Item | Value |
---|---|
geneid | 9918 |
ensemblid | ENSG00000010292.13 |
hgncid | 24305 |
symbol | NCAPD2 |
name | non-SMC condensin I complex subunit D2 |
refseq_nuc | NM_014865.4 |
refseq_prot | NP_055680.3 |
ensembl_nuc | ENST00000315579.10 |
ensembl_prot | ENSP00000325017.5 |
mane_status | MANE Select |
chr | chr12 |
start | 6494102 |
end | 6531955 |
strand | + |
ver | v1.2 |
region | chr12:6494102-6531955 |
region5000 | chr12:6489102-6536955 |
regionname0 | NCAPD2_chr12_6494102_6531955 |
regionname5000 | NCAPD2_chr12_6489102_6536955 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1401 | 210 | 71 | 41 | 72 | 3 | 23 | 60 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0002 | 1/1 | 1401 | 85 | 2 | 14 | 52 | 6 | 9 | 38 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0003 | 0/0 | 1401 | 78 | 4 | 7 | 56 | 3 | 8 | 37 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0004 | 0/0 | 1401 | 17 | 1 | 5 | 2 | 3 | 6 | 2 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0005 | 0/0 | 1401 | 12 | 0 | 0 | 10 | 0 | 2 | 9 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0006 | 0/0 | 1401 | 8 | 0 | 8 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0007 | 0/0 | 1401 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0008 | 0/0 | 1401 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0009 | 0/0 | 1401 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0010 | 0/0 | 1401 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0011 | 0/0 | 1401 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0012 | 0/0 | 1401 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0013 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0014 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0015 | 0/0 | 48 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(43): Show |
chr12 | 6489102 | 6536955 |
a0016 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0017 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MGHQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0018 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
a0019 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | MAPQM others(1396): Show |
chr12 | 6489102 | 6536955 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4203 | 123 | 41 | 29 | 38 | 3 | 12 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0001c0004 | 0/0 | 4203 | 58 | 14 | 8 | 28 | 0 | 8 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0001c0007 | 0/0 | 4203 | 12 | 10 | 2 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0001c0009 | 0/0 | 4203 | 7 | 0 | 1 | 6 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0001c0011 | 0/0 | 4203 | 4 | 4 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0001c0026 | 0/0 | 4203 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0001c0028 | 0/0 | 4203 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0001c0030 | 0/0 | 4203 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0001c0031 | 0/0 | 4203 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0001c0032 | 0/0 | 4203 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0001c0033 | 0/0 | 4203 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0002c0002 | 1/0 | 4203 | 81 | 2 | 13 | 50 | 6 | 9 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0002c0018 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0002c0019 | 0/0 | 4203 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0002c0021 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0002c0022 | 0/1 | 4203 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0003c0003 | 0/0 | 4203 | 70 | 3 | 6 | 51 | 3 | 7 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0003c0010 | 0/0 | 4203 | 6 | 0 | 0 | 5 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0003c0015 | 0/0 | 4203 | 2 | 1 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0004c0005 | 0/0 | 4203 | 17 | 1 | 5 | 2 | 3 | 6 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0005c0006 | 0/0 | 4203 | 12 | 0 | 0 | 10 | 0 | 2 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0006c0008 | 0/0 | 4203 | 8 | 0 | 8 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0007c0014 | 0/0 | 4203 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0007c0016 | 0/0 | 4203 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0008c0012 | 0/0 | 4203 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0009c0013 | 0/0 | 4203 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0010c0017 | 0/0 | 4203 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0011c0023 | 0/0 | 4203 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0012c0035 | 0/0 | 4203 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0013c0020 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0014c0027 | 0/0 | 4203 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0015c0034 | 0/0 | 4203 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0016c0029 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0017c0036 | 0/0 | 4203 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGG others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0018c0024 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 | ||
a0019c0025 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | ATGGC others(4198): Show |
chr12 | 6489102 | 6536955 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 4825 | 104 | 30 | 25 | 37 | 3 | 9 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0001t0003 | 0/0 | 4825 | 5 | 4 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0001t0006 | 0/0 | 4826 | 7 | 3 | 1 | 0 | 0 | 3 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4821): Show |
chr12 | 6489102 | 6536955 |
a0001c0001t0007 | 0/0 | 4824 | 6 | 3 | 2 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4819): Show |
chr12 | 6489102 | 6536955 |
a0001c0001t0015 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0004t0001 | 0/0 | 4825 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0004t0004 | 0/0 | 4825 | 41 | 0 | 7 | 27 | 0 | 7 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0004t0008 | 0/0 | 4825 | 6 | 5 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0004t0009 | 0/0 | 4825 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0004t0010 | 0/0 | 4826 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4821): Show |
chr12 | 6489102 | 6536955 |
a0001c0004t0011 | 0/0 | 4825 | 3 | 1 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0007t0004 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0007t0005 | 0/0 | 4826 | 9 | 7 | 2 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4821): Show |
chr12 | 6489102 | 6536955 |
a0001c0007t0012 | 0/0 | 4826 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4821): Show |
chr12 | 6489102 | 6536955 |
a0001c0009t0001 | 0/0 | 4825 | 7 | 0 | 1 | 6 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0011t0001 | 0/0 | 4825 | 4 | 4 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0026t0006 | 0/0 | 4826 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4821): Show |
chr12 | 6489102 | 6536955 |
a0001c0028t0009 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0030t0002 | 0/0 | 4825 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0031t0001 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0032t0016 | 0/0 | 4825 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0001c0033t0004 | 0/0 | 4825 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0002c0002t0001 | 1/0 | 4825 | 81 | 2 | 13 | 50 | 6 | 9 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0002c0018t0001 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0002c0019t0001 | 0/0 | 4825 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0002c0021t0001 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0002c0022t0002 | 0/1 | 4825 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0003c0003t0003 | 0/0 | 4825 | 66 | 3 | 5 | 48 | 3 | 7 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0003c0003t0013 | 0/0 | 4826 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4821): Show |
chr12 | 6489102 | 6536955 |
a0003c0003t0014 | 0/0 | 4824 | 2 | 0 | 1 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4819): Show |
chr12 | 6489102 | 6536955 |
a0003c0010t0001 | 0/0 | 4825 | 5 | 0 | 0 | 5 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0003c0010t0003 | 0/0 | 4825 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0003c0015t0003 | 0/0 | 4825 | 2 | 1 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0004c0005t0001 | 0/0 | 4825 | 17 | 1 | 5 | 2 | 3 | 6 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0005c0006t0003 | 0/0 | 4825 | 12 | 0 | 0 | 10 | 0 | 2 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0006c0008t0003 | 0/0 | 4825 | 8 | 0 | 8 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0007c0014t0001 | 0/0 | 4825 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0007c0016t0001 | 0/0 | 4825 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0008c0012t0006 | 0/0 | 4826 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4821): Show |
chr12 | 6489102 | 6536955 |
a0009c0013t0002 | 0/0 | 4825 | 3 | 3 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0010c0017t0003 | 0/0 | 4825 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0011c0023t0001 | 0/0 | 4825 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0012c0035t0001 | 0/0 | 4825 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0013c0020t0001 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0014c0027t0005 | 0/0 | 4826 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4821): Show |
chr12 | 6489102 | 6536955 |
a0015c0034t0005 | 0/0 | 4826 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4821): Show |
chr12 | 6489102 | 6536955 |
a0016c0029t0002 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0017c0036t0001 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0018c0024t0001 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
a0019c0025t0001 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | CCTTT others(4820): Show |
chr12 | 6489102 | 6536955 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0002g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0003g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0003g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0006g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0007g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0001t0015g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0009g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0009g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0010g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0010g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0010g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0011g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0011g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0004t0011g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0012g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0007t0012g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0009t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0011t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0011t0001g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0011t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0026t0006g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0028t0009g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0030t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0031t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0032t0016g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0001c0033t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 1 | 2 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0002 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0017 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0018t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0019t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0021t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0002c0022t0002g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0013g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0013g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0014g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0003t0014g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0010t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0015t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0003c0015t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0004c0005t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0005c0006t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0006c0008t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0007c0014t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0007c0014t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0007c0014t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0007c0016t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0007c0016t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0008c0012t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0008c0012t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0008c0012t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0009c0013t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0009c0013t0002g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0010c0017t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0010c0017t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0011c0023t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0012c0035t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0013c0020t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0014c0027t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0015c0034t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0016c0029t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0017c0036t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0018c0024t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
a0019c0025t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00099 | hp2 | a0004 | c0005 | t0001 | g0235 | EUR | GBR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0285 | EUR | GBR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00140 | hp2 | a0011 | c0023 | t0001 | g0149 | EUR | GBR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00280 | hp1 | a0003 | c0003 | t0003 | g0071 | EUR | FIN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00323 | hp1 | a0004 | c0005 | t0001 | g0233 | EUR | FIN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00323 | hp2 | a0003 | c0003 | t0003 | g0101 | EUR | FIN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00408 | hp2 | a0003 | c0003 | t0003 | g0086 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00423 | hp1 | a0003 | c0003 | t0003 | g0032 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00423 | hp2 | a0003 | c0003 | t0003 | g0075 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00438 | hp2 | a0005 | c0006 | t0003 | g0173 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00544 | hp2 | a0003 | c0003 | t0003 | g0046 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00558 | hp1 | a0001 | c0004 | t0004 | g0190 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00597 | hp2 | a0003 | c0003 | t0003 | g0012 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00609 | hp1 | a0003 | c0003 | t0003 | g0035 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00621 | hp1 | a0003 | c0003 | t0003 | g0065 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00642 | hp1 | a0001 | c0009 | t0001 | g0322 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00673 | hp1 | a0003 | c0010 | t0001 | g0094 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | CHS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00733 | hp1 | a0004 | c0005 | t0001 | g0232 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0115 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00735 | hp2 | a0006 | c0008 | t0003 | g0058 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01069 | hp1 | a0004 | c0005 | t0001 | g0238 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0343 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01070 | hp1 | a0003 | c0003 | t0014 | g0096 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0345 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01074 | hp2 | a0004 | c0005 | t0001 | g0246 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01081 | hp1 | a0002 | c0019 | t0001 | g0001 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01099 | hp1 | a0003 | c0003 | t0003 | g0098 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0326 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01106 | hp1 | a0006 | c0008 | t0003 | g0005 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0355 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01109 | hp1 | a0006 | c0008 | t0003 | g0005 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0348 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01168 | hp1 | a0003 | c0003 | t0003 | g0102 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01168 | hp2 | a0001 | c0004 | t0011 | g0388 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01169 | hp1 | a0003 | c0003 | t0003 | g0100 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01192 | hp2 | a0001 | c0007 | t0005 | g0265 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01243 | hp1 | a0001 | c0033 | t0004 | g0182 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01243 | hp2 | a0004 | c0005 | t0001 | g0243 | AMR | PUR | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01255 | hp1 | a0012 | c0035 | t0001 | g0240 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0327 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01257 | hp1 | a0006 | c0008 | t0003 | g0067 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01257 | hp2 | a0001 | c0004 | t0004 | g0198 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0152 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01258 | hp2 | a0001 | c0004 | t0004 | g0199 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01261 | hp1 | a0001 | c0007 | t0005 | g0263 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01261 | hp2 | a0003 | c0003 | t0003 | g0105 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0350 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01346 | hp2 | a0004 | c0005 | t0001 | g0231 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01358 | hp1 | a0001 | c0001 | t0006 | g0319 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01358 | hp2 | a0001 | c0004 | t0004 | g0200 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01361 | hp1 | a0006 | c0008 | t0003 | g0076 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0362 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0328 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0007 | EUR | IBS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0109 | EUR | IBS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0129 | EUR | IBS | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0337 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01884 | hp2 | a0001 | c0028 | t0009 | g0254 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01891 | hp1 | a0003 | c0015 | t0003 | g0092 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0372 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01928 | hp2 | a0006 | c0008 | t0003 | g0048 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01934 | hp2 | a0003 | c0003 | t0003 | g0099 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01943 | hp1 | a0001 | c0004 | t0004 | g0196 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01943 | hp2 | a0006 | c0008 | t0003 | g0005 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0321 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01952 | hp2 | a0001 | c0004 | t0004 | g0202 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01975 | hp1 | a0001 | c0001 | t0007 | g0003 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01975 | hp2 | a0006 | c0008 | t0003 | g0049 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0344 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01978 | hp2 | a0001 | c0004 | t0004 | g0211 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01981 | hp1 | a0001 | c0004 | t0004 | g0212 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0363 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01993 | hp1 | a0001 | c0001 | t0007 | g0025 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01993 | hp2 | a0003 | c0015 | t0003 | g0091 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02015 | hp2 | a0001 | c0004 | t0004 | g0019 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02027 | hp1 | a0003 | c0003 | t0003 | g0078 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02040 | hp2 | a0003 | c0003 | t0003 | g0064 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0359 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02055 | hp2 | a0001 | c0007 | t0012 | g0386 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02056 | hp2 | a0003 | c0003 | t0003 | g0088 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02071 | hp1 | a0003 | c0003 | t0003 | g0066 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02074 | hp1 | a0003 | c0010 | t0001 | g0081 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02080 | hp1 | a0010 | c0017 | t0003 | g0069 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02083 | hp1 | a0003 | c0003 | t0003 | g0034 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02083 | hp2 | a0002 | c0018 | t0001 | g0160 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02129 | hp1 | a0003 | c0010 | t0001 | g0054 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02132 | hp1 | a0003 | c0003 | t0003 | g0050 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02132 | hp2 | a0002 | c0021 | t0001 | g0121 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0377 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02155 | hp1 | a0003 | c0003 | t0003 | g0033 | EAS | CDX | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02155 | hp2 | a0003 | c0003 | t0003 | g0045 | EAS | CDX | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0370 | EAS | CDX | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0366 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0365 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0356 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0342 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0164 | AMR | PEL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02451 | hp1 | a0001 | c0004 | t0008 | g0217 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02451 | hp2 | a0001 | c0007 | t0005 | g0023 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02523 | hp2 | a0013 | c0020 | t0001 | g0141 | EAS | KHV | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02602 | hp1 | a0004 | c0005 | t0001 | g0244 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0174 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02615 | hp2 | a0014 | c0027 | t0005 | g0247 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02622 | hp1 | a0007 | c0014 | t0001 | g0284 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02622 | hp2 | a0001 | c0004 | t0010 | g0262 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0253 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02647 | hp1 | a0001 | c0007 | t0005 | g0022 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02647 | hp2 | a0008 | c0012 | t0006 | g0256 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02683 | hp1 | a0004 | c0005 | t0001 | g0242 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0373 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02717 | hp1 | a0001 | c0007 | t0005 | g0022 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02717 | hp2 | a0003 | c0003 | t0003 | g0077 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02738 | hp1 | a0003 | c0003 | t0003 | g0106 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02738 | hp2 | a0003 | c0003 | t0003 | g0103 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0349 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0257 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02818 | hp1 | a0001 | c0004 | t0010 | g0260 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0180 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02886 | hp2 | a0001 | c0004 | t0009 | g0229 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02895 | hp1 | a0001 | c0011 | t0001 | g0029 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02895 | hp2 | a0001 | c0007 | t0005 | g0268 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02896 | hp1 | a0001 | c0011 | t0001 | g0384 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02896 | hp2 | a0008 | c0012 | t0006 | g0252 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02897 | hp1 | a0001 | c0011 | t0001 | g0029 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02897 | hp2 | a0008 | c0012 | t0006 | g0248 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02922 | hp1 | a0001 | c0007 | t0005 | g0267 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0368 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0331 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0371 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02970 | hp1 | a0001 | c0004 | t0008 | g0216 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02970 | hp2 | a0015 | c0034 | t0005 | g0266 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0306 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03017 | hp2 | a0001 | c0004 | t0004 | g0206 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0369 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03041 | hp2 | a0001 | c0007 | t0004 | g0259 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03098 | hp1 | a0001 | c0004 | t0008 | g0214 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03098 | hp2 | a0001 | c0004 | t0008 | g0218 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03139 | hp1 | a0001 | c0004 | t0010 | g0261 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03139 | hp2 | a0001 | c0004 | t0009 | g0228 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03195 | hp1 | a0001 | c0007 | t0005 | g0023 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03195 | hp2 | a0001 | c0031 | t0001 | g0179 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0364 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03209 | hp2 | a0007 | c0016 | t0001 | g0283 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03225 | hp2 | a0009 | c0013 | t0002 | g0383 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03239 | hp1 | a0001 | c0030 | t0002 | g0291 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0354 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0336 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0325 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03486 | hp1 | a0007 | c0016 | t0001 | g0280 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03490 | hp1 | a0003 | c0003 | t0003 | g0072 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0250 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03491 | hp1 | a0004 | c0005 | t0001 | g0234 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0251 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0347 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03516 | hp1 | a0001 | c0001 | t0015 | g0367 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0381 | AFR | ESN | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03540 | hp1 | a0003 | c0003 | t0003 | g0089 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0333 | AFR | GWD | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03579 | hp1 | a0001 | c0011 | t0001 | g0385 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0339 | AFR | MSL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03654 | hp1 | a0004 | c0005 | t0001 | g0236 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03669 | hp1 | a0003 | c0003 | t0003 | g0053 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0249 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0324 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03688 | hp2 | a0005 | c0006 | t0003 | g0148 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03704 | hp1 | a0001 | c0004 | t0004 | g0185 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03704 | hp2 | a0003 | c0003 | t0003 | g0030 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03710 | hp2 | a0001 | c0026 | t0006 | g0258 | SAS | PJL | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0172 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0154 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03834 | hp1 | a0003 | c0003 | t0003 | g0004 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03927 | hp1 | a0001 | c0004 | t0004 | g0201 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03927 | hp2 | a0003 | c0003 | t0003 | g0070 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03942 | hp1 | a0003 | c0010 | t0003 | g0207 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0330 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0175 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04115 | hp2 | a0001 | c0004 | t0004 | g0210 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04184 | hp1 | a0004 | c0005 | t0001 | g0239 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04184 | hp2 | a0001 | c0004 | t0004 | g0204 | SAS | BEB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04199 | hp1 | a0001 | c0004 | t0011 | g0387 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04199 | hp2 | a0001 | c0004 | t0004 | g0203 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04204 | hp1 | a0001 | c0032 | t0016 | g0279 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04204 | hp2 | a0004 | c0005 | t0001 | g0241 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04228 | hp1 | a0005 | c0006 | t0003 | g0127 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0123 | SAS | STU | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0338 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18522 | hp2 | a0001 | c0004 | t0011 | g0018 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18612 | hp1 | a0001 | c0004 | t0004 | g0184 | EAS | CHB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18612 | hp2 | a0003 | c0003 | t0003 | g0052 | EAS | CHB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18906 | hp2 | a0007 | c0014 | t0001 | g0281 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18939 | hp2 | a0001 | c0004 | t0004 | g0197 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18940 | hp2 | a0001 | c0004 | t0004 | g0209 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18941 | hp1 | a0001 | c0004 | t0004 | g0224 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18944 | hp2 | a0005 | c0006 | t0003 | g0124 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18945 | hp1 | a0001 | c0009 | t0001 | g0380 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18946 | hp1 | a0003 | c0003 | t0003 | g0043 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18948 | hp1 | a0003 | c0003 | t0014 | g0082 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18950 | hp1 | a0001 | c0009 | t0001 | g0187 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18950 | hp2 | a0003 | c0010 | t0001 | g0080 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18951 | hp1 | a0005 | c0006 | t0003 | g0116 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18952 | hp1 | a0001 | c0004 | t0004 | g0226 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18952 | hp2 | a0003 | c0003 | t0003 | g0085 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18954 | hp1 | a0001 | c0004 | t0004 | g0183 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18954 | hp2 | a0003 | c0003 | t0003 | g0056 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18956 | hp1 | a0003 | c0003 | t0003 | g0012 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18957 | hp1 | a0003 | c0003 | t0003 | g0041 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18959 | hp2 | a0003 | c0003 | t0003 | g0062 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18960 | hp1 | a0005 | c0006 | t0003 | g0120 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18963 | hp2 | a0003 | c0003 | t0003 | g0040 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18965 | hp1 | a0003 | c0003 | t0003 | g0068 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18966 | hp1 | a0003 | c0003 | t0013 | g0087 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18966 | hp2 | a0001 | c0004 | t0004 | g0019 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18967 | hp1 | a0003 | c0003 | t0003 | g0093 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18968 | hp1 | a0001 | c0004 | t0004 | g0009 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18969 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18970 | hp1 | a0005 | c0006 | t0003 | g0125 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18970 | hp2 | a0001 | c0004 | t0004 | g0009 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18971 | hp1 | a0003 | c0003 | t0003 | g0039 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18971 | hp2 | a0001 | c0004 | t0004 | g0208 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18972 | hp1 | a0001 | c0004 | t0004 | g0193 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0376 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18973 | hp1 | a0003 | c0003 | t0003 | g0074 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18973 | hp2 | a0001 | c0004 | t0004 | g0227 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18974 | hp1 | a0003 | c0003 | t0003 | g0090 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18974 | hp2 | a0003 | c0003 | t0003 | g0061 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18975 | hp1 | a0003 | c0003 | t0003 | g0044 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18977 | hp2 | a0003 | c0003 | t0003 | g0057 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0382 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18978 | hp2 | a0005 | c0006 | t0003 | g0138 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18982 | hp1 | a0003 | c0003 | t0003 | g0036 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18984 | hp1 | a0003 | c0003 | t0003 | g0038 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18984 | hp2 | a0005 | c0006 | t0003 | g0014 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18986 | hp1 | a0016 | c0029 | t0002 | g0027 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18986 | hp2 | a0003 | c0003 | t0003 | g0055 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18988 | hp1 | a0003 | c0003 | t0003 | g0011 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18988 | hp2 | a0001 | c0004 | t0004 | g0191 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18989 | hp2 | a0001 | c0004 | t0004 | g0220 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18992 | hp2 | a0001 | c0004 | t0004 | g0221 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18995 | hp1 | a0005 | c0006 | t0003 | g0147 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18999 | hp1 | a0001 | c0009 | t0001 | g0205 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18999 | hp2 | a0003 | c0003 | t0003 | g0051 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19000 | hp1 | a0001 | c0004 | t0008 | g0213 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19002 | hp1 | a0005 | c0006 | t0003 | g0126 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19003 | hp1 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19004 | hp2 | a0001 | c0004 | t0004 | g0020 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19005 | hp1 | a0003 | c0003 | t0003 | g0011 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19010 | hp1 | a0001 | c0004 | t0004 | g0189 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19010 | hp2 | a0001 | c0009 | t0001 | g0188 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19012 | hp1 | a0001 | c0004 | t0004 | g0192 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19030 | hp2 | a0004 | c0005 | t0001 | g0245 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19043 | hp1 | a0009 | c0013 | t0002 | g0024 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19043 | hp2 | a0017 | c0036 | t0001 | g0378 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19054 | hp1 | a0003 | c0003 | t0003 | g0037 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19054 | hp2 | a0001 | c0004 | t0004 | g0194 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0379 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19058 | hp1 | a0001 | c0009 | t0001 | g0186 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19058 | hp2 | a0003 | c0003 | t0003 | g0059 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19060 | hp1 | a0003 | c0003 | t0003 | g0047 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19062 | hp1 | a0010 | c0017 | t0003 | g0063 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19063 | hp1 | a0018 | c0024 | t0001 | g0166 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19063 | hp2 | a0001 | c0004 | t0004 | g0223 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19066 | hp1 | a0005 | c0006 | t0003 | g0014 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19067 | hp1 | a0003 | c0003 | t0003 | g0084 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19068 | hp1 | a0004 | c0005 | t0001 | g0021 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0375 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19070 | hp2 | a0001 | c0004 | t0004 | g0222 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19074 | hp2 | a0019 | c0025 | t0001 | g0155 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19077 | hp2 | a0001 | c0004 | t0004 | g0195 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19078 | hp1 | a0001 | c0009 | t0001 | g0219 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19079 | hp1 | a0001 | c0004 | t0004 | g0020 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19079 | hp2 | a0003 | c0003 | t0003 | g0083 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19080 | hp1 | a0003 | c0003 | t0003 | g0079 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19081 | hp1 | a0003 | c0003 | t0013 | g0104 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19081 | hp2 | a0004 | c0005 | t0001 | g0021 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19083 | hp1 | a0003 | c0010 | t0001 | g0095 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19084 | hp2 | a0003 | c0003 | t0003 | g0031 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19087 | hp1 | a0001 | c0001 | t0007 | g0309 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19087 | hp2 | a0001 | c0004 | t0004 | g0225 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19091 | hp1 | a0001 | c0004 | t0004 | g0009 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19091 | hp2 | a0003 | c0003 | t0003 | g0060 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19240 | hp1 | a0001 | c0004 | t0009 | g0230 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA19240 | hp2 | a0009 | c0013 | t0002 | g0024 | AFR | YRI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20129 | hp1 | a0001 | c0004 | t0001 | g0018 | AFR | ASW | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20129 | hp2 | a0001 | c0007 | t0012 | g0269 | AFR | ASW | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20752 | hp1 | a0004 | c0005 | t0001 | g0237 | EUR | TSI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | TSI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20805 | hp2 | a0003 | c0003 | t0003 | g0097 | EUR | TSI | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20905 | hp1 | a0001 | c0004 | t0004 | g0181 | SAS | GIH | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0015 | SAS | GIH | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0374 | AMR | CLM | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02109 | hp2 | a0001 | c0004 | t0008 | g0215 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02486 | hp1 | a0001 | c0007 | t0005 | g0264 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0332 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0346 | AFR | ACB | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0351 | AFR | USA | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | USA | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA18955 | hp2 | a0003 | c0003 | t0003 | g0073 | EAS | JPT | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA21309 | hp1 | a0007 | c0014 | t0001 | g0282 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
NA21309 | hp2 | a0003 | c0003 | t0003 | g0042 | AFR | LWK | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
homoSapiens | chm13v2 | a0002 | c0022 | t0002 | g0176 | REF | REF | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0017 | REF | REF | NCAPD2_chr12_6489102_6536955 | NCAPD2 | chr12 | 6489102 | 6536955 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6495103 | C | G | 1 | a0017 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.5C>G | p.Ala2Gly | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/32 | 81/4825 | 5/4206 | 2/1401 | chr12 | 6495103 | |||
chr12:6495106 | C | A | 1 | a0017 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.8C>A | p.Pro3His | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/32 | 84/4825 | 8/4206 | 3/1401 | chr12 | 6495106 | |||
chr12:6495165 | G | T | 1 | a0012 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.67G>T | p.Val23Leu | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/32 | 143/4825 | 67/4206 | 23/1401 | chr12 | 6495165 | |||
chr12:6509734 | C | T | 1 | a0015 | 1 | HG02970.hp2 | stop_gained | HIGH | c.145C>T | p.Arg49* | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 3/32 | 221/4825 | 145/4206 | 49/1401 | chr12 | 6509734 | |||
chr12:6510118 | C | G | 13 | a0001 a0003 a0004 others(10): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
missense_variant | MODERATE | c.247C>G | p.Gln83Glu | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 4/32 | 323/4825 | 247/4206 | 83/1401 | chr12 | 6510118 | |||
chr12:6514329 | C | G | 1 | a0019 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.652C>G | p.Pro218Ala | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 7/32 | 728/4825 | 652/4206 | 218/1401 | chr12 | 6514329 | |||
chr12:6517440 | T | C | 1 | a0013 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1261T>C | p.Cys421Arg | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 11/32 | 1337/4825 | 1261/4206 | 421/1401 | chr12 | 6517440 | |||
chr12:6521008 | G | C | 1 | a0017 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1612G>C | p.Glu538Gln | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/32 | 1688/4825 | 1612/4206 | 538/1401 | chr12 | 6521008 | |||
chr12:6521803 | G | A | 1 | a0014 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1720G>A | p.Ala574Thr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/32 | 1796/4825 | 1720/4206 | 574/1401 | chr12 | 6521803 | |||
chr12:6521909 | G | C | 1 | a0010 | 2 | HG02080.hp1 NA19062.hp1 |
missense_variant | MODERATE | c.1826G>C | p.Arg609Thr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/32 | 1902/4825 | 1826/4206 | 609/1401 | chr12 | 6521909 | |||
chr12:6526108 | G | A | 2 | a0004 a0012 |
18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
missense_variant | MODERATE | c.2389G>A | p.Val797Met | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 19/32 | 2465/4825 | 2389/4206 | 797/1401 | chr12 | 6526108 | |||
chr12:6526311 | C | T | 1 | a0018 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.2506C>T | p.Pro836Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 20/32 | 2582/4825 | 2506/4206 | 836/1401 | chr12 | 6526311 | |||
chr12:6526312 | C | T | 1 | a0009 | 3 | HG03225.hp2 NA19043.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.2507C>T | p.Pro836Leu | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 20/32 | 2583/4825 | 2507/4206 | 836/1401 | chr12 | 6526312 | |||
chr12:6528985 | G | A | 1 | a0016 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.3518G>A | p.Arg1173His | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/32 | 3594/4825 | 3518/4206 | 1173/1401 | chr12 | 6528985 | |||
chr12:6529593 | G | T | 1 | a0007 | 5 | HG02622.hp1 HG03209.hp2 HG03486.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.3653G>T | p.Arg1218Leu | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 28/32 | 3729/4825 | 3653/4206 | 1218/1401 | chr12 | 6529593 | |||
chr12:6530815 | C | G | 4 | a0003 a0005 a0006 others(1): Show |
100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
missense_variant&splice_region_variant | MODERATE | c.3962C>G | p.Thr1321Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 30/32 | 4038/4825 | 3962/4206 | 1321/1401 | chr12 | 6530815 | |||
chr12:6530960 | A | G | 1 | a0008 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.4004A>G | p.Asn1335Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/32 | 4080/4825 | 4004/4206 | 1335/1401 | chr12 | 6530960 | |||
chr12:6531003 | T | A | 1 | a0011 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.4047T>A | p.His1349Gln | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/32 | 4123/4825 | 4047/4206 | 1349/1401 | chr12 | 6531003 | |||
