Item | Value |
---|---|
geneid | 10529 |
ensemblid | ENSG00000078114.19 |
hgncid | 16932 |
symbol | NEBL |
name | nebulette |
refseq_nuc | NM_006393.3 |
refseq_prot | NP_006384.1 |
ensembl_nuc | ENST00000377122.9 |
ensembl_prot | ENSP00000366326.4 |
mane_status | MANE Select |
chr | chr10 |
start | 20779973 |
end | 20897311 |
strand | - |
ver | v1.2 |
region | chr10:20779973-20897311 |
region5000 | chr10:20774973-20902311 |
regionname0 | NEBL_chr10_20779973_20897311 |
regionname5000 | NEBL_chr10_20774973_20902311 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1014 | 208 | 51 | 43 | 83 | 11 | 18 | 66 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0002 | 0/0 | 1014 | 57 | 28 | 3 | 21 | 0 | 5 | 17 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0003 | 0/0 | 1014 | 23 | 1 | 3 | 19 | 0 | 0 | 15 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0004 | 0/0 | 1014 | 21 | 0 | 0 | 20 | 0 | 1 | 14 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0005 | 0/0 | 1014 | 10 | 0 | 5 | 1 | 0 | 4 | 0 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0006 | 0/0 | 1014 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0007 | 0/0 | 1014 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0008 | 0/0 | 1014 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0009 | 0/0 | 1014 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0010 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0011 | 0/0 | 1014 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0012 | 0/0 | 1014 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0013 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0014 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
a0015 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | MRVPV others(1009): Show |
chr10 | 20774973 | 20902311 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3042 | 163 | 45 | 31 | 71 | 5 | 10 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0001c0003 | 0/1 | 3042 | 28 | 1 | 6 | 10 | 5 | 5 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0001c0006 | 0/0 | 3042 | 14 | 5 | 6 | 0 | 1 | 2 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0001c0013 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0001c0015 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0001c0016 | 0/0 | 3042 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0002c0002 | 0/0 | 3042 | 57 | 28 | 3 | 21 | 0 | 5 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0003c0004 | 0/0 | 3042 | 23 | 1 | 3 | 19 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0004c0005 | 0/0 | 3042 | 19 | 0 | 0 | 18 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0004c0011 | 0/0 | 3042 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0005c0007 | 0/0 | 3042 | 10 | 0 | 5 | 1 | 0 | 4 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0006c0008 | 0/0 | 3042 | 6 | 6 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0007c0009 | 0/0 | 3042 | 4 | 0 | 0 | 4 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0008c0010 | 0/0 | 3042 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0009c0012 | 0/0 | 3042 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0010c0020 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0011c0018 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0012c0014 | 0/0 | 3042 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0013c0021 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0014c0017 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 | ||
a0015c0019 | 0/0 | 3042 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATGAG others(3037): Show |
chr10 | 20774973 | 20902311 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 8925 | 32 | 4 | 14 | 13 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0002 | 0/0 | 8924 | 47 | 1 | 7 | 33 | 2 | 4 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0003 | 0/0 | 8924 | 3 | 0 | 1 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0004 | 0/0 | 8924 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0005 | 0/0 | 8924 | 15 | 7 | 1 | 7 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0007 | 0/0 | 8925 | 13 | 11 | 2 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0009 | 0/0 | 8924 | 6 | 0 | 0 | 6 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0013 | 0/0 | 8925 | 5 | 4 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0015 | 0/0 | 8924 | 4 | 4 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0016 | 0/0 | 8924 | 4 | 0 | 3 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0017 | 0/0 | 8924 | 3 | 3 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0018 | 0/0 | 8924 | 3 | 3 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0019 | 0/0 | 8924 | 3 | 0 | 0 | 3 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0020 | 0/0 | 8924 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0021 | 0/0 | 8925 | 2 | 0 | 0 | 0 | 0 | 2 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0022 | 0/0 | 8925 | 2 | 0 | 0 | 0 | 0 | 2 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0023 | 0/0 | 8924 | 2 | 0 | 0 | 0 | 2 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0024 | 0/0 | 8924 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0029 | 0/0 | 8925 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0030 | 0/0 | 8924 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0032 | 0/0 | 8925 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0033 | 0/0 | 8924 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0036 | 0/0 | 8924 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0039 | 0/0 | 8924 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0040 | 0/0 | 8925 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0044 | 0/0 | 8924 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0045 | 0/0 | 8924 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0046 | 0/0 | 8924 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0047 | 0/0 | 8924 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0048 | 0/0 | 8924 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0049 | 0/0 | 8925 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0001t0050 | 0/0 | 8924 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0003t0001 | 0/0 | 8925 | 25 | 1 | 5 | 10 | 5 | 4 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0003t0003 | 0/0 | 8924 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0003t0009 | 0/0 | 8924 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0003t0037 | 0/1 | 8925 | 1 | 0 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0006t0008 | 0/0 | 8925 | 4 | 4 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0006t0010 | 0/0 | 8924 | 9 | 1 | 6 | 0 | 1 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0006t0038 | 0/0 | 8924 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0013t0001 | 0/0 | 8925 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0001c0015t0002 | 0/0 | 8924 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0001c0016t0002 | 0/0 | 8924 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0002c0002t0001 | 0/0 | 8925 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0002c0002t0003 | 0/0 | 8924 | 21 | 0 | 0 | 19 | 0 | 2 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0002c0002t0004 | 0/0 | 8924 | 15 | 15 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0002c0002t0009 | 0/0 | 8924 | 3 | 0 | 0 | 2 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0002c0002t0011 | 0/0 | 8924 | 7 | 7 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0002c0002t0014 | 0/0 | 8924 | 5 | 1 | 3 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0002c0002t0026 | 0/0 | 8925 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0002c0002t0028 | 0/0 | 8925 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0002c0002t0034 | 0/0 | 8924 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0002c0002t0035 | 0/0 | 8924 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0002c0002t0042 | 0/0 | 8924 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0003c0004t0001 | 0/0 | 8925 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0003c0004t0002 | 0/0 | 8924 | 4 | 1 | 3 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0003c0004t0003 | 0/0 | 8924 | 3 | 0 | 0 | 3 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0003c0004t0006 | 0/0 | 8924 | 13 | 0 | 0 | 13 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0003c0004t0025 | 0/0 | 8925 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0004c0005t0001 | 0/0 | 8925 | 17 | 0 | 0 | 16 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0004c0005t0002 | 0/0 | 8924 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0004c0011t0001 | 0/0 | 8925 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0005c0007t0001 | 0/0 | 8925 | 4 | 0 | 2 | 1 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0005c0007t0012 | 0/0 | 8925 | 6 | 0 | 3 | 0 | 0 | 3 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0006c0008t0008 | 0/0 | 8925 | 6 | 6 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0007c0009t0003 | 0/0 | 8924 | 4 | 0 | 0 | 4 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0008c0010t0006 | 0/0 | 8924 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0009c0012t0041 | 0/0 | 8925 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0010c0020t0027 | 0/0 | 8925 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0011c0018t0001 | 0/0 | 8925 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0012c0014t0001 | 0/0 | 8925 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
a0013c0021t0043 | 0/0 | 8924 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0014c0017t0031 | 0/0 | 8924 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8919): Show |
chr10 | 20774973 | 20902311 |
a0015c0019t0001 | 0/0 | 8925 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | ATTTC others(8920): Show |
chr10 | 20774973 | 20902311 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0313 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0009g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0013g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0013g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0013g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0015g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0015g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0015g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0015g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0016g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0016g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0016g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0016g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0017g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0017g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0017g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0018g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0018g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0018g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0019g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0019g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0019g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0020g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0020g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0021g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0021g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0022g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0022g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0023g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0023g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0024g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0024g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0029g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0030g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0032g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0033g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0036g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0039g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0040g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0044g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0045g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0046g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0047g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0048g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0049g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0001t0050g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0009g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0003t0037g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0008g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0010g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0010g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0010g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0010g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0010g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0010g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0010g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0010g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0006t0038g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0013t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0015t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0001c0016t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0009g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0009g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0009g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0011g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0011g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0011g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0014g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0014g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0014g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0014g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0014g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0026g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0028g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0034g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0035g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0002c0002t0042g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0003c0004t0025g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0005t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0004c0011t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0005c0007t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0005c0007t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0005c0007t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0005c0007t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0005c0007t0012g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0005c0007t0012g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0005c0007t0012g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0005c0007t0012g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0005c0007t0012g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0005c0007t0012g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0006c0008t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0006c0008t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0006c0008t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0006c0008t0008g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0006c0008t0008g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0006c0008t0008g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0007c0009t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0007c0009t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0007c0009t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0007c0009t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0008c0010t0006g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0009c0012t0041g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0010c0020t0027g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0011c0018t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0012c0014t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0013c0021t0043g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0014c0017t0031g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
a0015c0019t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0009 | c0012 | t0041 | g0207 | EUR | GBR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00140 | hp2 | a0001 | c0001 | t0016 | g0155 | EUR | GBR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0091 | EUR | FIN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0246 | EUR | FIN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00408 | hp1 | a0002 | c0002 | t0003 | g0115 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00408 | hp2 | a0001 | c0003 | t0001 | g0110 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00438 | hp1 | a0003 | c0004 | t0006 | g0212 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00544 | hp1 | a0007 | c0009 | t0003 | g0030 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00558 | hp2 | a0004 | c0005 | t0001 | g0122 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00597 | hp2 | a0002 | c0002 | t0003 | g0033 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00621 | hp1 | a0010 | c0020 | t0027 | g0169 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00642 | hp1 | a0001 | c0001 | t0013 | g0189 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00642 | hp2 | a0001 | c0001 | t0007 | g0085 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00673 | hp1 | a0003 | c0004 | t0006 | g0208 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00673 | hp2 | a0004 | c0005 | t0001 | g0157 | EAS | CHS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01069 | hp1 | a0005 | c0007 | t0012 | g0047 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01070 | hp1 | a0002 | c0002 | t0014 | g0109 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01071 | hp1 | a0002 | c0002 | t0014 | g0108 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01081 | hp1 | a0005 | c0007 | t0001 | g0141 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01081 | hp2 | a0001 | c0001 | t0050 | g0329 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01106 | hp2 | a0011 | c0018 | t0001 | g0154 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01175 | hp1 | a0005 | c0007 | t0001 | g0069 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01175 | hp2 | a0001 | c0003 | t0009 | g0151 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0101 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01192 | hp2 | a0003 | c0004 | t0002 | g0057 | AMR | PUR | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01256 | hp1 | a0001 | c0001 | t0047 | g0245 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01257 | hp2 | a0005 | c0007 | t0012 | g0045 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01258 | hp2 | a0005 | c0007 | t0012 | g0046 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01261 | hp2 | a0001 | c0001 | t0016 | g0132 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01361 | hp1 | a0001 | c0001 | t0016 | g0232 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01361 | hp2 | a0012 | c0014 | t0001 | g0170 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01496 | hp1 | a0001 | c0001 | t0016 | g0131 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01496 | hp2 | a0001 | c0006 | t0010 | g0118 | AMR | CLM | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01515 | hp1 | a0001 | c0001 | t0023 | g0224 | EUR | IBS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01515 | hp2 | a0001 | c0003 | t0001 | g0089 | EUR | IBS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0173 | EUR | IBS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0126 | EUR | IBS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0088 | EUR | IBS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0125 | EUR | IBS | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01884 | hp1 | a0001 | c0001 | t0030 | g0198 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01884 | hp2 | a0001 | c0001 | t0017 | g0303 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01891 | hp1 | a0001 | c0006 | t0010 | g0149 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01928 | hp2 | a0001 | c0006 | t0010 | g0144 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0319 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01975 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0134 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0078 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01981 | hp2 | a0002 | c0002 | t0014 | g0027 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01993 | hp1 | a0001 | c0006 | t0010 | g0158 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG01993 | hp2 | a0003 | c0004 | t0002 | g0320 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02004 | hp2 | a0001 | c0006 | t0010 | g0143 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02015 | hp2 | a0003 | c0004 | t0006 | g0300 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02055 | hp1 | a0001 | c0001 | t0032 | g0190 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02055 | hp2 | a0001 | c0001 | t0018 | g0291 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02056 | hp2 | a0005 | c0007 | t0001 | g0012 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02074 | hp2 | a0001 | c0001 | t0049 | g0161 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02129 | hp2 | a0004 | c0005 | t0001 | g0011 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02132 | hp1 | a0003 | c0004 | t0003 | g0006 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02132 | hp2 | a0004 | c0005 | t0001 | g0160 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02135 | hp1 | a0004 | c0005 | t0001 | g0121 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0117 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0172 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02155 | hp1 | a0004 | c0005 | t0002 | g0164 | EAS | CDX | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02258 | hp1 | a0006 | c0008 | t0008 | g0310 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02258 | hp2 | a0002 | c0002 | t0034 | g0114 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02273 | hp1 | a0003 | c0004 | t0002 | g0015 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02293 | hp2 | a0001 | c0006 | t0010 | g0315 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02300 | hp1 | a0001 | c0006 | t0010 | g0080 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02451 | hp1 | a0001 | c0001 | t0018 | g0280 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02451 | hp2 | a0002 | c0002 | t0004 | g0259 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02523 | hp2 | a0001 | c0003 | t0001 | g0081 | EAS | KHV | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02572 | hp1 | a0001 | c0001 | t0017 | g0286 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02572 | hp2 | a0001 | c0006 | t0008 | g0302 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0306 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02622 | hp1 | a0002 | c0002 | t0004 | g0305 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02622 | hp2 | a0001 | c0001 | t0013 | g0185 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02630 | hp1 | a0002 | c0002 | t0011 | g0055 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02630 | hp2 | a0002 | c0002 | t0004 | g0263 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02698 | hp1 | a0005 | c0007 | t0012 | g0070 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02698 | hp2 | a0001 | c0001 | t0045 | g0142 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02717 | hp1 | a0002 | c0002 | t0004 | g0083 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02717 | hp2 | a0001 | c0001 | t0036 | g0290 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02723 | hp1 | a0002 | c0002 | t0004 | g0007 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02723 | hp2 | a0001 | c0006 | t0008 | g0281 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02735 | hp2 | a0005 | c0007 | t0012 | g0044 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0119 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02809 | hp1 | a0001 | c0006 | t0008 | g0184 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02809 | hp2 | a0006 | c0008 | t0008 | g0181 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02818 | hp1 | a0002 | c0002 | t0011 | g0056 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02886 | hp1 | a0006 | c0008 | t0008 | g0304 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0171 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0084 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02896 | hp2 | a0013 | c0021 | t0043 | g0196 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0059 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02965 | hp1 | a0002 | c0002 | t0035 | g0188 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0086 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02970 | hp2 | a0002 | c0002 | t0004 | g0219 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02976 | hp1 | a0001 | c0001 | t0039 | g0277 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02976 | hp2 | a0001 | c0001 | t0013 | g0197 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03041 | hp1 | a0001 | c0006 | t0008 | g0175 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03041 | hp2 | a0002 | c0002 | t0011 | g0288 | AFR | GWD | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0147 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03098 | hp2 | a0002 | c0002 | t0004 | g0287 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03130 | hp1 | a0002 | c0002 | t0004 | g0258 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0152 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03139 | hp1 | a0006 | c0008 | t0008 | g0309 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0098 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03195 | hp1 | a0001 | c0001 | t0040 | g0311 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0087 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03209 | hp1 | a0014 | c0017 | t0031 | g0250 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03209 | hp2 | a0002 | c0002 | t0011 | g0099 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03225 | hp2 | a0002 | c0002 | t0004 | g0285 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03486 | hp1 | a0006 | c0008 | t0008 | g0308 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03486 | hp2 | a0001 | c0001 | t0018 | g0289 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03491 | hp2 | a0001 | c0001 | t0022 | g0071 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03492 | hp1 | a0001 | c0006 | t0038 | g0124 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03492 | hp2 | a0001 | c0001 | t0022 | g0072 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03516 | hp1 | a0002 | c0002 | t0011 | g0183 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | ESN | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03579 | hp1 | a0002 | c0002 | t0011 | g0284 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03579 | hp2 | a0006 | c0008 | t0008 | g0307 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03688 | hp1 | a0002 | c0002 | t0009 | g0049 | SAS | STU | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03688 | hp2 | a0001 | c0001 | t0021 | g0100 | SAS | STU | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03704 | hp1 | a0001 | c0016 | t0002 | g0104 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03704 | hp2 | a0005 | c0007 | t0012 | g0043 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03710 | hp1 | a0001 | c0003 | t0003 | g0026 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03710 | hp2 | a0001 | c0006 | t0010 | g0166 | SAS | PJL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03927 | hp1 | a0001 | c0003 | t0001 | g0123 | SAS | BEB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | BEB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03942 | hp1 | a0002 | c0002 | t0003 | g0065 | SAS | BEB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03942 | hp2 | a0001 | c0001 | t0044 | g0205 | SAS | BEB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG04184 | hp1 | a0004 | c0005 | t0001 | g0162 | SAS | BEB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG04184 | hp2 | a0002 | c0002 | t0026 | g0013 | SAS | BEB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG04199 | hp1 | a0001 | c0001 | t0021 | g0136 | SAS | STU | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG04199 | hp2 | a0005 | c0007 | t0001 | g0068 | SAS | STU | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0018 | SAS | STU | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG04204 | hp2 | a0002 | c0002 | t0014 | g0167 | SAS | STU | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG04228 | hp1 | a0002 | c0002 | t0003 | g0041 | SAS | STU | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0097 | SAS | STU | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0096 | AFR | YRI | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18522 | hp2 | a0002 | c0002 | t0011 | g0177 | AFR | YRI | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18612 | hp1 | a0002 | c0002 | t0003 | g0039 | EAS | CHB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18612 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | CHB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18747 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | CHB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18747 | hp2 | a0001 | c0003 | t0001 | g0113 | EAS | CHB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18906 | hp1 | a0001 | c0001 | t0017 | g0278 | AFR | YRI | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18906 | hp2 | a0002 | c0002 | t0004 | g0262 | AFR | YRI | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0082 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18941 | hp2 | a0003 | c0004 | t0003 | g0006 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18943 | hp1 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18944 | hp1 | a0002 | c0002 | t0003 | g0037 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18944 | hp2 | a0015 | c0019 | t0001 | g0234 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18945 | hp1 | a0002 | c0002 | t0003 | g0036 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18945 | hp2 | a0004 | c0005 | t0001 | g0133 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18947 | hp2 | a0003 | c0004 | t0001 | g0298 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18948 | hp1 | a0004 | c0005 | t0001 | g0128 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18950 | hp1 | a0001 | c0001 | t0009 | g0040 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18950 | hp2 | a0001 | c0001 | t0019 | g0276 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18952 | hp1 | a0002 | c0002 | t0003 | g0106 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18952 | hp2 | a0003 | c0004 | t0006 | g0299 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18953 | hp2 | a0001 | c0001 | t0020 | g0200 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18954 | hp1 | a0004 | c0005 | t0001 | g0112 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18954 | hp2 | a0003 | c0004 | t0003 | g0255 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18956 | hp1 | a0002 | c0002 | t0003 | g0028 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18956 | hp2 | a0008 | c0010 | t0006 | g0004 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18960 | hp2 | a0004 | c0005 | t0001 | g0120 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18963 | hp1 | a0008 | c0010 | t0006 | g0004 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18963 | hp2 | a0004 | c0005 | t0001 | g0145 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18964 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18966 | hp1 | a0003 | c0004 | t0001 | g0297 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18966 | hp2 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18967 | hp2 | a0001 | c0013 | t0001 | g0163 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18968 | hp1 | a0004 | c0005 | t0001 | g0051 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18968 | hp2 | a0001 | c0001 | t0046 | g0223 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18969 | hp1 | a0001 | c0001 | t0020 | g0199 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18969 | hp2 | a0007 | c0009 | t0003 | g0029 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18970 | hp2 | a0003 | c0004 | t0006 | g0294 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18971 | hp1 | a0004 | c0011 | t0001 | g0003 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18971 | hp2 | a0003 | c0004 | t0006 | g0301 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18972 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18973 | hp1 | a0001 | c0001 | t0009 | g0075 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18974 | hp2 | a0002 | c0002 | t0003 | g0105 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18975 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18975 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18977 | hp2 | a0002 | c0002 | t0003 | g0061 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18982 | hp2 | a0003 | c0004 | t0006 | g0024 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18983 | hp2 | a0002 | c0002 | t0009 | g0035 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18984 | hp2 | a0007 | c0009 | t0003 | g0060 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18986 | hp1 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18986 | hp2 | a0001 | c0001 | t0009 | g0053 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18987 | hp1 | a0001 | c0001 | t0009 | g0067 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18989 | hp1 | a0004 | c0011 | t0001 | g0003 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18989 | hp2 | a0001 | c0001 | t0024 | g0324 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18990 | hp2 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18991 | hp2 | a0001 | c0001 | t0009 | g0076 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18992 | hp1 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18992 | hp2 | a0001 | c0001 | t0024 | g0227 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18997 | hp1 | a0004 | c0005 | t0001 | g0150 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18997 | hp2 | a0003 | c0004 | t0006 | g0272 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18998 | hp2 | a0003 | c0004 | t0025 | g0296 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18999 | hp1 | a0001 | c0015 | t0002 | g0242 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA18999 | hp2 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19001 | hp1 | a0002 | c0002 | t0003 | g0038 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19003 | hp1 | a0004 | c0005 | t0001 | g0092 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19003 | hp2 | a0003 | c0004 | t0006 | g0292 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19005 | hp2 | a0002 | c0002 | t0003 | g0293 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19006 | hp1 | a0001 | c0001 | t0019 | g0214 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19006 | hp2 | a0001 | c0001 | t0048 | g0103 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19009 | hp2 | a0007 | c0009 | t0003 | g0062 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19010 | hp1 | a0002 | c0002 | t0009 | g0032 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19011 | hp2 | a0003 | c0004 | t0006 | g0209 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19030 | hp1 | a0002 | c0002 | t0042 | g0178 | AFR | LWK | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19030 | hp2 | a0001 | c0001 | t0029 | g0279 | AFR | LWK | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0186 | AFR | LWK | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | LWK | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19056 | hp1 | a0001 | c0001 | t0019 | g0236 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19057 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19058 | hp1 | a0004 | c0005 | t0001 | g0156 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19062 | hp2 | a0003 | c0004 | t0006 | g0295 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19063 | hp2 | a0004 | c0005 | t0001 | g0146 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19064 | hp1 | a0002 | c0002 | t0003 | g0063 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19082 | hp1 | a0003 | c0004 | t0006 | g0008 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19082 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19083 | hp1 | a0004 | c0005 | t0001 | g0025 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19085 | hp2 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19087 | hp1 | a0001 | c0001 | t0009 | g0093 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19087 | hp2 | a0004 | c0005 | t0002 | g0135 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19088 | hp1 | a0003 | c0004 | t0006 | g0008 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19240 | hp1 | a0002 | c0002 | t0004 | g0174 | AFR | YRI | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA19240 | hp2 | a0002 | c0002 | t0004 | g0054 | AFR | YRI | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA20805 | hp1 | a0001 | c0006 | t0010 | g0148 | EUR | TSI | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA20805 | hp2 | a0001 | c0001 | t0023 | g0248 | EUR | TSI | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0217 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02109 | hp2 | a0001 | c0001 | t0033 | g0203 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02486 | hp1 | a0001 | c0001 | t0013 | g0187 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02486 | hp2 | a0001 | c0001 | t0015 | g0159 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02559 | hp1 | a0001 | c0001 | t0015 | g0079 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0328 | AFR | ACB | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03471 | hp1 | a0002 | c0002 | t0004 | g0261 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG03471 | hp2 | a0002 | c0002 | t0004 | g0007 | AFR | MSL | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG06807 | hp1 | a0002 | c0002 | t0004 | g0260 | AFR | USA | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
HG06807 | hp2 | a0002 | c0002 | t0014 | g0064 | AFR | USA | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA20300 | hp1 | a0003 | c0004 | t0002 | g0102 | AFR | USA | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0176 | AFR | USA | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | LWK | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
NA21309 | hp2 | a0002 | c0002 | t0028 | g0264 | AFR | LWK | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
homoSapiens | chm13v2 | a0001 | c0003 | t0037 | g0090 | REF | REF | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0313 | REF | REF | NEBL_chr10_20774973_20902311 | NEBL | chr10 | 20774973 | 20902311 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:20808518 | T | A | 1 | a0010 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.2753A>T | p.Asp918Val | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/28 | 2859/8925 | 2753/3045 | 918/1014 | chr10 | 20808518 | |||
chr10:20815684 | T | C | 3 | a0003 a0007 a0008 |
29 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(26): Show |
missense_variant | MODERATE | c.2182A>G | p.Thr728Ala | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/28 | 2288/8925 | 2182/3045 | 728/1014 | chr10 | 20815684 | |||
chr10:20817691 | A | G | 1 | a0006 | 6 | HG02258.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.2057T>C | p.Val686Ala | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/28 | 2163/8925 | 2057/3045 | 686/1014 | chr10 | 20817691 | |||
chr10:20819428 | C | T | 1 | a0012 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.2051G>A | p.Ser684Asn | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/28 | 2157/8925 | 2051/3045 | 684/1014 | chr10 | 20819428 | |||
chr10:20823208 | A | T | 2 | a0002 a0007 |
61 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(58): Show |
missense_variant&splice_region_variant | MODERATE | c.1962T>A | p.Asn654Lys | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/28 | 2068/8925 | 1962/3045 | 654/1014 | chr10 | 20823208 | |||
chr10:20826455 | T | C | 1 | a0014 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1861A>G | p.Ile621Val | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/28 | 1967/8925 | 1861/3045 | 621/1014 | chr10 | 20826455 | |||
chr10:20831215 | G | A | 1 | a0011 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1652C>T | p.Thr551Ile | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/28 | 1758/8925 | 1652/3045 | 551/1014 | chr10 | 20831215 | |||
chr10:20831255 | C | A | 1 | a0008 | 2 | NA18956.hp2 NA18963.hp1 |
missense_variant | MODERATE | c.1612G>T | p.Val538Leu | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/28 | 1718/8925 | 1612/3045 | 538/1014 | chr10 | 20831255 | |||
chr10:20840775 | G | C | 1 | a0015 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.1302C>G | p.Ile434Met | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/28 | 1408/8925 | 1302/3045 | 434/1014 | chr10 | 20840775 | |||
chr10:20845353 | C | G | 2 | a0005 a0010 |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
missense_variant | MODERATE | c.1132G>C | p.Asp378His | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/28 | 1238/8925 | 1132/3045 | 378/1014 | chr10 | 20845353 | |||
chr10:20850460 | T | C | 2 | a0005 a0010 |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
missense_variant | MODERATE | c.1051A>G | p.Met351Val | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/28 | 1157/8925 | 1051/3045 | 351/1014 | chr10 | 20850460 | |||
chr10:20868692 | G | T | 1 | a0004 | 21 | HG00558.hp2 HG00673.hp2 HG02129.hp2 others(18): Show |
