Item | Value |
---|---|
geneid | 10003 |
ensemblid | ENSG00000077616.11 |
hgncid | 14526 |
symbol | NAALAD2 |
name | N-acetylated alpha-linked acidic dipeptidase 2 |
refseq_nuc | NM_005467.4 |
refseq_prot | NP_005458.1 |
ensembl_nuc | ENST00000534061.6 |
ensembl_prot | ENSP00000432481.1 |
mane_status | MANE Select |
chr | chr11 |
start | 90134663 |
end | 90192894 |
strand | + |
ver | v1.2 |
region | chr11:90134663-90192894 |
region5000 | chr11:90129663-90197894 |
regionname0 | NAALAD2_chr11_90134663_90192894 |
regionname5000 | NAALAD2_chr11_90129663_90197894 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 740 | 274 | 47 | 48 | 138 | 11 | 28 | 112 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0002 | 0/0 | 740 | 42 | 17 | 7 | 2 | 1 | 15 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0003 | 0/0 | 740 | 14 | 1 | 3 | 9 | 0 | 1 | 5 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0004 | 0/0 | 740 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0005 | 0/0 | 740 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0006 | 0/0 | 740 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0007 | 0/0 | 740 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0008 | 0/0 | 740 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0009 | 0/0 | 740 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0010 | 0/0 | 740 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0011 | 0/0 | 740 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0012 | 0/0 | 399 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(394): Show |
chr11 | 90129663 | 90197894 |
a0013 | 0/0 | 740 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
a0014 | 0/0 | 740 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | MAESR others(735): Show |
chr11 | 90129663 | 90197894 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2220 | 148 | 25 | 29 | 70 | 6 | 16 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0001c0002 | 0/0 | 2220 | 117 | 16 | 17 | 67 | 5 | 12 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0001c0006 | 0/0 | 2220 | 6 | 5 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0001c0015 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0001c0016 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0001c0020 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0002c0003 | 0/0 | 2220 | 40 | 17 | 7 | 2 | 1 | 13 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0002c0009 | 0/0 | 2220 | 2 | 0 | 0 | 0 | 0 | 2 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0003c0004 | 0/0 | 2220 | 14 | 1 | 3 | 9 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0004c0005 | 0/0 | 2220 | 13 | 13 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0004c0021 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0005c0007 | 0/0 | 2220 | 6 | 5 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0005c0014 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0006c0008 | 0/0 | 2220 | 3 | 3 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0007c0011 | 0/0 | 2220 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0008c0010 | 0/0 | 2220 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0009c0018 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0010c0017 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0011c0022 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0012c0019 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0013c0013 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 | ||
a0014c0012 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | ATGGC others(2215): Show |
chr11 | 90129663 | 90197894 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/1 | 3466 | 69 | 20 | 17 | 22 | 3 | 5 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0001t0003 | 0/0 | 3466 | 44 | 2 | 3 | 34 | 0 | 5 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0001t0006 | 0/0 | 3466 | 19 | 0 | 8 | 3 | 3 | 5 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0001t0008 | 0/0 | 3466 | 7 | 1 | 1 | 4 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0001t0009 | 0/0 | 3466 | 5 | 0 | 0 | 5 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0001t0010 | 0/0 | 3466 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0001t0012 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0001t0013 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0002t0001 | 0/0 | 3466 | 73 | 5 | 12 | 47 | 2 | 7 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0002t0004 | 0/0 | 3466 | 20 | 9 | 2 | 9 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0002t0005 | 0/0 | 3466 | 16 | 2 | 2 | 4 | 3 | 5 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0002t0007 | 0/0 | 3466 | 6 | 0 | 0 | 6 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0002t0015 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0002t0016 | 0/0 | 3466 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0006t0001 | 0/0 | 3466 | 3 | 2 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0006t0004 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0006t0005 | 0/0 | 3466 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0015t0001 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0016t0002 | 0/0 | 3466 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0001c0020t0002 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0002c0003t0001 | 0/0 | 3466 | 29 | 10 | 6 | 2 | 1 | 10 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0002c0003t0004 | 0/0 | 3466 | 5 | 4 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0002c0003t0005 | 0/0 | 3466 | 3 | 3 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0002c0003t0007 | 0/0 | 3466 | 2 | 0 | 0 | 0 | 0 | 2 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0002c0003t0017 | 0/0 | 3438 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3433): Show |
chr11 | 90129663 | 90197894 |
a0002c0009t0001 | 0/0 | 3466 | 2 | 0 | 0 | 0 | 0 | 2 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0003c0004t0001 | 0/0 | 3466 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0003c0004t0004 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0003c0004t0005 | 0/0 | 3466 | 11 | 1 | 2 | 8 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0003c0004t0018 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0004c0005t0001 | 0/0 | 3466 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0004c0005t0004 | 0/0 | 3466 | 8 | 8 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0004c0005t0005 | 0/0 | 3466 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0004c0005t0014 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0004c0021t0011 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AAAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0005c0007t0001 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0005c0007t0005 | 0/0 | 3466 | 4 | 3 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0005c0007t0007 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0005c0014t0001 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0006c0008t0004 | 0/0 | 3466 | 3 | 3 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0007c0011t0002 | 0/0 | 3466 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0008c0010t0004 | 0/0 | 3466 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0009c0018t0006 | 0/0 | 3466 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0010c0017t0003 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0011c0022t0002 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0012c0019t0006 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0013c0013t0004 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
a0014c0012t0001 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | AGAGC others(3461): Show |
chr11 | 90129663 | 90197894 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0008g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0008g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0008g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0008g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0009g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0009g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0009g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0012g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0001t0013g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0007g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0015g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0002t0016g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0006t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0006t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0006t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0006t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0006t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0006t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0015t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0016t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0001c0020t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0007g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0007g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0003t0017g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0009t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0002c0009t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0005g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0003c0004t0018g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0005t0014g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0004c0021t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0005c0007t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0005c0007t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0005c0007t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0005c0007t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0005c0007t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0005c0007t0007g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0005c0014t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0006c0008t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0006c0008t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0006c0008t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0007c0011t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0007c0011t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0008c0010t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0008c0010t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0009c0018t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0010c0017t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0011c0022t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0012c0019t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0013c0013t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
a0014c0012t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0059 | EUR | GBR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | GBR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0215 | EUR | GBR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0171 | EUR | GBR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00323 | hp1 | a0001 | c0002 | t0005 | g0329 | EUR | FIN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0212 | EUR | FIN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00438 | hp2 | a0003 | c0004 | t0005 | g0236 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00544 | hp2 | a0002 | c0003 | t0001 | g0297 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00558 | hp2 | a0001 | c0001 | t0012 | g0109 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00609 | hp1 | a0007 | c0011 | t0002 | g0128 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00621 | hp2 | a0001 | c0001 | t0006 | g0183 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00639 | hp1 | a0002 | c0003 | t0001 | g0018 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00642 | hp2 | a0001 | c0002 | t0016 | g0332 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0177 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00738 | hp1 | a0001 | c0001 | t0006 | g0179 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00741 | hp1 | a0009 | c0018 | t0006 | g0178 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01069 | hp1 | a0002 | c0003 | t0001 | g0018 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01069 | hp2 | a0001 | c0001 | t0006 | g0172 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01071 | hp1 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0173 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01074 | hp1 | a0001 | c0002 | t0004 | g0260 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0338 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01081 | hp1 | a0005 | c0007 | t0005 | g0311 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01099 | hp1 | a0002 | c0003 | t0001 | g0273 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01106 | hp2 | a0001 | c0002 | t0005 | g0331 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01109 | hp2 | a0001 | c0006 | t0001 | g0321 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01168 | hp1 | a0002 | c0003 | t0017 | g0017 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0181 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01175 | hp2 | a0003 | c0004 | t0001 | g0242 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01192 | hp2 | a0002 | c0003 | t0001 | g0288 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0324 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01255 | hp1 | a0001 | c0002 | t0005 | g0019 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0182 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0074 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01261 | hp1 | a0001 | c0002 | t0004 | g0031 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01346 | hp1 | a0001 | c0001 | t0008 | g0137 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01346 | hp2 | a0003 | c0004 | t0005 | g0235 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01361 | hp2 | a0002 | c0003 | t0001 | g0282 | AMR | CLM | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01516 | hp1 | a0001 | c0002 | t0005 | g0330 | EUR | IBS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01516 | hp2 | a0001 | c0001 | t0006 | g0174 | EUR | IBS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01517 | hp1 | a0001 | c0002 | t0005 | g0328 | EUR | IBS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | IBS | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01891 | hp2 | a0002 | c0003 | t0001 | g0279 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01934 | hp2 | a0003 | c0004 | t0005 | g0231 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0285 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02015 | hp1 | a0002 | c0003 | t0001 | g0292 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02015 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02027 | hp2 | a0003 | c0004 | t0005 | g0246 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02055 | hp1 | a0006 | c0008 | t0004 | g0295 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02055 | hp2 | a0001 | c0002 | t0004 | g0257 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02056 | hp1 | a0001 | c0002 | t0004 | g0206 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0101 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02083 | hp2 | a0003 | c0004 | t0005 | g0237 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02129 | hp1 | a0003 | c0004 | t0004 | g0243 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02132 | hp2 | a0001 | c0001 | t0009 | g0170 | EAS | KHV | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02145 | hp2 | a0002 | c0003 | t0004 | g0261 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | CDX | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02155 | hp2 | a0001 | c0002 | t0004 | g0337 | EAS | CDX | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | CDX | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02165 | hp2 | a0001 | c0002 | t0004 | g0207 | EAS | CDX | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02258 | hp2 | a0003 | c0004 | t0005 | g0241 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02280 | hp1 | a0004 | c0005 | t0004 | g0267 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02300 | hp2 | a0001 | c0016 | t0002 | g0099 | AMR | PEL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02451 | hp1 | a0002 | c0003 | t0001 | g0281 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02451 | hp2 | a0004 | c0005 | t0004 | g0268 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0012 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02615 | hp2 | a0004 | c0005 | t0001 | g0253 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02622 | hp2 | a0001 | c0006 | t0001 | g0301 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02698 | hp1 | a0002 | c0003 | t0001 | g0269 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02717 | hp1 | a0001 | c0002 | t0004 | g0046 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02717 | hp2 | a0002 | c0003 | t0001 | g0299 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02723 | hp1 | a0004 | c0005 | t0004 | g0249 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02735 | hp1 | a0002 | c0003 | t0001 | g0293 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0225 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02738 | hp2 | a0002 | c0003 | t0001 | g0302 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02809 | hp1 | a0001 | c0006 | t0001 | g0300 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0278 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02818 | hp2 | a0002 | c0003 | t0005 | g0262 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02886 | hp1 | a0002 | c0003 | t0001 | g0276 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02886 | hp2 | a0004 | c0005 | t0001 | g0247 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02895 | hp1 | a0002 | c0003 | t0001 | g0271 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02895 | hp2 | a0004 | c0005 | t0014 | g0252 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02896 | hp1 | a0004 | c0005 | t0004 | g0266 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02896 | hp2 | a0001 | c0006 | t0004 | g0322 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02922 | hp1 | a0001 | c0002 | t0004 | g0256 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02922 | hp2 | a0008 | c0010 | t0004 | g0316 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02965 | hp1 | a0004 | c0005 | t0005 | g0248 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0163 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02970 | hp2 | a0002 | c0003 | t0004 | g0304 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02976 | hp1 | a0004 | c0005 | t0004 | g0264 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02976 | hp2 | a0001 | c0002 | t0004 | g0306 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03017 | hp1 | a0002 | c0003 | t0001 | g0294 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0030 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03041 | hp1 | a0004 | c0005 | t0004 | g0265 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03041 | hp2 | a0005 | c0007 | t0005 | g0313 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03098 | hp1 | a0001 | c0002 | t0004 | g0258 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03098 | hp2 | a0001 | c0002 | t0005 | g0320 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03130 | hp1 | a0004 | c0021 | t0011 | g0184 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03139 | hp2 | a0005 | c0014 | t0001 | g0315 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03195 | hp1 | a0001 | c0002 | t0004 | g0255 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03195 | hp2 | a0002 | c0003 | t0005 | g0016 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03209 | hp1 | a0002 | c0003 | t0004 | g0274 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03209 | hp2 | a0001 | c0001 | t0010 | g0164 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03225 | hp1 | a0001 | c0002 | t0005 | g0319 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03239 | hp1 | a0001 | c0002 | t0005 | g0327 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03239 | hp2 | a0002 | c0003 | t0007 | g0298 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03453 | hp1 | a0004 | c0005 | t0004 | g0250 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03453 | hp2 | a0001 | c0006 | t0005 | g0323 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03486 | hp1 | a0005 | c0007 | t0001 | g0317 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0309 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0011 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03491 | hp1 | a0002 | c0009 | t0001 | g0270 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0053 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0176 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0011 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03516 | hp1 | a0002 | c0003 | t0001 | g0275 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03516 | hp2 | a0005 | c0007 | t0005 | g0310 | AFR | ESN | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03540 | hp1 | a0004 | c0005 | t0004 | g0251 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03579 | hp1 | a0005 | c0007 | t0007 | g0312 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03579 | hp2 | a0001 | c0002 | t0004 | g0259 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03654 | hp2 | a0002 | c0003 | t0001 | g0017 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03669 | hp2 | a0002 | c0003 | t0001 | g0303 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03688 | hp1 | a0010 | c0017 | t0003 | g0086 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03688 | hp2 | a0002 | c0003 | t0001 | g0287 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03704 | hp2 | a0001 | c0002 | t0005 | g0326 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0305 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03831 | hp1 | a0002 | c0003 | t0004 | g0307 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03834 | hp1 | a0001 | c0002 | t0005 | g0019 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03834 | hp2 | a0003 | c0004 | t0018 | g0234 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03927 | hp2 | a0011 | c0022 | t0002 | g0127 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0062 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03942 | hp2 | a0002 | c0003 | t0001 | g0272 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG04115 | hp1 | a0012 | c0019 | t0006 | g0049 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG04115 | hp2 | a0001 | c0002 | t0005 | g0201 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0220 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG04184 | hp2 | a0013 | c0013 | t0004 | g0296 | SAS | BEB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG04204 | hp1 | a0002 | c0003 | t0001 | g0284 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0198 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG04228 | hp1 | a0001 | c0001 | t0008 | g0056 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG04228 | hp2 | a0002 | c0003 | t0007 | g0291 | SAS | STU | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18522 | hp1 | a0001 | c0002 | t0004 | g0047 | AFR | YRI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18522 | hp2 | a0005 | c0007 | t0005 | g0314 | AFR | YRI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | CHB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18747 | hp2 | a0014 | c0012 | t0001 | g0229 | EAS | CHB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18940 | hp1 | a0001 | c0001 | t0008 | g0114 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18941 | hp1 | a0001 | c0002 | t0007 | g0014 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18941 | hp2 | a0001 | c0001 | t0009 | g0005 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18944 | hp2 | a0001 | c0001 | t0008 | g0075 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18946 | hp2 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18951 | hp1 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18956 | hp2 | a0001 | c0002 | t0007 | g0020 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18957 | hp2 | a0003 | c0004 | t0005 | g0239 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18967 | hp2 | a0003 | c0004 | t0005 | g0244 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18973 | hp2 | a0003 | c0004 | t0005 | g0245 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18975 | hp2 | a0001 | c0002 | t0004 | g0227 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18977 | hp2 | a0007 | c0011 | t0002 | g0005 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18979 | hp2 | a0001 | c0002 | t0007 | g0029 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18985 | hp1 | a0001 | c0002 | t0005 | g0334 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18987 | hp2 | a0001 | c0015 | t0001 | g0001 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18992 | hp1 | a0001 | c0002 | t0015 | g0026 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18994 | hp2 | a0001 | c0001 | t0013 | g0009 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18995 | hp1 | a0001 | c0001 | t0008 | g0123 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18998 | hp2 | a0003 | c0004 | t0005 | g0238 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18999 | hp1 | a0001 | c0002 | t0007 | g0038 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19000 | hp2 | a0001 | c0002 | t0004 | g0188 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19006 | hp2 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19009 | hp2 | a0001 | c0002 | t0005 | g0335 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19043 | hp1 | a0001 | c0020 | t0002 | g0098 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19043 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19060 | hp1 | a0001 | c0002 | t0005 | g0192 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19060 | hp2 | a0001 | c0001 | t0009 | g0110 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19062 | hp2 | a0003 | c0004 | t0005 | g0240 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19063 | hp1 | a0001 | c0002 | t0007 | g0022 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19068 | hp2 | a0001 | c0002 | t0005 | g0336 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19079 | hp2 | a0001 | c0002 | t0004 | g0199 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19080 | hp1 | a0001 | c0002 | t0004 | g0187 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19081 | hp1 | a0001 | c0001 | t0008 | g0105 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19084 | hp1 | a0001 | c0002 | t0007 | g0014 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19085 | hp1 | a0001 | c0001 | t0009 | g0131 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19240 | hp1 | a0006 | c0008 | t0004 | g0289 | AFR | YRI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | YRI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0060 | AFR | ASW | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA20129 | hp2 | a0002 | c0003 | t0004 | g0283 | AFR | ASW | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA20805 | hp1 | a0002 | c0003 | t0001 | g0290 | EUR | TSI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0166 | EUR | TSI | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA20905 | hp1 | a0002 | c0009 | t0001 | g0308 | SAS | GIH | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA20905 | hp2 | a0001 | c0002 | t0005 | g0333 | SAS | GIH | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02109 | hp1 | a0001 | c0006 | t0005 | g0325 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02486 | hp1 | a0004 | c0005 | t0005 | g0263 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02486 | hp2 | a0002 | c0003 | t0001 | g0277 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02559 | hp1 | a0002 | c0003 | t0001 | g0286 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG02559 | hp2 | a0006 | c0008 | t0004 | g0230 | AFR | ACB | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
HG03471 | hp2 | a0002 | c0003 | t0005 | g0016 | AFR | MSL | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA20300 | hp1 | a0002 | c0003 | t0001 | g0280 | AFR | USA | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA20300 | hp2 | a0008 | c0010 | t0004 | g0318 | AFR | USA | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | LWK | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0118 | REF | REF | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0112 | REF | REF | NAALAD2_chr11_90129663_90197894 | NAALAD2 | chr11 | 90129663 | 90197894 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:90147362 | C | T | 1 | a0011 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.227C>T | p.Thr76Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/19 | 323/3466 | 227/2223 | 76/740 | chr11 | 90147362 | |||
chr11:90147436 | G | A | 1 | a0003 | 14 | HG00438.hp2 HG01175.hp2 HG01346.hp2 others(11): Show |
missense_variant | MODERATE | c.301G>A | p.Val101Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/19 | 397/3466 | 301/2223 | 101/740 | chr11 | 90147436 | |||
chr11:90150540 | A | G | 2 | a0005 a0008 |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
missense_variant | MODERATE | c.542A>G | p.Glu181Gly | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/19 | 638/3466 | 542/2223 | 181/740 | chr11 | 90150540 | |||
chr11:90150558 | C | T | 1 | a0004 | 14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
missense_variant | MODERATE | c.560C>T | p.Thr187Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/19 | 656/3466 | 560/2223 | 187/740 | chr11 | 90150558 | |||
chr11:90152299 | T | C | 1 | a0006 | 3 | HG02055.hp1 HG02559.hp2 NA19240.hp1 |
missense_variant&splice_region_variant | MODERATE | c.611T>C | p.Val204Ala | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/19 | 707/3466 | 611/2223 | 204/740 | chr11 | 90152299 | |||
chr11:90159272 | T | G | 1 | a0010 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.924T>G | p.Ser308Arg | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/19 | 1020/3466 | 924/2223 | 308/740 | chr11 | 90159272 | |||
chr11:90163031 | C | A | 1 | a0007 | 2 | HG00609.hp1 NA18977.hp2 |
missense_variant | MODERATE | c.1072C>A | p.Pro358Thr | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 9/19 | 1168/3466 | 1072/2223 | 358/740 | chr11 | 90163031 | |||
chr11:90163351 | T | A | 1 | a0009 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1117T>A | p.Phe373Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 10/19 | 1213/3466 | 1117/2223 | 373/740 | chr11 | 90163351 | |||