chr12:6531353 | G | A | 1 | a0006 | 8 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(5): Show |
missense_variant | MODERATE | c.4147G>A | p.Glu1383Lys | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 4223/4825 | 4147/4206 | 1383/1401 | chr12 | 6531353 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6510114 | T | C | 1 | a0002c0018 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.243T>C | p.Thr81Thr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 4/32 | 319/4825 | 243/4206 | 81/1401 | chr12 | 6510114 | |||
chr12:6510732 | T | C | 1 | a0003c0015 | 2 | HG01891.hp1 HG01993.hp2 |
synonymous_variant | LOW | c.366T>C | p.Tyr122Tyr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 5/32 | 442/4825 | 366/4206 | 122/1401 | chr12 | 6510732 | |||
chr12:6511229 | A | C | 1 | a0001c0033 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.564A>C | p.Ser188Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/32 | 640/4825 | 564/4206 | 188/1401 | chr12 | 6511229 | |||
chr12:6514334 | T | C | 1 | a0002c0019 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.657T>C | p.Thr219Thr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 7/32 | 733/4825 | 657/4206 | 219/1401 | chr12 | 6514334 | |||
chr12:6514875 | C | A | 1 | a0001c0026 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.942C>A | p.Ile314Ile | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/32 | 1018/4825 | 942/4206 | 314/1401 | chr12 | 6514875 | |||
chr12:6517616 | C | T | 1 | a0001c0032 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.1341C>T | p.Ala447Ala | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 12/32 | 1417/4825 | 1341/4206 | 447/1401 | chr12 | 6517616 | |||
chr12:6521091 | C | A | 1 | a0007c0016 | 2 | HG03209.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.1695C>A | p.Ile565Ile | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/32 | 1771/4825 | 1695/4206 | 565/1401 | chr12 | 6521091 | |||
chr12:6522003 | C | A | 14 | a0001c0001 a0001c0026 a0001c0028 others(11): Show |
234 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(231): Show |
synonymous_variant | LOW | c.1920C>A | p.Ile640Ile | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/32 | 1996/4825 | 1920/4206 | 640/1401 | chr12 | 6522003 | |||
chr12:6525651 | C | T | 1 | a0001c0030 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.2283C>T | p.Thr761Thr | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/32 | 2359/4825 | 2283/4206 | 761/1401 | chr12 | 6525651 | |||
chr12:6526188 | G | A | 1 | a0002c0021 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.2469G>A | p.Ser823Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 19/32 | 2545/4825 | 2469/4206 | 823/1401 | chr12 | 6526188 | |||
chr12:6528679 | T | C | 25 | a0001c0001 a0001c0004 a0001c0007 others(22): Show |
330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
splice_region_variant&synonymous_variant | LOW | c.3300T>C | p.Arg1100Arg | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 26/32 | 3376/4825 | 3300/4206 | 1100/1401 | chr12 | 6528679 | |||
chr12:6528775 | C | T | 2 | a0004c0005 a0012c0035 |
18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
synonymous_variant | LOW | c.3396C>T | p.Ser1132Ser | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 26/32 | 3472/4825 | 3396/4206 | 1132/1401 | chr12 | 6528775 | |||
chr12:6528950 | C | T | 7 | a0001c0001 a0001c0026 a0001c0030 others(4): Show |
133 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(130): Show |
synonymous_variant | LOW | c.3483C>T | p.Asn1161Asn | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/32 | 3559/4825 | 3483/4206 | 1161/1401 | chr12 | 6528950 | |||
chr12:6528977 | C | A | 1 | a0001c0031 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.3510C>A | p.Ile1170Ile | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/32 | 3586/4825 | 3510/4206 | 1170/1401 | chr12 | 6528977 | |||
chr12:6529922 | A | G | 22 | a0001c0001 a0001c0004 a0001c0007 others(19): Show |
326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
synonymous_variant | LOW | c.3801A>G | p.Val1267Val | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/32 | 3877/4825 | 3801/4206 | 1267/1401 | chr12 | 6529922 | |||
chr12:6529949 | T | G | 3 | a0001c0007 a0014c0027 a0015c0034 |
14 | HG01192.hp2 HG01261.hp1 HG02055.hp2 others(11): Show |
synonymous_variant | LOW | c.3828T>G | p.Pro1276Pro | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/32 | 3904/4825 | 3828/4206 | 1276/1401 | chr12 | 6529949 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6531496 | T | G | 1 | a0001c0001t0015 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*84T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 84 | chr12 | 6531496 | ||||||
chr12:6531503 | CT | C | 2 | a0001c0001t0007 a0003c0003t0014 |
8 | HG01070.hp1 HG01975.hp1 HG01993.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*99delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 99 | INFO_REALIGN_3_PRIME | chr12 | 6531503 | |||||
chr12:6531508 | T | TA | 2 | a0001c0004t0010 a0001c0007t0012 |
5 | HG02055.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*96_*97insA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 97 | chr12 | 6531508 | ||||||
chr12:6531509 | T | A | 2 | a0001c0004t0010 a0001c0007t0012 |
5 | HG02055.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*97T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 97 | chr12 | 6531509 | ||||||
chr12:6531509 | T | TA | 3 | a0001c0007t0005 a0014c0027t0005 a0015c0034t0005 |
11 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*97_*98insA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 98 | chr12 | 6531509 | ||||||
chr12:6531510 | T | A | 16 | a0001c0001t0002 a0001c0001t0015 a0001c0004t0004 others(13): Show |
174 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*98T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 98 | chr12 | 6531510 | ||||||
chr12:6531510 | T | TA | 4 | a0001c0001t0006 a0001c0026t0006 a0003c0003t0013 others(1): Show |
13 | HG01358.hp1 HG02630.hp2 HG02647.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*98_*99insA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 99 | chr12 | 6531510 | ||||||
chr12:6531511 | T | A | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(27): Show |
298 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*99T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 99 | chr12 | 6531511 | ||||||
chr12:6531528 | G | A | 1 | a0001c0007t0012 | 2 | HG02055.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*116G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 116 | chr12 | 6531528 | ||||||
chr12:6531678 | G | A | 2 | a0001c0004t0009 a0001c0028t0009 |
4 | HG01884.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*266G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 266 | chr12 | 6531678 | ||||||
chr12:6531744 | T | C | 11 | a0001c0004t0004 a0001c0004t0008 a0001c0004t0009 others(8): Show |
69 | HG00558.hp1 HG01192.hp2 HG01243.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*332T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 332 | chr12 | 6531744 | ||||||
chr12:6531810 | A | T | 9 | a0001c0001t0003 a0003c0003t0003 a0003c0003t0013 others(6): Show |
100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*398A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 398 | chr12 | 6531810 | ||||||
chr12:6531828 | C | T | 1 | a0001c0032t0016 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*416C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 32/32 | 416 | chr12 | 6531828 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:6494160 | A | C | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
splice_region_variant&intron_variant | LOW | c.-24+6A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494160 | |||||||
chr12:6494234 | A | G | 1 | a0001c0007t0012g0386 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-24+80A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494234 | |||||||
chr12:6494247 | A | G | 131 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(128): Show |
139 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.-24+93A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494247 | |||||||
chr12:6494307 | T | A | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.-24+153T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494307 | |||||||
chr12:6494307 | TTGTTAAG others(30): Show |
T | 172 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(169): Show |
183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.-24+211_-24+247del others(37): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr12 | 6494307 | ||||||
chr12:6494371 | G | T | 3 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+217G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494371 | |||||||
chr12:6494440 | T | C | 1 | a0003c0003t0003g0030 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-24+286T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494440 | |||||||
chr12:6494590 | G | T | 3 | a0001c0004t0009g0228 a0001c0004t0009g0229 a0001c0004t0009g0230 |
3 | HG02886.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-24+436G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494590 | |||||||
chr12:6494751 | G | A | 131 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(128): Show |
139 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.-23-325G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494751 | |||||||
chr12:6494910 | A | G | 310 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(307): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.-23-166A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6494910 | |||||||
chr12:6495019 | A | G | 12 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 others(9): Show |
14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23-57A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 1/31 | chr12 | 6495019 | |||||||
chr12:6495249 | T | G | 17 | a0004c0005t0001g0021 a0004c0005t0001g0231 a0004c0005t0001g0232 others(14): Show |
18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.127+24T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495249 | |||||||
chr12:6495252 | C | T | 120 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(117): Show |
128 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.127+27C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495252 | |||||||
chr12:6495287 | C | G | 1 | a0009c0013t0002g0383 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+62C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495287 | |||||||
chr12:6495920 | T | C | 1 | a0003c0003t0003g0031 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.127+695T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495920 | |||||||
chr12:6495939 | C | A | 128 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(125): Show |
135 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.127+714C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495939 | |||||||
chr12:6495989 | A | G | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+764A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6495989 | |||||||
chr12:6496021 | C | G | 1 | a0009c0013t0002g0383 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+796C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496021 | |||||||
chr12:6496039 | T | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(158): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.127+814T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496039 | |||||||
chr12:6496059 | C | CT | 142 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(139): Show |
153 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.127+850dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6496059 | ||||||
chr12:6496115 | T | C | 1 | a0002c0002t0001g0107 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.127+890T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496115 | |||||||
chr12:6496121 | G | A | 1 | a0001c0007t0004g0259 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127+896G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496121 | |||||||
chr12:6496217 | A | G | 310 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(307): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.127+992A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496217 | |||||||
chr12:6496348 | C | T | 17 | a0004c0005t0001g0021 a0004c0005t0001g0231 a0004c0005t0001g0232 others(14): Show |
18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.127+1123C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496348 | |||||||
chr12:6496375 | C | G | 131 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(128): Show |
139 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.127+1150C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496375 | |||||||
chr12:6496401 | G | C | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.127+1176G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496401 | |||||||
chr12:6496490 | T | A | 120 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(117): Show |
128 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.127+1265T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496490 | |||||||
chr12:6496529 | A | G | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.127+1304A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496529 | |||||||
chr12:6496539 | C | T | 1 | a0001c0001t0002g0382 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.127+1314C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496539 | |||||||
chr12:6496645 | G | A | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+1420G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496645 | |||||||
chr12:6496846 | G | A | 120 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(117): Show |
128 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.127+1621G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6496846 | |||||||
chr12:6497019 | G | A | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.127+1794G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497019 | |||||||
chr12:6497283 | T | G | 3 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+2058T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497283 | |||||||
chr12:6497299 | C | CTT | 18 | a0001c0009t0001g0219 a0004c0005t0001g0021 a0004c0005t0001g0231 others(15): Show |
19 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+2084_127+2085d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6497299 | ||||||
chr12:6497327 | G | A | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+2102G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497327 | |||||||
chr12:6497452 | C | G | 2 | a0003c0010t0001g0094 a0003c0010t0001g0095 |
2 | HG00673.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.127+2227C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497452 | |||||||
chr12:6497536 | T | A | 1 | a0002c0002t0001g0108 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.127+2311T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497536 | |||||||
chr12:6497562 | G | T | 1 | a0001c0001t0003g0381 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127+2337G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497562 | |||||||
chr12:6497620 | T | TTTG | 122 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(119): Show |
130 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.127+2411_127+2413d others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6497620 | ||||||
chr12:6497649 | T | TC | 389 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(386): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.127+2426dupC | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6497649 | ||||||
chr12:6497680 | C | T | 2 | a0001c0001t0002g0379 a0001c0009t0001g0380 |
2 | NA18945.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.127+2455C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497680 | |||||||
chr12:6497780 | G | A | 1 | a0003c0003t0003g0032 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.127+2555G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497780 | |||||||
chr12:6497852 | G | C | 172 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(169): Show |
183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.127+2627G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6497852 | |||||||
chr12:6497918 | C | CT | 122 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(119): Show |
130 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.127+2706dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6497918 | ||||||
chr12:6497918 | C | CTT | 11 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.127+2705_127+2706d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6497918 | ||||||
chr12:6498002 | G | C | 131 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(128): Show |
139 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.127+2777G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498002 | |||||||
chr12:6498198 | T | C | 30 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 others(27): Show |
33 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.127+2973T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498198 | |||||||
chr12:6498272 | A | G | 1 | a0001c0004t0008g0218 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127+3047A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498272 | |||||||
chr12:6498281 | A | G | 1 | a0001c0001t0002g0377 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.127+3056A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498281 | |||||||
chr12:6498478 | A | G | 1 | a0004c0005t0001g0246 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.127+3253A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498478 | |||||||
chr12:6498615 | C | CT | 25 | a0001c0001t0002g0375 a0001c0001t0002g0376 a0001c0007t0004g0259 others(22): Show |
27 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.127+3401dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6498615 | ||||||
chr12:6498694 | G | A | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+3469G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498694 | |||||||
chr12:6498732 | T | C | 131 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(128): Show |
139 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.127+3507T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498732 | |||||||
chr12:6498774 | A | AT | 30 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 others(27): Show |
33 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.127+3555dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6498774 | ||||||
chr12:6498855 | C | T | 1 | a0003c0015t0003g0092 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127+3630C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498855 | |||||||
chr12:6498879 | C | T | 1 | a0005c0006t0003g0173 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.127+3654C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498879 | |||||||
chr12:6498885 | T | C | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+3660T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6498885 | |||||||
chr12:6499203 | C | A | 1 | a0002c0002t0001g0109 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.127+3978C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499203 | |||||||
chr12:6499388 | G | A | 1 | a0001c0032t0016g0279 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.127+4163G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499388 | |||||||
chr12:6499403 | C | T | 2 | a0001c0001t0002g0373 a0001c0001t0002g0374 |
2 | HG01123.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.127+4178C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499403 | |||||||
chr12:6499411 | G | A | 1 | a0003c0003t0003g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.127+4186G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499411 | |||||||
chr12:6499441 | G | A | 12 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 others(9): Show |
14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.127+4216G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499441 | |||||||
chr12:6499554 | A | AT | 5 | a0001c0004t0008g0214 a0001c0004t0008g0215 a0001c0004t0008g0216 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+4337dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6499554 | ||||||
chr12:6499612 | G | A | 128 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(125): Show |
135 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.127+4387G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499612 | |||||||
chr12:6499701 | A | G | 1 | a0001c0007t0005g0264 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127+4476A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499701 | |||||||
chr12:6499724 | A | G | 1 | a0001c0007t0012g0386 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.127+4499A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499724 | |||||||
chr12:6499793 | G | A | 1 | a0004c0005t0001g0231 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.127+4568G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499793 | |||||||
chr12:6499860 | C | G | 2 | a0001c0001t0002g0371 a0001c0001t0002g0372 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127+4635C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499860 | |||||||
chr12:6499978 | C | T | 1 | a0001c0001t0002g0370 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.127+4753C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499978 | |||||||
chr12:6499994 | A | G | 1 | a0001c0001t0002g0369 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127+4769A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6499994 | |||||||
chr12:6500006 | C | G | 7 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(4): Show |
7 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+4781C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500006 | |||||||
chr12:6500154 | G | C | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02523.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.127+4929G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500154 | |||||||
chr12:6500337 | G | T | 111 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(108): Show |
118 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.127+5112G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500337 | |||||||
chr12:6500580 | C | G | 1 | a0002c0002t0001g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.127+5355C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500580 | |||||||
chr12:6500596 | T | C | 1 | a0001c0007t0012g0386 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.127+5371T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500596 | |||||||
