Item | Value |
---|---|
geneid | 374569 |
ensemblid | ENSG00000166183.16 |
hgncid | 20123 |
symbol | ASPG |
name | asparaginase |
refseq_nuc | NM_001080464.3 |
refseq_prot | NP_001073933.2 |
ensembl_nuc | ENST00000551177.6 |
ensembl_prot | ENSP00000450040.1 |
mane_status | MANE Select |
chr | chr14 |
start | 104085700 |
end | 104115582 |
strand | + |
ver | v1.2 |
region | chr14:104085700-104115582 |
region5000 | chr14:104080700-104120582 |
regionname0 | ASPG_chr14_104085700_104115582 |
regionname5000 | ASPG_chr14_104080700_104120582 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 573 | 153 | 25 | 45 | 51 | 11 | 20 | 34 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
a0002 | 0/1 | 573 | 153 | 54 | 25 | 53 | 1 | 19 | 41 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
a0003 | 0/0 | 573 | 51 | 8 | 8 | 27 | 4 | 4 | 14 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
a0004 | 0/0 | 573 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
a0005 | 0/0 | 573 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
a0006 | 0/0 | 573 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
a0007 | 0/0 | 573 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
a0008 | 0/0 | 573 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
a0009 | 0/0 | 573 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
a0010 | 0/0 | 573 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
a0011 | 0/0 | 573 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
a0012 | 0/0 | 573 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | MARAV others(568): Show |
chr14 | 104080700 | 104120582 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1719 | 138 | 16 | 43 | 49 | 10 | 19 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0001c0006 | 0/0 | 1719 | 5 | 2 | 1 | 1 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0001c0007 | 0/0 | 1719 | 5 | 5 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0001c0018 | 0/0 | 1719 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0001c0019 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0001c0022 | 0/0 | 1719 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0001c0024 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0001c0027 | 0/0 | 1719 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0002c0002 | 0/1 | 1719 | 85 | 12 | 15 | 45 | 0 | 12 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0002c0003 | 0/0 | 1719 | 57 | 31 | 10 | 8 | 1 | 7 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0002c0005 | 0/0 | 1719 | 6 | 6 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0002c0010 | 0/0 | 1719 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0002c0013 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0002c0016 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0002c0026 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0003c0004 | 0/0 | 1719 | 48 | 5 | 8 | 27 | 4 | 4 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0003c0009 | 0/0 | 1719 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0003c0025 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0004c0008 | 0/0 | 1719 | 3 | 2 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0005c0017 | 0/0 | 1719 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0006c0012 | 0/0 | 1719 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0007c0014 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0008c0020 | 0/0 | 1719 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0009c0021 | 0/0 | 1719 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0010c0011 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0011c0015 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 | ||
a0012c0023 | 0/0 | 1719 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | ATGGC others(1714): Show |
chr14 | 104080700 | 104120582 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4831 | 91 | 2 | 28 | 38 | 10 | 13 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0002 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0004 | 0/0 | 4831 | 18 | 5 | 9 | 0 | 0 | 4 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0005 | 1/0 | 4831 | 5 | 2 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0007 | 0/0 | 4831 | 7 | 3 | 0 | 4 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0010 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0011 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0014 | 0/0 | 4831 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0020 | 0/0 | 4831 | 2 | 0 | 0 | 1 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0024 | 0/0 | 4831 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0025 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0031 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0032 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0033 | 0/0 | 4831 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0034 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0035 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0001t0036 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0006t0002 | 0/0 | 4831 | 4 | 2 | 1 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0006t0028 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0007t0002 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0007t0008 | 0/0 | 4831 | 4 | 4 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0018t0001 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0019t0010 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0022t0001 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0024t0011 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0001c0027t0001 | 0/0 | 4831 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0002t0002 | 0/0 | 4831 | 71 | 6 | 15 | 39 | 0 | 11 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0002t0005 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0002t0008 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0002t0013 | 0/0 | 4831 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0002t0015 | 0/0 | 4831 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0002t0019 | 0/1 | 4831 | 2 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0002t0022 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0002t0027 | 0/0 | 4831 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0001 | 0/0 | 4831 | 14 | 0 | 4 | 7 | 0 | 3 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0002 | 0/0 | 4831 | 6 | 5 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0005 | 0/0 | 4831 | 7 | 6 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0006 | 0/0 | 4831 | 9 | 7 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0007 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0009 | 0/0 | 4831 | 6 | 0 | 2 | 0 | 1 | 3 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0010 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0011 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0016 | 0/0 | 4831 | 3 | 2 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0017 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0018 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0021 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0037 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0003t0038 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0005t0002 | 0/0 | 4831 | 4 | 4 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0005t0008 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0010t0002 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0013t0039 