chr11:90163539 | G | A | 1 | a0012 | 1 | HG04115.hp1 | stop_gained | HIGH | c.1200G>A | p.Trp400* | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/19 | 1296/3466 | 1200/2223 | 400/740 | chr11 | 90163539 | |||
chr11:90168986 | A | G | 4 | a0002 a0006 a0008 others(1): Show |
48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
missense_variant | MODERATE | c.1336A>G | p.Ile446Val | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/19 | 1432/3466 | 1336/2223 | 446/740 | chr11 | 90168986 | |||
chr11:90170086 | G | A | 1 | a0013 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1360G>A | p.Val454Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/19 | 1456/3466 | 1360/2223 | 454/740 | chr11 | 90170086 | |||
chr11:90178091 | A | T | 1 | a0014 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.1832A>T | p.Gln611Leu | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/19 | 1928/3466 | 1832/2223 | 611/740 | chr11 | 90178091 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:90135587 | G | A | 13 | a0001c0002 a0001c0006 a0001c0015 others(10): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
synonymous_variant | LOW | c.111G>A | p.Thr37Thr | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/19 | 207/3466 | 111/2223 | 37/740 | chr11 | 90135587 | |||
chr11:90150493 | A | G | 1 | a0001c0015 | 1 | NA18987.hp2 | synonymous_variant | LOW | c.495A>G | p.Val165Val | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/19 | 591/3466 | 495/2223 | 165/740 | chr11 | 90150493 | |||
chr11:90152369 | T | G | 1 | a0001c0016 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.681T>G | p.Pro227Pro | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/19 | 777/3466 | 681/2223 | 227/740 | chr11 | 90152369 | |||
chr11:90163000 | T | C | 1 | a0001c0006 | 6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.1041T>C | p.Asn347Asn | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 9/19 | 1137/3466 | 1041/2223 | 347/740 | chr11 | 90163000 | |||
chr11:90163596 | G | A | 1 | a0004c0005 | 13 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
synonymous_variant | LOW | c.1257G>A | p.Leu419Leu | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/19 | 1353/3466 | 1257/2223 | 419/740 | chr11 | 90163596 | |||
chr11:90168988 | A | C | 1 | a0002c0009 | 2 | HG03491.hp1 NA20905.hp1 |
synonymous_variant | LOW | c.1338A>C | p.Ile446Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/19 | 1434/3466 | 1338/2223 | 446/740 | chr11 | 90168988 | |||
chr11:90173875 | T | C | 1 | a0001c0020 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1462T>C | p.Leu488Leu | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/19 | 1558/3466 | 1462/2223 | 488/740 | chr11 | 90173875 | |||
chr11:90182973 | C | T | 1 | a0005c0014 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.1998C>T | p.Ile666Ile | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/19 | 2094/3466 | 1998/2223 | 666/740 | chr11 | 90182973 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:90134664 | G | A | 1 | a0004c0021t0011 | 1 | HG03130.hp1 | 5_prime_UTR_variant | MODIFIER | c.-95G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/19 | 95 | chr11 | 90134664 | ||||||
chr11:90134704 | C | T | 32 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0005 others(29): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
5_prime_UTR_variant | MODIFIER | c.-55C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/19 | 55 | chr11 | 90134704 | ||||||
chr11:90191813 | A | C | 1 | a0003c0004t0018 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 66 | chr11 | 90191813 | ||||||
chr11:90191821 | T | A | 1 | a0001c0001t0012 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*74T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 74 | chr11 | 90191821 | ||||||
chr11:90192011 | C | G | 6 | a0001c0001t0003 a0001c0001t0013 a0001c0002t0007 others(3): Show |
55 | HG00597.hp2 HG00673.hp1 HG01099.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*264C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 264 | chr11 | 90192011 | ||||||
chr11:90192066 | AAAACAGT others(21): Show |
A | 1 | a0002c0003t0017 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325_*352delGTTTGG others(22): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 325 | INFO_REALIGN_3_PRIME | chr11 | 90192066 | |||||
chr11:90192141 | T | C | 1 | a0001c0001t0009 | 5 | HG02015.hp2 HG02132.hp2 NA18941.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*394T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 394 | chr11 | 90192141 | ||||||
chr11:90192175 | A | T | 1 | a0001c0002t0016 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 428 | chr11 | 90192175 | ||||||
chr11:90192185 | T | C | 1 | a0004c0005t0014 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*438T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 438 | chr11 | 90192185 | ||||||
chr11:90192239 | G | A | 1 | a0001c0001t0010 | 2 | HG02965.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*492G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 492 | chr11 | 90192239 | ||||||
chr11:90192244 | T | G | 33 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(30): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*497T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 497 | chr11 | 90192244 | ||||||
chr11:90192594 | C | T | 20 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(17): Show |
179 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*847C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 847 | chr11 | 90192594 | ||||||
chr11:90192665 | G | A | 1 | a0001c0001t0013 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*918G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 918 | chr11 | 90192665 | ||||||
chr11:90192827 | C | A | 1 | a0001c0002t0015 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1080C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 19/19 | 1080 | chr11 | 90192827 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:90135107 | C | T | 1 | a0001c0001t0002g0338 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.82+267C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135107 | |||||||
chr11:90135260 | G | A | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.83-299G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135260 | |||||||
chr11:90135305 | T | A | 1 | a0001c0001t0002g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.83-254T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135305 | |||||||
chr11:90135414 | A | G | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.83-145A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135414 | |||||||
chr11:90135426 | T | G | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.83-133T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135426 | |||||||
chr11:90135446 | C | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.83-113C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135446 | |||||||
chr11:90135524 | G | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.83-35G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 1/18 | chr11 | 90135524 | |||||||
chr11:90135783 | T | C | 1 | a0012c0019t0006g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.194+113T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90135783 | |||||||
chr11:90135796 | CT | C | 85 | a0001c0001t0002g0052 a0001c0001t0003g0050 a0001c0001t0003g0051 others(82): Show |
87 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(84): Show |
intron_variant | MODIFIER | c.194+141delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90135796 | ||||||
chr11:90135796 | CTT | C | 97 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(94): Show |
108 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.194+140_194+141del others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90135796 | ||||||
chr11:90135870 | G | C | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+200G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90135870 | |||||||
chr11:90136293 | T | C | 7 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(4): Show |
7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+623T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136293 | |||||||
chr11:90136298 | A | G | 2 | a0001c0006t0004g0322 a0001c0006t0005g0323 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.194+628A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136298 | |||||||
chr11:90136446 | C | T | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+776C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136446 | |||||||
chr11:90136648 | C | T | 1 | a0001c0006t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.194+978C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136648 | |||||||
chr11:90136659 | A | C | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.194+989A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136659 | |||||||
chr11:90136836 | A | G | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+1166A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90136836 | |||||||
chr11:90137174 | CAG | C | 57 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(54): Show |
67 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.194+1508_194+1509d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90137174 | ||||||
chr11:90137186 | T | C | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.194+1516T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137186 | |||||||
chr11:90137223 | C | T | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+1553C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137223 | |||||||
chr11:90137242 | G | C | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+1572G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137242 | |||||||
chr11:90137411 | AT | A | 10 | a0001c0006t0001g0321 a0005c0007t0001g0317 a0005c0007t0005g0310 others(7): Show |
10 | HG01081.hp1 HG01109.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.194+1742delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137411 | |||||||
chr11:90137422 | T | A | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+1752T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137422 | |||||||
chr11:90137499 | A | T | 1 | a0001c0006t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.194+1829A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137499 | |||||||
chr11:90137582 | C | T | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(65): Show |
78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.194+1912C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137582 | |||||||
chr11:90137670 | C | T | 4 | a0001c0002t0004g0337 a0001c0002t0005g0334 a0001c0002t0005g0335 others(1): Show |
4 | HG02155.hp2 NA18985.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.194+2000C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137670 | |||||||
chr11:90137671 | T | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194+2001T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137671 | |||||||
chr11:90137862 | C | T | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+2192C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137862 | |||||||
chr11:90137891 | C | T | 2 | a0001c0001t0006g0182 a0001c0001t0006g0183 |
2 | HG00621.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.194+2221C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137891 | |||||||
chr11:90137943 | C | T | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(65): Show |
78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.194+2273C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137943 | |||||||
chr11:90137948 | A | C | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+2278A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137948 | |||||||
chr11:90137954 | A | T | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+2284A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137954 | |||||||
chr11:90137971 | A | G | 1 | a0014c0012t0001g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.194+2301A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90137971 | |||||||
chr11:90138010 | A | T | 16 | a0001c0001t0002g0175 a0001c0001t0003g0180 a0001c0001t0006g0012 others(13): Show |
17 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.194+2340A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138010 | |||||||
chr11:90138059 | C | G | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+2389C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138059 | |||||||
chr11:90138241 | T | G | 85 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(82): Show |
95 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.194+2571T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138241 | |||||||
chr11:90138315 | T | C | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+2645T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138315 | |||||||
chr11:90138410 | T | A | 4 | a0001c0002t0001g0309 a0002c0003t0004g0261 a0002c0003t0005g0016 others(1): Show |
5 | HG02145.hp2 HG02818.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.194+2740T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138410 | |||||||
chr11:90138500 | T | C | 27 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(24): Show |
28 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(25): Show |
intron_variant | MODIFIER | c.194+2830T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138500 | |||||||
chr11:90138585 | C | T | 1 | a0001c0001t0006g0011 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.194+2915C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138585 | |||||||
chr11:90138725 | C | CT | 37 | a0001c0001t0002g0010 a0001c0001t0002g0048 a0001c0001t0002g0136 others(34): Show |
38 | HG00621.hp2 HG01081.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.194+3089dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | C | CTT | 8 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 others(5): Show |
8 | HG00544.hp1 HG01993.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.194+3088_194+3089d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | C | CTTTTTTT others(5): Show |
1 | a0001c0002t0004g0337 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.194+3078_194+3089d others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | C | CTTTTTTT others(8): Show |
2 | a0001c0002t0005g0326 a0001c0002t0005g0327 |
2 | HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.194+3075_194+3089d others(17): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | C | CTTTTTTT others(9): Show |
4 | a0001c0002t0005g0019 a0001c0002t0005g0328 a0001c0002t0005g0329 others(1): Show |
5 | HG00323.hp1 HG01255.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+3074_194+3089d others(18): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | C | CTTTTTTT others(10): Show |
2 | a0001c0002t0005g0331 a0001c0002t0016g0332 |
2 | HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.194+3073_194+3089d others(19): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | C | CTTTTTTT others(11): Show |
1 | a0001c0002t0005g0333 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.194+3072_194+3089d others(20): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | CTTT | C | 10 | a0001c0002t0001g0309 a0001c0002t0004g0306 a0001c0006t0004g0322 others(7): Show |
11 | HG00639.hp1 HG01069.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.194+3087_194+3089d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | CTTTT | C | 42 | a0001c0002t0001g0324 a0001c0002t0004g0256 a0001c0002t0004g0257 others(39): Show |
43 | HG00544.hp2 HG01099.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.194+3086_194+3089d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | CTTTTT | C | 6 | a0001c0002t0001g0254 a0001c0002t0004g0255 a0002c0003t0001g0269 others(3): Show |
6 | HG02698.hp1 HG02895.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+3085_194+3089d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | CTTTTTTT | C | 12 | a0004c0005t0001g0247 a0004c0005t0004g0249 a0004c0005t0004g0250 others(9): Show |
12 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.194+3083_194+3089d others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | CTTTTTTT others(3): Show |
C | 25 | a0001c0002t0001g0004 a0001c0002t0001g0024 a0001c0002t0001g0025 others(22): Show |
26 | HG00597.hp1 HG01261.hp1 HG02683.hp2 others(23): Show |
intron_variant | MODIFIER | c.194+3080_194+3089d others(12): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0002g0054 a0001c0002t0001g0021 a0001c0002t0007g0020 others(3): Show |
6 | HG02027.hp2 HG02615.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.194+3079_194+3089d others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | CTTTTTTT others(5): Show |
C | 15 | a0001c0002t0001g0226 a0001c0002t0001g0228 a0001c0002t0001g0232 others(12): Show |
15 | HG00438.hp2 HG01175.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.194+3078_194+3089d others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | CTTTTTTT others(6): Show |
C | 49 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(46): Show |
59 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.194+3077_194+3089d others(15): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | CTTTTTTT others(9): Show |
C | 1 | a0001c0006t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.194+3074_194+3089d others(18): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138725 | CTTTTTTT others(12): Show |
C | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+3071_194+3089d others(21): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90138725 | ||||||
chr11:90138772 | A | G | 67 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(64): Show |
77 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.194+3102A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138772 | |||||||
chr11:90138800 | C | T | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194+3130C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138800 | |||||||
chr11:90138920 | A | G | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+3250A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90138920 | |||||||
chr11:90139058 | G | T | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.194+3388G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139058 | |||||||
chr11:90139075 | C | T | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.194+3405C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139075 | |||||||
chr11:90139146 | C | T | 1 | a0004c0005t0004g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.194+3476C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139146 | |||||||
chr11:90139226 | C | A | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+3556C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139226 | |||||||
chr11:90139249 | A | G | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.194+3579A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139249 | |||||||
chr11:90139253 | A | T | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.194+3583A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139253 | |||||||
chr11:90139294 | A | G | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+3624A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139294 | |||||||
chr11:90139321 | A | G | 7 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(4): Show |
7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+3651A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139321 | |||||||
chr11:90139388 | G | C | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.194+3718G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139388 | |||||||
chr11:90139489 | A | G | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.194+3819A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139489 | |||||||
chr11:90139518 | T | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.194+3848T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139518 | |||||||
chr11:90139579 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.194+3909G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139579 | |||||||
chr11:90139586 | T | C | 1 | a0001c0002t0004g0256 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.194+3916T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139586 | |||||||
chr11:90139813 | C | A | 1 | a0002c0003t0001g0269 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.194+4143C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139813 | |||||||
chr11:90139855 | CT | C | 8 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0003g0135 others(5): Show |
8 | HG00099.hp2 HG01255.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.194+4202delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90139855 | ||||||
chr11:90139855 | CTT | C | 14 | a0001c0002t0004g0255 a0004c0005t0001g0247 a0004c0005t0001g0253 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.194+4201_194+4202d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90139855 | ||||||
chr11:90139855 | CTTT | C | 172 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(169): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.194+4200_194+4202d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90139855 | ||||||
chr11:90139855 | CTTTT | C | 6 | a0001c0002t0001g0044 a0001c0002t0001g0185 a0001c0002t0001g0186 others(3): Show |
6 | HG02055.hp2 HG03491.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.194+4199_194+4202d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90139855 | ||||||
chr11:90139902 | G | A | 17 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(14): Show |
17 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.194+4232G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139902 | |||||||
chr11:90139940 | C | T | 20 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(17): Show |
21 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.194+4270C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139940 | |||||||
chr11:90139987 | C | T | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194+4317C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139987 | |||||||
chr11:90139995 | A | G | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.194+4325A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90139995 | |||||||
chr11:90140005 | C | T | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+4335C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140005 | |||||||
chr11:90140041 | T | C | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+4371T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140041 | |||||||
chr11:90140127 | A | G | 1 | a0001c0001t0006g0183 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.194+4457A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140127 | |||||||
chr11:90140137 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.194+4467A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140137 | |||||||
chr11:90140181 | C | T | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+4511C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140181 | |||||||
chr11:90140189 | C | A | 1 | a0001c0001t0002g0055 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.194+4519C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140189 | |||||||
chr11:90140221 | A | G | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.194+4551A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140221 | |||||||
chr11:90140305 | A | G | 5 | a0001c0001t0003g0130 a0001c0001t0003g0132 a0001c0001t0003g0133 others(2): Show |
5 | HG02129.hp2 HG02132.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+4635A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140305 | |||||||
chr11:90140418 | C | T | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.194+4748C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140418 | |||||||
chr11:90140447 | C | T | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.194+4777C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140447 | |||||||
chr11:90140450 | CT | C | 186 | a0001c0001t0002g0136 a0001c0002t0001g0001 a0001c0002t0001g0002 others(183): Show |
200 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.194+4790delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90140450 | ||||||
chr11:90140450 | CTT | C | 7 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(4): Show |
7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+4789_194+4790d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90140450 | ||||||
chr11:90140492 | GT | G | 10 | a0002c0003t0001g0271 a0002c0003t0001g0273 a0002c0003t0001g0275 others(7): Show |
10 | HG01099.hp1 HG01891.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.194+4830delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90140492 | ||||||
chr11:90140532 | A | G | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+4862A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140532 | |||||||
chr11:90140558 | A | G | 175 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(172): Show |
189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.194+4888A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140558 | |||||||
chr11:90140694 | G | T | 192 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(189): Show |
206 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.194+5024G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140694 | |||||||
chr11:90140791 | T | C | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0309 |
3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.194+5121T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140791 | |||||||
chr11:90140826 | A | G | 1 | a0001c0002t0005g0320 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.194+5156A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140826 | |||||||
chr11:90140865 | C | T | 1 | a0002c0003t0001g0018 | 2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.194+5195C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90140865 | |||||||
chr11:90141298 | T | G | 3 | a0001c0001t0006g0059 a0001c0001t0008g0060 a0001c0001t0008g0137 |
3 | HG00099.hp1 HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.194+5628T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141298 | |||||||
chr11:90141345 | C | G | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.194+5675C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141345 | |||||||
chr11:90141385 | A | T | 1 | a0001c0002t0001g0043 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.194+5715A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141385 | |||||||
chr11:90141434 | A | G | 1 | a0001c0002t0004g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.194+5764A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141434 | |||||||
chr11:90141447 | T | G | 1 | a0001c0001t0002g0338 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.194+5777T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141447 | |||||||
chr11:90141585 | C | G | 2 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
2 | NA19001.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.195-5745C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141585 | |||||||
chr11:90141594 | T | TTCTGTTT others(1): Show |
13 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(10): Show |
13 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.195-5735_195-5734i others(10): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90141594 | ||||||
chr11:90141594 | T | TTTTG | 249 | a0001c0001t0002g0048 a0001c0001t0002g0054 a0001c0001t0002g0064 others(246): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.195-5720_195-5717d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90141594 | ||||||
chr11:90141594 | T | TTTTGTTT others(1): Show |
8 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(5): Show |
8 | HG01074.hp1 HG01243.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.195-5724_195-5717d others(10): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90141594 | ||||||
chr11:90141636 | G | C | 1 | a0001c0001t0003g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.195-5694G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141636 | |||||||
chr11:90141688 | G | A | 8 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0302 others(5): Show |
9 | HG00639.hp1 HG01069.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.195-5642G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141688 | |||||||
chr11:90141703 | G | T | 10 | a0001c0006t0001g0321 a0005c0007t0001g0317 a0005c0007t0005g0310 others(7): Show |
10 | HG01081.hp1 HG01109.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-5627G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141703 | |||||||
chr11:90141713 | G | A | 1 | a0002c0003t0001g0284 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.195-5617G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141713 | |||||||
chr11:90141722 | T | C | 7 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(4): Show |
7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.195-5608T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141722 | |||||||
chr11:90141755 | G | A | 5 | a0001c0002t0001g0189 a0001c0002t0001g0190 a0001c0002t0001g0191 others(2): Show |
5 | HG00558.hp1 NA18982.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-5575G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141755 | |||||||
chr11:90141783 | T | G | 175 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(172): Show |
189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.195-5547T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141783 | |||||||
chr11:90141884 | T | G | 1 | a0001c0001t0002g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.195-5446T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141884 | |||||||
chr11:90141953 | G | A | 1 | a0001c0002t0005g0192 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.195-5377G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90141953 | |||||||
chr11:90142037 | G | A | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.195-5293G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142037 | |||||||
chr11:90142136 | G | A | 1 | a0002c0003t0001g0272 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.195-5194G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142136 | |||||||
chr11:90142162 | C | T | 5 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0004g0322 others(2): Show |
5 | HG02109.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.195-5168C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142162 | |||||||
chr11:90142185 | G | C | 46 | a0001c0002t0001g0309 a0001c0002t0004g0306 a0002c0003t0001g0017 others(43): Show |
48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.195-5145G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142185 | |||||||
chr11:90142268 | C | T | 2 | a0001c0001t0002g0162 a0001c0002t0001g0040 |
2 | HG02155.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.195-5062C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142268 | |||||||