chr12:6500598 | A | G | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+5373A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500598 | |||||||
chr12:6500802 | A | G | 2 | a0003c0015t0003g0091 a0003c0015t0003g0092 |
2 | HG01891.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.127+5577A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500802 | |||||||
chr12:6500952 | C | T | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+5727C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6500952 | |||||||
chr12:6501056 | CT | C | 158 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(155): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.127+5848delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501056 | ||||||
chr12:6501056 | CTT | C | 7 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(4): Show |
8 | HG02886.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+5847_127+5848d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501056 | ||||||
chr12:6501056 | CTTT | C | 11 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(8): Show |
11 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+5846_127+5848d others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501056 | ||||||
chr12:6501134 | C | G | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+5909C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501134 | |||||||
chr12:6501217 | C | T | 1 | a0003c0003t0003g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.127+5992C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501217 | |||||||
chr12:6501227 | A | AT | 49 | a0001c0004t0004g0009 a0001c0004t0004g0019 a0001c0004t0004g0184 others(46): Show |
59 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.127+6034dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | ||||||
chr12:6501227 | A | ATT | 38 | a0001c0004t0004g0020 a0001c0004t0004g0203 a0001c0004t0004g0204 others(35): Show |
42 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.127+6033_127+6034d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | ||||||
chr12:6501227 | AT | A | 61 | a0001c0001t0006g0257 a0001c0004t0001g0018 a0001c0004t0001g0180 others(58): Show |
66 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.127+6034delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | ||||||
chr12:6501227 | ATT | A | 14 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(11): Show |
14 | HG01070.hp1 HG01884.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.127+6033_127+6034d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | ||||||
chr12:6501227 | ATTTT | A | 23 | a0001c0001t0002g0278 a0001c0001t0002g0350 a0001c0001t0002g0351 others(20): Show |
23 | HG00597.hp1 HG01106.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.127+6031_127+6034d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | ||||||
chr12:6501227 | ATTTTT | A | 93 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(90): Show |
100 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.127+6030_127+6034d others(7): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | ||||||
chr12:6501227 | ATTTTTTT others(1): Show |
A | 10 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.127+6027_127+6034d others(10): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | ||||||
chr12:6501227 | ATTTTTTT others(2): Show |
A | 28 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0007t0004g0259 others(25): Show |
31 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+6026_127+6034d others(11): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6501227 | ||||||
chr12:6501259 | T | G | 128 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(125): Show |
135 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.127+6034T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501259 | |||||||
chr12:6501262 | G | T | 3 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+6037G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501262 | |||||||
chr12:6501265 | G | T | 3 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127+6040G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501265 | |||||||
chr12:6501277 | C | T | 17 | a0004c0005t0001g0021 a0004c0005t0001g0231 a0004c0005t0001g0232 others(14): Show |
18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.127+6052C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501277 | |||||||
chr12:6501319 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.127+6094C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501319 | |||||||
chr12:6501350 | G | C | 1 | a0001c0001t0002g0285 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.127+6125G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501350 | |||||||
chr12:6501479 | C | T | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+6254C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501479 | |||||||
chr12:6501489 | T | C | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.127+6264T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501489 | |||||||
chr12:6501560 | G | A | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.127+6335G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501560 | |||||||
chr12:6501567 | G | C | 1 | a0001c0004t0008g0218 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127+6342G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501567 | |||||||
chr12:6501600 | A | G | 2 | a0003c0003t0003g0072 a0003c0003t0003g0106 |
2 | HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.127+6375A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501600 | |||||||
chr12:6501794 | T | C | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.127+6569T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501794 | |||||||
chr12:6501901 | A | G | 1 | a0001c0004t0008g0213 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.127+6676A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501901 | |||||||
chr12:6501912 | T | C | 119 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(116): Show |
126 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.127+6687T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501912 | |||||||
chr12:6501954 | C | G | 1 | a0002c0002t0001g0108 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.127+6729C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6501954 | |||||||
chr12:6502002 | T | G | 1 | a0004c0005t0001g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127+6777T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502002 | |||||||
chr12:6502041 | C | T | 3 | a0001c0004t0004g0202 a0001c0004t0004g0212 a0001c0004t0008g0213 |
3 | HG01952.hp2 HG01981.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.127+6816C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502041 | |||||||
chr12:6502244 | T | C | 1 | a0001c0004t0008g0218 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127+7019T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502244 | |||||||
chr12:6502322 | G | A | 7 | a0001c0001t0002g0277 a0001c0001t0002g0289 a0001c0001t0002g0290 others(4): Show |
8 | HG01169.hp2 HG02809.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+7097G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502322 | |||||||
chr12:6502345 | A | G | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+7120A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502345 | |||||||
chr12:6502364 | T | G | 1 | a0001c0030t0002g0291 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.127+7139T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502364 | |||||||
chr12:6502447 | A | G | 1 | a0003c0003t0003g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.127+7222A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502447 | |||||||
chr12:6502503 | C | T | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-7214C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502503 | |||||||
chr12:6502534 | T | C | 10 | a0001c0007t0004g0259 a0001c0007t0005g0022 a0001c0007t0005g0023 others(7): Show |
12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-7183T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502534 | |||||||
chr12:6502553 | G | A | 172 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(169): Show |
183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.128-7164G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502553 | |||||||
chr12:6502674 | G | A | 1 | a0002c0002t0001g0112 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.128-7043G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502674 | |||||||
chr12:6502716 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.128-7001G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502716 | |||||||
chr12:6502789 | C | T | 45 | a0001c0004t0004g0009 a0001c0004t0004g0019 a0001c0004t0004g0020 others(42): Show |
49 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(46): Show |
intron_variant | MODIFIER | c.128-6928C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502789 | |||||||
chr12:6502798 | A | G | 310 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(307): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.128-6919A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502798 | |||||||
chr12:6502837 | T | TTTG | 286 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(283): Show |
305 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.128-6861_128-6859d others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6502837 | ||||||
chr12:6502837 | TTTG | T | 9 | a0001c0007t0004g0259 a0001c0007t0005g0022 a0001c0007t0005g0023 others(6): Show |
11 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.128-6861_128-6859d others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6502837 | ||||||
chr12:6502847 | T | TTG | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-6868_128-6867d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6502847 | ||||||
chr12:6502948 | G | A | 117 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(114): Show |
124 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.128-6769G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6502948 | |||||||
chr12:6503008 | C | CT | 54 | a0001c0004t0004g0201 a0001c0004t0004g0210 a0001c0004t0004g0211 others(51): Show |
57 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.128-6688dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6503008 | ||||||
chr12:6503008 | CT | C | 101 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(98): Show |
107 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.128-6688delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6503008 | ||||||
chr12:6503008 | CTT | C | 23 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(20): Show |
24 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.128-6689_128-6688d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6503008 | ||||||
chr12:6503014 | T | G | 7 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(4): Show |
7 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-6703T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503014 | |||||||
chr12:6503020 | T | G | 23 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(20): Show |
24 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.128-6697T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503020 | |||||||
chr12:6503024 | T | G | 23 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(20): Show |
24 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.128-6693T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503024 | |||||||
chr12:6503077 | C | G | 12 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 others(9): Show |
14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.128-6640C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503077 | |||||||
chr12:6503134 | C | T | 4 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(1): Show |
4 | HG02886.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-6583C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503134 | |||||||
chr12:6503293 | T | C | 1 | a0001c0001t0002g0361 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.128-6424T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503293 | |||||||
chr12:6503410 | C | T | 45 | a0001c0004t0004g0009 a0001c0004t0004g0019 a0001c0004t0004g0020 others(42): Show |
49 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(46): Show |
intron_variant | MODIFIER | c.128-6307C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503410 | |||||||
chr12:6503599 | G | A | 82 | a0001c0001t0002g0342 a0003c0003t0003g0004 a0003c0003t0003g0011 others(79): Show |
88 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.128-6118G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503599 | |||||||
chr12:6503676 | C | T | 2 | a0001c0001t0002g0340 a0001c0001t0002g0341 |
2 | NA18979.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.128-6041C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503676 | |||||||
chr12:6503717 | G | C | 92 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(89): Show |
99 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.128-6000G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503717 | |||||||
chr12:6503770 | A | AT | 11 | a0001c0004t0004g0211 a0002c0002t0001g0006 a0002c0002t0001g0111 others(8): Show |
13 | HG01978.hp2 NA18945.hp2 NA18953.hp2 others(10): Show |
intron_variant | MODIFIER | c.128-5931dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6503770 | ||||||
chr12:6503770 | AT | A | 153 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(150): Show |
163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.128-5931delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6503770 | ||||||
chr12:6503786 | T | A | 254 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(251): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.128-5931T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503786 | |||||||
chr12:6503787 | A | T | 46 | a0001c0004t0004g0009 a0001c0004t0004g0019 a0001c0004t0004g0020 others(43): Show |
50 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(47): Show |
intron_variant | MODIFIER | c.128-5930A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503787 | |||||||
chr12:6503904 | G | C | 3 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-5813G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503904 | |||||||
chr12:6503907 | G | A | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-5810G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503907 | |||||||
chr12:6503910 | A | G | 172 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(169): Show |
183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.128-5807A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6503910 | |||||||
chr12:6504003 | G | T | 57 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0004g0009 others(54): Show |
61 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.128-5714G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504003 | |||||||
chr12:6504092 | T | G | 1 | a0017c0036t0001g0378 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-5625T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504092 | |||||||
chr12:6504118 | G | A | 117 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(114): Show |
124 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.128-5599G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504118 | |||||||
chr12:6504155 | C | T | 1 | a0001c0007t0005g0267 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.128-5562C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504155 | |||||||
chr12:6504170 | C | CATATATA others(99): Show |
1 | a0001c0001t0006g0257 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.128-5528_128-5527i others(108): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504170 | ||||||
chr12:6504170 | CATATATA others(55): Show |
C | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.128-5534_128-5473d others(64): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504170 | ||||||
chr12:6504174 | TATATATA others(43): Show |
T | 48 | a0001c0004t0004g0009 a0001c0004t0004g0019 a0001c0004t0004g0020 others(45): Show |
52 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(49): Show |
intron_variant | MODIFIER | c.128-5535_128-5486d others(52): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504174 | ||||||
chr12:6504176 | TATATACA others(35): Show |
T | 3 | a0001c0004t0009g0228 a0001c0004t0009g0229 a0001c0004t0009g0230 |
3 | HG02886.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.128-5535_128-5494d others(44): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504176 | ||||||
chr12:6504176 | TATATACA others(41): Show |
T | 6 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0004g0184 others(3): Show |
6 | HG01243.hp1 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-5535_128-5488d others(50): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504176 | ||||||
chr12:6504180 | T | TACATATA others(87): Show |
1 | a0004c0005t0001g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.128-5520_128-5519i others(96): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504180 | ||||||
chr12:6504180 | T | TACATATA others(89): Show |
3 | a0004c0005t0001g0233 a0004c0005t0001g0237 a0012c0035t0001g0240 |
3 | HG00323.hp1 HG01255.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.128-5520_128-5519i others(98): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504180 | ||||||
chr12:6504180 | T | TACATATA others(115): Show |
1 | a0004c0005t0001g0246 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.128-5520_128-5519i others(124): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504180 | ||||||
chr12:6504182 | C | CAT | 24 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0007 others(21): Show |
27 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.128-5501_128-5500d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | ||||||
chr12:6504182 | C | CATAT | 11 | a0002c0002t0001g0006 a0002c0002t0001g0017 a0002c0002t0001g0108 others(8): Show |
11 | HG02015.hp1 HG02135.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.128-5503_128-5500d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | ||||||
chr12:6504182 | C | CATATAT | 7 | a0002c0002t0001g0002 a0002c0002t0001g0122 a0002c0002t0001g0137 others(4): Show |
7 | HG00621.hp2 HG00673.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-5505_128-5500d others(8): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | ||||||
chr12:6504182 | C | CATATATA others(1): Show |
4 | a0002c0002t0001g0008 a0002c0002t0001g0151 a0002c0002t0001g0157 others(1): Show |
6 | NA18941.hp2 NA18968.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-5507_128-5500d others(10): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | ||||||
chr12:6504182 | C | CATATATA others(3): Show |
1 | a0002c0002t0001g0002 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.128-5509_128-5500d others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | ||||||
chr12:6504182 | C | T | 1 | a0002c0002t0001g0165 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.128-5535C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504182 | |||||||
chr12:6504182 | CAT | C | 3 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0163 |
3 | HG02040.hp1 HG02258.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.128-5501_128-5500d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | ||||||
chr12:6504182 | CATAT | C | 2 | a0002c0002t0001g0001 a0002c0002t0001g0139 |
3 | HG00099.hp1 HG00741.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.128-5503_128-5500d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | ||||||
chr12:6504182 | CATATATA others(43): Show |
C | 1 | a0001c0001t0002g0330 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.128-5523_128-5474d others(52): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504182 | ||||||
chr12:6504184 | T | TATATATA others(85): Show |
1 | a0004c0005t0001g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.128-5520_128-5519i others(94): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504184 | ||||||
chr12:6504184 | T | TATATATA others(87): Show |
6 | a0004c0005t0001g0021 a0004c0005t0001g0234 a0004c0005t0001g0235 others(3): Show |
7 | HG00099.hp2 HG01243.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-5520_128-5519i others(96): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504184 | ||||||
chr12:6504184 | T | TATATATA others(117): Show |
2 | a0004c0005t0001g0231 a0004c0005t0001g0242 |
2 | HG01346.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.128-5520_128-5519i others(126): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504184 | ||||||
chr12:6504186 | T | TATATATA others(85): Show |
1 | a0004c0005t0001g0238 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.128-5520_128-5519i others(94): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504186 | ||||||
chr12:6504186 | TATATATA others(31): Show |
T | 2 | a0001c0007t0012g0269 a0001c0007t0012g0386 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.128-5511_128-5474d others(40): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504186 | ||||||
chr12:6504188 | T | TACATATA others(105): Show |
3 | a0008c0012t0006g0248 a0008c0012t0006g0252 a0008c0012t0006g0256 |
3 | HG02647.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.128-5528_128-5527i others(114): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504188 | ||||||
chr12:6504188 | T | TATATATA others(83): Show |
1 | a0004c0005t0001g0232 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.128-5520_128-5519i others(92): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504188 | ||||||
chr12:6504188 | T | TATATATA others(83): Show |
1 | a0004c0005t0001g0241 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.128-5520_128-5519i others(92): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504188 | ||||||
chr12:6504188 | TATATATA others(29): Show |
T | 7 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(4): Show |
7 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-5509_128-5474d others(38): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504188 | ||||||
chr12:6504190 | T | C | 1 | a0001c0001t0006g0257 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.128-5527T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504190 | |||||||
chr12:6504194 | TATATATA others(23): Show |
T | 1 | a0017c0036t0001g0378 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-5503_128-5474d others(32): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504194 | ||||||
chr12:6504196 | T | TATATACA others(83): Show |
1 | a0001c0001t0006g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.128-5516_128-5515i others(92): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504196 | ||||||