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0016t0006 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0002c0026t0006 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0003c0004t0003 | 0/0 | 4831 | 43 | 5 | 8 | 23 | 3 | 4 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0003c0004t0012 | 0/0 | 4831 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0003c0004t0026 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0003c0004t0030 | 0/0 | 4831 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0003c0009t0005 | 0/0 | 4831 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0003c0025t0003 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0004c0008t0004 | 0/0 | 4831 | 3 | 2 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0005c0017t0003 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0006c0012t0023 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0007c0014t0017 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0008c0020t0029 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0009c0021t0003 | 0/0 | 4831 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0010c0011t0023 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0011c0015t0002 | 0/0 | 4831 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
a0012c0023t0001 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | AGTCC others(4826): Show |
chr14 | 104080700 | 104120582 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 14 | 0 | 4 | 5 | 1 | 4 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0005g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0005g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0007g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0010g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0011g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0014g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0020g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0020g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0024g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0025g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0031g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0032g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0033g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0035g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0001t0036g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0006t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0006t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0006t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0006t0028g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0007t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0007t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0007t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0007t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0007t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0018t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0019t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0022t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0024t0011g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0001c0027t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0003 | 0/0 | 11 | 0 | 8 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0008g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0013g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0013g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0013g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0015g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0015g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0019g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0019g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0022g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0002t0027g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0055 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0009g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0009g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0009g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0009g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0009g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0010g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0010g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0011g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0016g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0016g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0017g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0017g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0018g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0018g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0021g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0021g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0037g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0003t0038g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0005t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0005t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0005t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0005t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0005t0008g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0010t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0013t0039g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0016t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0002c0026t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0002 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0007 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0012g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0026g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0004t0030g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0009t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0009t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0003c0025t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0004c0008t0004g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0005c0017t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0006c0012t0023g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0007c0014t0017g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0008c0020t0029g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0009c0021t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0010c0011t0023g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0011c0015t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