chr11:90142269 | G | A | 51 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(48): Show |
61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.195-5061G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142269 | |||||||
chr11:90142330 | G | C | 176 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(173): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.195-5000G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142330 | |||||||
chr11:90142363 | C | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-4967C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142363 | |||||||
chr11:90142496 | C | T | 70 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(67): Show |
80 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.195-4834C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142496 | |||||||
chr11:90142923 | C | T | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.195-4407C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142923 | |||||||
chr11:90142960 | C | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-4370C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142960 | |||||||
chr11:90142966 | G | A | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.195-4364G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142966 | |||||||
chr11:90142968 | A | G | 46 | a0001c0002t0001g0254 a0001c0002t0004g0306 a0002c0003t0001g0017 others(43): Show |
48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.195-4362A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90142968 | |||||||
chr11:90143143 | G | T | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.195-4187G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143143 | |||||||
chr11:90143170 | G | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-4160G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143170 | |||||||
chr11:90143188 | T | C | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(65): Show |
78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.195-4142T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143188 | |||||||
chr11:90143291 | T | C | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.195-4039T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143291 | |||||||
chr11:90143471 | G | A | 13 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(10): Show |
13 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.195-3859G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143471 | |||||||
chr11:90143522 | G | T | 1 | a0001c0006t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.195-3808G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143522 | |||||||
chr11:90143578 | A | G | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.195-3752A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143578 | |||||||
chr11:90143648 | C | T | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.195-3682C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143648 | |||||||
chr11:90143653 | C | T | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.195-3677C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143653 | |||||||
chr11:90143775 | A | C | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.195-3555A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143775 | |||||||
chr11:90143818 | T | C | 6 | a0001c0002t0004g0255 a0001c0002t0004g0256 a0001c0002t0004g0257 others(3): Show |
6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-3512T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143818 | |||||||
chr11:90143860 | T | A | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.195-3470T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143860 | |||||||
chr11:90143911 | G | A | 1 | a0003c0004t0018g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.195-3419G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90143911 | |||||||
chr11:90144012 | G | A | 1 | a0001c0002t0001g0193 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.195-3318G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144012 | |||||||
chr11:90144067 | A | G | 13 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(10): Show |
13 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.195-3263A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144067 | |||||||
chr11:90144071 | T | C | 1 | a0001c0006t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.195-3259T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144071 | |||||||
chr11:90144123 | C | G | 5 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0004g0322 others(2): Show |
5 | HG02109.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.195-3207C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144123 | |||||||
chr11:90144383 | A | T | 14 | a0003c0004t0001g0242 a0003c0004t0004g0243 a0003c0004t0005g0231 others(11): Show |
14 | HG00438.hp2 HG01175.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.195-2947A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144383 | |||||||
chr11:90144412 | G | A | 1 | a0001c0001t0003g0061 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.195-2918G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144412 | |||||||
chr11:90144460 | G | T | 1 | a0001c0001t0002g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.195-2870G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144460 | |||||||
chr11:90144570 | A | G | 1 | a0001c0001t0002g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.195-2760A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144570 | |||||||
chr11:90144619 | G | A | 2 | a0001c0001t0002g0136 a0001c0016t0002g0099 |
2 | HG02300.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.195-2711G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144619 | |||||||
chr11:90144690 | C | T | 1 | a0007c0011t0002g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.195-2640C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144690 | |||||||
chr11:90144704 | T | C | 1 | a0001c0002t0001g0309 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.195-2626T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144704 | |||||||
chr11:90144740 | T | TA | 7 | a0001c0001t0002g0100 a0001c0001t0002g0139 a0001c0001t0002g0147 others(4): Show |
7 | HG01243.hp2 HG02083.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.195-2575dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | ||||||
chr11:90144740 | T | TAAAAAA | 23 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(20): Show |
24 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(21): Show |
intron_variant | MODIFIER | c.195-2580_195-2575d others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | ||||||
chr11:90144740 | T | TAAAAAAA others(1): Show |
17 | a0001c0002t0004g0046 a0001c0002t0004g0047 a0002c0003t0001g0281 others(14): Show |
17 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.195-2582_195-2575d others(10): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | ||||||
chr11:90144740 | T | TAAAAAAA others(2): Show |
36 | a0001c0002t0004g0306 a0001c0006t0001g0300 a0001c0006t0001g0301 others(33): Show |
38 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.195-2583_195-2575d others(11): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | ||||||
chr11:90144740 | T | TAAAAAAA others(3): Show |
24 | a0001c0002t0001g0233 a0001c0002t0001g0309 a0001c0002t0004g0337 others(21): Show |
25 | HG00323.hp1 HG00642.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.195-2584_195-2575d others(12): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | ||||||
chr11:90144740 | T | TAAAAAAA others(4): Show |
9 | a0001c0002t0001g0324 a0001c0002t0005g0320 a0001c0002t0005g0326 others(6): Show |
9 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.195-2585_195-2575d others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | ||||||
chr11:90144740 | T | TAAAAAAA others(5): Show |
8 | a0001c0002t0001g0232 a0001c0002t0004g0256 a0001c0002t0004g0258 others(5): Show |
8 | HG01074.hp1 HG01081.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.195-2586_195-2575d others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | ||||||
chr11:90144740 | T | TAAAAAAA others(6): Show |
14 | a0001c0002t0001g0191 a0001c0002t0001g0221 a0001c0002t0001g0222 others(11): Show |
14 | HG00558.hp1 HG01109.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.195-2587_195-2575d others(15): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | ||||||
chr11:90144740 | T | TAAAAAAA others(7): Show |
36 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(33): Show |
46 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.195-2588_195-2575d others(16): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | ||||||
chr11:90144740 | T | TAAAAAAA others(8): Show |
18 | a0001c0002t0001g0185 a0001c0002t0001g0193 a0001c0002t0001g0194 others(15): Show |
18 | HG00621.hp1 HG00642.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-2589_195-2575d others(17): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | ||||||
chr11:90144740 | T | TAAAAAAA others(9): Show |
4 | a0003c0004t0005g0235 a0003c0004t0005g0236 a0003c0004t0005g0244 others(1): Show |
4 | HG00438.hp2 HG01346.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.195-2575_195-2574i others(18): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90144740 | ||||||
chr11:90144741 | A | T | 1 | a0001c0020t0002g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.195-2589A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144741 | |||||||
chr11:90144757 | G | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-2573G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144757 | |||||||
chr11:90144846 | G | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.195-2484G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144846 | |||||||
chr11:90144911 | G | A | 2 | a0001c0001t0002g0102 a0001c0001t0002g0149 |
2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.195-2419G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90144911 | |||||||
chr11:90145041 | T | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-2289T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145041 | |||||||
chr11:90145076 | G | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-2254G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145076 | |||||||
chr11:90145243 | C | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-2087C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145243 | |||||||
chr11:90145260 | T | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.195-2070T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145260 | |||||||
chr11:90145558 | T | C | 1 | a0001c0002t0001g0193 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.195-1772T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145558 | |||||||
chr11:90145636 | T | A | 1 | a0001c0002t0001g0193 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.195-1694T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145636 | |||||||
chr11:90145720 | G | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-1610G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145720 | |||||||
chr11:90145910 | A | G | 7 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(4): Show |
7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.195-1420A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145910 | |||||||
chr11:90145981 | T | G | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.195-1349T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90145981 | |||||||
chr11:90146028 | A | G | 1 | a0004c0005t0014g0252 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.195-1302A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146028 | |||||||
chr11:90146282 | T | TA | 8 | a0001c0001t0003g0062 a0001c0001t0003g0140 a0001c0006t0001g0300 others(5): Show |
8 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.195-1033dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146282 | ||||||
chr11:90146294 | A | G | 1 | a0001c0001t0003g0097 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.195-1036A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146294 | |||||||
chr11:90146343 | A | AT | 23 | a0001c0001t0002g0126 a0001c0001t0002g0145 a0001c0001t0002g0147 others(20): Show |
23 | HG00673.hp1 HG00735.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.195-954dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | ||||||
chr11:90146343 | AT | A | 53 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0055 others(50): Show |
54 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.195-954delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | ||||||
chr11:90146343 | ATTTTT | A | 32 | a0001c0002t0001g0309 a0001c0002t0001g0324 a0001c0002t0004g0257 others(29): Show |
32 | HG00544.hp2 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.195-958_195-954del others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | ||||||
chr11:90146343 | ATTTTTT | A | 54 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(51): Show |
57 | HG00323.hp1 HG00597.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.195-959_195-954del others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | ||||||
chr11:90146343 | ATTTTTTT | A | 22 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(19): Show |
23 | HG02280.hp1 HG02486.hp1 HG02683.hp2 others(20): Show |
intron_variant | MODIFIER | c.195-960_195-954del others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | ||||||
chr11:90146343 | ATTTTTTT others(1): Show |
A | 26 | a0001c0002t0001g0002 a0001c0002t0001g0186 a0001c0002t0001g0200 others(23): Show |
29 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.195-961_195-954del others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | ||||||
chr11:90146343 | ATTTTTTT others(2): Show |
A | 53 | a0001c0002t0001g0001 a0001c0002t0001g0013 a0001c0002t0001g0185 others(50): Show |
60 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.195-962_195-954del others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | ||||||
chr11:90146343 | ATTTTTTT others(9): Show |
A | 2 | a0001c0006t0004g0322 a0001c0006t0005g0323 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.195-969_195-954del others(16): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 90146343 | ||||||
chr11:90146513 | G | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-817G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146513 | |||||||
chr11:90146707 | C | T | 1 | a0012c0019t0006g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.195-623C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146707 | |||||||
chr11:90146936 | A | G | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.195-394A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146936 | |||||||
chr11:90146948 | A | G | 9 | a0001c0002t0005g0019 a0001c0002t0005g0326 a0001c0002t0005g0327 others(6): Show |
10 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-382A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90146948 | |||||||
chr11:90147065 | A | T | 14 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.195-265A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90147065 | |||||||
chr11:90147094 | T | G | 1 | a0003c0004t0005g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.195-236T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90147094 | |||||||
chr11:90147281 | C | A | 1 | a0002c0003t0001g0284 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.195-49C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90147281 | |||||||
chr11:90147301 | T | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.195-29T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 2/18 | chr11 | 90147301 | |||||||
chr11:90147537 | T | A | 1 | a0005c0007t0005g0311 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.381+21T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147537 | |||||||
chr11:90147663 | C | T | 3 | a0002c0003t0004g0261 a0002c0003t0005g0016 a0002c0003t0005g0262 |
4 | HG02145.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+147C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147663 | |||||||
chr11:90147677 | A | G | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.381+161A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147677 | |||||||
chr11:90147685 | T | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.381+169T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147685 | |||||||
chr11:90147687 | C | G | 2 | a0001c0002t0004g0046 a0001c0002t0004g0047 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.381+171C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147687 | |||||||
chr11:90147706 | A | T | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.381+190A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147706 | |||||||
chr11:90147794 | G | T | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.381+278G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147794 | |||||||
chr11:90147808 | G | A | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.381+292G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147808 | |||||||
chr11:90147929 | T | G | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.381+413T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90147929 | |||||||
chr11:90148003 | T | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.381+487T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148003 | |||||||
chr11:90148098 | C | T | 14 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.381+582C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148098 | |||||||
chr11:90148113 | G | A | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.381+597G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148113 | |||||||
chr11:90148118 | T | C | 2 | a0001c0001t0002g0064 a0001c0001t0002g0141 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.381+602T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148118 | |||||||
chr11:90148205 | C | T | 45 | a0001c0002t0004g0306 a0002c0003t0001g0017 a0002c0003t0001g0018 others(42): Show |
47 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.381+689C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148205 | |||||||
chr11:90148348 | T | C | 1 | a0001c0002t0004g0259 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.382-658T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148348 | |||||||
chr11:90148380 | G | A | 1 | a0001c0001t0002g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.382-626G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148380 | |||||||
chr11:90148463 | G | A | 1 | a0001c0001t0008g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.382-543G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148463 | |||||||
chr11:90148472 | G | A | 1 | a0003c0004t0005g0237 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.382-534G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148472 | |||||||
chr11:90148610 | C | T | 1 | a0002c0003t0004g0307 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.382-396C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148610 | |||||||
chr11:90148637 | A | T | 3 | a0004c0005t0004g0266 a0004c0005t0004g0267 a0004c0005t0004g0268 |
3 | HG02280.hp1 HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.382-369A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148637 | |||||||
chr11:90148647 | G | A | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382-359G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148647 | |||||||
chr11:90148723 | CA | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.382-275delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 90148723 | ||||||
chr11:90148738 | C | T | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.382-268C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148738 | |||||||
chr11:90148857 | C | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.382-149C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148857 | |||||||
chr11:90148887 | C | G | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0309 |
3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.382-119C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 3/18 | chr11 | 90148887 | |||||||
chr11:90149253 | C | T | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.483+146C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149253 | |||||||
chr11:90149291 | G | A | 2 | a0001c0002t0004g0023 a0001c0002t0004g0031 |
2 | HG01261.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.483+184G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149291 | |||||||
chr11:90149299 | G | C | 1 | a0002c0003t0001g0279 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.483+192G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149299 | |||||||
chr11:90149404 | G | T | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+297G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149404 | |||||||
chr11:90149464 | C | T | 14 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.483+357C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149464 | |||||||
chr11:90149465 | G | A | 1 | a0001c0001t0002g0154 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.483+358G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149465 | |||||||
chr11:90149487 | T | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.483+380T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149487 | |||||||
chr11:90149488 | G | C | 1 | a0001c0002t0001g0045 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.483+381G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149488 | |||||||
chr11:90149509 | C | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.483+402C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149509 | |||||||
chr11:90149587 | G | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.483+480G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149587 | |||||||
chr11:90149638 | A | G | 4 | a0003c0004t0005g0231 a0003c0004t0005g0235 a0003c0004t0005g0239 others(1): Show |
4 | HG01346.hp2 HG01934.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+531A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149638 | |||||||
chr11:90149728 | G | A | 6 | a0001c0001t0006g0053 a0001c0001t0006g0173 a0001c0001t0006g0176 others(3): Show |
6 | HG00735.hp1 HG00741.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+621G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149728 | |||||||
chr11:90149734 | G | A | 1 | a0002c0003t0004g0307 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.483+627G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90149734 | |||||||
chr11:90150203 | C | T | 2 | a0001c0002t0001g0324 a0001c0002t0004g0337 |
2 | HG01243.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.484-279C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90150203 | |||||||
chr11:90150236 | C | CAG | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.484-245_484-244dup others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 90150236 | ||||||
chr11:90150387 | A | C | 1 | a0001c0001t0002g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.484-95A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | chr11 | 90150387 | |||||||
chr11:90150427 | GTT | G | 191 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(188): Show |
205 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.484-45_484-44delTT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr11 | 90150427 | ||||||
chr11:90150622 | G | A | 2 | a0001c0001t0003g0009 a0001c0001t0013g0009 |
2 | NA18994.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.609+15G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90150622 | |||||||
chr11:90150632 | A | G | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.609+25A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90150632 | |||||||
chr11:90150717 | C | CT | 158 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(155): Show |
171 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.609+117dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 90150717 | ||||||
chr11:90150717 | C | CTT | 36 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(33): Show |
37 | HG00597.hp1 HG01074.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.609+116_609+117dup others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 90150717 | ||||||
chr11:90150725 | C | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.609+118C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90150725 | |||||||
chr11:90150773 | T | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.609+166T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90150773 | |||||||
chr11:90151090 | T | A | 178 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(175): Show |
192 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.609+483T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151090 | |||||||
chr11:90151144 | C | G | 1 | a0003c0004t0005g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.609+537C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151144 | |||||||
chr11:90151238 | C | T | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+631C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151238 | |||||||
chr11:90151246 | C | T | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.609+639C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151246 | |||||||
chr11:90151249 | A | G | 4 | a0001c0001t0003g0111 a0001c0001t0003g0124 a0001c0001t0003g0125 others(1): Show |
4 | HG00597.hp2 NA18747.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+642A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151249 | |||||||
chr11:90151272 | G | A | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+665G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151272 | |||||||
chr11:90151328 | T | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.609+721T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151328 | |||||||
chr11:90151341 | C | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.609+734C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151341 | |||||||
chr11:90151414 | C | T | 1 | a0001c0001t0003g0111 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.609+807C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151414 | |||||||
chr11:90151760 | G | A | 3 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 |
3 | HG01109.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.610-538G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151760 | |||||||
chr11:90151785 | A | T | 2 | a0001c0006t0004g0322 a0001c0006t0005g0323 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.610-513A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90151785 | |||||||
chr11:90152198 | G | A | 27 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(24): Show |
28 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(25): Show |
intron_variant | MODIFIER | c.610-100G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90152198 | |||||||
chr11:90152250 | C | G | 1 | a0001c0001t0002g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.610-48C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 5/18 | chr11 | 90152250 | |||||||
chr11:90152602 | A | C | 1 | a0001c0001t0002g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.796+118A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152602 | |||||||
chr11:90152618 | G | A | 1 | a0002c0003t0001g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.796+134G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152618 | |||||||
chr11:90152632 | A | T | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+148A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152632 | |||||||
chr11:90152635 | A | G | 7 | a0001c0002t0001g0254 a0001c0006t0001g0300 a0001c0006t0001g0301 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+151A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152635 | |||||||
chr11:90152783 | A | G | 46 | a0001c0002t0001g0309 a0001c0002t0004g0306 a0002c0003t0001g0017 others(43): Show |
48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.796+299A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152783 | |||||||
chr11:90152798 | A | G | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+314A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152798 | |||||||
chr11:90152802 | C | T | 1 | a0002c0003t0001g0279 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.796+318C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152802 | |||||||
chr11:90152854 | T | G | 2 | a0001c0002t0005g0328 a0001c0002t0005g0330 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.796+370T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152854 | |||||||
chr11:90152870 | C | CCGATAGA others(4): Show |
194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.796+386_796+387ins others(11): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152870 | |||||||
chr11:90152878 | A | T | 1 | a0001c0001t0006g0182 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.796+394A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152878 | |||||||
chr11:90152927 | A | G | 1 | a0001c0002t0004g0306 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.796+443A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152927 | |||||||
chr11:90152983 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.796+499G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90152983 | |||||||
chr11:90153116 | G | A | 96 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(93): Show |
107 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.796+632G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153116 | |||||||
chr11:90153151 | C | G | 4 | a0001c0002t0004g0256 a0001c0002t0004g0257 a0001c0002t0004g0258 others(1): Show |
4 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+667C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153151 | |||||||
chr11:90153229 | C | T | 96 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(93): Show |
107 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.796+745C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153229 | |||||||
chr11:90153430 | A | G | 2 | a0001c0006t0004g0322 a0001c0006t0005g0323 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796+946A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153430 | |||||||
chr11:90153525 | G | A | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.796+1041G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153525 | |||||||
chr11:90153637 | G | A | 1 | a0005c0007t0001g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.796+1153G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153637 | |||||||
chr11:90153642 | G | C | 1 | a0004c0005t0004g0249 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.796+1158G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153642 | |||||||
chr11:90153786 | T | G | 46 | a0001c0002t0001g0309 a0001c0002t0004g0306 a0002c0003t0001g0017 others(43): Show |
