Item | Value |
---|---|
geneid | 79841 |
ensemblid | ENSG00000165923.17 |
hgncid | 26296 |
symbol | AGBL2 |
name | AGBL carboxypeptidase 2 |
refseq_nuc | NM_024783.4 |
refseq_prot | NP_079059.2 |
ensembl_nuc | ENST00000525123.6 |
ensembl_prot | ENSP00000435582.1 |
mane_status | MANE Select |
chr | chr11 |
start | 47659591 |
end | 47715369 |
strand | - |
ver | v1.2 |
region | chr11:47659591-47715369 |
region5000 | chr11:47654591-47720369 |
regionname0 | AGBL2_chr11_47659591_47715369 |
regionname5000 | AGBL2_chr11_47654591_47720369 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 902 | 207 | 49 | 31 | 98 | 6 | 22 | 82 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0002 | 1/0 | 902 | 125 | 25 | 24 | 48 | 8 | 19 | 36 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0003 | 0/0 | 902 | 7 | 1 | 4 | 0 | 1 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0004 | 0/0 | 902 | 3 | 0 | 0 | 2 | 1 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0005 | 0/0 | 902 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0006 | 0/0 | 902 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0007 | 0/0 | 902 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0008 | 0/0 | 902 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0009 | 0/0 | 902 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0010 | 0/0 | 902 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0011 | 0/0 | 902 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0012 | 0/0 | 902 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
a0013 | 0/0 | 902 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | MFPAL others(897): Show |
chr11 | 47654591 | 47720369 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2706 | 207 | 49 | 31 | 98 | 6 | 22 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0002c0002 | 1/0 | 2706 | 119 | 22 | 23 | 46 | 8 | 19 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0002c0008 | 0/0 | 2706 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0002c0009 | 0/0 | 2706 | 2 | 0 | 1 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0002c0013 | 0/0 | 2706 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0002c0017 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0003c0003 | 0/0 | 2706 | 7 | 1 | 4 | 0 | 1 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0004c0005 | 0/0 | 2706 | 3 | 0 | 0 | 2 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0005c0004 | 0/0 | 2706 | 3 | 3 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0006c0006 | 0/0 | 2706 | 3 | 0 | 0 | 3 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0007c0007 | 0/0 | 2706 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0008c0014 | 0/0 | 2706 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0009c0011 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0010c0010 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0011c0015 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0012c0012 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 | ||
a0013c0016 | 0/0 | 2706 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | ATGTT others(2701): Show |
chr11 | 47654591 | 47720369 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3586 | 200 | 46 | 31 | 94 | 6 | 22 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0001c0001t0002 | 0/0 | 3586 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0001c0001t0003 | 0/0 | 3586 | 3 | 0 | 0 | 3 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0001c0001t0005 | 0/0 | 3586 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0001c0001t0006 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0002c0002t0001 | 1/0 | 3586 | 15 | 14 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0002c0002t0002 | 0/0 | 3586 | 103 | 8 | 23 | 46 | 8 | 18 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0002c0002t0007 | 0/0 | 3586 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0002c0008t0004 | 0/0 | 3586 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0002c0009t0002 | 0/0 | 3586 | 2 | 0 | 1 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0002c0013t0002 | 0/0 | 3586 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0002c0017t0002 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0003c0003t0002 | 0/0 | 3586 | 7 | 1 | 4 | 0 | 1 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0004c0005t0001 | 0/0 | 3586 | 3 | 0 | 0 | 2 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0005c0004t0002 | 0/0 | 3586 | 3 | 3 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0006c0006t0001 | 0/0 | 3586 | 3 | 0 | 0 | 3 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0007c0007t0001 | 0/0 | 3586 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0008c0014t0001 | 0/0 | 3586 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0009c0011t0001 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0010c0010t0001 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0011c0015t0001 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0012c0012t0001 | 0/0 | 3586 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
a0013c0016t0001 | 0/0 | 3586 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | AGACT others(3581): Show |
chr11 | 47654591 | 47720369 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0001c0001t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0344 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0002t0007g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0008t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0008t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0009t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0009t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0013t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0002c0017t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0003c0003t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0004c0005t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0004c0005t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0004c0005t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0005c0004t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0005c0004t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0005c0004t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0006c0006t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0006c0006t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0006c0006t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0007c0007t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0007c0007t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0008c0014t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0009c0011t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0010c0010t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0011c0015t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0012c0012t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
a0013c0016t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0039 | EUR | GBR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00099 | hp2 | a0003 | c0003 | t0002 | g0097 | EUR | GBR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | GBR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0051 | EUR | FIN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0331 | EUR | FIN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0017 | EUR | FIN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00544 | hp2 | a0002 | c0009 | t0002 | g0115 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00609 | hp1 | a0004 | c0005 | t0001 | g0306 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00639 | hp2 | a0003 | c0003 | t0002 | g0121 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0049 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | CHS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00735 | hp1 | a0003 | c0003 | t0002 | g0122 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0046 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0045 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0065 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0236 | AMR | PUR | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0100 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01261 | hp1 | a0003 | c0003 | t0002 | g0355 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0107 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0112 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0038 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0057 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0059 | EUR | IBS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0061 | EUR | IBS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0053 | EUR | IBS | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0234 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0052 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01978 | hp2 | a0002 | c0009 | t0002 | g0114 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0113 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0099 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0063 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02148 | hp2 | a0008 | c0014 | t0001 | g0223 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | CDX | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CDX | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02257 | hp1 | a0003 | c0003 | t0002 | g0109 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02258 | hp2 | a0007 | c0007 | t0001 | g0126 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0055 | AMR | PEL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0352 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02451 | hp2 | a0002 | c0017 | t0002 | g0235 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | KHV | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02572 | hp2 | a0009 | c0011 | t0001 | g0211 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0343 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0329 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0042 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02683 | hp2 | a0003 | c0003 | t0002 | g0110 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0330 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02723 | hp2 | a0005 | c0004 | t0002 | g0345 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0111 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0034 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02896 | hp1 | a0002 | c0008 | t0004 | g0351 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0054 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02965 | hp1 | a0010 | c0010 | t0001 | g0002 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02970 | hp1 | a0007 | c0007 | t0001 | g0125 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0350 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0020 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03098 | hp1 | a0002 | c0008 | t0004 | g0353 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03130 | hp2 | a0005 | c0004 | t0002 | g0347 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ESN | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0040 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03486 | hp2 | a0005 | c0004 | t0002 | g0346 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0098 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0103 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0060 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0026 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0028 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0021 | SAS | BEB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0033 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0117 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04204 | hp1 | a0002 | c0002 | t0007 | g0340 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18747 | hp1 | a0013 | c0016 | t0001 | g0171 | EAS | CHB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | CHB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18941 | hp1 | a0006 | c0006 | t0001 | g0304 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18970 | hp1 | a0006 | c0006 | t0001 | g0305 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18977 | hp1 | a0004 | c0005 | t0001 | g0273 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19005 | hp1 | a0002 | c0013 | t0002 | g0237 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19007 | hp2 | a0006 | c0006 | t0001 | g0292 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | YRI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0108 | AFR | ASW | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0325 | AFR | ASW | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | TSI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20752 | hp2 | a0004 | c0005 | t0001 | g0303 | EUR | TSI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0101 | EUR | TSI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0013 | EUR | TSI | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0041 | SAS | GIH | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | GIH | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01123 | hp1 | a0003 | c0003 | t0002 | g0096 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0047 | AMR | CLM | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03471 | hp1 | a0011 | c0015 | t0001 | g0342 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | USA | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
HG06807 | hp2 | a0012 | c0012 | t0001 | g0324 | AFR | USA | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | LWK | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0283 | REF | REF | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0344 | REF | REF | AGBL2_chr11_47654591_47720369 | AGBL2 | chr11 | 47654591 | 47720369 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47660227 | T | A | 1 | a0012 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.2655A>T | p.Arg885Ser | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 2950/3586 | 2655/2709 | 885/902 | chr11 | 47660227 | |||
chr11:47679976 | C | A | 9 | a0001 a0004 a0005 others(6): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
missense_variant | MODERATE | c.2013G>T | p.Met671Ile | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/19 | 2308/3586 | 2013/2709 | 671/902 | chr11 | 47679976 | |||
chr11:47690172 | C | A | 1 | a0008 | 1 | HG02148.hp2 | missense_variant | MODERATE | c.1535G>T | p.Arg512Leu | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1830/3586 | 1535/2709 | 512/902 | chr11 | 47690172 | |||
chr11:47690268 | A | G | 1 | a0004 | 3 | HG00609.hp1 NA18977.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.1439T>C | p.Leu480Pro | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1734/3586 | 1439/2709 | 480/902 | chr11 | 47690268 | |||
chr11:47690332 | C | A | 1 | a0011 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1375G>T | p.Ala459Ser | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1670/3586 | 1375/2709 | 459/902 | chr11 | 47690332 | |||
chr11:47690607 | G | A | 1 | a0013 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.1100C>T | p.Thr367Met | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1395/3586 | 1100/2709 | 367/902 | chr11 | 47690607 | |||
chr11:47690661 | C | T | 1 | a0003 | 7 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(4): Show |
missense_variant | MODERATE | c.1046G>A | p.Arg349His | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1341/3586 | 1046/2709 | 349/902 | chr11 | 47690661 | |||
chr11:47699497 | G | A | 1 | a0006 | 3 | NA18941.hp1 NA18970.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.643C>T | p.Pro215Ser | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/19 | 938/3586 | 643/2709 | 215/902 | chr11 | 47699497 | |||
chr11:47704575 | C | T | 1 | a0009 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.554G>A | p.Cys185Tyr | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/19 | 849/3586 | 554/2709 | 185/902 | chr11 | 47704575 | |||
chr11:47704602 | A | C | 1 | a0005 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.527T>G | p.Leu176Arg | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/19 | 822/3586 | 527/2709 | 176/902 | chr11 | 47704602 | |||
chr11:47705538 | C | T | 1 | a0010 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.383G>A | p.Arg128Gln | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/19 | 678/3586 | 383/2709 | 128/902 | chr11 | 47705538 | |||
chr11:47710389 | C | G | 1 | a0007 | 2 | HG02258.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.220G>C | p.Glu74Gln | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/19 | 515/3586 | 220/2709 | 74/902 | chr11 | 47710389 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47660326 | T | C | 1 | a0002c0008 | 2 | HG02896.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.2556A>G | p.Thr852Thr | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 2851/3586 | 2556/2709 | 852/902 | chr11 | 47660326 | |||
chr11:47690159 | G | A | 1 | a0002c0013 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.1548C>T | p.Ala516Ala | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/19 | 1843/3586 | 1548/2709 | 516/902 | chr11 | 47690159 | |||
chr11:47699456 | T | C | 1 | a0002c0009 | 2 | HG00544.hp2 HG01978.hp2 |
synonymous_variant | LOW | c.684A>G | p.Gln228Gln | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/19 | 979/3586 | 684/2709 | 228/902 | chr11 | 47699456 | |||
chr11:47705889 | G | A | 1 | a0002c0017 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.261C>T | p.His87His | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 5/19 | 556/3586 | 261/2709 | 87/902 | chr11 | 47705889 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47659661 | A | T | 1 | a0001c0001t0006 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 512 | chr11 | 47659661 | ||||||
chr11:47659708 | C | T | 1 | a0002c0008t0004 | 2 | HG02896.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*465G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 465 | chr11 | 47659708 | ||||||
chr11:47659725 | T | C | 1 | a0001c0001t0003 | 3 | HG02083.hp2 NA18747.hp2 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*448A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 448 | chr11 | 47659725 | ||||||
chr11:47659790 | C | A | 1 | a0001c0001t0005 | 2 | HG02622.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*383G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 383 | chr11 | 47659790 | ||||||
chr11:47659818 | T | G | 8 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0007 others(5): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*355A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 19/19 | 355 | chr11 | 47659818 | ||||||
chr11:47714691 | T | C | 1 | a0002c0002t0007 | 1 | HG04204.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-41A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 2/19 | chr11 | 47714691 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47660556 | A | AT | 220 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(217): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.2536-211dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47660556 | |||||||
chr11:47660696 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2536-350C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47660696 | |||||||
chr11:47660720 | A | AT | 336 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(333): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.2536-375dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47660720 | |||||||
chr11:47660850 | C | T | 115 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2536-504G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47660850 | |||||||
chr11:47661119 | T | C | 115 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2536-773A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661119 | |||||||
chr11:47661145 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2536-799T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661145 | |||||||
chr11:47661173 | A | T | 134 | a0001c0001t0001g0044 a0001c0001t0001g0136 a0001c0001t0001g0137 others(131): Show |
