0005c0006t0001g0290 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3544+1111C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17627544 | |||||||
chr6:17627601 | T | C | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.3544+1054A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17627601 | |||||||
chr6:17627654 | C | T | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.3544+1001G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17627654 | |||||||
chr6:17627964 | C | T | 1 | a0002c0010t0001g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3544+691G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17627964 | |||||||
chr6:17628088 | G | T | 1 | a0006c0007t0001g0115 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3544+567C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628088 | |||||||
chr6:17628089 | C | T | 1 | a0006c0007t0001g0115 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3544+566G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628089 | |||||||
chr6:17628153 | G | A | 1 | a0006c0007t0001g0123 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3544+502C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628153 | |||||||
chr6:17628208 | G | A | 2 | a0001c0014t0001g0118 a0001c0014t0003g0014 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3544+447C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628208 | |||||||
chr6:17628251 | G | A | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.3544+404C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628251 | |||||||
chr6:17628319 | G | A | 1 | a0003c0012t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3544+336C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628319 | |||||||
chr6:17628444 | T | C | 1 | a0003c0004t0001g0284 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3544+211A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628444 | |||||||
chr6:17628595 | T | TAAAACGA others(380): Show |
1 | a0001c0001t0001g0181 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3544+59_3544+60ins others(387): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628595 | |||||||
chr6:17628610 | T | TA | 229 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(226): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.3544+44dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628610 | |||||||
chr6:17628610 | T | TAA | 42 | a0001c0001t0007g0266 a0002c0002t0002g0050 a0002c0002t0002g0228 others(39): Show |
42 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.3544+43_3544+44dup others(2): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628610 | |||||||
chr6:17628619 | A | AT | 29 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(26): Show |
29 | HG00735.hp2 HG01109.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.3544+35_3544+36ins others(1): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628619 | |||||||
chr6:17628622 | T | A | 13 | a0001c0001t0001g0184 a0002c0010t0001g0053 a0002c0010t0001g0254 others(10): Show |
13 | HG01255.hp1 HG01928.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.3544+33A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 18/21 | chr6 | 17628622 | |||||||
chr6:17629558 | C | T | 1 | a0002c0002t0002g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2660-19G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17629558 | |||||||
chr6:17629768 | G | C | 2 | a0001c0014t0001g0118 a0001c0014t0003g0014 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2660-229C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17629768 | |||||||
chr6:17629964 | A | T | 10 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(7): Show |
10 | HG01167.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2660-425T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17629964 | |||||||
chr6:17630059 | G | A | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.2660-520C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630059 | |||||||
chr6:17630075 | G | A | 6 | a0004c0005t0001g0063 a0004c0005t0001g0064 a0004c0005t0001g0065 others(3): Show |
6 | HG00140.hp1 HG00738.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.2660-536C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630075 | |||||||
chr6:17630211 | A | G | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2660-672T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630211 | |||||||
chr6:17630221 | A | T | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2660-682T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630221 | |||||||
chr6:17630252 | T | A | 2 | a0005c0006t0001g0291 a0005c0006t0001g0305 |
2 | HG02004.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2660-713A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630252 | |||||||
chr6:17630280 | G | A | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2660-741C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630280 | |||||||
chr6:17630400 | T | C | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2660-861A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630400 | |||||||
chr6:17630594 | T | C | 2 | a0002c0002t0002g0221 a0002c0002t0002g0224 |
2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2660-1055A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630594 | |||||||
chr6:17630619 | C | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2660-1080G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630619 | |||||||
chr6:17630702 | CGGGAGAC others(10): Show |
C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2660-1180_2660-116 others(21): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630702 | |||||||
chr6:17630752 | GGAGGGGA | G | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2660-1220_2660-121 others(11): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630752 | |||||||
chr6:17630774 | GAGGAGAG others(12): Show |
G | 1 | a0002c0002t0004g0005 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2660-1254_2660-123 others(23): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630774 | |||||||
chr6:17630775 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2660-1236T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630775 | |||||||
chr6:17630786 | G | A | 4 | a0003c0004t0001g0081 a0003c0004t0001g0082 a0003c0004t0001g0083 others(1): Show |
4 | HG02622.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2660-1247C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630786 | |||||||
chr6:17630809 | GGAGAGAA | G | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2660-1277_2660-127 others(11): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630809 | |||||||
chr6:17630996 | A | C | 1 | a0002c0010t0001g0254 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2660-1457T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17630996 | |||||||
chr6:17631166 | T | C | 1 | a0001c0001t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2659+1484A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631166 | |||||||
chr6:17631178 | T | C | 2 | a0006c0007t0001g0117 a0006c0007t0001g0127 |
2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2659+1472A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631178 | |||||||
chr6:17631236 | CAT | C | 29 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0055 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.2659+1412_2659+141 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631236 | |||||||
chr6:17631244 | C | T | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2659+1406G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631244 | |||||||
chr6:17631333 | A | G | 35 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(32): Show |
35 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.2659+1317T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631333 | |||||||
chr6:17631688 | C | T | 3 | a0003c0004t0001g0302 a0003c0025t0001g0301 a0009c0027t0001g0306 |
3 | HG01192.hp2 HG01257.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2659+962G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631688 | |||||||
chr6:17631700 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2659+950G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631700 | |||||||
chr6:17631738 | G | A | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.2659+912C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631738 | |||||||
chr6:17631823 | T | G | 3 | a0006c0007t0001g0125 a0006c0007t0001g0189 a0006c0007t0001g0261 |
3 | HG01175.hp2 HG01358.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.2659+827A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631823 | |||||||
chr6:17631860 | G | A | 42 | a0001c0001t0001g0160 a0001c0003t0001g0095 a0001c0003t0001g0114 others(39): Show |
42 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2659+790C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631860 | |||||||
chr6:17631862 | G | C | 2 | a0001c0011t0001g0042 a0001c0011t0003g0002 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2659+788C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631862 | |||||||
chr6:17631882 | G | C | 3 | a0002c0002t0002g0046 a0002c0002t0002g0235 a0002c0002t0004g0003 |
3 | NA18953.hp2 NA18968.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2659+768C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631882 | |||||||
chr6:17631944 | C | T | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2659+706G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17631944 | |||||||
chr6:17632031 | T | C | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2659+619A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17632031 | |||||||
chr6:17632288 | A | C | 1 | a0002c0002t0002g0247 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2659+362T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17632288 | |||||||
chr6:17632308 | CAAACAAA others(9): Show |
C | 1 | a0001c0003t0001g0137 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2659+326_2659+341d others(18): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17632308 | |||||||
chr6:17632324 | AAAAC | A | 30 | a0003c0004t0001g0256 a0004c0005t0001g0039 a0004c0005t0001g0054 others(27): Show |
30 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.2659+322_2659+325d others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17632324 | |||||||
chr6:17632434 | C | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2659+216G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17632434 | |||||||
chr6:17632585 | A | AT | 5 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(2): Show |
5 | HG01496.hp1 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2659+64dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17632585 | |||||||
chr6:17632621 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2659+29G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 17/21 | chr6 | 17632621 | |||||||
chr6:17632846 | T | TA | 53 | a0001c0001t0001g0166 a0001c0001t0001g0170 a0001c0003t0001g0146 others(50): Show |
53 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
splice_region_variant&intron_variant | LOW | c.2465-3dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17632846 | |||||||
chr6:17632846 | T | TAA | 35 | a0002c0002t0002g0051 a0002c0002t0002g0224 a0002c0002t0005g0244 others(32): Show |
35 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(32): Show |
splice_region_variant&intron_variant | LOW | c.2465-4_2465-3dupTT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17632846 | |||||||
chr6:17632846 | T | TG | 17 | a0002c0002t0002g0047 a0002c0002t0002g0048 a0002c0002t0002g0050 others(14): Show |
17 | HG00597.hp1 HG02071.hp2 HG02132.hp1 others(14): Show |
splice_region_variant&intron_variant | LOW | c.2465-3_2465-2insC | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17632846 | |||||||
chr6:17632980 | G | A | 3 | a0002c0002t0005g0229 a0002c0002t0005g0244 a0002c0002t0020g0315 |
3 | HG02165.hp1 NA18984.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2465-136C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17632980 | |||||||
chr6:17633124 | CAT | C | 55 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(52): Show |
55 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2465-282_2465-281d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17633124 | |||||||
chr6:17633313 | T | A | 1 | a0015c0031t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2465-469A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17633313 | |||||||
chr6:17633472 | G | T | 7 | a0004c0005t0001g0056 a0004c0005t0001g0058 a0004c0005t0001g0059 others(4): Show |
7 | HG01109.hp2 NA18612.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.2465-628C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17633472 | |||||||
chr6:17633685 | C | A | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2465-841G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17633685 | |||||||
chr6:17633892 | ACT | A | 6 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(3): Show |
6 | HG01496.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2465-1050_2465-104 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17633892 | |||||||
chr6:17634211 | A | G | 1 | a0003c0025t0001g0301 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2465-1367T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634211 | |||||||
chr6:17634278 | G | C | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2465-1434C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634278 | |||||||
chr6:17634441 | A | AT | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01891.hp2 HG02280.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.2465-1598dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634441 | |||||||
chr6:17634441 | AT | A | 32 | a0001c0013t0001g0273 a0002c0002t0002g0227 a0003c0004t0001g0080 others(29): Show |
32 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.2465-1598delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634441 | |||||||
chr6:17634587 | C | T | 1 | a0003c0004t0001g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2465-1743G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634587 | |||||||
chr6:17634588 | G | C | 1 | a0005c0006t0001g0292 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2465-1744C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634588 | |||||||
chr6:17634635 | C | T | 2 | a0003c0004t0001g0081 a0003c0004t0001g0082 |
2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2465-1791G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634635 | |||||||
chr6:17634748 | A | G | 1 | a0004c0005t0001g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2465-1904T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634748 | |||||||
chr6:17634792 | T | G | 255 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(252): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.2465-1948A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634792 | |||||||
chr6:17634819 | G | A | 76 | a0001c0001t0001g0160 a0001c0003t0001g0095 a0001c0003t0001g0104 others(73): Show |
76 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2465-1975C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634819 | |||||||
chr6:17634858 | C | T | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2465-2014G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634858 | |||||||
chr6:17634860 | G | C | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2465-2016C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634860 | |||||||
chr6:17634900 | C | T | 2 | a0002c0010t0003g0007 a0002c0010t0003g0008 |
2 | HG01255.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2465-2056G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634900 | |||||||
chr6:17634944 | G | A | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2465-2100C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634944 | |||||||
chr6:17634979 | TA | T | 296 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(293): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2465-2136delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634979 | |||||||
chr6:17634980 | A | T | 1 | a0003c0004t0001g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2465-2136T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17634980 | |||||||
chr6:17635004 | G | C | 2 | a0001c0011t0001g0088 a0001c0011t0001g0089 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2464+2149C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635004 | |||||||
chr6:17635078 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2464+2075G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635078 | |||||||
chr6:17635098 | G | A | 35 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(32): Show |
35 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.2464+2055C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635098 | |||||||
chr6:17635103 | TC | T | 44 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(41): Show |
44 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2464+2049delG | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635103 | |||||||
chr6:17635104 | C | CT | 120 | a0001c0001t0001g0097 a0001c0001t0001g0101 a0001c0001t0001g0102 others(117): Show |
120 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2464+2048dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635104 | |||||||
chr6:17635104 | C | CTT | 19 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0166 others(16): Show |
19 | HG00280.hp1 HG00597.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.2464+2047_2464+204 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635104 | |||||||
chr6:17635104 | C | T | 12 | a0002c0002t0002g0215 a0002c0002t0002g0217 a0002c0002t0002g0233 others(9): Show |
12 | HG02135.hp1 HG02165.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2464+2049G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635104 | |||||||
chr6:17635104 | CT | C | 37 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0009g0307 others(34): Show |
37 | HG00323.hp2 HG01109.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.2464+2048delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635104 | |||||||
chr6:17635104 | CTTTT | C | 13 | a0002c0010t0001g0053 a0002c0010t0003g0007 a0002c0010t0003g0008 others(10): Show |
13 | HG00544.hp1 HG01255.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2464+2045_2464+204 others(8): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635104 | |||||||
chr6:17635104 | CTTTTT | C | 29 | a0002c0010t0001g0254 a0004c0005t0001g0039 a0004c0005t0001g0054 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.2464+2044_2464+204 others(9): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635104 | |||||||
chr6:17635104 | CTTTTTTT others(7): Show |
C | 3 | a0001c0003t0001g0134 a0001c0003t0001g0135 a0001c0003t0001g0143 |
3 | HG01099.hp1 HG03239.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2464+2035_2464+204 others(18): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635104 | |||||||
chr6:17635191 | G | A | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.2464+1962C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635191 | |||||||
chr6:17635281 | T | C | 3 | a0003c0004t0001g0302 a0003c0025t0001g0301 a0009c0027t0001g0306 |
3 | HG01192.hp2 HG01257.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2464+1872A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635281 | |||||||
chr6:17635356 | G | A | 1 | a0004c0005t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2464+1797C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635356 | |||||||
chr6:17635361 | G | A | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2464+1792C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635361 | |||||||
chr6:17635397 | C | T | 1 | a0002c0010t0015g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2464+1756G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635397 | |||||||
chr6:17635398 | C | T | 3 | a0002c0002t0002g0232 a0002c0010t0003g0007 a0002c0010t0003g0008 |
3 | HG01255.hp1 HG02970.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.2464+1755G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635398 | |||||||
chr6:17635399 | G | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0270 |
3 | NA18940.hp2 NA18956.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2464+1754C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635399 | |||||||
chr6:17635611 | G | A | 3 | a0002c0002t0001g0222 a0002c0002t0002g0234 a0002c0002t0002g0238 |
3 | HG02056.hp1 HG02071.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2464+1542C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635611 | |||||||
chr6:17635646 | G | A | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.2464+1507C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635646 | |||||||
chr6:17635740 | G | C | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.2464+1413C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635740 | |||||||
chr6:17635781 | G | A | 1 | a0001c0003t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2464+1372C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17635781 | |||||||
chr6:17636056 | G | A | 13 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(10): Show |
13 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.2464+1097C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17636056 | |||||||
chr6:17636334 | C | CA | 12 | a0001c0001t0001g0177 a0001c0001t0007g0178 a0001c0001t0007g0266 others(9): Show |
12 | HG01975.hp1 HG02027.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.2464+818dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17636334 | |||||||
chr6:17636334 | CA | C | 25 | a0001c0001t0001g0265 a0001c0001t0001g0270 a0001c0011t0001g0088 others(22): Show |
25 | HG00735.hp2 HG01192.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.2464+818delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17636334 | |||||||
chr6:17636350 | A | G | 1 | a0001c0021t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2464+803T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17636350 | |||||||
chr6:17636425 | G | C | 1 | a0001c0001t0018g0195 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2464+728C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17636425 | |||||||
chr6:17636580 | C | T | 1 | a0002c0002t0002g0215 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2464+573G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17636580 | |||||||
chr6:17636655 | C | G | 1 | a0001c0003t0001g0147 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2464+498G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17636655 | |||||||
chr6:17636780 | T | C | 1 | a0002c0002t0005g0237 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2464+373A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17636780 | |||||||
chr6:17637072 | C | T | 1 | a0003c0004t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2464+81G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 16/21 | chr6 | 17637072 | |||||||
chr6:17637775 | A | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
splice_region_variant&intron_variant | LOW | c.1847-5T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17637775 | |||||||
chr6:17637776 | A | G | 1 | a0002c0002t0002g0223 | 1 | NA18944.hp1 | splice_region_variant&intron_variant | LOW | c.1847-6T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17637776 | |||||||
chr6:17637784 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1847-14T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17637784 | |||||||
chr6:17637944 | A | G | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1847-174T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17637944 | |||||||
chr6:17638139 | A | G | 1 | a0003c0004t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1847-369T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17638139 | |||||||
chr6:17638233 | T | C | 1 | a0001c0003t0001g0144 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1847-463A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17638233 | |||||||
chr6:17638382 | C | T | 1 | a0003c0004t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1847-612G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17638382 | |||||||
chr6:17638802 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1847-1032A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17638802 | |||||||
chr6:17638934 | C | T | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1846+1005G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17638934 | |||||||
chr6:17639117 | G | A | 1 | a0001c0003t0021g0316 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1846+822C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17639117 | |||||||
chr6:17639147 | G | A | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1846+792C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17639147 | |||||||
chr6:17639222 | T | C | 4 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(1): Show |
4 | HG01884.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1846+717A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17639222 | |||||||
chr6:17639232 | G | C | 253 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(250): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.1846+707C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17639232 | |||||||
chr6:17639285 | G | C | 1 | a0001c0003t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1846+654C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17639285 | |||||||
chr6:17639655 | T | C | 11 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0001c0003t0001g0210 others(8): Show |