48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.796+1302T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90153786 | |||||||
chr11:90154030 | CCT | C | 194 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(191): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.796+1569_796+1570d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154030 | ||||||
chr11:90154030 | CCTCT | C | 117 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(114): Show |
128 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.796+1567_796+1570d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154030 | ||||||
chr11:90154030 | CCTCTCT | C | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.796+1565_796+1570d others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154030 | ||||||
chr11:90154051 | C | G | 2 | a0001c0002t0001g0232 a0001c0002t0001g0233 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.796+1567C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154051 | |||||||
chr11:90154065 | CTCTT | C | 65 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(62): Show |
75 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.796+1593_796+1596d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154065 | ||||||
chr11:90154073 | T | G | 31 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(28): Show |
32 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(29): Show |
intron_variant | MODIFIER | c.796+1589T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154073 | |||||||
chr11:90154126 | C | T | 1 | a0001c0020t0002g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.796+1642C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154126 | |||||||
chr11:90154154 | C | T | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.796+1670C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154154 | |||||||
chr11:90154192 | G | A | 1 | a0005c0007t0005g0310 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.796+1708G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154192 | |||||||
chr11:90154280 | G | C | 16 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(13): Show |
16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.796+1796G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154280 | |||||||
chr11:90154316 | T | G | 53 | a0001c0002t0001g0004 a0001c0002t0001g0024 a0001c0002t0001g0025 others(50): Show |
56 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.796+1832T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154316 | |||||||
chr11:90154324 | T | C | 46 | a0001c0002t0001g0309 a0001c0002t0004g0306 a0002c0003t0001g0017 others(43): Show |
48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.796+1840T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154324 | |||||||
chr11:90154478 | A | G | 1 | a0001c0001t0003g0097 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.796+1994A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154478 | |||||||
chr11:90154676 | T | G | 27 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(24): Show |
28 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+2192T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154676 | |||||||
chr11:90154773 | G | C | 2 | a0001c0002t0001g0202 a0001c0002t0001g0221 |
2 | NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.796+2289G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154773 | |||||||
chr11:90154830 | G | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.796+2346G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154830 | |||||||
chr11:90154842 | A | C | 14 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.796+2358A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154842 | |||||||
chr11:90154854 | AATATGTA others(73): Show |
A | 2 | a0004c0005t0001g0247 a0004c0005t0005g0248 |
2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.796+2403_796+2482d others(82): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154854 | ||||||
chr11:90154859 | G | A | 2 | a0001c0002t0004g0255 a0001c0002t0004g0259 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.796+2375G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154859 | |||||||
chr11:90154866 | T | G | 61 | a0001c0002t0001g0309 a0001c0002t0004g0306 a0001c0002t0004g0337 others(58): Show |
64 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.796+2382T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154866 | |||||||
chr11:90154873 | C | T | 1 | a0001c0001t0006g0174 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.796+2389C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154873 | |||||||
chr11:90154874 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.796+2390G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154874 | |||||||
chr11:90154879 | C | A | 1 | a0004c0005t0005g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.796+2395C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154879 | |||||||
chr11:90154882 | AAT | A | 165 | a0001c0001t0003g0077 a0001c0002t0001g0001 a0001c0002t0001g0002 others(162): Show |
178 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.796+2403_796+2404d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154882 | ||||||
chr11:90154882 | AATAT | A | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.796+2401_796+2404d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154882 | ||||||
chr11:90154882 | AATATATG others(45): Show |
A | 13 | a0002c0003t0004g0261 a0002c0003t0005g0262 a0004c0005t0001g0253 others(10): Show |
13 | HG02145.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.796+2403_796+2454d others(54): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154882 | ||||||
chr11:90154884 | T | TATATGTA others(18): Show |
2 | a0001c0001t0002g0073 a0001c0001t0003g0067 |
2 | NA18944.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.796+2454_796+2478d others(27): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154884 | ||||||
chr11:90154884 | TATATGTA others(18): Show |
T | 2 | a0001c0001t0003g0083 a0001c0001t0003g0090 |
2 | NA18977.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.796+2454_796+2478d others(27): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154884 | ||||||
chr11:90154896 | T | G | 1 | a0002c0003t0001g0305 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.796+2412T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154896 | |||||||
chr11:90154903 | C | T | 1 | a0001c0002t0004g0260 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.796+2419C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154903 | |||||||
chr11:90154909 | C | CATA | 105 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(102): Show |
116 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.796+2426_796+2428d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154909 | ||||||
chr11:90154909 | C | CATAAT | 13 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0076 others(10): Show |
13 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.796+2428_796+2429i others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154909 | ||||||
chr11:90154912 | ATGTATAT others(13): Show |
A | 14 | a0001c0002t0001g0037 a0001c0002t0001g0324 a0001c0002t0004g0255 others(11): Show |
14 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.796+2429_796+2448d others(22): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154912 | |||||||
chr11:90154912 | ATGTATAT others(15): Show |
A | 56 | a0001c0002t0004g0306 a0001c0002t0004g0337 a0001c0002t0005g0019 others(53): Show |
59 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.796+2429_796+2450d others(24): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154912 | |||||||
chr11:90154934 | C | CATA | 100 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(97): Show |
111 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.796+2451_796+2453d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154934 | ||||||
chr11:90154934 | C | CATAAT | 10 | a0001c0001t0003g0077 a0001c0002t0001g0028 a0001c0002t0001g0041 others(7): Show |
10 | HG01192.hp2 HG02922.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.796+2453_796+2454i others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154934 | ||||||
chr11:90154934 | C | CATATGTA others(21): Show |
1 | a0001c0001t0003g0092 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.796+2487_796+2514d others(30): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154934 | ||||||
chr11:90154934 | C | T | 14 | a0001c0002t0001g0037 a0001c0002t0001g0324 a0001c0002t0004g0255 others(11): Show |
14 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.796+2450C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154934 | |||||||
chr11:90154959 | CATA | C | 9 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0076 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2479_796+2481d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154959 | ||||||
chr11:90154962 | A | AAT | 120 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(117): Show |
124 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.796+2481_796+2482d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154962 | ||||||
chr11:90154993 | ATGTATG | A | 121 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(118): Show |
125 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.796+2513_796+2518d others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154993 | ||||||
chr11:90154993 | ATGTATGT others(1): Show |
A | 9 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0076 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2515_796+2522d others(10): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154993 | ||||||
chr11:90154995 | G | A | 4 | a0001c0002t0001g0027 a0001c0002t0001g0036 a0001c0002t0007g0020 others(1): Show |
4 | HG02451.hp2 NA18956.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+2511G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154995 | |||||||
chr11:90154996 | T | TATATATT others(15): Show |
1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.796+2514_796+2515i others(24): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | ||||||
chr11:90154996 | T | TATATATT others(71): Show |
1 | a0001c0002t0007g0014 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.796+2514_796+2515i others(80): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | ||||||
chr11:90154996 | T | TATATATT others(99): Show |
7 | a0001c0002t0001g0001 a0001c0002t0001g0204 a0001c0002t0001g0216 others(4): Show |
7 | HG00438.hp1 HG02165.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+2514_796+2515i others(108): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | ||||||
chr11:90154996 | T | TATATATT others(129): Show |
1 | a0003c0004t0005g0238 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.796+2514_796+2515i others(138): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | ||||||
chr11:90154996 | T | TATATATT others(127): Show |
35 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(32): Show |
43 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.796+2514_796+2515i others(136): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | ||||||
chr11:90154996 | T | TATATATT others(157): Show |
8 | a0001c0002t0001g0193 a0003c0004t0005g0231 a0003c0004t0005g0236 others(5): Show |
8 | HG00438.hp2 HG01934.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.796+2514_796+2515i others(166): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | ||||||
chr11:90154996 | T | TATATATT others(187): Show |
2 | a0001c0002t0001g0232 a0003c0004t0005g0245 |
2 | HG03139.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.796+2514_796+2515i others(196): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | ||||||
chr11:90154996 | T | TATATATT others(155): Show |
6 | a0001c0002t0001g0197 a0001c0002t0001g0203 a0001c0002t0001g0209 others(3): Show |
6 | HG00642.hp1 HG01943.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.796+2514_796+2515i others(164): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | ||||||
chr11:90154996 | T | TATATATT others(185): Show |
3 | a0001c0002t0001g0233 a0001c0002t0001g0309 a0003c0004t0005g0235 |
3 | HG01346.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.796+2514_796+2515i others(194): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | ||||||
chr11:90154996 | T | TATATATT others(183): Show |
3 | a0001c0002t0001g0208 a0003c0004t0001g0242 a0003c0004t0005g0241 |
3 | HG01175.hp2 HG01256.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.796+2514_796+2515i others(192): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | ||||||
chr11:90154996 | T | TATATATT others(211): Show |
1 | a0001c0002t0005g0201 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.796+2514_796+2515i others(220): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90154996 | ||||||
chr11:90154996 | T | TGTATATA others(17): Show |
3 | a0001c0002t0001g0027 a0001c0002t0001g0036 a0001c0002t0007g0020 |
3 | NA18956.hp2 NA18968.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.796+2512_796+2513i others(26): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154996 | |||||||
chr11:90154998 | T | TATATTAT others(13): Show |
1 | a0001c0002t0004g0206 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.796+2514_796+2515i others(22): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154998 | |||||||
chr11:90154998 | T | TATATTAT others(97): Show |
1 | a0001c0002t0001g0198 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.796+2514_796+2515i others(106): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154998 | |||||||
chr11:90154998 | T | TATATTAT others(125): Show |
1 | a0001c0002t0001g0226 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.796+2514_796+2515i others(134): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154998 | |||||||
chr11:90154999 | G | A | 72 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(69): Show |
82 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.796+2515G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90154999 | |||||||
chr11:90155001 | G | A | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.796+2517G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155001 | |||||||
chr11:90155018 | A | G | 203 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0076 others(200): Show |
217 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.796+2534A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155018 | |||||||
chr11:90155026 | A | AAT | 13 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(10): Show |
13 | HG02280.hp1 HG02486.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.796+2545_796+2546d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155026 | ||||||
chr11:90155026 | AATATGTA others(69): Show |
A | 6 | a0001c0001t0002g0048 a0001c0001t0002g0054 a0001c0001t0002g0138 others(3): Show |
6 | HG02615.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.796+2567_796+2642d others(78): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155026 | ||||||
chr11:90155029 | A | G | 1 | a0004c0005t0004g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.796+2545A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155029 | |||||||
chr11:90155031 | G | A | 1 | a0004c0005t0004g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.796+2547G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155031 | |||||||
chr11:90155031 | GTATA | G | 9 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0076 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2551_796+2554d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155031 | ||||||
chr11:90155037 | A | G | 1 | a0004c0005t0004g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.796+2553A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155037 | |||||||
chr11:90155043 | GTATATAT others(32): Show |
G | 1 | a0004c0005t0004g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.796+2574_796+2612d others(41): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155043 | ||||||
chr11:90155058 | A | G | 14 | a0001c0002t0001g0002 a0004c0005t0001g0247 a0004c0005t0001g0253 others(11): Show |
14 | HG02280.hp1 HG02300.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.796+2574A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155058 | |||||||
chr11:90155059 | T | TATACATA others(16): Show |
1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.796+2591_796+2592i others(25): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155059 | ||||||
chr11:90155061 | T | C | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.796+2577T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155061 | |||||||
chr11:90155066 | ATGTATAT others(4): Show |
A | 9 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0076 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2583_796+2593d others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155066 | |||||||
chr11:90155074 | ATG | A | 11 | a0001c0002t0004g0046 a0001c0002t0004g0047 a0005c0007t0001g0317 others(8): Show |
11 | HG01081.hp1 HG02717.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.796+2596_796+2597d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155074 | ||||||
chr11:90155082 | A | G | 12 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0076 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.796+2598A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155082 | |||||||
chr11:90155088 | ATT | A | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0309 |
3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.796+2605_796+2606d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155088 | |||||||
chr11:90155097 | G | A | 9 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0076 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2613G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155097 | |||||||
chr11:90155102 | C | CATA | 9 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0076 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+2619_796+2621d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155102 | ||||||
chr11:90155134 | G | A | 1 | a0005c0007t0001g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.796+2650G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155134 | |||||||
chr11:90155186 | GTA | G | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.796+2708_796+2709d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155186 | ||||||
chr11:90155200 | A | G | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.796+2716A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155200 | |||||||
chr11:90155230 | G | T | 2 | a0001c0001t0002g0064 a0001c0001t0002g0141 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.796+2746G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155230 | |||||||
chr11:90155256 | A | C | 1 | a0001c0002t0001g0030 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.796+2772A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155256 | |||||||
chr11:90155283 | TATGCATA others(4): Show |
T | 1 | a0001c0006t0005g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.796+2800_796+2810d others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155283 | |||||||
chr11:90155305 | G | GTATATAT others(24): Show |
2 | a0001c0006t0004g0322 a0001c0006t0005g0323 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796+2829_797-2802d others(33): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155305 | ||||||
chr11:90155316 | A | G | 1 | a0012c0019t0006g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.797-2829A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155316 | |||||||
chr11:90155336 | TTATA | T | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.797-2803_797-2800d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155336 | ||||||
chr11:90155352 | TTA | T | 49 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(46): Show |
59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2792_797-2791d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155352 | |||||||
chr11:90155353 | T | A | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG00140.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.797-2792T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155353 | |||||||
chr11:90155355 | C | A | 51 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(48): Show |
61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.797-2790C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155355 | |||||||
chr11:90155358 | G | A | 49 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(46): Show |
59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2787G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155358 | |||||||
chr11:90155364 | T | TATGTAAT others(35): Show |
1 | a0001c0001t0002g0152 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.797-2740_797-2699d others(44): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155364 | ||||||
chr11:90155364 | TATGTAAT others(35): Show |
T | 30 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(27): Show |
30 | HG00438.hp2 HG01074.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.797-2740_797-2699d others(44): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155364 | ||||||
chr11:90155365 | A | G | 49 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(46): Show |
59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2780A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155365 | |||||||
chr11:90155367 | G | A | 51 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(48): Show |
61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.797-2778G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155367 | |||||||
chr11:90155372 | A | T | 49 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(46): Show |
59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2773A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155372 | |||||||
chr11:90155373 | T | A | 49 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(46): Show |
59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2772T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155373 | |||||||
chr11:90155376 | C | T | 51 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(48): Show |
61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.797-2769C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155376 | |||||||
chr11:90155381 | T | A | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG00140.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.797-2764T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155381 | |||||||
chr11:90155385 | C | A | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG00140.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.797-2760C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155385 | |||||||
chr11:90155385 | C | T | 49 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(46): Show |
59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2760C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155385 | |||||||
chr11:90155388 | G | T | 49 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(46): Show |
59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2757G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155388 | |||||||
chr11:90155389 | T | A | 49 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(46): Show |
59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2756T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155389 | |||||||
chr11:90155390 | A | C | 49 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(46): Show |
59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2755A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155390 | |||||||
chr11:90155393 | A | G | 49 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(46): Show |
59 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.797-2752A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155393 | |||||||
chr11:90155395 | A | G | 3 | a0001c0001t0002g0066 a0001c0001t0002g0080 a0001c0001t0002g0139 |
3 | HG01243.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.797-2750A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155395 | |||||||
chr11:90155398 | A | T | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG00140.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.797-2747A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155398 | |||||||
chr11:90155399 | TATATATA | T | 52 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(49): Show |
62 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.797-2743_797-2737d others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155399 | ||||||
chr11:90155402 | A | G | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.797-2743A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155402 | |||||||
chr11:90155405 | T | A | 110 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(107): Show |
114 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.797-2740T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155405 | |||||||
chr11:90155405 | T | TTACATGT others(4): Show |
2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG00140.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.797-2740_797-2739i others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155405 | |||||||
chr11:90155406 | A | T | 112 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(109): Show |
116 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.797-2739A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155406 | |||||||
chr11:90155430 | GTAATATA | G | 7 | a0004c0005t0004g0264 a0004c0005t0004g0265 a0004c0005t0004g0266 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.797-2701_797-2695d others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155430 | ||||||
chr11:90155437 | A | ATAATATG others(21): Show |
7 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(4): Show |
7 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.797-2702_797-2701i others(30): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155437 | ||||||
chr11:90155443 | TATA | T | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.797-2698_797-2696d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155443 | ||||||
chr11:90155444 | A | G | 1 | a0001c0001t0009g0110 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.797-2701A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155444 | |||||||
chr11:90155459 | T | A | 16 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(13): Show |
16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-2686T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155459 | |||||||
chr11:90155471 | T | C | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.797-2674T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155471 | |||||||
chr11:90155472 | A | G | 1 | a0001c0001t0012g0109 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.797-2673A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155472 | |||||||
chr11:90155473 | C | A | 7 | a0002c0003t0001g0269 a0002c0003t0001g0288 a0002c0003t0001g0290 others(4): Show |
7 | HG01192.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.797-2672C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155473 | |||||||
chr11:90155477 | TATATATT others(7): Show |
T | 1 | a0001c0002t0007g0038 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.797-2651_797-2638d others(16): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155477 | ||||||
chr11:90155492 | ATATAT | A | 3 | a0001c0002t0001g0254 a0004c0005t0004g0266 a0004c0005t0004g0267 |
3 | HG02280.hp1 HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.797-2647_797-2643d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155492 | ||||||
chr11:90155538 | T | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.797-2607T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155538 | |||||||
chr11:90155547 | A | C | 2 | a0001c0001t0008g0123 a0001c0001t0012g0109 |
2 | HG00558.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.797-2598A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155547 | |||||||
chr11:90155566 | TA | T | 6 | a0004c0005t0004g0264 a0004c0005t0004g0265 a0004c0005t0004g0266 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.797-2577delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155566 | ||||||
chr11:90155573 | TAA | T | 19 | a0001c0001t0002g0175 a0001c0001t0003g0180 a0001c0001t0006g0012 others(16): Show |
20 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.797-2571_797-2570d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155573 | |||||||
chr11:90155574 | AAT | A | 17 | a0001c0001t0003g0151 a0001c0002t0001g0324 a0001c0002t0004g0255 others(14): Show |
17 | HG01074.hp1 HG01081.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.797-2564_797-2563d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155574 | ||||||
chr11:90155590 | ATATG | A | 16 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(13): Show |
16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-2552_797-2549d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155590 | ||||||
chr11:90155592 | ATG | A | 177 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(174): Show |
191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.797-2551_797-2550d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155592 | ||||||
chr11:90155594 | G | A | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.797-2551G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155594 | |||||||
chr11:90155600 | A | G | 65 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(62): Show |
75 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.797-2545A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155600 | |||||||
chr11:90155610 | CATATAAA others(14): Show |
C | 38 | a0001c0002t0004g0306 a0002c0003t0001g0017 a0002c0003t0001g0018 others(35): Show |
40 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.797-2529_797-2509d others(23): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155610 | ||||||
chr11:90155610 | CATATAAA others(16): Show |
C | 7 | a0002c0003t0001g0269 a0002c0003t0001g0288 a0002c0003t0001g0290 others(4): Show |
7 | HG01192.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.797-2529_797-2507d others(25): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155610 | ||||||
chr11:90155621 | CATATATA others(3): Show |
C | 128 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(125): Show |
139 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.797-2515_797-2506d others(12): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155621 | ||||||
chr11:90155621 | CATATATA others(5): Show |
C | 20 | a0001c0002t0001g0254 a0001c0002t0004g0255 a0001c0002t0004g0256 others(17): Show |
21 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.797-2515_797-2504d others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155621 | ||||||
chr11:90155630 | T | G | 1 | a0003c0004t0005g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.797-2515T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155630 | |||||||