134 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.2536-827T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661173 | |||||||
chr11:47661231 | C | T | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2536-885G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661231 | |||||||
chr11:47661469 | G | C | 2 | a0007c0007t0001g0125 a0007c0007t0001g0126 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2536-1123C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661469 | |||||||
chr11:47661509 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2536-1163G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661509 | |||||||
chr11:47661532 | G | C | 1 | a0001c0001t0001g0341 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2536-1186C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661532 | |||||||
chr11:47661611 | T | C | 11 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2536-1265A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661611 | |||||||
chr11:47661987 | T | C | 2 | a0002c0008t0004g0351 a0002c0008t0004g0353 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535+1039A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47661987 | |||||||
chr11:47662213 | A | G | 115 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2535+813T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662213 | |||||||
chr11:47662476 | G | T | 1 | a0002c0002t0002g0092 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2535+550C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662476 | |||||||
chr11:47662495 | CT | C | 219 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(216): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2535+530delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662495 | |||||||
chr11:47662499 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2535+527A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662499 | |||||||
chr11:47662519 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2535+507C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662519 | |||||||
chr11:47662898 | C | A | 350 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(347): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.2535+128G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662898 | |||||||
chr11:47662910 | C | A | 10 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2535+116G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 18/18 | chr11 | 47662910 | |||||||
chr11:47663356 | T | C | 115 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2449-244A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47663356 | |||||||
chr11:47663557 | C | CT | 27 | a0001c0001t0001g0299 a0002c0002t0002g0013 a0002c0002t0002g0015 others(24): Show |
27 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.2449-446dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47663557 | |||||||
chr11:47663557 | CT | C | 9 | a0001c0001t0001g0142 a0001c0001t0001g0186 a0001c0001t0001g0291 others(6): Show |
9 | HG01099.hp2 HG01261.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.2449-446delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47663557 | |||||||
chr11:47663802 | C | T | 221 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(218): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.2449-690G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47663802 | |||||||
chr11:47663942 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2449-830G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47663942 | |||||||
chr11:47664018 | C | T | 10 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0320 others(7): Show |
10 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2449-906G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664018 | |||||||
chr11:47664046 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2449-934C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664046 | |||||||
chr11:47664135 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2449-1023C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664135 | |||||||
chr11:47664175 | A | C | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2449-1063T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664175 | |||||||
chr11:47664189 | G | T | 11 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2449-1077C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664189 | |||||||
chr11:47664211 | TC | T | 7 | a0001c0001t0001g0314 a0001c0001t0001g0320 a0001c0001t0001g0321 others(4): Show |
7 | HG02258.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2449-1100delG | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664211 | |||||||
chr11:47664277 | C | T | 221 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(218): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.2449-1165G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664277 | |||||||
chr11:47664390 | G | C | 3 | a0002c0002t0002g0016 a0002c0002t0002g0031 a0002c0002t0002g0032 |
3 | HG02965.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2449-1278C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664390 | |||||||
chr11:47664414 | G | GT | 11 | a0001c0001t0001g0201 a0001c0001t0001g0261 a0001c0001t0001g0307 others(8): Show |
11 | HG00735.hp1 HG02572.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.2449-1303dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664414 | |||||||
chr11:47664498 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2449-1386C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664498 | |||||||
chr11:47664555 | C | T | 10 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2449-1443G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664555 | |||||||
chr11:47664605 | G | T | 1 | a0001c0001t0001g0266 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2449-1493C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664605 | |||||||
chr11:47664668 | C | G | 1 | a0002c0002t0002g0060 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2449-1556G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664668 | |||||||
chr11:47664759 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2449-1647A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664759 | |||||||
chr11:47664883 | T | TA | 6 | a0001c0001t0001g0243 a0001c0001t0001g0334 a0001c0001t0001g0335 others(3): Show |
6 | HG02897.hp1 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2449-1772_2449-177 others(5): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664883 | |||||||
chr11:47664884 | T | A | 16 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0134 others(13): Show |
16 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.2449-1772A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664884 | |||||||
chr11:47664890 | T | A | 151 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.2449-1778A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664890 | |||||||
chr11:47664890 | T | TA | 98 | a0001c0001t0001g0044 a0001c0001t0001g0199 a0001c0001t0001g0200 others(95): Show |
98 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2449-1779_2449-177 others(5): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664890 | |||||||
chr11:47664895 | A | T | 348 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(345): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2449-1783T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664895 | |||||||
chr11:47664896 | A | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0196 a0001c0001t0001g0229 others(1): Show |
4 | HG00741.hp1 HG02965.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2449-1784T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47664896 | |||||||
chr11:47665067 | T | C | 1 | a0008c0014t0001g0223 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2448+1889A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665067 | |||||||
chr11:47665247 | A | G | 1 | a0002c0002t0002g0043 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2448+1709T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665247 | |||||||
chr11:47665595 | A | G | 85 | a0001c0001t0001g0064 a0001c0001t0001g0123 a0001c0001t0001g0124 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2448+1361T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665595 | |||||||
chr11:47665781 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2448+1175T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665781 | |||||||
chr11:47665793 | T | C | 1 | a0002c0002t0001g0350 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2448+1163A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665793 | |||||||
chr11:47665831 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0015 a0002c0002t0002g0017 others(2): Show |
5 | HG00323.hp2 HG01496.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.2448+1125C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47665831 | |||||||
chr11:47666090 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2448+866T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666090 | |||||||
chr11:47666192 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2448+764C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666192 | |||||||
chr11:47666214 | C | T | 1 | a0011c0015t0001g0342 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2448+742G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666214 | |||||||
chr11:47666254 | C | A | 2 | a0001c0001t0001g0311 a0001c0001t0001g0312 |
2 | HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2448+702G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666254 | |||||||
chr11:47666256 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2448+700A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666256 | |||||||
chr11:47666295 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2448+661C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666295 | |||||||
chr11:47666313 | G | T | 10 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2448+643C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666313 | |||||||
chr11:47666333 | G | T | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2448+623C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666333 | |||||||
chr11:47666391 | C | CA | 114 | a0001c0001t0001g0128 a0002c0002t0002g0012 a0002c0002t0002g0013 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.2448+564dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666391 | |||||||
chr11:47666492 | C | T | 1 | a0002c0002t0002g0100 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2448+464G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666492 | |||||||
chr11:47666520 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2448+436A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666520 | |||||||
chr11:47666907 | G | A | 29 | a0001c0001t0001g0238 a0001c0001t0001g0243 a0001c0001t0001g0311 others(26): Show |
29 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.2448+49C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 17/18 | chr11 | 47666907 | |||||||
chr11:47667100 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2341-37A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667100 | |||||||
chr11:47667170 | A | AGCAGAGG others(4): Show |
1 | a0001c0001t0001g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2341-118_2341-108d others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667170 | |||||||
chr11:47667355 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2340+216G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667355 | |||||||
chr11:47667397 | C | T | 1 | a0002c0002t0007g0340 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2340+174G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667397 | |||||||
chr11:47667399 | C | T | 1 | a0002c0002t0002g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2340+172G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667399 | |||||||
chr11:47667416 | C | T | 1 | a0002c0002t0002g0070 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2340+155G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667416 | |||||||
chr11:47667435 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2340+136G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 16/18 | chr11 | 47667435 | |||||||
chr11:47667790 | G | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG01071.hp1 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2215-94C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47667790 | |||||||
chr11:47667791 | C | T | 115 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2215-95G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47667791 | |||||||
chr11:47667798 | G | A | 1 | a0002c0002t0002g0093 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2215-102C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47667798 | |||||||
chr11:47667880 | A | G | 1 | a0003c0003t0002g0122 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2215-184T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47667880 | |||||||
chr11:47668110 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2215-414C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668110 | |||||||
chr11:47668139 | G | A | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2215-443C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668139 | |||||||
chr11:47668153 | A | G | 6 | a0001c0001t0001g0158 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | HG03942.hp1 NA18952.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.2215-457T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668153 | |||||||
chr11:47668166 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2215-470C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668166 | |||||||
chr11:47668208 | C | CA | 98 | a0001c0001t0001g0064 a0001c0001t0001g0123 a0001c0001t0001g0124 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2215-513dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668208 | |||||||
chr11:47668208 | C | CAA | 10 | a0001c0001t0001g0160 a0001c0001t0001g0164 a0001c0001t0001g0182 others(7): Show |
10 | HG00673.hp1 HG01346.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.2215-514_2215-513d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668208 | |||||||
chr11:47668208 | CA | C | 115 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2215-513delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668208 | |||||||
chr11:47668291 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2214+550C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668291 | |||||||
chr11:47668298 | G | C | 1 | a0002c0002t0002g0065 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2214+543C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 15/18 | chr11 | 47668298 | |||||||
chr11:47669359 | C | A | 1 | a0001c0001t0001g0316 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2148-452G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47669359 | |||||||
chr11:47669487 | C | T | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2148-580G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47669487 | |||||||
chr11:47669551 | C | T | 1 | a0002c0002t0002g0052 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2148-644G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47669551 | |||||||
chr11:47669680 | TA | T | 132 | a0001c0001t0001g0044 a0001c0001t0001g0140 a0001c0001t0001g0196 others(129): Show |
132 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.2148-774delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47669680 | |||||||
chr11:47669701 | T | G | 1 | a0001c0001t0001g0246 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2148-794A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47669701 | |||||||
chr11:47670006 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2148-1099G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670006 | |||||||
chr11:47670332 | T | A | 2 | a0002c0002t0002g0023 a0002c0002t0002g0024 |
2 | NA18949.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.2148-1425A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670332 | |||||||
chr11:47670333 | A | T | 4 | a0001c0001t0001g0331 a0002c0002t0002g0016 a0002c0002t0002g0031 others(1): Show |
4 | HG00280.hp2 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2148-1426T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670333 | |||||||
chr11:47670427 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2148-1520C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670427 | |||||||
chr11:47670490 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2148-1583T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670490 | |||||||
chr11:47670491 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2148-1584A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670491 | |||||||
chr11:47670526 | C | T | 1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2148-1619G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670526 | |||||||
chr11:47670608 | C | T | 73 | a0001c0001t0001g0044 a0001c0001t0001g0239 a0001c0001t0001g0240 others(70): Show |
73 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.2148-1701G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670608 | |||||||
chr11:47670694 | T | TA | 193 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(190): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2148-1788dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670694 | |||||||
chr11:47670729 | C | T | 1 | a0001c0001t0001g0341 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2148-1822G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670729 | |||||||
chr11:47670804 | G | C | 1 | a0001c0001t0001g0272 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2148-1897C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670804 | |||||||
chr11:47670868 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2148-1961C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47670868 | |||||||
chr11:47671206 | G | T | 1 | a0006c0006t0001g0292 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2148-2299C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671206 | |||||||
chr11:47671332 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2148-2425A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671332 | |||||||
chr11:47671439 | G | A | 1 | a0002c0002t0002g0043 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2148-2532C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671439 | |||||||
chr11:47671529 | A | AAAAC | 120 | a0001c0001t0001g0044 a0001c0001t0001g0199 a0001c0001t0001g0200 others(117): Show |
120 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.2148-2626_2148-262 others(8): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671529 | |||||||
chr11:47671724 | T | TAATTCCC others(7): Show |
1 | a0001c0001t0001g0197 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2148-2831_2148-281 others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671724 | |||||||
chr11:47671950 | G | C | 1 | a0002c0002t0002g0062 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2148-3043C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47671950 | |||||||
chr11:47672101 | C | T | 3 | a0002c0002t0002g0023 a0002c0002t0002g0024 a0002c0002t0002g0025 |
3 | NA18949.hp2 NA19065.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2148-3194G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672101 | |||||||
chr11:47672202 | C | T | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2148-3295G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672202 | |||||||
chr11:47672292 | T | C | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02109.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2148-3385A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672292 | |||||||
chr11:47672321 | C | CT | 77 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(74): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.2148-3415dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672321 | |||||||
chr11:47672447 | T | C | 1 | a0002c0002t0002g0042 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2148-3540A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672447 | |||||||
chr11:47672474 | C | G | 1 | a0002c0002t0001g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2148-3567G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672474 | |||||||