a0012c0023t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00140 | hp2 | a0001 | c0027 | t0001 | g0136 | EUR | GBR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00280 | hp2 | a0002 | c0003 | t0009 | g0176 | EUR | FIN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00438 | hp1 | a0003 | c0004 | t0026 | g0002 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00438 | hp2 | a0001 | c0001 | t0007 | g0017 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00558 | hp1 | a0001 | c0001 | t0034 | g0001 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0212 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00597 | hp1 | a0003 | c0004 | t0003 | g0244 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00597 | hp2 | a0003 | c0004 | t0003 | g0026 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00609 | hp1 | a0003 | c0004 | t0003 | g0097 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00639 | hp1 | a0004 | c0008 | t0004 | g0021 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00642 | hp2 | a0002 | c0003 | t0009 | g0175 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00673 | hp2 | a0001 | c0006 | t0028 | g0138 | EAS | CHS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00733 | hp1 | a0002 | c0003 | t0005 | g0060 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00735 | hp1 | a0002 | c0003 | t0006 | g0233 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00735 | hp2 | a0001 | c0022 | t0001 | g0072 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG00741 | hp2 | a0003 | c0004 | t0003 | g0078 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01070 | hp1 | a0003 | c0004 | t0003 | g0007 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01074 | hp1 | a0002 | c0003 | t0016 | g0160 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01074 | hp2 | a0002 | c0003 | t0001 | g0019 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01081 | hp2 | a0003 | c0004 | t0003 | g0030 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01099 | hp2 | a0002 | c0003 | t0006 | g0055 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01106 | hp1 | a0003 | c0004 | t0003 | g0094 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01109 | hp1 | a0003 | c0004 | t0003 | g0007 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01167 | hp1 | a0002 | c0003 | t0001 | g0019 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01168 | hp1 | a0006 | c0012 | t0023 | g0230 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01243 | hp1 | a0003 | c0004 | t0003 | g0026 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01256 | hp2 | a0001 | c0001 | t0024 | g0040 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01257 | hp2 | a0003 | c0004 | t0003 | g0031 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01258 | hp1 | a0001 | c0001 | t0024 | g0040 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01258 | hp2 | a0003 | c0004 | t0003 | g0031 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0243 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01346 | hp1 | a0001 | c0001 | t0031 | g0143 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01433 | hp2 | a0001 | c0006 | t0002 | g0123 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01496 | hp1 | a0002 | c0003 | t0009 | g0172 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01515 | hp1 | a0003 | c0004 | t0003 | g0027 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01517 | hp2 | a0003 | c0004 | t0003 | g0027 | EUR | IBS | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01884 | hp1 | a0004 | c0008 | t0004 | g0021 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01884 | hp2 | a0002 | c0003 | t0005 | g0061 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01891 | hp2 | a0002 | c0003 | t0005 | g0059 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0195 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0196 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01978 | hp1 | a0002 | c0003 | t0001 | g0048 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02015 | hp2 | a0001 | c0018 | t0001 | g0036 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02027 | hp2 | a0001 | c0001 | t0007 | g0117 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02055 | hp1 | a0002 | c0003 | t0006 | g0232 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02055 | hp2 | a0002 | c0003 | t0018 | g0170 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02071 | hp2 | a0002 | c0003 | t0001 | g0019 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02074 | hp2 | a0003 | c0004 | t0003 | g0011 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02080 | hp1 | a0003 | c0004 | t0003 | g0076 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02083 | hp1 | a0003 | c0004 | t0003 | g0096 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02129 | hp1 | a0002 | c0003 | t0001 | g0048 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02132 | hp1 | a0002 | c0002 | t0013 | g0190 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02135 | hp1 | a0003 | c0004 | t0003 | g0093 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02145 | hp1 | a0002 | c0003 | t0010 | g0231 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02145 | hp2 | a0003 | c0025 | t0003 | g0086 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02155 | hp1 | a0003 | c0004 | t0003 | g0091 | EAS | CDX | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02165 | hp2 | a0001 | c0001 | t0036 | g0015 | EAS | CDX | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02257 | hp1 | a0001 | c0001 | t0035 | g0133 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02258 | hp1 | a0003 | c0004 | t0003 | g0104 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02258 | hp2 | a0002 | c0026 | t0006 | g0213 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02273 | hp1 | a0008 | c0020 | t0029 | g0056 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02280 | hp1 | a0002 | c0003 | t0006 | g0234 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02280 | hp2 | a0002 | c0010 | t0002 | g0050 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02300 | hp1 | a0002 | c0003 | t0001 | g0227 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0165 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02451 | hp2 | a0001 | c0019 | t0010 | g0238 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02523 | hp1 | a0003 | c0004 | t0003 | g0002 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02572 | hp1 | a0002 | c0003 | t0010 | g0154 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02572 | hp2 | a0002 | c0003 | t0002 | g0171 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0235 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0051 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02615 | hp2 | a0001 | c0007 | t0002 | g0241 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02622 | hp1 | a0002 | c0003 | t0017 | g0157 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02622 | hp2 | a0002 | c0003 | t0005 | g0062 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0065 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02630 | hp2 | a0001 | c0024 | t0011 | g0064 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02647 | hp1 | a0001 | c0001 | t0025 | g0236 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0166 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02698 | hp1 | a0002 | c0003 | t0009 | g0220 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02698 | hp2 | a0009 | c0021 | t0003 | g0067 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02717 | hp1 | a0002 | c0003 | t0017 | g0164 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02717 | hp2 | a0002 | c0003 | t0018 | g0174 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0237 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0211 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02735 | hp1 | a0002 | c0003 | t0009 | g0046 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02738 | hp1 | a0002 | c0003 | t0001 | g0203 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0202 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02809 | hp1 | a0002 | c0005 | t0002 | g0168 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02809 | hp2 | a0002 | c0013 | t0039 | g0161 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02818 | hp1 | a0010 | c0011 | t0023 | g0149 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02818 | hp2 | a0001 | c0006 | t0002 | g0034 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02886 | hp1 | a0002 | c0003 | t0006 | g0054 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0051 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02895 | hp1 | a0003 | c0004 | t0003 | g0030 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02895 | hp2 | a0002 | c0003 | t0002 | g0010 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02896 | hp1 | a0002 | c0003 | t0002 | g0010 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02897 | hp2 | a0011 | c0015 | t0002 | g0228 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02965 | hp1 | a0002 | c0003 | t0006 | g0053 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02965 | hp2 | a0002 | c0010 | t0002 | g0050 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02970 | hp1 | a0002 | c0016 | t0006 | g0205 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02970 | hp2 | a0002 | c0005 | t0002 | g0045 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02976 | hp1 | a0002 | c0003 | t0006 | g0054 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02976 | hp2 | a0001 | c0007 | t0008 | g0240 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03017 | hp1 | a0001 | c0001 | t0020 | g0005 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03041 | hp1 | a0002 | c0003 | t0006 | g0055 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03041 | hp2 | a0002 | c0005 | t0008 | g0221 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03098 | hp1 | a0003 | c0009 | t0005 | g0079 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03098 | hp2 | a0001 | c0001 | t0010 | g0239 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03130 | hp1 | a0002 | c0002 | t0019 | g0167 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03130 | hp2 | a0002 | c0003 | t0011 | g0159 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03139 | hp1 | a0002 | c0003 | t0016 | g0163 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03209 | hp1 | a0002 | c0003 | t0037 | g0162 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0080 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03225 | hp1 | a0002 | c0005 | t0008 | g0206 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03453 | hp1 | a0001 | c0007 | t0008 | g0082 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03453 | hp2 | a0002 | c0003 | t0002 | g0010 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03486 | hp1 | a0002 | c0002 | t0008 | g0047 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03486 | hp2 | a0002 | c0003 | t0021 | g0173 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03492 | hp2 | a0002 | c0003 | t0009 | g0046 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03516 | hp1 | a0004 | c0008 | t0004 | g0021 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03516 | hp2 | a0002 | c0003 | t0005 | g0177 | AFR | ESN | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03540 | hp2 | a0002 | c0003 | t0016 | g0158 | AFR | GWD | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03669 | hp1 | a0002 | c0003 | t0002 | g0200 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03669 | hp2 | a0003 | c0004 | t0003 | g0002 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03704 | hp2 | a0001 | c0001 | t0033 | g0134 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0198 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0188 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0092 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0218 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03927 | hp1 | a0003 | c0004 | t0003 | g0095 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0052 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03942 | hp1 | a0003 | c0004 | t0003 | g0100 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0052 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0217 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04184 | hp2 | a0002 | c0002 | t0027 | g0197 | SAS | BEB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0210 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0208 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04204 | hp2 | a0003 | c0004 | t0003 | g0007 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0201 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG04228 | hp2 | a0001 | c0006 | t0002 | g0124 | SAS | STU | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18522 | hp1 | a0001 | c0006 | t0002 | g0034 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18522 | hp2 | a0002 | c0002 | t0005 | g0169 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18612 | hp2 | a0003 | c0004 | t0003 | g0150 | EAS | CHB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18747 | hp1 | a0003 | c0004 | t0003 | g0002 | EAS | CHB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18747 | hp2 | a0003 | c0004 | t0003 | g0068 | EAS | CHB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18906 | hp1 | a0001 | c0007 | t0008 | g0081 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18906 | hp2 | a0002 | c0003 | t0005 | g0022 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18941 | hp2 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18943 | hp1 | a0002 | c0003 | t0001 | g0058 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18944 | hp1 | a0002 | c0002 | t0015 | g0043 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18949 | hp1 | a0002 | c0002 | t0013 | g0181 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18950 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18951 | hp2 | a0003 | c0004 | t0003 | g0107 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18952 | hp2 | a0002 | c0002 | t0015 | g0155 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18953 | hp1 | a0002 | c0003 | t0001 | g0189 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18954 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18964 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18966 | hp2 | a0002 | c0002 | t0015 | g0043 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18971 | hp1 | a0003 | c0004 | t0012 | g0012 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18971 | hp2 | a0002 | c0003 | t0007 | g0229 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0245 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18979 | hp2 | a0003 | c0004 | t0003 | g0002 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18985 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18985 | hp2 | a0001 | c0001 | t0014 | g0037 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18993 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18993 | hp2 | a0003 | c0004 | t0012 | g0012 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18995 | hp1 | a0003 | c0004 | t0003 | g0011 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19003 | hp1 | a0002 | c0002 | t0013 | g0191 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19003 | hp2 | a0003 | c0004 | t0003 | g0077 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19004 | hp1 | a0012 | c0023 | t0001 | g0109 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19005 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19005 | hp2 | a0003 | c0004 | t0012 | g0012 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19012 | hp1 | a0003 | c0004 | t0003 | g0002 