missense_variant | MODERATE | c.656C>A | p.Ala219Asp | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/28 | 762/8925 | 656/3045 | 219/1014 | chr10 | 20868692 | |||
chr10:20869761 | C | G | 1 | a0008 | 2 | NA18956.hp2 NA18963.hp1 |
missense_variant | MODERATE | c.561G>C | p.Gln187His | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 6/28 | 667/8925 | 561/3045 | 187/1014 | chr10 | 20869761 | |||
chr10:20889912 | T | C | 1 | a0013 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.191A>G | p.Lys64Arg | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/28 | 297/8925 | 191/3045 | 64/1014 | chr10 | 20889912 | |||
chr10:20889923 | C | G | 1 | a0009 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.180G>C | p.Lys60Asn | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/28 | 286/8925 | 180/3045 | 60/1014 | chr10 | 20889923 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:20785795 | T | C | 2 | a0001c0006 a0006c0008 |
20 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(17): Show |
synonymous_variant | LOW | c.2997A>G | p.Thr999Thr | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 3103/8925 | 2997/3045 | 999/1014 | chr10 | 20785795 | |||
chr10:20787250 | G | A | 1 | a0001c0016 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.2820C>T | p.His940His | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/28 | 2926/8925 | 2820/3045 | 940/1014 | chr10 | 20787250 | |||
chr10:20812827 | G | T | 1 | a0001c0015 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.2460C>A | p.Ala820Ala | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/28 | 2566/8925 | 2460/3045 | 820/1014 | chr10 | 20812827 | |||
chr10:20819448 | C | T | 4 | a0001c0003 a0001c0013 a0004c0005 others(1): Show |
48 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(45): Show |
synonymous_variant | LOW | c.2031G>A | p.Arg677Arg | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/28 | 2137/8925 | 2031/3045 | 677/1014 | chr10 | 20819448 | |||
chr10:20828578 | A | G | 1 | a0001c0013 | 1 | NA18967.hp2 | synonymous_variant | LOW | c.1728T>C | p.Asp576Asp | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/28 | 1834/8925 | 1728/3045 | 576/1014 | chr10 | 20828578 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:20780035 | G | C | 2 | a0001c0001t0018 a0001c0001t0039 |
4 | HG02055.hp2 HG02451.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5712C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 5712 | chr10 | 20780035 | ||||||
chr10:20780042 | T | G | 1 | a0001c0001t0024 | 2 | NA18989.hp2 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5705A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 5705 | chr10 | 20780042 | ||||||
chr10:20780243 | T | G | 21 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0009 others(18): Show |
104 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*5504A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 5504 | chr10 | 20780243 | ||||||
chr10:20780331 | G | C | 1 | a0002c0002t0035 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5416C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 5416 | chr10 | 20780331 | ||||||
chr10:20780375 | G | A | 1 | a0001c0001t0022 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5372C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 5372 | chr10 | 20780375 | ||||||
chr10:20780690 | T | C | 1 | a0001c0001t0036 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5057A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 5057 | chr10 | 20780690 | ||||||
chr10:20780831 | T | C | 1 | a0002c0002t0042 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4916A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 4916 | chr10 | 20780831 | ||||||
chr10:20780849 | G | A | 2 | a0001c0001t0032 a0001c0001t0046 |
2 | HG02055.hp1 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4898C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 4898 | chr10 | 20780849 | ||||||
chr10:20781464 | G | A | 2 | a0001c0006t0010 a0001c0006t0038 |
10 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4283C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 4283 | chr10 | 20781464 | ||||||
chr10:20781686 | C | G | 2 | a0003c0004t0006 a0008c0010t0006 |
15 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4061G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 4061 | chr10 | 20781686 | ||||||
chr10:20781728 | C | T | 11 | a0001c0001t0003 a0001c0001t0036 a0001c0001t0044 others(8): Show |
42 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*4019G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 4019 | chr10 | 20781728 | ||||||
chr10:20781764 | C | T | 21 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0013 others(18): Show |
87 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*3983G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 3983 | chr10 | 20781764 | ||||||
chr10:20782056 | A | G | 1 | a0002c0002t0011 | 7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3691T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 3691 | chr10 | 20782056 | ||||||
chr10:20782152 | T | C | 1 | a0013c0021t0043 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3595A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 3595 | chr10 | 20782152 | ||||||
chr10:20782262 | G | C | 32 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0009 others(29): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*3485C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 3485 | chr10 | 20782262 | ||||||
chr10:20782331 | A | G | 1 | a0001c0006t0038 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3416T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 3416 | chr10 | 20782331 | ||||||
chr10:20782483 | C | T | 1 | a0010c0020t0027 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3264G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 3264 | chr10 | 20782483 | ||||||
chr10:20782543 | T | C | 5 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0020 others(2): Show |
24 | HG00642.hp1 HG01891.hp2 HG01975.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3204A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 3204 | chr10 | 20782543 | ||||||
chr10:20782678 | C | T | 1 | a0001c0001t0033 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3069G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 3069 | chr10 | 20782678 | ||||||
chr10:20782761 | T | G | 1 | a0005c0007t0012 | 6 | HG01069.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2986A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 2986 | chr10 | 20782761 | ||||||
chr10:20783034 | G | A | 1 | a0001c0001t0020 | 2 | NA18953.hp2 NA18969.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2713C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 2713 | chr10 | 20783034 | ||||||
chr10:20783175 | A | AT | 2 | a0001c0006t0008 a0006c0008t0008 |
10 | HG02258.hp1 HG02572.hp2 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2571dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 2571 | chr10 | 20783175 | ||||||
chr10:20783286 | A | C | 1 | a0002c0002t0026 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2461T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 2461 | chr10 | 20783286 | ||||||
chr10:20783429 | T | C | 3 | a0001c0001t0017 a0003c0004t0006 a0008c0010t0006 |
18 | HG00438.hp1 HG00673.hp1 HG01884.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2318A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 2318 | chr10 | 20783429 | ||||||
chr10:20783628 | A | AT | 2 | a0001c0001t0013 a0001c0001t0032 |
6 | HG00642.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2118dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 2118 | chr10 | 20783628 | ||||||
chr10:20783672 | G | A | 17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0013 others(14): Show |
70 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2075C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 2075 | chr10 | 20783672 | ||||||
chr10:20783981 | T | G | 1 | a0001c0001t0047 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1766A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 1766 | chr10 | 20783981 | ||||||
chr10:20784012 | A | C | 1 | a0001c0001t0030 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1735T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 1735 | chr10 | 20784012 | ||||||
chr10:20784190 | G | A | 7 | a0001c0001t0003 a0001c0001t0048 a0001c0003t0003 others(4): Show |
38 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1557C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 1557 | chr10 | 20784190 | ||||||
chr10:20784259 | C | T | 1 | a0002c0002t0011 | 7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1488G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 1488 | chr10 | 20784259 | ||||||
chr10:20784323 | G | C | 1 | a0002c0002t0014 | 5 | HG01070.hp1 HG01071.hp1 HG01981.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1424C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 1424 | chr10 | 20784323 | ||||||
chr10:20784337 | G | C | 1 | a0001c0001t0050 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1410C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 1410 | chr10 | 20784337 | ||||||
chr10:20784358 | AT | A | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
219 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1388delA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 1388 | chr10 | 20784358 | ||||||
chr10:20784393 | A | G | 1 | a0001c0001t0021 | 2 | HG03688.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1354T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 1354 | chr10 | 20784393 | ||||||
chr10:20784521 | G | A | 1 | a0002c0002t0011 | 7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1226C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 1226 | chr10 | 20784521 | ||||||
chr10:20784592 | T | C | 28 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0016 others(25): Show |
131 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1155A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 1155 | chr10 | 20784592 | ||||||
chr10:20784609 | A | G | 1 | a0001c0001t0019 | 3 | NA18950.hp2 NA19006.hp1 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1138T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 1138 | chr10 | 20784609 | ||||||
chr10:20785091 | T | C | 2 | a0001c0001t0007 a0001c0001t0040 |
14 | HG00642.hp2 HG01192.hp1 HG02280.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*656A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 656 | chr10 | 20785091 | ||||||
chr10:20785177 | G | A | 2 | a0001c0001t0018 a0001c0001t0039 |
4 | HG02055.hp2 HG02451.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*570C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 570 | chr10 | 20785177 | ||||||
chr10:20785415 | A | G | 54 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(51): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*332T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 332 | chr10 | 20785415 | ||||||
chr10:20785420 | A | T | 1 | a0003c0004t0025 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*327T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 327 | chr10 | 20785420 | ||||||
chr10:20785526 | T | C | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0019 others(17): Show |
88 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*221A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 221 | chr10 | 20785526 | ||||||
chr10:20785662 | A | C | 1 | a0001c0001t0015 | 4 | HG02145.hp1 HG02486.hp2 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*85T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 28/28 | 85 | chr10 | 20785662 | ||||||
chr10:20897289 | G | A | 1 | a0001c0001t0050 | 1 | HG01081.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-84C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 1/28 | chr10 | 20897289 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:20785963 | T | C | 1 | a0001c0001t0002g0019 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2869-40A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/27 | chr10 | 20785963 | |||||||
chr10:20786155 | G | C | 313 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(310): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.2869-232C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/27 | chr10 | 20786155 | |||||||
chr10:20786196 | T | C | 1 | a0002c0002t0003g0293 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2869-273A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/27 | chr10 | 20786196 | |||||||
chr10:20786366 | T | C | 5 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2869-443A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/27 | chr10 | 20786366 | |||||||
chr10:20786410 | T | C | 82 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(79): Show |
83 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2869-487A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/27 | chr10 | 20786410 | |||||||
chr10:20786628 | C | T | 2 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
2 | HG03491.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2868+574G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/27 | chr10 | 20786628 | |||||||
chr10:20786710 | G | A | 2 | a0001c0003t0001g0088 a0001c0003t0001g0089 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2868+492C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/27 | chr10 | 20786710 | |||||||
chr10:20786741 | C | T | 13 | a0003c0004t0006g0008 a0003c0004t0006g0024 a0003c0004t0006g0208 others(10): Show |
15 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.2868+461G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/27 | chr10 | 20786741 | |||||||
chr10:20786812 | T | A | 1 | a0003c0004t0025g0296 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2868+390A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/27 | chr10 | 20786812 | |||||||
chr10:20786901 | A | G | 1 | a0001c0006t0008g0302 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2868+301T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/27 | chr10 | 20786901 | |||||||
chr10:20787171 | C | A | 103 | a0001c0001t0003g0253 a0001c0001t0003g0314 a0001c0001t0003g0319 others(100): Show |
108 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.2868+31G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 27/27 | chr10 | 20787171 | |||||||
chr10:20787356 | C | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0116 a0001c0001t0001g0139 |
3 | HG00733.hp1 HG00738.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2762-48G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20787356 | |||||||
chr10:20787372 | A | T | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2762-64T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20787372 | |||||||
chr10:20787378 | C | T | 89 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(86): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.2762-70G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20787378 | |||||||
chr10:20787571 | A | T | 16 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 others(13): Show |
18 | HG00438.hp1 HG00673.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.2762-263T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20787571 | |||||||
chr10:20787586 | CA | C | 19 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0302 others(16): Show |
19 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2762-279delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20787586 | |||||||
chr10:20787604 | C | T | 4 | a0001c0001t0018g0280 a0001c0001t0018g0289 a0001c0001t0018g0291 others(1): Show |
4 | HG02055.hp2 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2762-296G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20787604 | |||||||
chr10:20787636 | T | G | 5 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2762-328A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20787636 | |||||||
chr10:20787795 | G | A | 13 | a0003c0004t0006g0008 a0003c0004t0006g0024 a0003c0004t0006g0208 others(10): Show |
15 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.2762-487C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20787795 | |||||||
chr10:20787896 | G | A | 7 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2762-588C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20787896 | |||||||
chr10:20787943 | A | G | 13 | a0003c0004t0006g0008 a0003c0004t0006g0024 a0003c0004t0006g0208 others(10): Show |
15 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.2762-635T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20787943 | |||||||
chr10:20788103 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2762-795T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20788103 | |||||||
chr10:20788235 | G | A | 25 | a0001c0001t0005g0048 a0001c0001t0005g0096 a0001c0001t0005g0134 others(22): Show |
25 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.2762-927C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20788235 | |||||||
chr10:20788290 | C | T | 4 | a0003c0004t0006g0008 a0003c0004t0006g0292 a0003c0004t0006g0294 others(1): Show |
5 | NA18970.hp2 NA19003.hp2 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.2762-982G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20788290 | |||||||
chr10:20788432 | TAATA | T | 13 | a0003c0004t0006g0008 a0003c0004t0006g0024 a0003c0004t0006g0208 others(10): Show |
15 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.2762-1128_2762-112 others(8): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20788432 | |||||||
chr10:20788671 | T | C | 134 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(131): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.2762-1363A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20788671 | |||||||
chr10:20788706 | A | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(82): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.2762-1398T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20788706 | |||||||
chr10:20788765 | A | G | 13 | a0003c0004t0006g0008 a0003c0004t0006g0024 a0003c0004t0006g0208 others(10): Show |
15 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.2762-1457T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20788765 | |||||||
chr10:20789020 | C | T | 1 | a0001c0001t0015g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2762-1712G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789020 | |||||||
chr10:20789082 | G | T | 1 | a0001c0001t0013g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2762-1774C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789082 | |||||||
chr10:20789138 | C | G | 218 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0002g0005 others(215): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.2762-1830G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789138 | |||||||
chr10:20789254 | A | G | 43 | a0001c0001t0003g0253 a0001c0001t0003g0314 a0001c0001t0003g0319 others(40): Show |
44 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2762-1946T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789254 | |||||||
chr10:20789265 | T | C | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2762-1957A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789265 | |||||||
chr10:20789307 | A | C | 27 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 others(24): Show |
27 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.2762-1999T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789307 | |||||||
chr10:20789448 | T | C | 1 | a0004c0005t0001g0133 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2762-2140A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789448 | |||||||
chr10:20789493 | G | A | 67 | a0001c0001t0003g0253 a0001c0001t0003g0314 a0001c0001t0003g0319 others(64): Show |
68 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2762-2185C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789493 | |||||||
chr10:20789548 | G | A | 45 | a0001c0001t0009g0040 a0001c0001t0009g0053 a0001c0001t0009g0067 others(42): Show |
45 | HG00140.hp2 HG01175.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.2762-2240C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789548 | |||||||
chr10:20789611 | T | G | 214 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(211): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2762-2303A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789611 | |||||||
chr10:20789795 | A | G | 5 | a0002c0002t0004g0007 a0002c0002t0004g0054 a0002c0002t0004g0083 others(2): Show |
6 | HG02717.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2762-2487T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789795 | |||||||
chr10:20789853 | T | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2762-2545A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789853 | |||||||
chr10:20789868 | C | T | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2762-2560G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789868 | |||||||
chr10:20789872 | C | T | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2762-2564G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789872 | |||||||
chr10:20789878 | C | CACAT | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2762-2571_2762-257 others(8): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789878 | |||||||
chr10:20789886 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2762-2578G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789886 | |||||||
chr10:20789886 | CAT | C | 20 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0281 others(17): Show |
20 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.2762-2580_2762-257 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789886 | |||||||
chr10:20789888 | T | C | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2762-2580A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789888 | |||||||
chr10:20789909 | GTA | G | 6 | a0001c0001t0002g0020 a0001c0001t0002g0257 a0003c0004t0002g0015 others(3): Show |
6 | HG01192.hp2 HG01993.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.2762-2603_2762-260 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789909 | |||||||
chr10:20789911 | A | G | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2762-2603T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789911 | |||||||
chr10:20789929 | A | G | 133 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(130): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.2762-2621T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789929 | |||||||
chr10:20789953 | G | GTA | 5 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2762-2647_2762-264 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789953 | |||||||
chr10:20789968 | T | C | 1 | a0001c0001t0007g0328 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2762-2660A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789968 | |||||||
chr10:20789975 | A | T | 1 | a0001c0001t0024g0324 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2762-2667T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20789975 | |||||||
chr10:20790053 | T | C | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2762-2745A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790053 | |||||||
chr10:20790422 | G | A | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2762-3114C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790422 | |||||||
chr10:20790537 | G | T | 1 | a0001c0001t0002g0257 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2762-3229C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790537 | |||||||
chr10:20790545 | G | T | 1 | a0001c0001t0007g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2762-3237C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790545 | |||||||
chr10:20790549 | C | T | 1 | a0001c0006t0008g0281 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2762-3241G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790549 | |||||||
chr10:20790600 | C | CAA | 16 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 others(13): Show |
18 | HG00438.hp1 HG00673.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.2762-3294_2762-329 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790600 | |||||||
chr10:20790614 | C | A | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2762-3306G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790614 | |||||||
chr10:20790619 | C | A | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2762-3311G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790619 | |||||||
chr10:20790750 | G | C | 1 | a0002c0002t0028g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2762-3442C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790750 | |||||||
chr10:20790825 | T | C | 132 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(129): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.2762-3517A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790825 | |||||||
chr10:20790908 | C | A | 16 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 others(13): Show |
18 | HG00438.hp1 HG00673.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.2762-3600G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790908 | |||||||
chr10:20790911 | T | C | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2762-3603A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20790911 | |||||||
chr10:20791123 | T | C | 1 | a0001c0001t0013g0189 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2762-3815A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20791123 | |||||||
chr10:20791206 | C | G | 4 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2762-3898G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20791206 | |||||||
chr10:20791258 | A | G | 8 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2762-3950T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20791258 | |||||||
chr10:20791382 | A | G | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02074.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2762-4074T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20791382 | |||||||
chr10:20791438 | C | T | 1 | a0001c0001t0017g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2762-4130G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20791438 | |||||||
chr10:20791549 | C | T | 1 | a0001c0003t0001g0081 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2762-4241G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20791549 | |||||||
chr10:20791609 | A | G | 154 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(151): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2762-4301T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20791609 | |||||||
chr10:20791637 | A | C | 155 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(152): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.2762-4329T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20791637 | |||||||
chr10:20791743 | A | G | 43 | a0001c0001t0003g0253 a0001c0001t0003g0314 a0001c0001t0003g0319 others(40): Show |
44 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2762-4435T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20791743 | |||||||
chr10:20791832 | G | C | 1 | a0002c0002t0004g0083 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2762-4524C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20791832 | |||||||
chr10:20791957 | A | C | 1 | a0001c0001t0030g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2762-4649T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20791957 | |||||||
chr10:20792019 | G | T | 13 | a0003c0004t0006g0008 a0003c0004t0006g0024 a0003c0004t0006g0208 others(10): Show |
15 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.2762-4711C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20792019 | |||||||
chr10:20792072 | G | A | 10 | a0001c0006t0010g0080 a0001c0006t0010g0118 a0001c0006t0010g0143 others(7): Show |
10 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.2762-4764C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20792072 | |||||||
chr10:20792076 | G | A | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2762-4768C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20792076 | |||||||
chr10:20792123 | GA | G | 189 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(186): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.2762-4816delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20792123 | |||||||
chr10:20792123 | GAA | G | 6 | a0002c0002t0004g0007 a0002c0002t0004g0054 a0002c0002t0004g0083 others(3): Show |
7 | HG02717.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2762-4817_2762-481 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20792123 | |||||||
chr10:20792525 | G | A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2762-5217C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20792525 | |||||||
chr10:20792612 | G | T | 2 | a0001c0001t0015g0117 a0001c0001t0015g0159 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2762-5304C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20792612 | |||||||
chr10:20792803 | C | CA | 19 | a0001c0001t0002g0257 a0001c0001t0003g0314 a0002c0002t0011g0183 others(16): Show |
22 | HG00438.hp1 HG00558.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2762-5496dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20792803 | |||||||
chr10:20792803 | CA | C | 6 | a0001c0001t0002g0229 a0001c0001t0013g0185 a0001c0001t0013g0186 others(3): Show |
6 | HG00642.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2762-5496delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20792803 | |||||||
chr10:20792914 | G | A | 99 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(96): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.2762-5606C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20792914 | |||||||
chr10:20792985 | A | G | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2762-5677T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20792985 | |||||||
chr10:20793120 | T | C | 20 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0281 others(17): Show |
20 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.2762-5812A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20793120 | |||||||
chr10:20793202 | T | C | 1 | a0004c0005t0002g0164 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2762-5894A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20793202 | |||||||
chr10:20793331 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2762-6023T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20793331 | |||||||
chr10:20793557 | C | CT | 12 | a0001c0001t0018g0280 a0002c0002t0003g0028 a0002c0002t0011g0055 others(9): Show |
12 | HG02451.hp1 HG02630.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.2762-6250dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20793557 | |||||||
chr10:20793557 | CT | C | 13 | a0001c0001t0009g0053 a0001c0001t0047g0245 a0001c0006t0008g0175 others(10): Show |
13 | HG01256.hp1 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.2762-6250delA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20793557 | |||||||
chr10:20793584 | G | A | 3 | a0001c0001t0018g0280 a0001c0001t0018g0289 a0001c0001t0018g0291 |
3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2762-6276C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20793584 | |||||||
chr10:20793627 | C | T | 1 | a0003c0004t0002g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2762-6319G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20793627 | |||||||
chr10:20793826 | G | A | 1 | a0001c0001t0007g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2762-6518C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20793826 | |||||||
chr10:20794167 | G | A | 1 | a0001c0001t0002g0019 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2762-6859C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20794167 | |||||||
chr10:20794241 | C | T | 26 | a0001c0001t0005g0048 a0001c0001t0005g0096 a0001c0001t0005g0134 others(23): Show |
26 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.2762-6933G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20794241 | |||||||
chr10:20794268 | T | C | 6 | a0006c0008t0008g0181 a0006c0008t0008g0304 a0006c0008t0008g0307 others(3): Show |
6 | HG02258.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2762-6960A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20794268 | |||||||
chr10:20794332 | CTT | C | 39 | a0001c0001t0001g0204 a0001c0001t0001g0237 a0001c0003t0001g0017 others(36): Show |
40 | HG00408.hp2 HG00558.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.2762-7026_2762-702 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20794332 | |||||||
chr10:20794401 | A | G | 19 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0302 others(16): Show |
19 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2762-7093T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20794401 | |||||||
chr10:20794412 | T | C | 1 | a0001c0001t0007g0085 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2762-7104A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20794412 | |||||||
chr10:20794506 | T | G | 216 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0002g0005 others(213): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.2762-7198A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20794506 | |||||||
chr10:20794686 | A | G | 1 | a0004c0005t0002g0164 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2762-7378T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20794686 | |||||||
chr10:20794701 | A | G | 1 | a0001c0001t0017g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2762-7393T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20794701 | |||||||
chr10:20794814 | A | C | 16 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(13): Show |
19 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.2762-7506T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20794814 | |||||||
chr10:20794844 | G | A | 19 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0302 others(16): Show |
19 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2762-7536C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20794844 | |||||||
chr10:20795039 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2762-7731T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20795039 | |||||||
chr10:20795105 | C | A | 7 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2762-7797G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20795105 | |||||||
chr10:20795125 | G | GTT | 69 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(66): Show |
70 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.2762-7818_2762-781 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20795125 | |||||||
chr10:20795157 | A | C | 16 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(13): Show |
19 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.2762-7849T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20795157 | |||||||
chr10:20795176 | T | C | 15 | a0001c0001t0005g0048 a0001c0001t0005g0096 a0001c0001t0005g0134 others(12): Show |
15 | HG01891.hp2 HG01975.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2762-7868A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20795176 | |||||||
chr10:20795296 | G | A | 2 | a0001c0001t0005g0048 a0001c0001t0005g0134 |
2 | HG01891.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.2762-7988C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20795296 | |||||||
chr10:20795524 | T | A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2762-8216A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20795524 | |||||||
chr10:20795560 | A | ATG | 99 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0020 others(96): Show |
101 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.2762-8254_2762-825 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20795560 | |||||||
chr10:20795713 | A | C | 1 | a0001c0001t0004g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2762-8405T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20795713 | |||||||
chr10:20795782 | C | T | 1 | a0001c0003t0001g0077 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2762-8474G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20795782 | |||||||
chr10:20796133 | G | A | 7 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2762-8825C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796133 | |||||||
chr10:20796228 | T | C | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2762-8920A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796228 | |||||||
chr10:20796239 | C | T | 35 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0302 others(32): Show |
38 | HG00438.hp1 HG00673.hp1 HG01496.hp2 others(35): Show |
intron_variant | MODIFIER | c.2762-8931G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796239 | |||||||
chr10:20796264 | G | A | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2762-8956C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796264 | |||||||
chr10:20796320 | T | C | 1 | a0001c0001t0005g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2762-9012A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796320 | |||||||
chr10:20796367 | G | GA | 88 | a0001c0001t0001g0116 a0001c0001t0001g0237 a0001c0001t0001g0321 others(85): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2762-9060dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796367 | |||||||
chr10:20796367 | G | GAA | 18 | a0001c0001t0002g0216 a0001c0001t0002g0220 a0001c0001t0002g0233 others(15): Show |
18 | HG00438.hp1 HG01884.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.2762-9061_2762-906 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796367 | |||||||
chr10:20796367 | GA | G | 20 | a0001c0001t0001g0138 a0001c0001t0001g0317 a0001c0001t0007g0023 others(17): Show |
21 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.2762-9060delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796367 | |||||||
chr10:20796367 | GAA | G | 23 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(20): Show |
24 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.2762-9061_2762-906 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796367 | |||||||
chr10:20796367 | GAAA | G | 21 | a0001c0001t0005g0134 a0001c0001t0005g0217 a0001c0001t0018g0289 others(18): Show |
21 | HG01496.hp2 HG01928.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.2762-9062_2762-906 others(7): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796367 | |||||||
chr10:20796367 | GAAAAAAA | G | 9 | a0001c0001t0003g0253 a0001c0001t0003g0319 a0002c0002t0003g0016 others(6): Show |
9 | HG01934.hp2 NA18945.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.2762-9066_2762-906 others(11): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796367 | |||||||
chr10:20796367 | GAAAAAAA others(1): Show |
G | 25 | a0001c0001t0003g0314 a0001c0003t0003g0026 a0002c0002t0003g0001 others(22): Show |
26 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.2762-9067_2762-906 others(12): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796367 | |||||||
chr10:20796447 | C | A | 1 | a0001c0001t0039g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2762-9139G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796447 | |||||||
chr10:20796464 | A | T | 12 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0007g0023 others(9): Show |
12 | HG00642.hp2 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2762-9156T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796464 | |||||||
chr10:20796704 | C | T | 1 | a0002c0002t0035g0188 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2762-9396G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796704 | |||||||
chr10:20796736 | C | T | 2 | a0004c0005t0001g0092 a0004c0005t0001g0133 |
2 | NA18945.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2762-9428G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796736 | |||||||
chr10:20796751 | A | T | 2 | a0001c0001t0050g0329 a0009c0012t0041g0207 |
2 | HG00140.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2762-9443T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796751 | |||||||
chr10:20796776 | A | T | 1 | a0002c0002t0011g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2762-9468T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796776 | |||||||
chr10:20796809 | G | A | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2762-9501C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796809 | |||||||
chr10:20796883 | T | C | 1 | a0001c0001t0007g0152 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2762-9575A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796883 | |||||||
chr10:20796884 | A | G | 1 | a0001c0006t0008g0281 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2762-9576T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796884 | |||||||
chr10:20796999 | G | A | 1 | a0002c0002t0028g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2762-9691C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20796999 | |||||||
chr10:20797188 | T | C | 3 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0025g0296 |
3 | NA18947.hp2 NA18966.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2762-9880A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20797188 | |||||||
chr10:20797539 | G | A | 19 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0302 others(16): Show |
19 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2762-10231C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20797539 | |||||||
chr10:20797564 | A | G | 1 | a0001c0001t0009g0040 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2762-10256T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20797564 | |||||||
chr10:20797574 | A | T | 7 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(4): Show |
7 | HG02056.hp1 HG02074.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.2762-10266T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20797574 | |||||||
chr10:20797575 | C | T | 86 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(83): Show |
88 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.2762-10267G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20797575 | |||||||
chr10:20797578 | G | T | 9 | a0002c0002t0004g0174 a0002c0002t0004g0219 a0002c0002t0004g0258 others(6): Show |