chr11:47672558 | G | A | 1 | a0003c0003t0002g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2148-3651C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672558 | |||||||
chr11:47672560 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2148-3653G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672560 | |||||||
chr11:47672594 | C | T | 1 | a0002c0002t0002g0092 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2148-3687G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672594 | |||||||
chr11:47672614 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18968.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2148-3707G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672614 | |||||||
chr11:47672655 | G | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18968.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2148-3748C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47672655 | |||||||
chr11:47673022 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2148-4115C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673022 | |||||||
chr11:47673147 | C | T | 221 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(218): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.2147+4124G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673147 | |||||||
chr11:47673379 | A | G | 135 | a0001c0001t0001g0044 a0001c0001t0001g0136 a0001c0001t0001g0137 others(132): Show |
135 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.2147+3892T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673379 | |||||||
chr11:47673581 | T | C | 336 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(333): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.2147+3690A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673581 | |||||||
chr11:47673793 | C | CA | 162 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(159): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.2147+3477dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673793 | |||||||
chr11:47673793 | C | CAA | 15 | a0001c0001t0001g0128 a0001c0001t0001g0142 a0001c0001t0001g0160 others(12): Show |
15 | HG00673.hp1 HG01175.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.2147+3476_2147+347 others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673793 | |||||||
chr11:47673793 | CA | C | 117 | a0001c0001t0001g0140 a0001c0001t0001g0203 a0002c0002t0001g0003 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.2147+3477delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673793 | |||||||
chr11:47673826 | G | A | 4 | a0002c0002t0002g0070 a0002c0002t0002g0077 a0002c0002t0002g0079 others(1): Show |
4 | HG00438.hp1 NA18964.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2147+3445C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673826 | |||||||
chr11:47673956 | G | A | 115 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2147+3315C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47673956 | |||||||
chr11:47674041 | G | A | 1 | a0002c0002t0002g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2147+3230C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674041 | |||||||
chr11:47674068 | G | C | 1 | a0002c0002t0002g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2147+3203C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674068 | |||||||
chr11:47674122 | A | G | 2 | a0002c0002t0001g0350 a0002c0002t0001g0352 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2147+3149T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674122 | |||||||
chr11:47674151 | G | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.2147+3120C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674151 | |||||||
chr11:47674155 | C | G | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.2147+3116G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674155 | |||||||
chr11:47674288 | G | A | 82 | a0002c0002t0002g0012 a0002c0002t0002g0014 a0002c0002t0002g0018 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2147+2983C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674288 | |||||||
chr11:47674522 | G | A | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2147+2749C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674522 | |||||||
chr11:47674566 | CA | C | 17 | a0001c0001t0001g0175 a0001c0001t0001g0196 a0001c0001t0001g0197 others(14): Show |
17 | HG00735.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.2147+2704delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674566 | |||||||
chr11:47674566 | CAA | C | 91 | a0001c0001t0001g0064 a0001c0001t0001g0123 a0001c0001t0001g0124 others(88): Show |
91 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.2147+2703_2147+270 others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674566 | |||||||
chr11:47674566 | CAAA | C | 241 | a0001c0001t0001g0044 a0001c0001t0001g0140 a0001c0001t0001g0142 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2147+2702_2147+270 others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674566 | |||||||
chr11:47674571 | A | G | 1 | a0002c0002t0002g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2147+2700T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674571 | |||||||
chr11:47674662 | A | T | 115 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2147+2609T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674662 | |||||||
chr11:47674765 | C | T | 2 | a0002c0002t0001g0350 a0002c0002t0001g0352 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2147+2506G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674765 | |||||||
chr11:47674875 | C | G | 3 | a0001c0001t0001g0212 a0001c0001t0001g0220 a0001c0001t0001g0354 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2147+2396G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47674875 | |||||||
chr11:47675044 | A | T | 81 | a0002c0002t0002g0012 a0002c0002t0002g0014 a0002c0002t0002g0018 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.2147+2227T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675044 | |||||||
chr11:47675126 | TG | T | 6 | a0001c0001t0001g0158 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | HG03942.hp1 NA18952.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.2147+2144delC | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675126 | |||||||
chr11:47675184 | T | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0297 |
2 | NA18987.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.2147+2087A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675184 | |||||||
chr11:47675194 | C | G | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02109.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2147+2077G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675194 | |||||||
chr11:47675199 | C | CT | 8 | a0001c0001t0001g0231 a0001c0001t0001g0247 a0001c0001t0001g0249 others(5): Show |
8 | HG02056.hp1 HG03471.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.2147+2071dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675199 | |||||||
chr11:47675199 | CT | C | 129 | a0001c0001t0001g0064 a0001c0001t0001g0123 a0001c0001t0001g0124 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.2147+2071delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675199 | |||||||
chr11:47675199 | CTT | C | 17 | a0001c0001t0001g0142 a0001c0001t0001g0208 a0001c0001t0001g0230 others(14): Show |
17 | HG01257.hp2 HG01943.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2147+2070_2147+207 others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675199 | |||||||
chr11:47675199 | CTTTT | C | 110 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.2147+2068_2147+207 others(8): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675199 | |||||||
chr11:47675199 | CTTTTTTT others(6): Show |
C | 3 | a0005c0004t0002g0345 a0005c0004t0002g0346 a0005c0004t0002g0347 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2147+2059_2147+207 others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675199 | |||||||
chr11:47675270 | G | A | 1 | a0002c0002t0002g0105 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2147+2001C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675270 | |||||||
chr11:47675375 | G | GT | 171 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.2147+1895dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675375 | |||||||
chr11:47675375 | G | GTT | 43 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0137 others(40): Show |
43 | HG01071.hp1 HG01109.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.2147+1894_2147+189 others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675375 | |||||||
chr11:47675375 | GT | G | 95 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0015 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.2147+1895delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675375 | |||||||
chr11:47675500 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2147+1771G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675500 | |||||||
chr11:47675695 | T | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG01071.hp1 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2147+1576A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47675695 | |||||||
chr11:47676041 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2147+1230G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676041 | |||||||
chr11:47676142 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2147+1129C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676142 | |||||||
chr11:47676429 | A | G | 3 | a0005c0004t0002g0345 a0005c0004t0002g0346 a0005c0004t0002g0347 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2147+842T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676429 | |||||||
chr11:47676557 | C | G | 1 | a0002c0002t0001g0352 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2147+714G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676557 | |||||||
chr11:47676726 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2147+545C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676726 | |||||||
chr11:47676810 | T | G | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2147+461A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676810 | |||||||
chr11:47676813 | C | CA | 14 | a0001c0001t0001g0182 a0001c0001t0001g0188 a0001c0001t0001g0190 others(11): Show |
14 | HG00735.hp1 HG01175.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2147+457dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676813 | |||||||
chr11:47676813 | CA | C | 136 | a0001c0001t0001g0044 a0001c0001t0001g0140 a0001c0001t0001g0151 others(133): Show |
136 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.2147+457delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676813 | |||||||
chr11:47676886 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2147+385C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47676886 | |||||||
chr11:47677237 | A | T | 1 | a0001c0001t0001g0194 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2147+34T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47677237 | |||||||
chr11:47677245 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2147+26T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 14/18 | chr11 | 47677245 | |||||||
chr11:47677450 | T | G | 1 | a0001c0001t0001g0157 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2017-49A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47677450 | |||||||
chr11:47677475 | C | T | 1 | a0002c0002t0002g0029 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2017-74G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47677475 | |||||||
chr11:47677738 | C | A | 6 | a0001c0001t0001g0243 a0001c0001t0001g0334 a0001c0001t0001g0335 others(3): Show |
6 | HG02897.hp1 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2017-337G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47677738 | |||||||
chr11:47677846 | C | A | 30 | a0002c0002t0002g0013 a0002c0002t0002g0015 a0002c0002t0002g0016 others(27): Show |
30 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2017-445G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47677846 | |||||||
chr11:47677880 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2017-479G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47677880 | |||||||
chr11:47678241 | C | T | 1 | a0002c0002t0002g0026 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2017-840G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678241 | |||||||
chr11:47678288 | C | CTATTT | 22 | a0001c0001t0001g0216 a0001c0001t0001g0220 a0001c0001t0001g0311 others(19): Show |
22 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.2017-892_2017-888d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | |||||||
chr11:47678288 | C | CTATTTTA others(3): Show |
9 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2017-897_2017-888d others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | |||||||
chr11:47678288 | C | CTATTTTA others(8): Show |
6 | a0001c0001t0001g0315 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG01496.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2017-902_2017-888d others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | |||||||
chr11:47678288 | C | CTATTTTA others(13): Show |
1 | a0001c0001t0001g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2017-907_2017-888d others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | |||||||
chr11:47678288 | CTATTT | C | 167 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(164): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2017-892_2017-888d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | |||||||
chr11:47678288 | CTATTTTA others(3): Show |
C | 4 | a0001c0001t0001g0293 a0005c0004t0002g0345 a0005c0004t0002g0346 others(1): Show |
4 | HG02723.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-897_2017-888d others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | |||||||
chr11:47678288 | CTATTTTA others(8): Show |
C | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0139 others(1): Show |
4 | HG01081.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-902_2017-888d others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | |||||||
chr11:47678288 | CTATTTTA others(18): Show |
C | 1 | a0001c0001t0001g0300 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2017-912_2017-888d others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678288 | |||||||
chr11:47678330 | A | ATTATTAT others(9): Show |
1 | a0002c0002t0002g0029 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2017-930_2017-929i others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678330 | |||||||
chr11:47678330 | A | ATTTTTTT others(6): Show |
1 | a0002c0002t0002g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2017-930_2017-929i others(15): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678330 | |||||||
chr11:47678331 | T | C | 89 | a0001c0001t0001g0064 a0001c0001t0001g0123 a0001c0001t0001g0124 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2017-930A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678331 | |||||||
chr11:47678335 | A | ATT | 32 | a0002c0002t0002g0022 a0002c0002t0002g0027 a0002c0002t0002g0030 others(29): Show |
32 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.2017-936_2017-935d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | ATTTTATT others(18): Show |
5 | a0002c0002t0002g0039 a0002c0002t0002g0040 a0002c0002t0002g0061 others(2): Show |
5 | HG00099.hp1 HG00544.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.2017-935_2017-934i others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | ATTTTATT others(19): Show |
1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2017-935_2017-934i others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | ATTTTATT others(16): Show |
1 | a0002c0002t0002g0070 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2017-935_2017-934i others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | ATTTTATT others(17): Show |
1 | a0002c0002t0002g0069 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2017-935_2017-934i others(26): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | ATTTTATT others(18): Show |
6 | a0002c0002t0002g0026 a0002c0002t0002g0028 a0002c0002t0002g0041 others(3): Show |
6 | HG02074.hp2 HG03669.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.2017-935_2017-934i others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | ATTTTATT others(19): Show |
2 | a0002c0002t0002g0014 a0002c0002t0002g0033 |
2 | HG02738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2017-935_2017-934i others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | ATTTTATT others(16): Show |
2 | a0002c0002t0002g0071 a0003c0003t0002g0121 |
2 | HG00639.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.2017-935_2017-934i others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | ATTTTATT others(17): Show |
10 | a0002c0002t0002g0012 a0002c0002t0002g0042 a0002c0002t0002g0066 others(7): Show |
10 | HG00735.hp1 HG01261.hp1 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.2017-935_2017-934i others(26): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | ATTTTATT others(18): Show |
4 | a0002c0002t0002g0072 a0002c0002t0002g0080 a0002c0002t0002g0089 others(1): Show |
4 | HG02257.hp1 NA18990.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-935_2017-934i others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | ATTTTATT others(19): Show |
1 | a0003c0003t0002g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2017-935_2017-934i others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | ATTTTATT others(20): Show |
1 | a0003c0003t0002g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2017-935_2017-934i others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678335 | A | T | 2 | a0002c0002t0002g0029 a0002c0002t0002g0111 |
2 | HG02735.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2017-934T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678335 | |||||||
chr11:47678338 | A | ATTATTTT others(11): Show |
2 | a0002c0002t0002g0102 a0002c0002t0002g0106 |
2 | NA18971.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2017-938_2017-937i others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | |||||||
chr11:47678338 | A | ATTATTTT others(16): Show |
1 | a0002c0013t0002g0237 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2017-938_2017-937i others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | |||||||
chr11:47678338 | A | ATTTTTTT others(4): Show |
1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2017-938_2017-937i others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | |||||||
chr11:47678338 | A | ATTTTTTT others(12): Show |
3 | a0002c0002t0002g0067 a0002c0002t0002g0073 a0002c0002t0002g0105 |
3 | HG00609.hp2 NA18942.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2017-938_2017-937i others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | |||||||
chr11:47678338 | A | ATTTTTTT others(14): Show |
4 | a0002c0002t0002g0018 a0002c0002t0002g0019 a0002c0002t0002g0020 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-938_2017-937i others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | |||||||
chr11:47678338 | A | ATTTTTTT others(15): Show |
1 | a0002c0002t0002g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2017-938_2017-937i others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | |||||||
chr11:47678338 | A | T | 36 | a0002c0002t0002g0012 a0002c0002t0002g0014 a0002c0002t0002g0026 others(33): Show |
36 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.2017-937T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678338 | |||||||
chr11:47678343 | A | ATTATTAT others(21): Show |
1 | a0002c0002t0002g0022 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2017-943_2017-942i others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | |||||||
chr11:47678343 | A | ATTATTAT others(20): Show |
1 | a0002c0002t0002g0083 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2017-943_2017-942i others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | |||||||
chr11:47678343 | A | ATTATTAT others(22): Show |
2 | a0002c0002t0002g0027 a0002c0002t0002g0030 |
2 | NA18956.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2017-943_2017-942i others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | |||||||