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19030 | hp1 | a0003 | c0004 | t0003 | g0102 | AFR | LWK | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19030 | hp2 | a0002 | c0002 | t0022 | g0041 | AFR | LWK | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19043 | hp1 | a0002 | c0002 | t0022 | g0041 | AFR | LWK | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19043 | hp2 | a0002 | c0003 | t0021 | g0178 | AFR | LWK | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19060 | hp1 | a0001 | c0001 | t0014 | g0037 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19065 | hp2 | a0003 | c0004 | t0003 | g0090 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19066 | hp2 | a0003 | c0004 | t0003 | g0002 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19080 | hp1 | a0003 | c0004 | t0003 | g0002 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19083 | hp2 | a0001 | c0001 | t0032 | g0112 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19085 | hp1 | a0003 | c0004 | t0003 | g0011 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19085 | hp2 | a0003 | c0004 | t0003 | g0002 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19089 | hp1 | a0003 | c0004 | t0003 | g0002 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19240 | hp1 | a0003 | c0004 | t0003 | g0103 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA19240 | hp2 | a0002 | c0003 | t0005 | g0022 | AFR | YRI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20129 | hp1 | a0002 | c0005 | t0002 | g0045 | AFR | ASW | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20129 | hp2 | a0002 | c0003 | t0038 | g0044 | AFR | ASW | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20752 | hp1 | a0003 | c0004 | t0003 | g0007 | EUR | TSI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20752 | hp2 | a0003 | c0004 | t0030 | g0002 | EUR | TSI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20905 | hp1 | a0002 | c0003 | t0001 | g0204 | SAS | GIH | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20905 | hp2 | a0002 | c0003 | t0001 | g0209 | SAS | GIH | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0070 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG01123 | hp2 | a0005 | c0017 | t0003 | g0222 | AMR | CLM | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02109 | hp1 | a0002 | c0005 | t0002 | g0215 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02109 | hp2 | a0007 | c0014 | t0017 | g0044 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02486 | hp1 | a0003 | c0009 | t0005 | g0099 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02486 | hp2 | a0003 | c0004 | t0003 | g0098 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02559 | hp1 | a0002 | c0003 | t0006 | g0053 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | ACB | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03471 | hp1 | a0002 | c0002 | t0008 | g0047 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG03471 | hp2 | a0002 | c0003 | t0002 | g0010 | AFR | MSL | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0216 | AFR | USA | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0066 | AFR | USA | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | USA | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
NA20300 | hp2 | a0001 | c0007 | t0008 | g0071 | AFR | USA | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
homoSapiens | chm13v2 | a0002 | c0002 | t0019 | g0223 | REF | REF | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0063 | REF | REF | ASPG_chr14_104080700_104120582 | ASPG | chr14 | 104080700 | 104120582 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104093496 | C | A | 2 | a0006 a0010 |
2 | HG01168.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.197C>A | p.Ala66Asp | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/16 | 268/4831 | 197/1722 | 66/573 | chr14 | 104093496 | |||
chr14:104093582 | T | C | 6 | a0002 a0005 a0006 others(3): Show |
157 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(154): Show |
missense_variant | MODERATE | c.283T>C | p.Cys95Arg | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/16 | 354/4831 | 283/1722 | 95/573 | chr14 | 104093582 | |||
chr14:104093585 | C | G | 6 | a0002 a0005 a0006 others(3): Show |
157 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(154): Show |
missense_variant | MODERATE | c.286C>G | p.Leu96Val | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/16 | 357/4831 | 286/1722 | 96/573 | chr14 | 104093585 | |||
chr14:104103668 | C | T | 1 | a0012 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.746C>T | p.Ala249Val | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/16 | 817/4831 | 746/1722 | 249/573 | chr14 | 104103668 | |||
chr14:104104476 | C | A | 1 | a0004 | 3 | HG00639.hp1 HG01884.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.926C>A | p.Ala309Glu | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/16 | 997/4831 | 926/1722 | 309/573 | chr14 | 104104476 | |||
chr14:104104717 | C | G | 3 | a0003 a0005 a0009 |
53 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
missense_variant | MODERATE | c.1032C>G | p.Ser344Arg | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/16 | 1103/4831 | 1032/1722 | 344/573 | chr14 | 104104717 | |||
chr14:104106827 | T | C | 1 | a0007 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1202T>C | p.Val401Ala | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 11/16 | 1273/4831 | 1202/1722 | 401/573 | chr14 | 104106827 | |||
chr14:104106865 | G | A | 1 | a0009 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1240G>A | p.Val414Met | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 11/16 | 1311/4831 | 1240/1722 | 414/573 | chr14 | 104106865 | |||
chr14:104107270 | T | C | 1 | a0008 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.1358T>C | p.Leu453Pro | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/16 | 1429/4831 | 1358/1722 | 453/573 | chr14 | 104107270 | |||
chr14:104109266 | G | C | 1 | a0011 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.1471G>C | p.Ala491Pro | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/16 | 1542/4831 | 1471/1722 | 491/573 | chr14 | 104109266 | |||
chr14:104109269 | T | C | 1 | a0011 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.1474T>C | p.Ser492Pro | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/16 | 1545/4831 | 1474/1722 | 492/573 | chr14 | 104109269 | |||
chr14:104111978 | T | A | 1 | a0010 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1679T>A | p.Val560Asp | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 15/16 | 1750/4831 | 1679/1722 | 560/573 | chr14 | 104111978 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104085812 | C | G | 1 | a0001c0027 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.42C>G | p.Val14Val | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/16 | 113/4831 | 42/1722 | 14/573 | chr14 | 104085812 | |||
chr14:104085818 | C | T | 2 | a0002c0010 a0002c0026 |
3 | HG02258.hp2 HG02280.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.48C>T | p.Thr16Thr | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/16 | 119/4831 | 48/1722 | 16/573 | chr14 | 104085818 | |||
chr14:104093515 | T | C | 12 | a0002c0002 a0002c0003 a0002c0005 others(9): Show |
157 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(154): Show |
synonymous_variant | LOW | c.216T>C | p.Ile72Ile | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/16 | 287/4831 | 216/1722 | 72/573 | chr14 | 104093515 | |||