11 | HG01255.hp2 HG01496.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.1846+284A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17639655 | |||||||
chr6:17639691 | A | G | 1 | a0002c0002t0002g0241 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1846+248T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17639691 | |||||||
chr6:17639725 | A | C | 3 | a0004c0005t0001g0072 a0004c0005t0001g0073 a0004c0005t0001g0074 |
3 | HG00323.hp1 HG01981.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1846+214T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 15/21 | chr6 | 17639725 | |||||||
chr6:17640086 | T | A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(7): Show |
10 | HG01167.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1721-22A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17640086 | |||||||
chr6:17640314 | G | A | 12 | a0003c0004t0001g0080 a0003c0004t0001g0081 a0003c0004t0001g0082 others(9): Show |
12 | HG01109.hp1 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1721-250C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17640314 | |||||||
chr6:17640577 | A | G | 1 | a0016c0024t0001g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1721-513T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17640577 | |||||||
chr6:17640608 | C | T | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1721-544G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17640608 | |||||||
chr6:17640650 | G | C | 13 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(10): Show |
13 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1721-586C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17640650 | |||||||
chr6:17640740 | T | G | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1721-676A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17640740 | |||||||
chr6:17640761 | C | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1721-697G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17640761 | |||||||
chr6:17640783 | A | AT | 61 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(58): Show |
61 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1721-720dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17640783 | |||||||
chr6:17641112 | C | T | 8 | a0004c0005t0001g0068 a0004c0005t0001g0069 a0004c0005t0001g0070 others(5): Show |
8 | HG00323.hp1 HG01928.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1721-1048G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641112 | |||||||
chr6:17641130 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-1066G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641130 | |||||||
chr6:17641253 | C | T | 1 | a0008c0015t0001g0085 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1721-1189G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641253 | |||||||
chr6:17641270 | C | T | 98 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(95): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1721-1206G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641270 | |||||||
chr6:17641311 | C | A | 1 | a0001c0003t0001g0272 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1721-1247G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641311 | |||||||
chr6:17641344 | G | A | 1 | a0002c0010t0001g0254 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1721-1280C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641344 | |||||||
chr6:17641365 | T | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1721-1301A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641365 | |||||||
chr6:17641582 | G | A | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1721-1518C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641582 | |||||||
chr6:17641684 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1721-1620A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641684 | |||||||
chr6:17641728 | G | A | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1721-1664C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641728 | |||||||
chr6:17641787 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1721-1723C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641787 | |||||||
chr6:17641838 | C | T | 1 | a0004c0005t0001g0072 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1721-1774G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641838 | |||||||
chr6:17641842 | A | ACT | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1721-1780_1721-177 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641842 | |||||||
chr6:17641851 | G | GA | 60 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0101 others(57): Show |
60 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1721-1788dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641851 | |||||||
chr6:17641859 | G | A | 309 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(306): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1721-1795C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17641859 | |||||||
chr6:17642241 | A | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1721-2177T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17642241 | |||||||
chr6:17642376 | AAGAC | A | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1721-2316_1721-231 others(8): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17642376 | |||||||
chr6:17642786 | A | C | 1 | a0001c0001t0003g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1721-2722T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17642786 | |||||||
chr6:17642987 | A | G | 1 | a0002c0010t0015g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1721-2923T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17642987 | |||||||
chr6:17643229 | C | T | 255 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(252): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1720+2838G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17643229 | |||||||
chr6:17643244 | G | A | 3 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0003g0002 |
3 | HG02280.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1720+2823C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17643244 | |||||||
chr6:17643488 | C | G | 1 | a0004c0005t0001g0074 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1720+2579G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17643488 | |||||||
chr6:17643512 | C | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1720+2555G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17643512 | |||||||
chr6:17643964 | T | C | 4 | a0004c0005t0001g0063 a0004c0005t0001g0064 a0004c0005t0001g0065 others(1): Show |
4 | HG00140.hp1 HG00738.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+2103A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17643964 | |||||||
chr6:17644028 | T | C | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1720+2039A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644028 | |||||||
chr6:17644073 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1720+1994T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644073 | |||||||
chr6:17644076 | C | T | 1 | a0001c0001t0003g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1720+1991G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644076 | |||||||
chr6:17644161 | A | G | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1720+1906T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644161 | |||||||
chr6:17644214 | T | G | 144 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(141): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1720+1853A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644214 | |||||||
chr6:17644215 | T | A | 3 | a0005c0006t0006g0312 a0005c0006t0006g0313 a0005c0006t0010g0311 |
3 | NA18612.hp2 NA18968.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1720+1852A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644215 | |||||||
chr6:17644253 | C | T | 1 | a0001c0001t0018g0195 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1720+1814G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644253 | |||||||
chr6:17644260 | C | T | 1 | a0006c0007t0001g0189 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1720+1807G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644260 | |||||||
chr6:17644270 | A | G | 1 | a0002c0002t0002g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1720+1797T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644270 | |||||||
chr6:17644325 | C | T | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1720+1742G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644325 | |||||||
chr6:17644332 | CACTGCTA others(7): Show |
C | 1 | a0007c0008t0001g0202 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1720+1721_1720+173 others(18): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644332 | |||||||
chr6:17644646 | T | TA | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+1420dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644646 | |||||||
chr6:17644811 | C | T | 3 | a0001c0003t0001g0095 a0001c0003t0001g0114 a0001c0003t0003g0013 |
3 | NA18965.hp1 NA18986.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1720+1256G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644811 | |||||||
chr6:17644814 | G | A | 1 | a0006c0007t0001g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1720+1253C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644814 | |||||||
chr6:17644852 | G | A | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1720+1215C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644852 | |||||||
chr6:17644916 | T | A | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1720+1151A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644916 | |||||||
chr6:17644969 | C | T | 1 | a0003c0012t0001g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1720+1098G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17644969 | |||||||
chr6:17645016 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1720+1051G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645016 | |||||||
chr6:17645080 | G | A | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1720+987C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645080 | |||||||
chr6:17645211 | C | G | 1 | a0005c0006t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1720+856G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645211 | |||||||
chr6:17645230 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1720+837C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645230 | |||||||
chr6:17645242 | C | CA | 35 | a0001c0001t0001g0166 a0001c0001t0001g0180 a0001c0001t0001g0193 others(32): Show |
35 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.1720+824dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645242 | |||||||
chr6:17645242 | CA | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(13): Show |
16 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1720+824delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645242 | |||||||
chr6:17645303 | C | CT | 13 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(10): Show |
13 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1720+763dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645303 | |||||||
chr6:17645448 | C | T | 1 | a0006c0007t0001g0110 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1720+619G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645448 | |||||||
chr6:17645452 | T | C | 1 | a0002c0010t0001g0254 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1720+615A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645452 | |||||||
chr6:17645467 | C | CT | 12 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(9): Show |
12 | HG01175.hp2 HG01358.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1720+599dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645467 | |||||||
chr6:17645467 | CT | C | 110 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(107): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1720+599delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645467 | |||||||
chr6:17645646 | A | G | 6 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(3): Show |
6 | HG01496.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+421T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645646 | |||||||
chr6:17645937 | G | A | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1720+130C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17645937 | |||||||
chr6:17646025 | T | C | 7 | a0003c0004t0001g0080 a0003c0004t0001g0257 a0003c0012t0001g0275 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1720+42A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 14/21 | chr6 | 17646025 | |||||||
chr6:17646268 | C | T | 1 | a0002c0002t0002g0223 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1633-114G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646268 | |||||||
chr6:17646293 | C | A | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1633-139G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646293 | |||||||
chr6:17646321 | C | A | 1 | a0004c0005t0001g0066 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1633-167G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646321 | |||||||
chr6:17646325 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1633-171C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646325 | |||||||
chr6:17646340 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1633-186A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646340 | |||||||
chr6:17646345 | C | A | 42 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(39): Show |
42 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1633-191G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646345 | |||||||
chr6:17646369 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1633-215C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646369 | |||||||
chr6:17646373 | A | G | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1633-219T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646373 | |||||||
chr6:17646389 | G | A | 1 | a0005c0006t0001g0283 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1633-235C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646389 | |||||||
chr6:17646407 | T | C | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1633-253A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646407 | |||||||
chr6:17646509 | A | C | 1 | a0002c0002t0005g0237 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1633-355T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646509 | |||||||
chr6:17646511 | A | G | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1633-357T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646511 | |||||||
chr6:17646696 | G | A | 1 | a0002c0002t0002g0232 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1633-542C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646696 | |||||||
chr6:17646727 | T | G | 2 | a0003c0004t0001g0080 a0003c0004t0001g0257 |
2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1633-573A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646727 | |||||||
chr6:17646918 | C | CT | 178 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(175): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1633-765dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646918 | |||||||
chr6:17646918 | C | CTT | 9 | a0001c0001t0001g0130 a0001c0001t0001g0173 a0001c0001t0018g0195 others(6): Show |
9 | HG00438.hp1 HG01175.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1633-766_1633-765d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646918 | |||||||
chr6:17646918 | CT | C | 10 | a0001c0001t0009g0307 a0001c0001t0009g0308 a0002c0002t0002g0047 others(7): Show |
10 | HG00597.hp1 HG02004.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1633-765delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646918 | |||||||
chr6:17646936 | T | A | 1 | a0002c0002t0005g0237 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1633-782A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646936 | |||||||
chr6:17646965 | C | T | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1633-811G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646965 | |||||||
chr6:17646977 | G | A | 1 | a0003c0004t0001g0302 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1633-823C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17646977 | |||||||
chr6:17647051 | C | T | 1 | a0004c0005t0003g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1632+756G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17647051 | |||||||
chr6:17647185 | T | C | 1 | a0003c0004t0001g0286 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1632+622A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17647185 | |||||||
chr6:17647415 | A | C | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1632+392T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17647415 | |||||||
chr6:17647427 | G | A | 1 | a0002c0002t0002g0215 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1632+380C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17647427 | |||||||
chr6:17647628 | C | T | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1632+179G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 13/21 | chr6 | 17647628 | |||||||
chr6:17648112 | T | C | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1534-207A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648112 | |||||||
chr6:17648244 | G | A | 2 | a0003c0004t0001g0285 a0003c0004t0001g0286 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1534-339C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648244 | |||||||
chr6:17648355 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1534-450C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648355 | |||||||
chr6:17648367 | A | G | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1534-462T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648367 | |||||||
chr6:17648422 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1534-517C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648422 | |||||||
chr6:17648488 | G | A | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1534-583C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648488 | |||||||
chr6:17648553 | G | T | 1 | a0001c0011t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1533+610C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648553 | |||||||
chr6:17648603 | C | A | 6 | a0001c0001t0001g0111 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG01069.hp2 HG01981.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533+560G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648603 | |||||||
chr6:17648608 | C | G | 15 | a0002c0002t0002g0215 a0002c0002t0002g0216 a0002c0002t0002g0217 others(12): Show |
15 | HG00558.hp1 HG02135.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.1533+555G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648608 | |||||||
chr6:17648619 | AAAAT | A | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533+540_1533+543d others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648619 | |||||||
chr6:17648644 | A | T | 11 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
11 | HG01891.hp2 HG02074.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1533+519T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648644 | |||||||
chr6:17648667 | G | A | 2 | a0003c0004t0001g0080 a0003c0004t0001g0257 |
2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1533+496C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648667 | |||||||
chr6:17648795 | A | AC | 55 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(52): Show |
55 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.1533+367dupG | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648795 | |||||||
chr6:17648802 | CA | C | 136 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(133): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1533+360delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648802 | |||||||
chr6:17648871 | T | C | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1533+292A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17648871 | |||||||
chr6:17649037 | TTC | T | 3 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0003g0002 |
3 | HG02280.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1533+124_1533+125d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17649037 | |||||||
chr6:17649153 | G | A | 4 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(1): Show |
4 | HG01884.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533+10C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 12/21 | chr6 | 17649153 | |||||||
chr6:17649420 | G | T | 11 | a0001c0003t0001g0133 a0001c0003t0001g0136 a0001c0003t0001g0141 others(8): Show |
11 | HG00609.hp2 HG02080.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.1396-120C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17649420 | |||||||
chr6:17649454 | A | G | 1 | a0001c0001t0018g0195 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1396-154T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17649454 | |||||||
chr6:17649502 | C | T | 1 | a0017c0030t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1396-202G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17649502 | |||||||
chr6:17649570 | A | AGTT | 306 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(303): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1396-273_1396-271d others(5): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17649570 | |||||||
chr6:17649579 | A | C | 1 | a0001c0001t0001g0267 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1396-279T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17649579 | |||||||
chr6:17649902 | C | T | 1 | a0001c0001t0013g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1396-602G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17649902 | |||||||
chr6:17650089 | C | G | 255 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(252): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1396-789G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650089 | |||||||
chr6:17650122 | T | C | 1 | a0002c0002t0020g0315 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1396-822A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650122 | |||||||
chr6:17650124 | T | C | 1 | a0002c0002t0020g0315 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1396-824A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650124 | |||||||
chr6:17650215 | C | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1396-915G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650215 | |||||||
chr6:17650321 | A | T | 15 | a0006c0007t0001g0103 a0006c0007t0001g0107 a0006c0007t0001g0108 others(12): Show |
15 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1396-1021T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650321 | |||||||
chr6:17650334 | A | G | 1 | a0001c0014t0003g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1396-1034T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650334 | |||||||
chr6:17650400 | G | A | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1396-1100C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650400 | |||||||
chr6:17650654 | T | TAAAACCT others(327): Show |
1 | a0003c0004t0001g0090 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1396-1355_1396-135 others(338): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650654 | |||||||
chr6:17650654 | T | TAAAACCT others(328): Show |
1 | a0003c0004t0003g0009 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1396-1355_1396-135 others(339): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650654 | |||||||
chr6:17650654 | T | TAAAACCT others(329): Show |
3 | a0003c0004t0001g0092 a0003c0004t0001g0093 a0003c0004t0001g0094 |
3 | HG01975.hp1 HG02698.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1396-1355_1396-135 others(340): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650654 | |||||||
chr6:17650654 | T | TAAAACCT others(330): Show |
2 | a0003c0004t0003g0010 a0003c0004t0003g0031 |
2 | HG02027.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1396-1355_1396-135 others(341): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650654 | |||||||
chr6:17650654 | T | TAAAACCT others(337): Show |
1 | a0003c0004t0001g0091 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1396-1355_1396-135 others(348): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650654 | |||||||
chr6:17650814 | T | A | 1 | a0002c0002t0002g0226 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1396-1514A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650814 | |||||||
chr6:17650838 | C | T | 10 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(7): Show |
10 | HG01167.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1396-1538G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17650838 | |||||||
chr6:17651081 | T | C | 2 | a0001c0001t0001g0097 a0001c0021t0001g0098 |
2 | HG01361.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1396-1781A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17651081 | |||||||
chr6:17651206 | G | C | 1 | a0006c0007t0001g0109 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1396-1906C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17651206 | |||||||
chr6:17651245 | G | C | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1396-1945C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17651245 | |||||||
chr6:17651511 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1396-2211C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17651511 | |||||||