chr11:47678343 | A | ATTATTTT others(19): Show |
3 | a0002c0002t0002g0094 a0002c0002t0002g0098 a0002c0002t0002g0103 |
3 | HG03491.hp2 HG03492.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2017-943_2017-942i others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | |||||||
chr11:47678343 | A | ATTATTTT others(20): Show |
12 | a0002c0002t0002g0068 a0002c0002t0002g0076 a0002c0002t0002g0077 others(9): Show |
12 | HG00408.hp1 HG00438.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.2017-943_2017-942i others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | |||||||
chr11:47678343 | A | ATTATTTT others(21): Show |
11 | a0002c0002t0002g0074 a0002c0002t0002g0075 a0002c0002t0002g0082 others(8): Show |
11 | HG00673.hp2 HG01358.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.2017-943_2017-942i others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | |||||||
chr11:47678343 | A | ATTATTTT others(22): Show |
1 | a0002c0002t0002g0090 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2017-943_2017-942i others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | |||||||
chr11:47678343 | A | ATTTTATT others(26): Show |
1 | a0002c0002t0002g0107 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2017-943_2017-942i others(35): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | |||||||
chr11:47678343 | A | T | 50 | a0002c0002t0002g0012 a0002c0002t0002g0014 a0002c0002t0002g0018 others(47): Show |
50 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.2017-942T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678343 | |||||||
chr11:47678459 | G | A | 2 | a0007c0007t0001g0125 a0007c0007t0001g0126 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2017-1058C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678459 | |||||||
chr11:47678602 | G | C | 1 | a0002c0013t0002g0237 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2017-1201C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678602 | |||||||
chr11:47678616 | G | T | 82 | a0002c0002t0002g0012 a0002c0002t0002g0014 a0002c0002t0002g0018 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.2017-1215C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678616 | |||||||
chr11:47678794 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2016+1179C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678794 | |||||||
chr11:47678812 | G | C | 350 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(347): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.2016+1161C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678812 | |||||||
chr11:47678988 | G | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0031 a0002c0002t0002g0032 |
3 | HG02965.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2016+985C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47678988 | |||||||
chr11:47679037 | C | T | 1 | a0002c0002t0002g0050 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2016+936G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679037 | |||||||
chr11:47679058 | C | CA | 20 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0199 others(17): Show |
20 | HG01099.hp1 HG01257.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.2016+914dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | |||||||
chr11:47679058 | C | CAA | 20 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0140 others(17): Show |
20 | HG01243.hp1 HG01261.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2016+913_2016+914d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | |||||||
chr11:47679058 | C | CAAA | 34 | a0001c0001t0001g0242 a0001c0001t0001g0244 a0001c0001t0001g0260 others(31): Show |
34 | HG00280.hp2 HG00597.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.2016+912_2016+914d others(5): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | |||||||
chr11:47679058 | C | CAAAA | 39 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0245 others(36): Show |
39 | HG00408.hp2 HG00544.hp1 HG01978.hp1 others(36): Show |
intron_variant | MODIFIER | c.2016+911_2016+914d others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | |||||||
chr11:47679058 | C | CAAAAA | 7 | a0001c0001t0001g0044 a0001c0001t0001g0212 a0001c0001t0001g0246 others(4): Show |
7 | HG00609.hp1 HG00741.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.2016+910_2016+914d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | |||||||
chr11:47679058 | C | CAAAAAA | 7 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0220 others(4): Show |
7 | HG02818.hp2 HG03486.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.2016+909_2016+914d others(8): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | |||||||
chr11:47679058 | CA | C | 73 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(70): Show |
73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.2016+914delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | |||||||
chr11:47679058 | CAA | C | 125 | a0001c0001t0001g0064 a0001c0001t0001g0123 a0001c0001t0001g0124 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.2016+913_2016+914d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679058 | |||||||
chr11:47679076 | A | G | 28 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(25): Show |
28 | HG00673.hp1 HG00733.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2016+897T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679076 | |||||||
chr11:47679341 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2016+632A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679341 | |||||||
chr11:47679561 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2016+412T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679561 | |||||||
chr11:47679636 | A | G | 4 | a0002c0002t0002g0085 a0002c0002t0002g0090 a0002c0002t0002g0119 others(1): Show |
4 | HG02083.hp1 NA18944.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2016+337T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 13/18 | chr11 | 47679636 | |||||||
chr11:47680077 | G | GA | 7 | a0001c0001t0001g0151 a0001c0001t0001g0181 a0001c0001t0001g0213 others(4): Show |
7 | HG02738.hp2 NA18940.hp1 NA18944.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1916-5dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680077 | |||||||
chr11:47680089 | A | C | 10 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0036 others(7): Show |
10 | HG00280.hp1 HG01123.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1916-16T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680089 | |||||||
chr11:47680267 | T | C | 115 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1916-194A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680267 | |||||||
chr11:47680378 | G | A | 1 | a0010c0010t0001g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1916-305C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680378 | |||||||
chr11:47680514 | C | G | 1 | a0001c0001t0001g0341 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1916-441G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680514 | |||||||
chr11:47680576 | C | G | 10 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0320 others(7): Show |
10 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1916-503G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680576 | |||||||
chr11:47680747 | C | T | 1 | a0003c0003t0002g0110 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1916-674G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680747 | |||||||
chr11:47680786 | G | GAAACA | 76 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0199 others(73): Show |
76 | HG00099.hp1 HG00280.hp1 HG01123.hp2 others(73): Show |
intron_variant | MODIFIER | c.1916-718_1916-714d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | |||||||
chr11:47680786 | G | GAAACAAA others(3): Show |
148 | a0001c0001t0001g0064 a0001c0001t0001g0123 a0001c0001t0001g0124 others(145): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1916-723_1916-714d others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | |||||||
chr11:47680786 | G | GAAACAAA others(8): Show |
88 | a0001c0001t0001g0044 a0001c0001t0001g0135 a0001c0001t0001g0142 others(85): Show |
88 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1916-728_1916-714d others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | |||||||
chr11:47680786 | G | GAAACAAA others(13): Show |
5 | a0001c0001t0001g0244 a0001c0001t0001g0260 a0001c0001t0001g0263 others(2): Show |
5 | HG02083.hp2 HG03831.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1916-733_1916-714d others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | |||||||
chr11:47680786 | G | GAAACAAA others(18): Show |
1 | a0001c0001t0001g0274 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1916-738_1916-714d others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | |||||||
chr11:47680786 | GAAACA | G | 18 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0206 others(15): Show |
18 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1916-718_1916-714d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680786 | |||||||
chr11:47680795 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1916-722G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680795 | |||||||
chr11:47680843 | A | G | 103 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0238 others(100): Show |
103 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1916-770T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47680843 | |||||||
chr11:47681377 | CA | C | 11 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1915+591delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47681377 | |||||||
chr11:47681624 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1915+345G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47681624 | |||||||
chr11:47681759 | G | A | 25 | a0002c0002t0002g0013 a0002c0002t0002g0015 a0002c0002t0002g0017 others(22): Show |
25 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1915+210C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 12/18 | chr11 | 47681759 | |||||||
chr11:47682219 | A | G | 1 | a0002c0002t0002g0014 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1789-124T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682219 | |||||||
chr11:47682256 | C | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02109.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1789-161G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682256 | |||||||
chr11:47682303 | GT | G | 25 | a0001c0001t0001g0064 a0002c0002t0002g0013 a0002c0002t0002g0015 others(22): Show |
25 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1789-209delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682303 | |||||||
chr11:47682305 | T | A | 25 | a0001c0001t0001g0064 a0002c0002t0002g0013 a0002c0002t0002g0015 others(22): Show |
25 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1789-210A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682305 | |||||||
chr11:47682306 | A | G | 25 | a0001c0001t0001g0064 a0002c0002t0002g0013 a0002c0002t0002g0015 others(22): Show |
25 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1789-211T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682306 | |||||||
chr11:47682391 | T | C | 116 | a0001c0001t0001g0064 a0002c0002t0002g0012 a0002c0002t0002g0013 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1789-296A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682391 | |||||||
chr11:47682648 | T | G | 116 | a0001c0001t0001g0064 a0002c0002t0002g0012 a0002c0002t0002g0013 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1789-553A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682648 | |||||||
chr11:47682859 | G | A | 1 | a0002c0002t0002g0100 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1789-764C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682859 | |||||||
chr11:47682930 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1789-835A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47682930 | |||||||
chr11:47683177 | C | T | 4 | a0002c0002t0001g0350 a0002c0002t0001g0352 a0002c0008t0004g0351 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1789-1082G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683177 | |||||||
chr11:47683191 | C | T | 3 | a0002c0002t0002g0054 a0002c0002t0002g0063 a0002c0002t0002g0065 |
3 | HG01175.hp2 HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1789-1096G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683191 | |||||||
chr11:47683463 | C | A | 220 | a0001c0001t0001g0044 a0001c0001t0001g0123 a0001c0001t0001g0124 others(217): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1789-1368G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683463 | |||||||
chr11:47683851 | G | A | 9 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(6): Show |
9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1789-1756C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683851 | |||||||
chr11:47683928 | T | TA | 20 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0001g0238 others(17): Show |
20 | HG00597.hp1 HG01261.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.1789-1834dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683928 | |||||||
chr11:47683928 | TA | T | 80 | a0001c0001t0001g0151 a0001c0001t0001g0271 a0001c0001t0001g0287 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1789-1834delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683928 | |||||||
chr11:47683978 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1789-1883G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47683978 | |||||||
chr11:47684024 | G | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02109.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1788+1869C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684024 | |||||||
chr11:47684081 | TACCCCAT others(9): Show |
T | 1 | a0009c0011t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1788+1796_1788+181 others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684081 | |||||||
chr11:47684511 | G | A | 1 | a0003c0003t0002g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1788+1382C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684511 | |||||||
chr11:47684534 | C | T | 116 | a0001c0001t0001g0064 a0002c0002t0002g0012 a0002c0002t0002g0013 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1788+1359G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684534 | |||||||
chr11:47684589 | A | G | 220 | a0001c0001t0001g0044 a0001c0001t0001g0123 a0001c0001t0001g0124 others(217): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1788+1304T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684589 | |||||||
chr11:47684739 | A | G | 116 | a0001c0001t0001g0064 a0002c0002t0002g0012 a0002c0002t0002g0013 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1788+1154T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684739 | |||||||
chr11:47684813 | C | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0031 a0002c0002t0002g0032 |
3 | HG02965.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1788+1080G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47684813 | |||||||
chr11:47685063 | AG | A | 116 | a0001c0001t0001g0064 a0002c0002t0002g0012 a0002c0002t0002g0013 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1788+829delC | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685063 | |||||||
chr11:47685198 | C | T | 3 | a0005c0004t0002g0345 a0005c0004t0002g0346 a0005c0004t0002g0347 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1788+695G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685198 | |||||||
chr11:47685201 | C | T | 3 | a0003c0003t0002g0109 a0003c0003t0002g0121 a0003c0003t0002g0122 |
3 | HG00639.hp2 HG00735.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1788+692G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685201 | |||||||
chr11:47685385 | A | G | 2 | a0007c0007t0001g0125 a0007c0007t0001g0126 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1788+508T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685385 | |||||||
chr11:47685432 | T | C | 1 | a0002c0002t0002g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1788+461A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685432 | |||||||
chr11:47685525 | G | A | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1788+368C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685525 | |||||||
chr11:47685604 | T | C | 116 | a0001c0001t0001g0064 a0002c0002t0002g0012 a0002c0002t0002g0013 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1788+289A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685604 | |||||||
chr11:47685699 | G | T | 1 | a0001c0001t0001g0300 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1788+194C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685699 | |||||||
chr11:47685741 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1788+152G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 11/18 | chr11 | 47685741 | |||||||
chr11:47686178 | G | A | 2 | a0002c0002t0002g0016 a0002c0002t0002g0031 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1632-129C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686178 | |||||||
chr11:47686294 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1632-245C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686294 | |||||||
chr11:47686376 | C | T | 1 | a0002c0002t0002g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1632-327G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686376 | |||||||
chr11:47686447 | G | GT | 72 | a0001c0001t0001g0064 a0001c0001t0001g0151 a0001c0001t0001g0192 others(69): Show |
72 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1632-399dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686447 | |||||||
chr11:47686447 | G | GTT | 10 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(7): Show |
10 | HG00642.hp1 HG01081.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1632-400_1632-399d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686447 | |||||||
chr11:47686447 | G | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0139 |
3 | HG02257.hp2 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1632-398C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686447 | |||||||
chr11:47686447 | GT | G | 65 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0128 others(62): Show |
65 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1632-399delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686447 | |||||||
chr11:47686580 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1632-531C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686580 | |||||||
chr11:47686674 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1632-625T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686674 | |||||||
chr11:47686678 | T | C | 336 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(333): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1632-629A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686678 | |||||||
chr11:47686688 | C | T | 2 | a0001c0001t0005g0329 a0001c0001t0005g0330 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1632-639G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686688 | |||||||
chr11:47686731 | T | C | 336 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(333): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1632-682A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686731 | |||||||
chr11:47686959 | C | CA | 207 | a0001c0001t0001g0064 a0001c0001t0001g0123 a0001c0001t0001g0124 others(204): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1632-911dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686959 | |||||||
chr11:47686980 | T | A | 1 | a0002c0002t0001g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1632-931A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686980 | |||||||
chr11:47686999 | G | T | 2 | a0001c0001t0001g0269 a0001c0001t0001g0299 |
2 | NA18953.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1632-950C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47686999 | |||||||
chr11:47687141 | AT | A | 110 | a0001c0001t0001g0064 a0002c0002t0002g0012 a0002c0002t0002g0013 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1632-1093delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687141 | |||||||