chr14:104095551 | C | T | 1 | a0001c0007 | 5 | HG02615.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
synonymous_variant | LOW | c.324C>T | p.His108His | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/16 | 395/4831 | 324/1722 | 108/573 | chr14 | 104095551 | |||
chr14:104095599 | G | C | 1 | a0003c0009 | 2 | HG02486.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.372G>C | p.Ser124Ser | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/16 | 443/4831 | 372/1722 | 124/573 | chr14 | 104095599 | |||
chr14:104097595 | G | T | 8 | a0001c0006 a0001c0007 a0002c0002 others(5): Show |
105 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(102): Show |
synonymous_variant | LOW | c.471G>T | p.Leu157Leu | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/16 | 542/4831 | 471/1722 | 157/573 | chr14 | 104097595 | |||
chr14:104098909 | C | T | 1 | a0001c0024 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.570C>T | p.Asp190Asp | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/16 | 641/4831 | 570/1722 | 190/573 | chr14 | 104098909 | |||
chr14:104103591 | C | T | 1 | a0002c0005 | 6 | HG02109.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.669C>T | p.Asp223Asp | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/16 | 740/4831 | 669/1722 | 223/573 | chr14 | 104103591 | |||
chr14:104103597 | G | A | 1 | a0001c0018 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.675G>A | p.Lys225Lys | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/16 | 746/4831 | 675/1722 | 225/573 | chr14 | 104103597 | |||
chr14:104104396 | G | A | 2 | a0001c0019 a0002c0013 |
2 | HG02451.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.846G>A | p.Glu282Glu | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/16 | 917/4831 | 846/1722 | 282/573 | chr14 | 104104396 | |||
chr14:104104429 | C | T | 1 | a0001c0022 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.879C>T | p.Ile293Ile | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/16 | 950/4831 | 879/1722 | 293/573 | chr14 | 104104429 | |||
chr14:104109253 | G | C | 1 | a0002c0016 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.1458G>C | p.Leu486Leu | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/16 | 1529/4831 | 1458/1722 | 486/573 | chr14 | 104109253 | |||
chr14:104109268 | C | T | 1 | a0011c0015 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.1473C>T | p.Ala491Ala | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/16 | 1544/4831 | 1473/1722 | 491/573 | chr14 | 104109268 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104085711 | C | G | 6 | a0002c0003t0016 a0002c0003t0017 a0002c0003t0037 others(3): Show |
9 | HG01074.hp1 HG02109.hp2 HG02622.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-60C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/16 | 60 | chr14 | 104085711 | ||||||
chr14:104112721 | C | T | 1 | a0001c0001t0036 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*177C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 177 | chr14 | 104112721 | ||||||
chr14:104112752 | C | T | 1 | a0001c0001t0024 | 2 | HG01256.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*208C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 208 | chr14 | 104112752 | ||||||
chr14:104112810 | T | G | 1 | a0002c0003t0037 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266T>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 266 | chr14 | 104112810 | ||||||
chr14:104112873 | C | G | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(54): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*329C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 329 | chr14 | 104112873 | ||||||
chr14:104112877 | A | G | 5 | a0001c0001t0010 a0001c0019t0010 a0002c0003t0010 others(2): Show |
6 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*333A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 333 | chr14 | 104112877 | ||||||
chr14:104112907 | A | C | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(61): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*363A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 363 | chr14 | 104112907 | ||||||
chr14:104112951 | C | A | 1 | a0002c0003t0018 | 2 | HG02055.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*407C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 407 | chr14 | 104112951 | ||||||
chr14:104113127 | C | T | 1 | a0001c0001t0025 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 583 | chr14 | 104113127 | ||||||
chr14:104113273 | T | A | 1 | a0003c0004t0012 | 3 | NA18971.hp1 NA18993.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*729T>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 729 | chr14 | 104113273 | ||||||
chr14:104113279 | G | A | 6 | a0003c0004t0003 a0003c0004t0012 a0003c0004t0026 others(3): Show |
50 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*735G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 735 | chr14 | 104113279 | ||||||
chr14:104113451 | C | T | 1 | a0001c0001t0035 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 907 | chr14 | 104113451 | ||||||
chr14:104113493 | C | T | 1 | a0002c0002t0015 | 3 | NA18944.hp1 NA18952.hp2 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*949C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 949 | chr14 | 104113493 | ||||||
chr14:104113695 | G | C | 1 | a0002c0003t0009 | 6 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1151G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 1151 | chr14 | 104113695 | ||||||
chr14:104113818 | C | T | 2 | a0006c0012t0023 a0010c0011t0023 |
2 | HG01168.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1274C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 1274 | chr14 | 104113818 | ||||||
chr14:104114049 | C | T | 1 | a0002c0002t0022 | 2 | NA19030.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1505C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 1505 | chr14 | 104114049 | ||||||
chr14:104114057 | C | T | 17 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0020 others(14): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1513C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 1513 | chr14 | 104114057 | ||||||
chr14:104114263 | C | T | 2 | a0001c0001t0014 a0003c0004t0030 |
4 | NA18941.hp2 NA18985.hp2 NA19060.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1719C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 1719 | chr14 | 104114263 | ||||||
chr14:104114735 | C | T | 3 | a0001c0001t0004 a0004c0008t0004 a0008c0020t0029 |
22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2191C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2191 | chr14 | 104114735 | ||||||
chr14:104114750 | G | A | 1 | a0002c0002t0027 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2206G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2206 | chr14 | 104114750 | ||||||
chr14:104114852 | C | T | 2 | a0002c0003t0009 a0002c0003t0021 |
8 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2308C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2308 | chr14 | 104114852 | ||||||
chr14:104115209 | G | C | 1 | a0001c0001t0031 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2665G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2665 | chr14 | 104115209 | ||||||
chr14:104115233 | T | A | 2 | a0001c0001t0032 a0002c0002t0013 |
4 | HG02132.hp1 NA18949.hp1 NA19003.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2689T>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2689 | chr14 | 104115233 | ||||||