chr6:17651629 | G | A | 1 | a0003c0012t0001g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1396-2329C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17651629 | |||||||
chr6:17651650 | T | C | 4 | a0003c0004t0001g0081 a0003c0004t0001g0082 a0003c0004t0001g0083 others(1): Show |
4 | HG02622.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-2350A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17651650 | |||||||
chr6:17651676 | G | A | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1396-2376C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17651676 | |||||||
chr6:17651694 | A | C | 4 | a0003c0004t0001g0081 a0003c0004t0001g0082 a0003c0004t0001g0083 others(1): Show |
4 | HG02622.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-2394T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17651694 | |||||||
chr6:17651911 | C | T | 1 | a0001c0003t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1396-2611G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17651911 | |||||||
chr6:17651963 | C | CACAT | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1396-2667_1396-266 others(8): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17651963 | |||||||
chr6:17652103 | A | T | 5 | a0003c0012t0001g0275 a0003c0012t0001g0277 a0003c0012t0001g0278 others(2): Show |
5 | HG01109.hp1 HG01243.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-2803T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652103 | |||||||
chr6:17652120 | C | A | 1 | a0002c0002t0002g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1396-2820G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652120 | |||||||
chr6:17652157 | C | T | 1 | a0006c0007t0001g0115 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1396-2857G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652157 | |||||||
chr6:17652178 | A | G | 1 | a0009c0027t0001g0306 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1396-2878T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652178 | |||||||
chr6:17652247 | TTTTC | T | 55 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(52): Show |
55 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.1396-2951_1396-294 others(8): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652247 | |||||||
chr6:17652318 | G | A | 1 | a0005c0006t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1396-3018C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652318 | |||||||
chr6:17652344 | A | C | 2 | a0001c0003t0001g0126 a0001c0003t0001g0272 |
2 | NA18984.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1396-3044T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652344 | |||||||
chr6:17652376 | C | T | 1 | a0006c0007t0001g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1396-3076G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652376 | |||||||
chr6:17652574 | A | T | 147 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(144): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1396-3274T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652574 | |||||||
chr6:17652634 | G | A | 98 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(95): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1396-3334C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652634 | |||||||
chr6:17652937 | G | A | 9 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(6): Show |
9 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1396-3637C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652937 | |||||||
chr6:17652956 | G | A | 1 | a0013c0020t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1396-3656C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17652956 | |||||||
chr6:17653081 | T | C | 1 | a0002c0002t0002g0258 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1396-3781A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17653081 | |||||||
chr6:17653489 | T | A | 1 | a0001c0003t0001g0262 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1396-4189A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17653489 | |||||||
chr6:17653583 | G | A | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1396-4283C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17653583 | |||||||
chr6:17653688 | G | A | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1396-4388C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17653688 | |||||||
chr6:17653807 | G | A | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1396-4507C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17653807 | |||||||
chr6:17653949 | C | T | 8 | a0001c0001t0001g0156 a0001c0001t0001g0166 a0001c0001t0001g0167 others(5): Show |
8 | NA18939.hp2 NA18941.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396-4649G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17653949 | |||||||
chr6:17653982 | A | T | 42 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(39): Show |
42 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1396-4682T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17653982 | |||||||
chr6:17654046 | A | C | 1 | a0001c0001t0001g0193 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1396-4746T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654046 | |||||||
chr6:17654095 | G | A | 1 | a0001c0003t0001g0271 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1396-4795C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654095 | |||||||
chr6:17654106 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1396-4806G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654106 | |||||||
chr6:17654324 | AT | A | 44 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(41): Show |
44 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1396-5025delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654324 | |||||||
chr6:17654367 | G | A | 3 | a0002c0002t0002g0247 a0002c0002t0002g0248 a0002c0002t0004g0026 |
3 | HG00642.hp1 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1396-5067C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654367 | |||||||
chr6:17654418 | T | A | 1 | a0002c0002t0002g0219 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1396-5118A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654418 | |||||||
chr6:17654424 | C | T | 5 | a0002c0002t0002g0046 a0002c0002t0002g0049 a0002c0002t0002g0235 others(2): Show |
5 | HG00438.hp2 NA18953.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-5124G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654424 | |||||||
chr6:17654477 | A | G | 1 | a0001c0003t0001g0192 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1396-5177T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654477 | |||||||
chr6:17654520 | C | A | 1 | a0005c0017t0003g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1396-5220G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654520 | |||||||
chr6:17654589 | C | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1396-5289G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654589 | |||||||
chr6:17654609 | C | T | 2 | a0003c0004t0001g0081 a0003c0004t0001g0082 |
2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1396-5309G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654609 | |||||||
chr6:17654874 | CATA | C | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1396-5577_1396-557 others(7): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17654874 | |||||||
chr6:17655022 | A | C | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396-5722T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655022 | |||||||
chr6:17655040 | C | A | 4 | a0003c0004t0001g0090 a0003c0004t0001g0092 a0003c0004t0001g0094 others(1): Show |
4 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-5740G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655040 | |||||||
chr6:17655071 | ATATACTG others(12): Show |
A | 1 | a0013c0020t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1396-5790_1396-577 others(23): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655071 | |||||||
chr6:17655074 | T | C | 1 | a0006c0007t0001g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1396-5774A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655074 | |||||||
chr6:17655133 | C | G | 1 | a0002c0002t0002g0218 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1396-5833G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655133 | |||||||
chr6:17655158 | T | C | 1 | a0008c0015t0001g0086 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1396-5858A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655158 | |||||||
chr6:17655278 | G | A | 29 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0055 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1396-5978C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655278 | |||||||
chr6:17655422 | GC | G | 55 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(52): Show |
55 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.1396-6123delG | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655422 | |||||||
chr6:17655458 | C | CT | 209 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(206): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1396-6159dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655458 | |||||||
chr6:17655458 | CT | C | 13 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(10): Show |
13 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1396-6159delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655458 | |||||||
chr6:17655513 | G | A | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395+6140C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655513 | |||||||
chr6:17655542 | C | G | 1 | a0002c0002t0005g0229 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1395+6111G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655542 | |||||||
chr6:17655578 | C | T | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1395+6075G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655578 | |||||||
chr6:17655665 | G | A | 1 | a0001c0001t0003g0012 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1395+5988C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655665 | |||||||
chr6:17655736 | T | A | 1 | a0001c0001t0001g0264 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1395+5917A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17655736 | |||||||
chr6:17656084 | A | G | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1395+5569T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17656084 | |||||||
chr6:17656110 | CAGG | C | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1395+5540_1395+554 others(7): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17656110 | |||||||
chr6:17656151 | GC | G | 29 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0055 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1395+5501delG | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17656151 | |||||||
chr6:17656346 | T | C | 4 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(1): Show |
4 | HG01884.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+5307A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17656346 | |||||||
chr6:17656364 | T | C | 1 | a0001c0003t0001g0144 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1395+5289A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17656364 | |||||||
chr6:17656373 | T | C | 1 | a0003c0012t0001g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1395+5280A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17656373 | |||||||
chr6:17656564 | G | C | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1395+5089C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17656564 | |||||||
chr6:17656671 | T | A | 11 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0169 others(8): Show |
11 | HG00558.hp2 HG01069.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1395+4982A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17656671 | |||||||
chr6:17656802 | C | G | 289 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1395+4851G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17656802 | |||||||
chr6:17657151 | T | A | 1 | a0002c0002t0002g0235 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1395+4502A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657151 | |||||||
chr6:17657192 | A | G | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395+4461T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657192 | |||||||
chr6:17657259 | T | C | 3 | a0002c0010t0001g0053 a0002c0010t0003g0007 a0002c0010t0003g0008 |
3 | HG01255.hp1 HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1395+4394A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657259 | |||||||
chr6:17657276 | T | G | 4 | a0003c0004t0001g0081 a0003c0004t0001g0082 a0003c0004t0001g0083 others(1): Show |
4 | HG02622.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395+4377A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657276 | |||||||
chr6:17657385 | T | TA | 41 | a0002c0010t0001g0254 a0002c0010t0003g0007 a0002c0010t0003g0008 others(38): Show |
41 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.1395+4267dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657385 | |||||||
chr6:17657393 | T | A | 11 | a0002c0010t0001g0053 a0003c0004t0001g0090 a0003c0004t0001g0091 others(8): Show |
11 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1395+4260A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657393 | |||||||
chr6:17657394 | A | T | 1 | a0002c0010t0001g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1395+4259T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657394 | |||||||
chr6:17657400 | A | T | 40 | a0002c0010t0001g0254 a0002c0010t0003g0007 a0002c0010t0003g0008 others(37): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.1395+4253T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657400 | |||||||
chr6:17657401 | T | A | 44 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(41): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1395+4252A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657401 | |||||||
chr6:17657401 | T | TA | 7 | a0001c0001t0009g0307 a0001c0011t0001g0041 a0001c0011t0001g0042 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1395+4251dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657401 | |||||||
chr6:17657401 | TA | T | 7 | a0001c0003t0001g0141 a0003c0004t0001g0081 a0003c0004t0001g0082 others(4): Show |
7 | HG00735.hp2 HG02622.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1395+4251delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657401 | |||||||
chr6:17657408 | A | T | 1 | a0001c0003t0001g0119 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1395+4245T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657408 | |||||||
chr6:17657409 | A | T | 110 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0101 others(107): Show |
110 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1395+4244T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657409 | |||||||
chr6:17657420 | T | C | 253 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(250): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.1395+4233A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657420 | |||||||
chr6:17657433 | G | T | 3 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0003g0002 |
3 | HG02280.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1395+4220C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657433 | |||||||
chr6:17657491 | G | A | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1395+4162C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657491 | |||||||
chr6:17657510 | G | T | 1 | a0006c0007t0001g0115 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1395+4143C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657510 | |||||||
chr6:17657615 | G | A | 1 | a0002c0002t0002g0238 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1395+4038C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657615 | |||||||
chr6:17657777 | ATATTAG | A | 57 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(54): Show |
57 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1395+3870_1395+387 others(10): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657777 | |||||||
chr6:17657801 | T | C | 1 | a0001c0003t0001g0150 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1395+3852A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657801 | |||||||
chr6:17657865 | T | G | 3 | a0004c0005t0001g0058 a0004c0005t0001g0067 a0004c0005t0001g0253 |
3 | NA18971.hp2 NA18999.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1395+3788A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657865 | |||||||
chr6:17657923 | C | T | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+3730G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17657923 | |||||||
chr6:17658102 | G | T | 29 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0055 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1395+3551C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658102 | |||||||
chr6:17658126 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1395+3527C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658126 | |||||||
chr6:17658136 | A | G | 1 | a0017c0030t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1395+3517T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658136 | |||||||
chr6:17658159 | G | A | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+3494C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658159 | |||||||
chr6:17658230 | C | T | 11 | a0001c0003t0001g0133 a0001c0003t0001g0136 a0001c0003t0001g0141 others(8): Show |
11 | HG00609.hp2 HG02080.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.1395+3423G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658230 | |||||||
chr6:17658417 | A | G | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1395+3236T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658417 | |||||||
chr6:17658529 | C | T | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395+3124G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658529 | |||||||
chr6:17658648 | G | A | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1395+3005C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658648 | |||||||
chr6:17658698 | T | C | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1395+2955A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658698 | |||||||
chr6:17658710 | T | C | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1395+2943A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658710 | |||||||
chr6:17658772 | T | C | 10 | a0002c0002t0002g0216 a0002c0002t0002g0217 a0002c0002t0002g0218 others(7): Show |
10 | HG00558.hp1 HG02135.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395+2881A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658772 | |||||||
chr6:17658950 | C | T | 3 | a0002c0010t0015g0274 a0003c0012t0001g0275 a0019c0029t0001g0276 |
3 | HG02735.hp2 HG03540.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1395+2703G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658950 | |||||||
chr6:17658951 | G | A | 1 | a0002c0010t0001g0254 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1395+2702C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17658951 | |||||||
chr6:17659006 | T | C | 2 | a0003c0012t0001g0275 a0019c0029t0001g0276 |
2 | HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1395+2647A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17659006 | |||||||
chr6:17659063 | C | T | 1 | a0015c0031t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1395+2590G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17659063 | |||||||
chr6:17659213 | G | A | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1395+2440C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17659213 | |||||||
chr6:17659305 | G | A | 1 | a0003c0004t0001g0286 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1395+2348C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17659305 | |||||||
chr6:17659418 | A | G | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1395+2235T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17659418 | |||||||
chr6:17659528 | A | G | 10 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0001g0172 others(7): Show |
10 | HG01257.hp1 HG01928.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.1395+2125T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17659528 | |||||||
chr6:17659683 | G | A | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1395+1970C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17659683 | |||||||
chr6:17659755 | G | A | 1 | a0003c0004t0001g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1395+1898C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17659755 | |||||||
chr6:17659761 | G | A | 1 | a0006c0007t0001g0105 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1395+1892C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17659761 | |||||||
chr6:17659770 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1395+1883G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17659770 | |||||||
chr6:17660024 | G | T | 65 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(62): Show |
65 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1395+1629C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660024 | |||||||
chr6:17660165 | A | G | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1395+1488T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660165 | |||||||
chr6:17660247 | G | A | 1 | a0005c0006t0003g0037 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1395+1406C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660247 | |||||||
chr6:17660248 | C | T | 1 | a0005c0006t0003g0037 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1395+1405G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660248 | |||||||
chr6:17660386 | A | G | 1 | a0005c0006t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1395+1267T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660386 | |||||||
chr6:17660453 | A | G | 5 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(2): Show |
5 | HG01496.hp1 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+1200T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660453 | |||||||
chr6:17660526 | G | A | 1 | a0001c0003t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1395+1127C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660526 | |||||||
chr6:17660579 | T | C | 3 | a0002c0002t0002g0247 a0002c0002t0002g0248 a0002c0002t0004g0026 |
3 | HG00642.hp1 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1395+1074A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660579 | |||||||
chr6:17660596 | A | G | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1395+1057T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660596 | |||||||
chr6:17660656 | A | G | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1395+997T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660656 | |||||||
chr6:17660922 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1395+731G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660922 | |||||||
chr6:17660956 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1395+697C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17660956 | |||||||
chr6:17661081 | G | A | 2 | a0001c0001t0001g0264 a0001c0001t0003g0020 |
2 | HG02083.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1395+572C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17661081 | |||||||
chr6:17661329 | C | T | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1395+324G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17661329 | |||||||
chr6:17661388 | T | C | 45 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(42): Show |
45 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1395+265A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17661388 | |||||||
chr6:17661511 | T | A | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1395+142A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17661511 | |||||||
chr6:17661512 | G | A | 312 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(309): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1395+141C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 11/21 | chr6 | 17661512 | |||||||
chr6:17661962 | T | C | 1 | a0002c0010t0003g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1268+56A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 10/21 | chr6 | 17661962 | |||||||
chr6:17662193 | T | C | 4 | a0001c0009t0001g0149 a0001c0009t0003g0016 a0001c0009t0003g0017 others(1): Show |
4 | HG02145.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-123A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17662193 | |||||||
chr6:17662451 | G | A | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1216-381C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17662451 | |||||||
chr6:17662949 | T | C | 1 | a0004c0005t0001g0062 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1216-879A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17662949 | |||||||
chr6:17662979 | C | T | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1216-909G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17662979 | |||||||
chr6:17663224 | GAA | G | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0011t0001g0041 others(4): Show |
7 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1216-1156_1216-115 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663224 | |||||||
chr6:17663230 | A | T | 6 | a0001c0001t0001g0045 a0003c0012t0001g0275 a0003c0012t0001g0277 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1216-1160T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663230 | |||||||