chr11:47687142 | T | A | 3 | a0002c0002t0002g0099 a0002c0002t0002g0101 a0002c0002t0002g0112 |
3 | HG01358.hp1 HG02055.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1632-1093A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687142 | |||||||
chr11:47687363 | C | T | 346 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(343): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1632-1314G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687363 | |||||||
chr11:47687614 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1632-1565C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687614 | |||||||
chr11:47687660 | C | T | 116 | a0001c0001t0001g0064 a0002c0002t0002g0012 a0002c0002t0002g0013 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1632-1611G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687660 | |||||||
chr11:47687807 | C | CT | 55 | a0001c0001t0001g0064 a0001c0001t0001g0294 a0002c0002t0002g0013 others(52): Show |
55 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1632-1759dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687807 | |||||||
chr11:47687890 | C | T | 2 | a0007c0007t0001g0125 a0007c0007t0001g0126 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1632-1841G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47687890 | |||||||
chr11:47688078 | G | A | 28 | a0001c0001t0001g0064 a0002c0002t0002g0013 a0002c0002t0002g0015 others(25): Show |
28 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1631+1998C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688078 | |||||||
chr11:47688136 | A | T | 1 | a0002c0002t0002g0060 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1631+1940T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688136 | |||||||
chr11:47688159 | G | A | 346 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(343): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1631+1917C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688159 | |||||||
chr11:47688173 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1631+1903C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688173 | |||||||
chr11:47688461 | A | G | 21 | a0002c0002t0002g0014 a0002c0002t0002g0022 a0002c0002t0002g0023 others(18): Show |
21 | HG00099.hp1 HG00544.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1631+1615T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688461 | |||||||
chr11:47688473 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1631+1603A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688473 | |||||||
chr11:47688699 | T | C | 10 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1631+1377A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688699 | |||||||
chr11:47688762 | T | G | 3 | a0002c0002t0002g0016 a0002c0002t0002g0031 a0002c0002t0002g0032 |
3 | HG02965.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1631+1314A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688762 | |||||||
chr11:47688783 | A | C | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02109.hp2 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1631+1293T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688783 | |||||||
chr11:47688892 | T | A | 3 | a0002c0002t0002g0234 a0002c0002t0002g0236 a0002c0017t0002g0235 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1631+1184A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47688892 | |||||||
chr11:47689172 | G | C | 2 | a0002c0002t0002g0098 a0002c0002t0002g0103 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1631+904C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689172 | |||||||
chr11:47689302 | A | AT | 81 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(78): Show |
81 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1631+773dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689302 | |||||||
chr11:47689302 | AT | A | 102 | a0001c0001t0001g0044 a0001c0001t0001g0206 a0001c0001t0001g0238 others(99): Show |
102 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1631+773delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689302 | |||||||
chr11:47689469 | T | C | 102 | a0001c0001t0001g0044 a0001c0001t0001g0238 a0001c0001t0001g0239 others(99): Show |
102 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1631+607A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689469 | |||||||
chr11:47689485 | A | T | 1 | a0001c0001t0001g0183 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1631+591T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689485 | |||||||
chr11:47689957 | C | T | 1 | a0002c0002t0002g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1631+119G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689957 | |||||||
chr11:47689992 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1631+84C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 10/18 | chr11 | 47689992 | |||||||
chr11:47691084 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.849-226A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691084 | |||||||
chr11:47691097 | T | C | 3 | a0002c0002t0002g0035 a0002c0002t0002g0036 a0002c0002t0002g0037 |
3 | HG01255.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.849-239A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691097 | |||||||
chr11:47691099 | C | CA | 182 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(179): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.849-242dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691099 | |||||||
chr11:47691099 | C | CAA | 143 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0128 others(140): Show |
143 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.849-243_849-242dup others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691099 | |||||||
chr11:47691099 | C | CAAA | 10 | a0001c0001t0001g0239 a0001c0001t0001g0331 a0002c0002t0002g0058 others(7): Show |
10 | HG00280.hp2 HG01192.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-244_849-242dup others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691099 | |||||||
chr11:47691205 | A | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG00597.hp1 NA18962.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.849-347T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691205 | |||||||
chr11:47691211 | C | G | 2 | a0002c0002t0002g0098 a0002c0002t0002g0103 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.849-353G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691211 | |||||||
chr11:47691447 | C | A | 28 | a0001c0001t0001g0064 a0002c0002t0002g0013 a0002c0002t0002g0015 others(25): Show |
28 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.849-589G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691447 | |||||||
chr11:47691581 | G | A | 2 | a0002c0008t0004g0351 a0002c0008t0004g0353 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.848+522C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691581 | |||||||
chr11:47691640 | G | A | 28 | a0001c0001t0001g0064 a0002c0002t0002g0013 a0002c0002t0002g0015 others(25): Show |
28 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.848+463C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691640 | |||||||
chr11:47691710 | G | GAAAAAAA others(6): Show |
1 | a0004c0005t0001g0306 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.848+380_848+392dup others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691710 | |||||||
chr11:47691725 | A | AATATATA others(13): Show |
1 | a0010c0010t0001g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.848+377_848+378ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691725 | |||||||
chr11:47691727 | A | T | 3 | a0001c0001t0001g0348 a0001c0001t0001g0349 a0010c0010t0001g0002 |
3 | HG02896.hp2 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.848+376T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691727 | |||||||
chr11:47691729 | A | AAAAAAAA others(35): Show |
1 | a0003c0003t0002g0110 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(42): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(39): Show |
1 | a0003c0003t0002g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(46): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(32): Show |
1 | a0002c0002t0002g0107 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(36): Show |
1 | a0002c0002t0002g0012 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(43): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(35): Show |
1 | a0002c0002t0002g0112 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(42): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(22): Show |
1 | a0002c0002t0002g0040 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(34): Show |
1 | a0003c0003t0002g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(41): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(36): Show |
1 | a0002c0002t0002g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(43): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(23): Show |
1 | a0002c0002t0002g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(31): Show |
1 | a0002c0002t0002g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(38): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(33): Show |
4 | a0002c0002t0002g0070 a0002c0002t0002g0101 a0003c0003t0002g0097 others(1): Show |
4 | HG00099.hp2 HG00735.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(40): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0307 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(22): Show |
3 | a0002c0002t0002g0032 a0002c0002t0002g0039 a0002c0002t0002g0061 |
3 | HG00099.hp1 HG01517.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(15): Show |
1 | a0002c0002t0002g0106 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0261 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(25): Show |
1 | a0002c0002t0002g0055 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(32): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(27): Show |
1 | a0002c0002t0002g0030 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(34): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(31): Show |
1 | a0002c0002t0002g0090 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(38): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(39): Show |
1 | a0002c0002t0002g0089 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(46): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(14): Show |
1 | a0002c0002t0002g0102 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(26): Show |
1 | a0002c0002t0002g0022 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(33): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(32): Show |
1 | a0002c0002t0002g0092 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(34): Show |
1 | a0002c0002t0002g0066 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(41): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(36): Show |
1 | a0002c0002t0002g0073 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(43): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(13): Show |
1 | a0006c0006t0001g0305 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(21): Show |
1 | a0002c0002t0002g0031 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(23): Show |
1 | a0002c0002t0002g0076 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(27): Show |
1 | a0002c0002t0002g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(34): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(29): Show |
2 | a0002c0002t0002g0029 a0002c0002t0002g0085 |
2 | HG02083.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(36): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(31): Show |
2 | a0002c0002t0002g0108 a0002c0002t0002g0117 |
2 | HG04199.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(38): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(33): Show |
1 | a0002c0002t0002g0082 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(40): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(35): Show |
1 | a0002c0002t0002g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(42): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(37): Show |
1 | a0002c0002t0002g0093 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(44): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(39): Show |
1 | a0002c0002t0002g0071 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(46): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(41): Show |
1 | a0002c0002t0002g0033 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(48): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(45): Show |
1 | a0002c0002t0002g0091 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(52): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(12): Show |
1 | a0006c0006t0001g0304 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0264 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(28): Show |
1 | a0002c0002t0002g0083 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(35): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(30): Show |
3 | a0002c0002t0002g0084 a0002c0002t0002g0104 a0003c0003t0002g0121 |
3 | HG00639.hp2 HG01169.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(37): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(32): Show |
2 | a0002c0002t0002g0041 a0002c0002t0002g0068 |
2 | HG00408.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(34): Show |
1 | a0002c0002t0002g0051 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(41): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0317 a0001c0001t0002g0241 |
2 | HG02886.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(15): Show |
7 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0327 others(4): Show |
7 | HG00323.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0254 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(21): Show |
1 | a0002c0002t0002g0042 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(23): Show |
2 | a0002c0002t0002g0016 a0002c0002t0002g0118 |
2 | HG02071.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(25): Show |
1 | a0002c0002t0002g0113 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(32): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(29): Show |
1 | a0001c0001t0001g0064 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(36): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(33): Show |
3 | a0002c0002t0002g0078 a0002c0002t0002g0079 a0002c0002t0002g0116 |
3 | HG02523.hp2 NA19009.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(40): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(35): Show |
1 | a0002c0002t0002g0021 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(42): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(37): Show |
1 | a0002c0002t0002g0087 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(44): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(12): Show |
5 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0239 others(2): Show |
5 | HG02300.hp1 NA18953.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(14): Show |
4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0270 others(1): Show |
4 | HG00544.hp1 NA18947.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0203 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(16): Show |
5 | a0001c0001t0001g0253 a0001c0001t0005g0330 a0002c0002t0002g0015 others(2): Show |
5 | HG01496.hp2 HG02004.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0331 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(22): Show |
3 | a0002c0002t0002g0028 a0002c0002t0002g0063 a0002c0009t0002g0114 |
3 | HG01978.hp2 HG02145.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(24): Show |
4 | a0001c0001t0001g0202 a0002c0002t0002g0035 a0002c0002t0002g0036 others(1): Show |
4 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(26): Show |
5 | a0001c0001t0001g0246 a0002c0002t0002g0047 a0002c0002t0002g0052 others(2): Show |
5 | HG01123.hp2 HG01517.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(33): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(28): Show |
2 | a0002c0002t0002g0059 a0002c0002t0002g0060 |
2 | HG01515.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(35): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(32): Show |
1 | a0002c0002t0002g0069 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(34): Show |
1 | a0002c0002t0002g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(41): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(9): Show |
8 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0196 others(5): Show |
8 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(16): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(11): Show |
2 | a0001c0001t0001g0169 a0001c0001t0001g0267 |
2 | HG03710.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(13): Show |
7 | a0001c0001t0001g0240 a0001c0001t0001g0281 a0001c0001t0001g0284 others(4): Show |
7 | HG02148.hp1 NA18945.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(15): Show |
5 | a0001c0001t0001g0207 a0001c0001t0001g0256 a0001c0001t0001g0319 others(2): Show |
5 | HG00609.hp2 HG01071.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(17): Show |
3 | a0001c0001t0001g0298 a0002c0002t0002g0049 a0004c0005t0001g0273 |
3 | HG00408.hp2 HG00642.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0201 a0002c0002t0002g0023 |
2 | HG02572.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(26): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(21): Show |
3 | a0001c0001t0001g0200 a0002c0002t0002g0024 a0002c0002t0002g0062 |
3 | HG02109.hp2 HG03669.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(23): Show |
1 | a0002c0002t0002g0014 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(27): Show |
2 | a0002c0002t0002g0072 a0002c0002t0002g0119 |
2 | NA18944.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(34): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(29): Show |
1 | a0002c0002t0002g0081 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(36): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(31): Show |
4 | a0002c0002t0002g0074 a0002c0002t0002g0088 a0002c0002t0002g0120 others(1): Show |
4 | HG02451.hp2 NA18993.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(38): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(33): Show |
3 | a0002c0002t0002g0020 a0002c0002t0002g0025 a0002c0002t0002g0067 |
3 | HG03017.hp2 NA18942.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(40): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(35): Show |
1 | a0001c0001t0001g0287 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(42): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(37): Show |
1 | a0002c0002t0002g0094 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(44): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(8): Show |
7 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0170 others(4): Show |
7 | HG02293.hp2 HG02897.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(15): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(10): Show |
3 | a0001c0001t0001g0134 a0001c0001t0001g0161 a0001c0001t0001g0282 |
3 | HG01109.hp1 NA18941.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0242 |
2 | HG01192.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(14): Show |
4 | a0001c0001t0001g0244 a0001c0001t0001g0272 a0001c0001t0001g0309 others(1): Show |
4 | HG02056.hp1 HG03831.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(16): Show |
5 | a0001c0001t0001g0247 a0001c0001t0001g0259 a0001c0001t0001g0275 others(2): Show |
5 | HG01099.hp2 HG01169.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(18): Show |
2 | a0001c0001t0001g0212 a0001c0001t0001g0286 |
2 | HG02273.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0289 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(22): Show |
1 | a0002c0002t0002g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(24): Show |
1 | a0002c0002t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(26): Show |
1 | a0002c0002t0002g0026 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(33): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(32): Show |
2 | a0002c0002t0002g0095 a0002c0002t0002g0100 |
2 | HG01258.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(7): Show |
2 | a0001c0001t0001g0184 a0001c0001t0001g0338 |