chr11:90155631 | A | T | 1 | a0003c0004t0005g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.797-2514A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155631 | |||||||
chr11:90155655 | GTATGTAT others(42): Show |
G | 1 | a0004c0005t0004g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.797-2486_797-2438d others(51): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155655 | ||||||
chr11:90155659 | GTAT | G | 8 | a0001c0002t0001g0217 a0001c0006t0001g0300 a0001c0006t0001g0301 others(5): Show |
8 | HG00609.hp2 HG01109.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.797-2478_797-2476d others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155659 | ||||||
chr11:90155659 | GTATTATT others(38): Show |
G | 178 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(175): Show |
192 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.797-2478_797-2434d others(47): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155659 | ||||||
chr11:90155665 | TTATTGTA others(42): Show |
T | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.797-2478_797-2430d others(51): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155665 | ||||||
chr11:90155674 | GTATGTAA others(54): Show |
G | 1 | a0001c0002t0001g0217 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.797-2464_797-2404d others(63): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155674 | ||||||
chr11:90155691 | ACATATGT others(12): Show |
A | 1 | a0002c0003t0001g0302 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.797-2453_797-2435d others(21): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155691 | |||||||
chr11:90155704 | TTATTATT others(12): Show |
T | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.797-2438_797-2420d others(21): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155704 | ||||||
chr11:90155733 | A | T | 5 | a0001c0002t0001g0189 a0001c0002t0001g0190 a0001c0002t0001g0191 others(2): Show |
5 | HG00558.hp1 NA18982.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.797-2412A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155733 | |||||||
chr11:90155734 | C | T | 170 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(167): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.797-2411C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155734 | |||||||
chr11:90155735 | A | G | 170 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(167): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.797-2410A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155735 | |||||||
chr11:90155753 | A | T | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(65): Show |
78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.797-2392A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155753 | |||||||
chr11:90155758 | T | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-2387T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155758 | |||||||
chr11:90155842 | A | G | 5 | a0001c0002t0001g0214 a0001c0006t0001g0300 a0001c0006t0001g0301 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.797-2303A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155842 | |||||||
chr11:90155843 | TGTTA | T | 5 | a0001c0002t0001g0214 a0001c0006t0001g0300 a0001c0006t0001g0301 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.797-2301_797-2298d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155843 | |||||||
chr11:90155845 | TTA | T | 188 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(185): Show |
202 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.797-2292_797-2291d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155845 | ||||||
chr11:90155847 | A | ATATATTA others(37): Show |
1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.797-2293_797-2292i others(46): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155847 | ||||||
chr11:90155854 | T | TTATATTA others(27): Show |
2 | a0001c0001t0003g0082 a0001c0001t0003g0092 |
2 | HG02698.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.797-2278_797-2245d others(36): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155854 | ||||||
chr11:90155877 | G | A | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.797-2268G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155877 | |||||||
chr11:90155877 | GTATATGT others(32): Show |
G | 1 | a0001c0006t0005g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.797-2257_797-2219d others(41): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90155877 | ||||||
chr11:90155885 | A | T | 46 | a0001c0002t0001g0309 a0001c0002t0004g0306 a0002c0003t0001g0017 others(43): Show |
48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.797-2260A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155885 | |||||||
chr11:90155929 | A | G | 16 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(13): Show |
16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-2216A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155929 | |||||||
chr11:90155933 | G | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-2212G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90155933 | |||||||
chr11:90156030 | G | T | 1 | a0001c0001t0002g0073 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.797-2115G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156030 | |||||||
chr11:90156044 | T | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-2101T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156044 | |||||||
chr11:90156048 | C | G | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.797-2097C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156048 | |||||||
chr11:90156188 | T | A | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.797-1957T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156188 | |||||||
chr11:90156205 | A | C | 14 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.797-1940A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156205 | |||||||
chr11:90156270 | C | T | 16 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(13): Show |
16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-1875C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156270 | |||||||
chr11:90156301 | A | G | 2 | a0001c0001t0008g0123 a0001c0001t0012g0109 |
2 | HG00558.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.797-1844A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156301 | |||||||
chr11:90156501 | G | A | 1 | a0001c0001t0008g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.797-1644G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156501 | |||||||
chr11:90156693 | C | G | 6 | a0001c0002t0004g0255 a0001c0002t0004g0256 a0001c0002t0004g0257 others(3): Show |
6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.797-1452C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156693 | |||||||
chr11:90156737 | A | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-1408A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156737 | |||||||
chr11:90156876 | A | C | 14 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.797-1269A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156876 | |||||||
chr11:90156924 | T | G | 3 | a0001c0001t0002g0055 a0001c0001t0002g0057 a0001c0001t0002g0155 |
3 | HG00099.hp2 HG01106.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.797-1221T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156924 | |||||||
chr11:90156966 | G | A | 1 | a0001c0002t0001g0203 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.797-1179G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90156966 | |||||||
chr11:90157049 | A | C | 1 | a0001c0002t0001g0213 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.797-1096A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157049 | |||||||
chr11:90157075 | G | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-1070G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157075 | |||||||
chr11:90157365 | C | A | 2 | a0001c0006t0004g0322 a0001c0006t0005g0323 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.797-780C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157365 | |||||||
chr11:90157367 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.797-778A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157367 | |||||||
chr11:90157367 | A | T | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.797-778A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157367 | |||||||
chr11:90157506 | C | G | 1 | a0001c0002t0004g0259 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.797-639C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157506 | |||||||
chr11:90157560 | A | G | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.797-585A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157560 | |||||||
chr11:90157691 | A | G | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-454A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157691 | |||||||
chr11:90157728 | C | CT | 191 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(188): Show |
205 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.797-406dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | 90157728 | ||||||
chr11:90157878 | G | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.797-267G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157878 | |||||||
chr11:90157996 | G | T | 1 | a0001c0006t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.797-149G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90157996 | |||||||
chr11:90158010 | C | T | 14 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.797-135C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90158010 | |||||||
chr11:90158023 | A | G | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.797-122A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | chr11 | 90158023 | |||||||
chr11:90158333 | A | G | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.890+95A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90158333 | |||||||
chr11:90158371 | C | T | 1 | a0006c0008t0004g0295 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.890+133C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90158371 | |||||||
chr11:90158558 | G | A | 6 | a0001c0002t0004g0255 a0001c0002t0004g0256 a0001c0002t0004g0257 others(3): Show |
6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.890+320G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90158558 | |||||||
chr11:90158599 | G | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.890+361G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90158599 | |||||||
chr11:90159041 | A | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.891-198A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159041 | |||||||
chr11:90159082 | T | G | 177 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(174): Show |
191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.891-157T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159082 | |||||||
chr11:90159098 | C | T | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.891-141C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159098 | |||||||
chr11:90159113 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.891-126T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159113 | |||||||
chr11:90159123 | T | G | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.891-116T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159123 | |||||||
chr11:90159131 | T | C | 2 | a0001c0001t0002g0064 a0001c0001t0002g0141 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.891-108T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159131 | |||||||
chr11:90159141 | T | C | 1 | a0001c0006t0001g0301 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.891-98T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 7/18 | chr11 | 90159141 | |||||||
chr11:90159359 | A | C | 3 | a0001c0001t0006g0012 a0001c0001t0006g0171 a0001c0001t0006g0172 |
4 | HG00140.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.989+22A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159359 | |||||||
chr11:90159391 | C | T | 14 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.989+54C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159391 | |||||||
chr11:90159407 | TTCTGCCA | T | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.989+71_989+77delTC others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159407 | |||||||
chr11:90159413 | C | T | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.989+76C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159413 | |||||||
chr11:90159452 | A | G | 2 | a0001c0006t0004g0322 a0001c0006t0005g0323 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.989+115A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159452 | |||||||
chr11:90159552 | A | G | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.989+215A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159552 | |||||||
chr11:90159635 | A | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.989+298A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159635 | |||||||
chr11:90159679 | T | C | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.989+342T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159679 | |||||||
chr11:90159680 | G | A | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.989+343G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159680 | |||||||
chr11:90159725 | C | T | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.989+388C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159725 | |||||||
chr11:90159776 | C | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.989+439C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159776 | |||||||
chr11:90159916 | T | TGCACTTG others(65): Show |
2 | a0003c0004t0001g0242 a0003c0004t0005g0244 |
2 | HG01175.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.989+637_989+638ins others(72): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159916 | ||||||
chr11:90159936 | A | G | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.989+599A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90159936 | |||||||
chr11:90159953 | T | TA | 10 | a0001c0001t0002g0064 a0001c0001t0002g0142 a0001c0001t0002g0156 others(7): Show |
10 | HG00673.hp1 HG00738.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.989+639dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159953 | ||||||
chr11:90159953 | TA | T | 24 | a0001c0001t0002g0134 a0001c0001t0003g0051 a0001c0001t0003g0072 others(21): Show |
24 | HG01069.hp2 HG01081.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.989+639delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159953 | ||||||
chr11:90159953 | TAA | T | 84 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(81): Show |
87 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.989+638_989+639del others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159953 | ||||||
chr11:90159953 | TAAA | T | 15 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(12): Show |
16 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.989+637_989+639del others(3): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159953 | ||||||
chr11:90159954 | A | AAAAAAAA others(65): Show |
1 | a0001c0002t0001g0214 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.989+638_989+639ins others(72): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159954 | ||||||
chr11:90159954 | A | AAAAAAAA others(64): Show |
5 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0219 others(2): Show |
5 | HG00673.hp2 HG01109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.989+637_989+638ins others(71): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159954 | ||||||
chr11:90159955 | A | AAAAAAAA others(64): Show |
3 | a0001c0002t0001g0210 a0001c0002t0001g0217 a0001c0002t0001g0222 |
3 | HG00609.hp2 HG01257.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.989+638_989+639ins others(71): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159955 | ||||||
chr11:90159955 | A | AAAAAAAA others(63): Show |
53 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(50): Show |
61 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.989+637_989+638ins others(70): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159955 | ||||||
chr11:90159955 | A | AAAAAAAA others(62): Show |
1 | a0001c0002t0001g0208 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.989+636_989+637ins others(69): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159955 | ||||||
chr11:90159955 | A | AAAAAAAA others(63): Show |
2 | a0001c0002t0001g0202 a0001c0002t0001g0221 |
2 | NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.989+627_989+628ins others(70): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159955 | ||||||
chr11:90159956 | A | AAAAAAAA others(62): Show |
3 | a0001c0002t0001g0190 a0001c0002t0001g0212 a0003c0004t0005g0239 |
3 | HG00323.hp2 NA18957.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.989+637_989+638ins others(69): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90159956 | ||||||
chr11:90160057 | G | T | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.989+720G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160057 | |||||||
chr11:90160087 | A | G | 1 | a0001c0001t0003g0095 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.989+750A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160087 | |||||||
chr11:90160352 | A | C | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.989+1015A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160352 | |||||||
chr11:90160441 | C | T | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.989+1104C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160441 | |||||||
chr11:90160796 | A | T | 1 | a0009c0018t0006g0178 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.989+1459A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160796 | |||||||
chr11:90160836 | A | G | 178 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(175): Show |
192 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.989+1499A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160836 | |||||||
chr11:90160926 | C | A | 1 | a0001c0002t0001g0228 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.989+1589C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160926 | |||||||
chr11:90160927 | A | C | 1 | a0001c0002t0001g0228 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.989+1590A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160927 | |||||||
chr11:90160928 | T | A | 1 | a0001c0002t0001g0228 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.989+1591T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160928 | |||||||
chr11:90160971 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.989+1634C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90160971 | |||||||
chr11:90161013 | T | G | 2 | a0001c0002t0001g0027 a0001c0002t0001g0032 |
2 | NA18968.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.989+1676T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161013 | |||||||
chr11:90161052 | T | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.989+1715T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161052 | |||||||
chr11:90161126 | G | C | 65 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(62): Show |
75 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.989+1789G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161126 | |||||||
chr11:90161165 | C | G | 1 | a0001c0001t0002g0161 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.990-1784C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161165 | |||||||
chr11:90161171 | C | T | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.990-1778C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161171 | |||||||
chr11:90161351 | G | A | 2 | a0001c0002t0004g0023 a0001c0002t0004g0031 |
2 | HG01261.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.990-1598G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161351 | |||||||
chr11:90161416 | T | C | 1 | a0008c0010t0004g0316 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.990-1533T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161416 | |||||||
chr11:90161435 | A | G | 6 | a0001c0002t0004g0255 a0001c0002t0004g0256 a0001c0002t0004g0257 others(3): Show |
6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.990-1514A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161435 | |||||||
chr11:90161504 | G | A | 1 | a0001c0002t0001g0021 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.990-1445G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161504 | |||||||
chr11:90161523 | C | A | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.990-1426C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161523 | |||||||
chr11:90161642 | C | T | 9 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(6): Show |
9 | HG01081.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.990-1307C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161642 | |||||||
chr11:90161833 | A | G | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.990-1116A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161833 | |||||||
chr11:90161857 | C | T | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.990-1092C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161857 | |||||||
chr11:90161925 | GA | G | 196 | a0001c0001t0002g0048 a0001c0001t0002g0054 a0001c0001t0002g0081 others(193): Show |
210 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.990-1011delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90161925 | ||||||
chr11:90161941 | T | A | 1 | a0001c0002t0001g0228 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.990-1008T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161941 | |||||||
chr11:90161978 | T | C | 1 | a0005c0007t0005g0311 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.990-971T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90161978 | |||||||
chr11:90162086 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.990-863A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162086 | |||||||
chr11:90162359 | G | A | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.990-590G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162359 | |||||||
chr11:90162401 | G | T | 1 | a0002c0003t0001g0287 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.990-548G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162401 | |||||||
chr11:90162466 | T | C | 2 | a0001c0006t0004g0322 a0001c0006t0005g0323 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.990-483T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162466 | |||||||
chr11:90162475 | A | C | 3 | a0001c0001t0002g0066 a0001c0001t0002g0080 a0001c0001t0002g0139 |
3 | HG01243.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.990-474A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162475 | |||||||
chr11:90162682 | A | T | 14 | a0004c0005t0001g0247 a0004c0005t0001g0253 a0004c0005t0004g0249 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.990-267A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162682 | |||||||
chr11:90162772 | A | G | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.990-177A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162772 | |||||||
chr11:90162780 | C | T | 1 | a0004c0005t0004g0267 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.990-169C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162780 | |||||||
chr11:90162851 | C | CATAATAA others(25): Show |
2 | a0001c0001t0006g0174 a0001c0001t0006g0179 |
2 | HG00738.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.990-84_990-53dupAT others(30): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 90162851 | ||||||
chr11:90162873 | A | G | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.990-76A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 8/18 | chr11 | 90162873 | |||||||
chr11:90163249 | A | G | 65 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(62): Show |
75 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1076-61A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 9/18 | chr11 | 90163249 | |||||||
chr11:90163289 | C | T | 231 | a0001c0001t0002g0048 a0001c0001t0002g0054 a0001c0001t0002g0065 others(228): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1076-21C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 9/18 | chr11 | 90163289 | |||||||
chr11:90163448 | C | A | 1 | a0001c0001t0002g0113 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1195+19C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 10/18 | chr11 | 90163448 | |||||||
chr11:90163449 | T | A | 1 | a0001c0001t0002g0113 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1195+20T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 10/18 | chr11 | 90163449 | |||||||
chr11:90163472 | A | C | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1195+43A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 10/18 | chr11 | 90163472 | |||||||
chr11:90163514 | G | A | 1 | a0001c0001t0003g0180 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1196-21G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 10/18 | chr11 | 90163514 | |||||||
chr11:90164026 | T | A | 2 | a0001c0001t0008g0105 a0001c0001t0008g0114 |
2 | NA18940.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1278+409T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90164026 | |||||||
chr11:90164092 | C | A | 1 | a0001c0001t0003g0130 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1278+475C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90164092 | |||||||
chr11:90164403 | G | A | 2 | a0001c0002t0001g0204 a0001c0002t0001g0218 |
2 | NA18990.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1278+786G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90164403 | |||||||
chr11:90164590 | TTAATAA | T | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1278+981_1278+986d others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90164590 | ||||||
chr11:90164793 | T | C | 4 | a0001c0002t0004g0256 a0001c0002t0004g0257 a0001c0002t0004g0258 others(1): Show |
4 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278+1176T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90164793 | |||||||
chr11:90164821 | G | T | 2 | a0001c0006t0001g0300 a0001c0006t0001g0321 |
2 | HG01109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1278+1204G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90164821 | |||||||
chr11:90165062 | C | T | 1 | a0006c0008t0004g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1278+1445C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165062 | |||||||
chr11:90165163 | C | T | 1 | a0001c0006t0005g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1278+1546C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165163 | |||||||
chr11:90165246 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1278+1629G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165246 | |||||||
chr11:90165299 | A | G | 1 | a0001c0001t0003g0061 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1278+1682A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165299 | |||||||
chr11:90165300 | T | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1278+1683T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165300 | |||||||
chr11:90165318 | C | A | 1 | a0001c0001t0008g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1278+1701C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165318 | |||||||
chr11:90165322 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1278+1705G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165322 | |||||||
chr11:90165414 | G | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1278+1797G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165414 | |||||||
chr11:90165417 | A | G | 1 | a0001c0001t0002g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1278+1800A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165417 | |||||||
chr11:90165419 | C | T | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1278+1802C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165419 | |||||||
chr11:90165514 | G | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1278+1897G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165514 | |||||||
chr11:90165635 | C | T | 24 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0272 others(21): Show |
25 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1278+2018C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165635 | |||||||
chr11:90165673 | G | T | 148 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(145): Show |
161 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1278+2056G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165673 | |||||||
chr11:90165798 | A | G | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1278+2181A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165798 | |||||||
chr11:90165874 | A | C | 1 | a0005c0007t0001g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1278+2257A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165874 | |||||||
chr11:90165905 | G | A | 4 | a0001c0001t0002g0048 a0001c0001t0002g0138 a0001c0001t0010g0163 others(1): Show |
4 | HG02965.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+2288G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90165905 | |||||||
chr11:90166104 | C | CTGGCCTA others(33): Show |
1 | a0001c0002t0001g0228 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1278+2489_1278+252 others(44): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90166104 | ||||||
chr11:90166247 | CTCTG | C | 44 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0269 others(41): Show |
46 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1278+2636_1278+263 others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90166247 | ||||||
chr11:90166253 | CTGTG | C | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0309 |
3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1278+2640_1278+264 others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90166253 | ||||||
chr11:90166293 | C | G | 2 | a0008c0010t0004g0316 a0008c0010t0004g0318 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1279-2636C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166293 | |||||||
chr11:90166319 | A | G | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.1279-2610A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166319 | |||||||
chr11:90166324 | A | T | 1 | a0001c0002t0004g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1279-2605A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166324 | |||||||
chr11:90166334 | C | T | 18 | a0001c0001t0002g0142 a0001c0001t0002g0145 a0001c0002t0001g0324 others(15): Show |
18 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1279-2595C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166334 | |||||||
chr11:90166523 | T | C | 5 | a0002c0003t0001g0287 a0002c0003t0001g0297 a0002c0003t0007g0291 others(2): Show |
5 | HG00544.hp2 HG03239.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-2406T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166523 | |||||||