chr6:17663232 | T | C | 6 | a0001c0001t0001g0045 a0003c0012t0001g0275 a0003c0012t0001g0277 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1216-1162A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663232 | |||||||
chr6:17663232 | T | TAC | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1216-1164_1216-116 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663232 | |||||||
chr6:17663232 | TAC | T | 128 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0099 others(125): Show |
128 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1216-1164_1216-116 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663232 | |||||||
chr6:17663232 | TACAC | T | 19 | a0001c0001t0009g0307 a0001c0001t0009g0308 a0001c0003t0001g0104 others(16): Show |
19 | HG00735.hp2 HG01192.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1216-1166_1216-116 others(8): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663232 | |||||||
chr6:17663233 | A | G | 2 | a0004c0005t0001g0054 a0004c0005t0001g0252 |
2 | HG00280.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1216-1163T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663233 | |||||||
chr6:17663254 | C | CAT | 3 | a0006c0007t0001g0107 a0006c0007t0001g0108 a0006c0007t0001g0109 |
3 | HG00140.hp2 HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1216-1185_1216-118 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663254 | |||||||
chr6:17663256 | C | T | 8 | a0001c0003t0001g0124 a0001c0003t0001g0134 a0001c0003t0001g0135 others(5): Show |
8 | HG00140.hp2 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1216-1186G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663256 | |||||||
chr6:17663258 | C | T | 68 | a0001c0003t0001g0095 a0001c0003t0001g0104 a0001c0003t0001g0114 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1216-1188G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663258 | |||||||
chr6:17663258 | CACAT | C | 19 | a0005c0006t0001g0280 a0005c0006t0001g0283 a0005c0006t0001g0287 others(16): Show |
19 | HG00099.hp2 HG00639.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1216-1192_1216-118 others(8): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663258 | |||||||
chr6:17663260 | C | CACACATA others(3): Show |
2 | a0004c0005t0001g0055 a0004c0005t0001g0069 |
2 | HG01074.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1216-1191_1216-119 others(14): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663260 | |||||||
chr6:17663260 | C | CACATATA others(1): Show |
27 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0056 others(24): Show |
27 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1216-1191_1216-119 others(12): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663260 | |||||||
chr6:17663260 | C | T | 210 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(207): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1216-1190G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663260 | |||||||
chr6:17663260 | CAT | C | 4 | a0001c0011t0001g0088 a0001c0011t0001g0089 a0005c0006t0001g0281 others(1): Show |
4 | HG00408.hp1 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-1192_1216-119 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663260 | |||||||
chr6:17663262 | T | C | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01891.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1216-1192A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663262 | |||||||
chr6:17663584 | A | G | 1 | a0002c0010t0015g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1216-1514T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663584 | |||||||
chr6:17663644 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1216-1574A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663644 | |||||||
chr6:17663662 | A | G | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1215+1577T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663662 | |||||||
chr6:17663741 | T | C | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1215+1498A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663741 | |||||||
chr6:17663780 | A | T | 1 | a0001c0003t0021g0316 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1215+1459T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663780 | |||||||
chr6:17663930 | C | CCA | 3 | a0001c0003t0001g0262 a0002c0002t0014g0213 a0017c0030t0001g0138 |
3 | HG03654.hp1 HG04184.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1215+1307_1215+130 others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663930 | |||||||
chr6:17663941 | A | C | 247 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(244): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1215+1298T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663941 | |||||||
chr6:17663947 | C | A | 12 | a0001c0001t0001g0187 a0001c0001t0009g0307 a0001c0001t0009g0308 others(9): Show |
12 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1215+1292G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17663947 | |||||||
chr6:17664019 | T | A | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1215+1220A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17664019 | |||||||
chr6:17664066 | C | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1215+1173G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17664066 | |||||||
chr6:17664088 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1215+1151T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17664088 | |||||||
chr6:17664179 | C | T | 247 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(244): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1215+1060G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17664179 | |||||||
chr6:17664343 | G | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+896C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17664343 | |||||||
chr6:17664353 | C | T | 4 | a0001c0013t0001g0206 a0001c0013t0001g0273 a0001c0013t0003g0023 others(1): Show |
4 | NA18950.hp2 NA18960.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+886G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17664353 | |||||||
chr6:17664446 | C | T | 1 | a0008c0015t0001g0086 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1215+793G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17664446 | |||||||
chr6:17664945 | C | T | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1215+294G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17664945 | |||||||
chr6:17665052 | C | CAAAAAAA others(1): Show |
52 | a0002c0002t0001g0222 a0002c0002t0002g0047 a0002c0002t0002g0048 others(49): Show |
52 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1215+179_1215+186d others(10): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17665052 | |||||||
chr6:17665052 | C | CAAAAAAA others(3): Show |
7 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(4): Show |
7 | HG02258.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+177_1215+186d others(12): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17665052 | |||||||
chr6:17665052 | C | CAAAAAAA others(4): Show |
2 | a0007c0008t0001g0200 a0007c0008t0003g0022 |
2 | HG02145.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1215+176_1215+186d others(13): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17665052 | |||||||
chr6:17665052 | C | CAAAAAAA others(5): Show |
16 | a0001c0001t0001g0163 a0003c0004t0001g0079 a0003c0004t0001g0081 others(13): Show |
16 | HG00323.hp2 HG00735.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1215+175_1215+186d others(14): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17665052 | |||||||
chr6:17665052 | C | CAAAAAAA others(6): Show |
45 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(42): Show |
45 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1215+174_1215+186d others(15): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17665052 | |||||||
chr6:17665052 | C | CAAAAAAA others(7): Show |
81 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(78): Show |
81 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1215+186_1215+187i others(16): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17665052 | |||||||
chr6:17665052 | C | CAAAAAAA others(8): Show |
81 | a0001c0001t0001g0148 a0001c0001t0001g0157 a0001c0001t0001g0170 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.1215+186_1215+187i others(17): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17665052 | |||||||
chr6:17665052 | C | CAAAAAAA others(9): Show |
18 | a0001c0001t0001g0044 a0001c0003t0001g0095 a0001c0003t0001g0136 others(15): Show |
18 | HG00408.hp2 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1215+186_1215+187i others(18): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17665052 | |||||||
chr6:17665052 | C | CAAAAAAA others(10): Show |
3 | a0001c0001t0001g0045 a0001c0003t0003g0013 a0001c0011t0001g0089 |
3 | HG01891.hp2 HG02886.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1215+186_1215+187i others(19): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17665052 | |||||||
chr6:17665052 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1215+186_1215+187i others(20): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17665052 | |||||||
chr6:17665126 | A | G | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1215+113T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 9/21 | chr6 | 17665126 | |||||||
chr6:17665454 | C | A | 1 | a0001c0001t0013g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1069-69G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665454 | |||||||
chr6:17665460 | C | T | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-75G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665460 | |||||||
chr6:17665554 | T | C | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1069-169A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665554 | |||||||
chr6:17665574 | C | T | 268 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(265): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1069-189G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665574 | |||||||
chr6:17665614 | G | A | 9 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(6): Show |
9 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-229C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665614 | |||||||
chr6:17665650 | T | C | 1 | a0003c0004t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1069-265A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665650 | |||||||
chr6:17665656 | A | G | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1069-271T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665656 | |||||||
chr6:17665724 | G | T | 86 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(83): Show |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1069-339C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665724 | |||||||
chr6:17665736 | T | A | 1 | a0001c0003t0003g0025 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1069-351A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665736 | |||||||
chr6:17665771 | A | G | 247 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(244): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1069-386T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665771 | |||||||
chr6:17665816 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1069-431G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665816 | |||||||
chr6:17665834 | G | A | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069-449C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665834 | |||||||
chr6:17665860 | G | GT | 8 | a0001c0001t0013g0038 a0001c0003t0001g0121 a0001c0009t0001g0164 others(5): Show |
8 | HG00597.hp1 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1069-476dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665860 | |||||||
chr6:17665987 | C | CT | 7 | a0001c0001t0001g0157 a0001c0003t0003g0025 a0001c0011t0001g0041 others(4): Show |
7 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-603dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17665987 | |||||||
chr6:17666004 | A | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1069-619T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17666004 | |||||||
chr6:17666054 | G | A | 2 | a0007c0008t0001g0197 a0007c0008t0001g0198 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1069-669C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17666054 | |||||||
chr6:17666108 | T | C | 1 | a0001c0003t0001g0192 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1069-723A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17666108 | |||||||
chr6:17666390 | C | T | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1069-1005G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17666390 | |||||||
chr6:17666458 | G | A | 2 | a0001c0001t0001g0097 a0001c0021t0001g0098 |
2 | HG01361.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1069-1073C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17666458 | |||||||
chr6:17666563 | T | C | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1069-1178A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17666563 | |||||||
chr6:17666862 | T | C | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1069-1477A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17666862 | |||||||
chr6:17666953 | T | C | 3 | a0006c0007t0001g0107 a0006c0007t0001g0108 a0006c0007t0001g0109 |
3 | HG00140.hp2 HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1069-1568A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17666953 | |||||||
chr6:17667289 | T | C | 1 | a0003c0004t0001g0091 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1068+1686A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17667289 | |||||||
chr6:17667347 | T | C | 1 | a0005c0017t0003g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1068+1628A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17667347 | |||||||
chr6:17667396 | T | C | 1 | a0001c0001t0017g0116 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1068+1579A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17667396 | |||||||
chr6:17667404 | C | G | 255 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(252): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1068+1571G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17667404 | |||||||
chr6:17667452 | C | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1068+1523G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17667452 | |||||||
chr6:17667676 | T | C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG00558.hp2 NA18980.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1068+1299A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17667676 | |||||||
chr6:17667753 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1068+1222G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17667753 | |||||||
chr6:17667802 | C | A | 1 | a0001c0011t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1068+1173G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17667802 | |||||||
chr6:17667802 | C | T | 5 | a0001c0009t0001g0139 a0001c0009t0001g0149 a0001c0009t0003g0016 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1068+1173G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17667802 | |||||||
chr6:17668069 | C | CTTTT | 13 | a0002c0002t0002g0052 a0002c0002t0002g0245 a0002c0002t0002g0246 others(10): Show |
13 | HG00438.hp2 HG00642.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1068+902_1068+905d others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668069 | |||||||
chr6:17668069 | C | CTTTTT | 35 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(32): Show |
35 | HG00558.hp1 HG00597.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1068+901_1068+905d others(7): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668069 | |||||||
chr6:17668069 | C | CTTTTTT | 8 | a0002c0002t0002g0218 a0002c0002t0002g0225 a0002c0002t0002g0228 others(5): Show |
8 | HG02071.hp2 HG03017.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.1068+900_1068+905d others(8): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668069 | |||||||
chr6:17668069 | CT | C | 52 | a0001c0001t0001g0156 a0001c0001t0001g0166 a0001c0001t0009g0307 others(49): Show |
52 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1068+905delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668069 | |||||||
chr6:17668069 | CTT | C | 151 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(148): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1068+904_1068+905d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668069 | |||||||
chr6:17668161 | C | T | 1 | a0004c0005t0001g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1068+814G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668161 | |||||||
chr6:17668222 | C | T | 1 | a0003c0012t0001g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1068+753G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668222 | |||||||
chr6:17668242 | A | AT | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068+732dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668242 | |||||||
chr6:17668315 | A | G | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1068+660T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668315 | |||||||
chr6:17668375 | T | C | 1 | a0001c0003t0003g0032 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1068+600A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668375 | |||||||
chr6:17668450 | A | G | 2 | a0001c0011t0001g0088 a0001c0011t0001g0089 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1068+525T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668450 | |||||||
chr6:17668610 | C | T | 6 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(3): Show |
6 | HG01496.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+365G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668610 | |||||||
chr6:17668637 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1068+338C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668637 | |||||||
chr6:17668713 | C | T | 1 | a0004c0005t0003g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1068+262G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668713 | |||||||
chr6:17668776 | T | A | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1068+199A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668776 | |||||||
chr6:17668782 | G | A | 11 | a0002c0002t0002g0052 a0002c0002t0002g0245 a0002c0002t0002g0246 others(8): Show |
11 | HG00642.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1068+193C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668782 | |||||||
chr6:17668829 | C | T | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068+146G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 8/21 | chr6 | 17668829 | |||||||
chr6:17669031 | G | GA | 43 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(40): Show |
43 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(40): Show |
splice_region_variant&intron_variant | LOW | c.1015-4dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 7/21 | chr6 | 17669031 | |||||||
chr6:17669031 | GA | G | 59 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(56): Show |
59 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
splice_region_variant&intron_variant | LOW | c.1015-4delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 7/21 | chr6 | 17669031 | |||||||
chr6:17669081 | C | CT | 31 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0179 others(28): Show |
31 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1015-54dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 7/21 | chr6 | 17669081 | |||||||
chr6:17669141 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0268 |
2 | HG00639.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1015-113G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 7/21 | chr6 | 17669141 | |||||||
chr6:17669243 | T | A | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1014+50A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 7/21 | chr6 | 17669243 | |||||||
chr6:17669736 | A | G | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.853-190T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17669736 | |||||||
chr6:17669801 | A | G | 1 | a0002c0010t0001g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.853-255T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17669801 | |||||||
chr6:17669853 | G | A | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.853-307C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17669853 | |||||||
chr6:17669937 | T | C | 1 | a0003c0004t0001g0299 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.853-391A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17669937 | |||||||
chr6:17670045 | G | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-499C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670045 | |||||||
chr6:17670074 | C | A | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.853-528G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670074 | |||||||
chr6:17670092 | T | C | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.853-546A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670092 | |||||||
chr6:17670095 | C | CA | 24 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(21): Show |
24 | HG00438.hp2 HG00735.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.853-550dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670095 | |||||||
chr6:17670095 | CA | C | 169 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(166): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.853-550delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670095 | |||||||
chr6:17670095 | CAA | C | 6 | a0001c0001t0001g0102 a0001c0001t0001g0174 a0001c0032t0001g0205 others(3): Show |
6 | HG00280.hp2 HG02004.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-551_853-550del others(2): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670095 | |||||||
chr6:17670095 | CAAAA | C | 20 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(17): Show |
20 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.853-553_853-550del others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670095 | |||||||
chr6:17670095 | CAAAAAAA others(3): Show |
C | 1 | a0003c0004t0001g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.853-559_853-550del others(10): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670095 | |||||||
chr6:17670095 | CAAAAAAA others(4): Show |
C | 1 | a0003c0004t0001g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.853-560_853-550del others(11): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670095 | |||||||
chr6:17670130 | G | A | 58 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0101 others(55): Show |
58 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.853-584C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670130 | |||||||
chr6:17670208 | C | T | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.853-662G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670208 | |||||||
chr6:17670268 | A | T | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.853-722T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670268 | |||||||
chr6:17670363 | C | A | 4 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(1): Show |
4 | HG01884.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-817G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670363 | |||||||
chr6:17670717 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.853-1171A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670717 | |||||||
chr6:17670740 | AT | A | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.853-1195delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670740 | |||||||
chr6:17670749 | A | T | 1 | a0004c0005t0001g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.853-1203T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670749 | |||||||
chr6:17670865 | C | T | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.853-1319G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670865 | |||||||
chr6:17670866 | G | A | 1 | a0005c0017t0003g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.853-1320C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670866 | |||||||
chr6:17670935 | C | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.853-1389G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670935 | |||||||
chr6:17670958 | G | A | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.853-1412C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670958 | |||||||
chr6:17670971 | C | T | 1 | a0001c0003t0001g0150 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.853-1425G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670971 | |||||||
chr6:17670999 | T | C | 1 | a0002c0010t0001g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.853-1453A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17670999 | |||||||
chr6:17671137 | T | C | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.853-1591A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17671137 | |||||||
chr6:17671298 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.853-1752C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17671298 | |||||||
chr6:17671366 | T | A | 5 | a0007c0008t0001g0200 a0007c0008t0001g0201 a0007c0008t0001g0202 others(2): Show |
5 | HG02615.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-1820A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17671366 | |||||||
chr6:17671433 | T | C | 1 | a0003c0012t0001g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.853-1887A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17671433 | |||||||