chr14:104115323 | G | C | 14 | a0001c0001t0002 a0001c0001t0032 a0001c0001t0033 others(11): Show |
100 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2779G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2779 | chr14 | 104115323 | ||||||
chr14:104115344 | G | A | 1 | a0001c0006t0028 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2800G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2800 | chr14 | 104115344 | ||||||
chr14:104115359 | G | A | 1 | a0003c0004t0012 | 3 | NA18971.hp1 NA18993.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2815G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2815 | chr14 | 104115359 | ||||||
chr14:104115385 | C | T | 4 | a0001c0007t0008 a0002c0002t0008 a0002c0002t0022 others(1): Show |
10 | HG02976.hp2 HG03041.hp2 HG03225.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2841C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2841 | chr14 | 104115385 | ||||||
chr14:104115388 | C | G | 9 | a0001c0001t0011 a0001c0001t0025 a0001c0024t0011 others(6): Show |
18 | HG00735.hp1 HG01099.hp2 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2844C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2844 | chr14 | 104115388 | ||||||
chr14:104115389 | G | C | 1 | a0001c0001t0034 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2845G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2845 | chr14 | 104115389 | ||||||
chr14:104115423 | A | G | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(17): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2879A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2879 | chr14 | 104115423 | ||||||
chr14:104115503 | T | C | 1 | a0002c0002t0027 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2959T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 2959 | chr14 | 104115503 | ||||||
chr14:104115547 | C | A | 1 | a0008c0020t0029 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3003C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 16/16 | 3003 | chr14 | 104115547 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104085866 | C | T | 1 | a0001c0001t0007g0245 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.82+14C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104085866 | |||||||
chr14:104085964 | G | A | 1 | a0002c0003t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.82+112G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104085964 | |||||||
chr14:104085983 | G | A | 5 | a0002c0003t0005g0022 a0002c0003t0005g0059 a0002c0003t0005g0060 others(2): Show |
6 | HG00733.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+131G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104085983 | |||||||
chr14:104085986 | C | G | 1 | a0003c0004t0003g0244 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.82+134C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104085986 | |||||||
chr14:104086045 | A | G | 116 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(113): Show |
164 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(161): Show |
intron_variant | MODIFIER | c.82+193A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086045 | |||||||
chr14:104086132 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
6 | HG00438.hp2 NA18947.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+280A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086132 | |||||||
chr14:104086265 | A | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(248): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.82+413A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086265 | |||||||
chr14:104086299 | G | C | 1 | a0002c0003t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82+447G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086299 | |||||||
chr14:104086583 | G | A | 1 | a0009c0021t0003g0067 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.82+731G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086583 | |||||||
chr14:104086749 | C | T | 1 | a0003c0004t0003g0150 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.82+897C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086749 | |||||||
chr14:104086849 | C | T | 4 | a0002c0002t0002g0003 a0002c0002t0002g0057 a0002c0002t0002g0242 others(1): Show |
15 | HG00738.hp2 HG01192.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.82+997C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086849 | |||||||
chr14:104086859 | A | G | 17 | a0001c0001t0004g0056 a0001c0001t0004g0235 a0001c0001t0010g0239 others(14): Show |
22 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.82+1007A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086859 | |||||||
chr14:104086877 | G | A | 3 | a0002c0002t0002g0156 a0002c0002t0015g0043 a0002c0002t0015g0155 |
4 | NA18944.hp1 NA18952.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1025G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086877 | |||||||
chr14:104086983 | C | T | 1 | a0002c0003t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82+1131C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104086983 | |||||||
chr14:104087184 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(185): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.82+1332A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087184 | |||||||
chr14:104087225 | TCTC | T | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.82+1376_82+1378del others(3): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104087225 | ||||||
chr14:104087228 | C | G | 1 | a0002c0003t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82+1376C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087228 | |||||||
chr14:104087229 | C | T | 10 | a0001c0001t0004g0056 a0001c0001t0004g0235 a0001c0001t0010g0239 others(7): Show |
12 | HG00639.hp1 HG01884.hp1 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.82+1377C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087229 | |||||||
chr14:104087273 | G | A | 10 | a0002c0003t0011g0159 a0002c0003t0016g0158 a0002c0003t0016g0160 others(7): Show |
10 | HG01074.hp1 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.82+1421G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087273 | |||||||
chr14:104087320 | T | C | 4 | a0002c0002t0002g0165 a0002c0002t0002g0166 a0002c0002t0019g0167 others(1): Show |
4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1468T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087320 | |||||||
chr14:104087535 | G | A | 1 | a0002c0003t0010g0231 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.82+1683G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087535 | |||||||
chr14:104087707 | G | A | 83 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(80): Show |
126 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.82+1855G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087707 | |||||||
chr14:104087797 | C | T | 1 | a0001c0001t0005g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.82+1945C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087797 | |||||||
chr14:104087805 | C | T | 1 | a0002c0003t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82+1953C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087805 | |||||||
chr14:104087844 | G | A | 2 | a0001c0001t0001g0108 a0012c0023t0001g0109 |
2 | HG03017.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.82+1992G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104087844 | |||||||