2 | HG03540.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(14): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(9): Show |
5 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0167 others(2): Show |
5 | HG02135.hp1 NA18522.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(16): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(11): Show |
5 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0001g0158 others(2): Show |
5 | HG02135.hp2 HG03453.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(13): Show |
3 | a0001c0001t0001g0147 a0001c0001t0001g0293 a0001c0001t0001g0310 |
3 | HG03704.hp2 NA18991.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(15): Show |
6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0276 others(3): Show |
6 | HG01257.hp2 HG02280.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(17): Show |
4 | a0001c0001t0001g0220 a0001c0001t0001g0248 a0002c0002t0002g0045 others(1): Show |
4 | HG01070.hp1 HG01081.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(21): Show |
3 | a0001c0001t0001g0205 a0002c0002t0002g0065 a0002c0009t0002g0115 |
3 | HG00544.hp2 HG01175.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(28): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(29): Show |
1 | a0002c0002t0002g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(36): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(31): Show |
2 | a0002c0002t0002g0098 a0002c0002t0002g0103 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(38): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(33): Show |
2 | a0002c0002t0002g0019 a0002c0002t0002g0086 |
2 | HG01071.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(40): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(6): Show |
2 | a0002c0002t0002g0234 a0002c0002t0002g0236 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(8): Show |
5 | a0001c0001t0001g0141 a0001c0001t0001g0176 a0001c0001t0001g0177 others(2): Show |
5 | HG00323.hp1 HG01433.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(15): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(10): Show |
5 | a0001c0001t0001g0148 a0001c0001t0001g0163 a0001c0001t0001g0187 others(2): Show |
5 | HG01175.hp1 HG04115.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(12): Show |
5 | a0001c0001t0001g0135 a0001c0001t0001g0145 a0001c0001t0001g0230 others(2): Show |
5 | HG02132.hp2 HG02155.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0209 a0001c0001t0001g0271 |
2 | HG04199.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(16): Show |
8 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0252 others(5): Show |
8 | HG01255.hp1 HG02293.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(18): Show |
2 | a0001c0001t0001g0199 a0001c0001t0001g0255 |
2 | HG02071.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0288 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(27): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0238 a0002c0002t0007g0340 |
2 | HG02818.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(24): Show |
1 | a0003c0003t0002g0355 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(32): Show |
1 | a0002c0002t0002g0018 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(39): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(14): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(9): Show |
9 | a0001c0001t0001g0129 a0001c0001t0001g0152 a0001c0001t0001g0183 others(6): Show |
9 | HG02735.hp1 HG02976.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(16): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(11): Show |
5 | a0001c0001t0001g0162 a0001c0001t0001g0224 a0001c0001t0001g0231 others(2): Show |
5 | HG00597.hp1 HG02572.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0188 a0001c0001t0001g0341 |
2 | NA19077.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0155 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(17): Show |
4 | a0001c0001t0001g0268 a0001c0001t0001g0312 a0002c0002t0002g0043 others(1): Show |
4 | HG01081.hp1 HG01243.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0332 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(26): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(8): Show |
3 | a0001c0001t0001g0142 a0001c0001t0001g0339 a0007c0007t0001g0126 |
3 | HG01943.hp2 HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(15): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(12): Show |
6 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0157 others(3): Show |
6 | HG02630.hp1 HG04204.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0266 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(16): Show |
3 | a0001c0001t0001g0245 a0001c0001t0001g0295 a0001c0001t0001g0315 |
3 | HG02145.hp2 NA18957.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0159 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(31): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(30): Show |
1 | a0013c0016t0001g0171 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(37): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(7): Show |
4 | a0001c0001t0001g0138 a0001c0001t0001g0146 a0001c0001t0001g0173 others(1): Show |
4 | HG00733.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(14): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(9): Show |
4 | a0001c0001t0001g0149 a0001c0001t0001g0165 a0001c0001t0001g0228 others(1): Show |
4 | HG02056.hp2 HG02148.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(16): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(11): Show |
1 | a0002c0002t0001g0352 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(18): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(15): Show |
2 | a0001c0001t0001g0160 a0001c0001t0001g0251 |
2 | HG00673.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(17): Show |
1 | a0005c0004t0002g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0226 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(30): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0320 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(32): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(15): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(10): Show |
2 | a0001c0001t0001g0197 a0001c0001t0001g0322 |
2 | HG03471.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(14): Show |
1 | a0002c0002t0002g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(16): Show |
3 | a0001c0001t0001g0321 a0001c0001t0001g0328 a0012c0012t0001g0324 |
3 | HG02886.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(23): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(22): Show |
1 | a0005c0004t0002g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(29): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0214 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(10): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(5): Show |
2 | a0001c0001t0001g0137 a0001c0001t0001g0213 |
2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0144 a0001c0001t0001g0194 |
2 | NA18966.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(16): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0300 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0323 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(22): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0044 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(24): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAT others(6): Show |
1 | a0007c0007t0001g0125 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAT others(10): Show |
2 | a0001c0001t0001g0172 a0001c0001t0001g0313 |
2 | HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(17): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAT others(12): Show |
2 | a0001c0001t0001g0326 a0001c0001t0006g0325 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(19): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAT others(14): Show |
1 | a0001c0001t0001g0233 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAAAT others(18): Show |
1 | a0002c0008t0004g0353 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(25): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAATA others(1): Show |
6 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG01109.hp2 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(8): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAATA others(3): Show |
1 | a0002c0002t0001g0003 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(10): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAAATA others(13): Show |
2 | a0001c0001t0001g0133 a0001c0001t0001g0143 |
2 | NA18968.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.848+373_848+374ins others(20): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAATAT others(6): Show |
4 | a0002c0002t0001g0004 a0002c0002t0001g0006 a0002c0002t0001g0008 others(1): Show |
4 | HG02630.hp2 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+373_848+374ins others(13): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAAATAT others(14): Show |
1 | a0002c0008t0004g0351 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAAATATA others(3): Show |
3 | a0001c0001t0001g0164 a0001c0001t0001g0192 a0002c0002t0001g0007 |
3 | HG01346.hp1 HG01358.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.848+373_848+374ins others(10): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | AAATATAT others(14): Show |
1 | a0001c0001t0001g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.848+373_848+374ins others(21): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691729 | A | T | 4 | a0001c0001t0001g0301 a0001c0001t0001g0348 a0001c0001t0001g0349 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+374T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691729 | |||||||
chr11:47691731 | T | A | 3 | a0001c0001t0001g0318 a0002c0002t0002g0058 a0004c0005t0001g0306 |
3 | HG00609.hp1 HG01192.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.848+372A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691731 | |||||||
chr11:47691733 | T | A | 2 | a0001c0001t0001g0318 a0002c0002t0002g0058 |
2 | HG01192.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.848+370A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691733 | |||||||
chr11:47691735 | T | A | 1 | a0002c0002t0002g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.848+368A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47691735 | |||||||
chr11:47692002 | C | T | 1 | a0002c0002t0007g0340 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.848+101G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 9/18 | chr11 | 47692002 | |||||||
chr11:47692404 | C | CT | 48 | a0001c0001t0001g0064 a0001c0001t0001g0127 a0001c0001t0001g0128 others(45): Show |
48 | HG00438.hp2 HG00642.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.695-149dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692404 | |||||||
chr11:47692404 | C | CTTT | 51 | a0001c0001t0001g0205 a0001c0001t0001g0240 a0001c0001t0001g0242 others(48): Show |
51 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.695-151_695-149dup others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692404 | |||||||
chr11:47692404 | C | CTTTT | 52 | a0001c0001t0001g0044 a0001c0001t0001g0199 a0001c0001t0001g0200 others(49): Show |
52 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.695-152_695-149dup others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692404 | |||||||
chr11:47692404 | CT | C | 80 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0208 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.695-149delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692404 | |||||||
chr11:47692404 | CTTTTTTT others(5): Show |
C | 2 | a0007c0007t0001g0125 a0007c0007t0001g0126 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.695-160_695-149del others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692404 | |||||||
chr11:47692430 | G | T | 1 | a0001c0001t0001g0190 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.695-174C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692430 | |||||||
chr11:47692499 | C | T | 2 | a0002c0002t0001g0350 a0002c0002t0001g0352 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.695-243G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692499 | |||||||
chr11:47692537 | G | A | 1 | a0003c0003t0002g0122 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.695-281C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692537 | |||||||
chr11:47692603 | G | A | 10 | a0001c0001t0001g0130 a0001c0001t0001g0134 a0001c0001t0001g0158 others(7): Show |
10 | HG02135.hp1 HG03942.hp1 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.695-347C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692603 | |||||||
chr11:47692659 | G | A | 1 | a0002c0009t0002g0115 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.695-403C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47692659 | |||||||
chr11:47693058 | G | A | 127 | a0001c0001t0001g0044 a0001c0001t0001g0136 a0001c0001t0001g0137 others(124): Show |
127 | HG00280.hp2 HG00544.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.695-802C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693058 | |||||||
chr11:47693213 | G | C | 3 | a0001c0001t0001g0212 a0001c0001t0001g0220 a0001c0001t0001g0354 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.695-957C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693213 | |||||||
chr11:47693538 | TGA | T | 220 | a0001c0001t0001g0044 a0001c0001t0001g0123 a0001c0001t0001g0124 others(217): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.695-1284_695-1283d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693538 | |||||||
chr11:47693817 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.695-1561C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693817 | |||||||
chr11:47693933 | T | G | 2 | a0002c0002t0002g0038 a0002c0002t0002g0039 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.695-1677A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693933 | |||||||
chr11:47693935 | A | T | 2 | a0002c0002t0002g0038 a0002c0002t0002g0039 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.695-1679T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693935 | |||||||
chr11:47693972 | T | C | 116 | a0001c0001t0001g0064 a0002c0002t0002g0012 a0002c0002t0002g0013 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.695-1716A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47693972 | |||||||
chr11:47694022 | T | C | 28 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(25): Show |
28 | HG01071.hp1 HG01099.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.695-1766A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694022 | |||||||
chr11:47694030 | T | C | 1 | a0001c0001t0001g0275 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.695-1774A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694030 | |||||||
chr11:47694143 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | NA18952.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.695-1887A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694143 | |||||||
chr11:47694229 | C | CA | 86 | a0001c0001t0001g0132 a0001c0001t0001g0149 a0001c0001t0001g0199 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.695-1974dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694229 | |||||||
chr11:47694391 | C | G | 1 | a0002c0002t0001g0007 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.695-2135G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694391 | |||||||
chr11:47694432 | C | G | 3 | a0001c0001t0001g0164 a0001c0001t0001g0192 a0001c0001t0001g0229 |
3 | HG00741.hp1 HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.695-2176G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694432 | |||||||
chr11:47694772 | G | C | 84 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(81): Show |
84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.695-2516C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694772 | |||||||
chr11:47694829 | T | G | 86 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(83): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.695-2573A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694829 | |||||||
chr11:47694875 | G | A | 3 | a0001c0001t0001g0212 a0001c0001t0001g0220 a0001c0001t0001g0354 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.695-2619C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694875 | |||||||
chr11:47694920 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.695-2664C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694920 | |||||||
chr11:47694969 | T | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-2713A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47694969 | |||||||
chr11:47695048 | G | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG00597.hp1 NA18962.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.695-2792C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695048 | |||||||
chr11:47695137 | G | C | 1 | a0002c0002t0002g0026 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.695-2881C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695137 | |||||||
chr11:47695423 | C | A | 83 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.695-3167G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695423 | |||||||
chr11:47695454 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.695-3198C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695454 | |||||||
chr11:47695475 | C | CA | 215 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0128 others(212): Show |
215 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.695-3220dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695475 | |||||||
chr11:47695475 | C | CAA | 40 | a0001c0001t0001g0190 a0001c0001t0001g0199 a0001c0001t0001g0200 others(37): Show |
40 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.695-3221_695-3220d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695475 | |||||||
chr11:47695501 | G | C | 1 | a0010c0010t0001g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.695-3245C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695501 | |||||||
chr11:47695650 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.695-3394A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47695650 | |||||||
chr11:47696026 | A | G | 9 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(6): Show |
9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+3420T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696026 | |||||||
chr11:47696027 | AAAAAAAA others(3): Show |
A | 9 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(6): Show |
9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+3409_694+3418d others(12): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696027 | |||||||
chr11:47696029 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.694+3417T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696029 | |||||||
chr11:47696030 | A | G | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+3416T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696030 | |||||||
chr11:47696036 | A | AAAG | 12 | a0001c0001t0001g0129 a0001c0001t0001g0169 a0001c0001t0001g0202 others(9): Show |
12 | HG01071.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.694+3409_694+3410i others(5): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696036 | |||||||
chr11:47696036 | A | AAG | 58 | a0001c0001t0001g0044 a0001c0001t0001g0124 a0001c0001t0001g0143 others(55): Show |
58 | HG00408.hp1 HG00544.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.694+3409_694+3410i others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696036 | |||||||
chr11:47696036 | A | G | 7 | a0001c0001t0001g0155 a0001c0001t0001g0228 a0001c0001t0001g0272 others(4): Show |
7 | HG00140.hp2 HG02056.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+3410T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696036 | |||||||
chr11:47696037 | G | A | 79 | a0001c0001t0001g0044 a0001c0001t0001g0124 a0001c0001t0001g0129 others(76): Show |
79 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.694+3409C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696037 | |||||||
chr11:47696037 | G | GA | 247 | a0001c0001t0001g0064 a0001c0001t0001g0123 a0001c0001t0001g0130 others(244): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.694+3408dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696037 | |||||||