chr11:90166561 | C | T | 16 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(13): Show |
16 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1279-2368C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166561 | |||||||
chr11:90166571 | C | T | 1 | a0002c0003t0001g0280 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1279-2358C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166571 | |||||||
chr11:90166588 | C | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1279-2341C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166588 | |||||||
chr11:90166695 | C | T | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0309 |
3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1279-2234C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166695 | |||||||
chr11:90166727 | C | T | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279-2202C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166727 | |||||||
chr11:90166743 | G | A | 7 | a0001c0002t0001g0324 a0001c0002t0004g0255 a0001c0002t0004g0256 others(4): Show |
7 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279-2186G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166743 | |||||||
chr11:90166743 | G | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1279-2186G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166743 | |||||||
chr11:90166849 | A | AG | 177 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(174): Show |
191 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.1279-2080_1279-207 others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166849 | |||||||
chr11:90166942 | G | A | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1279-1987G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90166942 | |||||||
chr11:90167024 | G | A | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1279-1905G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167024 | |||||||
chr11:90167061 | C | T | 5 | a0001c0001t0002g0048 a0001c0001t0002g0138 a0001c0001t0002g0146 others(2): Show |
5 | HG02965.hp2 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-1868C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167061 | |||||||
chr11:90167115 | C | A | 2 | a0001c0006t0004g0322 a0001c0006t0005g0323 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1279-1814C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167115 | |||||||
chr11:90167128 | G | T | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1279-1801G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167128 | |||||||
chr11:90167132 | C | A | 6 | a0001c0002t0004g0255 a0001c0002t0004g0256 a0001c0002t0004g0257 others(3): Show |
6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279-1797C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167132 | |||||||
chr11:90167133 | C | G | 1 | a0001c0020t0002g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1279-1796C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167133 | |||||||
chr11:90167138 | C | T | 12 | a0002c0003t0001g0269 a0002c0003t0001g0288 a0002c0003t0001g0290 others(9): Show |
13 | HG01192.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1279-1791C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167138 | |||||||
chr11:90167160 | C | T | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1279-1769C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167160 | |||||||
chr11:90167161 | G | A | 14 | a0003c0004t0001g0242 a0003c0004t0004g0243 a0003c0004t0005g0231 others(11): Show |
14 | HG00438.hp2 HG01175.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279-1768G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167161 | |||||||
chr11:90167177 | T | G | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-1752T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167177 | |||||||
chr11:90167208 | ACCGGGGC others(8): Show |
A | 1 | a0001c0002t0007g0029 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1279-1719_1279-170 others(19): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90167208 | ||||||
chr11:90167230 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1279-1699C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167230 | |||||||
chr11:90167308 | G | A | 51 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(48): Show |
61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1279-1621G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167308 | |||||||
chr11:90167309 | C | T | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0309 |
3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1279-1620C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167309 | |||||||
chr11:90167316 | G | A | 2 | a0001c0006t0004g0322 a0001c0006t0005g0323 |
2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1279-1613G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167316 | |||||||
chr11:90167379 | C | T | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1279-1550C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167379 | |||||||
chr11:90167393 | T | G | 1 | a0001c0001t0002g0052 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1279-1536T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167393 | |||||||
chr11:90167405 | C | T | 151 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(148): Show |
164 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1279-1524C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167405 | |||||||
chr11:90167461 | G | C | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279-1468G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167461 | |||||||
chr11:90167462 | A | C | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(65): Show |
78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1279-1467A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167462 | |||||||
chr11:90167481 | C | T | 6 | a0001c0002t0004g0255 a0001c0002t0004g0256 a0001c0002t0004g0257 others(3): Show |
6 | HG01074.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279-1448C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167481 | |||||||
chr11:90167528 | C | T | 1 | a0001c0006t0001g0300 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1279-1401C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167528 | |||||||
chr11:90167568 | C | T | 193 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(190): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.1279-1361C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167568 | |||||||
chr11:90167569 | G | A | 1 | a0011c0022t0002g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1279-1360G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167569 | |||||||
chr11:90167614 | T | C | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1279-1315T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167614 | |||||||
chr11:90167763 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1279-1166A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167763 | |||||||
chr11:90167776 | G | T | 44 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0269 others(41): Show |
46 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1279-1153G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167776 | |||||||
chr11:90167800 | G | T | 1 | a0001c0002t0001g0044 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1279-1129G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167800 | |||||||
chr11:90167821 | C | G | 1 | a0001c0002t0001g0204 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1279-1108C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167821 | |||||||
chr11:90167827 | T | A | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1279-1102T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167827 | |||||||
chr11:90167850 | GCAATCGG others(17): Show |
G | 4 | a0001c0002t0001g0254 a0001c0002t0004g0255 a0001c0002t0004g0259 others(1): Show |
4 | HG02109.hp1 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279-1059_1279-103 others(28): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90167850 | ||||||
chr11:90167879 | C | T | 2 | a0001c0002t0004g0199 a0001c0002t0004g0227 |
2 | NA18975.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1279-1050C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167879 | |||||||
chr11:90167913 | T | G | 15 | a0001c0002t0004g0306 a0004c0005t0001g0247 a0004c0005t0001g0253 others(12): Show |
15 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1279-1016T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167913 | |||||||
chr11:90167949 | C | T | 194 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(191): Show |
208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.1279-980C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167949 | |||||||
chr11:90167960 | T | G | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-969T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167960 | |||||||
chr11:90167969 | T | C | 1 | a0001c0002t0001g0212 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1279-960T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167969 | |||||||
chr11:90167990 | G | A | 61 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0319 others(58): Show |
64 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1279-939G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90167990 | |||||||
chr11:90168083 | G | A | 1 | a0001c0001t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1279-846G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168083 | |||||||
chr11:90168120 | A | AC | 61 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0319 others(58): Show |
64 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1279-806dupC | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 90168120 | ||||||
chr11:90168176 | G | A | 1 | a0003c0004t0004g0243 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1279-753G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168176 | |||||||
chr11:90168214 | A | C | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1279-715A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168214 | |||||||
chr11:90168306 | C | G | 1 | a0001c0002t0004g0260 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1279-623C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168306 | |||||||
chr11:90168329 | C | G | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279-600C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168329 | |||||||
chr11:90168352 | C | T | 3 | a0004c0005t0001g0253 a0004c0005t0004g0249 a0004c0005t0004g0250 |
3 | HG02615.hp2 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1279-577C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168352 | |||||||
chr11:90168390 | C | T | 15 | a0001c0002t0004g0306 a0004c0005t0001g0247 a0004c0005t0001g0253 others(12): Show |
15 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1279-539C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168390 | |||||||
chr11:90168404 | G | A | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0309 |
3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1279-525G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168404 | |||||||
chr11:90168458 | G | A | 1 | a0001c0001t0003g0083 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1279-471G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168458 | |||||||
chr11:90168517 | TAAAA | T | 7 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(4): Show |
7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279-411_1279-408d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168517 | |||||||
chr11:90168600 | G | C | 1 | a0001c0001t0002g0115 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1279-329G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168600 | |||||||
chr11:90168634 | C | T | 2 | a0002c0003t0001g0282 a0002c0003t0001g0286 |
2 | HG01361.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1279-295C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168634 | |||||||
chr11:90168654 | C | T | 7 | a0002c0003t0001g0269 a0002c0003t0001g0288 a0002c0003t0001g0290 others(4): Show |
7 | HG01192.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279-275C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168654 | |||||||
chr11:90168665 | T | C | 1 | a0001c0002t0001g0024 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1279-264T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168665 | |||||||
chr11:90168679 | G | A | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0309 |
3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1279-250G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168679 | |||||||
chr11:90168711 | T | C | 7 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(4): Show |
7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279-218T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168711 | |||||||
chr11:90168857 | A | G | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1279-72A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168857 | |||||||
chr11:90168866 | A | G | 5 | a0001c0002t0004g0306 a0004c0005t0001g0253 a0004c0005t0004g0249 others(2): Show |
5 | HG02615.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-63A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 11/18 | chr11 | 90168866 | |||||||
chr11:90169108 | A | G | 187 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(184): Show |
201 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1342+116A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169108 | |||||||
chr11:90169143 | A | G | 1 | a0008c0010t0004g0316 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1342+151A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169143 | |||||||
chr11:90169181 | T | A | 5 | a0001c0001t0002g0073 a0001c0001t0002g0103 a0001c0001t0002g0156 others(2): Show |
5 | NA18940.hp1 NA18944.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1342+189T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169181 | |||||||
chr11:90169300 | A | AT | 179 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(176): Show |
193 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1342+309dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 90169300 | ||||||
chr11:90169363 | G | A | 1 | a0001c0001t0003g0106 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1342+371G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169363 | |||||||
chr11:90169390 | A | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1342+398A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169390 | |||||||
chr11:90169448 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1342+456G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169448 | |||||||
chr11:90169454 | A | T | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1342+462A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169454 | |||||||
chr11:90169507 | C | CA | 6 | a0001c0001t0006g0074 a0001c0002t0001g0030 a0001c0002t0001g0039 others(3): Show |
6 | HG00621.hp1 HG01257.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1342+528dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 90169507 | ||||||
chr11:90169507 | C | CAA | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1342+527_1342+528d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 90169507 | ||||||
chr11:90169507 | CAAAAA | C | 7 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(4): Show |
7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1342+524_1342+528d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr11 | 90169507 | ||||||
chr11:90169527 | G | T | 2 | a0002c0003t0001g0285 a0002c0003t0001g0293 |
2 | HG01978.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1342+535G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169527 | |||||||
chr11:90169590 | C | A | 1 | a0001c0006t0005g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1343-479C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169590 | |||||||
chr11:90169601 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1343-468G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169601 | |||||||
chr11:90169633 | C | G | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1343-436C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169633 | |||||||
chr11:90169675 | G | A | 7 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(4): Show |
7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1343-394G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169675 | |||||||
chr11:90169814 | G | A | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1343-255G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169814 | |||||||
chr11:90169882 | G | C | 8 | a0001c0001t0002g0055 a0001c0001t0002g0057 a0001c0001t0002g0107 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1343-187G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169882 | |||||||
chr11:90169888 | T | G | 1 | a0001c0001t0006g0011 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1343-181T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169888 | |||||||
chr11:90169916 | A | T | 1 | a0001c0002t0001g0198 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1343-153A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169916 | |||||||
chr11:90169926 | C | A | 1 | a0001c0001t0003g0135 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1343-143C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 12/18 | chr11 | 90169926 | |||||||
chr11:90170166 | C | T | 188 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(185): Show |
202 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1410+30C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170166 | |||||||
chr11:90170237 | G | A | 144 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(141): Show |
157 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1410+101G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170237 | |||||||
chr11:90170717 | G | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1410+581G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170717 | |||||||
chr11:90170836 | C | T | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1410+700C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170836 | |||||||
chr11:90170877 | A | G | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1410+741A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170877 | |||||||
chr11:90170905 | A | G | 8 | a0001c0002t0004g0306 a0004c0005t0001g0247 a0004c0005t0001g0253 others(5): Show |
8 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1410+769A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170905 | |||||||
chr11:90170977 | G | T | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0309 |
3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1410+841G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90170977 | |||||||
chr11:90171070 | C | A | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(65): Show |
78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1410+934C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171070 | |||||||
chr11:90171126 | A | C | 1 | a0001c0002t0001g0225 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1410+990A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171126 | |||||||
chr11:90171168 | A | G | 61 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0319 others(58): Show |
64 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1410+1032A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171168 | |||||||
chr11:90171369 | C | T | 2 | a0001c0002t0001g0193 a0001c0002t0001g0203 |
2 | HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1410+1233C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171369 | |||||||
chr11:90171383 | C | G | 2 | a0002c0003t0001g0269 a0002c0003t0001g0290 |
2 | HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1410+1247C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171383 | |||||||
chr11:90171421 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1410+1285T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171421 | |||||||
chr11:90171461 | G | A | 2 | a0001c0001t0003g0069 a0001c0001t0003g0072 |
2 | NA19074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1410+1325G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171461 | |||||||
chr11:90171494 | G | T | 1 | a0001c0001t0002g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1410+1358G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171494 | |||||||
chr11:90171518 | T | A | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1410+1382T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171518 | |||||||
chr11:90171538 | T | C | 155 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(152): Show |
168 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.1410+1402T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171538 | |||||||
chr11:90171548 | G | T | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1410+1412G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171548 | |||||||
chr11:90171578 | A | G | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1410+1442A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171578 | |||||||
chr11:90171809 | A | T | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1410+1673A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171809 | |||||||
chr11:90171891 | C | T | 73 | a0001c0002t0004g0306 a0001c0002t0004g0337 a0001c0002t0005g0019 others(70): Show |
76 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1410+1755C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171891 | |||||||
chr11:90171937 | A | G | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1410+1801A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90171937 | |||||||
chr11:90171983 | AAAAAAAG others(9): Show |
A | 49 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0269 others(46): Show |
51 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.1411-1826_1411-181 others(20): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 90171983 | ||||||
chr11:90172042 | C | T | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411-1782C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172042 | |||||||
chr11:90172043 | G | A | 73 | a0001c0002t0004g0306 a0001c0002t0004g0337 a0001c0002t0005g0019 others(70): Show |
76 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1411-1781G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172043 | |||||||
chr11:90172068 | T | C | 334 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0010 others(331): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1411-1756T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172068 | |||||||
chr11:90172068 | T | G | 3 | a0001c0002t0001g0025 a0001c0002t0001g0043 a0001c0002t0015g0026 |
3 | NA18974.hp2 NA18992.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1411-1756T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172068 | |||||||
chr11:90172071 | T | G | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(65): Show |
78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1411-1753T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172071 | |||||||
chr11:90172142 | G | A | 2 | a0001c0002t0004g0023 a0001c0002t0004g0031 |
2 | HG01261.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1411-1682G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172142 | |||||||
chr11:90172226 | C | T | 1 | a0001c0001t0006g0011 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1411-1598C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172226 | |||||||
chr11:90172257 | AG | A | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411-1564delG | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr11 | 90172257 | ||||||
chr11:90172262 | G | A | 2 | a0001c0002t0004g0046 a0001c0002t0004g0047 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1411-1562G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172262 | |||||||
chr11:90172350 | C | T | 3 | a0001c0002t0005g0334 a0001c0002t0005g0335 a0001c0002t0005g0336 |
3 | NA18985.hp1 NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1411-1474C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172350 | |||||||
chr11:90172421 | G | A | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1411-1403G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172421 | |||||||
chr11:90172431 | G | C | 1 | a0001c0001t0002g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1411-1393G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172431 | |||||||
chr11:90172442 | A | G | 6 | a0001c0001t0003g0180 a0001c0001t0006g0012 a0001c0001t0006g0171 others(3): Show |
7 | HG00140.hp2 HG00738.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411-1382A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172442 | |||||||
chr11:90172455 | G | C | 148 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(145): Show |
161 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1411-1369G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172455 | |||||||
chr11:90172518 | C | G | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411-1306C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172518 | |||||||
chr11:90172643 | T | G | 1 | a0001c0002t0005g0333 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1411-1181T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172643 | |||||||
chr11:90172716 | G | A | 12 | a0001c0002t0004g0306 a0004c0005t0001g0247 a0004c0005t0001g0253 others(9): Show |
12 | HG02486.hp1 HG02615.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1411-1108G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172716 | |||||||
chr11:90172838 | A | G | 1 | a0002c0003t0001g0271 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1411-986A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172838 | |||||||
chr11:90172979 | A | G | 1 | a0001c0001t0003g0094 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1411-845A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172979 | |||||||
chr11:90172996 | T | G | 337 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0010 others(334): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1411-828T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90172996 | |||||||
chr11:90173083 | A | G | 7 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(4): Show |
7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411-741A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173083 | |||||||
chr11:90173137 | A | G | 3 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 |
3 | HG01109.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1411-687A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173137 | |||||||
chr11:90173186 | T | C | 7 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(4): Show |
7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411-638T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173186 | |||||||
chr11:90173188 | C | T | 1 | a0002c0003t0001g0271 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1411-636C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173188 | |||||||
chr11:90173247 | T | C | 1 | a0002c0003t0001g0297 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1411-577T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173247 | |||||||
chr11:90173248 | T | C | 2 | a0001c0002t0004g0255 a0001c0002t0004g0259 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1411-576T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173248 | |||||||
chr11:90173337 | G | A | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1411-487G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173337 | |||||||
chr11:90173348 | A | G | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0309 |
3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1411-476A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173348 | |||||||
chr11:90173430 | T | C | 3 | a0001c0001t0003g0009 a0001c0001t0003g0144 a0001c0001t0013g0009 |
3 | NA18967.hp1 NA18994.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1411-394T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173430 | |||||||
chr11:90173543 | A | G | 1 | a0001c0006t0001g0301 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1411-281A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173543 | |||||||
chr11:90173716 | C | T | 3 | a0001c0002t0001g0254 a0003c0004t0001g0242 a0003c0004t0005g0241 |
3 | HG01175.hp2 HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1411-108C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 13/18 | chr11 | 90173716 | |||||||
chr11:90173928 | T | TA | 3 | a0001c0001t0006g0059 a0001c0001t0008g0060 a0001c0001t0008g0137 |
3 | HG00099.hp1 HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1502+14dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90173928 | ||||||
chr11:90174149 | C | T | 27 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(24): Show |
28 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(25): Show |
intron_variant | MODIFIER | c.1502+234C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174149 | |||||||
chr11:90174150 | G | A | 1 | a0002c0003t0001g0273 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1502+235G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174150 | |||||||
chr11:90174188 | G | A | 46 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0269 others(43): Show |
48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1502+273G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174188 | |||||||
chr11:90174199 | C | T | 7 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(4): Show |
7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502+284C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174199 | |||||||
chr11:90174219 | T | C | 177 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(174): Show |
191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1502+304T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174219 | |||||||
chr11:90174496 | A | C | 12 | a0001c0002t0004g0306 a0004c0005t0001g0247 a0004c0005t0001g0253 others(9): Show |
12 | HG02486.hp1 HG02615.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1502+581A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174496 | |||||||
chr11:90174527 | A | T | 1 | a0001c0002t0004g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1502+612A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174527 | |||||||
chr11:90174608 | T | A | 2 | a0001c0002t0001g0193 a0001c0002t0001g0203 |
2 | HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1502+693T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174608 | |||||||
chr11:90174729 | TTTTTA | T | 3 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0309 |
3 | HG02723.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1502+819_1502+823d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90174729 | ||||||
chr11:90174746 | C | A | 170 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(167): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1502+831C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174746 | |||||||