9 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2762-10270C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20797578 | |||||||
chr10:20797603 | C | G | 200 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(197): Show |
206 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.2762-10295G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20797603 | |||||||
chr10:20797793 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2762-10485T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20797793 | |||||||
chr10:20797977 | C | A | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2761+10533G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20797977 | |||||||
chr10:20798110 | C | CA | 73 | a0001c0001t0001g0140 a0001c0001t0001g0237 a0001c0001t0002g0005 others(70): Show |
74 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2761+10399dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798110 | |||||||
chr10:20798110 | CA | C | 92 | a0001c0001t0003g0253 a0001c0001t0003g0314 a0001c0001t0003g0319 others(89): Show |
97 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2761+10399delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798110 | |||||||
chr10:20798110 | CAA | C | 21 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0281 others(18): Show |
21 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2761+10398_2761+10 others(8): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798110 | |||||||
chr10:20798306 | A | G | 1 | a0002c0002t0028g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2761+10204T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798306 | |||||||
chr10:20798334 | T | C | 16 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(13): Show |
19 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.2761+10176A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798334 | |||||||
chr10:20798474 | C | CAT | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2761+10034_2761+10 others(8): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798474 | |||||||
chr10:20798556 | T | C | 71 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(68): Show |
72 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2761+9954A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798556 | |||||||
chr10:20798609 | G | A | 5 | a0001c0003t0001g0066 a0001c0003t0001g0078 a0001c0003t0001g0081 others(2): Show |
5 | HG00408.hp2 HG01981.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.2761+9901C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798609 | |||||||
chr10:20798677 | T | A | 2 | a0005c0007t0001g0069 a0005c0007t0001g0141 |
2 | HG01081.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2761+9833A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798677 | |||||||
chr10:20798756 | T | C | 10 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0281 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2761+9754A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798756 | |||||||
chr10:20798827 | A | G | 7 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2761+9683T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798827 | |||||||
chr10:20798943 | T | C | 1 | a0002c0002t0003g0038 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2761+9567A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20798943 | |||||||
chr10:20799045 | GCTAGATG others(6): Show |
G | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+9452_2761+946 others(17): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799045 | |||||||
chr10:20799080 | T | C | 1 | a0001c0001t0039g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2761+9430A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799080 | |||||||
chr10:20799165 | T | G | 1 | a0002c0002t0003g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2761+9345A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799165 | |||||||
chr10:20799192 | G | A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+9318C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799192 | |||||||
chr10:20799211 | A | G | 20 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0281 others(17): Show |
20 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.2761+9299T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799211 | |||||||
chr10:20799261 | T | A | 20 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0281 others(17): Show |
20 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.2761+9249A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799261 | |||||||
chr10:20799276 | A | G | 16 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(13): Show |
19 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.2761+9234T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799276 | |||||||
chr10:20799538 | C | G | 38 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0003g0253 others(35): Show |
39 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.2761+8972G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799538 | |||||||
chr10:20799719 | T | C | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2761+8791A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799719 | |||||||
chr10:20799729 | G | A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+8781C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799729 | |||||||
chr10:20799782 | T | C | 4 | a0003c0004t0002g0015 a0003c0004t0002g0057 a0003c0004t0002g0102 others(1): Show |
4 | HG01192.hp2 HG01993.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.2761+8728A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799782 | |||||||
chr10:20799810 | C | T | 191 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(188): Show |
197 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.2761+8700G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799810 | |||||||
chr10:20799824 | C | T | 5 | a0002c0002t0004g0007 a0002c0002t0004g0054 a0002c0002t0004g0083 others(2): Show |
6 | HG02717.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2761+8686G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799824 | |||||||
chr10:20799872 | G | A | 22 | a0001c0001t0005g0048 a0001c0001t0005g0096 a0001c0001t0005g0134 others(19): Show |
22 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2761+8638C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799872 | |||||||
chr10:20799898 | C | G | 1 | a0001c0001t0001g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2761+8612G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799898 | |||||||
chr10:20799924 | C | CGT | 88 | a0001c0001t0001g0237 a0001c0001t0001g0283 a0001c0001t0002g0005 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2761+8584_2761+858 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799924 | |||||||
chr10:20799924 | CGT | C | 29 | a0001c0001t0005g0048 a0001c0001t0005g0096 a0001c0001t0005g0134 others(26): Show |
29 | HG00642.hp1 HG01496.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.2761+8584_2761+858 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799924 | |||||||
chr10:20799950 | A | T | 7 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2761+8560T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799950 | |||||||
chr10:20799959 | AAG | A | 19 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0302 others(16): Show |
19 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2761+8549_2761+855 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799959 | |||||||
chr10:20799968 | C | T | 1 | a0002c0002t0028g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2761+8542G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20799968 | |||||||
chr10:20800105 | T | C | 87 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(84): Show |
89 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.2761+8405A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20800105 | |||||||
chr10:20800347 | A | AC | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2761+8162dupG | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20800347 | |||||||
chr10:20800502 | C | A | 7 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2761+8008G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20800502 | |||||||
chr10:20800638 | T | C | 1 | a0002c0002t0003g0028 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2761+7872A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20800638 | |||||||
chr10:20800680 | G | A | 16 | a0001c0001t0009g0067 a0003c0004t0003g0006 a0003c0004t0003g0255 others(13): Show |
19 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.2761+7830C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20800680 | |||||||
chr10:20800715 | GA | G | 114 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(111): Show |
116 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.2761+7794delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20800715 | |||||||
chr10:20800764 | G | A | 13 | a0001c0001t0001g0140 a0001c0001t0001g0168 a0001c0001t0001g0206 others(10): Show |
14 | HG00280.hp1 HG01256.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2761+7746C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20800764 | |||||||
chr10:20800900 | A | G | 1 | a0002c0002t0004g0083 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2761+7610T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20800900 | |||||||
chr10:20801021 | G | A | 1 | a0001c0001t0007g0152 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2761+7489C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20801021 | |||||||
chr10:20801226 | C | T | 198 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(195): Show |
204 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2761+7284G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20801226 | |||||||
chr10:20801416 | C | T | 1 | a0001c0001t0009g0075 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2761+7094G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20801416 | |||||||
chr10:20801633 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2761+6877G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20801633 | |||||||
chr10:20801689 | G | T | 1 | a0001c0001t0036g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2761+6821C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20801689 | |||||||
chr10:20801695 | T | C | 1 | a0002c0002t0003g0036 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2761+6815A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20801695 | |||||||
chr10:20801727 | G | A | 12 | a0001c0001t0005g0048 a0001c0001t0005g0134 a0001c0001t0005g0180 others(9): Show |
12 | HG01891.hp2 HG01975.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2761+6783C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20801727 | |||||||
chr10:20801759 | C | T | 1 | a0001c0001t0009g0040 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2761+6751G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20801759 | |||||||
chr10:20801792 | C | T | 1 | a0001c0001t0030g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2761+6718G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20801792 | |||||||
chr10:20801884 | T | C | 3 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0025g0296 |
3 | NA18947.hp2 NA18966.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2761+6626A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20801884 | |||||||
chr10:20801929 | C | T | 3 | a0001c0001t0018g0280 a0001c0001t0018g0289 a0001c0001t0018g0291 |
3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2761+6581G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20801929 | |||||||
chr10:20802016 | T | C | 1 | a0001c0001t0039g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2761+6494A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802016 | |||||||
chr10:20802033 | A | G | 19 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0302 others(16): Show |
19 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2761+6477T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802033 | |||||||
chr10:20802097 | C | T | 1 | a0002c0002t0004g0262 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2761+6413G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802097 | |||||||
chr10:20802113 | C | T | 1 | a0006c0008t0008g0310 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2761+6397G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802113 | |||||||
chr10:20802171 | G | T | 1 | a0001c0001t0009g0076 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2761+6339C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802171 | |||||||
chr10:20802178 | A | G | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+6332T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802178 | |||||||
chr10:20802451 | AG | A | 16 | a0001c0001t0004g0179 a0002c0002t0004g0007 a0002c0002t0004g0054 others(13): Show |
17 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.2761+6058delC | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802451 | |||||||
chr10:20802491 | C | G | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2761+6019G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802491 | |||||||
chr10:20802512 | T | C | 10 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0281 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2761+5998A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802512 | |||||||
chr10:20802693 | T | C | 1 | a0001c0001t0046g0223 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2761+5817A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802693 | |||||||
chr10:20802715 | T | C | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2761+5795A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802715 | |||||||
chr10:20802774 | C | G | 7 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2761+5736G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802774 | |||||||
chr10:20802802 | A | G | 19 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0302 others(16): Show |
19 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2761+5708T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802802 | |||||||
chr10:20802893 | G | A | 28 | a0001c0001t0004g0179 a0001c0001t0015g0079 a0001c0001t0015g0117 others(25): Show |
29 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(26): Show |
intron_variant | MODIFIER | c.2761+5617C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20802893 | |||||||
chr10:20803224 | T | C | 1 | a0002c0002t0028g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2761+5286A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803224 | |||||||
chr10:20803484 | C | G | 69 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(66): Show |
70 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.2761+5026G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803484 | |||||||
chr10:20803487 | C | T | 3 | a0001c0001t0001g0140 a0001c0003t0001g0021 a0001c0003t0001g0123 |
3 | HG01975.hp1 HG01978.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2761+5023G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803487 | |||||||
chr10:20803707 | A | G | 1 | a0001c0013t0001g0163 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2761+4803T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803707 | |||||||
chr10:20803808 | G | GA | 8 | a0001c0001t0004g0179 a0001c0006t0008g0281 a0002c0002t0004g0007 others(5): Show |
9 | HG02717.hp1 HG02723.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2761+4701dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803808 | |||||||
chr10:20803808 | G | GAA | 96 | a0001c0001t0001g0237 a0001c0001t0001g0283 a0001c0001t0002g0005 others(93): Show |
97 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.2761+4700_2761+470 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803808 | |||||||
chr10:20803808 | G | GAAAA | 14 | a0002c0002t0011g0183 a0003c0004t0006g0008 a0003c0004t0006g0024 others(11): Show |
16 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.2761+4698_2761+470 others(8): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803808 | |||||||
chr10:20803812 | A | AAT | 5 | a0001c0001t0007g0085 a0001c0001t0018g0280 a0001c0001t0018g0289 others(2): Show |
5 | HG00642.hp2 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2761+4696_2761+469 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803812 | |||||||
chr10:20803813 | AT | A | 3 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0302 |
3 | HG02572.hp2 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2761+4696delA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803813 | |||||||
chr10:20803814 | T | A | 201 | a0001c0001t0001g0237 a0001c0001t0001g0283 a0001c0001t0002g0005 others(198): Show |
207 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.2761+4696A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803814 | |||||||
chr10:20803816 | T | A | 155 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0153 others(152): Show |
160 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.2761+4694A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803816 | |||||||
chr10:20803818 | T | A | 86 | a0001c0001t0002g0153 a0001c0001t0002g0273 a0001c0001t0004g0179 others(83): Show |
89 | HG00438.hp1 HG00642.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.2761+4692A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803818 | |||||||
chr10:20803820 | T | A | 30 | a0001c0001t0005g0048 a0001c0001t0013g0197 a0001c0001t0020g0199 others(27): Show |
30 | HG00438.hp1 HG01496.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.2761+4690A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803820 | |||||||
chr10:20803822 | T | A | 18 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0302 others(15): Show |
18 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.2761+4688A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803822 | |||||||
chr10:20803824 | T | A | 11 | a0001c0006t0008g0175 a0001c0006t0008g0184 a0001c0006t0008g0302 others(8): Show |
11 | HG01496.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.2761+4686A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803824 | |||||||
chr10:20803846 | T | C | 3 | a0001c0001t0018g0280 a0001c0001t0018g0289 a0001c0001t0018g0291 |
3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2761+4664A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803846 | |||||||
chr10:20803857 | T | G | 10 | a0002c0002t0004g0174 a0002c0002t0004g0219 a0002c0002t0004g0258 others(7): Show |
10 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2761+4653A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803857 | |||||||
chr10:20803997 | A | C | 1 | a0001c0001t0003g0314 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2761+4513T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20803997 | |||||||
chr10:20804317 | C | G | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+4193G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804317 | |||||||
chr10:20804342 | C | T | 1 | a0001c0006t0008g0302 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2761+4168G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804342 | |||||||
chr10:20804390 | G | A | 10 | a0001c0006t0010g0080 a0001c0006t0010g0118 a0001c0006t0010g0143 others(7): Show |
10 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.2761+4120C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804390 | |||||||
chr10:20804392 | G | C | 1 | a0001c0003t0001g0050 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2761+4118C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804392 | |||||||
chr10:20804402 | C | T | 37 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0003g0253 others(34): Show |
38 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2761+4108G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804402 | |||||||
chr10:20804513 | T | C | 6 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2761+3997A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804513 | |||||||
chr10:20804518 | T | A | 23 | a0001c0001t0004g0179 a0002c0002t0004g0007 a0002c0002t0004g0054 others(20): Show |
24 | HG02451.hp2 HG02622.hp1 HG02630.hp1 others(21): Show |
intron_variant | MODIFIER | c.2761+3992A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804518 | |||||||
chr10:20804555 | A | G | 1 | a0001c0006t0008g0281 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2761+3955T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804555 | |||||||
chr10:20804586 | T | C | 1 | a0003c0004t0002g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2761+3924A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804586 | |||||||
chr10:20804654 | T | C | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2761+3856A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804654 | |||||||
chr10:20804686 | G | A | 20 | a0001c0001t0040g0311 a0001c0006t0008g0175 a0001c0006t0008g0184 others(17): Show |
20 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.2761+3824C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804686 | |||||||
chr10:20804727 | T | C | 1 | a0002c0002t0028g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2761+3783A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804727 | |||||||
chr10:20804735 | T | C | 1 | a0004c0005t0001g0156 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2761+3775A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804735 | |||||||
chr10:20804770 | T | G | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2761+3740A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804770 | |||||||
chr10:20804804 | C | T | 1 | a0003c0004t0002g0102 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2761+3706G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20804804 | |||||||
chr10:20805033 | G | C | 1 | a0001c0013t0001g0163 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2761+3477C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805033 | |||||||
chr10:20805041 | C | G | 1 | a0001c0015t0002g0242 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2761+3469G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805041 | |||||||
chr10:20805088 | T | A | 1 | a0001c0001t0001g0206 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2761+3422A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805088 | |||||||
chr10:20805114 | T | A | 6 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2761+3396A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805114 | |||||||
chr10:20805122 | A | C | 8 | a0002c0002t0004g0174 a0002c0002t0004g0219 a0002c0002t0004g0258 others(5): Show |
8 | HG02451.hp2 HG02630.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2761+3388T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805122 | |||||||
chr10:20805130 | G | A | 21 | a0001c0001t0005g0048 a0001c0001t0005g0096 a0001c0001t0005g0134 others(18): Show |
21 | HG00642.hp1 HG01891.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.2761+3380C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805130 | |||||||
chr10:20805131 | T | C | 2 | a0001c0001t0005g0048 a0001c0001t0005g0134 |
2 | HG01891.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.2761+3379A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805131 | |||||||
chr10:20805183 | A | T | 1 | a0001c0003t0001g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2761+3327T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805183 | |||||||
chr10:20805263 | T | C | 6 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2761+3247A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805263 | |||||||
chr10:20805288 | T | C | 16 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(13): Show |
19 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.2761+3222A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805288 | |||||||
chr10:20805348 | C | T | 67 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(64): Show |
68 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.2761+3162G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805348 | |||||||
chr10:20805352 | T | C | 16 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(13): Show |
19 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.2761+3158A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805352 | |||||||
chr10:20805573 | C | T | 1 | a0004c0005t0002g0135 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2761+2937G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805573 | |||||||
chr10:20805718 | T | C | 3 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0017g0303 |
3 | HG01884.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2761+2792A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805718 | |||||||
chr10:20805722 | G | A | 4 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(1): Show |
4 | HG01993.hp1 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2761+2788C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805722 | |||||||
chr10:20805768 | G | A | 9 | a0001c0001t0005g0180 a0001c0001t0005g0182 a0001c0001t0005g0191 others(6): Show |
9 | NA18953.hp2 NA18964.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.2761+2742C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805768 | |||||||
chr10:20805777 | T | C | 6 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2761+2733A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805777 | |||||||
chr10:20805816 | G | A | 1 | a0013c0021t0043g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2761+2694C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805816 | |||||||
chr10:20805836 | C | T | 6 | a0001c0006t0010g0080 a0001c0006t0010g0118 a0001c0006t0010g0143 others(3): Show |
6 | HG01496.hp2 HG01928.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.2761+2674G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805836 | |||||||
chr10:20805852 | CA | C | 180 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(177): Show |
185 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.2761+2657delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805852 | |||||||
chr10:20805852 | CAA | C | 16 | a0001c0001t0004g0179 a0002c0002t0004g0007 a0002c0002t0004g0054 others(13): Show |
17 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.2761+2656_2761+265 others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805852 | |||||||
chr10:20805902 | T | C | 6 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2761+2608A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805902 | |||||||
chr10:20805911 | G | A | 1 | a0001c0006t0008g0302 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2761+2599C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805911 | |||||||
chr10:20805935 | T | C | 1 | a0006c0008t0008g0309 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2761+2575A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20805935 | |||||||
chr10:20806074 | A | G | 1 | a0001c0001t0015g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2761+2436T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806074 | |||||||
chr10:20806092 | TC | T | 7 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2761+2417delG | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806092 | |||||||
chr10:20806158 | A | G | 69 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(66): Show |
70 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.2761+2352T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806158 | |||||||
chr10:20806182 | G | A | 1 | a0001c0001t0004g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2761+2328C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806182 | |||||||
chr10:20806250 | C | T | 3 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0025g0296 |
3 | NA18947.hp2 NA18966.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2761+2260G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806250 | |||||||
chr10:20806264 | C | T | 3 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 |
3 | HG02145.hp1 HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2761+2246G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806264 | |||||||
chr10:20806265 | C | G | 3 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 |
3 | HG02145.hp1 HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2761+2245G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806265 | |||||||
chr10:20806304 | A | T | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+2206T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806304 | |||||||
chr10:20806548 | A | G | 10 | a0001c0006t0010g0080 a0001c0006t0010g0118 a0001c0006t0010g0143 others(7): Show |
10 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.2761+1962T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806548 | |||||||
chr10:20806556 | G | A | 1 | a0001c0001t0036g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2761+1954C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806556 | |||||||
chr10:20806586 | G | C | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+1924C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806586 | |||||||
chr10:20806681 | G | A | 9 | a0002c0002t0004g0174 a0002c0002t0004g0219 a0002c0002t0004g0258 others(6): Show |
9 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2761+1829C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806681 | |||||||
chr10:20806696 | T | C | 1 | a0001c0001t0003g0253 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2761+1814A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806696 | |||||||
chr10:20806721 | G | C | 21 | a0001c0001t0036g0290 a0001c0001t0040g0311 a0001c0006t0008g0175 others(18): Show |
21 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2761+1789C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806721 | |||||||
chr10:20806771 | A | T | 1 | a0011c0018t0001g0154 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2761+1739T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806771 | |||||||
chr10:20806798 | A | G | 7 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2761+1712T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806798 | |||||||
chr10:20806854 | C | G | 68 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(65): Show |
69 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.2761+1656G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20806854 | |||||||
chr10:20807064 | G | A | 1 | a0001c0001t0030g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2761+1446C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807064 | |||||||
chr10:20807183 | A | T | 3 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 |
3 | HG02145.hp1 HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2761+1327T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807183 | |||||||
chr10:20807221 | G | A | 16 | a0001c0001t0004g0179 a0002c0002t0004g0007 a0002c0002t0004g0054 others(13): Show |
17 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.2761+1289C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807221 | |||||||
chr10:20807222 | C | A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+1288G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807222 | |||||||
chr10:20807222 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2761+1288G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807222 | |||||||
chr10:20807589 | C | A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+921G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807589 | |||||||
chr10:20807642 | G | T | 1 | a0002c0002t0011g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2761+868C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807642 | |||||||
chr10:20807651 | T | G | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+859A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807651 | |||||||
chr10:20807653 | G | C | 1 | a0001c0001t0005g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2761+857C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807653 | |||||||
chr10:20807662 | C | G | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+848G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807662 | |||||||
chr10:20807666 | AT | A | 59 | a0001c0001t0003g0314 a0001c0001t0003g0319 a0001c0001t0005g0048 others(56): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2761+843delA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807666 | |||||||
chr10:20807719 | C | T | 1 | a0001c0001t0039g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2761+791G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807719 | |||||||
chr10:20807768 | G | C | 9 | a0001c0001t0001g0073 a0001c0001t0001g0116 a0001c0001t0001g0137 others(6): Show |
9 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.2761+742C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807768 | |||||||
chr10:20807787 | A | G | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2761+723T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807787 | |||||||
chr10:20807916 | T | C | 74 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(71): Show |
75 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.2761+594A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807916 | |||||||
chr10:20807967 | T | C | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2761+543A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807967 | |||||||
chr10:20807981 | T | TA | 22 | a0001c0001t0005g0048 a0001c0001t0005g0134 a0001c0001t0005g0180 others(19): Show |
22 | HG00280.hp1 HG00642.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.2761+528dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807981 | |||||||
chr10:20807981 | TA | T | 17 | a0001c0001t0002g0173 a0001c0001t0039g0277 a0002c0002t0004g0174 others(14): Show |
17 | HG01516.hp1 HG02451.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.2761+528delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807981 | |||||||
chr10:20807999 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2761+511G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20807999 | |||||||
chr10:20808055 | C | A | 1 | a0002c0002t0028g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2761+455G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20808055 | |||||||
chr10:20808192 | G | A | 59 | a0001c0001t0003g0314 a0001c0001t0003g0319 a0001c0001t0005g0048 others(56): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2761+318C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20808192 | |||||||
chr10:20808230 | A | T | 7 | a0001c0001t0004g0179 a0002c0002t0004g0007 a0002c0002t0004g0054 others(4): Show |
8 | HG02717.hp1 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2761+280T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20808230 | |||||||
chr10:20808283 | G | C | 71 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(68): Show |
72 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2761+227C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 26/27 | chr10 | 20808283 | |||||||
chr10:20808686 | G | A | 3 | a0001c0003t0003g0026 a0002c0002t0003g0041 a0002c0002t0003g0065 |
3 | HG03710.hp1 HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2612-27C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20808686 | |||||||
chr10:20808840 | A | G | 204 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0237 others(201): Show |
210 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.2612-181T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20808840 | |||||||
chr10:20809130 | A | C | 16 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(13): Show |
19 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.2612-471T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20809130 | |||||||
chr10:20809189 | A | T | 2 | a0001c0001t0007g0052 a0001c0001t0007g0087 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2612-530T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20809189 | |||||||
chr10:20809223 | A | T | 1 | a0002c0002t0003g0061 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2612-564T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20809223 | |||||||
chr10:20809247 | C | G | 12 | a0001c0001t0005g0048 a0001c0001t0005g0134 a0001c0001t0005g0180 others(9): Show |
12 | HG01891.hp2 HG01975.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2611+559G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20809247 | |||||||
chr10:20809315 | T | C | 4 | a0001c0003t0001g0097 a0001c0003t0001g0119 a0001c0003t0001g0125 others(1): Show |
4 | HG01516.hp2 HG01517.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.2611+491A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20809315 | |||||||
chr10:20809339 | T | C | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2611+467A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20809339 | |||||||
chr10:20809454 | T | C | 3 | a0001c0001t0018g0280 a0001c0001t0018g0289 a0001c0001t0018g0291 |
3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2611+352A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20809454 | |||||||
chr10:20809504 | T | G | 5 | a0003c0004t0006g0208 a0003c0004t0006g0209 a0003c0004t0006g0212 others(2): Show |
6 | HG00438.hp1 HG00673.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.2611+302A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20809504 | |||||||
chr10:20809654 | T | C | 1 | a0001c0006t0010g0315 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2611+152A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20809654 | |||||||
chr10:20809718 | AC | A | 5 | a0001c0001t0013g0185 a0001c0001t0013g0186 a0001c0001t0013g0187 others(2): Show |
5 | HG00642.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2611+87delG | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20809718 | |||||||
chr10:20809746 | C | T | 16 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(13): Show |
19 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.2611+60G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 25/27 | chr10 | 20809746 | |||||||
chr10:20809950 | G | GA | 24 | a0001c0001t0001g0325 a0001c0001t0009g0076 a0001c0001t0018g0289 others(21): Show |
27 | HG00438.hp1 HG00673.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.2519-53dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20809950 | |||||||
chr10:20809950 | G | GAA | 88 | a0001c0001t0001g0237 a0001c0001t0002g0005 a0001c0001t0002g0019 others(85): Show |
90 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.2519-54_2519-53dup others(2): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20809950 | |||||||
chr10:20809950 | GA | G | 10 | a0001c0001t0039g0277 a0001c0006t0010g0080 a0001c0006t0010g0118 others(7): Show |
10 | HG01496.hp2 HG01928.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.2519-53delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20809950 | |||||||
chr10:20810107 | C | A | 4 | a0001c0001t0040g0311 a0001c0006t0008g0175 a0001c0006t0008g0184 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2519-209G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20810107 | |||||||
chr10:20810301 | T | G | 15 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(12): Show |
18 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.2519-403A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20810301 | |||||||
chr10:20810340 | G | T | 12 | a0001c0001t0001g0074 a0005c0007t0001g0012 a0005c0007t0001g0068 others(9): Show |
12 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2519-442C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20810340 | |||||||
chr10:20810348 | T | C | 2 | a0001c0001t0022g0071 a0001c0001t0022g0072 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2519-450A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20810348 | |||||||
chr10:20810368 | C | CA | 40 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0003g0314 others(37): Show |
41 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2519-471dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20810368 | |||||||
chr10:20810421 | T | C | 1 | a0001c0001t0004g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2519-523A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20810421 | |||||||
chr10:20810476 | G | C | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2519-578C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20810476 | |||||||
chr10:20810697 | A | G | 1 | a0001c0001t0005g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2519-799T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20810697 | |||||||
chr10:20810900 | A | G | 1 | a0002c0002t0028g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2519-1002T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20810900 | |||||||
chr10:20810975 | G | A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2519-1077C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20810975 | |||||||
chr10:20811126 | A | G | 21 | a0001c0001t0040g0311 a0001c0006t0008g0175 a0001c0006t0008g0184 others(18): Show |
21 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2519-1228T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20811126 | |||||||
chr10:20811274 | C | T | 1 | a0001c0003t0001g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2519-1376G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20811274 | |||||||
chr10:20811356 | T | C | 19 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(16): Show |
22 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2518+1413A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20811356 | |||||||
chr10:20811409 | T | C | 3 | a0001c0001t0018g0280 a0001c0001t0018g0289 a0001c0001t0018g0291 |
3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2518+1360A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20811409 | |||||||
chr10:20811657 | T | A | 1 | a0002c0002t0003g0107 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2518+1112A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20811657 | |||||||
chr10:20811982 | A | G | 22 | a0001c0001t0040g0311 a0001c0006t0008g0175 a0001c0006t0008g0184 others(19): Show |
22 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.2518+787T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20811982 | |||||||
chr10:20812075 | A | T | 1 | a0004c0005t0001g0011 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2518+694T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20812075 | |||||||
chr10:20812162 | T | C | 1 | a0001c0001t0017g0286 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2518+607A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20812162 | |||||||