chr6:17671449 | G | A | 1 | a0002c0002t0002g0049 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.853-1903C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17671449 | |||||||
chr6:17671460 | A | C | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-1914T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17671460 | |||||||
chr6:17671594 | C | T | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.853-2048G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17671594 | |||||||
chr6:17671641 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.853-2095A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17671641 | |||||||
chr6:17671677 | C | T | 1 | a0002c0002t0002g0258 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.853-2131G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17671677 | |||||||
chr6:17671816 | T | C | 1 | a0001c0003t0001g0271 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.853-2270A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17671816 | |||||||
chr6:17671911 | G | A | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0179 others(2): Show |
5 | NA18940.hp2 NA18947.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-2365C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17671911 | |||||||
chr6:17672013 | T | TA | 4 | a0003c0004t0001g0079 a0003c0004t0001g0081 a0003c0004t0001g0083 others(1): Show |
4 | HG02572.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-2468dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17672013 | |||||||
chr6:17672232 | C | T | 1 | a0003c0012t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.852+2673G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17672232 | |||||||
chr6:17672248 | A | G | 1 | a0001c0003t0001g0150 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.852+2657T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17672248 | |||||||
chr6:17672451 | C | T | 1 | a0013c0020t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.852+2454G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17672451 | |||||||
chr6:17672658 | T | C | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.852+2247A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17672658 | |||||||
chr6:17673106 | C | T | 2 | a0001c0011t0001g0088 a0001c0011t0001g0089 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.852+1799G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17673106 | |||||||
chr6:17673137 | C | T | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.852+1768G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17673137 | |||||||
chr6:17673138 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.852+1767C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17673138 | |||||||
chr6:17673268 | C | G | 1 | a0005c0006t0006g0313 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.852+1637G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17673268 | |||||||
chr6:17673272 | C | T | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.852+1633G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17673272 | |||||||
chr6:17673495 | A | G | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.852+1410T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17673495 | |||||||
chr6:17673628 | G | A | 1 | a0002c0010t0001g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.852+1277C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17673628 | |||||||
chr6:17674265 | T | C | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.852+640A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17674265 | |||||||
chr6:17674348 | A | C | 4 | a0003c0004t0001g0090 a0003c0004t0001g0092 a0003c0004t0001g0094 others(1): Show |
4 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+557T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17674348 | |||||||
chr6:17674396 | A | C | 1 | a0002c0002t0002g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.852+509T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17674396 | |||||||
chr6:17674397 | G | C | 1 | a0003c0004t0001g0094 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.852+508C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17674397 | |||||||
chr6:17674437 | T | C | 1 | a0002c0010t0001g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.852+468A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 5/21 | chr6 | 17674437 | |||||||
chr6:17675088 | T | G | 1 | a0008c0015t0001g0085 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.724-55A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 4/21 | chr6 | 17675088 | |||||||
chr6:17675147 | T | C | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.723+82A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 4/21 | chr6 | 17675147 | |||||||
chr6:17675155 | G | GA | 19 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(16): Show |
19 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.723+73dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 4/21 | chr6 | 17675155 | |||||||
chr6:17675889 | G | A | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.335-119C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17675889 | |||||||
chr6:17675962 | AT | A | 3 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0001g0299 |
3 | HG03579.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.335-193delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17675962 | |||||||
chr6:17676178 | C | G | 2 | a0003c0004t0001g0302 a0009c0027t0001g0306 |
2 | HG01192.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.335-408G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676178 | |||||||
chr6:17676239 | A | G | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.335-469T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676239 | |||||||
chr6:17676365 | T | C | 4 | a0003c0012t0001g0275 a0003c0012t0001g0277 a0003c0012t0001g0279 others(1): Show |
4 | HG01243.hp2 HG02735.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-595A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676365 | |||||||
chr6:17676405 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.335-635G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676405 | |||||||
chr6:17676427 | T | C | 3 | a0004c0005t0001g0063 a0004c0005t0001g0064 a0004c0005t0001g0065 |
3 | HG00140.hp1 HG00738.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.335-657A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676427 | |||||||
chr6:17676437 | G | GAATA | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.335-668_335-667ins others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676437 | |||||||
chr6:17676562 | A | G | 1 | a0005c0006t0001g0283 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.335-792T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676562 | |||||||
chr6:17676597 | A | G | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.335-827T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676597 | |||||||
chr6:17676708 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.335-938C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676708 | |||||||
chr6:17676753 | A | G | 1 | a0003c0012t0001g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.335-983T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676753 | |||||||
chr6:17676872 | G | C | 3 | a0004c0005t0001g0063 a0004c0005t0001g0064 a0004c0005t0001g0065 |
3 | HG00140.hp1 HG00738.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.335-1102C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676872 | |||||||
chr6:17676970 | G | T | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.335-1200C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17676970 | |||||||
chr6:17677090 | A | G | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.335-1320T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17677090 | |||||||
chr6:17677155 | C | G | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.335-1385G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17677155 | |||||||
chr6:17677216 | A | G | 1 | a0002c0002t0004g0027 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.335-1446T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17677216 | |||||||
chr6:17677415 | G | A | 3 | a0001c0003t0001g0126 a0001c0003t0001g0260 a0001c0003t0001g0272 |
3 | HG02083.hp2 NA18984.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.335-1645C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17677415 | |||||||
chr6:17677490 | T | G | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.335-1720A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17677490 | |||||||
chr6:17677559 | C | G | 1 | a0005c0006t0001g0290 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.335-1789G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17677559 | |||||||
chr6:17677730 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.335-1960A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17677730 | |||||||
chr6:17677732 | CT | C | 299 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(296): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.335-1963delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17677732 | |||||||
chr6:17677732 | CTT | C | 6 | a0001c0001t0013g0038 a0001c0003t0001g0142 a0001c0014t0001g0118 others(3): Show |
6 | HG00642.hp1 HG01070.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.335-1964_335-1963d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17677732 | |||||||
chr6:17678352 | C | CA | 28 | a0001c0003t0001g0124 a0001c0003t0001g0147 a0001c0003t0001g0192 others(25): Show |
28 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.335-2583dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAA | 7 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0200 others(4): Show |
7 | HG02145.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.335-2585_335-2583d others(5): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAA | 45 | a0001c0001t0009g0308 a0002c0002t0002g0047 a0002c0002t0002g0048 others(42): Show |
45 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.335-2587_335-2583d others(7): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAAA | 10 | a0001c0001t0009g0307 a0001c0009t0001g0161 a0002c0002t0001g0222 others(7): Show |
10 | HG02056.hp1 HG02071.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.335-2588_335-2583d others(8): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAAAA others(5): Show |
2 | a0001c0009t0001g0139 a0001c0009t0001g0164 |
2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.335-2594_335-2583d others(14): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAAAA others(7): Show |
3 | a0001c0009t0001g0149 a0001c0009t0003g0016 a0013c0020t0001g0191 |
3 | HG02055.hp1 HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.335-2596_335-2583d others(16): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0151 a0001c0001t0001g0162 a0001c0009t0003g0017 others(1): Show |
4 | HG02451.hp2 HG02717.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-2597_335-2583d others(17): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0040 a0001c0001t0001g0152 a0001c0001t0001g0163 |
3 | HG01167.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.335-2598_335-2583d others(18): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0154 a0003c0004t0001g0302 a0009c0027t0001g0306 |
3 | HG01192.hp2 HG02258.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.335-2600_335-2583d others(20): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAAAA others(13): Show |
3 | a0003c0004t0001g0299 a0003c0004t0001g0300 a0003c0025t0001g0301 |
3 | HG01257.hp2 HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.335-2602_335-2583d others(22): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAAAA others(14): Show |
2 | a0003c0004t0001g0298 a0003c0004t0001g0303 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.335-2603_335-2583d others(23): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0003g0021 a0003c0004t0001g0284 |
2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.335-2604_335-2583d others(24): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAAAA others(18): Show |
3 | a0001c0001t0001g0153 a0001c0001t0003g0033 a0003c0004t0001g0296 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.335-2583_335-2582i others(27): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | C | CAAAAAAA others(19): Show |
2 | a0003c0004t0001g0295 a0003c0004t0001g0297 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.335-2583_335-2582i others(28): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | CA | C | 50 | a0001c0001t0001g0099 a0001c0001t0001g0111 a0001c0001t0001g0130 others(47): Show |
50 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.335-2583delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678352 | CAA | C | 12 | a0001c0001t0001g0096 a0001c0001t0001g0102 a0001c0001t0001g0160 others(9): Show |
12 | HG01070.hp1 HG01361.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.335-2584_335-2583d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678352 | |||||||
chr6:17678536 | C | T | 4 | a0003c0004t0001g0081 a0003c0004t0001g0082 a0003c0004t0001g0083 others(1): Show |
4 | HG02622.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.335-2766G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678536 | |||||||
chr6:17678539 | T | C | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.335-2769A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678539 | |||||||
chr6:17678569 | C | T | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.335-2799G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678569 | |||||||
chr6:17678826 | TC | T | 6 | a0001c0001t0001g0157 a0001c0003t0001g0134 a0001c0003t0001g0135 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.335-3057delG | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678826 | |||||||
chr6:17678888 | A | G | 9 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(6): Show |
9 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.335-3118T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678888 | |||||||
chr6:17678947 | TA | T | 245 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(242): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.335-3178delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678947 | |||||||
chr6:17678947 | TAA | T | 9 | a0001c0003t0001g0095 a0001c0009t0001g0161 a0003c0004t0001g0295 others(6): Show |
9 | HG01074.hp2 HG01496.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.335-3179_335-3178d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678947 | |||||||
chr6:17678971 | TAAC | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.335-3204_335-3202d others(5): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17678971 | |||||||
chr6:17679218 | C | T | 1 | a0003c0012t0001g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.335-3448G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17679218 | |||||||
chr6:17679349 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.335-3579T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17679349 | |||||||
chr6:17679476 | G | C | 97 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(94): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.335-3706C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17679476 | |||||||
chr6:17679848 | C | T | 1 | a0001c0009t0001g0161 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.335-4078G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17679848 | |||||||
chr6:17679884 | G | C | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.335-4114C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17679884 | |||||||
chr6:17679914 | C | A | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.335-4144G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17679914 | |||||||
chr6:17680053 | G | A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(7): Show |
10 | HG01167.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.335-4283C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17680053 | |||||||
chr6:17680125 | C | T | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.335-4355G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17680125 | |||||||
chr6:17680272 | T | C | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.335-4502A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17680272 | |||||||
chr6:17680276 | C | T | 2 | a0002c0010t0003g0007 a0002c0010t0003g0008 |
2 | HG01255.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.335-4506G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17680276 | |||||||
chr6:17680378 | T | C | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.335-4608A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17680378 | |||||||
chr6:17680713 | C | T | 1 | a0002c0002t0002g0242 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.335-4943G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17680713 | |||||||
chr6:17680731 | C | A | 10 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(7): Show |
10 | HG01167.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.335-4961G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17680731 | |||||||
chr6:17680950 | T | C | 9 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(6): Show |
9 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.335-5180A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17680950 | |||||||
chr6:17681045 | A | G | 4 | a0003c0012t0001g0275 a0003c0012t0001g0277 a0003c0012t0001g0279 others(1): Show |
4 | HG01243.hp2 HG02735.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-5275T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17681045 | |||||||
chr6:17681071 | GAGTATTA others(3): Show |
G | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.335-5311_335-5302d others(12): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17681071 | |||||||
chr6:17681181 | A | G | 1 | a0006c0007t0001g0103 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.335-5411T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17681181 | |||||||
chr6:17681211 | TA | T | 96 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(93): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.335-5442delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17681211 | |||||||
chr6:17681401 | A | AT | 289 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.335-5632_335-5631i others(3): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17681401 | |||||||
chr6:17681441 | C | T | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.335-5671G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17681441 | |||||||
chr6:17681519 | T | C | 3 | a0004c0005t0001g0062 a0004c0005t0001g0066 a0004c0005t0016g0212 |
3 | HG00544.hp1 NA18946.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.335-5749A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17681519 | |||||||
chr6:17681641 | A | G | 1 | a0001c0009t0001g0164 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.335-5871T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17681641 | |||||||
chr6:17681737 | G | A | 11 | a0001c0003t0001g0133 a0001c0003t0001g0136 a0001c0003t0001g0141 others(8): Show |
11 | HG00609.hp2 HG02080.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.335-5967C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17681737 | |||||||
chr6:17681965 | T | C | 1 | a0002c0002t0002g0050 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.335-6195A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17681965 | |||||||
chr6:17681972 | C | G | 1 | a0005c0006t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.335-6202G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17681972 | |||||||
chr6:17682172 | T | C | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.334+6224A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682172 | |||||||
chr6:17682240 | T | TA | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.334+6155dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682240 | |||||||
chr6:17682253 | C | T | 1 | a0004c0005t0001g0061 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.334+6143G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682253 | |||||||
chr6:17682488 | T | C | 1 | a0003c0012t0001g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.334+5908A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682488 | |||||||
chr6:17682491 | A | G | 146 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(143): Show |
146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.334+5905T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682491 | |||||||
chr6:17682604 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.334+5792G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682604 | |||||||
chr6:17682684 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.334+5712A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682684 | |||||||
chr6:17682691 | T | G | 1 | a0001c0001t0013g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.334+5705A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682691 | |||||||
chr6:17682800 | C | T | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.334+5596G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682800 | |||||||
chr6:17682811 | G | A | 1 | a0005c0006t0001g0287 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.334+5585C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682811 | |||||||
chr6:17682815 | G | A | 13 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(10): Show |
13 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.334+5581C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682815 | |||||||
chr6:17682862 | G | C | 1 | a0003c0004t0001g0256 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.334+5534C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682862 | |||||||
chr6:17682891 | G | A | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.334+5505C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682891 | |||||||
chr6:17682917 | A | T | 1 | a0003c0004t0001g0256 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.334+5479T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682917 | |||||||
chr6:17682925 | G | GA | 31 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(28): Show |
31 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.334+5470dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682925 | |||||||
chr6:17682925 | G | GAA | 130 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0101 others(127): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.334+5469_334+5470d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682925 | |||||||
chr6:17682925 | G | GAAA | 18 | a0001c0001t0001g0096 a0001c0001t0001g0148 a0001c0001t0001g0180 others(15): Show |
18 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.334+5468_334+5470d others(5): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682925 | |||||||
chr6:17682925 | GA | G | 11 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0003g0002 others(8): Show |
11 | HG02280.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.334+5470delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682925 | |||||||
chr6:17682928 | A | G | 58 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(55): Show |
58 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.334+5468T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682928 | |||||||
chr6:17682935 | A | AAC | 8 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.334+5460_334+5461i others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682935 | |||||||
chr6:17682940 | A | C | 18 | a0005c0006t0001g0281 a0005c0006t0001g0283 a0005c0006t0001g0287 others(15): Show |
18 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.334+5456T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682940 | |||||||
chr6:17682977 | T | C | 289 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.334+5419A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17682977 | |||||||
chr6:17683099 | TGA | T | 3 | a0002c0010t0001g0053 a0002c0010t0003g0007 a0002c0010t0003g0008 |
3 | HG01255.hp1 HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.334+5295_334+5296d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683099 | |||||||
chr6:17683102 | A | T | 3 | a0002c0010t0001g0053 a0002c0010t0003g0007 a0002c0010t0003g0008 |
3 | HG01255.hp1 HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.334+5294T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683102 | |||||||
chr6:17683323 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.334+5073T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683323 | |||||||
chr6:17683490 | G | A | 153 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(150): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.334+4906C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683490 | |||||||
chr6:17683581 | G | A | 1 | a0001c0003t0003g0015 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.334+4815C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683581 | |||||||
chr6:17683588 | T | C | 1 | a0001c0001t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.334+4808A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683588 | |||||||
chr6:17683636 | T | C | 1 | a0004c0005t0001g0057 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.334+4760A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683636 | |||||||
chr6:17683718 | A | AC | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.334+4677dupG | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683718 | |||||||
chr6:17683798 | T | A | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.334+4598A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683798 | |||||||