chr12:6504196 | TATATATA others(21): Show |
T | 101 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(98): Show |
108 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.128-5501_128-5474d others(30): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504196 | ||||||
chr12:6504197 | A | G | 1 | a0001c0007t0005g0263 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.128-5520A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504197 | |||||||
chr12:6504198 | T | C | 3 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-5519T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504198 | |||||||
chr12:6504198 | T | TATACATA others(79): Show |
2 | a0001c0001t0006g0255 a0001c0028t0009g0254 |
2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.128-5516_128-5515i others(88): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504198 | ||||||
chr12:6504198 | TATATATA others(19): Show |
T | 12 | a0001c0001t0002g0027 a0001c0001t0002g0320 a0001c0001t0002g0335 others(9): Show |
12 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-5499_128-5474d others(28): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504198 | ||||||
chr12:6504199 | A | G | 9 | a0001c0007t0004g0259 a0001c0007t0005g0022 a0001c0007t0005g0023 others(6): Show |
11 | HG01192.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.128-5518A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504199 | |||||||
chr12:6504200 | T | C | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.128-5517T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504200 | |||||||
chr12:6504202 | T | C | 2 | a0001c0001t0002g0375 a0001c0001t0002g0376 |
2 | NA18972.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.128-5515T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504202 | |||||||
chr12:6504202 | T | TATATATA others(117): Show |
1 | a0001c0001t0006g0249 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.128-5506_128-5505i others(126): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504202 | ||||||
chr12:6504204 | T | C | 4 | a0001c0001t0006g0253 a0008c0012t0006g0248 a0008c0012t0006g0252 others(1): Show |
4 | HG02630.hp2 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-5513T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504204 | |||||||
chr12:6504204 | T | TACATATA others(103): Show |
1 | a0001c0026t0006g0258 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.128-5512_128-5511i others(112): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504204 | ||||||
chr12:6504204 | T | TATATATA others(115): Show |
2 | a0001c0001t0006g0250 a0001c0001t0006g0251 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.128-5506_128-5505i others(124): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504204 | ||||||
chr12:6504206 | T | C | 2 | a0001c0001t0006g0255 a0001c0028t0009g0254 |
2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.128-5511T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504206 | |||||||
chr12:6504208 | TATATATA others(9): Show |
T | 3 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-5499_128-5484d others(18): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504208 | ||||||
chr12:6504212 | T | C | 2 | a0004c0005t0001g0236 a0004c0005t0001g0242 |
2 | HG02683.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.128-5505T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504212 | |||||||
chr12:6504212 | T | TAG | 4 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0117 others(1): Show |
4 | HG02165.hp2 NA18945.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-5504_128-5503i others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504212 | ||||||
chr12:6504214 | T | C | 14 | a0004c0005t0001g0021 a0004c0005t0001g0231 a0004c0005t0001g0233 others(11): Show |
15 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.128-5503T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504214 | |||||||
chr12:6504215 | A | ACACATAT others(55): Show |
3 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-5502_128-5501i others(64): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504215 | |||||||
chr12:6504216 | T | C | 13 | a0004c0005t0001g0021 a0004c0005t0001g0231 a0004c0005t0001g0233 others(10): Show |
14 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.128-5501T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504216 | |||||||
chr12:6504216 | TAG | T | 8 | a0001c0007t0004g0259 a0001c0007t0005g0022 a0001c0007t0005g0023 others(5): Show |
9 | HG01192.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-5499_128-5498d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504216 | ||||||
chr12:6504217 | A | G | 3 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-5500A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504217 | |||||||
chr12:6504218 | G | C | 5 | a0001c0004t0011g0387 a0001c0004t0011g0388 a0004c0005t0001g0232 others(2): Show |
5 | HG00733.hp1 HG01074.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-5499G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504218 | |||||||
chr12:6504218 | G | T | 29 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(26): Show |
30 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.128-5499G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504218 | |||||||
chr12:6504220 | T | C | 4 | a0001c0004t0011g0387 a0001c0004t0011g0388 a0004c0005t0001g0232 others(1): Show |
4 | HG00733.hp1 HG01168.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-5497T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504220 | |||||||
chr12:6504222 | T | C | 1 | a0001c0007t0005g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.128-5495T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504222 | |||||||
chr12:6504224 | G | C | 9 | a0001c0007t0004g0259 a0001c0007t0005g0022 a0001c0007t0005g0023 others(6): Show |
10 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-5493G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504224 | |||||||
chr12:6504224 | G | T | 43 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(40): Show |
44 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.128-5493G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504224 | |||||||
chr12:6504226 | T | G | 1 | a0002c0002t0001g0006 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.128-5491T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504226 | |||||||
chr12:6504228 | T | C | 3 | a0001c0001t0002g0363 a0001c0011t0001g0029 a0001c0011t0001g0384 |
4 | HG01981.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-5489T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504228 | |||||||
chr12:6504228 | T | TATATATA others(27): Show |
2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.128-5482_128-5481i others(36): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6504228 | ||||||
chr12:6504230 | T | C | 64 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(61): Show |
69 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.128-5487T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504230 | |||||||
chr12:6504230 | T | G | 4 | a0002c0002t0001g0007 a0002c0002t0001g0118 a0002c0002t0001g0134 others(1): Show |
6 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-5487T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504230 | |||||||
chr12:6504232 | T | C | 113 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(110): Show |
121 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.128-5485T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504232 | |||||||
chr12:6504233 | A | G | 3 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0014c0027t0005g0247 |
3 | HG02615.hp2 NA18977.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.128-5484A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504233 | |||||||
chr12:6504234 | T | C | 117 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(114): Show |
124 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.128-5483T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504234 | |||||||
chr12:6504239 | A | G | 3 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-5478A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504239 | |||||||
chr12:6504424 | G | A | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.128-5293G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504424 | |||||||
chr12:6504453 | C | T | 1 | a0001c0001t0002g0336 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.128-5264C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504453 | |||||||
chr12:6504598 | G | A | 1 | a0001c0007t0012g0386 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.128-5119G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504598 | |||||||
chr12:6504924 | T | G | 2 | a0003c0003t0003g0037 a0003c0003t0003g0038 |
2 | NA18984.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.128-4793T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504924 | |||||||
chr12:6504933 | C | T | 5 | a0007c0014t0001g0281 a0007c0014t0001g0282 a0007c0014t0001g0284 others(2): Show |
5 | HG02622.hp1 HG03209.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-4784C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504933 | |||||||
chr12:6504990 | T | C | 117 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(114): Show |
124 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.128-4727T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6504990 | |||||||
chr12:6505015 | A | G | 45 | a0001c0004t0004g0009 a0001c0004t0004g0019 a0001c0004t0004g0020 others(42): Show |
49 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(46): Show |
intron_variant | MODIFIER | c.128-4702A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505015 | |||||||
chr12:6505220 | C | T | 12 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 others(9): Show |
14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.128-4497C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505220 | |||||||
chr12:6505290 | T | C | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-4427T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505290 | |||||||
chr12:6505300 | A | G | 1 | a0002c0002t0001g0168 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.128-4417A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505300 | |||||||
chr12:6505304 | G | A | 3 | a0001c0004t0009g0228 a0001c0004t0009g0229 a0001c0004t0009g0230 |
3 | HG02886.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.128-4413G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505304 | |||||||
chr12:6505355 | C | T | 17 | a0004c0005t0001g0021 a0004c0005t0001g0231 a0004c0005t0001g0232 others(14): Show |
18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.128-4362C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505355 | |||||||
chr12:6505361 | C | T | 1 | a0002c0002t0001g0129 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.128-4356C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505361 | |||||||
chr12:6505391 | C | T | 3 | a0001c0004t0004g0198 a0001c0004t0004g0199 a0001c0004t0004g0200 |
3 | HG01257.hp2 HG01258.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.128-4326C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505391 | |||||||
chr12:6505575 | G | A | 1 | a0004c0005t0001g0232 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.128-4142G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505575 | |||||||
chr12:6505656 | C | T | 17 | a0004c0005t0001g0021 a0004c0005t0001g0231 a0004c0005t0001g0232 others(14): Show |
18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.128-4061C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505656 | |||||||
chr12:6505688 | A | T | 4 | a0001c0004t0009g0228 a0001c0004t0009g0229 a0001c0004t0009g0230 others(1): Show |
4 | HG02886.hp2 HG03139.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-4029A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505688 | |||||||
chr12:6505779 | C | T | 1 | a0001c0001t0015g0367 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.128-3938C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505779 | |||||||
chr12:6505846 | C | CAG | 311 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(308): Show |
332 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.128-3870_128-3869d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6505846 | ||||||
chr12:6505986 | G | T | 57 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0004g0009 others(54): Show |
61 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.128-3731G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6505986 | |||||||
chr12:6506036 | G | A | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.128-3681G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506036 | |||||||
chr12:6506041 | C | T | 1 | a0001c0001t0002g0339 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.128-3676C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506041 | |||||||
chr12:6506361 | G | T | 32 | a0001c0004t0004g0009 a0001c0004t0004g0019 a0001c0004t0004g0020 others(29): Show |
36 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.128-3356G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506361 | |||||||
chr12:6506446 | C | T | 20 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 others(17): Show |
21 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.128-3271C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506446 | |||||||
chr12:6506470 | G | A | 1 | a0003c0003t0003g0039 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.128-3247G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506470 | |||||||
chr12:6506482 | C | T | 1 | a0003c0003t0003g0086 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.128-3235C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506482 | |||||||
chr12:6506515 | A | G | 310 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(307): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.128-3202A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506515 | |||||||
chr12:6506518 | A | G | 1 | a0003c0003t0003g0038 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.128-3199A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506518 | |||||||
chr12:6506522 | A | G | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.128-3195A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506522 | |||||||
chr12:6506552 | T | C | 14 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(11): Show |
15 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.128-3165T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506552 | |||||||
chr12:6506695 | A | T | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-3022A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506695 | |||||||
chr12:6506709 | G | A | 8 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(5): Show |
8 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-3008G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506709 | |||||||
chr12:6506715 | C | A | 1 | a0001c0004t0008g0213 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.128-3002C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506715 | |||||||
chr12:6506784 | G | A | 1 | a0007c0016t0001g0280 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.128-2933G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506784 | |||||||
chr12:6506921 | G | A | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.128-2796G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506921 | |||||||
chr12:6506954 | G | T | 48 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(45): Show |
50 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-2763G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506954 | |||||||
chr12:6506972 | A | C | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.128-2745A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6506972 | |||||||
chr12:6507057 | G | A | 310 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(307): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.128-2660G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507057 | |||||||
chr12:6507090 | T | G | 2 | a0002c0002t0001g0117 a0019c0025t0001g0155 |
2 | NA18955.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.128-2627T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507090 | |||||||
chr12:6507157 | T | G | 3 | a0002c0002t0001g0007 a0002c0002t0001g0118 a0002c0002t0001g0152 |
5 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-2560T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507157 | |||||||
chr12:6507341 | C | T | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-2376C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507341 | |||||||
chr12:6507554 | G | A | 2 | a0001c0001t0002g0350 a0001c0001t0002g0351 |
2 | HG01346.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.128-2163G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507554 | |||||||
chr12:6507840 | C | T | 1 | a0001c0004t0004g0221 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.128-1877C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507840 | |||||||
chr12:6507841 | GA | G | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-1869delA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6507841 | ||||||
chr12:6507869 | G | A | 1 | a0001c0001t0002g0342 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.128-1848G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6507869 | |||||||
chr12:6508043 | T | G | 3 | a0003c0003t0003g0040 a0003c0003t0003g0073 a0003c0003t0003g0090 |
3 | NA18955.hp2 NA18963.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.128-1674T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508043 | |||||||
chr12:6508183 | G | A | 1 | a0002c0002t0001g0112 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.128-1534G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508183 | |||||||
chr12:6508185 | T | C | 310 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(307): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.128-1532T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508185 | |||||||
chr12:6508206 | T | C | 310 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(307): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.128-1511T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508206 | |||||||
chr12:6508340 | A | G | 3 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.128-1377A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508340 | |||||||
chr12:6508393 | C | T | 291 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(288): Show |
310 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.128-1324C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508393 | |||||||
chr12:6508533 | A | G | 1 | a0001c0007t0012g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.128-1184A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508533 | |||||||
chr12:6508902 | C | T | 1 | a0001c0004t0008g0217 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.128-815C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6508902 | |||||||
chr12:6509023 | C | T | 1 | a0001c0001t0002g0328 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.128-694C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6509023 | |||||||
chr12:6509074 | C | CTT | 16 | a0004c0005t0001g0021 a0004c0005t0001g0231 a0004c0005t0001g0232 others(13): Show |
17 | HG00099.hp2 HG00733.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.128-629_128-628dup others(2): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6509074 | ||||||
chr12:6509074 | CT | C | 25 | a0001c0001t0002g0025 a0001c0001t0002g0289 a0001c0001t0002g0293 others(22): Show |
25 | HG00642.hp2 HG01168.hp2 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.128-628delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6509074 | ||||||
chr12:6509138 | G | GT | 4 | a0001c0004t0008g0214 a0001c0004t0008g0215 a0001c0004t0008g0216 others(1): Show |
4 | HG02109.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-578dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | 6509138 | ||||||
chr12:6509188 | G | A | 1 | a0002c0021t0001g0121 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.128-529G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6509188 | |||||||
chr12:6509490 | G | A | 1 | a0001c0033t0004g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.128-227G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6509490 | |||||||
chr12:6509508 | C | T | 5 | a0003c0003t0003g0064 a0003c0003t0003g0065 a0003c0003t0003g0085 others(2): Show |
5 | HG00621.hp1 HG02040.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-209C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6509508 | |||||||
chr12:6509705 | C | T | 81 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(78): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.128-12C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | chr12 | 6509705 | |||||||
chr12:6509888 | T | C | 106 | a0001c0004t0011g0387 a0001c0004t0011g0388 a0001c0007t0012g0269 others(103): Show |
114 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.203+96T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 3/31 | chr12 | 6509888 | |||||||
chr12:6509915 | TCTA | T | 129 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(126): Show |
136 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.203+126_203+128del others(3): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr12 | 6509915 | ||||||
chr12:6509998 | C | T | 4 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(1): Show |
4 | HG02886.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-77C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 3/31 | chr12 | 6509998 | |||||||
chr12:6510151 | G | A | 1 | a0001c0004t0008g0217 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.262+18G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 4/31 | chr12 | 6510151 | |||||||
chr12:6510236 | T | A | 1 | a0001c0007t0012g0386 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.262+103T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 4/31 | chr12 | 6510236 | |||||||
chr12:6510236 | T | C | 83 | a0001c0004t0011g0387 a0001c0004t0011g0388 a0003c0003t0003g0004 others(80): Show |
89 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.262+103T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 4/31 | chr12 | 6510236 | |||||||
chr12:6510857 | G | C | 11 | a0001c0004t0004g0009 a0001c0004t0004g0020 a0001c0004t0004g0189 others(8): Show |
14 | NA18941.hp1 NA18952.hp1 NA18968.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+47G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 5/31 | chr12 | 6510857 | |||||||
chr12:6510971 | C | T | 1 | a0003c0003t0014g0096 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.445-139C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 5/31 | chr12 | 6510971 | |||||||