chr11:47696185 | CA | C | 236 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0128 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.694+3260delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696185 | |||||||
chr11:47696185 | CAA | C | 105 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(102): Show |
105 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.694+3259_694+3260d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696185 | |||||||
chr11:47696466 | G | A | 1 | a0002c0002t0002g0072 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.694+2980C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696466 | |||||||
chr11:47696557 | C | T | 3 | a0005c0004t0002g0345 a0005c0004t0002g0346 a0005c0004t0002g0347 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.694+2889G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696557 | |||||||
chr11:47696634 | A | G | 3 | a0005c0004t0002g0345 a0005c0004t0002g0346 a0005c0004t0002g0347 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.694+2812T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47696634 | |||||||
chr11:47697150 | C | A | 336 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(333): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.694+2296G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697150 | |||||||
chr11:47697248 | G | T | 336 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(333): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.694+2198C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697248 | |||||||
chr11:47697399 | C | T | 2 | a0002c0002t0002g0045 a0002c0002t0002g0046 |
2 | HG01070.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.694+2047G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697399 | |||||||
chr11:47697540 | CT | C | 120 | a0001c0001t0001g0044 a0001c0001t0001g0128 a0001c0001t0001g0132 others(117): Show |
120 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.694+1905delA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697540 | |||||||
chr11:47697540 | CTT | C | 206 | a0001c0001t0001g0064 a0001c0001t0001g0123 a0001c0001t0001g0124 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.694+1904_694+1905d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697540 | |||||||
chr11:47697631 | T | C | 350 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(347): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.694+1815A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697631 | |||||||
chr11:47697641 | G | C | 1 | a0002c0008t0004g0353 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.694+1805C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697641 | |||||||
chr11:47697740 | G | T | 1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.694+1706C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697740 | |||||||
chr11:47697835 | C | A | 1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.694+1611G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697835 | |||||||
chr11:47697842 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0155 |
2 | HG00140.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.694+1604C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47697842 | |||||||
chr11:47698042 | A | G | 8 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.694+1404T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698042 | |||||||
chr11:47698121 | C | CA | 10 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.694+1324dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698121 | |||||||
chr11:47698127 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.694+1319C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698127 | |||||||
chr11:47698168 | A | AT | 118 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0129 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.694+1277dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698168 | |||||||
chr11:47698168 | A | ATT | 99 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(96): Show |
99 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.694+1276_694+1277d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698168 | |||||||
chr11:47698168 | A | ATTT | 22 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(19): Show |
22 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.694+1275_694+1277d others(5): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698168 | |||||||
chr11:47698235 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.694+1211G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698235 | |||||||
chr11:47698676 | A | G | 117 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0002c0002t0002g0012 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.694+770T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698676 | |||||||
chr11:47698889 | C | T | 1 | a0002c0002t0002g0026 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.694+557G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698889 | |||||||
chr11:47698925 | G | T | 1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.694+521C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698925 | |||||||
chr11:47698936 | A | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.694+510T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698936 | |||||||
chr11:47698957 | T | C | 117 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0002c0002t0002g0012 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.694+489A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698957 | |||||||
chr11:47698966 | C | CA | 9 | a0001c0001t0001g0064 a0002c0002t0002g0016 a0002c0002t0002g0021 others(6): Show |
9 | HG00438.hp2 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+479dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698966 | |||||||
chr11:47698966 | CA | C | 15 | a0001c0001t0001g0198 a0001c0001t0001g0240 a0001c0001t0001g0268 others(12): Show |
15 | HG00408.hp2 HG00733.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.694+479delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698966 | |||||||
chr11:47698966 | CAA | C | 197 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(194): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.694+478_694+479del others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698966 | |||||||
chr11:47698966 | CAAA | C | 9 | a0001c0001t0001g0199 a0001c0001t0001g0213 a0001c0001t0001g0214 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+477_694+479del others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47698966 | |||||||
chr11:47699442 | A | T | 1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | splice_region_variant&intron_variant | LOW | c.694+4T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 8/18 | chr11 | 47699442 | |||||||
chr11:47699667 | A | C | 1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-114T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699667 | |||||||
chr11:47699668 | C | A | 1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-115G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699668 | |||||||
chr11:47699728 | A | G | 1 | a0002c0002t0002g0102 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.587-175T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699728 | |||||||
chr11:47699740 | G | A | 1 | a0002c0002t0002g0087 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.587-187C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699740 | |||||||
chr11:47699760 | G | A | 101 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(98): Show |
101 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.587-207C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699760 | |||||||
chr11:47699975 | T | G | 4 | a0002c0002t0002g0067 a0002c0002t0002g0069 a0002c0002t0002g0088 others(1): Show |
4 | HG02074.hp2 NA18940.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-422A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699975 | |||||||
chr11:47699992 | C | CTAT | 117 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0002c0002t0002g0012 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.587-442_587-440dup others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47699992 | |||||||
chr11:47700060 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.587-507G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700060 | |||||||
chr11:47700259 | G | A | 2 | a0001c0001t0001g0313 a0001c0001t0001g0326 |
2 | HG01261.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.587-706C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700259 | |||||||
chr11:47700293 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.587-740G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700293 | |||||||
chr11:47700334 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.587-781A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700334 | |||||||
chr11:47700357 | T | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0195 |
2 | HG02132.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.587-804A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700357 | |||||||
chr11:47700439 | T | A | 1 | a0001c0001t0001g0293 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.587-886A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700439 | |||||||
chr11:47700513 | A | G | 2 | a0001c0001t0005g0329 a0001c0001t0005g0330 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.587-960T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700513 | |||||||
chr11:47700544 | G | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.587-991C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700544 | |||||||
chr11:47700591 | AAAAC | A | 198 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(195): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.587-1042_587-1039d others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700591 | |||||||
chr11:47700596 | AAACAAAC others(1): Show |
A | 3 | a0001c0001t0001g0212 a0001c0001t0001g0220 a0001c0001t0001g0354 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.587-1051_587-1044d others(10): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700596 | |||||||
chr11:47700600 | AAACC | A | 16 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(13): Show |
16 | HG02071.hp2 NA18957.hp2 NA18967.hp2 others(13): Show |
intron_variant | MODIFIER | c.587-1051_587-1048d others(6): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700600 | |||||||
chr11:47700608 | A | C | 3 | a0001c0001t0001g0212 a0001c0001t0001g0220 a0001c0001t0001g0354 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.587-1055T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700608 | |||||||
chr11:47700839 | A | T | 1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-1286T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700839 | |||||||
chr11:47700891 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.587-1338G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700891 | |||||||
chr11:47700939 | A | T | 1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-1386T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700939 | |||||||
chr11:47700940 | T | C | 1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-1387A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700940 | |||||||
chr11:47700941 | C | T | 1 | a0002c0002t0002g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-1388G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47700941 | |||||||
chr11:47701019 | G | A | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-1466C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701019 | |||||||
chr11:47701055 | C | CA | 16 | a0001c0001t0001g0128 a0001c0001t0001g0209 a0001c0001t0001g0260 others(13): Show |
16 | HG01261.hp2 HG02486.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.587-1503dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701055 | |||||||
chr11:47701246 | G | A | 127 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0313 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.587-1693C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701246 | |||||||
chr11:47701267 | G | A | 117 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0002c0002t0002g0012 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.587-1714C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701267 | |||||||
chr11:47701271 | C | G | 117 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0002c0002t0002g0012 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.587-1718G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701271 | |||||||
chr11:47701418 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.587-1865G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701418 | |||||||
chr11:47701451 | C | T | 1 | a0002c0002t0002g0112 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.587-1898G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701451 | |||||||
chr11:47701469 | C | CA | 9 | a0001c0001t0001g0149 a0001c0001t0001g0198 a0001c0001t0001g0201 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-1917dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701469 | |||||||
chr11:47701469 | CA | C | 119 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0152 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.587-1917delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701469 | |||||||
chr11:47701469 | CAA | C | 7 | a0002c0002t0002g0013 a0002c0002t0002g0068 a0002c0002t0002g0069 others(4): Show |
7 | HG00408.hp1 HG01258.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.587-1918_587-1917d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701469 | |||||||
chr11:47701858 | C | T | 6 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(3): Show |
6 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-2305G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701858 | |||||||
chr11:47701886 | G | C | 1 | a0001c0001t0001g0143 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.587-2333C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701886 | |||||||
chr11:47701960 | G | A | 86 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(83): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.587-2407C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701960 | |||||||
chr11:47701973 | CA | C | 337 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(334): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.587-2421delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701973 | |||||||
chr11:47701988 | A | G | 117 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0002c0002t0002g0012 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.587-2435T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47701988 | |||||||
chr11:47702261 | G | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0031 a0002c0002t0002g0032 |
3 | HG02965.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.586+2282C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702261 | |||||||
chr11:47702386 | A | G | 219 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(216): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.586+2157T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702386 | |||||||
chr11:47702702 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.586+1841G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702702 | |||||||
chr11:47702805 | C | T | 1 | a0002c0002t0002g0031 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586+1738G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702805 | |||||||
chr11:47702843 | T | C | 1 | a0002c0002t0002g0090 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.586+1700A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702843 | |||||||
chr11:47702929 | C | T | 3 | a0005c0004t0002g0345 a0005c0004t0002g0346 a0005c0004t0002g0347 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.586+1614G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47702929 | |||||||
chr11:47703246 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.586+1297C>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703246 | |||||||
chr11:47703454 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.586+1089T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703454 | |||||||
chr11:47703754 | C | T | 84 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(81): Show |
84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.586+789G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703754 | |||||||
chr11:47703925 | C | CA | 40 | a0001c0001t0001g0044 a0001c0001t0001g0197 a0001c0001t0001g0198 others(37): Show |
40 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.586+617dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703925 | |||||||
chr11:47703940 | A | AAC | 77 | a0001c0001t0001g0261 a0002c0002t0002g0012 a0002c0002t0002g0014 others(74): Show |
77 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.586+602_586+603ins others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703940 | |||||||
chr11:47703941 | C | A | 79 | a0001c0001t0001g0261 a0002c0002t0002g0012 a0002c0002t0002g0014 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.586+602G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703941 | |||||||
chr11:47703942 | A | C | 1 | a0001c0001t0001g0143 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.586+601T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703942 | |||||||
chr11:47703962 | G | A | 10 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+581C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703962 | |||||||
chr11:47703984 | C | G | 4 | a0002c0002t0002g0038 a0002c0002t0002g0039 a0002c0002t0002g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+559G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47703984 | |||||||
chr11:47704137 | C | T | 2 | a0007c0007t0001g0125 a0007c0007t0001g0126 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.586+406G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47704137 | |||||||
chr11:47704387 | G | C | 1 | a0002c0002t0002g0061 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.586+156C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47704387 | |||||||
chr11:47704439 | C | T | 2 | a0002c0008t0004g0351 a0002c0008t0004g0353 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.586+104G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47704439 | |||||||
chr11:47704482 | C | CA | 17 | a0001c0001t0001g0224 a0001c0001t0001g0297 a0001c0001t0001g0301 others(14): Show |
17 | HG01175.hp2 HG01255.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.586+60dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47704482 | |||||||
chr11:47704482 | CA | C | 12 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(9): Show |
12 | HG01943.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.586+60delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 7/18 | chr11 | 47704482 | |||||||
chr11:47704844 | T | G | 1 | a0002c0002t0002g0092 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.401-116A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/18 | chr11 | 47704844 | |||||||
chr11:47705062 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.401-334A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/18 | chr11 | 47705062 | |||||||
chr11:47705313 | G | GA | 333 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(330): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.400+207dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/18 | chr11 | 47705313 | |||||||
chr11:47705336 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.400+185G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/18 | chr11 | 47705336 | |||||||
chr11:47705425 | C | G | 86 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(83): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.400+96G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 6/18 | chr11 | 47705425 | |||||||
chr11:47705641 | C | CA | 112 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
splice_region_variant&intron_variant | LOW | c.287-8dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 5/18 | chr11 | 47705641 | |||||||
chr11:47705641 | C | CAA | 85 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(82): Show |