chr6:17683812 | C | T | 3 | a0002c0002t0002g0250 a0002c0002t0002g0251 a0002c0002t0004g0028 |
3 | HG02109.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.334+4584G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683812 | |||||||
chr6:17683821 | T | C | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.334+4575A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683821 | |||||||
chr6:17683898 | T | C | 1 | a0002c0010t0015g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.334+4498A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683898 | |||||||
chr6:17683920 | G | A | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.334+4476C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17683920 | |||||||
chr6:17684097 | T | A | 3 | a0001c0003t0001g0124 a0001c0003t0001g0147 a0001c0003t0021g0316 |
3 | HG00408.hp2 NA18962.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.334+4299A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17684097 | |||||||
chr6:17684324 | C | T | 7 | a0001c0009t0001g0139 a0001c0009t0001g0149 a0001c0009t0001g0161 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.334+4072G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17684324 | |||||||
chr6:17684450 | G | A | 1 | a0001c0003t0001g0119 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.334+3946C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17684450 | |||||||
chr6:17684515 | C | G | 2 | a0007c0008t0001g0201 a0007c0008t0001g0203 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.334+3881G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17684515 | |||||||
chr6:17684568 | C | T | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.334+3828G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17684568 | |||||||
chr6:17684648 | A | T | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.334+3748T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17684648 | |||||||
chr6:17684660 | T | C | 1 | a0006c0007t0001g0261 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.334+3736A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17684660 | |||||||
chr6:17684728 | A | G | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.334+3668T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17684728 | |||||||
chr6:17684910 | T | C | 7 | a0001c0009t0001g0139 a0001c0009t0001g0149 a0001c0009t0001g0161 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.334+3486A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17684910 | |||||||
chr6:17684913 | G | A | 2 | a0006c0007t0001g0110 a0006c0007t0001g0115 |
2 | HG01069.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.334+3483C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17684913 | |||||||
chr6:17685033 | T | C | 5 | a0001c0003t0001g0131 a0001c0003t0001g0137 a0001c0003t0001g0142 others(2): Show |
5 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.334+3363A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685033 | |||||||
chr6:17685145 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.334+3251T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685145 | |||||||
chr6:17685238 | GTCATGT | G | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.334+3152_334+3157d others(8): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685238 | |||||||
chr6:17685245 | G | A | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.334+3151C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685245 | |||||||
chr6:17685246 | C | A | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.334+3150G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685246 | |||||||
chr6:17685272 | G | C | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.334+3124C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685272 | |||||||
chr6:17685285 | C | T | 9 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(6): Show |
9 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.334+3111G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685285 | |||||||
chr6:17685418 | G | A | 1 | a0002c0010t0001g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.334+2978C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685418 | |||||||
chr6:17685503 | C | T | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.334+2893G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685503 | |||||||
chr6:17685548 | C | CA | 40 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(37): Show |
40 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.334+2847dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685548 | |||||||
chr6:17685548 | CA | C | 43 | a0001c0001t0001g0102 a0001c0001t0001g0160 a0002c0002t0002g0052 others(40): Show |
43 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.334+2847delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685548 | |||||||
chr6:17685706 | T | C | 10 | a0002c0002t0002g0216 a0002c0002t0002g0217 a0002c0002t0002g0218 others(7): Show |
10 | HG00558.hp1 HG02135.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.334+2690A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685706 | |||||||
chr6:17685743 | T | C | 8 | a0004c0005t0001g0068 a0004c0005t0001g0069 a0004c0005t0001g0070 others(5): Show |
8 | HG00323.hp1 HG01928.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.334+2653A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685743 | |||||||
chr6:17685940 | T | C | 2 | a0001c0014t0001g0118 a0001c0014t0003g0014 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.334+2456A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685940 | |||||||
chr6:17685953 | T | C | 1 | a0005c0006t0001g0289 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.334+2443A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685953 | |||||||
chr6:17685974 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.334+2422C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17685974 | |||||||
chr6:17686153 | AAAAG | A | 233 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.334+2239_334+2242d others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686153 | |||||||
chr6:17686297 | C | T | 1 | a0001c0001t0013g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.334+2099G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686297 | |||||||
chr6:17686298 | G | A | 2 | a0003c0012t0001g0275 a0019c0029t0001g0276 |
2 | HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.334+2098C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686298 | |||||||
chr6:17686329 | A | T | 43 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(40): Show |
43 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.334+2067T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686329 | |||||||
chr6:17686389 | C | T | 2 | a0002c0002t0002g0225 a0002c0002t0002g0226 |
2 | HG00558.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.334+2007G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686389 | |||||||
chr6:17686400 | T | C | 1 | a0001c0009t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.334+1996A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686400 | |||||||
chr6:17686445 | G | C | 2 | a0003c0012t0001g0277 a0003c0012t0001g0279 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.334+1951C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686445 | |||||||
chr6:17686458 | C | T | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.334+1938G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686458 | |||||||
chr6:17686524 | T | G | 19 | a0005c0006t0001g0281 a0005c0006t0001g0283 a0005c0006t0001g0287 others(16): Show |
19 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.334+1872A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686524 | |||||||
chr6:17686676 | T | C | 1 | a0013c0020t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.334+1720A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686676 | |||||||
chr6:17686697 | A | G | 2 | a0001c0001t0001g0097 a0001c0021t0001g0098 |
2 | HG01361.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.334+1699T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686697 | |||||||
chr6:17686707 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.334+1689A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686707 | |||||||
chr6:17686719 | A | AT | 7 | a0005c0006t0001g0287 a0005c0006t0001g0289 a0005c0006t0001g0304 others(4): Show |
7 | NA18612.hp2 NA18952.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.334+1676dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686719 | |||||||
chr6:17686719 | A | T | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334+1677T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686719 | |||||||
chr6:17686822 | T | A | 1 | a0001c0003t0003g0013 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.334+1574A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686822 | |||||||
chr6:17686843 | C | T | 29 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0055 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.334+1553G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686843 | |||||||
chr6:17686880 | C | CG | 5 | a0001c0001t0001g0111 a0001c0001t0001g0185 a0001c0001t0001g0269 others(2): Show |
5 | HG01069.hp2 HG01981.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.334+1515_334+1516i others(3): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686880 | |||||||
chr6:17686881 | C | G | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.334+1515G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686881 | |||||||
chr6:17686892 | G | A | 2 | a0003c0012t0001g0275 a0019c0029t0001g0276 |
2 | HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.334+1504C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686892 | |||||||
chr6:17686895 | G | A | 1 | a0002c0002t0001g0222 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.334+1501C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686895 | |||||||
chr6:17686900 | A | AG | 17 | a0001c0001t0001g0130 a0001c0001t0001g0166 a0001c0001t0003g0018 others(14): Show |
17 | HG00438.hp1 HG00438.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.334+1495dupC | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686900 | |||||||
chr6:17686903 | G | A | 1 | a0019c0029t0001g0276 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.334+1493C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686903 | |||||||
chr6:17686907 | C | T | 11 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(8): Show |
11 | HG00735.hp2 HG01167.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.334+1489G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17686907 | |||||||
chr6:17687066 | T | C | 1 | a0001c0003t0001g0095 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.334+1330A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17687066 | |||||||
chr6:17687189 | C | T | 1 | a0008c0015t0001g0085 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.334+1207G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17687189 | |||||||
chr6:17687221 | C | A | 1 | a0002c0002t0002g0051 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.334+1175G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17687221 | |||||||
chr6:17687744 | G | C | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.334+652C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17687744 | |||||||
chr6:17687798 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.334+598G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17687798 | |||||||
chr6:17688031 | A | G | 13 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(10): Show |
13 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.334+365T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17688031 | |||||||
chr6:17688105 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.334+291C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17688105 | |||||||
chr6:17688193 | G | C | 29 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0055 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.334+203C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17688193 | |||||||
chr6:17688195 | C | A | 1 | a0003c0004t0001g0286 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.334+201G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17688195 | |||||||
chr6:17688366 | T | C | 2 | a0007c0008t0001g0197 a0007c0008t0001g0198 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.334+30A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 2/21 | chr6 | 17688366 | |||||||
chr6:17688823 | A | C | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.112-205T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17688823 | |||||||
chr6:17689055 | C | G | 33 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.112-437G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689055 | |||||||
chr6:17689071 | TA | T | 95 | a0001c0003t0001g0126 a0001c0003t0001g0260 a0001c0003t0001g0272 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.112-454delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689071 | |||||||
chr6:17689089 | G | T | 2 | a0002c0010t0003g0007 a0002c0010t0003g0008 |
2 | HG01255.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.112-471C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689089 | |||||||
chr6:17689223 | T | TAAAAATA others(3): Show |
8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-615_112-606dup others(10): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689223 | |||||||
chr6:17689280 | A | G | 4 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(1): Show |
4 | HG01884.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-662T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689280 | |||||||
chr6:17689285 | G | A | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.112-667C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689285 | |||||||
chr6:17689323 | G | T | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.112-705C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689323 | |||||||
chr6:17689408 | T | C | 1 | a0002c0002t0005g0237 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.112-790A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689408 | |||||||
chr6:17689413 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.112-795T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689413 | |||||||
chr6:17689416 | C | CA | 13 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(10): Show |
13 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-799dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689416 | |||||||
chr6:17689416 | CA | C | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.112-799delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689416 | |||||||
chr6:17689475 | T | C | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.112-857A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689475 | |||||||
chr6:17689539 | C | CT | 62 | a0001c0001t0001g0170 a0002c0002t0001g0222 a0002c0002t0002g0046 others(59): Show |
62 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.112-922dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689539 | |||||||
chr6:17689597 | T | C | 1 | a0005c0006t0001g0281 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.112-979A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689597 | |||||||
chr6:17689598 | G | A | 1 | a0005c0006t0001g0281 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.112-980C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689598 | |||||||
chr6:17689600 | G | A | 1 | a0005c0006t0001g0281 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.112-982C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689600 | |||||||
chr6:17689602 | T | C | 1 | a0005c0006t0001g0281 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.112-984A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689602 | |||||||
chr6:17689625 | C | G | 10 | a0002c0002t0002g0216 a0002c0002t0002g0217 a0002c0002t0002g0218 others(7): Show |
10 | HG00558.hp1 HG02135.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.112-1007G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17689625 | |||||||
chr6:17690162 | C | T | 1 | a0001c0003t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.112-1544G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17690162 | |||||||
chr6:17690228 | T | C | 1 | a0011c0033t0001g0140 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.112-1610A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17690228 | |||||||
chr6:17690245 | G | A | 1 | a0002c0010t0001g0254 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.112-1627C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17690245 | |||||||
chr6:17690270 | T | TGAACCCG others(20): Show |
29 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0055 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.112-1679_112-1653d others(29): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17690270 | |||||||
chr6:17690431 | G | C | 1 | a0004c0005t0001g0070 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.112-1813C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17690431 | |||||||
chr6:17690659 | G | C | 1 | a0003c0004t0001g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.112-2041C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17690659 | |||||||
chr6:17690708 | C | A | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.112-2090G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17690708 | |||||||
chr6:17691040 | G | A | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.112-2422C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691040 | |||||||
chr6:17691175 | G | A | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.112-2557C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691175 | |||||||
chr6:17691205 | T | C | 2 | a0006c0007t0001g0110 a0006c0007t0001g0115 |
2 | HG01069.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.112-2587A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691205 | |||||||
chr6:17691270 | T | C | 2 | a0003c0004t0001g0080 a0003c0004t0001g0257 |
2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.112-2652A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691270 | |||||||
chr6:17691289 | C | T | 1 | a0006c0022t0001g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.112-2671G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691289 | |||||||
chr6:17691434 | A | C | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.112-2816T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691434 | |||||||
chr6:17691539 | T | C | 1 | a0003c0012t0001g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.112-2921A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691539 | |||||||
chr6:17691594 | G | A | 1 | a0004c0005t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.112-2976C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691594 | |||||||
chr6:17691626 | A | G | 1 | a0013c0020t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.112-3008T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691626 | |||||||
chr6:17691660 | G | A | 1 | a0005c0006t0001g0294 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.112-3042C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691660 | |||||||
chr6:17691822 | A | AT | 67 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0101 others(64): Show |
67 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.112-3205dupA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691822 | |||||||
chr6:17691838 | A | G | 2 | a0002c0002t0002g0218 a0002c0002t0002g0243 |
2 | HG02135.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.112-3220T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17691838 | |||||||
chr6:17692003 | T | G | 1 | a0002c0002t0002g0238 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.112-3385A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17692003 | |||||||
chr6:17692287 | T | C | 1 | a0005c0006t0001g0294 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.112-3669A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17692287 | |||||||
chr6:17692478 | C | A | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.112-3860G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17692478 | |||||||
chr6:17692535 | G | T | 1 | a0005c0006t0001g0294 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.112-3917C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17692535 | |||||||
chr6:17692563 | T | C | 1 | a0002c0010t0015g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.112-3945A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17692563 | |||||||
chr6:17692586 | T | C | 1 | a0002c0010t0001g0254 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.112-3968A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17692586 | |||||||
chr6:17693105 | A | G | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.112-4487T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693105 | |||||||
chr6:17693156 | C | A | 4 | a0001c0003t0001g0134 a0001c0003t0001g0135 a0001c0003t0001g0143 others(1): Show |
4 | HG01074.hp1 HG01099.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-4538G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693156 | |||||||
chr6:17693183 | T | TAC | 18 | a0001c0001t0013g0038 a0001c0001t0018g0195 a0001c0003t0001g0260 others(15): Show |
18 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.112-4567_112-4566d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | T | TACAC | 54 | a0001c0001t0001g0268 a0001c0001t0003g0018 a0001c0001t0009g0307 others(51): Show |
54 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.112-4569_112-4566d others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | T | TACACAC | 26 | a0001c0001t0001g0101 a0001c0001t0001g0148 a0001c0001t0001g0165 others(23): Show |
26 | HG00609.hp1 HG01175.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.112-4571_112-4566d others(8): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | T | TACACACA others(1): Show |
96 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0099 others(93): Show |
96 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.112-4573_112-4566d others(10): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | T | TACACACA others(3): Show |
23 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0102 others(20): Show |
23 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.112-4575_112-4566d others(12): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | T | TACACACA others(5): Show |
17 | a0001c0001t0001g0045 a0001c0001t0001g0151 a0001c0001t0001g0170 others(14): Show |
17 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.112-4577_112-4566d others(14): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | T | TACACACA others(7): Show |
8 | a0001c0001t0001g0040 a0001c0001t0001g0130 a0001c0001t0001g0152 others(5): Show |
8 | HG00438.hp1 HG02074.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-4579_112-4566d others(16): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | T | TACACACA others(9): Show |
2 | a0001c0001t0001g0193 a0005c0017t0003g0036 |
2 | HG01243.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.112-4581_112-4566d others(18): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | T | TACACACA others(11): Show |
1 | a0003c0004t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112-4583_112-4566d others(20): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | T | TACACACA others(13): Show |
1 | a0001c0001t0001g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.112-4585_112-4566d others(22): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | T | TACACACA others(15): Show |
2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01167.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.112-4587_112-4566d others(24): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | TAC | T | 23 | a0002c0002t0002g0221 a0002c0002t0002g0224 a0002c0010t0001g0053 others(20): Show |
23 | HG00323.hp2 HG00735.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.112-4567_112-4566d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | TACAC | T | 28 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0055 others(25): Show |
28 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.112-4569_112-4566d others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | TACACACA others(1): Show |
T | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-4573_112-4566d others(10): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | TACACACA others(3): Show |
T | 1 | a0004c0005t0003g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.112-4575_112-4566d others(12): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693183 | TACACACA others(15): Show |
T | 2 | a0002c0010t0003g0007 a0002c0010t0003g0008 |
2 | HG01255.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.112-4587_112-4566d others(24): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693183 | |||||||
chr6:17693463 | C | T | 2 | a0001c0001t0001g0097 a0001c0021t0001g0098 |
2 | HG01361.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.112-4845G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693463 | |||||||
chr6:17693565 | A | C | 1 | a0002c0002t0002g0223 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.112-4947T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693565 | |||||||
chr6:17693652 | C | T | 1 | a0015c0031t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.112-5034G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693652 | |||||||
chr6:17693653 | G | A | 42 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(39): Show |
42 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.112-5035C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693653 | |||||||