chr10:20812201 | G | A | 6 | a0001c0006t0010g0080 a0001c0006t0010g0118 a0001c0006t0010g0143 others(3): Show |
6 | HG01496.hp2 HG01928.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.2518+568C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20812201 | |||||||
chr10:20812326 | T | TA | 19 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(16): Show |
22 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2518+442_2518+443i others(3): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20812326 | |||||||
chr10:20812350 | C | A | 5 | a0001c0001t0013g0185 a0001c0001t0013g0186 a0001c0001t0013g0187 others(2): Show |
5 | HG00642.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2518+419G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20812350 | |||||||
chr10:20812388 | C | T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0116 a0001c0001t0001g0139 others(3): Show |
6 | HG00733.hp1 HG00738.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2518+381G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20812388 | |||||||
chr10:20812444 | G | A | 9 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(6): Show |
9 | HG01891.hp2 HG01975.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.2518+325C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20812444 | |||||||
chr10:20812494 | T | C | 203 | a0001c0001t0001g0204 a0001c0001t0001g0237 a0001c0001t0001g0282 others(200): Show |
209 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.2518+275A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20812494 | |||||||
chr10:20812579 | T | C | 19 | a0003c0004t0003g0006 a0003c0004t0003g0255 a0003c0004t0006g0008 others(16): Show |
22 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2518+190A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20812579 | |||||||
chr10:20812613 | G | A | 1 | a0004c0005t0001g0156 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2518+156C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 24/27 | chr10 | 20812613 | |||||||
chr10:20813035 | G | A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2347-95C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 23/27 | chr10 | 20813035 | |||||||
chr10:20813083 | AAGTCTGG others(6): Show |
A | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2347-156_2347-144d others(15): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 23/27 | chr10 | 20813083 | |||||||
chr10:20813130 | T | A | 1 | a0002c0002t0003g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2347-190A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 23/27 | chr10 | 20813130 | |||||||
chr10:20813390 | AC | A | 27 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(24): Show |
27 | HG00642.hp1 HG01891.hp2 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.2347-451delG | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 23/27 | chr10 | 20813390 | |||||||
chr10:20813430 | A | T | 1 | a0001c0001t0045g0142 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2347-490T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 23/27 | chr10 | 20813430 | |||||||
chr10:20813478 | T | C | 86 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2346+461A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 23/27 | chr10 | 20813478 | |||||||
chr10:20813810 | C | G | 2 | a0001c0001t0021g0100 a0001c0001t0021g0136 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2346+129G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 23/27 | chr10 | 20813810 | |||||||
chr10:20813855 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2346+84C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 23/27 | chr10 | 20813855 | |||||||
chr10:20813861 | A | T | 1 | a0001c0001t0007g0085 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2346+78T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 23/27 | chr10 | 20813861 | |||||||
chr10:20813895 | C | G | 18 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(15): Show |
21 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.2346+44G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 23/27 | chr10 | 20813895 | |||||||
chr10:20814238 | T | A | 18 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(15): Show |
21 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.2242-195A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814238 | |||||||
chr10:20814257 | A | C | 1 | a0001c0001t0030g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2242-214T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814257 | |||||||
chr10:20814293 | A | C | 2 | a0001c0001t0007g0052 a0001c0001t0007g0087 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2242-250T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814293 | |||||||
chr10:20814318 | A | G | 1 | a0001c0001t0036g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2242-275T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814318 | |||||||
chr10:20814319 | A | G | 22 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(19): Show |
25 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.2242-276T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814319 | |||||||
chr10:20814321 | C | A | 3 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 |
3 | HG02145.hp1 HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2242-278G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814321 | |||||||
chr10:20814323 | C | T | 22 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(19): Show |
25 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.2242-280G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814323 | |||||||
chr10:20814335 | T | A | 1 | a0001c0001t0002g0271 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2242-292A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814335 | |||||||
chr10:20814345 | C | A | 27 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(24): Show |
27 | HG00642.hp1 HG01891.hp2 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.2242-302G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814345 | |||||||
chr10:20814350 | C | T | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2242-307G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814350 | |||||||
chr10:20814359 | G | C | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2242-316C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814359 | |||||||
chr10:20814391 | T | A | 1 | a0001c0001t0002g0226 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2242-348A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814391 | |||||||
chr10:20814443 | A | AT | 21 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(18): Show |
24 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.2242-401dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814443 | |||||||
chr10:20814445 | T | TA | 12 | a0001c0001t0002g0216 a0001c0001t0005g0172 a0002c0002t0003g0038 others(9): Show |
12 | HG02145.hp2 HG02630.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.2242-403dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814445 | |||||||
chr10:20814445 | TA | T | 10 | a0001c0001t0001g0137 a0001c0001t0002g0173 a0001c0001t0002g0226 others(7): Show |
10 | HG01069.hp2 HG01516.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.2242-403delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814445 | |||||||
chr10:20814446 | A | T | 1 | a0003c0004t0006g0300 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2242-403T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814446 | |||||||
chr10:20814471 | G | C | 15 | a0002c0002t0004g0007 a0002c0002t0004g0054 a0002c0002t0004g0083 others(12): Show |
16 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.2242-428C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814471 | |||||||
chr10:20814599 | A | C | 12 | a0001c0001t0005g0048 a0001c0001t0005g0134 a0001c0001t0005g0180 others(9): Show |
12 | HG01891.hp2 HG01975.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2242-556T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814599 | |||||||
chr10:20814609 | T | TACACACA others(3): Show |
2 | a0002c0002t0011g0056 a0002c0002t0011g0288 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2242-567_2242-566i others(12): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814609 | |||||||
chr10:20814609 | T | TACACACA others(5): Show |
6 | a0002c0002t0011g0055 a0002c0002t0011g0099 a0002c0002t0011g0177 others(3): Show |
6 | HG02630.hp1 HG03209.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2242-567_2242-566i others(14): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814609 | |||||||
chr10:20814609 | T | TACACACA others(9): Show |
2 | a0001c0001t0015g0117 a0001c0001t0015g0159 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2242-567_2242-566i others(18): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814609 | |||||||
chr10:20814609 | T | TACACACA others(11): Show |
1 | a0001c0001t0015g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2242-567_2242-566i others(20): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814609 | |||||||
chr10:20814617 | T | C | 11 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(8): Show |
11 | HG02145.hp1 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2242-574A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814617 | |||||||
chr10:20814617 | T | TACAC | 2 | a0002c0002t0003g0001 a0002c0002t0003g0115 |
3 | HG00408.hp1 NA18975.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.2242-578_2242-575d others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814617 | |||||||
chr10:20814617 | T | TACACACA others(1): Show |
32 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0002g0275 others(29): Show |
32 | HG00597.hp2 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.2242-582_2242-575d others(10): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814617 | |||||||
chr10:20814617 | T | TACACACA others(3): Show |
21 | a0001c0001t0002g0211 a0001c0001t0002g0222 a0001c0001t0002g0228 others(18): Show |
22 | HG00621.hp1 HG00733.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.2242-584_2242-575d others(12): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814617 | |||||||
chr10:20814617 | T | TACACACA others(5): Show |
88 | a0001c0001t0001g0204 a0001c0001t0001g0237 a0001c0001t0002g0005 others(85): Show |
92 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.2242-586_2242-575d others(14): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814617 | |||||||
chr10:20814617 | T | TACACACA others(7): Show |
37 | a0001c0001t0001g0206 a0001c0001t0002g0235 a0001c0001t0002g0240 others(34): Show |
37 | HG00597.hp1 HG00642.hp1 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.2242-588_2242-575d others(16): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814617 | |||||||
chr10:20814617 | T | TACACACA others(9): Show |
13 | a0001c0001t0005g0180 a0001c0001t0005g0182 a0001c0001t0005g0191 others(10): Show |
13 | HG02258.hp1 HG02809.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.2242-590_2242-575d others(18): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814617 | |||||||
chr10:20814617 | T | TACACACA others(6): Show |
1 | a0001c0001t0002g0226 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2242-575_2242-574i others(15): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814617 | |||||||
chr10:20814617 | TACACACA others(3): Show |
T | 3 | a0001c0001t0018g0280 a0001c0001t0018g0289 a0001c0001t0018g0291 |
3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2242-584_2242-575d others(12): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814617 | |||||||
chr10:20814661 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2242-618A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814661 | |||||||
chr10:20814750 | A | T | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2242-707T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814750 | |||||||
chr10:20814763 | A | ACT | 26 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 others(23): Show |
29 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2242-722_2242-721d others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814763 | |||||||
chr10:20814844 | A | G | 22 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(19): Show |
25 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.2241+781T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814844 | |||||||
chr10:20814974 | G | A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2241+651C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20814974 | |||||||
chr10:20815155 | T | G | 3 | a0003c0004t0006g0292 a0003c0004t0006g0294 a0003c0004t0006g0295 |
3 | NA18970.hp2 NA19003.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2241+470A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20815155 | |||||||
chr10:20815244 | G | C | 1 | a0001c0001t0004g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2241+381C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20815244 | |||||||
chr10:20815271 | T | C | 1 | a0001c0001t0039g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2241+354A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20815271 | |||||||
chr10:20815438 | T | C | 22 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(19): Show |
25 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.2241+187A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20815438 | |||||||
chr10:20815557 | G | A | 23 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(20): Show |
26 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.2241+68C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20815557 | |||||||
chr10:20815591 | T | C | 1 | a0004c0005t0001g0133 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2241+34A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 22/27 | chr10 | 20815591 | |||||||
chr10:20815722 | C | T | 22 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(19): Show |
25 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.2149-5G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20815722 | |||||||
chr10:20815765 | A | T | 207 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(204): Show |
213 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.2149-48T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20815765 | |||||||
chr10:20815817 | G | A | 6 | a0006c0008t0008g0181 a0006c0008t0008g0304 a0006c0008t0008g0307 others(3): Show |
6 | HG02258.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2149-100C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20815817 | |||||||
chr10:20815833 | A | G | 3 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 |
3 | HG02145.hp1 HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2149-116T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20815833 | |||||||
chr10:20815856 | T | C | 22 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(19): Show |
25 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.2149-139A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20815856 | |||||||
chr10:20815903 | G | A | 9 | a0002c0002t0004g0174 a0002c0002t0004g0219 a0002c0002t0004g0258 others(6): Show |
9 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2149-186C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20815903 | |||||||
chr10:20815925 | T | C | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2149-208A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20815925 | |||||||
chr10:20816058 | G | C | 1 | a0001c0001t0013g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2149-341C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816058 | |||||||
chr10:20816122 | A | G | 4 | a0007c0009t0003g0029 a0007c0009t0003g0030 a0007c0009t0003g0060 others(1): Show |
4 | HG00544.hp1 NA18969.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149-405T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816122 | |||||||
chr10:20816363 | G | C | 31 | a0001c0006t0008g0281 a0002c0002t0003g0001 a0002c0002t0003g0016 others(28): Show |
32 | HG00408.hp1 HG00597.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2149-646C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816363 | |||||||
chr10:20816373 | C | T | 1 | a0001c0016t0002g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2149-656G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816373 | |||||||
chr10:20816435 | C | T | 1 | a0001c0001t0013g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2149-718G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816435 | |||||||
chr10:20816539 | G | A | 1 | a0001c0016t0002g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2149-822C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816539 | |||||||
chr10:20816761 | C | T | 1 | a0002c0002t0011g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2148+839G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816761 | |||||||
chr10:20816762 | G | A | 31 | a0001c0006t0008g0281 a0002c0002t0003g0001 a0002c0002t0003g0016 others(28): Show |
32 | HG00408.hp1 HG00597.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2148+838C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816762 | |||||||
chr10:20816816 | C | T | 15 | a0002c0002t0004g0007 a0002c0002t0004g0054 a0002c0002t0004g0083 others(12): Show |
16 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.2148+784G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816816 | |||||||
chr10:20816820 | C | G | 1 | a0015c0019t0001g0234 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2148+780G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816820 | |||||||
chr10:20816890 | A | G | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2148+710T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816890 | |||||||
chr10:20816903 | G | A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2148+697C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20816903 | |||||||
chr10:20817155 | G | A | 1 | a0001c0001t0036g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2148+445C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20817155 | |||||||
chr10:20817195 | C | T | 3 | a0001c0001t0018g0280 a0001c0001t0018g0289 a0001c0001t0018g0291 |
3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2148+405G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20817195 | |||||||
chr10:20817320 | T | C | 7 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 others(4): Show |
7 | HG02145.hp1 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+280A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20817320 | |||||||
chr10:20817332 | A | T | 7 | a0001c0001t0001g0140 a0001c0006t0010g0080 a0001c0006t0010g0118 others(4): Show |
7 | HG01496.hp2 HG01928.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+268T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20817332 | |||||||
chr10:20817391 | T | C | 3 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 |
3 | HG02145.hp2 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2148+209A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 21/27 | chr10 | 20817391 | |||||||
chr10:20817740 | C | G | 3 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 |
3 | HG02145.hp1 HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2056-48G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20817740 | |||||||
chr10:20817911 | CT | C | 4 | a0001c0001t0004g0179 a0001c0001t0005g0201 a0001c0001t0005g0202 others(1): Show |
4 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2056-220delA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20817911 | |||||||
chr10:20818042 | T | C | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2056-350A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20818042 | |||||||
chr10:20818075 | G | A | 8 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(5): Show |
8 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.2056-383C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20818075 | |||||||
chr10:20818320 | G | C | 1 | a0001c0001t0039g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2056-628C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20818320 | |||||||
chr10:20818364 | A | G | 1 | a0013c0021t0043g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2056-672T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20818364 | |||||||
chr10:20818392 | T | C | 1 | a0001c0001t0009g0040 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2056-700A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20818392 | |||||||
chr10:20818444 | G | A | 1 | a0001c0001t0044g0205 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2056-752C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20818444 | |||||||
chr10:20818558 | C | A | 8 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(5): Show |
8 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.2055+866G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20818558 | |||||||
chr10:20818641 | A | C | 2 | a0001c0001t0039g0277 a0014c0017t0031g0250 |
2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2055+783T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20818641 | |||||||
chr10:20818937 | G | A | 3 | a0001c0001t0002g0243 a0001c0001t0003g0253 a0001c0015t0002g0242 |
3 | NA18964.hp2 NA18979.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2055+487C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20818937 | |||||||
chr10:20819242 | G | A | 1 | a0001c0001t0002g0274 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2055+182C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20819242 | |||||||
chr10:20819299 | T | C | 26 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0002g0015 others(23): Show |
29 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2055+125A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20819299 | |||||||
chr10:20819318 | C | T | 208 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0204 others(205): Show |
214 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.2055+106G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 20/27 | chr10 | 20819318 | |||||||
chr10:20819603 | T | C | 2 | a0001c0001t0002g0257 a0001c0001t0049g0161 |
2 | HG02074.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1963-87A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20819603 | |||||||
chr10:20819607 | T | C | 2 | a0002c0002t0003g0063 a0002c0002t0003g0111 |
2 | NA18747.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1963-91A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20819607 | |||||||
chr10:20819714 | T | TTTG | 14 | a0001c0001t0040g0311 a0001c0006t0008g0175 a0001c0006t0008g0184 others(11): Show |
14 | HG02258.hp1 HG02572.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1963-201_1963-199d others(5): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20819714 | |||||||
chr10:20819777 | T | C | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1963-261A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20819777 | |||||||
chr10:20819852 | A | G | 27 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0002g0015 others(24): Show |
30 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1963-336T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20819852 | |||||||
chr10:20819919 | G | A | 1 | a0005c0007t0012g0047 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1963-403C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20819919 | |||||||
chr10:20819921 | T | C | 87 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(84): Show |
89 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1963-405A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20819921 | |||||||
chr10:20819941 | T | G | 1 | a0002c0002t0003g0293 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1963-425A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20819941 | |||||||
chr10:20819973 | A | G | 6 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1963-457T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20819973 | |||||||
chr10:20820130 | C | T | 120 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(117): Show |
123 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1963-614G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20820130 | |||||||
chr10:20820308 | T | G | 313 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(310): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1963-792A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20820308 | |||||||
chr10:20820598 | G | C | 1 | a0001c0001t0036g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1963-1082C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20820598 | |||||||
chr10:20820637 | C | A | 1 | a0001c0001t0007g0328 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1963-1121G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20820637 | |||||||
chr10:20820684 | G | C | 86 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(83): Show |
88 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1963-1168C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20820684 | |||||||
chr10:20820783 | C | G | 23 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(20): Show |
26 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1963-1267G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20820783 | |||||||
chr10:20820810 | G | A | 2 | a0001c0003t0001g0088 a0001c0003t0001g0089 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1963-1294C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20820810 | |||||||
chr10:20820922 | T | G | 1 | a0001c0001t0005g0134 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1963-1406A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20820922 | |||||||
chr10:20820977 | C | T | 30 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0022 others(27): Show |
31 | HG00408.hp1 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1963-1461G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20820977 | |||||||
chr10:20821023 | C | T | 75 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(72): Show |
76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1963-1507G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20821023 | |||||||
chr10:20821099 | T | C | 6 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1963-1583A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20821099 | |||||||
chr10:20821406 | G | A | 1 | a0005c0007t0001g0012 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1962+1802C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20821406 | |||||||
chr10:20821516 | A | T | 1 | a0001c0001t0039g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1962+1692T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20821516 | |||||||
chr10:20821521 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1962+1687A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20821521 | |||||||
chr10:20821535 | A | G | 1 | a0002c0002t0003g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1962+1673T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20821535 | |||||||
chr10:20821696 | C | T | 2 | a0001c0001t0017g0278 a0001c0001t0017g0303 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1962+1512G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20821696 | |||||||
chr10:20821705 | A | G | 8 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(5): Show |
8 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1962+1503T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20821705 | |||||||
chr10:20821732 | G | A | 1 | a0001c0003t0003g0026 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1962+1476C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20821732 | |||||||
chr10:20821974 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1962+1234G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20821974 | |||||||
chr10:20822190 | C | T | 1 | a0001c0001t0015g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1962+1018G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822190 | |||||||
chr10:20822237 | A | G | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1962+971T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822237 | |||||||
chr10:20822238 | T | C | 1 | a0001c0001t0002g0252 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1962+970A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822238 | |||||||
chr10:20822279 | A | G | 6 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1962+929T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822279 | |||||||
chr10:20822326 | T | C | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1962+882A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822326 | |||||||
chr10:20822357 | C | A | 200 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(197): Show |
206 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1962+851G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822357 | |||||||
chr10:20822359 | A | G | 1 | a0002c0002t0011g0284 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1962+849T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822359 | |||||||
chr10:20822549 | A | G | 11 | a0001c0001t0040g0311 a0001c0006t0008g0175 a0001c0006t0008g0184 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1962+659T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822549 | |||||||
chr10:20822573 | T | A | 1 | a0001c0001t0039g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1962+635A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822573 | |||||||
chr10:20822574 | A | G | 1 | a0001c0001t0004g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1962+634T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822574 | |||||||
chr10:20822586 | T | C | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1962+622A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822586 | |||||||
chr10:20822645 | TATA | T | 6 | a0001c0001t0013g0185 a0001c0001t0013g0186 a0001c0001t0013g0187 others(3): Show |
6 | HG00642.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1962+560_1962+562d others(5): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822645 | |||||||
chr10:20822652 | TATATATA others(18): Show |
T | 73 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(70): Show |
74 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1962+531_1962+555d others(27): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822652 | |||||||
chr10:20822655 | ATATAGAT others(10): Show |
A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1962+536_1962+552d others(19): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822655 | |||||||
chr10:20822929 | T | G | 19 | a0001c0001t0040g0311 a0001c0006t0008g0175 a0001c0006t0008g0184 others(16): Show |
19 | HG02258.hp1 HG02572.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.1962+279A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822929 | |||||||
chr10:20822958 | C | T | 1 | a0001c0001t0039g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1962+250G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822958 | |||||||
chr10:20822964 | T | A | 1 | a0001c0001t0002g0243 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1962+244A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822964 | |||||||
chr10:20822995 | A | G | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1962+213T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20822995 | |||||||
chr10:20823005 | A | C | 6 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1962+203T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20823005 | |||||||
chr10:20823092 | C | T | 1 | a0001c0003t0009g0151 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1962+116G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20823092 | |||||||
chr10:20823105 | A | G | 2 | a0005c0007t0001g0069 a0005c0007t0001g0141 |
2 | HG01081.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1962+103T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20823105 | |||||||
chr10:20823182 | A | T | 103 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(100): Show |
107 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.1962+26T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 19/27 | chr10 | 20823182 | |||||||
chr10:20823374 | G | C | 8 | a0002c0002t0011g0055 a0002c0002t0011g0056 a0002c0002t0011g0099 others(5): Show |
8 | HG02630.hp1 HG02818.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1870-74C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20823374 | |||||||
chr10:20823609 | C | T | 1 | a0002c0002t0003g0033 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1870-309G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20823609 | |||||||
chr10:20823730 | C | G | 6 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1870-430G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20823730 | |||||||
chr10:20823989 | T | C | 11 | a0001c0001t0040g0311 a0001c0006t0008g0175 a0001c0006t0008g0184 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1870-689A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20823989 | |||||||
chr10:20824010 | A | C | 22 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0002g0015 others(19): Show |
25 | HG00438.hp1 HG00673.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.1870-710T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20824010 | |||||||
chr10:20824011 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1870-711C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20824011 | |||||||
chr10:20824015 | A | G | 1 | a0001c0001t0005g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1870-715T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20824015 | |||||||
chr10:20824610 | T | C | 1 | a0001c0001t0017g0286 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1870-1310A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20824610 | |||||||
chr10:20824656 | T | C | 17 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 others(14): Show |
17 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1870-1356A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20824656 | |||||||
chr10:20824804 | C | A | 1 | a0001c0001t0003g0314 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1870-1504G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20824804 | |||||||
chr10:20824949 | C | A | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1869+1498G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20824949 | |||||||
chr10:20824971 | C | T | 11 | a0001c0001t0040g0311 a0001c0006t0008g0175 a0001c0006t0008g0184 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1869+1476G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20824971 | |||||||
chr10:20825034 | C | G | 22 | a0001c0001t0004g0179 a0001c0001t0005g0180 a0001c0001t0005g0182 others(19): Show |
22 | HG00642.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1869+1413G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825034 | |||||||
chr10:20825043 | C | T | 1 | a0001c0001t0002g0019 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1869+1404G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825043 | |||||||
chr10:20825310 | G | A | 1 | a0002c0002t0004g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1869+1137C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825310 | |||||||
chr10:20825395 | G | A | 18 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0003g0006 others(15): Show |
21 | HG00438.hp1 HG00673.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.1869+1052C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825395 | |||||||
chr10:20825591 | T | C | 207 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0204 others(204): Show |
213 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1869+856A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825591 | |||||||
chr10:20825592 | G | A | 1 | a0002c0002t0011g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1869+855C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825592 | |||||||
chr10:20825663 | C | CA | 23 | a0001c0001t0002g0247 a0001c0001t0040g0311 a0001c0006t0008g0175 others(20): Show |
23 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1869+783dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825663 | |||||||
chr10:20825743 | A | G | 1 | a0013c0021t0043g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1869+704T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825743 | |||||||
chr10:20825778 | G | A | 3 | a0001c0001t0018g0280 a0001c0001t0018g0289 a0001c0001t0018g0291 |
3 | HG02055.hp2 HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1869+669C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825778 | |||||||
chr10:20825851 | C | T | 207 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0204 others(204): Show |
213 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1869+596G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825851 | |||||||
chr10:20825852 | T | G | 1 | a0002c0002t0003g0016 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1869+595A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825852 | |||||||
chr10:20825854 | G | A | 2 | a0001c0001t0023g0224 a0001c0001t0023g0248 |
2 | HG01515.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1869+593C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825854 | |||||||
chr10:20825903 | G | A | 1 | a0001c0006t0010g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1869+544C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825903 | |||||||
chr10:20825933 | A | G | 29 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 others(26): Show |
32 | HG00438.hp1 HG00673.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1869+514T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825933 | |||||||
chr10:20825984 | T | C | 22 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0002g0015 others(19): Show |
25 | HG00438.hp1 HG00673.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+463A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20825984 | |||||||
chr10:20826021 | T | G | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1869+426A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20826021 | |||||||
chr10:20826051 | C | T | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1869+396G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20826051 | |||||||
chr10:20826280 | T | C | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1869+167A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20826280 | |||||||
chr10:20826296 | A | C | 6 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869+151T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20826296 | |||||||
chr10:20826395 | T | G | 4 | a0002c0002t0003g0001 a0002c0002t0003g0063 a0002c0002t0003g0111 others(1): Show |
5 | HG00408.hp1 NA18747.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1869+52A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20826395 | |||||||
chr10:20826403 | T | C | 207 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0204 others(204): Show |
213 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1869+44A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 18/27 | chr10 | 20826403 | |||||||
chr10:20826565 | T | C | 1 | a0001c0006t0008g0281 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1777-26A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20826565 | |||||||
chr10:20826679 | A | C | 157 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0204 others(154): Show |
162 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1777-140T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20826679 | |||||||
chr10:20826730 | A | G | 2 | a0001c0001t0007g0101 a0001c0001t0007g0152 |
2 | HG01192.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1777-191T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20826730 | |||||||
chr10:20826949 | T | A | 1 | a0002c0002t0011g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1777-410A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20826949 | |||||||
chr10:20826977 | T | G | 147 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0204 others(144): Show |
150 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1777-438A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20826977 | |||||||
chr10:20827202 | G | C | 3 | a0002c0002t0003g0105 a0002c0002t0003g0106 a0002c0002t0003g0107 |
3 | NA18952.hp1 NA18974.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1777-663C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20827202 | |||||||
chr10:20827414 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1777-875A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20827414 | |||||||
chr10:20827634 | G | C | 1 | a0001c0001t0036g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1776+896C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20827634 | |||||||
chr10:20827726 | A | G | 207 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0204 others(204): Show |
213 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1776+804T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20827726 | |||||||
chr10:20827737 | C | A | 2 | a0001c0001t0001g0282 a0002c0002t0004g0305 |
2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1776+793G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20827737 | |||||||
chr10:20827798 | T | G | 1 | a0001c0001t0024g0324 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1776+732A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20827798 | |||||||
chr10:20827915 | C | T | 1 | a0001c0001t0009g0093 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1776+615G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20827915 | |||||||
chr10:20827990 | C | G | 320 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0031 others(317): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1776+540G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20827990 | |||||||
chr10:20828004 | C | T | 10 | a0001c0001t0040g0311 a0001c0006t0008g0175 a0001c0006t0008g0184 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1776+526G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20828004 | |||||||
chr10:20828080 | T | TA | 41 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0048g0103 others(38): Show |
42 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1776+449dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20828080 | |||||||
chr10:20828120 | A | G | 2 | a0001c0001t0001g0168 a0004c0011t0001g0003 |