chr12:6510997 | C | T | 2 | a0002c0002t0001g0109 a0011c0023t0001g0149 |
2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.445-113C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 5/31 | chr12 | 6510997 | |||||||
chr12:6511329 | G | T | 232 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(229): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.587+77G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511329 | |||||||
chr12:6511334 | G | GT | 9 | a0001c0001t0002g0341 a0001c0009t0001g0219 a0002c0002t0001g0165 others(6): Show |
9 | HG02056.hp1 HG02074.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.587+92dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6511334 | ||||||
chr12:6511340 | T | G | 1 | a0001c0004t0011g0387 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.587+88T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511340 | |||||||
chr12:6511343 | T | G | 5 | a0002c0002t0001g0008 a0002c0002t0001g0122 a0002c0002t0001g0137 others(2): Show |
7 | HG00621.hp2 NA18941.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.587+91T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511343 | |||||||
chr12:6511346 | T | G | 5 | a0002c0002t0001g0008 a0002c0002t0001g0122 a0002c0002t0001g0137 others(2): Show |
7 | HG00621.hp2 NA18941.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.587+94T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511346 | |||||||
chr12:6511386 | G | A | 2 | a0002c0002t0001g0117 a0009c0013t0002g0383 |
2 | HG03225.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.587+134G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511386 | |||||||
chr12:6511436 | A | G | 304 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(301): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.587+184A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511436 | |||||||
chr12:6511457 | C | T | 17 | a0004c0005t0001g0021 a0004c0005t0001g0231 a0004c0005t0001g0232 others(14): Show |
18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.587+205C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511457 | |||||||
chr12:6511472 | A | G | 2 | a0001c0011t0001g0029 a0001c0011t0001g0384 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.587+220A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511472 | |||||||
chr12:6511541 | C | A | 1 | a0001c0001t0002g0296 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.587+289C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511541 | |||||||
chr12:6511552 | C | G | 1 | a0003c0003t0003g0068 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.587+300C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511552 | |||||||
chr12:6511613 | G | A | 235 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(232): Show |
250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.587+361G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511613 | |||||||
chr12:6511753 | G | A | 1 | a0003c0003t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.587+501G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511753 | |||||||
chr12:6511866 | G | A | 1 | a0001c0004t0009g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.587+614G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511866 | |||||||
chr12:6511980 | G | A | 1 | a0001c0004t0004g0201 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.587+728G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6511980 | |||||||
chr12:6512056 | T | C | 2 | a0001c0007t0012g0269 a0001c0007t0012g0386 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.587+804T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512056 | |||||||
chr12:6512085 | C | T | 152 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(149): Show |
161 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.587+833C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512085 | |||||||
chr12:6512112 | A | T | 1 | a0001c0001t0002g0346 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587+860A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512112 | |||||||
chr12:6512114 | A | C | 1 | a0001c0001t0002g0346 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587+862A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512114 | |||||||
chr12:6512146 | C | T | 1 | a0001c0007t0012g0386 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.587+894C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512146 | |||||||
chr12:6512188 | C | T | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.587+936C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512188 | |||||||
chr12:6512272 | C | CA | 12 | a0001c0004t0008g0213 a0001c0009t0001g0219 a0002c0002t0001g0130 others(9): Show |
12 | HG01192.hp1 HG02622.hp1 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.587+1041dupA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512272 | ||||||
chr12:6512272 | CA | C | 22 | a0001c0001t0002g0362 a0001c0004t0001g0018 a0001c0004t0001g0180 others(19): Show |
24 | HG01192.hp2 HG01261.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.587+1041delA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512272 | ||||||
chr12:6512272 | CAA | C | 221 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(218): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.587+1040_587+1041d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512272 | ||||||
chr12:6512276 | A | G | 2 | a0003c0003t0003g0061 a0003c0003t0003g0084 |
2 | NA18974.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.587+1024A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512276 | |||||||
chr12:6512292 | A | T | 2 | a0001c0001t0002g0326 a0001c0001t0002g0327 |
2 | HG01099.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.587+1040A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512292 | |||||||
chr12:6512308 | TAGAC | T | 3 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.587+1066_587+1069d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512308 | ||||||
chr12:6512314 | G | A | 1 | a0001c0001t0002g0330 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.587+1062G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512314 | |||||||
chr12:6512314 | GACAGACA others(1): Show |
G | 4 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(1): Show |
4 | HG02886.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+1070_587+1077d others(10): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512314 | ||||||
chr12:6512318 | GACAA | G | 7 | a0001c0001t0002g0354 a0001c0004t0004g0181 a0001c0004t0008g0214 others(4): Show |
7 | HG02109.hp2 HG02451.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+1070_587+1073d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6512318 | ||||||
chr12:6512398 | A | G | 1 | a0001c0011t0001g0385 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.587+1146A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512398 | |||||||
chr12:6512475 | A | G | 129 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(126): Show |
136 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.587+1223A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512475 | |||||||
chr12:6512485 | C | T | 1 | a0003c0003t0003g0060 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.587+1233C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512485 | |||||||
chr12:6512535 | C | T | 1 | a0001c0007t0012g0386 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.587+1283C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512535 | |||||||
chr12:6512680 | A | G | 4 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(1): Show |
4 | HG02886.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+1428A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512680 | |||||||
chr12:6512716 | C | T | 1 | a0001c0004t0009g0228 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.587+1464C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512716 | |||||||
chr12:6512945 | A | G | 304 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(301): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.588-1320A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6512945 | |||||||
chr12:6513065 | TAA | T | 11 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(8): Show |
11 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.588-1198_588-1197d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513065 | ||||||
chr12:6513180 | T | C | 244 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(241): Show |
261 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.588-1085T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513180 | |||||||
chr12:6513232 | T | C | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.588-1033T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513232 | |||||||
chr12:6513239 | C | T | 1 | a0004c0005t0001g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.588-1026C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513239 | |||||||
chr12:6513361 | T | C | 7 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0144 others(4): Show |
7 | HG00438.hp1 HG00673.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.588-904T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513361 | |||||||
chr12:6513444 | G | A | 1 | a0003c0003t0003g0103 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.588-821G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513444 | |||||||
chr12:6513622 | T | C | 1 | a0002c0002t0001g0112 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.588-643T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513622 | |||||||
chr12:6513715 | C | CT | 9 | a0001c0001t0006g0253 a0001c0001t0006g0255 a0001c0001t0006g0257 others(6): Show |
9 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.588-532dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | C | CTTTTTTT others(7): Show |
2 | a0001c0004t0010g0260 a0001c0004t0010g0261 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.588-545_588-532dup others(14): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | C | CTTTTTTT others(8): Show |
13 | a0001c0004t0010g0262 a0001c0007t0005g0268 a0004c0005t0001g0021 others(10): Show |
14 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-546_588-532dup others(15): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | C | CTTTTTTT others(9): Show |
9 | a0001c0007t0004g0259 a0001c0007t0005g0023 a0001c0007t0005g0267 others(6): Show |
10 | HG00733.hp1 HG01243.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.588-547_588-532dup others(16): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | C | CTTTTTTT others(10): Show |
7 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0007t0005g0263 others(4): Show |
7 | HG01099.hp2 HG01192.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.588-548_588-532dup others(17): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | C | CTTTTTTT others(11): Show |
20 | a0001c0001t0002g0010 a0001c0001t0002g0293 a0001c0001t0002g0294 others(17): Show |
23 | HG01069.hp2 HG01081.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.588-549_588-532dup others(18): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | C | CTTTTTTT others(12): Show |
47 | a0001c0001t0002g0003 a0001c0001t0002g0025 a0001c0001t0002g0026 others(44): Show |
52 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.588-532_588-531ins others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | C | CTTTTTTT others(13): Show |
24 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(21): Show |
24 | HG00642.hp1 HG01358.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.588-532_588-531ins others(20): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | C | CTTTTTTT others(14): Show |
14 | a0001c0001t0002g0273 a0001c0001t0002g0274 a0001c0001t0002g0275 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.588-532_588-531ins others(21): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | C | CTTTTTTT others(15): Show |
4 | a0001c0001t0002g0336 a0001c0001t0002g0338 a0001c0001t0002g0339 others(1): Show |
4 | HG03453.hp1 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-532_588-531ins others(22): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0360 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.588-532_588-531ins others(24): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | C | CTTTTTTT others(27): Show |
1 | a0001c0007t0012g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588-532_588-531ins others(34): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | CT | C | 80 | a0001c0001t0002g0298 a0001c0004t0011g0388 a0003c0003t0003g0004 others(77): Show |
86 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.588-532delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513715 | CTTTT | C | 52 | a0001c0004t0004g0009 a0001c0004t0004g0019 a0001c0004t0004g0020 others(49): Show |
56 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(53): Show |
intron_variant | MODIFIER | c.588-535_588-532del others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | 6513715 | ||||||
chr12:6513735 | T | C | 304 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(301): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.588-530T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513735 | |||||||
chr12:6513747 | G | C | 10 | a0001c0007t0004g0259 a0001c0007t0005g0022 a0001c0007t0005g0023 others(7): Show |
12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.588-518G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513747 | |||||||
chr12:6513751 | T | C | 1 | a0001c0007t0012g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588-514T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513751 | |||||||
chr12:6513784 | C | T | 3 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.588-481C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513784 | |||||||
chr12:6513842 | A | T | 7 | a0002c0002t0001g0007 a0002c0002t0001g0015 a0002c0002t0001g0109 others(4): Show |
10 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.588-423A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513842 | |||||||
chr12:6513931 | G | A | 119 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(116): Show |
129 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.588-334G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6513931 | |||||||
chr12:6514041 | T | A | 3 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0352 |
3 | NA18944.hp1 NA19000.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.588-224T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6514041 | |||||||
chr12:6514138 | A | G | 1 | a0003c0003t0003g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.588-127A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6514138 | |||||||
chr12:6514216 | A | G | 118 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(115): Show |
125 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.588-49A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6514216 | |||||||
chr12:6514223 | T | C | 248 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(245): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.588-42T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | chr12 | 6514223 | |||||||
chr12:6514625 | C | T | 1 | a0002c0002t0001g0157 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.839+38C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 8/31 | chr12 | 6514625 | |||||||
chr12:6514945 | G | A | 1 | a0003c0003t0003g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.987+25G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6514945 | |||||||
chr12:6514973 | T | C | 118 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(115): Show |
125 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.987+53T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6514973 | |||||||
chr12:6515200 | T | C | 5 | a0007c0014t0001g0281 a0007c0014t0001g0282 a0007c0014t0001g0284 others(2): Show |
5 | HG02622.hp1 HG03209.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+280T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515200 | |||||||
chr12:6515269 | C | T | 126 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(123): Show |
133 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.987+349C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515269 | |||||||
chr12:6515374 | G | A | 10 | a0001c0007t0004g0259 a0001c0007t0005g0022 a0001c0007t0005g0023 others(7): Show |
12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.987+454G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515374 | |||||||
chr12:6515401 | T | C | 1 | a0001c0001t0002g0355 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.987+481T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515401 | |||||||
chr12:6515465 | G | A | 1 | a0001c0033t0004g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.987+545G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515465 | |||||||
chr12:6515500 | C | A | 1 | a0004c0005t0001g0235 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.987+580C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515500 | |||||||
chr12:6515572 | T | C | 1 | a0001c0001t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.987+652T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515572 | |||||||
chr12:6515640 | A | G | 94 | a0001c0004t0011g0387 a0001c0004t0011g0388 a0002c0002t0001g0163 others(91): Show |
101 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.987+720A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515640 | |||||||
chr12:6515843 | T | C | 3 | a0007c0014t0001g0281 a0007c0014t0001g0282 a0007c0014t0001g0284 |
3 | HG02622.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.987+923T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515843 | |||||||
chr12:6515844 | A | AG | 3 | a0007c0014t0001g0281 a0007c0014t0001g0282 a0007c0014t0001g0284 |
3 | HG02622.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.987+924_987+925ins others(1): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515844 | |||||||
chr12:6515877 | G | A | 2 | a0001c0007t0012g0269 a0001c0007t0012g0386 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.988-951G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515877 | |||||||
chr12:6515964 | A | G | 258 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(255): Show |
275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.988-864A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6515964 | |||||||
chr12:6516050 | G | T | 5 | a0001c0004t0008g0215 a0001c0004t0008g0216 a0001c0004t0008g0217 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.988-778G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516050 | |||||||
chr12:6516065 | G | A | 1 | a0001c0001t0002g0350 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.988-763G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516065 | |||||||
chr12:6516067 | G | A | 8 | a0003c0003t0003g0012 a0003c0003t0003g0035 a0003c0003t0003g0039 others(5): Show |
9 | HG00597.hp2 HG00609.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-761G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516067 | |||||||
chr12:6516073 | G | C | 2 | a0003c0003t0003g0072 a0003c0003t0003g0106 |
2 | HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.988-755G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516073 | |||||||
chr12:6516119 | C | T | 104 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(101): Show |
111 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.988-709C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516119 | |||||||
chr12:6516145 | G | A | 116 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(113): Show |
123 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.988-683G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516145 | |||||||
chr12:6516167 | A | G | 262 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(259): Show |
280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.988-661A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516167 | |||||||
chr12:6516206 | C | A | 5 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 others(2): Show |
6 | HG02622.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.988-622C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516206 | |||||||
chr12:6516216 | C | A | 5 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 others(2): Show |
6 | HG02622.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.988-612C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516216 | |||||||
chr12:6516245 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.988-583T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516245 | |||||||
chr12:6516317 | T | C | 38 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(35): Show |
42 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.988-511T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516317 | |||||||
chr12:6516318 | ATGGT | A | 38 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(35): Show |
42 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.988-509_988-506del others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516318 | |||||||
chr12:6516324 | AAATCCT | A | 38 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(35): Show |
42 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.988-503_988-498del others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516324 | |||||||
chr12:6516704 | A | G | 2 | a0001c0001t0002g0340 a0001c0001t0002g0341 |
2 | NA18979.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.988-124A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516704 | |||||||
chr12:6516763 | T | C | 6 | a0007c0014t0001g0281 a0007c0014t0001g0282 a0007c0014t0001g0284 others(3): Show |
6 | HG02622.hp1 HG03209.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.988-65T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 9/31 | chr12 | 6516763 | |||||||
chr12:6517033 | A | G | 5 | a0001c0001t0002g0028 a0001c0001t0002g0343 a0001c0001t0002g0345 others(2): Show |
6 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1185+8A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 10/31 | chr12 | 6517033 | |||||||
chr12:6517066 | C | T | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1185+41C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 10/31 | chr12 | 6517066 | |||||||
chr12:6517203 | G | C | 308 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(305): Show |
330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1186-162G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 10/31 | chr12 | 6517203 | |||||||
chr12:6517698 | C | T | 1 | a0002c0002t0001g0129 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1408+15C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 12/31 | chr12 | 6517698 | |||||||