chr11:90174866 | T | G | 1 | a0001c0002t0004g0306 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1502+951T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90174866 | |||||||
chr11:90175044 | G | GATGGGGT others(5): Show |
1 | a0001c0006t0005g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-926_1503-925i others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175044 | ||||||
chr11:90175049 | C | G | 1 | a0001c0006t0005g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-923C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175049 | |||||||
chr11:90175051 | C | A | 1 | a0001c0006t0005g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-921C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175051 | |||||||
chr11:90175053 | C | A | 1 | a0001c0006t0005g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-919C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175053 | |||||||
chr11:90175056 | C | T | 1 | a0001c0006t0005g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-916C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175056 | |||||||
chr11:90175058 | T | A | 1 | a0001c0006t0005g0325 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1503-914T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175058 | |||||||
chr11:90175284 | A | T | 1 | a0002c0003t0001g0293 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1503-688A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175284 | |||||||
chr11:90175408 | T | C | 1 | a0001c0002t0004g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1503-564T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175408 | |||||||
chr11:90175554 | G | T | 46 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0269 others(43): Show |
48 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1503-418G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175554 | |||||||
chr11:90175600 | T | C | 177 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(174): Show |
191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1503-372T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175600 | |||||||
chr11:90175619 | GT | G | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(65): Show |
78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1503-349delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175619 | ||||||
chr11:90175836 | T | A | 2 | a0001c0002t0004g0046 a0001c0002t0004g0047 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1503-136T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175836 | |||||||
chr11:90175928 | A | ATG | 13 | a0001c0001t0002g0081 a0001c0001t0002g0138 a0001c0001t0003g0051 others(10): Show |
13 | HG01099.hp2 HG01256.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1503-21_1503-20dup others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175928 | ||||||
chr11:90175928 | A | ATGTGTG | 80 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(77): Show |
83 | HG00597.hp1 HG00639.hp1 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.1503-25_1503-20dup others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175928 | ||||||
chr11:90175928 | A | ATGTGTGT others(1): Show |
74 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(71): Show |
84 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1503-27_1503-20dup others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175928 | ||||||
chr11:90175928 | A | ATGTGTGT others(3): Show |
21 | a0001c0002t0001g0224 a0001c0002t0004g0337 a0001c0002t0005g0019 others(18): Show |
22 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1503-29_1503-20dup others(10): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175928 | ||||||
chr11:90175928 | A | ATGTGTGT others(7): Show |
1 | a0001c0002t0001g0211 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1503-33_1503-20dup others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175928 | ||||||
chr11:90175928 | A | G | 10 | a0001c0001t0002g0175 a0001c0001t0006g0053 a0001c0001t0006g0059 others(7): Show |
10 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1503-44A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | chr11 | 90175928 | |||||||
chr11:90175929 | T | TGTGC | 3 | a0005c0007t0005g0310 a0005c0007t0005g0313 a0005c0007t0005g0314 |
3 | HG03041.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1503-40_1503-39ins others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175929 | ||||||
chr11:90175931 | T | TGC | 4 | a0005c0007t0001g0317 a0005c0007t0005g0311 a0005c0007t0007g0312 others(1): Show |
4 | HG01081.hp1 HG03139.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503-40_1503-39ins others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 90175931 | ||||||
chr11:90176196 | G | A | 1 | a0001c0001t0002g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1593+134G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176196 | |||||||
chr11:90176221 | G | A | 7 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(4): Show |
7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1593+159G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176221 | |||||||
chr11:90176306 | T | C | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1593+244T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176306 | |||||||
chr11:90176451 | A | G | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1593+389A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176451 | |||||||
chr11:90176700 | G | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1593+638G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176700 | |||||||
chr11:90176740 | A | T | 1 | a0001c0001t0002g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1593+678A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176740 | |||||||
chr11:90176800 | T | C | 1 | a0008c0010t0004g0316 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1593+738T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176800 | |||||||
chr11:90176853 | C | G | 1 | a0001c0002t0007g0029 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1593+791C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176853 | |||||||
chr11:90176890 | C | T | 176 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(173): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1593+828C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176890 | |||||||
chr11:90176937 | A | C | 4 | a0001c0001t0003g0006 a0001c0001t0003g0071 a0001c0001t0003g0094 others(1): Show |
5 | HG02040.hp2 NA18968.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1593+875A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176937 | |||||||
chr11:90176957 | T | G | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1593+895T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176957 | |||||||
chr11:90176966 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1594-887T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176966 | |||||||
chr11:90176968 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1594-885T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90176968 | |||||||
chr11:90177057 | C | T | 3 | a0001c0002t0001g0034 a0001c0002t0001g0039 a0001c0002t0001g0044 |
3 | NA18943.hp2 NA19076.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1594-796C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177057 | |||||||
chr11:90177164 | C | T | 3 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 |
3 | HG01109.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1594-689C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177164 | |||||||
chr11:90177313 | C | CT | 15 | a0001c0001t0002g0108 a0001c0001t0002g0150 a0001c0001t0006g0096 others(12): Show |
15 | HG01099.hp1 HG01891.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.1594-526dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177313 | ||||||
chr11:90177313 | CT | C | 32 | a0001c0001t0002g0058 a0001c0001t0002g0156 a0001c0001t0003g0084 others(29): Show |
33 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(30): Show |
intron_variant | MODIFIER | c.1594-526delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177313 | ||||||
chr11:90177401 | C | T | 7 | a0002c0003t0001g0269 a0002c0003t0001g0288 a0002c0003t0001g0290 others(4): Show |
7 | HG01192.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594-452C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177401 | |||||||
chr11:90177526 | C | T | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1594-327C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177526 | |||||||
chr11:90177527 | G | A | 1 | a0001c0001t0003g0091 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1594-326G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177527 | |||||||
chr11:90177560 | A | G | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1594-293A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177560 | |||||||
chr11:90177586 | G | GT | 37 | a0001c0001t0002g0008 a0001c0001t0002g0048 a0001c0001t0002g0052 others(34): Show |
37 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1594-229dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GT | G | 41 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0064 others(38): Show |
41 | HG00597.hp2 HG00639.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.1594-229delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTT | G | 17 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0054 others(14): Show |
19 | HG00544.hp1 HG01081.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1594-230_1594-229d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTT | G | 7 | a0002c0003t0001g0018 a0002c0003t0001g0302 a0002c0009t0001g0270 others(4): Show |
8 | HG00639.hp1 HG01069.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1594-232_1594-229d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTT | G | 23 | a0001c0001t0002g0157 a0001c0002t0004g0306 a0002c0003t0001g0017 others(20): Show |
23 | HG01168.hp1 HG01261.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.1594-233_1594-229d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTTT | G | 22 | a0002c0003t0001g0269 a0002c0003t0001g0272 a0002c0003t0001g0276 others(19): Show |
22 | HG00544.hp2 HG01192.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1594-234_1594-229d others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTTTT others(3): Show |
G | 11 | a0001c0002t0001g0021 a0001c0002t0001g0035 a0001c0002t0001g0036 others(8): Show |
11 | HG00597.hp1 HG03130.hp1 HG03453.hp2 others(8): Show |
intron_variant | MODIFIER | c.1594-238_1594-229d others(12): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTTTT others(4): Show |
G | 32 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(29): Show |
33 | HG01109.hp1 HG01261.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1594-239_1594-229d others(13): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTTTT others(5): Show |
G | 36 | a0001c0001t0006g0012 a0001c0001t0006g0171 a0001c0001t0006g0172 others(33): Show |
45 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1594-240_1594-229d others(14): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTTTT others(6): Show |
G | 40 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0203 others(37): Show |
41 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1594-241_1594-229d others(15): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTTTT others(7): Show |
G | 1 | a0001c0002t0001g0208 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1594-242_1594-229d others(16): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTTTT others(10): Show |
G | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1594-245_1594-229d others(19): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTTTT others(11): Show |
G | 1 | a0005c0007t0005g0310 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1594-246_1594-229d others(20): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTTTT others(12): Show |
G | 6 | a0005c0007t0001g0317 a0005c0007t0005g0311 a0005c0007t0005g0313 others(3): Show |
6 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1594-247_1594-229d others(21): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTTTT others(14): Show |
G | 1 | a0002c0003t0001g0273 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1594-249_1594-229d others(23): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177586 | GTTTTTTT others(17): Show |
G | 3 | a0003c0004t0005g0237 a0003c0004t0005g0238 a0003c0004t0005g0245 |
3 | HG02083.hp2 NA18973.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1594-252_1594-229d others(26): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177586 | ||||||
chr11:90177677 | TC | T | 176 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(173): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1594-174delC | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr11 | 90177677 | ||||||
chr11:90177683 | G | A | 7 | a0005c0007t0001g0317 a0005c0007t0005g0310 a0005c0007t0005g0311 others(4): Show |
7 | HG01081.hp1 HG03041.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594-170G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 15/18 | chr11 | 90177683 | |||||||
chr11:90178242 | C | A | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858+125C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178242 | |||||||
chr11:90178255 | TAAAAC | T | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858+142_1858+146d others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90178255 | ||||||
chr11:90178312 | T | A | 1 | a0001c0002t0001g0032 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1858+195T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178312 | |||||||
chr11:90178425 | A | G | 1 | a0005c0007t0007g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1858+308A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178425 | |||||||
chr11:90178453 | T | C | 186 | a0001c0001t0002g0048 a0001c0001t0002g0138 a0001c0001t0010g0163 others(183): Show |
200 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1858+336T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178453 | |||||||
chr11:90178454 | G | A | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858+337G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178454 | |||||||
chr11:90178467 | C | T | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1858+350C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178467 | |||||||
chr11:90178485 | T | C | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1858+368T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178485 | |||||||
chr11:90178498 | C | T | 3 | a0001c0001t0002g0048 a0001c0001t0010g0163 a0001c0001t0010g0164 |
3 | HG02965.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1858+381C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178498 | |||||||
chr11:90178534 | G | A | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(65): Show |
78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1858+417G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178534 | |||||||
chr11:90178661 | G | T | 1 | a0001c0006t0001g0301 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1858+544G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178661 | |||||||
chr11:90178670 | C | CA | 6 | a0001c0001t0002g0119 a0001c0001t0002g0148 a0001c0001t0002g0160 others(3): Show |
6 | HG00597.hp2 HG00741.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858+568dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90178670 | ||||||
chr11:90178670 | CA | C | 71 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0006g0096 others(68): Show |
81 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1858+568delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90178670 | ||||||
chr11:90178699 | A | G | 1 | a0001c0002t0001g0210 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1858+582A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178699 | |||||||
chr11:90178766 | G | A | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1858+649G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90178766 | |||||||
chr11:90179087 | C | T | 1 | a0003c0004t0004g0243 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1858+970C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179087 | |||||||
chr11:90179151 | A | G | 184 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(181): Show |
198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1858+1034A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179151 | |||||||
chr11:90179280 | C | G | 5 | a0001c0001t0003g0106 a0001c0001t0003g0111 a0001c0001t0003g0130 others(2): Show |
5 | HG02129.hp2 HG02132.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858+1163C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179280 | |||||||
chr11:90179308 | T | C | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858+1191T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179308 | |||||||
chr11:90179333 | G | A | 1 | a0001c0001t0006g0096 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1858+1216G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179333 | |||||||
chr11:90179449 | T | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1858+1332T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179449 | |||||||
chr11:90179484 | T | C | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0013 others(65): Show |
78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1858+1367T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179484 | |||||||
chr11:90179567 | T | A | 8 | a0001c0002t0004g0306 a0004c0005t0001g0247 a0004c0005t0001g0253 others(5): Show |
8 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1858+1450T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179567 | |||||||
chr11:90179619 | T | G | 1 | a0004c0005t0004g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1858+1502T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179619 | |||||||
chr11:90179705 | C | G | 1 | a0001c0002t0007g0029 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1858+1588C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179705 | |||||||
chr11:90179784 | T | TA | 176 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(173): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1858+1668dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90179784 | ||||||
chr11:90179864 | T | G | 177 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(174): Show |
191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1858+1747T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90179864 | |||||||
chr11:90180066 | G | GATGA | 3 | a0001c0001t0003g0135 a0001c0002t0004g0255 a0001c0002t0004g0259 |
3 | HG03195.hp1 HG03579.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1859-1527_1859-152 others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90180066 | ||||||
chr11:90180066 | GATGA | G | 176 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(173): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1859-1527_1859-152 others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90180066 | ||||||
chr11:90180088 | T | C | 4 | a0001c0001t0002g0119 a0001c0001t0002g0148 a0001c0001t0002g0160 others(1): Show |
4 | HG00741.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1859-1532T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180088 | |||||||
chr11:90180138 | T | A | 9 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0076 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1859-1482T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180138 | |||||||
chr11:90180200 | C | T | 176 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(173): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1859-1420C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180200 | |||||||
chr11:90180301 | C | T | 176 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(173): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1859-1319C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180301 | |||||||
chr11:90180359 | A | G | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1859-1261A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180359 | |||||||
chr11:90180561 | A | G | 163 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(160): Show |
176 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.1859-1059A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180561 | |||||||
chr11:90180816 | A | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1859-804A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90180816 | |||||||
chr11:90181060 | T | C | 7 | a0002c0003t0001g0271 a0002c0003t0001g0273 a0002c0003t0001g0276 others(4): Show |
7 | HG01099.hp1 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1859-560T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90181060 | |||||||
chr11:90181236 | AT | A | 11 | a0001c0002t0004g0306 a0004c0005t0001g0247 a0004c0005t0001g0253 others(8): Show |
11 | HG02486.hp1 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1859-375delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr11 | 90181236 | ||||||
chr11:90181250 | T | A | 1 | a0001c0001t0002g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1859-370T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90181250 | |||||||
chr11:90181588 | A | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1859-32A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90181588 | |||||||
chr11:90181618 | A | T | 1 | a0007c0011t0002g0128 | 1 | HG00609.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1859-2A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 16/18 | chr11 | 90181618 | |||||||
chr11:90181719 | T | C | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(26): Show |
30 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(27): Show |
intron_variant | MODIFIER | c.1940+18T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181719 | |||||||
chr11:90181725 | TTAAA | T | 6 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1940+25_1940+28del others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181725 | |||||||
chr11:90181725 | TTAAAAA | T | 42 | a0002c0003t0001g0017 a0002c0003t0001g0269 a0002c0003t0001g0271 others(39): Show |
43 | HG00544.hp2 HG01099.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.1940+25_1940+30del others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181725 | |||||||
chr11:90181726 | TA | T | 30 | a0001c0001t0002g0066 a0001c0001t0002g0100 a0001c0001t0002g0129 others(27): Show |
30 | HG00597.hp2 HG01081.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.1940+41delA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90181726 | ||||||
chr11:90181726 | TAA | T | 14 | a0001c0001t0003g0072 a0001c0002t0004g0255 a0001c0002t0004g0259 others(11): Show |
14 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.1940+40_1940+41del others(2): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90181726 | ||||||
chr11:90181726 | TAAAAA | T | 107 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(104): Show |
120 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1940+37_1940+41del others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90181726 | ||||||
chr11:90181727 | A | T | 1 | a0001c0001t0008g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1940+26A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181727 | |||||||
chr11:90181728 | A | T | 3 | a0004c0005t0004g0266 a0004c0005t0004g0267 a0004c0005t0004g0268 |
3 | HG02280.hp1 HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1940+27A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181728 | |||||||
chr11:90181732 | A | T | 27 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0024 others(24): Show |
28 | HG00597.hp1 HG01261.hp1 HG02602.hp2 others(25): Show |
intron_variant | MODIFIER | c.1940+31A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181732 | |||||||
chr11:90181733 | A | T | 4 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0033 others(1): Show |
4 | NA18943.hp1 NA18956.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.1940+32A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181733 | |||||||
chr11:90181772 | A | C | 176 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(173): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1940+71A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181772 | |||||||
chr11:90181779 | T | C | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1940+78T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181779 | |||||||
chr11:90181837 | A | G | 4 | a0001c0002t0001g0197 a0001c0002t0001g0208 a0001c0002t0001g0209 others(1): Show |
4 | HG00642.hp1 HG01256.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1940+136A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181837 | |||||||
chr11:90181844 | C | A | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1940+143C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181844 | |||||||
chr11:90181878 | A | C | 176 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(173): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1940+177A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181878 | |||||||
chr11:90181965 | T | TG | 9 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0076 others(6): Show |
9 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1940+268dupG | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90181965 | ||||||
chr11:90181974 | C | T | 1 | a0003c0004t0005g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1940+273C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90181974 | |||||||
chr11:90182009 | G | A | 2 | a0001c0002t0004g0255 a0001c0002t0004g0259 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1940+308G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182009 | |||||||
chr11:90182082 | G | A | 7 | a0002c0003t0001g0273 a0002c0003t0001g0276 a0002c0003t0001g0277 others(4): Show |
7 | HG01099.hp1 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1940+381G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182082 | |||||||
chr11:90182112 | A | G | 1 | a0001c0002t0005g0320 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1940+411A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182112 | |||||||
chr11:90182141 | G | C | 1 | a0002c0003t0001g0299 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1940+440G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182141 | |||||||
chr11:90182222 | T | C | 13 | a0001c0002t0004g0337 a0001c0002t0005g0019 a0001c0002t0005g0326 others(10): Show |
14 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1940+521T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182222 | |||||||
chr11:90182249 | A | C | 1 | a0001c0001t0003g0087 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1940+548A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182249 | |||||||
chr11:90182271 | A | T | 3 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 |
3 | HG01109.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1940+570A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182271 | |||||||
chr11:90182279 | ATG | A | 3 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 |
3 | HG01109.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1940+582_1940+583d others(4): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90182279 | ||||||
chr11:90182287 | A | G | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1940+586A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182287 | |||||||
chr11:90182340 | A | G | 4 | a0001c0002t0001g0197 a0001c0002t0001g0208 a0001c0002t0001g0209 others(1): Show |
4 | HG00642.hp1 HG01256.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1941-576A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182340 | |||||||
chr11:90182398 | G | C | 2 | a0001c0002t0005g0319 a0001c0002t0005g0320 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1941-518G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182398 | |||||||
chr11:90182474 | A | G | 5 | a0001c0001t0002g0048 a0001c0001t0002g0138 a0001c0001t0002g0146 others(2): Show |
5 | HG02965.hp2 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1941-442A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182474 | |||||||
chr11:90182476 | C | G | 172 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(169): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1941-440C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182476 | |||||||
chr11:90182499 | C | T | 172 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(169): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1941-417C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182499 | |||||||
chr11:90182510 | T | A | 1 | a0001c0006t0001g0301 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1941-406T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182510 | |||||||
chr11:90182523 | T | C | 47 | a0001c0006t0004g0322 a0002c0003t0001g0017 a0002c0003t0001g0018 others(44): Show |
49 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1941-393T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182523 | |||||||
chr11:90182577 | T | C | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1941-339T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182577 | |||||||
chr11:90182635 | T | TAGAA | 172 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(169): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1941-280_1941-277d others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr11 | 90182635 | ||||||
chr11:90182708 | A | T | 176 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(173): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1941-208A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182708 | |||||||
chr11:90182849 | T | G | 1 | a0004c0021t0011g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1941-67T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182849 | |||||||
chr11:90182885 | C | G | 172 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(169): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1941-31C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182885 | |||||||
chr11:90182912 | G | C | 172 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(169): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
splice_region_variant&intron_variant | LOW | c.1941-4G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 17/18 | chr11 | 90182912 | |||||||
chr11:90183026 | G | A | 1 | a0001c0001t0003g0061 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2033+18G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183026 | |||||||
chr11:90183058 | A | G | 3 | a0001c0001t0006g0059 a0001c0001t0008g0060 a0001c0001t0008g0137 |
3 | HG00099.hp1 HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2033+50A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183058 | |||||||
chr11:90183179 | T | G | 2 | a0001c0002t0001g0036 a0001c0002t0007g0038 |
2 | NA18991.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2033+171T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183179 | |||||||