3 | NA18971.hp1 NA18989.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1776+410T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20828120 | |||||||
chr10:20828133 | T | C | 1 | a0001c0001t0002g0020 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1776+397A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20828133 | |||||||
chr10:20828160 | T | C | 6 | a0002c0002t0004g0007 a0002c0002t0004g0054 a0002c0002t0004g0083 others(3): Show |
7 | HG02717.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1776+370A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20828160 | |||||||
chr10:20828311 | C | T | 1 | a0003c0004t0006g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1776+219G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 17/27 | chr10 | 20828311 | |||||||
chr10:20828745 | T | C | 22 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0002g0015 others(19): Show |
25 | HG00438.hp1 HG00673.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.1672-111A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20828745 | |||||||
chr10:20828759 | C | T | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1672-125G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20828759 | |||||||
chr10:20828765 | C | CAG | 76 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(73): Show |
77 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1672-133_1672-132d others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20828765 | |||||||
chr10:20828766 | A | AGG | 22 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0002g0015 others(19): Show |
25 | HG00438.hp1 HG00673.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.1672-133_1672-132i others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20828766 | |||||||
chr10:20828783 | G | C | 1 | a0002c0002t0011g0183 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1672-149C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20828783 | |||||||
chr10:20829053 | A | G | 3 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0033g0203 |
3 | HG02109.hp2 HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1672-419T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829053 | |||||||
chr10:20829077 | A | T | 1 | a0001c0001t0017g0286 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1672-443T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829077 | |||||||
chr10:20829134 | A | C | 3 | a0001c0001t0015g0079 a0001c0001t0015g0117 a0001c0001t0015g0159 |
3 | HG02145.hp1 HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1672-500T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829134 | |||||||
chr10:20829184 | A | T | 4 | a0001c0003t0001g0097 a0001c0003t0001g0119 a0001c0003t0001g0125 others(1): Show |
4 | HG01516.hp2 HG01517.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1672-550T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829184 | |||||||
chr10:20829220 | A | G | 1 | a0001c0003t0001g0077 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1672-586T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829220 | |||||||
chr10:20829244 | T | C | 55 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0002c0002t0003g0001 others(52): Show |
59 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1672-610A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829244 | |||||||
chr10:20829378 | T | C | 6 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1672-744A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829378 | |||||||
chr10:20829427 | G | A | 8 | a0002c0002t0004g0174 a0002c0002t0004g0219 a0002c0002t0004g0258 others(5): Show |
8 | HG02451.hp2 HG02630.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1672-793C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829427 | |||||||
chr10:20829439 | G | T | 36 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0002c0002t0003g0001 others(33): Show |
37 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.1672-805C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829439 | |||||||
chr10:20829449 | G | T | 1 | a0001c0001t0015g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1672-815C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829449 | |||||||
chr10:20829454 | GA | G | 32 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0002c0002t0003g0001 others(29): Show |
33 | HG00408.hp1 HG00544.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1672-821delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829454 | |||||||
chr10:20829455 | A | G | 4 | a0002c0002t0003g0033 a0002c0002t0003g0065 a0002c0002t0014g0027 others(1): Show |
4 | HG00597.hp2 HG01981.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1672-821T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829455 | |||||||
chr10:20829509 | C | T | 79 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(76): Show |
80 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1672-875G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829509 | |||||||
chr10:20829535 | A | G | 1 | a0004c0005t0001g0133 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1672-901T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829535 | |||||||
chr10:20829540 | A | G | 71 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(68): Show |
72 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1672-906T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829540 | |||||||
chr10:20829557 | A | G | 169 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0204 others(166): Show |
174 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1672-923T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829557 | |||||||
chr10:20829558 | C | T | 71 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(68): Show |
72 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1672-924G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829558 | |||||||
chr10:20829598 | TA | T | 54 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0002c0002t0003g0001 others(51): Show |
58 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1672-965delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829598 | |||||||
chr10:20829654 | C | T | 49 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0002c0002t0003g0001 others(46): Show |
52 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1672-1020G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829654 | |||||||
chr10:20829767 | C | G | 1 | a0001c0001t0036g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1672-1133G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20829767 | |||||||
chr10:20830012 | T | C | 64 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0015g0079 others(61): Show |
67 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.1671+1184A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830012 | |||||||
chr10:20830076 | G | C | 2 | a0001c0001t0005g0048 a0001c0001t0005g0134 |
2 | HG01891.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1671+1120C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830076 | |||||||
chr10:20830103 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1671+1093C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830103 | |||||||
chr10:20830117 | C | T | 1 | a0001c0001t0036g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1671+1079G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830117 | |||||||
chr10:20830464 | A | C | 2 | a0001c0001t0013g0186 a0001c0001t0032g0190 |
2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1671+732T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830464 | |||||||
chr10:20830504 | A | T | 1 | a0001c0006t0008g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1671+692T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830504 | |||||||
chr10:20830552 | C | G | 1 | a0002c0002t0003g0016 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1671+644G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830552 | |||||||
chr10:20830619 | A | G | 52 | a0001c0001t0001g0129 a0001c0001t0002g0020 a0001c0001t0004g0179 others(49): Show |
52 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(49): Show |
intron_variant | MODIFIER | c.1671+577T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830619 | |||||||
chr10:20830673 | G | A | 1 | a0009c0012t0041g0207 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1671+523C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830673 | |||||||
chr10:20830717 | CA | C | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1671+478delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830717 | |||||||
chr10:20830734 | C | CA | 54 | a0001c0001t0002g0221 a0001c0001t0004g0179 a0001c0001t0005g0048 others(51): Show |
55 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.1671+461dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830734 | |||||||
chr10:20830734 | CA | C | 11 | a0001c0001t0040g0311 a0001c0006t0008g0281 a0001c0006t0008g0302 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1671+461delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830734 | |||||||
chr10:20830908 | A | G | 2 | a0001c0006t0008g0175 a0002c0002t0004g0174 |
2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1671+288T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830908 | |||||||
chr10:20830912 | T | TA | 11 | a0001c0001t0005g0134 a0001c0001t0005g0193 a0001c0001t0007g0101 others(8): Show |
11 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.1671+283dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830912 | |||||||
chr10:20830912 | T | TAA | 68 | a0001c0001t0002g0019 a0001c0001t0004g0179 a0001c0001t0005g0048 others(65): Show |
70 | HG00621.hp1 HG00642.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.1671+282_1671+283d others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830912 | |||||||
chr10:20830912 | T | TAAA | 73 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(70): Show |
75 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1671+281_1671+283d others(5): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830912 | |||||||
chr10:20830912 | T | TAAAA | 16 | a0001c0001t0002g0173 a0001c0001t0002g0211 a0001c0001t0002g0246 others(13): Show |
17 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1671+280_1671+283d others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830912 | |||||||
chr10:20830912 | TA | T | 14 | a0001c0001t0001g0127 a0001c0001t0007g0023 a0001c0001t0007g0084 others(11): Show |
14 | HG01081.hp2 HG01168.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.1671+283delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830912 | |||||||
chr10:20830912 | TAAAAAAA others(3): Show |
T | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1671+274_1671+283d others(12): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20830912 | |||||||
chr10:20831042 | G | A | 1 | a0001c0001t0029g0279 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1671+154C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20831042 | |||||||
chr10:20831092 | T | C | 1 | a0001c0001t0036g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1671+104A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20831092 | |||||||
chr10:20831167 | G | A | 1 | a0001c0001t0029g0279 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1671+29C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20831167 | |||||||
chr10:20831187 | A | G | 164 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(161): Show |
169 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1671+9T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 16/27 | chr10 | 20831187 | |||||||
chr10:20831398 | G | A | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1560+75C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 15/27 | chr10 | 20831398 | |||||||
chr10:20831802 | G | C | 1 | a0001c0001t0003g0253 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1450-219C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20831802 | |||||||
chr10:20831848 | C | G | 1 | a0001c0006t0008g0281 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1450-265G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20831848 | |||||||
chr10:20831918 | T | C | 2 | a0002c0002t0003g0041 a0002c0002t0003g0065 |
2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1450-335A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20831918 | |||||||
chr10:20832138 | G | A | 4 | a0001c0001t0007g0052 a0001c0001t0007g0087 a0001c0001t0007g0101 others(1): Show |
4 | HG01192.hp1 HG02280.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450-555C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20832138 | |||||||
chr10:20832140 | A | T | 1 | a0001c0001t0004g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1450-557T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20832140 | |||||||
chr10:20832225 | C | T | 2 | a0001c0001t0007g0052 a0001c0001t0007g0087 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1450-642G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20832225 | |||||||
chr10:20832407 | A | G | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1450-824T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20832407 | |||||||
chr10:20832427 | G | GT | 13 | a0001c0001t0001g0127 a0005c0007t0001g0012 a0005c0007t0001g0068 others(10): Show |
13 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1450-845dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20832427 | |||||||
chr10:20832611 | TA | T | 23 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0140 others(20): Show |
23 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.1450-1029delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20832611 | |||||||
chr10:20832612 | A | T | 11 | a0001c0001t0007g0023 a0001c0001t0007g0059 a0001c0001t0007g0084 others(8): Show |
11 | HG00642.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1450-1029T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20832612 | |||||||
chr10:20832640 | A | C | 40 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(37): Show |
40 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.1450-1057T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20832640 | |||||||
chr10:20832791 | C | T | 2 | a0001c0001t0007g0052 a0001c0001t0007g0087 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1450-1208G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20832791 | |||||||
chr10:20832799 | C | G | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1450-1216G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20832799 | |||||||
chr10:20833018 | C | T | 1 | a0001c0001t0015g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1450-1435G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20833018 | |||||||
chr10:20833354 | A | C | 3 | a0001c0001t0007g0086 a0001c0001t0007g0098 a0001c0001t0007g0147 |
3 | HG02970.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1450-1771T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20833354 | |||||||
chr10:20833419 | T | G | 52 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(49): Show |
53 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.1450-1836A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20833419 | |||||||
chr10:20833518 | T | C | 52 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(49): Show |
53 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.1450-1935A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20833518 | |||||||
chr10:20833520 | C | A | 1 | a0001c0003t0001g0066 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1450-1937G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20833520 | |||||||
chr10:20833709 | T | C | 1 | a0001c0001t0036g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1449+1804A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20833709 | |||||||
chr10:20833749 | C | G | 1 | a0001c0001t0009g0053 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1449+1764G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20833749 | |||||||
chr10:20833755 | C | CA | 13 | a0003c0004t0006g0299 a0003c0004t0006g0301 a0005c0007t0001g0012 others(10): Show |
13 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1449+1757dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20833755 | |||||||
chr10:20833786 | T | C | 1 | a0001c0001t0024g0324 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1449+1727A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20833786 | |||||||
chr10:20833967 | G | A | 1 | a0015c0019t0001g0234 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1449+1546C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20833967 | |||||||
chr10:20833979 | T | C | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+1534A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20833979 | |||||||
chr10:20834031 | C | T | 164 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(161): Show |
169 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1449+1482G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20834031 | |||||||
chr10:20834047 | T | C | 12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0116 others(9): Show |
13 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1449+1466A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20834047 | |||||||
chr10:20834256 | T | C | 5 | a0001c0001t0017g0278 a0001c0001t0036g0290 a0001c0001t0039g0277 others(2): Show |
5 | HG02717.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+1257A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20834256 | |||||||
chr10:20834355 | G | A | 5 | a0001c0001t0017g0278 a0001c0001t0036g0290 a0001c0001t0039g0277 others(2): Show |
5 | HG02717.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+1158C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20834355 | |||||||
chr10:20834664 | A | G | 11 | a0001c0001t0015g0306 a0001c0001t0040g0311 a0001c0006t0008g0281 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1449+849T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20834664 | |||||||
chr10:20834673 | A | G | 164 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(161): Show |
169 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1449+840T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20834673 | |||||||
chr10:20834737 | T | C | 2 | a0001c0006t0008g0175 a0002c0002t0004g0174 |
2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1449+776A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20834737 | |||||||
chr10:20834794 | A | G | 2 | a0001c0001t0007g0101 a0001c0001t0007g0152 |
2 | HG01192.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1449+719T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20834794 | |||||||
chr10:20834896 | G | T | 163 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(160): Show |
168 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.1449+617C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20834896 | |||||||
chr10:20835209 | T | C | 1 | a0001c0006t0008g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1449+304A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20835209 | |||||||
chr10:20835355 | T | A | 11 | a0001c0001t0015g0306 a0001c0001t0040g0311 a0001c0006t0008g0281 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1449+158A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 14/27 | chr10 | 20835355 | |||||||
chr10:20835833 | A | G | 11 | a0001c0001t0015g0306 a0001c0001t0040g0311 a0001c0006t0008g0281 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1339-210T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20835833 | |||||||
chr10:20836051 | T | C | 1 | a0015c0019t0001g0234 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1339-428A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836051 | |||||||
chr10:20836127 | C | A | 3 | a0001c0001t0017g0278 a0001c0001t0036g0290 a0001c0001t0039g0277 |
3 | HG02717.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1339-504G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836127 | |||||||
chr10:20836156 | T | A | 1 | a0001c0001t0017g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1339-533A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836156 | |||||||
chr10:20836262 | G | A | 1 | a0001c0001t0002g0273 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1339-639C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836262 | |||||||
chr10:20836284 | G | A | 1 | a0001c0001t0015g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1339-661C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836284 | |||||||
chr10:20836334 | A | G | 28 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(25): Show |
28 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1339-711T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836334 | |||||||
chr10:20836371 | C | T | 11 | a0001c0001t0015g0306 a0001c0001t0040g0311 a0001c0006t0008g0281 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1339-748G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836371 | |||||||
chr10:20836428 | G | T | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1339-805C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836428 | |||||||
chr10:20836559 | G | C | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1339-936C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836559 | |||||||
chr10:20836616 | G | A | 1 | a0001c0001t0023g0248 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1339-993C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836616 | |||||||
chr10:20836779 | C | A | 2 | a0001c0001t0007g0085 a0002c0002t0011g0099 |
2 | HG00642.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1339-1156G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836779 | |||||||
chr10:20836830 | T | A | 82 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(79): Show |
85 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1339-1207A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836830 | |||||||
chr10:20836998 | A | G | 84 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(81): Show |
87 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1339-1375T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20836998 | |||||||
chr10:20837060 | G | A | 1 | a0002c0002t0004g0259 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1339-1437C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20837060 | |||||||
chr10:20837151 | G | T | 6 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1339-1528C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20837151 | |||||||
chr10:20837316 | A | T | 1 | a0002c0002t0003g0039 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1339-1693T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20837316 | |||||||
chr10:20837642 | C | T | 1 | a0002c0002t0034g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1339-2019G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20837642 | |||||||
chr10:20837769 | G | A | 1 | a0012c0014t0001g0170 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1339-2146C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20837769 | |||||||
chr10:20837839 | C | T | 1 | a0002c0002t0004g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1339-2216G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20837839 | |||||||
chr10:20837883 | T | C | 2 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
2 | HG03491.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1339-2260A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20837883 | |||||||
chr10:20837981 | A | G | 7 | a0001c0001t0005g0180 a0001c0001t0005g0182 a0001c0001t0005g0191 others(4): Show |
7 | NA18964.hp1 NA18972.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1339-2358T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20837981 | |||||||
chr10:20838129 | C | T | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1339-2506G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20838129 | |||||||
chr10:20838293 | A | C | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1338+2446T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20838293 | |||||||
chr10:20838365 | A | G | 1 | a0004c0005t0001g0160 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1338+2374T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20838365 | |||||||
chr10:20838437 | G | C | 3 | a0001c0001t0049g0161 a0004c0005t0001g0162 a0004c0005t0002g0164 |
3 | HG02074.hp2 HG02155.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1338+2302C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20838437 | |||||||
chr10:20838661 | A | T | 2 | a0001c0003t0001g0021 a0001c0003t0001g0123 |
2 | HG01975.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1338+2078T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20838661 | |||||||
chr10:20838762 | C | T | 1 | a0006c0008t0008g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1338+1977G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20838762 | |||||||
chr10:20838853 | A | G | 28 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(25): Show |
28 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1338+1886T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20838853 | |||||||
chr10:20838865 | A | G | 1 | a0001c0001t0021g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1338+1874T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20838865 | |||||||
chr10:20838934 | T | G | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1338+1805A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20838934 | |||||||
chr10:20838935 | A | G | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1338+1804T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20838935 | |||||||
chr10:20839154 | C | T | 2 | a0001c0001t0005g0048 a0001c0001t0005g0134 |
2 | HG01891.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1338+1585G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20839154 | |||||||
chr10:20839240 | T | C | 6 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1338+1499A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20839240 | |||||||
chr10:20839316 | G | A | 1 | a0001c0001t0036g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1338+1423C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20839316 | |||||||
chr10:20839320 | C | T | 1 | a0003c0004t0006g0024 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1338+1419G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20839320 | |||||||
chr10:20839435 | C | T | 1 | a0001c0006t0010g0080 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1338+1304G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20839435 | |||||||
chr10:20839477 | A | C | 1 | a0002c0002t0003g0115 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1338+1262T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20839477 | |||||||
chr10:20839528 | C | T | 1 | a0002c0002t0004g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1338+1211G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20839528 | |||||||
chr10:20839702 | G | C | 1 | a0001c0001t0001g0325 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1338+1037C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20839702 | |||||||
chr10:20839831 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1338+908G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20839831 | |||||||
chr10:20839880 | T | A | 163 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(160): Show |
168 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.1338+859A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20839880 | |||||||
chr10:20840029 | C | T | 2 | a0002c0002t0009g0032 a0002c0002t0009g0035 |
2 | NA18983.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1338+710G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20840029 | |||||||
chr10:20840110 | T | C | 2 | a0001c0001t0007g0059 a0001c0001t0007g0084 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1338+629A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20840110 | |||||||
chr10:20840659 | T | C | 13 | a0002c0002t0001g0010 a0002c0002t0042g0178 a0005c0007t0001g0012 others(10): Show |
13 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1338+80A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 13/27 | chr10 | 20840659 | |||||||
chr10:20840913 | T | C | 1 | a0001c0006t0008g0281 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1228-64A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20840913 | |||||||
chr10:20840952 | C | A | 82 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(79): Show |
85 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1228-103G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20840952 | |||||||
chr10:20841045 | A | G | 1 | a0001c0003t0001g0081 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1228-196T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20841045 | |||||||
chr10:20841271 | A | C | 84 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(81): Show |
87 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1228-422T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20841271 | |||||||
chr10:20841409 | T | C | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1228-560A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20841409 | |||||||
chr10:20841802 | T | C | 5 | a0002c0002t0003g0001 a0002c0002t0003g0022 a0002c0002t0003g0063 others(2): Show |
6 | HG00408.hp1 NA18747.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-953A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20841802 | |||||||
chr10:20841862 | C | A | 1 | a0004c0005t0001g0122 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1228-1013G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20841862 | |||||||
chr10:20842018 | A | G | 1 | a0002c0002t0034g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1228-1169T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20842018 | |||||||
chr10:20842250 | C | A | 5 | a0002c0002t0003g0036 a0002c0002t0003g0038 a0002c0002t0003g0061 others(2): Show |
5 | NA18945.hp1 NA18977.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-1401G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20842250 | |||||||
chr10:20842403 | G | T | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1228-1554C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20842403 | |||||||
chr10:20842540 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1228-1691G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20842540 | |||||||
chr10:20842580 | T | C | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1228-1731A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20842580 | |||||||
chr10:20842687 | A | T | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1228-1838T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20842687 | |||||||
chr10:20842696 | A | G | 1 | a0002c0002t0003g0115 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1228-1847T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20842696 | |||||||
chr10:20842781 | T | C | 14 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0116 others(11): Show |
15 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1228-1932A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20842781 | |||||||
chr10:20843027 | T | G | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1228-2178A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20843027 | |||||||
chr10:20843219 | T | C | 11 | a0001c0001t0015g0306 a0001c0001t0040g0311 a0001c0006t0008g0281 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1227+2039A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20843219 | |||||||
chr10:20843343 | TATAGCAG others(9): Show |
T | 1 | a0001c0001t0015g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1227+1899_1227+191 others(20): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20843343 | |||||||
chr10:20843381 | G | C | 1 | a0001c0001t0023g0248 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1227+1877C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20843381 | |||||||
chr10:20843548 | T | TA | 165 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(162): Show |
170 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.1227+1709dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20843548 | |||||||
chr10:20843644 | T | G | 1 | a0004c0005t0001g0133 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1227+1614A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20843644 | |||||||
chr10:20843658 | A | C | 82 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(79): Show |
85 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1227+1600T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20843658 | |||||||
chr10:20843793 | T | C | 1 | a0001c0003t0001g0021 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1227+1465A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20843793 | |||||||
chr10:20843870 | C | T | 2 | a0004c0005t0001g0160 a0004c0005t0002g0135 |
2 | HG02132.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1227+1388G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20843870 | |||||||
chr10:20843902 | G | A | 10 | a0001c0001t0015g0306 a0001c0001t0040g0311 a0001c0006t0008g0302 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1227+1356C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20843902 | |||||||
chr10:20843937 | C | T | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1227+1321G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20843937 | |||||||
chr10:20844176 | C | T | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1227+1082G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20844176 | |||||||
chr10:20844253 | T | C | 12 | a0001c0006t0008g0281 a0005c0007t0001g0012 a0005c0007t0001g0068 others(9): Show |
12 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1227+1005A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20844253 | |||||||
chr10:20844437 | C | G | 81 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(78): Show |
84 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1227+821G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20844437 | |||||||
chr10:20844513 | T | TA | 79 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(76): Show |
81 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.1227+744dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20844513 | |||||||
chr10:20844657 | G | A | 164 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(161): Show |
169 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1227+601C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20844657 | |||||||
chr10:20844990 | C | T | 6 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1227+268G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20844990 | |||||||
chr10:20845144 | A | C | 1 | a0002c0002t0004g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1227+114T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20845144 | |||||||
chr10:20845179 | T | C | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1227+79A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 12/27 | chr10 | 20845179 | |||||||
chr10:20845374 | A | C | 3 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 |
3 | HG02145.hp2 HG02895.hp1 NA18522.hp1 |
splice_region_variant&intron_variant | LOW | c.1117-6T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20845374 | |||||||
chr10:20845438 | G | C | 1 | a0013c0021t0043g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1117-70C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20845438 | |||||||
chr10:20845717 | C | G | 1 | a0004c0005t0001g0011 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1117-349G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20845717 | |||||||
chr10:20845836 | T | C | 1 | a0002c0002t0011g0284 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1117-468A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20845836 | |||||||
chr10:20845940 | A | G | 7 | a0001c0001t0017g0278 a0001c0001t0018g0289 a0001c0001t0018g0291 others(4): Show |
7 | HG02055.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117-572T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20845940 | |||||||
chr10:20846036 | G | A | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1117-668C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846036 | |||||||
chr10:20846041 | T | C | 1 | a0001c0001t0001g0326 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1117-673A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846041 | |||||||
chr10:20846083 | A | G | 12 | a0001c0001t0015g0306 a0001c0001t0017g0303 a0001c0001t0040g0311 others(9): Show |
12 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1117-715T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846083 | |||||||
chr10:20846236 | G | A | 3 | a0001c0003t0001g0018 a0001c0003t0001g0091 a0001c0003t0003g0026 |
3 | HG00280.hp1 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1117-868C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846236 | |||||||
chr10:20846291 | A | G | 28 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(25): Show |
28 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1117-923T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846291 | |||||||
chr10:20846307 | G | C | 6 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1117-939C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846307 | |||||||
chr10:20846430 | A | T | 1 | a0002c0002t0026g0013 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1117-1062T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846430 | |||||||
chr10:20846455 | T | C | 19 | a0001c0001t0017g0286 a0002c0002t0001g0010 a0002c0002t0004g0007 others(16): Show |
20 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1117-1087A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846455 | |||||||
chr10:20846501 | A | G | 2 | a0001c0003t0001g0021 a0001c0003t0001g0123 |
2 | HG01975.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1117-1133T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846501 | |||||||
chr10:20846626 | T | C | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1117-1258A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846626 | |||||||
chr10:20846677 | G | A | 12 | a0001c0001t0015g0306 a0001c0001t0017g0303 a0001c0001t0040g0311 others(9): Show |
12 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1117-1309C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846677 | |||||||
chr10:20846687 | G | C | 82 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(79): Show |
85 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1117-1319C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846687 | |||||||
chr10:20846729 | G | A | 1 | a0002c0002t0003g0033 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1117-1361C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846729 | |||||||
chr10:20846849 | G | GA | 11 | a0001c0001t0001g0014 a0001c0001t0002g0266 a0001c0001t0005g0180 others(8): Show |
11 | HG00621.hp2 HG02135.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.1117-1482dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20846849 | |||||||
chr10:20847238 | T | C | 12 | a0001c0001t0015g0306 a0001c0001t0017g0303 a0001c0001t0040g0311 others(9): Show |
12 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1117-1870A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20847238 | |||||||
chr10:20847322 | A | G | 2 | a0001c0001t0001g0325 a0001c0001t0024g0324 |
2 | NA18989.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1117-1954T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20847322 | |||||||
chr10:20847347 | G | A | 1 | a0001c0001t0017g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1117-1979C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20847347 | |||||||
chr10:20847352 | G | A | 1 | a0001c0001t0015g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1117-1984C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20847352 | |||||||
chr10:20847389 | G | C | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1117-2021C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20847389 | |||||||
chr10:20847515 | G | A | 80 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(77): Show |
83 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1117-2147C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20847515 | |||||||
chr10:20847604 | G | A | 2 | a0001c0001t0002g0130 a0001c0013t0001g0163 |
2 | NA18967.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1117-2236C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20847604 | |||||||
chr10:20847710 | G | A | 6 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1117-2342C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20847710 | |||||||
chr10:20847723 | G | A | 10 | a0001c0001t0015g0306 a0001c0001t0040g0311 a0001c0006t0008g0302 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-2355C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20847723 | |||||||
chr10:20847928 | C | T | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1116+2467G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20847928 | |||||||
chr10:20848184 | G | T | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116+2211C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848184 | |||||||
chr10:20848265 | G | A | 40 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(37): Show |
40 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.1116+2130C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848265 | |||||||
chr10:20848424 | C | T | 1 | a0001c0001t0002g0267 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1116+1971G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848424 | |||||||
chr10:20848510 | C | T | 1 | a0002c0002t0011g0183 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1116+1885G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848510 | |||||||
chr10:20848511 | G | A | 1 | a0002c0002t0011g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1116+1884C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848511 | |||||||
chr10:20848541 | G | A | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1116+1854C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848541 | |||||||
chr10:20848543 | G | T | 1 | a0002c0002t0004g0259 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1116+1852C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848543 | |||||||
chr10:20848621 | G | GAACT | 40 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(37): Show |