chr6:17693657 | C | CGGGCAGA others(9): Show |
8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-5055_112-5040d others(18): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693657 | |||||||
chr6:17693666 | C | A | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.112-5048G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693666 | |||||||
chr6:17693723 | T | C | 10 | a0001c0001t0001g0040 a0001c0001t0001g0151 a0001c0001t0001g0152 others(7): Show |
10 | HG01167.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.112-5105A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693723 | |||||||
chr6:17693793 | G | GA | 6 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(3): Show |
6 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-5176dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693793 | |||||||
chr6:17693895 | C | T | 1 | a0017c0030t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.112-5277G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17693895 | |||||||
chr6:17694066 | G | A | 2 | a0003c0012t0001g0275 a0019c0029t0001g0276 |
2 | HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.112-5448C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694066 | |||||||
chr6:17694075 | G | A | 2 | a0003c0004t0001g0083 a0016c0024t0001g0084 |
2 | HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.112-5457C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694075 | |||||||
chr6:17694223 | C | T | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.112-5605G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694223 | |||||||
chr6:17694251 | T | C | 1 | a0001c0003t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.112-5633A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694251 | |||||||
chr6:17694256 | G | C | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.112-5638C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694256 | |||||||
chr6:17694324 | T | C | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.112-5706A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694324 | |||||||
chr6:17694387 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.112-5769C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694387 | |||||||
chr6:17694397 | G | A | 1 | a0005c0006t0001g0290 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.112-5779C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694397 | |||||||
chr6:17694423 | C | T | 1 | a0003c0012t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.112-5805G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694423 | |||||||
chr6:17694427 | C | A | 1 | a0001c0003t0001g0155 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.112-5809G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694427 | |||||||
chr6:17694531 | C | G | 1 | a0004c0005t0001g0087 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.112-5913G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694531 | |||||||
chr6:17694541 | T | C | 1 | a0001c0003t0001g0262 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.112-5923A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694541 | |||||||
chr6:17694611 | C | T | 12 | a0003c0004t0001g0080 a0003c0004t0001g0081 a0003c0004t0001g0082 others(9): Show |
12 | HG01109.hp1 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.112-5993G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694611 | |||||||
chr6:17694706 | C | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.112-6088G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694706 | |||||||
chr6:17694710 | G | A | 9 | a0003c0004t0001g0295 a0003c0004t0001g0296 a0003c0004t0001g0297 others(6): Show |
9 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.112-6092C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694710 | |||||||
chr6:17694794 | T | G | 1 | a0002c0002t0002g0242 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.112-6176A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694794 | |||||||
chr6:17694908 | C | T | 2 | a0001c0011t0001g0088 a0001c0011t0001g0089 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.112-6290G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694908 | |||||||
chr6:17694966 | G | A | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.112-6348C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694966 | |||||||
chr6:17694982 | G | GA | 152 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(149): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.112-6365dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694982 | |||||||
chr6:17694982 | GAA | G | 40 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0004c0005t0001g0039 others(37): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.112-6366_112-6365d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694982 | |||||||
chr6:17694992 | A | G | 1 | a0002c0002t0001g0222 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.112-6374T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17694992 | |||||||
chr6:17695474 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.112-6856T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17695474 | |||||||
chr6:17695491 | T | C | 1 | a0003c0004t0003g0010 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.112-6873A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17695491 | |||||||
chr6:17695498 | T | C | 1 | a0001c0003t0003g0032 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.112-6880A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17695498 | |||||||
chr6:17695564 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.112-6946T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17695564 | |||||||
chr6:17695627 | T | C | 55 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0101 others(52): Show |
55 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.112-7009A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17695627 | |||||||
chr6:17695648 | A | C | 2 | a0001c0011t0001g0088 a0001c0011t0001g0089 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.112-7030T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17695648 | |||||||
chr6:17695834 | C | T | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.112-7216G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17695834 | |||||||
chr6:17695881 | C | T | 1 | a0002c0002t0002g0258 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.112-7263G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17695881 | |||||||
chr6:17695941 | G | A | 1 | a0002c0010t0012g0004 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.112-7323C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17695941 | |||||||
chr6:17695996 | G | A | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-7378C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17695996 | |||||||
chr6:17696003 | C | T | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-7385G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17696003 | |||||||
chr6:17696140 | C | A | 1 | a0006c0007t0001g0103 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.112-7522G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17696140 | |||||||
chr6:17696314 | T | C | 4 | a0001c0001t0001g0102 a0001c0001t0001g0160 a0006c0022t0001g0159 others(1): Show |
4 | HG01070.hp1 HG01358.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-7696A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17696314 | |||||||
chr6:17696342 | C | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0003g0019 |
3 | NA18978.hp2 NA18983.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.112-7724G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17696342 | |||||||
chr6:17696493 | C | T | 6 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0001c0013t0001g0206 others(3): Show |
6 | NA18950.hp2 NA18960.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.112-7875G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17696493 | |||||||
chr6:17696522 | G | A | 8 | a0005c0006t0001g0287 a0005c0006t0001g0289 a0005c0006t0001g0304 others(5): Show |
8 | NA18612.hp2 NA18952.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-7904C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17696522 | |||||||
chr6:17696552 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.112-7934C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17696552 | |||||||
chr6:17696761 | AT | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.112-8144delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17696761 | |||||||
chr6:17696862 | C | A | 2 | a0008c0015t0001g0085 a0008c0015t0001g0086 |
2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.112-8244G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17696862 | |||||||
chr6:17696943 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.112-8325G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17696943 | |||||||
chr6:17697070 | CA | C | 18 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(15): Show |
18 | HG00323.hp2 HG01192.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.112-8453delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697070 | |||||||
chr6:17697070 | CAA | C | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.112-8454_112-8453d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697070 | |||||||
chr6:17697160 | G | A | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-8542C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697160 | |||||||
chr6:17697185 | G | C | 1 | a0008c0015t0001g0086 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.112-8567C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697185 | |||||||
chr6:17697395 | G | C | 1 | a0002c0002t0020g0315 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.112-8777C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697395 | |||||||
chr6:17697523 | T | A | 1 | a0002c0002t0002g0219 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.111+8754A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697523 | |||||||
chr6:17697547 | C | G | 2 | a0003c0004t0001g0080 a0003c0004t0001g0257 |
2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.111+8730G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697547 | |||||||
chr6:17697642 | C | T | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.111+8635G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697642 | |||||||
chr6:17697731 | A | C | 2 | a0001c0001t0001g0102 a0010c0026t0003g0011 |
2 | HG01358.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.111+8546T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697731 | |||||||
chr6:17697732 | C | T | 98 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(95): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.111+8545G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697732 | |||||||
chr6:17697732 | CTCTATAA others(37): Show |
C | 1 | a0001c0009t0001g0161 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.111+8501_111+8544d others(46): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697732 | |||||||
chr6:17697870 | T | A | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.111+8407A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17697870 | |||||||
chr6:17698052 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.111+8225G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698052 | |||||||
chr6:17698152 | G | A | 1 | a0001c0001t0003g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.111+8125C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698152 | |||||||
chr6:17698225 | G | A | 21 | a0005c0006t0001g0280 a0005c0006t0001g0281 a0005c0006t0001g0283 others(18): Show |
21 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.111+8052C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698225 | |||||||
chr6:17698342 | CAGTGCTT others(116): Show |
C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7812_111+7934d others(2): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698342 | |||||||
chr6:17698343 | A | G | 1 | a0004c0005t0001g0062 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.111+7934T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698343 | |||||||
chr6:17698362 | C | G | 1 | a0001c0003t0003g0032 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.111+7915G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698362 | |||||||
chr6:17698417 | C | T | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.111+7860G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698417 | |||||||
chr6:17698418 | C | T | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.111+7859G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698418 | |||||||
chr6:17698466 | T | C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7811A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698466 | |||||||
chr6:17698467 | G | A | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7810C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698467 | |||||||
chr6:17698474 | C | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7803G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698474 | |||||||
chr6:17698476 | C | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7801G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698476 | |||||||
chr6:17698485 | C | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7792G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698485 | |||||||
chr6:17698490 | G | A | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7787C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698490 | |||||||
chr6:17698495 | T | C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7782A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698495 | |||||||
chr6:17698503 | C | G | 4 | a0003c0004t0001g0091 a0003c0004t0001g0093 a0003c0004t0003g0010 others(1): Show |
4 | HG02027.hp2 HG02135.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+7774G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698503 | |||||||
chr6:17698504 | C | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7773G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698504 | |||||||
chr6:17698505 | G | A | 1 | a0005c0006t0001g0283 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.111+7772C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698505 | |||||||
chr6:17698509 | T | C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7768A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698509 | |||||||
chr6:17698513 | C | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7764G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698513 | |||||||
chr6:17698521 | A | G | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7756T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698521 | |||||||
chr6:17698524 | G | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7753C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698524 | |||||||
chr6:17698532 | A | C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7745T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698532 | |||||||
chr6:17698542 | T | G | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7735A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698542 | |||||||
chr6:17698545 | C | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7732G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698545 | |||||||
chr6:17698549 | T | C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7728A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698549 | |||||||
chr6:17698563 | C | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7714G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698563 | |||||||
chr6:17698577 | G | A | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7700C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698577 | |||||||
chr6:17698580 | T | C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7697A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698580 | |||||||
chr6:17698594 | G | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7683C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698594 | |||||||
chr6:17698598 | C | T | 2 | a0002c0002t0014g0213 a0002c0010t0002g0220 |
2 | HG02559.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.111+7679G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698598 | |||||||
chr6:17698599 | G | A | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.111+7678C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698599 | |||||||
chr6:17698606 | T | C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7671A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698606 | |||||||
chr6:17698607 | G | A | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7670C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698607 | |||||||
chr6:17698609 | G | A | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7668C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698609 | |||||||
chr6:17698610 | C | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7667G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698610 | |||||||
chr6:17698611 | A | G | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7666T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698611 | |||||||
chr6:17698618 | G | A | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7659C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698618 | |||||||
chr6:17698618 | G | C | 1 | a0005c0006t0001g0283 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.111+7659C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698618 | |||||||
chr6:17698635 | G | A | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7642C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698635 | |||||||
chr6:17698637 | C | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7640G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698637 | |||||||
chr6:17698642 | G | A | 1 | a0006c0007t0001g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.111+7635C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698642 | |||||||
chr6:17698652 | G | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7625C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698652 | |||||||
chr6:17698655 | G | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7622C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698655 | |||||||
chr6:17698661 | C | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7616G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698661 | |||||||
chr6:17698663 | G | A | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7614C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698663 | |||||||
chr6:17698674 | C | A | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7603G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698674 | |||||||
chr6:17698692 | C | CATGCCAT others(115): Show |
1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7584_111+7585i others(124): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698692 | |||||||
chr6:17698693 | G | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7584C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698693 | |||||||
chr6:17698695 | G | A | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7582C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698695 | |||||||
chr6:17698701 | A | G | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7576T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698701 | |||||||
chr6:17698725 | A | G | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+7552T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698725 | |||||||
chr6:17698737 | C | CA | 19 | a0001c0001t0001g0185 a0001c0001t0018g0195 a0001c0003t0001g0145 others(16): Show |
19 | HG00741.hp2 HG01109.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.111+7539dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698737 | |||||||
chr6:17698737 | CA | C | 63 | a0001c0001t0001g0148 a0001c0001t0001g0186 a0001c0001t0001g0188 others(60): Show |
63 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.111+7539delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698737 | |||||||
chr6:17698793 | C | T | 1 | a0002c0010t0015g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.111+7484G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698793 | |||||||
chr6:17698800 | G | A | 1 | a0003c0012t0001g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.111+7477C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17698800 | |||||||
chr6:17699091 | G | T | 98 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(95): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.111+7186C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699091 | |||||||
chr6:17699189 | AT | A | 250 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(247): Show |
250 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.111+7087delA | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699189 | |||||||
chr6:17699189 | ATT | A | 7 | a0002c0002t0002g0219 a0004c0005t0001g0056 a0004c0005t0001g0070 others(4): Show |
7 | HG00140.hp2 HG01928.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+7086_111+7087d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699189 | |||||||
chr6:17699198 | T | C | 3 | a0001c0003t0001g0146 a0003c0012t0001g0277 a0003c0012t0001g0279 |
3 | HG01243.hp2 HG06807.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.111+7079A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699198 | |||||||
chr6:17699310 | C | T | 1 | a0006c0007t0001g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111+6967G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699310 | |||||||
chr6:17699324 | G | A | 1 | a0002c0010t0001g0254 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.111+6953C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699324 | |||||||
chr6:17699397 | T | C | 110 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(107): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.111+6880A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699397 | |||||||
chr6:17699443 | A | G | 1 | a0001c0001t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.111+6834T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699443 | |||||||
chr6:17699481 | C | CA | 104 | a0001c0001t0009g0307 a0001c0001t0009g0308 a0001c0003t0003g0025 others(101): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.111+6795dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699481 | |||||||
chr6:17699481 | C | CAAAA | 11 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(8): Show |
11 | HG01192.hp2 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+6792_111+6795d others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699481 | |||||||
chr6:17699870 | C | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.111+6407G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699870 | |||||||
chr6:17699880 | C | T | 1 | a0004c0005t0001g0056 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.111+6397G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17699880 | |||||||
chr6:17700003 | C | T | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.111+6274G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700003 | |||||||
chr6:17700027 | C | G | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.111+6250G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700027 | |||||||
chr6:17700092 | AACTTCTG others(17): Show |
A | 1 | a0005c0006t0003g0037 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.111+6161_111+6184d others(26): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700092 | |||||||
chr6:17700200 | A | C | 55 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(52): Show |
55 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.111+6077T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700200 | |||||||
chr6:17700237 | C | CAT | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+6038_111+6039d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700237 | |||||||
chr6:17700273 | T | C | 1 | a0007c0008t0001g0203 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.111+6004A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700273 | |||||||
chr6:17700283 | A | G | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.111+5994T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700283 | |||||||
chr6:17700320 | C | T | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.111+5957G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700320 | |||||||
chr6:17700462 | C | T | 1 | a0003c0004t0001g0079 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.111+5815G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700462 | |||||||
chr6:17700807 | T | G | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.111+5470A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700807 | |||||||
chr6:17700883 | T | A | 4 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(1): Show |
4 | HG01884.hp2 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+5394A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700883 | |||||||
chr6:17700945 | A | G | 1 | a0002c0010t0015g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.111+5332T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17700945 | |||||||
chr6:17701191 | C | T | 4 | a0003c0012t0001g0275 a0003c0012t0001g0277 a0003c0012t0001g0279 others(1): Show |
4 | HG01243.hp2 HG02735.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+5086G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701191 | |||||||
chr6:17701224 | T | TA | 11 | a0001c0001t0001g0194 a0003c0004t0001g0080 a0003c0004t0001g0091 others(8): Show |