chr12:6517994 | T | C | 1 | a0004c0005t0001g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1589+35T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6517994 | |||||||
chr12:6518120 | T | G | 1 | a0002c0002t0001g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1589+161T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518120 | |||||||
chr12:6518190 | G | A | 308 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(305): Show |
330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1589+231G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518190 | |||||||
chr12:6518218 | C | T | 1 | a0002c0002t0001g0015 | 2 | HG01074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1589+259C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518218 | |||||||
chr12:6518402 | A | G | 1 | a0001c0001t0002g0307 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1589+443A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518402 | |||||||
chr12:6518492 | A | G | 3 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1589+533A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518492 | |||||||
chr12:6518503 | A | AGTTTTTT others(9): Show |
5 | a0001c0001t0006g0253 a0001c0001t0006g0257 a0001c0028t0009g0254 others(2): Show |
5 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1589+545_1589+560d others(18): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518503 | ||||||
chr12:6518504 | G | GT | 23 | a0001c0009t0001g0187 a0001c0009t0001g0188 a0001c0009t0001g0205 others(20): Show |
23 | HG00438.hp2 HG00642.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1589+575dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTT | 14 | a0001c0004t0004g0190 a0001c0004t0004g0191 a0001c0004t0004g0192 others(11): Show |
14 | HG00558.hp1 HG01257.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1589+571_1589+575d others(7): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(2): Show |
25 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0277 others(22): Show |
27 | HG00408.hp1 HG00741.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.1589+550_1589+551i others(11): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(3): Show |
29 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0285 others(26): Show |
33 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1589+550_1589+551i others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(4): Show |
10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0297 others(7): Show |
11 | HG00733.hp2 HG01934.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1589+550_1589+551i others(13): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(5): Show |
5 | a0001c0001t0002g0278 a0001c0001t0002g0320 a0001c0001t0002g0330 others(2): Show |
5 | HG01069.hp2 HG01346.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589+550_1589+551i others(14): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(6): Show |
3 | a0001c0001t0002g0317 a0001c0001t0002g0345 a0001c0001t0002g0365 |
3 | HG00639.hp1 HG01071.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(15): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(7): Show |
1 | a0001c0001t0002g0287 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1589+550_1589+551i others(16): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(8): Show |
2 | a0001c0001t0003g0368 a0001c0001t0003g0381 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(17): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(9): Show |
1 | a0001c0001t0003g0321 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1589+550_1589+551i others(18): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(10): Show |
1 | a0001c0001t0003g0359 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1589+550_1589+551i others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(11): Show |
3 | a0001c0001t0002g0337 a0001c0001t0002g0338 a0001c0001t0002g0372 |
3 | HG01884.hp1 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(20): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(12): Show |
1 | a0001c0001t0002g0339 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1589+550_1589+551i others(21): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(13): Show |
3 | a0001c0001t0002g0335 a0001c0001t0002g0348 a0001c0001t0002g0366 |
3 | HG01109.hp2 HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(22): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(17): Show |
2 | a0001c0001t0002g0336 a0001c0001t0003g0325 |
2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(26): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(19): Show |
2 | a0001c0001t0007g0306 a0001c0001t0007g0356 |
2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(28): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(21): Show |
2 | a0001c0001t0007g0364 a0001c0001t0015g0367 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(30): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(22): Show |
2 | a0001c0001t0002g0331 a0001c0001t0002g0333 |
2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(31): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(25): Show |
1 | a0001c0001t0002g0334 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1589+550_1589+551i others(34): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(27): Show |
2 | a0001c0001t0002g0292 a0001c0001t0002g0332 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(36): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(34): Show |
2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(43): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(35): Show |
3 | a0001c0001t0002g0270 a0001c0001t0002g0275 a0001c0001t0002g0276 |
3 | HG02145.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1589+550_1589+551i others(44): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(39): Show |
1 | a0001c0001t0002g0271 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1589+550_1589+551i others(48): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTGT others(41): Show |
1 | a0001c0001t0002g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1589+550_1589+551i others(50): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTT | 11 | a0001c0004t0004g0181 a0001c0004t0004g0184 a0001c0004t0004g0195 others(8): Show |
11 | HG01243.hp1 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1589+570_1589+575d others(8): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT | 9 | a0001c0004t0004g0183 a0001c0004t0004g0197 a0001c0004t0004g0200 others(6): Show |
9 | HG01358.hp2 HG01361.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1589+569_1589+575d others(9): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(2): Show |
11 | a0001c0001t0002g0357 a0001c0031t0001g0179 a0004c0005t0001g0021 others(8): Show |
12 | HG00323.hp1 HG00733.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.1589+567_1589+575d others(11): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(3): Show |
10 | a0001c0001t0002g0295 a0001c0004t0001g0018 a0001c0004t0001g0180 others(7): Show |
10 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1589+566_1589+575d others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(4): Show |
5 | a0001c0007t0012g0269 a0003c0003t0003g0042 a0003c0003t0003g0077 others(2): Show |
5 | HG01255.hp1 HG02717.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589+565_1589+575d others(13): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(5): Show |
1 | a0007c0014t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1589+564_1589+575d others(14): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(10): Show |
3 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0026t0006g0258 |
3 | HG03490.hp2 HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1589+557_1589+558i others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0006g0251 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1589+557_1589+558i others(20): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(6): Show |
5 | a0003c0015t0003g0091 a0003c0015t0003g0092 a0004c0005t0001g0231 others(2): Show |
5 | HG01346.hp2 HG01891.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1589+563_1589+575d others(15): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(7): Show |
1 | a0003c0003t0003g0032 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1589+562_1589+575d others(16): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0006g0255 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1589+560_1589+561i others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(9): Show |
1 | a0003c0003t0003g0072 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1589+560_1589+575d others(18): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(10): Show |
11 | a0003c0003t0003g0004 a0003c0003t0003g0033 a0003c0003t0003g0050 others(8): Show |
13 | HG00408.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1589+559_1589+575d others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(11): Show |
16 | a0001c0001t0002g0371 a0003c0003t0003g0012 a0003c0003t0003g0034 others(13): Show |
17 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.1589+558_1589+575d others(20): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(12): Show |
13 | a0003c0003t0003g0036 a0003c0003t0003g0037 a0003c0003t0003g0040 others(10): Show |
14 | HG02056.hp2 HG03669.hp1 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.1589+557_1589+575d others(21): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(13): Show |
1 | a0005c0006t0003g0126 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1589+556_1589+575d others(22): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(14): Show |
3 | a0005c0006t0003g0120 a0005c0006t0003g0138 a0005c0006t0003g0147 |
3 | NA18960.hp1 NA18978.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1589+555_1589+575d others(23): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(15): Show |
6 | a0003c0003t0003g0045 a0003c0003t0003g0074 a0003c0003t0003g0106 others(3): Show |
6 | HG02129.hp1 HG02155.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589+554_1589+575d others(24): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(16): Show |
5 | a0003c0003t0003g0011 a0003c0003t0003g0039 a0003c0003t0003g0060 others(2): Show |
6 | NA18948.hp1 NA18952.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589+553_1589+575d others(25): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(17): Show |
5 | a0003c0003t0003g0055 a0003c0003t0003g0056 a0003c0003t0003g0059 others(2): Show |
5 | HG00621.hp1 HG02040.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1589+552_1589+575d others(26): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(18): Show |
1 | a0003c0003t0003g0057 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1589+551_1589+575d others(27): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(21): Show |
2 | a0003c0003t0003g0101 a0003c0003t0013g0104 |
2 | HG00323.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1589+548_1589+575d others(30): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(22): Show |
1 | a0006c0008t0003g0005 | 3 | HG01106.hp1 HG01109.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1589+547_1589+575d others(31): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(23): Show |
2 | a0003c0003t0003g0105 a0006c0008t0003g0058 |
2 | HG00735.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1589+546_1589+575d others(32): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | G | GTTTTTTT others(25): Show |
1 | a0003c0003t0003g0031 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1589+575_1589+576i others(34): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | GTT | G | 9 | a0001c0007t0005g0022 a0001c0007t0005g0023 a0001c0007t0005g0263 others(6): Show |
11 | HG00423.hp2 HG01070.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1589+574_1589+575d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | GTTT | G | 8 | a0001c0001t0002g0296 a0001c0001t0002g0310 a0001c0001t0002g0323 others(5): Show |
8 | HG01099.hp1 HG02080.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1589+573_1589+575d others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | GTTTT | G | 12 | a0001c0004t0004g0009 a0001c0004t0004g0020 a0001c0004t0004g0189 others(9): Show |
15 | HG00544.hp2 NA18941.hp1 NA18946.hp1 others(12): Show |
intron_variant | MODIFIER | c.1589+572_1589+575d others(6): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518504 | GTTTTTTT others(3): Show |
G | 1 | a0001c0004t0004g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1589+566_1589+575d others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518504 | ||||||
chr12:6518505 | T | TTTTTTTT others(8): Show |
1 | a0008c0012t0006g0252 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1589+560_1589+561i others(17): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518505 | ||||||
chr12:6518508 | T | TTTGTTTT others(3): Show |
2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1589+551_1589+552i others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518508 | ||||||
chr12:6518508 | T | TTTTTTTT others(3): Show |
1 | a0001c0004t0010g0260 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1589+558_1589+559i others(12): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518508 | ||||||
chr12:6518511 | T | G | 1 | a0018c0024t0001g0166 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1589+552T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518511 | |||||||
chr12:6518513 | T | G | 5 | a0001c0001t0002g0296 a0001c0001t0002g0310 a0001c0001t0002g0323 others(2): Show |
5 | HG02080.hp2 HG02293.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589+554T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518513 | |||||||
chr12:6518515 | T | G | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1589+556T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518515 | |||||||
chr12:6518517 | T | TTTTTTTT others(10): Show |
1 | a0003c0010t0003g0207 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1589+574_1589+575i others(19): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518517 | ||||||
chr12:6518519 | T | G | 2 | a0001c0001t0002g0329 a0001c0001t0002g0361 |
2 | NA18990.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1589+560T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518519 | |||||||
chr12:6518525 | T | G | 1 | a0001c0004t0010g0261 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1589+566T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518525 | |||||||
chr12:6518533 | T | TTTTTTTT others(7): Show |
1 | a0004c0005t0001g0235 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1589+575_1589+576i others(16): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6518533 | ||||||
chr12:6518630 | C | T | 3 | a0001c0001t0002g0315 a0010c0017t0003g0063 a0010c0017t0003g0069 |
3 | HG02071.hp2 HG02080.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1589+671C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518630 | |||||||
chr12:6518723 | A | G | 308 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(305): Show |
330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1589+764A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518723 | |||||||
chr12:6518809 | C | T | 5 | a0001c0001t0002g0285 a0001c0001t0002g0304 a0001c0001t0002g0346 others(2): Show |
5 | HG00140.hp1 HG01081.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1589+850C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518809 | |||||||
chr12:6518833 | T | C | 1 | a0002c0002t0001g0111 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1589+874T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518833 | |||||||
chr12:6518949 | G | A | 3 | a0001c0004t0009g0228 a0001c0004t0009g0229 a0001c0004t0009g0230 |
3 | HG02886.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1589+990G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518949 | |||||||
chr12:6518967 | C | G | 5 | a0001c0001t0002g0028 a0001c0001t0002g0343 a0001c0001t0002g0345 others(2): Show |
6 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589+1008C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518967 | |||||||
chr12:6518972 | A | G | 5 | a0001c0001t0002g0028 a0001c0001t0002g0343 a0001c0001t0002g0345 others(2): Show |
6 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1589+1013A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518972 | |||||||
chr12:6518982 | T | C | 104 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(101): Show |
111 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1589+1023T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6518982 | |||||||
chr12:6519029 | GC | G | 5 | a0001c0004t0008g0214 a0001c0004t0008g0215 a0001c0004t0008g0216 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589+1071delC | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519029 | |||||||
chr12:6519031 | G | A | 1 | a0014c0027t0005g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1589+1072G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519031 | |||||||
chr12:6519033 | C | A | 2 | a0001c0007t0012g0269 a0001c0007t0012g0386 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1589+1074C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519033 | |||||||
chr12:6519111 | C | T | 1 | a0003c0010t0001g0054 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1589+1152C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519111 | |||||||
chr12:6519133 | G | C | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1589+1174G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519133 | |||||||
chr12:6519195 | T | C | 3 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1589+1236T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519195 | |||||||
chr12:6519267 | A | C | 3 | a0001c0001t0007g0306 a0001c0001t0007g0356 a0001c0001t0007g0364 |
3 | HG02258.hp1 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1589+1308A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519267 | |||||||
chr12:6519315 | C | T | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1589+1356C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519315 | |||||||
chr12:6519382 | A | G | 1 | a0007c0014t0001g0281 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1589+1423A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519382 | |||||||
chr12:6519484 | C | T | 1 | a0002c0002t0001g0111 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1590-1502C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519484 | |||||||
chr12:6519609 | T | C | 3 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1590-1377T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519609 | |||||||
chr12:6519947 | G | C | 220 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(217): Show |
234 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1590-1039G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519947 | |||||||
chr12:6519954 | T | C | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1590-1032T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6519954 | |||||||
chr12:6520100 | A | G | 309 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(306): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.1590-886A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520100 | |||||||
chr12:6520115 | A | C | 1 | a0004c0005t0001g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1590-871A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520115 | |||||||
chr12:6520181 | T | TA | 159 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(156): Show |
171 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.1590-794dupA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6520181 | ||||||
chr12:6520181 | T | TAA | 33 | a0001c0001t0002g0278 a0001c0001t0002g0358 a0001c0001t0006g0257 others(30): Show |
35 | HG00438.hp2 HG02027.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1590-795_1590-794d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6520181 | ||||||
chr12:6520191 | A | AT | 8 | a0001c0004t0009g0228 a0001c0004t0009g0229 a0001c0004t0009g0230 others(5): Show |
9 | HG00673.hp2 HG02523.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1590-795_1590-794i others(3): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520191 | |||||||
chr12:6520192 | AT | A | 8 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(5): Show |
8 | HG02055.hp2 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1590-793delT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520192 | |||||||
chr12:6520193 | T | A | 212 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(209): Show |
226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1590-793T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520193 | |||||||
chr12:6520195 | T | A | 32 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(29): Show |
32 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1590-791T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520195 | |||||||
chr12:6520265 | A | G | 1 | a0003c0003t0003g0038 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1590-721A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520265 | |||||||
chr12:6520304 | T | G | 3 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1590-682T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520304 | |||||||
chr12:6520322 | G | A | 2 | a0001c0007t0012g0269 a0001c0007t0012g0386 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1590-664G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520322 | |||||||
chr12:6520379 | ACCACAGG others(15): Show |
A | 93 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(90): Show |
100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1590-589_1590-568d others(24): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6520379 | ||||||
chr12:6520389 | CACACCAT others(59): Show |
C | 11 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(8): Show |
11 | HG01884.hp2 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1590-589_1590-524d others(68): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | 6520389 | ||||||
chr12:6520397 | T | C | 7 | a0002c0002t0001g0006 a0002c0002t0001g0132 a0002c0002t0001g0133 others(4): Show |
9 | NA18945.hp2 NA18953.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.1590-589T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520397 | |||||||
chr12:6520439 | A | G | 1 | a0003c0003t0003g0051 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1590-547A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520439 | |||||||
chr12:6520491 | C | T | 1 | a0001c0004t0008g0214 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1590-495C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520491 | |||||||