40 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.1116+1770_1116+177 others(8): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848621 | |||||||
chr10:20848817 | A | G | 205 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0204 others(202): Show |
211 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1116+1578T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848817 | |||||||
chr10:20848846 | T | G | 1 | a0001c0001t0013g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1116+1549A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848846 | |||||||
chr10:20848891 | A | G | 169 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(166): Show |
174 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.1116+1504T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848891 | |||||||
chr10:20848972 | T | C | 82 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(79): Show |
85 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1116+1423A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20848972 | |||||||
chr10:20849005 | G | T | 1 | a0002c0002t0003g0022 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1116+1390C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849005 | |||||||
chr10:20849104 | A | G | 1 | a0001c0001t0017g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1116+1291T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849104 | |||||||
chr10:20849107 | A | G | 40 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(37): Show |
40 | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.1116+1288T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849107 | |||||||
chr10:20849160 | G | A | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1116+1235C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849160 | |||||||
chr10:20849252 | G | C | 6 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1116+1143C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849252 | |||||||
chr10:20849439 | G | C | 1 | a0002c0002t0011g0284 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1116+956C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849439 | |||||||
chr10:20849645 | G | A | 167 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(164): Show |
172 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.1116+750C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849645 | |||||||
chr10:20849666 | T | C | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116+729A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849666 | |||||||
chr10:20849696 | A | G | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1116+699T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849696 | |||||||
chr10:20849758 | G | T | 1 | a0001c0003t0001g0077 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1116+637C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849758 | |||||||
chr10:20849824 | C | T | 1 | a0001c0001t0002g0216 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1116+571G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849824 | |||||||
chr10:20849847 | T | C | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116+548A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20849847 | |||||||
chr10:20850118 | G | C | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116+277C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20850118 | |||||||
chr10:20850136 | T | C | 1 | a0001c0001t0005g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1116+259A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20850136 | |||||||
chr10:20850200 | G | C | 1 | a0001c0001t0002g0019 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1116+195C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20850200 | |||||||
chr10:20850323 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0002g0235 |
2 | HG01257.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1116+72G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 11/27 | chr10 | 20850323 | |||||||
chr10:20850599 | G | A | 12 | a0001c0001t0007g0176 a0001c0001t0017g0278 a0001c0001t0018g0289 others(9): Show |
12 | HG02055.hp2 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1009-97C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20850599 | |||||||
chr10:20850754 | A | T | 81 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(78): Show |
84 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1009-252T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20850754 | |||||||
chr10:20850983 | T | C | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1009-481A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20850983 | |||||||
chr10:20851073 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1009-571A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851073 | |||||||
chr10:20851104 | G | A | 2 | a0001c0001t0021g0100 a0001c0001t0021g0136 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1009-602C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851104 | |||||||
chr10:20851116 | G | C | 6 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1009-614C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851116 | |||||||
chr10:20851117 | A | C | 3 | a0001c0001t0009g0040 a0001c0001t0009g0067 a0001c0001t0009g0076 |
3 | NA18950.hp1 NA18987.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1009-615T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851117 | |||||||
chr10:20851119 | T | C | 1 | a0004c0005t0001g0092 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1009-617A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851119 | |||||||
chr10:20851163 | T | A | 1 | a0001c0001t0015g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1009-661A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851163 | |||||||
chr10:20851326 | A | C | 296 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(293): Show |
304 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.1009-824T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851326 | |||||||
chr10:20851405 | T | C | 1 | a0002c0002t0034g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1009-903A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851405 | |||||||
chr10:20851484 | T | C | 1 | a0004c0005t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1009-982A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851484 | |||||||
chr10:20851497 | C | T | 17 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0018g0289 others(14): Show |
18 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.1009-995G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851497 | |||||||
chr10:20851547 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1008+998C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851547 | |||||||
chr10:20851603 | G | A | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008+942C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851603 | |||||||
chr10:20851619 | C | CA | 24 | a0001c0001t0009g0093 a0001c0001t0013g0197 a0001c0001t0018g0291 others(21): Show |
25 | HG00558.hp2 HG00621.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1008+925dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851619 | |||||||
chr10:20851619 | C | CAAA | 15 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(12): Show |
16 | HG01069.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1008+923_1008+925d others(5): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851619 | |||||||
chr10:20851663 | T | C | 1 | a0014c0017t0031g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1008+882A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851663 | |||||||
chr10:20851677 | C | T | 1 | a0001c0006t0008g0302 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1008+868G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851677 | |||||||
chr10:20851804 | T | C | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008+741A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851804 | |||||||
chr10:20851839 | T | A | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008+706A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851839 | |||||||
chr10:20851865 | C | T | 2 | a0002c0002t0004g0007 a0002c0002t0004g0285 |
3 | HG02723.hp1 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1008+680G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851865 | |||||||
chr10:20851895 | G | T | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008+650C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851895 | |||||||
chr10:20851947 | G | T | 1 | a0001c0003t0001g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1008+598C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851947 | |||||||
chr10:20851970 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1008+575T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851970 | |||||||
chr10:20851988 | C | CT | 299 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(296): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1008+556dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20851988 | |||||||
chr10:20852054 | A | T | 274 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(271): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1008+491T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20852054 | |||||||
chr10:20852087 | T | A | 1 | a0001c0001t0004g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1008+458A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20852087 | |||||||
chr10:20852312 | C | T | 8 | a0002c0002t0004g0219 a0002c0002t0004g0258 a0002c0002t0004g0259 others(5): Show |
8 | HG02451.hp2 HG02630.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1008+233G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20852312 | |||||||
chr10:20852469 | G | A | 1 | a0012c0014t0001g0170 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1008+76C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20852469 | |||||||
chr10:20852477 | G | A | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008+68C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20852477 | |||||||
chr10:20852511 | AG | A | 81 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(78): Show |
85 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1008+33delC | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20852511 | |||||||
chr10:20852527 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008+18C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20852527 | |||||||
chr10:20852540 | T | C | 310 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(307): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
splice_region_variant&intron_variant | LOW | c.1008+5A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20852540 | |||||||
chr10:20852541 | G | A | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.1008+4C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 10/27 | chr10 | 20852541 | |||||||
chr10:20852923 | C | G | 298 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(295): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.904-274G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20852923 | |||||||
chr10:20853075 | A | C | 1 | a0008c0010t0006g0004 | 2 | NA18956.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.904-426T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20853075 | |||||||
chr10:20853151 | G | A | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-502C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20853151 | |||||||
chr10:20853415 | C | T | 10 | a0001c0001t0007g0023 a0001c0001t0007g0059 a0001c0001t0007g0084 others(7): Show |
10 | HG00642.hp2 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.904-766G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20853415 | |||||||
chr10:20853630 | A | G | 4 | a0001c0001t0007g0052 a0001c0001t0007g0087 a0001c0001t0007g0101 others(1): Show |
4 | HG01192.hp1 HG02280.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-981T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20853630 | |||||||
chr10:20853631 | TA | T | 4 | a0001c0001t0007g0052 a0001c0001t0007g0087 a0001c0001t0007g0101 others(1): Show |
4 | HG01192.hp1 HG02280.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-983delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20853631 | |||||||
chr10:20853913 | C | A | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-1264G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20853913 | |||||||
chr10:20854148 | C | A | 1 | a0001c0001t0001g0312 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.904-1499G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854148 | |||||||
chr10:20854188 | T | C | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-1539A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854188 | |||||||
chr10:20854201 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-1552C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854201 | |||||||
chr10:20854206 | T | TG | 4 | a0001c0001t0015g0117 a0001c0006t0010g0158 a0002c0002t0003g0105 others(1): Show |
4 | HG01175.hp1 HG01993.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.904-1558dupC | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854206 | |||||||
chr10:20854539 | A | T | 309 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(306): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.904-1890T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854539 | |||||||
chr10:20854554 | T | C | 1 | a0001c0001t0002g0254 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.904-1905A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854554 | |||||||
chr10:20854561 | C | CT | 72 | a0001c0001t0001g0014 a0001c0001t0001g0282 a0001c0001t0001g0283 others(69): Show |
73 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.904-1913dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854561 | |||||||
chr10:20854561 | C | CTT | 11 | a0001c0001t0004g0179 a0001c0001t0005g0195 a0001c0001t0013g0186 others(8): Show |
11 | HG00621.hp1 HG01175.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.904-1914_904-1913d others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854561 | |||||||
chr10:20854561 | CT | C | 14 | a0001c0001t0017g0303 a0001c0006t0008g0302 a0002c0002t0003g0293 others(11): Show |
15 | HG01884.hp2 HG02015.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.904-1913delA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854561 | |||||||
chr10:20854596 | G | T | 1 | a0001c0001t0002g0019 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.904-1947C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854596 | |||||||
chr10:20854636 | C | T | 1 | a0001c0001t0016g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.904-1987G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854636 | |||||||
chr10:20854655 | C | T | 1 | a0001c0006t0038g0124 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.904-2006G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854655 | |||||||
chr10:20854776 | G | A | 1 | a0002c0002t0034g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.904-2127C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854776 | |||||||
chr10:20854793 | G | A | 5 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-2144C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854793 | |||||||
chr10:20854842 | G | C | 1 | a0001c0001t0016g0132 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.904-2193C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854842 | |||||||
chr10:20854846 | G | A | 1 | a0001c0006t0038g0124 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.904-2197C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854846 | |||||||
chr10:20854952 | C | T | 1 | a0002c0002t0003g0033 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.904-2303G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20854952 | |||||||
chr10:20855070 | G | A | 5 | a0002c0002t0014g0064 a0002c0002t0014g0108 a0002c0002t0014g0109 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-2421C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855070 | |||||||
chr10:20855160 | C | T | 9 | a0001c0001t0007g0176 a0001c0001t0017g0278 a0001c0001t0039g0277 others(6): Show |
9 | HG02630.hp1 HG02818.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.904-2511G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855160 | |||||||
chr10:20855166 | T | G | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-2517A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855166 | |||||||
chr10:20855184 | G | A | 1 | a0001c0001t0007g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.904-2535C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855184 | |||||||
chr10:20855194 | A | C | 1 | a0001c0016t0002g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.904-2545T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855194 | |||||||
chr10:20855227 | T | TA | 18 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0002g0256 others(15): Show |
19 | HG01934.hp1 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.904-2579dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855227 | |||||||
chr10:20855227 | T | TAA | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-2580_904-2579d others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855227 | |||||||
chr10:20855308 | T | A | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.904-2659A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855308 | |||||||
chr10:20855379 | G | A | 2 | a0001c0001t0013g0197 a0001c0001t0030g0198 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.904-2730C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855379 | |||||||
chr10:20855521 | A | AAAC | 3 | a0001c0003t0001g0119 a0001c0016t0002g0104 a0002c0002t0003g0039 |
3 | HG02738.hp1 HG03704.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.903+2718_903+2719i others(5): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855521 | |||||||
chr10:20855522 | A | AAC | 143 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(140): Show |
146 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.903+2717_903+2718i others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855522 | |||||||
chr10:20855525 | C | A | 146 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(143): Show |
149 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.903+2715G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855525 | |||||||
chr10:20855525 | CA | C | 13 | a0001c0001t0002g0211 a0002c0002t0003g0293 a0003c0004t0001g0297 others(10): Show |
14 | HG02015.hp2 HG02735.hp1 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.903+2714delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855525 | |||||||
chr10:20855526 | A | C | 41 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0009g0075 others(38): Show |
42 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.903+2714T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855526 | |||||||
chr10:20855531 | A | C | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.903+2709T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855531 | |||||||
chr10:20855553 | G | A | 159 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(156): Show |
163 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.903+2687C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855553 | |||||||
chr10:20855577 | C | T | 5 | a0004c0005t0001g0112 a0004c0005t0001g0120 a0004c0005t0001g0145 others(2): Show |
5 | NA18954.hp1 NA18960.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.903+2663G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855577 | |||||||
chr10:20855745 | T | C | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.903+2495A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855745 | |||||||
chr10:20855793 | G | A | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+2447C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855793 | |||||||
chr10:20855828 | A | C | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.903+2412T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855828 | |||||||
chr10:20855857 | G | A | 298 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(295): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.903+2383C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855857 | |||||||
chr10:20855883 | T | A | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.903+2357A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855883 | |||||||
chr10:20855955 | A | T | 1 | a0001c0001t0002g0274 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.903+2285T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20855955 | |||||||
chr10:20856052 | C | T | 38 | a0001c0003t0001g0017 a0001c0003t0001g0042 a0001c0003t0001g0050 others(35): Show |
39 | HG00408.hp2 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.903+2188G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20856052 | |||||||
chr10:20856143 | G | A | 1 | a0002c0002t0003g0036 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.903+2097C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20856143 | |||||||
chr10:20856192 | T | C | 75 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0140 others(72): Show |
76 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.903+2048A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20856192 | |||||||
chr10:20856634 | A | G | 4 | a0001c0001t0018g0289 a0001c0001t0018g0291 a0001c0001t0036g0290 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.903+1606T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20856634 | |||||||
chr10:20856682 | A | G | 3 | a0001c0001t0002g0020 a0001c0006t0008g0175 a0002c0002t0004g0174 |
3 | HG03041.hp1 NA18983.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.903+1558T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20856682 | |||||||
chr10:20856897 | C | T | 144 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(141): Show |
147 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.903+1343G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20856897 | |||||||
chr10:20856975 | C | T | 1 | a0001c0006t0008g0302 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.903+1265G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20856975 | |||||||
chr10:20857026 | A | C | 1 | a0001c0001t0002g0231 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.903+1214T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857026 | |||||||
chr10:20857191 | A | G | 1 | a0001c0001t0017g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.903+1049T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857191 | |||||||
chr10:20857337 | G | A | 18 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0168 others(15): Show |
18 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.903+903C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857337 | |||||||
chr10:20857451 | A | G | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.903+789T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857451 | |||||||
chr10:20857458 | G | T | 3 | a0001c0001t0018g0289 a0001c0001t0018g0291 a0001c0001t0036g0290 |
3 | HG02055.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.903+782C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857458 | |||||||
chr10:20857526 | T | A | 1 | a0002c0002t0035g0188 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.903+714A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857526 | |||||||
chr10:20857567 | A | T | 1 | a0001c0001t0015g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.903+673T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857567 | |||||||
chr10:20857583 | G | T | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02074.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.903+657C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857583 | |||||||
chr10:20857673 | C | T | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.903+567G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857673 | |||||||
chr10:20857775 | C | T | 9 | a0001c0001t0005g0180 a0001c0001t0005g0182 a0001c0001t0005g0191 others(6): Show |
9 | NA18953.hp2 NA18964.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.903+465G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857775 | |||||||
chr10:20857836 | C | T | 7 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0006g0008 others(4): Show |
8 | NA18947.hp2 NA18966.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.903+404G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857836 | |||||||
chr10:20857861 | A | G | 1 | a0002c0002t0004g0258 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.903+379T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857861 | |||||||
chr10:20857980 | G | A | 3 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 |
3 | HG02145.hp2 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.903+260C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20857980 | |||||||
chr10:20858092 | C | G | 1 | a0002c0002t0035g0188 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.903+148G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20858092 | |||||||
chr10:20858214 | C | T | 2 | a0001c0006t0008g0175 a0002c0002t0004g0174 |
2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.903+26G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20858214 | |||||||
chr10:20858215 | G | A | 32 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0009g0040 others(29): Show |
33 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.903+25C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 9/27 | chr10 | 20858215 | |||||||
chr10:20858418 | A | G | 1 | a0001c0001t0002g0273 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.799-74T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20858418 | |||||||
chr10:20858441 | T | A | 173 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(170): Show |
178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.799-97A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20858441 | |||||||
chr10:20858489 | G | A | 76 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(73): Show |
79 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.799-145C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20858489 | |||||||
chr10:20858568 | A | G | 1 | a0001c0001t0030g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.799-224T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20858568 | |||||||
chr10:20858591 | T | C | 189 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(186): Show |
194 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.799-247A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20858591 | |||||||
chr10:20858596 | T | C | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.799-252A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20858596 | |||||||
chr10:20858665 | A | G | 1 | a0004c0005t0001g0156 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.799-321T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20858665 | |||||||
chr10:20858682 | A | C | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.799-338T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20858682 | |||||||
chr10:20858683 | T | C | 10 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0017g0286 others(7): Show |
11 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.799-339A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20858683 | |||||||
chr10:20858730 | C | A | 2 | a0001c0001t0007g0052 a0001c0001t0007g0087 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.799-386G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20858730 | |||||||
chr10:20858829 | T | C | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.799-485A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20858829 | |||||||
chr10:20859037 | C | G | 1 | a0001c0001t0002g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.798+676G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859037 | |||||||
chr10:20859044 | A | G | 6 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.798+669T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859044 | |||||||
chr10:20859062 | G | A | 1 | a0002c0002t0028g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.798+651C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859062 | |||||||
chr10:20859065 | C | G | 1 | a0002c0002t0034g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.798+648G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859065 | |||||||
chr10:20859077 | A | T | 4 | a0001c0001t0017g0278 a0001c0001t0039g0277 a0001c0006t0008g0175 others(1): Show |
4 | HG02976.hp1 HG03041.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+636T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859077 | |||||||
chr10:20859141 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+572C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859141 | |||||||
chr10:20859158 | C | G | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+555G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859158 | |||||||
chr10:20859266 | T | A | 162 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(159): Show |
166 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.798+447A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859266 | |||||||
chr10:20859301 | A | G | 1 | a0001c0006t0008g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.798+412T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859301 | |||||||
chr10:20859476 | C | A | 4 | a0001c0001t0017g0278 a0001c0001t0039g0277 a0001c0006t0008g0175 others(1): Show |
4 | HG02976.hp1 HG03041.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+237G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859476 | |||||||
chr10:20859624 | C | A | 4 | a0001c0001t0018g0289 a0001c0001t0018g0291 a0001c0001t0036g0290 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+89G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859624 | |||||||
chr10:20859650 | C | T | 1 | a0001c0001t0002g0268 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.798+63G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859650 | |||||||
chr10:20859655 | C | A | 150 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(147): Show |
154 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.798+58G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 8/27 | chr10 | 20859655 | |||||||
chr10:20859857 | T | A | 1 | a0006c0008t0008g0309 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.685-31A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20859857 | |||||||
chr10:20859953 | G | A | 1 | a0001c0001t0029g0279 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.685-127C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20859953 | |||||||
chr10:20860086 | C | G | 179 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0204 others(176): Show |
185 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.685-260G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860086 | |||||||
chr10:20860131 | A | T | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.685-305T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860131 | |||||||
chr10:20860248 | C | T | 2 | a0001c0001t0013g0197 a0001c0006t0010g0166 |
2 | HG02976.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.685-422G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860248 | |||||||
chr10:20860499 | A | G | 3 | a0002c0002t0003g0105 a0002c0002t0003g0106 a0002c0002t0003g0107 |
3 | NA18952.hp1 NA18974.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.685-673T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860499 | |||||||
chr10:20860523 | A | C | 1 | a0001c0001t0002g0269 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.685-697T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860523 | |||||||
chr10:20860561 | C | CA | 58 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0002g0210 others(55): Show |
59 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.685-736dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860561 | |||||||
chr10:20860561 | C | CAA | 61 | a0001c0001t0001g0014 a0001c0001t0001g0116 a0001c0001t0001g0129 others(58): Show |
63 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.685-737_685-736dup others(2): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860561 | |||||||
chr10:20860561 | C | CAAA | 45 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0168 others(42): Show |
45 | HG00408.hp2 HG00673.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.685-738_685-736dup others(3): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860561 | |||||||
chr10:20860561 | C | CAAAA | 16 | a0001c0001t0001g0127 a0001c0001t0001g0140 a0001c0001t0002g0153 others(13): Show |
16 | HG00140.hp2 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.685-739_685-736dup others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860561 | |||||||
chr10:20860561 | CAAAAAG | C | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.685-741_685-736del others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860561 | |||||||
chr10:20860561 | CAAAAAGA others(3): Show |
C | 6 | a0001c0003t0001g0042 a0001c0003t0001g0050 a0001c0003t0001g0094 others(3): Show |
6 | NA18612.hp2 NA18747.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.685-745_685-736del others(10): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860561 | |||||||
chr10:20860561 | CAAAAAGA others(4): Show |
C | 1 | a0001c0001t0002g0225 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.685-746_685-736del others(11): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860561 | |||||||
chr10:20860564 | AAAG | A | 9 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0017g0286 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-741_685-739del others(3): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860564 | |||||||
chr10:20860566 | AG | A | 14 | a0001c0001t0001g0237 a0001c0001t0017g0278 a0001c0001t0017g0303 others(11): Show |
14 | HG01261.hp1 HG01515.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.685-741delC | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860566 | |||||||
chr10:20860567 | G | A | 253 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(250): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.685-741C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860567 | |||||||
chr10:20860616 | T | C | 2 | a0002c0002t0003g0063 a0002c0002t0003g0111 |
2 | NA18747.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.685-790A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860616 | |||||||
chr10:20860836 | C | A | 1 | a0001c0001t0015g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.685-1010G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860836 | |||||||
chr10:20860906 | G | A | 1 | a0013c0021t0043g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.685-1080C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860906 | |||||||
chr10:20860925 | A | G | 9 | a0001c0001t0017g0286 a0001c0001t0018g0289 a0001c0001t0018g0291 others(6): Show |
10 | HG02055.hp2 HG02572.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.685-1099T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860925 | |||||||
chr10:20860982 | A | G | 300 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(297): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.685-1156T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860982 | |||||||
chr10:20860999 | C | G | 10 | a0001c0001t0007g0023 a0001c0001t0007g0059 a0001c0001t0007g0084 others(7): Show |
10 | HG00642.hp2 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-1173G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20860999 | |||||||
chr10:20861027 | T | A | 28 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(25): Show |
28 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.685-1201A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861027 | |||||||
chr10:20861054 | A | C | 2 | a0001c0001t0016g0155 a0011c0018t0001g0154 |
2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.685-1228T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861054 | |||||||
chr10:20861060 | C | CT | 28 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(25): Show |
28 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.685-1235dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861060 | |||||||
chr10:20861142 | G | C | 1 | a0001c0013t0001g0163 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.685-1316C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861142 | |||||||
chr10:20861146 | G | A | 1 | a0001c0013t0001g0163 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.685-1320C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861146 | |||||||
chr10:20861148 | G | C | 1 | a0001c0013t0001g0163 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.685-1322C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861148 | |||||||
chr10:20861151 | A | T | 1 | a0001c0013t0001g0163 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.685-1325T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861151 | |||||||
chr10:20861152 | C | G | 1 | a0001c0013t0001g0163 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.685-1326G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861152 | |||||||
chr10:20861153 | A | T | 1 | a0001c0013t0001g0163 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.685-1327T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861153 | |||||||
chr10:20861154 | A | T | 1 | a0001c0013t0001g0163 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.685-1328T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861154 | |||||||
chr10:20861204 | G | T | 1 | a0001c0001t0007g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.685-1378C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861204 | |||||||
chr10:20861279 | G | T | 37 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0009g0040 others(34): Show |
38 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.685-1453C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861279 | |||||||
chr10:20861332 | C | T | 1 | a0002c0002t0004g0287 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.685-1506G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861332 | |||||||
chr10:20861469 | G | A | 248 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(245): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.685-1643C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861469 | |||||||
chr10:20861471 | G | A | 1 | a0002c0002t0014g0027 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.685-1645C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861471 | |||||||
chr10:20861493 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.685-1667G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861493 | |||||||
chr10:20861605 | G | C | 11 | a0001c0001t0015g0306 a0001c0001t0040g0311 a0001c0006t0008g0281 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-1779C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861605 | |||||||
chr10:20861814 | A | T | 4 | a0001c0001t0007g0052 a0001c0001t0007g0087 a0001c0001t0007g0101 others(1): Show |
4 | HG01192.hp1 HG02280.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-1988T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861814 | |||||||
chr10:20861820 | T | C | 9 | a0001c0001t0007g0176 a0001c0001t0017g0278 a0001c0001t0039g0277 others(6): Show |
9 | HG02630.hp1 HG02818.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-1994A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861820 | |||||||
chr10:20861854 | G | A | 145 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(142): Show |
148 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.685-2028C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861854 | |||||||
chr10:20861984 | T | C | 272 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(269): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.685-2158A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20861984 | |||||||
chr10:20862116 | T | A | 1 | a0010c0020t0027g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.685-2290A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862116 | |||||||
chr10:20862131 | C | T | 3 | a0003c0004t0002g0015 a0003c0004t0002g0057 a0003c0004t0002g0102 |
3 | HG01192.hp2 HG02273.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.685-2305G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862131 | |||||||
chr10:20862159 | C | T | 271 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(268): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.685-2333G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862159 | |||||||
chr10:20862299 | A | G | 9 | a0001c0001t0005g0180 a0001c0001t0005g0182 a0001c0001t0005g0191 others(6): Show |
9 | NA18953.hp2 NA18964.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-2473T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862299 | |||||||
chr10:20862366 | T | C | 5 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-2540A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862366 | |||||||
chr10:20862496 | C | G | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-2670G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862496 | |||||||
chr10:20862517 | G | A | 77 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(74): Show |
80 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.685-2691C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862517 | |||||||
chr10:20862567 | T | A | 4 | a0001c0001t0017g0278 a0001c0001t0039g0277 a0001c0006t0008g0175 others(1): Show |
4 | HG02976.hp1 HG03041.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-2741A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862567 | |||||||
chr10:20862673 | T | C | 1 | a0002c0002t0034g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.685-2847A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862673 | |||||||
chr10:20862756 | A | C | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.685-2930T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862756 | |||||||
chr10:20862862 | C | T | 77 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(74): Show |
80 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.685-3036G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862862 | |||||||
chr10:20862874 | A | AT | 6 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.685-3049dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862874 | |||||||