85 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(82): Show |
splice_region_variant&intron_variant | LOW | c.287-9_287-8dupTT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 5/18 | chr11 | 47705641 | |||||||
chr11:47705641 | C | CAAA | 20 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(17): Show |
20 | HG00408.hp2 HG02071.hp2 HG02523.hp1 others(17): Show |
splice_region_variant&intron_variant | LOW | c.287-10_287-8dupTTT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 5/18 | chr11 | 47705641 | |||||||
chr11:47705924 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02135.hp1 | splice_region_variant&intron_variant | LOW | c.233-7T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47705924 | |||||||
chr11:47706038 | A | C | 101 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(98): Show |
101 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.233-121T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706038 | |||||||
chr11:47706196 | C | T | 14 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(11): Show |
14 | HG01071.hp1 HG01099.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.233-279G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706196 | |||||||
chr11:47706245 | G | A | 2 | a0007c0007t0001g0125 a0007c0007t0001g0126 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.233-328C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706245 | |||||||
chr11:47706472 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0224 |
2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.233-555G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706472 | |||||||
chr11:47706497 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.233-580G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706497 | |||||||
chr11:47706522 | A | T | 100 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(97): Show |
100 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.233-605T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706522 | |||||||
chr11:47706524 | A | T | 1 | a0002c0009t0002g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.233-607T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706524 | |||||||
chr11:47706824 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.233-907C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706824 | |||||||
chr11:47706889 | TC | T | 112 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(109): Show |
112 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.233-973delG | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706889 | |||||||
chr11:47706890 | C | CA | 76 | a0001c0001t0001g0142 a0002c0002t0001g0005 a0002c0002t0001g0007 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.233-974_233-973ins others(1): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | |||||||
chr11:47706890 | C | CAA | 17 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(14): Show |
17 | HG01071.hp2 HG01261.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.233-974_233-973ins others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | |||||||
chr11:47706890 | C | CAAA | 7 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(4): Show |
7 | HG01109.hp2 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-974_233-973ins others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | |||||||
chr11:47706890 | C | CAT | 77 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(74): Show |
77 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.233-974_233-973ins others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | |||||||
chr11:47706890 | C | CATA | 8 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0148 others(5): Show |
8 | HG00597.hp1 HG00741.hp1 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.233-974_233-973ins others(3): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | |||||||
chr11:47706890 | CCA | C | 3 | a0001c0001t0001g0299 a0001c0001t0001g0307 a0001c0001t0001g0312 |
3 | HG01243.hp1 NA18972.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.233-975_233-974del others(2): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | |||||||
chr11:47706890 | CCAAAAAA others(7): Show |
C | 3 | a0002c0002t0002g0023 a0002c0002t0002g0024 a0002c0002t0002g0025 |
3 | NA18949.hp2 NA19065.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.233-987_233-974del others(14): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706890 | |||||||
chr11:47706891 | C | A | 231 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.233-974G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706891 | |||||||
chr11:47706891 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.233-974G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47706891 | |||||||
chr11:47707024 | T | TA | 97 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(94): Show |
97 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.233-1108dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707024 | |||||||
chr11:47707024 | T | TAA | 8 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(5): Show |
8 | HG01884.hp1 HG02559.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-1109_233-1108d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707024 | |||||||
chr11:47707024 | TA | T | 199 | a0001c0001t0001g0044 a0001c0001t0001g0123 a0001c0001t0001g0124 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.233-1108delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707024 | |||||||
chr11:47707024 | TAA | T | 12 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
12 | HG01070.hp2 HG01943.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.233-1109_233-1108d others(4): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707024 | |||||||
chr11:47707065 | G | A | 85 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.233-1148C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707065 | |||||||
chr11:47707203 | C | G | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.233-1286G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707203 | |||||||
chr11:47707372 | C | T | 103 | a0001c0001t0001g0141 a0001c0001t0001g0238 a0001c0001t0001g0239 others(100): Show |
103 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.233-1455G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707372 | |||||||
chr11:47707432 | G | C | 3 | a0001c0001t0001g0212 a0001c0001t0001g0220 a0001c0001t0001g0354 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.233-1515C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707432 | |||||||
chr11:47707572 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.233-1655G>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707572 | |||||||
chr11:47707599 | G | A | 1 | a0002c0002t0001g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.233-1682C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707599 | |||||||
chr11:47707628 | G | A | 92 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0002c0002t0002g0012 others(89): Show |
92 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.233-1711C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707628 | |||||||
chr11:47707692 | T | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG01071.hp1 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.233-1775A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707692 | |||||||
chr11:47707768 | C | T | 2 | a0001c0001t0001g0311 a0001c0001t0001g0312 |
2 | HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.233-1851G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47707768 | |||||||
chr11:47708098 | C | T | 14 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.233-2181G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708098 | |||||||
chr11:47708218 | C | T | 114 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0002c0002t0002g0012 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.232+2159G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708218 | |||||||
chr11:47708269 | A | T | 330 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(327): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.232+2108T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708269 | |||||||
chr11:47708343 | C | T | 5 | a0002c0002t0002g0018 a0002c0002t0002g0019 a0002c0002t0002g0020 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+2034G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708343 | |||||||
chr11:47708471 | CCTTTA | C | 6 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG00597.hp2 NA18947.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+1901_232+1905d others(7): Show |
AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708471 | |||||||
chr11:47708514 | T | G | 3 | a0001c0001t0001g0341 a0002c0002t0001g0350 a0002c0002t0001g0352 |
3 | HG02451.hp1 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.232+1863A>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708514 | |||||||
chr11:47708590 | C | T | 34 | a0002c0002t0002g0012 a0002c0002t0002g0066 a0002c0002t0002g0067 others(31): Show |
34 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.232+1787G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708590 | |||||||
chr11:47708596 | G | A | 133 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(130): Show |
133 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.232+1781C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708596 | |||||||
chr11:47708598 | G | A | 3 | a0005c0004t0002g0345 a0005c0004t0002g0346 a0005c0004t0002g0347 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.232+1779C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708598 | |||||||
chr11:47708808 | G | A | 1 | a0004c0005t0001g0306 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.232+1569C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708808 | |||||||
chr11:47708812 | C | CA | 16 | a0001c0001t0001g0209 a0001c0001t0001g0221 a0001c0001t0001g0222 others(13): Show |
16 | HG01109.hp2 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.232+1564dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708812 | |||||||
chr11:47708812 | CA | C | 11 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
11 | HG00323.hp2 HG02132.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.232+1564delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708812 | |||||||
chr11:47708857 | C | T | 1 | a0002c0002t0002g0015 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+1520G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47708857 | |||||||
chr11:47709085 | G | A | 2 | a0001c0001t0005g0329 a0001c0001t0005g0330 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.232+1292C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709085 | |||||||
chr11:47709213 | C | T | 16 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(13): Show |
16 | HG02071.hp2 NA18957.hp2 NA18967.hp2 others(13): Show |
intron_variant | MODIFIER | c.232+1164G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709213 | |||||||
chr11:47709399 | A | C | 1 | a0001c0001t0001g0333 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.232+978T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709399 | |||||||
chr11:47709465 | A | C | 1 | a0001c0001t0001g0133 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.232+912T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709465 | |||||||
chr11:47709499 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.232+878A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709499 | |||||||
chr11:47709589 | C | CT | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG01175.hp1 HG01192.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+787dupA | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709589 | |||||||
chr11:47709674 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.232+703C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709674 | |||||||
chr11:47709699 | T | C | 3 | a0002c0002t0002g0234 a0002c0002t0002g0236 a0002c0017t0002g0235 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.232+678A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709699 | |||||||
chr11:47709778 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.232+599T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709778 | |||||||
chr11:47709836 | G | C | 28 | a0001c0001t0001g0238 a0001c0001t0001g0243 a0001c0001t0001g0311 others(25): Show |
28 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.232+541C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709836 | |||||||
chr11:47709871 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.232+506C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47709871 | |||||||
chr11:47710155 | C | T | 1 | a0009c0011t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.232+222G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47710155 | |||||||
chr11:47710183 | C | T | 1 | a0002c0002t0002g0066 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.232+194G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47710183 | |||||||
chr11:47710299 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.232+78C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 4/18 | chr11 | 47710299 | |||||||
chr11:47710753 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.98-242A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47710753 | |||||||
chr11:47710852 | G | A | 1 | a0002c0002t0001g0350 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.98-341C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47710852 | |||||||
chr11:47710909 | C | CA | 9 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(6): Show |
9 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-399dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47710909 | |||||||
chr11:47710909 | CA | C | 322 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(319): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.98-399delT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47710909 | |||||||
chr11:47710909 | CAA | C | 8 | a0001c0001t0001g0212 a0001c0001t0001g0242 a0001c0001t0001g0243 others(5): Show |
8 | HG02897.hp1 HG03209.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-400_98-399delTT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47710909 | |||||||
chr11:47711031 | A | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.98-520T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711031 | |||||||
chr11:47711323 | G | C | 2 | a0007c0007t0001g0125 a0007c0007t0001g0126 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.98-812C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711323 | |||||||
chr11:47711431 | C | T | 1 | a0002c0002t0001g0001 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.98-920G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711431 | |||||||
chr11:47711432 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.98-921G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711432 | |||||||
chr11:47711690 | T | C | 1 | a0009c0011t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.98-1179A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711690 | |||||||
chr11:47711717 | T | A | 11 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.98-1206A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711717 | |||||||
chr11:47711814 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.98-1303G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711814 | |||||||
chr11:47711942 | G | A | 55 | a0002c0002t0002g0012 a0002c0002t0002g0066 a0002c0002t0002g0067 others(52): Show |
55 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.98-1431C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47711942 | |||||||
chr11:47712090 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.98-1579T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712090 | |||||||
chr11:47712366 | C | T | 1 | a0002c0002t0002g0116 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.98-1855G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712366 | |||||||
chr11:47712531 | G | A | 2 | a0002c0009t0002g0114 a0002c0009t0002g0115 |
2 | HG00544.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.97+1753C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712531 | |||||||
chr11:47712606 | T | C | 2 | a0002c0008t0004g0351 a0002c0008t0004g0353 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.97+1678A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712606 | |||||||
chr11:47712792 | C | G | 2 | a0007c0007t0001g0125 a0007c0007t0001g0126 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.97+1492G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712792 | |||||||
chr11:47712793 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.97+1491T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712793 | |||||||
chr11:47712825 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.97+1459T>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712825 | |||||||
chr11:47712892 | G | A | 114 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0002c0002t0002g0012 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.97+1392C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712892 | |||||||
chr11:47712990 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.97+1294G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47712990 | |||||||
chr11:47713164 | A | T | 1 | a0002c0002t0002g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.97+1120T>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47713164 | |||||||
chr11:47713284 | C | T | 3 | a0005c0004t0002g0345 a0005c0004t0002g0346 a0005c0004t0002g0347 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.97+1000G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47713284 | |||||||
chr11:47713344 | C | CA | 31 | a0001c0001t0001g0222 a0001c0001t0001g0224 a0001c0001t0001g0225 others(28): Show |
31 | HG00140.hp1 HG00544.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.97+939dupT | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47713344 | |||||||
chr11:47713581 | T | A | 350 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(347): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.97+703A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47713581 | |||||||
chr11:47713602 | T | A | 216 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 others(213): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.97+682A>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47713602 | |||||||
chr11:47714074 | C | T | 1 | a0001c0001t0001g0341 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.97+210G>A | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 3/18 | chr11 | 47714074 | |||||||
chr11:47714452 | G | A | 1 | a0002c0013t0002g0237 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.34-105C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 2/18 | chr11 | 47714452 | |||||||
chr11:47714471 | T | C | 101 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(98): Show |
101 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.34-124A>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 2/18 | chr11 | 47714471 | |||||||
chr11:47714762 | C | G | 330 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0123 others(327): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.-100-12G>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47714762 | |||||||
chr11:47714765 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-100-15C>T | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47714765 | |||||||
chr11:47714766 | A | G | 1 | a0002c0002t0002g0012 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-100-16T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47714766 | |||||||
chr11:47714936 | A | G | 10 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(7): Show |
10 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-100-186T>C | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47714936 | |||||||
chr11:47714988 | G | C | 1 | a0003c0003t0002g0355 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-101+187C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47714988 | |||||||
chr11:47715152 | G | C | 1 | a0002c0002t0002g0022 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-101+23C>G | AGBL2 | ENSG00000165923.17 | transcript | ENST00000525123.6 | protein_coding | 1/18 | chr11 | 47715152 |