chr11:90183189 | T | G | 4 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2033+181T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183189 | |||||||
chr11:90183227 | T | G | 172 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(169): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2033+219T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183227 | |||||||
chr11:90183316 | C | T | 172 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(169): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2033+308C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183316 | |||||||
chr11:90183328 | TC | T | 9 | a0001c0002t0004g0306 a0004c0005t0001g0247 a0004c0005t0001g0253 others(6): Show |
9 | HG02615.hp2 HG02723.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2033+321delC | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183328 | |||||||
chr11:90183394 | G | A | 184 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(181): Show |
198 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.2033+386G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183394 | |||||||
chr11:90183477 | C | A | 7 | a0001c0002t0001g0013 a0001c0002t0001g0194 a0001c0002t0001g0204 others(4): Show |
8 | NA18939.hp2 NA18956.hp1 NA18978.hp2 others(5): Show |
intron_variant | MODIFIER | c.2033+469C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183477 | |||||||
chr11:90183494 | G | A | 173 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(170): Show |
187 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.2033+486G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183494 | |||||||
chr11:90183502 | C | T | 1 | a0001c0006t0005g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+494C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183502 | |||||||
chr11:90183585 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2033+577C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183585 | |||||||
chr11:90183700 | T | C | 175 | a0001c0001t0002g0064 a0001c0002t0001g0001 a0001c0002t0001g0002 others(172): Show |
189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.2033+692T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183700 | |||||||
chr11:90183740 | T | G | 1 | a0004c0005t0004g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2033+732T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183740 | |||||||
chr11:90183857 | G | C | 1 | a0001c0001t0003g0180 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2033+849G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183857 | |||||||
chr11:90183940 | C | G | 2 | a0001c0002t0001g0232 a0001c0002t0001g0233 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2033+932C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90183940 | |||||||
chr11:90184094 | A | G | 144 | a0001c0001t0002g0064 a0001c0002t0001g0001 a0001c0002t0001g0002 others(141): Show |
157 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.2033+1086A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184094 | |||||||
chr11:90184162 | T | C | 1 | a0001c0002t0005g0192 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2033+1154T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184162 | |||||||
chr11:90184417 | A | G | 22 | a0001c0002t0001g0324 a0001c0002t0004g0306 a0001c0002t0005g0319 others(19): Show |
22 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.2033+1409A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184417 | |||||||
chr11:90184475 | G | A | 15 | a0001c0001t0003g0077 a0001c0002t0001g0324 a0001c0002t0005g0319 others(12): Show |
15 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2033+1467G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184475 | |||||||
chr11:90184487 | G | A | 8 | a0001c0001t0003g0077 a0001c0020t0002g0098 a0005c0007t0001g0317 others(5): Show |
8 | HG01081.hp1 HG03041.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.2033+1479G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184487 | |||||||
chr11:90184524 | G | A | 1 | a0002c0003t0001g0293 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2033+1516G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184524 | |||||||
chr11:90184531 | G | A | 228 | a0001c0001t0002g0048 a0001c0001t0002g0054 a0001c0001t0002g0064 others(225): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.2033+1523G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184531 | |||||||
chr11:90184595 | CT | C | 10 | a0001c0001t0003g0077 a0001c0006t0001g0300 a0001c0006t0001g0321 others(7): Show |
10 | HG01081.hp1 HG01109.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2033+1588delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184595 | |||||||
chr11:90184691 | T | A | 2 | a0001c0006t0001g0321 a0004c0005t0001g0247 |
2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2033+1683T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184691 | |||||||
chr11:90184701 | G | A | 42 | a0001c0001t0002g0126 a0001c0001t0002g0161 a0001c0001t0008g0056 others(39): Show |
43 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.2033+1693G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184701 | |||||||
chr11:90184702 | C | A | 1 | a0001c0002t0001g0195 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2033+1694C>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184702 | |||||||
chr11:90184715 | G | A | 23 | a0001c0001t0002g0100 a0001c0001t0002g0162 a0001c0001t0006g0012 others(20): Show |
24 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2033+1707G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184715 | |||||||
chr11:90184723 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2033+1715T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184723 | |||||||
chr11:90184739 | T | C | 30 | a0001c0001t0002g0158 a0001c0001t0002g0175 a0001c0001t0003g0063 others(27): Show |
31 | HG00099.hp1 HG00597.hp1 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.2033+1731T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184739 | |||||||
chr11:90184760 | G | A | 50 | a0001c0001t0006g0101 a0001c0001t0008g0056 a0001c0002t0001g0001 others(47): Show |
58 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2033+1752G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184760 | |||||||
chr11:90184792 | G | A | 9 | a0001c0002t0004g0256 a0001c0002t0004g0257 a0001c0002t0004g0258 others(6): Show |
9 | HG01074.hp1 HG01109.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2033+1784G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184792 | |||||||
chr11:90184800 | T | A | 12 | a0001c0002t0005g0019 a0001c0002t0005g0326 a0001c0002t0005g0327 others(9): Show |
13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2033+1792T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184800 | |||||||
chr11:90184882 | G | C | 1 | a0004c0005t0004g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2033+1874G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184882 | |||||||
chr11:90184898 | A | G | 56 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(53): Show |
58 | HG00673.hp1 HG01099.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.2033+1890A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90184898 | |||||||
chr11:90185072 | A | T | 2 | a0004c0005t0005g0263 a0004c0021t0011g0184 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2033+2064A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185072 | |||||||
chr11:90185205 | G | A | 232 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(229): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.2033+2197G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185205 | |||||||
chr11:90185241 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2033+2233A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185241 | |||||||
chr11:90185451 | G | A | 12 | a0001c0001t0006g0101 a0003c0004t0005g0231 a0003c0004t0005g0235 others(9): Show |
12 | HG00438.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.2033+2443G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185451 | |||||||
chr11:90185515 | T | G | 39 | a0001c0001t0008g0060 a0001c0002t0001g0040 a0001c0002t0001g0197 others(36): Show |
40 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.2033+2507T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185515 | |||||||
chr11:90185555 | T | A | 1 | a0001c0002t0004g0258 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2033+2547T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185555 | |||||||
chr11:90185644 | G | A | 2 | a0001c0002t0004g0046 a0001c0002t0004g0047 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2033+2636G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185644 | |||||||
chr11:90185648 | A | G | 1 | a0001c0002t0004g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2033+2640A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185648 | |||||||
chr11:90185766 | A | T | 1 | a0001c0006t0005g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+2758A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185766 | |||||||
chr11:90185850 | G | C | 50 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(47): Show |
52 | HG00597.hp2 HG00673.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2033+2842G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185850 | |||||||
chr11:90185858 | C | CT | 51 | a0001c0001t0002g0054 a0001c0001t0002g0064 a0001c0001t0002g0065 others(48): Show |
51 | HG01074.hp1 HG01081.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.2033+2866dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | ||||||
chr11:90185858 | C | CTT | 10 | a0001c0002t0004g0258 a0001c0002t0005g0329 a0001c0006t0001g0300 others(7): Show |
11 | HG00323.hp1 HG01109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2033+2865_2033+286 others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | ||||||
chr11:90185858 | C | CTTT | 13 | a0001c0002t0005g0019 a0001c0002t0005g0326 a0001c0002t0005g0327 others(10): Show |
14 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.2033+2864_2033+286 others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | ||||||
chr11:90185858 | C | CTTTT | 6 | a0002c0003t0001g0277 a0002c0003t0001g0278 a0002c0003t0001g0279 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2033+2863_2033+286 others(8): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | ||||||
chr11:90185858 | C | CTTTTT | 31 | a0001c0001t0008g0060 a0001c0002t0001g0040 a0001c0002t0001g0197 others(28): Show |
32 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.2033+2862_2033+286 others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | ||||||
chr11:90185858 | CT | C | 17 | a0001c0001t0002g0113 a0001c0001t0002g0156 a0001c0001t0006g0101 others(14): Show |
17 | HG00438.hp2 HG01934.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.2033+2866delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185858 | ||||||
chr11:90185873 | T | A | 1 | a0001c0006t0005g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+2865T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185873 | |||||||
chr11:90185873 | TTA | T | 47 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0051 others(44): Show |
49 | HG00597.hp2 HG00673.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.2033+2870_2033+287 others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90185873 | ||||||
chr11:90185874 | T | A | 2 | a0001c0001t0002g0104 a0001c0002t0001g0220 |
2 | HG02148.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2033+2866T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185874 | |||||||
chr11:90185911 | G | T | 1 | a0001c0006t0005g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+2903G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185911 | |||||||
chr11:90185949 | T | C | 41 | a0001c0001t0008g0056 a0001c0001t0008g0075 a0001c0001t0008g0123 others(38): Show |
49 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.2033+2941T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185949 | |||||||
chr11:90185979 | G | C | 144 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(141): Show |
150 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.2033+2971G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90185979 | |||||||
chr11:90186028 | T | A | 3 | a0001c0002t0004g0256 a0001c0002t0004g0257 a0001c0002t0004g0260 |
3 | HG01074.hp1 HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2033+3020T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186028 | |||||||
chr11:90186029 | A | T | 1 | a0004c0005t0004g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2033+3021A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186029 | |||||||
chr11:90186184 | C | G | 1 | a0001c0002t0005g0329 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2033+3176C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186184 | |||||||
chr11:90186454 | G | C | 12 | a0001c0002t0005g0019 a0001c0002t0005g0326 a0001c0002t0005g0327 others(9): Show |
13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2033+3446G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186454 | |||||||
chr11:90186502 | T | C | 1 | a0005c0007t0001g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2033+3494T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186502 | |||||||
chr11:90186505 | A | C | 1 | a0001c0001t0002g0169 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2033+3497A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186505 | |||||||
chr11:90186515 | GATTTATA others(14): Show |
G | 2 | a0001c0002t0001g0232 a0001c0002t0001g0309 |
2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2033+3508_2033+352 others(25): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186515 | |||||||
chr11:90186635 | G | A | 12 | a0001c0002t0005g0019 a0001c0002t0005g0326 a0001c0002t0005g0327 others(9): Show |
13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2033+3627G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186635 | |||||||
chr11:90186729 | G | T | 9 | a0001c0002t0005g0019 a0001c0002t0005g0326 a0001c0002t0005g0327 others(6): Show |
10 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.2033+3721G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186729 | |||||||
chr11:90186730 | T | A | 234 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(231): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.2033+3722T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186730 | |||||||
chr11:90186811 | A | C | 5 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(2): Show |
5 | HG01109.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2033+3803A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186811 | |||||||
chr11:90186829 | A | T | 1 | a0005c0007t0005g0314 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2033+3821A>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186829 | |||||||
chr11:90186897 | A | G | 12 | a0001c0002t0005g0019 a0001c0002t0005g0326 a0001c0002t0005g0327 others(9): Show |
13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2033+3889A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186897 | |||||||
chr11:90186915 | G | A | 125 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(122): Show |
130 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.2033+3907G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186915 | |||||||
chr11:90186941 | A | G | 1 | a0001c0006t0005g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+3933A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186941 | |||||||
chr11:90186942 | A | C | 1 | a0001c0001t0002g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2033+3934A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186942 | |||||||
chr11:90186952 | T | G | 2 | a0002c0003t0004g0274 a0008c0010t0004g0316 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2033+3944T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186952 | |||||||
chr11:90186969 | C | G | 3 | a0001c0002t0005g0334 a0001c0002t0005g0335 a0001c0002t0005g0336 |
3 | NA18985.hp1 NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2033+3961C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90186969 | |||||||
chr11:90187009 | G | A | 2 | a0001c0001t0006g0053 a0001c0001t0006g0176 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2033+4001G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187009 | |||||||
chr11:90187010 | A | G | 1 | a0003c0004t0018g0234 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2033+4002A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187010 | |||||||
chr11:90187017 | T | C | 9 | a0001c0001t0002g0055 a0001c0001t0002g0057 a0001c0001t0002g0107 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.2033+4009T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187017 | |||||||
chr11:90187022 | A | G | 1 | a0001c0006t0005g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+4014A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187022 | |||||||
chr11:90187063 | T | A | 1 | a0001c0006t0005g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+4055T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187063 | |||||||
chr11:90187150 | A | G | 4 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(1): Show |
4 | HG01109.hp2 HG02622.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2033+4142A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187150 | |||||||
chr11:90187199 | T | C | 1 | a0001c0006t0005g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2033+4191T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187199 | |||||||
chr11:90187304 | C | T | 1 | a0001c0006t0005g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2034-4254C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187304 | |||||||
chr11:90187313 | C | CACATTTT others(92): Show |
1 | a0001c0002t0005g0319 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2034-4148_2034-414 others(103): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90187313 | ||||||
chr11:90187348 | G | T | 1 | a0001c0006t0005g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2034-4210G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187348 | |||||||
chr11:90187426 | T | C | 87 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(84): Show |
91 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.2034-4132T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187426 | |||||||
chr11:90187532 | CTT | C | 34 | a0001c0001t0003g0088 a0001c0001t0006g0011 a0001c0001t0006g0012 others(31): Show |
36 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.2034-4022_2034-402 others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90187532 | ||||||
chr11:90187537 | T | C | 93 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(90): Show |
97 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.2034-4021T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187537 | |||||||
chr11:90187570 | A | G | 3 | a0001c0002t0004g0199 a0001c0002t0004g0207 a0001c0002t0004g0227 |
3 | HG02165.hp2 NA18975.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2034-3988A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187570 | |||||||
chr11:90187757 | C | G | 88 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(85): Show |
92 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.2034-3801C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187757 | |||||||
chr11:90187888 | A | G | 1 | a0001c0006t0005g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2034-3670A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187888 | |||||||
chr11:90187986 | C | T | 2 | a0001c0001t0002g0048 a0001c0001t0002g0141 |
2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2034-3572C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90187986 | |||||||
chr11:90188064 | C | T | 92 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(89): Show |
96 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.2034-3494C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188064 | |||||||
chr11:90188367 | C | G | 1 | a0004c0005t0004g0251 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2034-3191C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188367 | |||||||
chr11:90188444 | T | C | 1 | a0001c0002t0001g0254 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2034-3114T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188444 | |||||||
chr11:90188496 | G | T | 140 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(137): Show |
146 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.2034-3062G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188496 | |||||||
chr11:90188518 | G | A | 2 | a0002c0003t0001g0285 a0002c0003t0001g0293 |
2 | HG01978.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.2034-3040G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188518 | |||||||
chr11:90188551 | T | A | 1 | a0001c0002t0001g0215 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2034-3007T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188551 | |||||||
chr11:90188574 | A | G | 1 | a0001c0001t0002g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2034-2984A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188574 | |||||||
chr11:90188825 | T | A | 1 | a0004c0005t0004g0251 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2034-2733T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188825 | |||||||
chr11:90188859 | C | G | 14 | a0001c0002t0005g0019 a0001c0002t0005g0320 a0001c0002t0005g0326 others(11): Show |
15 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.2034-2699C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188859 | |||||||
chr11:90188986 | G | T | 143 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(140): Show |
148 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.2034-2572G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90188986 | |||||||
chr11:90189034 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2034-2524T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189034 | |||||||
chr11:90189062 | A | G | 27 | a0001c0001t0003g0088 a0001c0001t0006g0011 a0001c0001t0006g0012 others(24): Show |
29 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.2034-2496A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189062 | |||||||
chr11:90189125 | G | A | 2 | a0001c0002t0001g0232 a0001c0002t0001g0309 |
2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2034-2433G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189125 | |||||||
chr11:90189135 | A | AT | 43 | a0001c0002t0001g0040 a0001c0002t0001g0197 a0001c0002t0001g0209 others(40): Show |
44 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.2034-2422dupT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90189135 | ||||||
chr11:90189147 | G | A | 1 | a0003c0004t0005g0235 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2034-2411G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189147 | |||||||
chr11:90189249 | A | G | 47 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0006g0053 others(44): Show |
50 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2034-2309A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189249 | |||||||
chr11:90189255 | C | G | 55 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(52): Show |
57 | HG00597.hp2 HG00673.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.2034-2303C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189255 | |||||||
chr11:90189280 | AT | A | 36 | a0001c0001t0008g0060 a0001c0002t0001g0040 a0001c0002t0001g0197 others(33): Show |
36 | HG00544.hp2 HG00642.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.2034-2277delT | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189280 | |||||||
chr11:90189498 | G | A | 1 | a0002c0003t0005g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2034-2060G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189498 | |||||||
chr11:90189531 | G | A | 1 | a0001c0002t0001g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2034-2027G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189531 | |||||||
chr11:90189561 | G | A | 3 | a0002c0003t0005g0016 a0002c0003t0005g0262 a0003c0004t0005g0241 |
4 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2034-1997G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189561 | |||||||
chr11:90189718 | G | A | 12 | a0001c0002t0005g0019 a0001c0002t0005g0326 a0001c0002t0005g0327 others(9): Show |
13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2034-1840G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189718 | |||||||
chr11:90189737 | C | G | 39 | a0001c0001t0008g0060 a0001c0002t0001g0040 a0001c0002t0001g0197 others(36): Show |
39 | HG00544.hp2 HG00642.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.2034-1821C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189737 | |||||||
chr11:90189748 | C | T | 2 | a0001c0001t0003g0084 a0001c0001t0003g0095 |
2 | NA18970.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.2034-1810C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189748 | |||||||
chr11:90189769 | C | CA | 41 | a0001c0001t0008g0060 a0001c0002t0001g0030 a0001c0002t0001g0040 others(38): Show |
41 | HG00544.hp2 HG00642.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.2034-1777dupA | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90189769 | ||||||
chr11:90189769 | C | CAA | 68 | a0001c0001t0006g0059 a0001c0001t0008g0056 a0001c0001t0008g0075 others(65): Show |
78 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.2034-1778_2034-177 others(6): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90189769 | ||||||
chr11:90189778 | A | AG | 3 | a0002c0003t0001g0269 a0002c0003t0001g0288 a0002c0003t0001g0290 |
3 | HG01192.hp2 HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2034-1780_2034-177 others(5): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189778 | |||||||
chr11:90189805 | A | G | 1 | a0004c0005t0014g0252 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2034-1753A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189805 | |||||||
chr11:90189857 | G | T | 2 | a0001c0002t0001g0232 a0001c0002t0001g0309 |
2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2034-1701G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90189857 | |||||||
chr11:90190049 | T | G | 1 | a0002c0003t0001g0280 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2034-1509T>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190049 | |||||||
chr11:90190082 | G | A | 1 | a0002c0003t0001g0284 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2034-1476G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190082 | |||||||
chr11:90190114 | G | T | 163 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(160): Show |
175 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.2034-1444G>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190114 | |||||||
chr11:90190200 | C | CACA | 213 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(210): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2034-1356_2034-135 others(7): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90190200 | ||||||
chr11:90190317 | T | C | 12 | a0001c0002t0005g0019 a0001c0002t0005g0326 a0001c0002t0005g0327 others(9): Show |
13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2034-1241T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190317 | |||||||
chr11:90190349 | A | C | 2 | a0004c0005t0005g0263 a0004c0021t0011g0184 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2034-1209A>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190349 | |||||||
chr11:90190437 | G | C | 12 | a0001c0002t0005g0019 a0001c0002t0005g0326 a0001c0002t0005g0327 others(9): Show |
13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2034-1121G>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190437 | |||||||
chr11:90190712 | C | G | 167 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0050 others(164): Show |
179 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.2034-846C>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190712 | |||||||
chr11:90190731 | G | A | 2 | a0001c0001t0006g0174 a0001c0001t0006g0179 |
2 | HG00738.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2034-827G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190731 | |||||||
chr11:90190769 | GTCATTAA | G | 6 | a0001c0002t0001g0232 a0001c0002t0001g0309 a0001c0006t0001g0300 others(3): Show |
6 | HG01109.hp2 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2034-773_2034-767d others(9): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90190769 | ||||||
chr11:90190833 | C | T | 12 | a0001c0002t0005g0019 a0001c0002t0005g0326 a0001c0002t0005g0327 others(9): Show |
13 | HG00323.hp1 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2034-725C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190833 | |||||||
chr11:90190964 | T | C | 4 | a0001c0002t0005g0319 a0001c0006t0005g0325 a0004c0005t0005g0248 others(1): Show |
4 | HG02109.hp1 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2034-594T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90190964 | |||||||
chr11:90191100 | A | G | 2 | a0001c0002t0005g0320 a0001c0006t0005g0323 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2034-458A>G | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191100 | |||||||
chr11:90191151 | T | C | 1 | a0002c0003t0001g0288 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2034-407T>C | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191151 | |||||||
chr11:90191270 | C | T | 1 | a0002c0003t0001g0280 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2034-288C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191270 | |||||||
chr11:90191288 | T | A | 1 | a0003c0004t0005g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2034-270T>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191288 | |||||||
chr11:90191300 | T | TAAAAGAA others(314): Show |
4 | a0001c0006t0001g0300 a0001c0006t0001g0301 a0001c0006t0001g0321 others(1): Show |
4 | HG01109.hp2 HG02622.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2034-244_2034-243i others(323): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90191300 | ||||||
chr11:90191300 | T | TAAAAGAA others(333): Show |
1 | a0001c0002t0001g0232 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2034-244_2034-243i others(342): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90191300 | ||||||
chr11:90191300 | T | TAAAAGAA others(339): Show |
1 | a0001c0002t0001g0309 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2034-244_2034-243i others(348): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr11 | 90191300 | ||||||
chr11:90191461 | G | A | 3 | a0002c0003t0005g0016 a0002c0003t0005g0262 a0003c0004t0005g0241 |
4 | HG02258.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2034-97G>A | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191461 | |||||||
chr11:90191479 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2034-79C>T | NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 18/18 | chr11 | 90191479 |