chr10:20862917 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.685-3091C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862917 | |||||||
chr10:20862951 | T | C | 1 | a0001c0001t0005g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.685-3125A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20862951 | |||||||
chr10:20863101 | G | A | 77 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(74): Show |
80 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.685-3275C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20863101 | |||||||
chr10:20863292 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.685-3466C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20863292 | |||||||
chr10:20863345 | C | T | 3 | a0003c0004t0006g0292 a0003c0004t0006g0294 a0003c0004t0006g0295 |
3 | NA18970.hp2 NA19003.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.685-3519G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20863345 | |||||||
chr10:20863608 | C | T | 77 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(74): Show |
80 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.685-3782G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20863608 | |||||||
chr10:20863713 | CA | C | 25 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0134 others(22): Show |
25 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.685-3888delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20863713 | |||||||
chr10:20863893 | T | C | 300 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(297): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.685-4067A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20863893 | |||||||
chr10:20863926 | G | A | 1 | a0006c0008t0008g0310 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.685-4100C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20863926 | |||||||
chr10:20864031 | T | C | 1 | a0002c0002t0004g0305 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.685-4205A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20864031 | |||||||
chr10:20864271 | T | C | 4 | a0001c0001t0017g0278 a0001c0001t0039g0277 a0001c0006t0008g0175 others(1): Show |
4 | HG02976.hp1 HG03041.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+4393A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20864271 | |||||||
chr10:20864399 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.684+4265G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20864399 | |||||||
chr10:20864536 | C | T | 2 | a0001c0001t0001g0116 a0001c0003t0001g0002 |
3 | HG00738.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.684+4128G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20864536 | |||||||
chr10:20864778 | C | G | 14 | a0001c0001t0004g0179 a0001c0001t0005g0201 a0001c0001t0005g0202 others(11): Show |
14 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.684+3886G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20864778 | |||||||
chr10:20864893 | C | G | 5 | a0001c0001t0017g0278 a0001c0001t0039g0277 a0001c0006t0008g0175 others(2): Show |
5 | HG02976.hp1 HG03041.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+3771G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20864893 | |||||||
chr10:20864940 | T | C | 2 | a0001c0006t0010g0148 a0001c0006t0010g0149 |
2 | HG01891.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.684+3724A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20864940 | |||||||
chr10:20865223 | C | T | 244 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(241): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.684+3441G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20865223 | |||||||
chr10:20865239 | ATACC | A | 77 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(74): Show |
80 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.684+3421_684+3424d others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20865239 | |||||||
chr10:20865342 | G | A | 299 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(296): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.684+3322C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20865342 | |||||||
chr10:20865365 | C | T | 9 | a0001c0001t0007g0176 a0001c0001t0017g0278 a0001c0001t0039g0277 others(6): Show |
9 | HG02630.hp1 HG02818.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.684+3299G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20865365 | |||||||
chr10:20865518 | C | T | 2 | a0001c0003t0001g0017 a0012c0014t0001g0170 |
2 | HG01361.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.684+3146G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20865518 | |||||||
chr10:20865638 | C | T | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.684+3026G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20865638 | |||||||
chr10:20865688 | C | T | 1 | a0004c0005t0002g0135 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.684+2976G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20865688 | |||||||
chr10:20865811 | G | T | 78 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(75): Show |
81 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.684+2853C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20865811 | |||||||
chr10:20866381 | T | C | 2 | a0001c0001t0016g0155 a0011c0018t0001g0154 |
2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.684+2283A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20866381 | |||||||
chr10:20866421 | T | C | 2 | a0003c0004t0003g0006 a0003c0004t0003g0255 |
3 | HG02132.hp1 NA18941.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.684+2243A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20866421 | |||||||
chr10:20866559 | T | C | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.684+2105A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20866559 | |||||||
chr10:20866568 | G | A | 1 | a0001c0006t0010g0158 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.684+2096C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20866568 | |||||||
chr10:20866707 | G | A | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.684+1957C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20866707 | |||||||
chr10:20866876 | C | T | 1 | a0001c0006t0008g0302 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.684+1788G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20866876 | |||||||
chr10:20867036 | G | A | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.684+1628C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20867036 | |||||||
chr10:20867248 | G | A | 39 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(36): Show |
40 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.684+1416C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20867248 | |||||||
chr10:20867273 | A | T | 4 | a0001c0001t0017g0278 a0001c0001t0039g0277 a0001c0006t0008g0175 others(1): Show |
4 | HG02976.hp1 HG03041.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+1391T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20867273 | |||||||
chr10:20867318 | C | T | 145 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(142): Show |
148 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.684+1346G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20867318 | |||||||
chr10:20867634 | T | C | 1 | a0001c0001t0005g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.684+1030A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20867634 | |||||||
chr10:20867746 | G | A | 1 | a0002c0002t0003g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.684+918C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20867746 | |||||||
chr10:20867756 | G | A | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.684+908C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20867756 | |||||||
chr10:20867788 | T | C | 300 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(297): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.684+876A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20867788 | |||||||
chr10:20868050 | A | AT | 6 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.684+613dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868050 | |||||||
chr10:20868052 | T | TA | 172 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0034 others(169): Show |
177 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.684+611dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868052 | |||||||
chr10:20868052 | T | TAA | 10 | a0001c0001t0001g0014 a0001c0001t0001g0282 a0001c0001t0001g0283 others(7): Show |
10 | HG00621.hp2 HG01934.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.684+610_684+611dup others(2): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868052 | |||||||
chr10:20868052 | T | TAAAAA | 26 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(23): Show |
26 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.684+607_684+611dup others(5): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868052 | |||||||
chr10:20868052 | TA | T | 13 | a0001c0001t0001g0127 a0001c0003t0001g0119 a0002c0002t0003g0293 others(10): Show |
14 | HG01168.hp1 HG02015.hp2 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.684+611delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868052 | |||||||
chr10:20868054 | A | G | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.684+610T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868054 | |||||||
chr10:20868068 | C | T | 1 | a0002c0002t0003g0022 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.684+596G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868068 | |||||||
chr10:20868098 | C | T | 1 | a0005c0007t0001g0012 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.684+566G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868098 | |||||||
chr10:20868099 | G | A | 19 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0168 others(16): Show |
19 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+565C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868099 | |||||||
chr10:20868310 | C | CTG | 19 | a0001c0001t0002g0019 a0001c0001t0005g0048 a0001c0001t0005g0096 others(16): Show |
19 | HG01891.hp2 HG02015.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+352_684+353dup others(2): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868310 | |||||||
chr10:20868310 | C | CTGTG | 5 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+350_684+353dup others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868310 | |||||||
chr10:20868310 | C | CTGTGTG | 9 | a0003c0004t0001g0297 a0003c0004t0001g0298 a0003c0004t0006g0008 others(6): Show |
10 | NA18947.hp2 NA18952.hp2 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.684+348_684+353dup others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868310 | |||||||
chr10:20868310 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0029g0279 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.684+344_684+353dup others(10): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868310 | |||||||
chr10:20868310 | C | CTGTGTGT others(5): Show |
3 | a0001c0001t0001g0283 a0001c0001t0018g0280 a0002c0002t0011g0288 |
3 | HG02280.hp2 HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.684+342_684+353dup others(12): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868310 | |||||||
chr10:20868310 | C | CTGTGTGT others(7): Show |
1 | a0001c0001t0001g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.684+340_684+353dup others(14): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868310 | |||||||
chr10:20868310 | CTG | C | 223 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(220): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.684+352_684+353del others(2): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868310 | |||||||
chr10:20868563 | T | C | 220 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(217): Show |
225 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.684+101A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 7/27 | chr10 | 20868563 | |||||||
chr10:20868834 | CA | C | 252 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0073 others(249): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.583-70delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 6/27 | chr10 | 20868834 | |||||||
chr10:20868845 | AAAAT | A | 27 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.583-84_583-81delAT others(2): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 6/27 | chr10 | 20868845 | |||||||
chr10:20868848 | AT | A | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.583-84delA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 6/27 | chr10 | 20868848 | |||||||
chr10:20869127 | T | C | 1 | a0001c0003t0001g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.583-362A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 6/27 | chr10 | 20869127 | |||||||
chr10:20869280 | G | A | 24 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0134 others(21): Show |
24 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.582+460C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 6/27 | chr10 | 20869280 | |||||||
chr10:20869287 | T | G | 2 | a0001c0006t0008g0175 a0002c0002t0004g0174 |
2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.582+453A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 6/27 | chr10 | 20869287 | |||||||
chr10:20869435 | A | G | 1 | a0001c0001t0017g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.582+305T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 6/27 | chr10 | 20869435 | |||||||
chr10:20869489 | T | C | 1 | a0001c0001t0045g0142 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.582+251A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 6/27 | chr10 | 20869489 | |||||||
chr10:20869569 | C | A | 7 | a0001c0001t0007g0176 a0001c0001t0018g0280 a0002c0002t0011g0055 others(4): Show |
7 | HG02451.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.582+171G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 6/27 | chr10 | 20869569 | |||||||
chr10:20869998 | T | G | 1 | a0001c0001t0005g0048 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.481-157A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20869998 | |||||||
chr10:20870239 | T | C | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.481-398A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20870239 | |||||||
chr10:20870307 | A | C | 300 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(297): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.481-466T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20870307 | |||||||
chr10:20870325 | C | CA | 109 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0073 others(106): Show |
111 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.481-485dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20870325 | |||||||
chr10:20870325 | C | CAA | 84 | a0001c0001t0001g0034 a0001c0001t0001g0127 a0001c0001t0001g0129 others(81): Show |
86 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.481-486_481-485dup others(2): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20870325 | |||||||
chr10:20870325 | CA | C | 13 | a0001c0001t0002g0226 a0001c0001t0002g0271 a0002c0002t0003g0293 others(10): Show |
14 | HG02015.hp2 HG03491.hp1 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.481-485delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20870325 | |||||||
chr10:20870417 | T | C | 1 | a0010c0020t0027g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.481-576A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20870417 | |||||||
chr10:20870795 | A | G | 55 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0004g0179 others(52): Show |
56 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.481-954T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20870795 | |||||||
chr10:20870871 | A | G | 2 | a0001c0001t0018g0289 a0001c0001t0018g0291 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.481-1030T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20870871 | |||||||
chr10:20870907 | C | T | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.481-1066G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20870907 | |||||||
chr10:20871077 | T | C | 1 | a0001c0006t0008g0302 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.481-1236A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20871077 | |||||||
chr10:20871100 | T | C | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.481-1259A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20871100 | |||||||
chr10:20871508 | C | T | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-1667G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20871508 | |||||||
chr10:20871971 | T | C | 1 | a0001c0001t0030g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.481-2130A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20871971 | |||||||
chr10:20872023 | C | T | 77 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(74): Show |
80 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.481-2182G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20872023 | |||||||
chr10:20872082 | C | T | 1 | a0001c0003t0001g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.481-2241G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20872082 | |||||||
chr10:20872317 | C | T | 6 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-2476G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20872317 | |||||||
chr10:20872490 | T | A | 1 | a0001c0001t0004g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.481-2649A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20872490 | |||||||
chr10:20872499 | A | G | 319 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0031 others(316): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.481-2658T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20872499 | |||||||
chr10:20872559 | C | T | 1 | a0001c0001t0002g0019 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.481-2718G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20872559 | |||||||
chr10:20872746 | G | A | 1 | a0001c0001t0040g0311 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.481-2905C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20872746 | |||||||
chr10:20872748 | G | C | 1 | a0004c0005t0001g0156 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.481-2907C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20872748 | |||||||
chr10:20872872 | C | T | 1 | a0001c0001t0015g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.481-3031G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20872872 | |||||||
chr10:20873072 | T | G | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.481-3231A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20873072 | |||||||
chr10:20873095 | C | A | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.481-3254G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20873095 | |||||||
chr10:20873113 | A | C | 1 | a0001c0001t0002g0225 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.481-3272T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20873113 | |||||||
chr10:20873312 | C | T | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.481-3471G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20873312 | |||||||
chr10:20873598 | T | C | 2 | a0001c0001t0040g0311 a0002c0002t0001g0010 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.481-3757A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20873598 | |||||||
chr10:20873608 | T | C | 1 | a0002c0002t0003g0293 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.481-3767A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20873608 | |||||||
chr10:20873666 | A | C | 6 | a0001c0003t0001g0066 a0001c0003t0001g0078 a0001c0003t0001g0081 others(3): Show |
6 | HG00408.hp2 HG01981.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-3825T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20873666 | |||||||
chr10:20874331 | A | G | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.481-4490T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20874331 | |||||||
chr10:20874341 | T | C | 27 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.481-4500A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20874341 | |||||||
chr10:20874592 | G | C | 1 | a0001c0001t0033g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.481-4751C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20874592 | |||||||
chr10:20874653 | A | C | 7 | a0001c0001t0007g0176 a0001c0001t0018g0280 a0002c0002t0011g0055 others(4): Show |
7 | HG02451.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-4812T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20874653 | |||||||
chr10:20874741 | A | AT | 12 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(9): Show |
13 | HG00544.hp1 HG02015.hp2 NA18947.hp2 others(10): Show |
intron_variant | MODIFIER | c.481-4901dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20874741 | |||||||
chr10:20874755 | T | G | 5 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-4914A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20874755 | |||||||
chr10:20874758 | A | G | 299 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(296): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.481-4917T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20874758 | |||||||
chr10:20874906 | G | GT | 8 | a0002c0002t0004g0219 a0002c0002t0004g0258 a0002c0002t0004g0259 others(5): Show |
8 | HG02451.hp2 HG02630.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-5066dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20874906 | |||||||
chr10:20874940 | T | C | 86 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(83): Show |
89 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.481-5099A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20874940 | |||||||
chr10:20874988 | C | T | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.481-5147G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20874988 | |||||||
chr10:20875075 | G | A | 1 | a0001c0001t0002g0218 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.481-5234C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875075 | |||||||
chr10:20875083 | C | T | 5 | a0002c0002t0014g0027 a0002c0002t0014g0064 a0002c0002t0014g0108 others(2): Show |
5 | HG01070.hp1 HG01071.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-5242G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875083 | |||||||
chr10:20875164 | A | G | 2 | a0005c0007t0001g0069 a0005c0007t0001g0141 |
2 | HG01081.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.481-5323T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875164 | |||||||
chr10:20875196 | T | G | 1 | a0002c0002t0034g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.481-5355A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875196 | |||||||
chr10:20875208 | A | C | 1 | a0006c0008t0008g0307 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.481-5367T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875208 | |||||||
chr10:20875223 | G | T | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.481-5382C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875223 | |||||||
chr10:20875276 | A | T | 1 | a0001c0001t0040g0311 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.481-5435T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875276 | |||||||
chr10:20875428 | A | G | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+5366T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875428 | |||||||
chr10:20875456 | T | G | 5 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+5338A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875456 | |||||||
chr10:20875521 | G | A | 1 | a0001c0001t0015g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.480+5273C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875521 | |||||||
chr10:20875718 | T | TAGCCAGC others(17): Show |
1 | a0001c0001t0017g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.480+5052_480+5075d others(26): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875718 | |||||||
chr10:20875818 | G | T | 300 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(297): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.480+4976C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875818 | |||||||
chr10:20875908 | T | C | 1 | a0001c0001t0003g0314 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.480+4886A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875908 | |||||||
chr10:20875980 | A | G | 6 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0054 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+4814T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20875980 | |||||||
chr10:20876041 | G | T | 1 | a0005c0007t0012g0044 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.480+4753C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876041 | |||||||
chr10:20876079 | C | G | 1 | a0001c0001t0030g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.480+4715G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876079 | |||||||
chr10:20876194 | C | T | 3 | a0001c0001t0018g0289 a0001c0001t0018g0291 a0001c0001t0036g0290 |
3 | HG02055.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.480+4600G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876194 | |||||||
chr10:20876232 | G | C | 77 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(74): Show |
80 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.480+4562C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876232 | |||||||
chr10:20876401 | T | G | 1 | a0002c0002t0003g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.480+4393A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876401 | |||||||
chr10:20876415 | C | T | 1 | a0002c0002t0011g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.480+4379G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876415 | |||||||
chr10:20876543 | A | G | 1 | a0001c0001t0046g0223 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.480+4251T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876543 | |||||||
chr10:20876612 | G | A | 1 | a0001c0006t0010g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.480+4182C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876612 | |||||||
chr10:20876631 | T | G | 2 | a0001c0001t0002g0257 a0001c0001t0049g0161 |
2 | HG02074.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.480+4163A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876631 | |||||||
chr10:20876643 | C | T | 108 | a0001c0001t0001g0014 a0001c0001t0001g0073 a0001c0001t0001g0074 others(105): Show |
110 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.480+4151G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876643 | |||||||
chr10:20876791 | T | A | 39 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0002g0019 others(36): Show |
40 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.480+4003A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876791 | |||||||
chr10:20876950 | C | G | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480+3844G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20876950 | |||||||
chr10:20877029 | T | C | 27 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.480+3765A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877029 | |||||||
chr10:20877140 | C | T | 6 | a0001c0001t0001g0140 a0001c0006t0010g0080 a0001c0006t0010g0118 others(3): Show |
6 | HG01496.hp2 HG01928.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+3654G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877140 | |||||||
chr10:20877181 | G | C | 2 | a0001c0001t0020g0199 a0001c0001t0020g0200 |
2 | NA18953.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.480+3613C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877181 | |||||||
chr10:20877281 | T | C | 3 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 |
3 | HG02145.hp2 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.480+3513A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877281 | |||||||
chr10:20877297 | T | A | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480+3497A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877297 | |||||||
chr10:20877323 | C | T | 5 | a0001c0001t0017g0278 a0001c0001t0039g0277 a0001c0006t0008g0175 others(2): Show |
5 | HG02896.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+3471G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877323 | |||||||
chr10:20877387 | C | T | 5 | a0001c0001t0017g0278 a0001c0001t0039g0277 a0001c0006t0008g0175 others(2): Show |
5 | HG02896.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+3407G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877387 | |||||||
chr10:20877481 | G | A | 311 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(308): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.480+3313C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877481 | |||||||
chr10:20877485 | T | A | 1 | a0001c0006t0038g0124 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.480+3309A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877485 | |||||||
chr10:20877486 | C | A | 1 | a0001c0001t0013g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.480+3308G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877486 | |||||||
chr10:20877498 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.480+3296A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877498 | |||||||
chr10:20877591 | A | C | 1 | a0004c0005t0001g0133 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.480+3203T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877591 | |||||||
chr10:20877613 | G | A | 1 | a0001c0001t0005g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.480+3181C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877613 | |||||||
chr10:20877725 | C | T | 146 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(143): Show |
149 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.480+3069G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20877725 | |||||||
chr10:20878081 | T | A | 1 | a0004c0005t0001g0092 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.480+2713A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878081 | |||||||
chr10:20878082 | C | A | 24 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0134 others(21): Show |
24 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.480+2712G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878082 | |||||||
chr10:20878085 | T | C | 3 | a0001c0001t0018g0289 a0001c0001t0018g0291 a0001c0001t0036g0290 |
3 | HG02055.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.480+2709A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878085 | |||||||
chr10:20878240 | A | G | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.480+2554T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878240 | |||||||
chr10:20878444 | A | G | 30 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(27): Show |
30 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.480+2350T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878444 | |||||||
chr10:20878457 | G | T | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.480+2337C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878457 | |||||||
chr10:20878529 | C | T | 1 | a0001c0001t0023g0224 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.480+2265G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878529 | |||||||
chr10:20878549 | T | C | 2 | a0001c0001t0018g0280 a0002c0002t0011g0288 |
2 | HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.480+2245A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878549 | |||||||
chr10:20878787 | A | G | 149 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(146): Show |
152 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.480+2007T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878787 | |||||||
chr10:20878790 | A | C | 1 | a0001c0001t0045g0142 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.480+2004T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878790 | |||||||
chr10:20878939 | T | C | 4 | a0002c0002t0014g0064 a0002c0002t0014g0108 a0002c0002t0014g0109 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+1855A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878939 | |||||||
chr10:20878958 | C | T | 1 | a0004c0005t0001g0011 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.480+1836G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878958 | |||||||
chr10:20878967 | C | T | 1 | a0001c0001t0046g0223 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.480+1827G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20878967 | |||||||
chr10:20879174 | C | G | 27 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.480+1620G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879174 | |||||||
chr10:20879290 | G | A | 4 | a0001c0001t0018g0289 a0001c0001t0018g0291 a0001c0001t0036g0290 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+1504C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879290 | |||||||
chr10:20879309 | G | T | 1 | a0001c0001t0003g0314 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.480+1485C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879309 | |||||||
chr10:20879449 | A | C | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.480+1345T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879449 | |||||||
chr10:20879468 | C | T | 27 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.480+1326G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879468 | |||||||
chr10:20879594 | T | C | 1 | a0001c0001t0018g0289 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.480+1200A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879594 | |||||||
chr10:20879635 | A | G | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+1159T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879635 | |||||||
chr10:20879637 | T | A | 27 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0096 others(24): Show |
27 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.480+1157A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879637 | |||||||
chr10:20879689 | C | A | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.480+1105G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879689 | |||||||
chr10:20879821 | A | G | 1 | a0001c0001t0017g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.480+973T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879821 | |||||||
chr10:20879828 | A | T | 1 | a0005c0007t0001g0012 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.480+966T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879828 | |||||||
chr10:20879992 | G | C | 5 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0285 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+802C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20879992 | |||||||
chr10:20880064 | T | A | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.480+730A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880064 | |||||||
chr10:20880091 | G | A | 8 | a0002c0002t0004g0219 a0002c0002t0004g0258 a0002c0002t0004g0259 others(5): Show |
8 | HG02451.hp2 HG02630.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+703C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880091 | |||||||
chr10:20880102 | C | T | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.480+692G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880102 | |||||||
chr10:20880163 | C | T | 76 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(73): Show |
79 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.480+631G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880163 | |||||||
chr10:20880186 | A | C | 301 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(298): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.480+608T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880186 | |||||||
chr10:20880190 | G | A | 1 | a0001c0001t0009g0093 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.480+604C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880190 | |||||||
chr10:20880216 | G | T | 5 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+578C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880216 | |||||||
chr10:20880229 | T | C | 301 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(298): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.480+565A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880229 | |||||||
chr10:20880242 | T | C | 2 | a0001c0006t0008g0175 a0002c0002t0004g0174 |
2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.480+552A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880242 | |||||||
chr10:20880320 | A | G | 1 | a0002c0002t0026g0013 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.480+474T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880320 | |||||||
chr10:20880330 | A | G | 1 | a0002c0002t0003g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.480+464T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880330 | |||||||
chr10:20880347 | G | A | 1 | a0001c0001t0015g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.480+447C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 5/27 | chr10 | 20880347 | |||||||
chr10:20880994 | T | G | 13 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0116 others(10): Show |
14 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.370-90A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20880994 | |||||||
chr10:20881132 | T | C | 3 | a0001c0001t0005g0096 a0001c0001t0005g0171 a0001c0001t0005g0172 |
3 | HG02145.hp2 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.370-228A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20881132 | |||||||
chr10:20881155 | T | C | 3 | a0001c0001t0002g0220 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02056.hp1 HG02135.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.370-251A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20881155 | |||||||
chr10:20881172 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.370-268C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20881172 | |||||||
chr10:20881455 | A | G | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | HG02074.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.370-551T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20881455 | |||||||
chr10:20881589 | T | C | 1 | a0005c0007t0012g0047 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.370-685A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20881589 | |||||||
chr10:20881646 | A | G | 2 | a0001c0001t0001g0321 a0001c0001t0001g0323 |
2 | HG00544.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.370-742T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20881646 | |||||||
chr10:20881990 | C | T | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.370-1086G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20881990 | |||||||
chr10:20882086 | G | A | 4 | a0001c0003t0001g0042 a0001c0003t0001g0050 a0001c0003t0001g0094 others(1): Show |
4 | NA18612.hp2 NA18966.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-1182C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882086 | |||||||
chr10:20882111 | G | A | 78 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(75): Show |
81 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.370-1207C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882111 | |||||||
chr10:20882169 | A | G | 11 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(8): Show |
11 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-1265T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882169 | |||||||
chr10:20882232 | G | T | 5 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0285 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-1328C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882232 | |||||||
chr10:20882317 | A | G | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.370-1413T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882317 | |||||||
chr10:20882330 | G | A | 5 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0285 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.370-1426C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882330 | |||||||
chr10:20882339 | AAAAGGAA others(11): Show |
A | 22 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(19): Show |
23 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.370-1453_370-1436d others(20): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882339 | |||||||
chr10:20882624 | C | G | 1 | a0001c0016t0002g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.370-1720G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882624 | |||||||
chr10:20882738 | C | CA | 20 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0005g0048 others(17): Show |
20 | HG01891.hp2 HG01975.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.370-1835dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882738 | |||||||
chr10:20882738 | C | CAA | 6 | a0001c0001t0017g0278 a0001c0001t0017g0286 a0001c0001t0039g0277 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.370-1836_370-1835d others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882738 | |||||||
chr10:20882738 | CA | C | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.370-1835delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882738 | |||||||
chr10:20882799 | A | G | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.370-1895T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882799 | |||||||
chr10:20882920 | G | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.370-2016C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882920 | |||||||
chr10:20882925 | G | A | 289 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(286): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.370-2021C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882925 | |||||||
chr10:20882973 | A | G | 1 | a0001c0001t0005g0048 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.370-2069T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882973 | |||||||
chr10:20882987 | C | T | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.370-2083G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20882987 | |||||||
chr10:20883203 | A | G | 4 | a0001c0001t0018g0289 a0001c0001t0018g0291 a0001c0001t0036g0290 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-2299T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20883203 | |||||||