chr12:6520492 | G | A | 1 | a0004c0005t0001g0231 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1590-494G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520492 | |||||||
chr12:6520670 | T | A | 1 | a0002c0002t0001g0134 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1590-316T>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520670 | |||||||
chr12:6520717 | C | G | 5 | a0007c0014t0001g0281 a0007c0014t0001g0282 a0007c0014t0001g0284 others(2): Show |
5 | HG02622.hp1 HG03209.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1590-269C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520717 | |||||||
chr12:6520918 | A | C | 1 | a0002c0002t0001g0161 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1590-68A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | chr12 | 6520918 | |||||||
chr12:6521312 | C | T | 1 | a0001c0001t0002g0288 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1714+202C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521312 | |||||||
chr12:6521313 | G | A | 3 | a0001c0004t0009g0228 a0001c0004t0009g0229 a0001c0004t0009g0230 |
3 | HG02886.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1714+203G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521313 | |||||||
chr12:6521461 | T | C | 104 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(101): Show |
111 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1715-337T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521461 | |||||||
chr12:6521570 | C | A | 6 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 others(3): Show |
6 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1715-228C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521570 | |||||||
chr12:6521584 | A | AG | 314 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(311): Show |
336 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1715-213dupG | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr12 | 6521584 | ||||||
chr12:6521692 | AAAG | A | 4 | a0003c0003t0003g0030 a0003c0003t0003g0072 a0003c0003t0003g0106 others(1): Show |
4 | HG02738.hp1 HG03490.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1715-99_1715-97del others(3): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr12 | 6521692 | ||||||
chr12:6521748 | C | A | 1 | a0007c0014t0001g0281 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1715-50C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521748 | |||||||
chr12:6521748 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1715-50C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521748 | |||||||
chr12:6521750 | C | T | 1 | a0001c0033t0004g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1715-48C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 14/31 | chr12 | 6521750 | |||||||
chr12:6522051 | C | G | 1 | a0002c0021t0001g0121 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1954+14C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522051 | |||||||
chr12:6522142 | C | T | 1 | a0002c0002t0001g0177 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1954+105C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522142 | |||||||
chr12:6522183 | G | A | 34 | a0003c0003t0003g0004 a0003c0003t0003g0012 a0003c0003t0003g0035 others(31): Show |
39 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1954+146G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522183 | |||||||
chr12:6522229 | C | T | 1 | a0003c0003t0003g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1954+192C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522229 | |||||||
chr12:6522238 | ATCTTGGA others(2): Show |
A | 2 | a0001c0001t0002g0026 a0001c0001t0002g0342 |
3 | HG00741.hp1 HG01496.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1954+206_1954+214d others(11): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | INFO_REALIGN_3_PRIME | chr12 | 6522238 | ||||||
chr12:6522344 | T | C | 1 | a0001c0001t0002g0302 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1954+307T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522344 | |||||||
chr12:6522457 | G | A | 314 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(311): Show |
336 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1955-371G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522457 | |||||||
chr12:6522559 | G | A | 116 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(113): Show |
123 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1955-269G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522559 | |||||||
chr12:6522568 | G | A | 5 | a0001c0004t0008g0214 a0001c0004t0008g0215 a0001c0004t0008g0216 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1955-260G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522568 | |||||||
chr12:6522722 | G | A | 103 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(100): Show |
110 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1955-106G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 15/31 | chr12 | 6522722 | |||||||
chr12:6523054 | A | C | 1 | a0001c0001t0002g0362 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2129+52A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 16/31 | chr12 | 6523054 | |||||||
chr12:6523095 | A | C | 3 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2129+93A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 16/31 | chr12 | 6523095 | |||||||
chr12:6523238 | C | T | 1 | a0014c0027t0005g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2130-24C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 16/31 | chr12 | 6523238 | |||||||
chr12:6523398 | G | GT | 8 | a0001c0009t0001g0188 a0001c0009t0001g0205 a0002c0002t0001g0111 others(5): Show |
8 | HG01123.hp1 HG02056.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.2214+69dupT | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6523398 | ||||||
chr12:6523398 | G | GTT | 18 | a0001c0001t0002g0292 a0001c0004t0004g0224 a0004c0005t0001g0021 others(15): Show |
19 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2214+68_2214+69dup others(2): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6523398 | ||||||
chr12:6523398 | G | GTTT | 52 | a0001c0004t0004g0009 a0001c0004t0004g0019 a0001c0004t0004g0020 others(49): Show |
57 | HG00558.hp1 HG01168.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.2214+67_2214+69dup others(3): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6523398 | ||||||
chr12:6523398 | G | GTTTT | 201 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(198): Show |
215 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.2214+66_2214+69dup others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6523398 | ||||||
chr12:6523398 | G | GTTTTT | 35 | a0001c0001t0002g0274 a0001c0001t0002g0278 a0001c0001t0002g0308 others(32): Show |
37 | HG00621.hp1 HG01123.hp2 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.2214+65_2214+69dup others(5): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6523398 | ||||||
chr12:6523484 | G | A | 1 | a0003c0003t0003g0086 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2214+138G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523484 | |||||||
chr12:6523643 | C | T | 1 | a0004c0005t0001g0238 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2214+297C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523643 | |||||||
chr12:6523650 | A | G | 4 | a0002c0002t0001g0109 a0002c0002t0001g0164 a0002c0002t0001g0170 others(1): Show |
4 | HG00140.hp2 HG00639.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2214+304A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523650 | |||||||
chr12:6523725 | T | G | 1 | a0002c0002t0001g0142 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2214+379T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523725 | |||||||
chr12:6523759 | A | G | 36 | a0001c0001t0002g0292 a0001c0004t0001g0018 a0001c0004t0001g0180 others(33): Show |
39 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.2214+413A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523759 | |||||||
chr12:6523803 | C | A | 93 | a0003c0003t0003g0004 a0003c0003t0003g0011 a0003c0003t0003g0012 others(90): Show |
100 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.2214+457C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523803 | |||||||
chr12:6523882 | G | A | 3 | a0002c0002t0001g0168 a0002c0002t0001g0171 a0013c0020t0001g0141 |
3 | HG00438.hp1 HG02523.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.2214+536G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6523882 | |||||||
chr12:6524066 | G | A | 8 | a0003c0003t0003g0037 a0003c0003t0003g0038 a0003c0003t0003g0041 others(5): Show |
8 | NA18948.hp1 NA18954.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.2214+720G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524066 | |||||||
chr12:6524345 | A | G | 1 | a0001c0004t0004g0197 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2214+999A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524345 | |||||||
chr12:6524369 | G | A | 5 | a0001c0009t0001g0186 a0001c0009t0001g0187 a0001c0009t0001g0188 others(2): Show |
5 | NA18950.hp1 NA18999.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.2214+1023G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524369 | |||||||
chr12:6524394 | A | G | 1 | a0002c0002t0001g0163 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2214+1048A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524394 | |||||||
chr12:6524414 | C | T | 10 | a0001c0007t0004g0259 a0001c0007t0005g0022 a0001c0007t0005g0023 others(7): Show |
12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2214+1068C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524414 | |||||||
chr12:6524455 | T | C | 35 | a0001c0001t0002g0292 a0001c0004t0001g0018 a0001c0004t0001g0180 others(32): Show |
39 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.2214+1109T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524455 | |||||||
chr12:6524648 | C | CA | 137 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(134): Show |
146 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.2215-912dupA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6524648 | ||||||
chr12:6524648 | C | CAA | 14 | a0001c0001t0002g0293 a0001c0001t0002g0298 a0001c0001t0002g0311 others(11): Show |
14 | HG01168.hp2 HG01433.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.2215-913_2215-912d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6524648 | ||||||
chr12:6524648 | CA | C | 19 | a0001c0004t0004g0196 a0001c0004t0008g0214 a0001c0004t0008g0216 others(16): Show |
20 | HG00323.hp1 HG01943.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2215-912delA | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr12 | 6524648 | ||||||
chr12:6524709 | A | C | 4 | a0001c0001t0002g0296 a0001c0001t0002g0310 a0001c0001t0002g0323 others(1): Show |
4 | HG02080.hp2 HG02293.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.2215-874A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524709 | |||||||
chr12:6524817 | C | T | 3 | a0001c0011t0001g0029 a0001c0011t0001g0384 a0001c0011t0001g0385 |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2215-766C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524817 | |||||||
chr12:6524936 | T | G | 1 | a0001c0004t0004g0190 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2215-647T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6524936 | |||||||
chr12:6525286 | C | T | 3 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2215-297C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6525286 | |||||||
chr12:6525323 | C | G | 12 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 others(9): Show |
14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2215-260C>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6525323 | |||||||
chr12:6525526 | A | C | 2 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2215-57A>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 17/31 | chr12 | 6525526 | |||||||
chr12:6525818 | G | T | 1 | a0003c0003t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2348+102G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/31 | chr12 | 6525818 | |||||||
chr12:6525848 | T | C | 1 | a0001c0004t0004g0181 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2348+132T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/31 | chr12 | 6525848 | |||||||
chr12:6525950 | A | G | 1 | a0001c0004t0004g0206 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2349-118A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/31 | chr12 | 6525950 | |||||||
chr12:6526000 | A | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0019 a0001c0004t0004g0020 others(36): Show |
43 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.2349-68A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/31 | chr12 | 6526000 | |||||||
chr12:6526039 | C | T | 4 | a0001c0001t0006g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(1): Show |
4 | HG03490.hp2 HG03492.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2349-29C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 18/31 | chr12 | 6526039 | |||||||
chr12:6526208 | G | A | 17 | a0004c0005t0001g0021 a0004c0005t0001g0231 a0004c0005t0001g0232 others(14): Show |
18 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.2481+8G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 19/31 | chr12 | 6526208 | |||||||
chr12:6526242 | C | T | 2 | a0001c0001t0002g0323 a0001c0001t0007g0309 |
2 | NA19085.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2481+42C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 19/31 | chr12 | 6526242 | |||||||
chr12:6526266 | A | G | 1 | a0001c0001t0002g0336 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2482-21A>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 19/31 | chr12 | 6526266 | |||||||
chr12:6526401 | A | T | 314 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(311): Show |
336 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.2566+30A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 20/31 | chr12 | 6526401 | |||||||
chr12:6526629 | G | C | 10 | a0001c0007t0004g0259 a0001c0007t0005g0022 a0001c0007t0005g0023 others(7): Show |
12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2734+14G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 21/31 | chr12 | 6526629 | |||||||
chr12:6526643 | G | A | 1 | a0003c0003t0003g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2734+28G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 21/31 | chr12 | 6526643 | |||||||
chr12:6526727 | G | A | 1 | a0004c0005t0001g0239 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2734+112G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 21/31 | chr12 | 6526727 | |||||||
chr12:6527135 | G | A | 4 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(1): Show |
4 | HG02886.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2907+72G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527135 | |||||||
chr12:6527219 | C | T | 1 | a0001c0004t0004g0181 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2907+156C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527219 | |||||||
chr12:6527226 | G | A | 51 | a0001c0004t0004g0009 a0001c0004t0004g0019 a0001c0004t0004g0020 others(48): Show |
55 | HG00558.hp1 HG01243.hp1 HG01257.hp2 others(52): Show |
intron_variant | MODIFIER | c.2907+163G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527226 | |||||||
chr12:6527244 | C | A | 2 | a0001c0007t0012g0269 a0001c0007t0012g0386 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2907+181C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527244 | |||||||
chr12:6527549 | A | T | 2 | a0010c0017t0003g0063 a0010c0017t0003g0069 |
2 | HG02080.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2908-228A>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527549 | |||||||
chr12:6527572 | G | A | 1 | a0001c0004t0001g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2908-205G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527572 | |||||||
chr12:6527702 | T | C | 1 | a0011c0023t0001g0149 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2908-75T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527702 | |||||||
chr12:6527733 | T | C | 1 | a0003c0003t0003g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2908-44T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 22/31 | chr12 | 6527733 | |||||||
chr12:6528108 | G | A | 1 | a0001c0001t0002g0305 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3143+17G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 24/31 | chr12 | 6528108 | |||||||
chr12:6528110 | A | AC | 21 | a0001c0001t0002g0310 a0001c0001t0002g0312 a0001c0001t0002g0315 others(18): Show |
21 | HG01192.hp1 HG01243.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.3143+24dupC | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 24/31 | INFO_REALIGN_3_PRIME | chr12 | 6528110 | ||||||
chr12:6528114 | C | A | 1 | a0007c0014t0001g0281 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3143+23C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 24/31 | chr12 | 6528114 | |||||||
chr12:6528434 | G | A | 1 | a0002c0002t0001g0163 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3299+106G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 25/31 | chr12 | 6528434 | |||||||
chr12:6528586 | T | C | 1 | a0001c0009t0001g0322 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3300-93T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 25/31 | chr12 | 6528586 | |||||||
chr12:6528936 | G | C | 1 | a0003c0003t0003g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3478-9G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 26/31 | chr12 | 6528936 | |||||||
chr12:6529081 | C | T | 2 | a0001c0007t0012g0269 a0001c0007t0012g0386 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3572+42C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529081 | |||||||
chr12:6529184 | C | T | 107 | a0001c0031t0001g0179 a0003c0003t0003g0004 a0003c0003t0003g0011 others(104): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.3572+145C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529184 | |||||||
chr12:6529383 | G | T | 4 | a0001c0004t0009g0228 a0001c0004t0009g0229 a0001c0004t0009g0230 others(1): Show |
4 | HG01884.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3573-130G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529383 | |||||||
chr12:6529393 | CAG | C | 12 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 others(9): Show |
14 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3573-119_3573-118d others(4): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529393 | |||||||
chr12:6529450 | G | A | 1 | a0002c0002t0001g0143 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3573-63G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529450 | |||||||
chr12:6529481 | C | T | 1 | a0002c0018t0001g0160 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3573-32C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529481 | |||||||
chr12:6529500 | C | T | 126 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0025 others(123): Show |
133 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.3573-13C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 27/31 | chr12 | 6529500 | |||||||
chr12:6529727 | T | C | 20 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(17): Show |
20 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.3654-48T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 28/31 | chr12 | 6529727 | |||||||
chr12:6529736 | G | A | 3 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3654-39G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 28/31 | chr12 | 6529736 | |||||||
chr12:6530056 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3837+98G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530056 | |||||||
chr12:6530121 | T | TCCAGTTC others(334): Show |
1 | a0002c0002t0001g0115 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3837+177_3837+178i others(343): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr12 | 6530121 | ||||||
chr12:6530125 | G | A | 3 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 |
3 | HG02886.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3837+167G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530125 | |||||||
chr12:6530224 | G | C | 1 | a0002c0002t0001g0146 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3837+266G>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530224 | |||||||
chr12:6530271 | C | T | 1 | a0003c0003t0003g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3837+313C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530271 | |||||||
chr12:6530272 | T | C | 1 | a0003c0003t0003g0040 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3837+314T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530272 | |||||||
chr12:6530330 | T | G | 1 | a0002c0002t0001g0163 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3838-361T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530330 | |||||||
chr12:6530440 | T | C | 4 | a0001c0004t0009g0228 a0001c0004t0009g0229 a0001c0004t0009g0230 others(1): Show |
4 | HG01884.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3838-251T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530440 | |||||||
chr12:6530544 | T | C | 1 | a0002c0002t0001g0156 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3838-147T>C | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530544 | |||||||
chr12:6530595 | T | G | 1 | a0001c0007t0012g0386 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3838-96T>G | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 29/31 | chr12 | 6530595 | |||||||
chr12:6530873 | G | T | 3 | a0001c0004t0010g0260 a0001c0004t0010g0261 a0001c0004t0010g0262 |
3 | HG02622.hp2 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3965-48G>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 30/31 | chr12 | 6530873 | |||||||
chr12:6531097 | C | A | 1 | a0001c0009t0001g0188 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.4120+21C>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/31 | chr12 | 6531097 | |||||||
chr12:6531101 | G | A | 113 | a0001c0004t0001g0018 a0001c0004t0001g0180 a0001c0004t0011g0018 others(110): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.4120+25G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/31 | chr12 | 6531101 | |||||||
chr12:6531212 | G | A | 10 | a0001c0007t0004g0259 a0001c0007t0005g0022 a0001c0007t0005g0023 others(7): Show |
12 | HG01192.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.4121-115G>A | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/31 | chr12 | 6531212 | |||||||
chr12:6531277 | C | T | 1 | a0001c0001t0002g0285 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4121-50C>T | NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 31/31 | chr12 | 6531277 |