11 | HG00735.hp2 HG01361.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+5052dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701224 | |||||||
chr6:17701275 | A | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | NA18947.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.111+5002T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701275 | |||||||
chr6:17701397 | C | T | 4 | a0003c0012t0001g0275 a0003c0012t0001g0277 a0003c0012t0001g0279 others(1): Show |
4 | HG01243.hp2 HG02735.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+4880G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701397 | |||||||
chr6:17701540 | T | G | 1 | a0013c0020t0001g0191 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.111+4737A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701540 | |||||||
chr6:17701556 | G | A | 29 | a0004c0005t0001g0039 a0004c0005t0001g0054 a0004c0005t0001g0055 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.111+4721C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701556 | |||||||
chr6:17701593 | G | A | 1 | a0016c0024t0001g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.111+4684C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701593 | |||||||
chr6:17701622 | T | C | 6 | a0002c0010t0015g0274 a0007c0008t0001g0200 a0007c0008t0001g0201 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+4655A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701622 | |||||||
chr6:17701652 | C | T | 2 | a0001c0001t0009g0307 a0001c0001t0009g0308 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.111+4625G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701652 | |||||||
chr6:17701660 | C | CA | 59 | a0001c0003t0001g0104 a0001c0003t0001g0271 a0002c0002t0001g0222 others(56): Show |
59 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.111+4616dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701660 | |||||||
chr6:17701660 | CA | C | 149 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(146): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.111+4616delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701660 | |||||||
chr6:17701676 | A | T | 5 | a0003c0012t0001g0275 a0003c0012t0001g0277 a0003c0012t0001g0278 others(2): Show |
5 | HG01109.hp1 HG01243.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+4601T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701676 | |||||||
chr6:17701692 | G | A | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.111+4585C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701692 | |||||||
chr6:17701706 | C | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01167.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.111+4571G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701706 | |||||||
chr6:17701726 | C | G | 1 | a0001c0003t0001g0147 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.111+4551G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701726 | |||||||
chr6:17701831 | T | TG | 7 | a0002c0010t0003g0008 a0004c0005t0001g0057 a0004c0005t0001g0060 others(4): Show |
7 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+4445_111+4446i others(3): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701831 | |||||||
chr6:17701831 | T | TGG | 9 | a0004c0005t0001g0063 a0004c0005t0001g0064 a0004c0005t0001g0065 others(6): Show |
9 | HG00140.hp1 HG00544.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+4445_111+4446i others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701831 | |||||||
chr6:17701831 | T | TGGG | 7 | a0004c0005t0001g0039 a0004c0005t0001g0055 a0004c0005t0001g0071 others(4): Show |
7 | HG00323.hp1 HG01074.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+4445_111+4446i others(5): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701831 | |||||||
chr6:17701832 | C | CGG | 19 | a0001c0003t0001g0095 a0001c0003t0001g0141 a0001c0003t0001g0142 others(16): Show |
19 | HG01070.hp2 HG01358.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.111+4443_111+4444d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701832 | |||||||
chr6:17701832 | C | CGGG | 26 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0003t0001g0122 others(23): Show |
26 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+4442_111+4444d others(5): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701832 | |||||||
chr6:17701832 | C | CGGGG | 22 | a0001c0001t0001g0043 a0001c0001t0001g0111 a0001c0001t0001g0130 others(19): Show |
22 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.111+4441_111+4444d others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701832 | |||||||
chr6:17701832 | C | CGGGGGGG others(5): Show |
1 | a0003c0004t0001g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.111+4433_111+4444d others(14): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701832 | |||||||
chr6:17701832 | C | CGGGGGGG others(7): Show |
1 | a0003c0004t0001g0091 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.111+4444_111+4445i others(16): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701832 | |||||||
chr6:17701832 | C | CGGGGGGG others(8): Show |
1 | a0001c0011t0003g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.111+4444_111+4445i others(17): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701832 | |||||||
chr6:17701832 | C | CGGGGGGG others(10): Show |
1 | a0003c0004t0001g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.111+4444_111+4445i others(19): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701832 | |||||||
chr6:17701832 | C | G | 30 | a0002c0010t0003g0007 a0002c0010t0003g0008 a0004c0005t0001g0039 others(27): Show |
30 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.111+4445G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701832 | |||||||
chr6:17701835 | G | T | 4 | a0003c0012t0001g0275 a0003c0012t0001g0277 a0003c0012t0001g0278 others(1): Show |
4 | HG01109.hp1 HG02735.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+4442C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701835 | |||||||
chr6:17701838 | G | C | 1 | a0004c0005t0001g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.111+4439C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701838 | |||||||
chr6:17701842 | G | A | 57 | a0001c0001t0009g0307 a0001c0001t0009g0308 a0001c0003t0001g0104 others(54): Show |
57 | HG00438.hp2 HG00558.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.111+4435C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701842 | |||||||
chr6:17701842 | G | C | 1 | a0005c0006t0001g0290 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.111+4435C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701842 | |||||||
chr6:17701842 | G | GA | 3 | a0002c0002t0002g0047 a0002c0002t0002g0052 a0002c0002t0020g0315 |
3 | HG00597.hp1 HG02809.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.111+4434_111+4435i others(3): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701842 | |||||||
chr6:17701843 | G | A | 58 | a0001c0003t0001g0104 a0001c0003t0001g0271 a0002c0002t0001g0222 others(55): Show |
58 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.111+4434C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701843 | |||||||
chr6:17701843 | G | GA | 3 | a0001c0001t0001g0096 a0001c0001t0001g0187 a0001c0001t0013g0038 |
3 | HG02109.hp2 NA18971.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.111+4433_111+4434i others(3): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701843 | |||||||
chr6:17701844 | G | A | 61 | a0001c0001t0001g0096 a0001c0001t0001g0187 a0001c0001t0013g0038 others(58): Show |
61 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.111+4433C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701844 | |||||||
chr6:17701844 | G | GA | 15 | a0001c0009t0001g0164 a0001c0009t0003g0017 a0001c0009t0011g0001 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+4432dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701844 | |||||||
chr6:17701844 | G | GAA | 46 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0171 others(43): Show |
46 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.111+4431_111+4432d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701844 | |||||||
chr6:17701844 | G | GGAA | 20 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(17): Show |
20 | HG00544.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.111+4432_111+4433i others(5): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701844 | |||||||
chr6:17701844 | G | GGGGGGGG others(3): Show |
1 | a0008c0015t0001g0086 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.111+4432_111+4433i others(12): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701844 | |||||||
chr6:17701844 | GA | G | 14 | a0004c0005t0001g0058 a0004c0005t0001g0059 a0004c0005t0001g0060 others(11): Show |
14 | HG00140.hp1 HG00544.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.111+4432delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701844 | |||||||
chr6:17701844 | GAA | G | 11 | a0004c0005t0001g0039 a0004c0005t0001g0056 a0004c0005t0001g0057 others(8): Show |
11 | HG00323.hp1 HG01928.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+4431_111+4432d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701844 | |||||||
chr6:17701844 | GAAA | G | 3 | a0004c0005t0001g0054 a0004c0005t0001g0055 a0004c0005t0001g0252 |
3 | HG00280.hp2 HG01074.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.111+4430_111+4432d others(5): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701844 | |||||||
chr6:17701845 | A | G | 63 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(60): Show |
63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.111+4432T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701845 | |||||||
chr6:17701846 | A | G | 40 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(37): Show |
40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.111+4431T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701846 | |||||||
chr6:17701847 | A | G | 23 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(20): Show |
23 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.111+4430T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701847 | |||||||
chr6:17701848 | A | G | 9 | a0001c0001t0001g0043 a0001c0011t0001g0041 a0001c0011t0003g0002 others(6): Show |
9 | HG00323.hp2 HG01978.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.111+4429T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701848 | |||||||
chr6:17701914 | T | TAGCTCTA others(5): Show |
1 | a0002c0002t0002g0046 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.111+4351_111+4362d others(14): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701914 | |||||||
chr6:17701957 | A | C | 58 | a0001c0003t0001g0104 a0001c0003t0001g0271 a0002c0002t0001g0222 others(55): Show |
58 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.111+4320T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701957 | |||||||
chr6:17701963 | C | A | 1 | a0005c0006t0003g0037 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.111+4314G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701963 | |||||||
chr6:17701965 | A | C | 1 | a0005c0006t0003g0037 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.111+4312T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701965 | |||||||
chr6:17701967 | C | A | 1 | a0005c0006t0003g0037 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.111+4310G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701967 | |||||||
chr6:17701970 | A | C | 1 | a0005c0006t0003g0037 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.111+4307T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701970 | |||||||
chr6:17701971 | C | A | 1 | a0005c0006t0003g0037 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.111+4306G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701971 | |||||||
chr6:17701974 | C | T | 3 | a0001c0001t0009g0307 a0001c0001t0009g0308 a0008c0015t0001g0085 |
3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.111+4303G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17701974 | |||||||
chr6:17702020 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.111+4257C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702020 | |||||||
chr6:17702052 | A | G | 56 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(53): Show |
56 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.111+4225T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702052 | |||||||
chr6:17702076 | TAAG | T | 55 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(52): Show |
55 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.111+4198_111+4200d others(5): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702076 | |||||||
chr6:17702183 | C | T | 1 | a0001c0001t0013g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.111+4094G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702183 | |||||||
chr6:17702202 | A | T | 1 | a0001c0001t0001g0194 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.111+4075T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702202 | |||||||
chr6:17702235 | A | C | 1 | a0006c0007t0001g0103 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.111+4042T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702235 | |||||||
chr6:17702256 | C | A | 1 | a0001c0001t0001g0188 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.111+4021G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702256 | |||||||
chr6:17702263 | T | C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+4014A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702263 | |||||||
chr6:17702462 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.111+3815G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702462 | |||||||
chr6:17702591 | G | C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+3686C>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702591 | |||||||
chr6:17702598 | C | A | 1 | a0006c0007t0001g0189 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.111+3679G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702598 | |||||||
chr6:17702599 | C | G | 2 | a0001c0001t0001g0102 a0010c0026t0003g0011 |
2 | HG01358.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.111+3678G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702599 | |||||||
chr6:17702617 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.111+3660T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702617 | |||||||
chr6:17702637 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.111+3640A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702637 | |||||||
chr6:17702650 | T | C | 1 | a0005c0006t0003g0037 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.111+3627A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702650 | |||||||
chr6:17702651 | G | T | 1 | a0005c0006t0003g0037 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.111+3626C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702651 | |||||||
chr6:17702812 | C | A | 8 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(5): Show |
8 | HG00323.hp2 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+3465G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702812 | |||||||
chr6:17702841 | T | C | 310 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.111+3436A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702841 | |||||||
chr6:17702933 | C | CTCACGCC others(38): Show |
34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.111+3299_111+3343d others(47): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702933 | |||||||
chr6:17702980 | C | T | 2 | a0002c0002t0002g0245 a0002c0002t0002g0246 |
2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.111+3297G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17702980 | |||||||
chr6:17703044 | A | C | 1 | a0015c0031t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.111+3233T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703044 | |||||||
chr6:17703059 | G | T | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.111+3218C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703059 | |||||||
chr6:17703074 | T | C | 2 | a0001c0011t0001g0088 a0001c0011t0001g0089 |
2 | HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.111+3203A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703074 | |||||||
chr6:17703096 | G | A | 1 | a0001c0001t0003g0020 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.111+3181C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703096 | |||||||
chr6:17703152 | C | A | 5 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0001g0088 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.111+3125G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703152 | |||||||
chr6:17703197 | C | CA | 20 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0003g0021 others(17): Show |
20 | HG00323.hp1 HG01361.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.111+3079dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703197 | |||||||
chr6:17703197 | CA | C | 8 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0021t0001g0098 others(5): Show |
8 | HG00323.hp2 HG01361.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+3079delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703197 | |||||||
chr6:17703205 | AAAAAAAA others(4): Show |
A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.111+3061_111+3071d others(13): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703205 | |||||||
chr6:17703216 | T | A | 1 | a0002c0002t0001g0222 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.111+3061A>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703216 | |||||||
chr6:17703331 | T | C | 55 | a0002c0002t0001g0222 a0002c0002t0002g0046 a0002c0002t0002g0047 others(52): Show |
55 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.111+2946A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703331 | |||||||
chr6:17703413 | T | C | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.111+2864A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703413 | |||||||
chr6:17703425 | C | G | 3 | a0002c0010t0001g0053 a0002c0010t0003g0007 a0002c0010t0003g0008 |
3 | HG01255.hp1 HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.111+2852G>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703425 | |||||||
chr6:17703641 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.111+2636G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703641 | |||||||
chr6:17703655 | T | TA | 43 | a0002c0002t0001g0222 a0002c0002t0002g0047 a0002c0002t0002g0048 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.111+2621dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703655 | |||||||
chr6:17703655 | T | TAA | 11 | a0002c0002t0002g0052 a0002c0002t0002g0245 a0002c0002t0002g0246 others(8): Show |
11 | HG00642.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+2620_111+2621d others(4): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703655 | |||||||
chr6:17703655 | TA | T | 35 | a0002c0010t0001g0053 a0002c0010t0001g0254 a0002c0010t0003g0007 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.111+2621delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703655 | |||||||
chr6:17703964 | A | C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+2313T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17703964 | |||||||
chr6:17704144 | T | C | 3 | a0005c0006t0001g0291 a0005c0006t0001g0292 a0005c0006t0001g0305 |
3 | HG00639.hp1 HG02004.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.111+2133A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704144 | |||||||
chr6:17704174 | T | C | 288 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.111+2103A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704174 | |||||||
chr6:17704197 | C | T | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.111+2080G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704197 | |||||||
chr6:17704291 | C | CA | 13 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0196 others(10): Show |
13 | HG01361.hp1 HG01928.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.111+1985dupT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704291 | |||||||
chr6:17704291 | CA | C | 36 | a0001c0003t0001g0095 a0001c0003t0001g0272 a0002c0010t0001g0053 others(33): Show |
36 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.111+1985delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704291 | |||||||
chr6:17704493 | G | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG01891.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.111+1784C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704493 | |||||||
chr6:17704545 | A | T | 1 | a0004c0005t0001g0252 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.111+1732T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704545 | |||||||
chr6:17704670 | A | T | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+1607T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704670 | |||||||
chr6:17704671 | C | A | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+1606G>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704671 | |||||||
chr6:17704672 | A | C | 1 | a0002c0002t0014g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.111+1605T>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704672 | |||||||
chr6:17704730 | CA | C | 206 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(203): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.111+1546delT | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704730 | |||||||
chr6:17704759 | CTTTT | C | 17 | a0003c0004t0001g0090 a0003c0004t0001g0091 a0003c0004t0001g0092 others(14): Show |
17 | HG00323.hp2 HG01192.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.111+1514_111+1517d others(6): Show |
NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704759 | |||||||
chr6:17704830 | G | A | 1 | a0002c0002t0002g0258 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.111+1447C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704830 | |||||||
chr6:17704995 | G | T | 3 | a0001c0011t0001g0041 a0001c0011t0001g0042 a0001c0011t0003g0002 |
3 | HG02280.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.111+1282C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17704995 | |||||||
chr6:17705013 | T | C | 145 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0097 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.111+1264A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705013 | |||||||
chr6:17705026 | G | A | 9 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(6): Show |
9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.111+1251C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705026 | |||||||
chr6:17705057 | C | T | 1 | a0012c0019t0003g0035 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.111+1220G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705057 | |||||||
chr6:17705169 | C | T | 1 | a0005c0006t0001g0280 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.111+1108G>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705169 | |||||||
chr6:17705284 | G | A | 12 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0001c0003t0001g0210 others(9): Show |
12 | HG01255.hp2 HG01496.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.111+993C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705284 | |||||||
chr6:17705372 | T | C | 1 | a0003c0004t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.111+905A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705372 | |||||||
chr6:17705409 | T | C | 1 | a0001c0001t0009g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.111+868A>G | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705409 | |||||||
chr6:17705499 | T | G | 1 | a0003c0012t0001g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.111+778A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705499 | |||||||
chr6:17705508 | G | A | 1 | a0004c0005t0016g0212 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.111+769C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705508 | |||||||
chr6:17705585 | T | TG | 78 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0267 others(75): Show |
78 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.111+691dupC | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705585 | |||||||
chr6:17705589 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.111+688C>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705589 | |||||||
chr6:17705596 | A | G | 5 | a0007c0008t0001g0197 a0007c0008t0001g0198 a0007c0008t0001g0199 others(2): Show |
5 | HG02145.hp1 HG02258.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+681T>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705596 | |||||||
chr6:17705750 | T | G | 1 | a0002c0010t0015g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.111+527A>C | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705750 | |||||||
chr6:17705865 | G | A | 5 | a0003c0012t0001g0275 a0003c0012t0001g0277 a0003c0012t0001g0278 others(2): Show |
5 | HG01109.hp1 HG01243.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+412C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705865 | |||||||
chr6:17705900 | A | T | 1 | a0004c0005t0001g0039 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.111+377T>A | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17705900 | |||||||
chr6:17706173 | G | A | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.111+104C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17706173 | |||||||
chr6:17706262 | G | A | 34 | a0003c0004t0001g0284 a0003c0004t0001g0285 a0003c0004t0001g0286 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.111+15C>T | NUP153 | ENSG00000124789.12 | transcript | ENST00000262077.3 | protein_coding | 1/21 | chr6 | 17706262 |