chr10:20883250 | T | G | 3 | a0001c0003t0001g0097 a0001c0003t0001g0125 a0001c0003t0001g0126 |
3 | HG01516.hp2 HG01517.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.370-2346A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20883250 | |||||||
chr10:20883278 | A | G | 22 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(19): Show |
23 | HG00621.hp1 HG01069.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.370-2374T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20883278 | |||||||
chr10:20883542 | G | A | 2 | a0001c0001t0018g0289 a0001c0001t0018g0291 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.370-2638C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20883542 | |||||||
chr10:20883560 | C | G | 2 | a0001c0006t0008g0175 a0002c0002t0004g0174 |
2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.370-2656G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20883560 | |||||||
chr10:20883735 | T | C | 1 | a0002c0002t0003g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.370-2831A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20883735 | |||||||
chr10:20883849 | G | A | 1 | a0001c0001t0002g0268 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.370-2945C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20883849 | |||||||
chr10:20883861 | CACTTTAG others(22): Show |
C | 3 | a0001c0001t0018g0289 a0001c0001t0018g0291 a0001c0001t0036g0290 |
3 | HG02055.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.370-2986_370-2958d others(31): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20883861 | |||||||
chr10:20884091 | G | A | 1 | a0009c0012t0041g0207 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.370-3187C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20884091 | |||||||
chr10:20884253 | T | G | 77 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(74): Show |
80 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.370-3349A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20884253 | |||||||
chr10:20884340 | G | A | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.370-3436C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20884340 | |||||||
chr10:20884375 | C | T | 1 | a0001c0006t0008g0281 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.370-3471G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20884375 | |||||||
chr10:20884462 | T | A | 152 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(149): Show |
155 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.370-3558A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20884462 | |||||||
chr10:20884492 | T | C | 1 | a0003c0004t0006g0301 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.370-3588A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20884492 | |||||||
chr10:20884649 | G | C | 10 | a0001c0001t0015g0306 a0001c0001t0040g0311 a0001c0006t0008g0302 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.369+3448C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20884649 | |||||||
chr10:20884719 | G | C | 1 | a0001c0001t0001g0322 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.369+3378C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20884719 | |||||||
chr10:20884729 | T | C | 1 | a0010c0020t0027g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.369+3368A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20884729 | |||||||
chr10:20884764 | T | C | 293 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(290): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.369+3333A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20884764 | |||||||
chr10:20884961 | T | C | 5 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0285 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+3136A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20884961 | |||||||
chr10:20885068 | A | AAT | 51 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0004g0179 others(48): Show |
52 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.369+3028_369+3029i others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885068 | |||||||
chr10:20885252 | GC | G | 6 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+2844delG | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885252 | |||||||
chr10:20885278 | A | T | 1 | a0007c0009t0003g0029 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.369+2819T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885278 | |||||||
chr10:20885279 | A | G | 6 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+2818T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885279 | |||||||
chr10:20885343 | T | C | 169 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(166): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.369+2754A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885343 | |||||||
chr10:20885361 | G | A | 6 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+2736C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885361 | |||||||
chr10:20885685 | C | T | 1 | a0002c0002t0003g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.369+2412G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885685 | |||||||
chr10:20885696 | T | C | 1 | a0004c0005t0002g0135 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.369+2401A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885696 | |||||||
chr10:20885743 | T | G | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.369+2354A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885743 | |||||||
chr10:20885881 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.369+2216C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885881 | |||||||
chr10:20885895 | T | A | 6 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+2202A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885895 | |||||||
chr10:20885981 | T | G | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.369+2116A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885981 | |||||||
chr10:20885987 | G | C | 1 | a0001c0001t0030g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.369+2110C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20885987 | |||||||
chr10:20886088 | C | T | 35 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0134 others(32): Show |
36 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.369+2009G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20886088 | |||||||
chr10:20886104 | A | G | 78 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(75): Show |
81 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.369+1993T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20886104 | |||||||
chr10:20886145 | A | C | 1 | a0005c0007t0001g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.369+1952T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20886145 | |||||||
chr10:20886187 | AT | A | 5 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+1909delA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20886187 | |||||||
chr10:20886201 | G | T | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+1896C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20886201 | |||||||
chr10:20886248 | C | T | 1 | a0001c0003t0001g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.369+1849G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20886248 | |||||||
chr10:20886249 | G | A | 2 | a0001c0006t0008g0175 a0002c0002t0004g0174 |
2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.369+1848C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20886249 | |||||||
chr10:20886395 | G | A | 1 | a0004c0005t0001g0157 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.369+1702C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20886395 | |||||||
chr10:20886792 | C | G | 1 | a0001c0003t0001g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.369+1305G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20886792 | |||||||
chr10:20886874 | A | C | 77 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(74): Show |
80 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.369+1223T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20886874 | |||||||
chr10:20886876 | G | A | 1 | a0001c0006t0008g0281 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.369+1221C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20886876 | |||||||
chr10:20887009 | T | A | 1 | a0012c0014t0001g0170 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.369+1088A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887009 | |||||||
chr10:20887025 | G | C | 5 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0018g0280 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+1072C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887025 | |||||||
chr10:20887111 | G | C | 1 | a0001c0006t0008g0281 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.369+986C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887111 | |||||||
chr10:20887210 | T | C | 25 | a0001c0001t0001g0139 a0001c0001t0004g0179 a0001c0001t0005g0048 others(22): Show |
25 | HG00642.hp1 HG00733.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.369+887A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887210 | |||||||
chr10:20887213 | T | G | 24 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0134 others(21): Show |
24 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.369+884A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887213 | |||||||
chr10:20887222 | AATGAGTT others(4): Show |
A | 1 | a0001c0001t0002g0273 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.369+864_369+874del others(11): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887222 | |||||||
chr10:20887223 | ATGAGTTT others(3): Show |
A | 76 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(73): Show |
79 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.369+864_369+873del others(10): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887223 | |||||||
chr10:20887411 | C | CT | 34 | a0001c0001t0001g0327 a0001c0001t0002g0213 a0001c0001t0002g0215 others(31): Show |
34 | HG00438.hp1 HG00621.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.369+685dupA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887411 | |||||||
chr10:20887411 | CT | C | 32 | a0001c0001t0001g0140 a0001c0001t0002g0269 a0001c0001t0005g0193 others(29): Show |
34 | HG00738.hp2 HG01361.hp2 HG01978.hp2 others(31): Show |
intron_variant | MODIFIER | c.369+685delA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887411 | |||||||
chr10:20887411 | CTT | C | 129 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(126): Show |
131 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.369+684_369+685del others(2): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887411 | |||||||
chr10:20887411 | CTTT | C | 6 | a0001c0001t0001g0127 a0001c0001t0016g0131 a0001c0001t0016g0132 others(3): Show |
6 | HG01070.hp1 HG01168.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+683_369+685del others(3): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887411 | |||||||
chr10:20887422 | T | A | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.369+675A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887422 | |||||||
chr10:20887492 | C | T | 3 | a0001c0006t0008g0175 a0002c0002t0004g0174 a0013c0021t0043g0196 |
3 | HG02896.hp2 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.369+605G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887492 | |||||||
chr10:20887535 | C | T | 1 | a0004c0005t0001g0011 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.369+562G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887535 | |||||||
chr10:20887578 | G | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.369+519C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887578 | |||||||
chr10:20887622 | G | A | 1 | a0001c0003t0003g0026 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.369+475C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887622 | |||||||
chr10:20887722 | A | T | 1 | a0001c0001t0017g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.369+375T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887722 | |||||||
chr10:20887831 | C | T | 11 | a0001c0001t0007g0176 a0001c0001t0017g0278 a0001c0001t0039g0277 others(8): Show |
11 | HG02630.hp1 HG02818.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.369+266G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887831 | |||||||
chr10:20887990 | T | C | 1 | a0004c0005t0001g0128 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.369+107A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20887990 | |||||||
chr10:20888016 | G | A | 290 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(287): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.369+81C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 4/27 | chr10 | 20888016 | |||||||
chr10:20888214 | G | GA | 29 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0004g0179 others(26): Show |
29 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.259-8dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20888214 | |||||||
chr10:20888227 | GA | G | 167 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(164): Show |
170 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.259-21delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20888227 | |||||||
chr10:20888325 | A | C | 1 | a0002c0002t0003g0293 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.259-118T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20888325 | |||||||
chr10:20888629 | G | T | 1 | a0001c0001t0002g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.259-422C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20888629 | |||||||
chr10:20888730 | T | C | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-523A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20888730 | |||||||
chr10:20888779 | A | T | 4 | a0001c0001t0002g0210 a0003c0004t0006g0208 a0003c0004t0006g0209 others(1): Show |
5 | HG00438.hp2 HG00673.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-572T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20888779 | |||||||
chr10:20888865 | T | C | 212 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(209): Show |
217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.259-658A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20888865 | |||||||
chr10:20889000 | C | A | 1 | a0001c0001t0013g0189 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.259-793G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889000 | |||||||
chr10:20889032 | C | T | 78 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(75): Show |
81 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.258+813G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889032 | |||||||
chr10:20889075 | T | C | 1 | a0013c0021t0043g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.258+770A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889075 | |||||||
chr10:20889128 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0139 |
3 | HG00733.hp1 HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.258+717C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889128 | |||||||
chr10:20889172 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0321 a0001c0001t0001g0322 others(1): Show |
5 | HG00544.hp2 HG02523.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+673C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889172 | |||||||
chr10:20889271 | T | C | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.258+574A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889271 | |||||||
chr10:20889324 | T | C | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+521A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889324 | |||||||
chr10:20889339 | T | C | 28 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0134 others(25): Show |
28 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.258+506A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889339 | |||||||
chr10:20889367 | T | C | 1 | a0001c0001t0007g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258+478A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889367 | |||||||
chr10:20889455 | T | C | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.258+390A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889455 | |||||||
chr10:20889483 | A | G | 2 | a0001c0001t0009g0075 a0001c0001t0009g0076 |
2 | NA18973.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.258+362T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889483 | |||||||
chr10:20889495 | T | C | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+350A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889495 | |||||||
chr10:20889601 | A | G | 30 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0004g0179 others(27): Show |
30 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.258+244T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889601 | |||||||
chr10:20889645 | G | A | 290 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(287): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.258+200C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889645 | |||||||
chr10:20889662 | T | G | 4 | a0001c0001t0018g0289 a0001c0001t0018g0291 a0001c0001t0036g0290 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+183A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 3/27 | chr10 | 20889662 | |||||||
chr10:20889998 | T | A | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-49A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20889998 | |||||||
chr10:20890019 | A | T | 7 | a0001c0001t0013g0185 a0001c0001t0013g0186 a0001c0001t0013g0187 others(4): Show |
7 | HG00642.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-70T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890019 | |||||||
chr10:20890103 | A | G | 4 | a0001c0001t0018g0289 a0001c0001t0018g0291 a0001c0001t0036g0290 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-154T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890103 | |||||||
chr10:20890164 | C | T | 1 | a0001c0001t0017g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.154-215G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890164 | |||||||
chr10:20890231 | A | T | 283 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(280): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.154-282T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890231 | |||||||
chr10:20890266 | T | C | 1 | a0001c0001t0002g0270 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.154-317A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890266 | |||||||
chr10:20890316 | C | T | 15 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0116 others(12): Show |
16 | HG00733.hp1 HG00738.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-367G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890316 | |||||||
chr10:20890399 | G | C | 5 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-450C>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890399 | |||||||
chr10:20890429 | C | T | 5 | a0001c0001t0017g0286 a0002c0002t0004g0007 a0002c0002t0004g0285 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-480G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890429 | |||||||
chr10:20890664 | C | T | 10 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(7): Show |
10 | HG00621.hp1 HG01069.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-715G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890664 | |||||||
chr10:20890752 | C | T | 192 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(189): Show |
196 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.154-803G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890752 | |||||||
chr10:20890828 | T | C | 1 | a0003c0004t0006g0301 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.154-879A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890828 | |||||||
chr10:20890956 | C | T | 2 | a0004c0005t0001g0162 a0004c0005t0002g0164 |
2 | HG02155.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.154-1007G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20890956 | |||||||
chr10:20891067 | T | C | 197 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(194): Show |
201 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.154-1118A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20891067 | |||||||
chr10:20891107 | T | A | 83 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(80): Show |
86 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.154-1158A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20891107 | |||||||
chr10:20891156 | C | T | 25 | a0001c0001t0004g0179 a0001c0001t0005g0048 a0001c0001t0005g0134 others(22): Show |
25 | HG00642.hp1 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.154-1207G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20891156 | |||||||
chr10:20891324 | T | G | 1 | a0001c0001t0002g0271 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.154-1375A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20891324 | |||||||
chr10:20891328 | A | T | 1 | a0001c0001t0001g0206 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.154-1379T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20891328 | |||||||
chr10:20891437 | T | C | 2 | a0001c0001t0001g0325 a0001c0001t0024g0324 |
2 | NA18989.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.154-1488A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20891437 | |||||||
chr10:20891566 | C | A | 1 | a0002c0002t0011g0099 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.154-1617G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20891566 | |||||||
chr10:20891659 | C | G | 2 | a0004c0005t0001g0160 a0004c0005t0002g0135 |
2 | HG02132.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.154-1710G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20891659 | |||||||
chr10:20891690 | T | C | 1 | a0003c0004t0006g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.154-1741A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20891690 | |||||||
chr10:20891822 | T | G | 1 | a0001c0001t0002g0273 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.154-1873A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20891822 | |||||||
chr10:20891958 | A | G | 276 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(273): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.154-2009T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20891958 | |||||||
chr10:20892046 | T | C | 1 | a0005c0007t0001g0012 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.154-2097A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892046 | |||||||
chr10:20892057 | C | A | 7 | a0001c0001t0005g0180 a0001c0001t0005g0182 a0001c0001t0005g0191 others(4): Show |
7 | NA18964.hp1 NA18972.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-2108G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892057 | |||||||
chr10:20892179 | C | A | 8 | a0001c0001t0013g0185 a0001c0001t0013g0186 a0001c0001t0013g0187 others(5): Show |
8 | HG00642.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-2230G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892179 | |||||||
chr10:20892228 | C | T | 4 | a0001c0001t0018g0289 a0001c0001t0018g0291 a0001c0001t0036g0290 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-2279G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892228 | |||||||
chr10:20892230 | C | T | 1 | a0001c0001t0033g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.154-2281G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892230 | |||||||
chr10:20892327 | A | C | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.154-2378T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892327 | |||||||
chr10:20892401 | C | T | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-2452G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892401 | |||||||
chr10:20892550 | T | C | 1 | a0001c0001t0002g0274 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.154-2601A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892550 | |||||||
chr10:20892616 | T | C | 291 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(288): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.154-2667A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892616 | |||||||
chr10:20892672 | C | T | 4 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(1): Show |
4 | HG02630.hp1 HG02818.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-2723G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892672 | |||||||
chr10:20892774 | G | A | 76 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(73): Show |
79 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.154-2825C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892774 | |||||||
chr10:20892778 | G | T | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.154-2829C>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892778 | |||||||
chr10:20892799 | G | A | 1 | a0001c0001t0032g0190 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.154-2850C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892799 | |||||||
chr10:20892845 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.154-2896C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892845 | |||||||
chr10:20892862 | T | A | 1 | a0002c0002t0014g0027 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.154-2913A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20892862 | |||||||
chr10:20893105 | C | A | 1 | a0001c0001t0002g0275 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.154-3156G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20893105 | |||||||
chr10:20893368 | A | G | 80 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(77): Show |
83 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.154-3419T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20893368 | |||||||
chr10:20893518 | A | G | 1 | a0002c0002t0011g0288 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.153+3440T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20893518 | |||||||
chr10:20893606 | A | G | 5 | a0006c0008t0008g0304 a0006c0008t0008g0307 a0006c0008t0008g0308 others(2): Show |
5 | HG02258.hp1 HG02886.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+3352T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20893606 | |||||||
chr10:20893688 | T | C | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.153+3270A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20893688 | |||||||
chr10:20893796 | A | G | 14 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(11): Show |
14 | HG00621.hp1 HG01069.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.153+3162T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20893796 | |||||||
chr10:20893871 | G | A | 1 | a0001c0001t0021g0100 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.153+3087C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20893871 | |||||||
chr10:20894435 | A | G | 253 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(250): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.153+2523T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894435 | |||||||
chr10:20894585 | C | T | 289 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(286): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.153+2373G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894585 | |||||||
chr10:20894637 | G | A | 40 | a0001c0001t0004g0179 a0001c0001t0005g0171 a0001c0001t0005g0172 others(37): Show |
40 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.153+2321C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894637 | |||||||
chr10:20894680 | C | T | 178 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(175): Show |
182 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.153+2278G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894680 | |||||||
chr10:20894731 | G | A | 10 | a0005c0007t0001g0012 a0005c0007t0001g0068 a0005c0007t0001g0069 others(7): Show |
10 | HG00621.hp1 HG01069.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+2227C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894731 | |||||||
chr10:20894750 | T | TA | 122 | a0001c0001t0001g0014 a0001c0001t0001g0073 a0001c0001t0001g0074 others(119): Show |
124 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.153+2207dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894750 | |||||||
chr10:20894750 | T | TAA | 6 | a0001c0001t0001g0129 a0001c0001t0005g0195 a0001c0001t0015g0159 others(3): Show |
6 | HG01261.hp2 HG02074.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+2206_153+2207d others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894750 | |||||||
chr10:20894750 | TA | T | 53 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0204 others(50): Show |
55 | HG00544.hp1 HG00597.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.153+2207delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894750 | |||||||
chr10:20894769 | AT | A | 4 | a0001c0001t0007g0176 a0002c0002t0011g0055 a0002c0002t0011g0056 others(1): Show |
4 | HG02630.hp1 HG02818.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+2188delA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894769 | |||||||
chr10:20894820 | T | G | 12 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0017g0286 others(9): Show |
13 | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.153+2138A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894820 | |||||||
chr10:20894910 | T | C | 1 | a0004c0005t0001g0160 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.153+2048A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894910 | |||||||
chr10:20894916 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0002g0130 a0001c0013t0001g0163 |
3 | NA18967.hp2 NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.153+2042C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894916 | |||||||
chr10:20894925 | T | TC | 4 | a0001c0001t0004g0179 a0001c0001t0005g0172 a0001c0001t0005g0194 others(1): Show |
4 | HG02145.hp2 HG02886.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+2032dupG | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894925 | |||||||
chr10:20894926 | CT | C | 10 | a0001c0001t0005g0180 a0001c0001t0013g0185 a0001c0001t0013g0186 others(7): Show |
10 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+2031delA | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894926 | |||||||
chr10:20894926 | CTAAAAAA others(4): Show |
C | 1 | a0001c0001t0013g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+2021_153+2031d others(13): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894926 | |||||||
chr10:20894927 | T | A | 4 | a0001c0001t0004g0179 a0001c0001t0005g0172 a0001c0001t0005g0194 others(1): Show |
4 | HG02145.hp2 HG02886.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+2031A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894927 | |||||||
chr10:20894927 | T | C | 11 | a0001c0001t0005g0171 a0001c0001t0005g0182 a0001c0001t0005g0191 others(8): Show |
11 | HG02109.hp2 HG02809.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.153+2031A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894927 | |||||||
chr10:20894927 | T | TA | 17 | a0001c0001t0002g0216 a0001c0001t0002g0240 a0001c0001t0002g0267 others(14): Show |
17 | HG00544.hp1 HG00558.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.153+2030dupT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894927 | |||||||
chr10:20894927 | TA | T | 24 | a0001c0001t0001g0206 a0001c0001t0001g0237 a0001c0001t0001g0282 others(21): Show |
25 | HG00280.hp1 HG01256.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.153+2030delT | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894927 | |||||||
chr10:20894928 | A | C | 10 | a0001c0001t0005g0180 a0001c0001t0013g0185 a0001c0001t0013g0186 others(7): Show |
10 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+2030T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894928 | |||||||
chr10:20894934 | A | T | 1 | a0002c0002t0014g0027 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.153+2024T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894934 | |||||||
chr10:20894938 | A | C | 1 | a0001c0001t0013g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+2020T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894938 | |||||||
chr10:20894998 | T | C | 26 | a0001c0001t0004g0179 a0001c0001t0005g0171 a0001c0001t0005g0172 others(23): Show |
26 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.153+1960A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20894998 | |||||||
chr10:20895031 | C | T | 9 | a0001c0001t0013g0185 a0001c0001t0013g0186 a0001c0001t0013g0187 others(6): Show |
9 | HG00642.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+1927G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895031 | |||||||
chr10:20895042 | C | A | 17 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0017g0278 others(14): Show |
18 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.153+1916G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895042 | |||||||
chr10:20895235 | A | G | 2 | a0001c0001t0017g0278 a0001c0001t0039g0277 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.153+1723T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895235 | |||||||
chr10:20895323 | A | T | 1 | a0001c0001t0017g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.153+1635T>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895323 | |||||||
chr10:20895324 | C | A | 1 | a0001c0001t0017g0303 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.153+1634G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895324 | |||||||
chr10:20895469 | T | A | 4 | a0001c0001t0016g0131 a0001c0001t0016g0132 a0001c0001t0050g0329 others(1): Show |
4 | HG01081.hp2 HG01261.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+1489A>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895469 | |||||||
chr10:20895475 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.153+1483A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895475 | |||||||
chr10:20895484 | G | A | 44 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0004g0179 others(41): Show |
44 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(41): Show |
intron_variant | MODIFIER | c.153+1474C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895484 | |||||||
chr10:20895532 | C | T | 1 | a0001c0001t0015g0306 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153+1426G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895532 | |||||||
chr10:20895537 | C | A | 1 | a0002c0002t0042g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.153+1421G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895537 | |||||||
chr10:20895748 | TTGTGCTT others(6): Show |
T | 1 | a0013c0021t0043g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.153+1197_153+1209d others(15): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895748 | |||||||
chr10:20895952 | A | C | 298 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(295): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.153+1006T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20895952 | |||||||
chr10:20896018 | T | C | 9 | a0001c0001t0017g0286 a0001c0001t0018g0289 a0001c0001t0018g0291 others(6): Show |
10 | HG02055.hp2 HG02572.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.153+940A>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896018 | |||||||
chr10:20896052 | C | T | 1 | a0005c0007t0001g0012 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.153+906G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896052 | |||||||
chr10:20896070 | C | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(157): Show |
163 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.153+888G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896070 | |||||||
chr10:20896095 | C | G | 33 | a0001c0001t0004g0179 a0001c0001t0005g0180 a0001c0001t0005g0182 others(30): Show |
33 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.153+863G>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896095 | |||||||
chr10:20896123 | A | G | 161 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(158): Show |
164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.153+835T>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896123 | |||||||
chr10:20896127 | T | G | 9 | a0001c0001t0017g0286 a0001c0001t0018g0289 a0001c0001t0018g0291 others(6): Show |
10 | HG02055.hp2 HG02572.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.153+831A>C | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896127 | |||||||
chr10:20896328 | G | A | 1 | a0001c0001t0005g0134 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.153+630C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896328 | |||||||
chr10:20896380 | C | CAACAA | 4 | a0001c0001t0007g0101 a0003c0004t0002g0015 a0003c0004t0002g0057 others(1): Show |
4 | HG01192.hp1 HG01192.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+573_153+577dup others(5): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896380 | |||||||
chr10:20896392 | C | T | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+566G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896392 | |||||||
chr10:20896483 | C | CAT | 15 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(12): Show |
15 | HG00642.hp1 HG02055.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.153+473_153+474dup others(2): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | C | CATAT | 3 | a0001c0013t0001g0163 a0002c0002t0011g0183 a0004c0005t0001g0162 |
3 | HG03516.hp1 HG04184.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.153+471_153+474dup others(4): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | C | CATATAT | 33 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(30): Show |
34 | HG00140.hp2 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.153+469_153+474dup others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | C | CATATATA others(1): Show |
32 | a0001c0001t0001g0116 a0001c0001t0001g0127 a0001c0001t0001g0129 others(29): Show |
32 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.153+467_153+474dup others(8): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | C | CATATATA others(3): Show |
56 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0005g0096 others(53): Show |
56 | HG00280.hp1 HG00642.hp2 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.153+465_153+474dup others(10): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | C | CATATATA others(5): Show |
32 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0005g0048 others(29): Show |
33 | HG00544.hp1 HG00597.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.153+463_153+474dup others(12): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | C | CATATATA others(7): Show |
7 | a0001c0001t0007g0023 a0001c0003t0003g0026 a0002c0002t0003g0022 others(4): Show |
7 | HG02622.hp1 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+461_153+474dup others(14): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | C | CATATATA others(9): Show |
5 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0017g0303 others(2): Show |
5 | HG01884.hp2 HG01975.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+459_153+474dup others(16): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | C | CATATATA others(11): Show |
3 | a0001c0003t0001g0017 a0001c0006t0008g0302 a0002c0002t0003g0016 |
3 | HG01433.hp1 HG02572.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.153+457_153+474dup others(18): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | C | CATATATA others(13): Show |
4 | a0001c0001t0001g0014 a0002c0002t0026g0013 a0003c0004t0002g0015 others(1): Show |
4 | HG00621.hp2 HG02056.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+455_153+474dup others(20): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | C | CATATATA others(15): Show |
1 | a0004c0005t0001g0011 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.153+453_153+474dup others(22): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | CAT | C | 16 | a0001c0001t0001g0009 a0001c0001t0001g0316 a0001c0001t0001g0317 others(13): Show |
17 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.153+473_153+474del others(2): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | CATATAT | C | 4 | a0001c0001t0005g0171 a0001c0001t0005g0172 a0001c0001t0007g0328 others(1): Show |
4 | HG01361.hp2 HG02145.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+469_153+474del others(6): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | CATATATA others(7): Show |
C | 1 | a0004c0011t0001g0003 | 2 | NA18971.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.153+461_153+474del others(14): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | CATATATA others(11): Show |
C | 93 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(90): Show |
97 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.153+457_153+474del others(18): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896483 | CATATATA others(13): Show |
C | 11 | a0002c0002t0003g0293 a0003c0004t0001g0297 a0003c0004t0001g0298 others(8): Show |
12 | HG02015.hp2 NA18947.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+455_153+474del others(20): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896483 | |||||||
chr10:20896487 | T | TATATATA others(11): Show |
1 | a0002c0002t0014g0167 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.153+470_153+471ins others(18): Show |
NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896487 | |||||||
chr10:20896595 | C | A | 31 | a0001c0001t0004g0179 a0001c0001t0005g0180 a0001c0001t0005g0182 others(28): Show |
31 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.153+363G>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896595 | |||||||
chr10:20896732 | G | A | 103 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0237 others(100): Show |
108 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.153+226C>T | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896732 | |||||||
chr10:20896779 | C | T | 1 | a0002c0002t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153+179G>A | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896779 | |||||||
chr10:20896892 | A | C | 300 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0034 others(297): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.153+66T>G | NEBL | ENSG00000078114.19 | transcript | ENST00000377122.9 | protein_coding | 2/27 | chr10 | 20896892 |