chr14:104088098 | C | T | 1 | a0002c0003t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82+2246C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088098 | |||||||
chr14:104088103 | C | G | 10 | a0002c0003t0011g0159 a0002c0003t0016g0158 a0002c0003t0016g0160 others(7): Show |
10 | HG01074.hp1 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.82+2251C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088103 | |||||||
chr14:104088347 | C | T | 11 | a0001c0001t0001g0148 a0002c0003t0011g0159 a0002c0003t0016g0158 others(8): Show |
11 | HG01074.hp1 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.82+2495C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088347 | |||||||
chr14:104088502 | G | A | 3 | a0002c0002t0005g0169 a0002c0005t0002g0045 a0002c0005t0002g0168 |
4 | HG02809.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+2650G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088502 | |||||||
chr14:104088584 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(185): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.82+2732C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088584 | |||||||
chr14:104088643 | G | A | 3 | a0002c0002t0002g0165 a0002c0002t0002g0166 a0002c0002t0019g0167 |
3 | HG02451.hp1 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.82+2791G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088643 | |||||||
chr14:104088784 | G | A | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.82+2932G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088784 | |||||||
chr14:104088788 | A | G | 2 | a0002c0003t0002g0010 a0011c0015t0002g0228 |
5 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+2936A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088788 | |||||||
chr14:104088856 | G | A | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.82+3004G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088856 | |||||||
chr14:104088887 | G | C | 1 | a0003c0004t0003g0068 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.82+3035G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088887 | |||||||
chr14:104088975 | T | C | 5 | a0002c0003t0005g0022 a0002c0003t0005g0059 a0002c0003t0005g0060 others(2): Show |
6 | HG00733.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+3123T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088975 | |||||||
chr14:104088984 | A | G | 81 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(78): Show |
124 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.82+3132A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104088984 | |||||||
chr14:104089002 | C | T | 1 | a0002c0003t0001g0227 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.82+3150C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089002 | |||||||
chr14:104089096 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0073 others(60): Show |
95 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.82+3244C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089096 | |||||||
chr14:104089116 | G | T | 93 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(90): Show |
136 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.82+3264G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089116 | |||||||
chr14:104089169 | C | T | 6 | a0001c0001t0010g0239 a0001c0001t0011g0237 a0001c0001t0025g0236 others(3): Show |
6 | HG02451.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+3317C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089169 | |||||||
chr14:104089216 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.82+3364G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089216 | |||||||
chr14:104089240 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.82+3388C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089240 | |||||||
chr14:104089327 | A | C | 1 | a0001c0001t0001g0042 | 2 | NA18963.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.83-3306A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089327 | |||||||
chr14:104089359 | C | CA | 17 | a0002c0002t0002g0165 a0002c0002t0002g0166 a0002c0002t0008g0047 others(14): Show |
20 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.83-3264dupA | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089359 | ||||||
chr14:104089468 | G | A | 3 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0001c0019t0010g0238 |
3 | HG02451.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.83-3165G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089468 | |||||||
chr14:104089571 | C | T | 2 | a0006c0012t0023g0230 a0010c0011t0023g0149 |
2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.83-3062C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089571 | |||||||
chr14:104089640 | G | A | 3 | a0001c0001t0004g0024 a0001c0001t0004g0069 a0001c0001t0004g0070 |
4 | HG01081.hp1 HG01123.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2993G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089640 | |||||||
chr14:104089792 | T | A | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-2841T>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089792 | |||||||
chr14:104089854 | A | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0146 others(1): Show |
7 | HG00423.hp2 HG02040.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-2779A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089854 | |||||||
chr14:104089872 | G | C | 120 | a0001c0001t0001g0226 a0001c0001t0002g0110 a0001c0001t0004g0056 others(117): Show |
169 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(166): Show |
intron_variant | MODIFIER | c.83-2761G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089872 | |||||||
chr14:104089900 | A | G | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-2733A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104089900 | |||||||
chr14:104089947 | C | CA | 48 | a0001c0001t0001g0111 a0001c0001t0004g0056 a0001c0001t0004g0208 others(45): Show |
69 | HG00280.hp2 HG00558.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.83-2659dupA | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | ||||||
chr14:104089947 | C | CAA | 23 | a0001c0001t0004g0235 a0001c0001t0010g0239 a0002c0002t0002g0003 others(20): Show |
36 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.83-2660_83-2659dup others(2): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | ||||||
chr14:104089947 | C | CAAA | 26 | a0002c0002t0002g0004 a0002c0002t0002g0018 a0002c0002t0002g0049 others(23): Show |
37 | HG00609.hp2 HG01074.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.83-2661_83-2659dup others(3): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | ||||||
chr14:104089947 | C | CAAAA | 7 | a0002c0002t0002g0179 a0002c0002t0002g0180 a0002c0002t0002g0242 others(4): Show |
8 | HG01978.hp1 HG02129.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-2662_83-2659dup others(4): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | ||||||
chr14:104089947 | CA | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(93): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.83-2659delA | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | ||||||
chr14:104089947 | CAA | C | 8 | a0001c0001t0001g0108 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
8 | HG01346.hp1 HG01891.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-2660_83-2659del others(2): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | ||||||
chr14:104089947 | CAAA | C | 5 | a0002c0003t0005g0022 a0002c0003t0005g0060 a0002c0003t0005g0061 others(2): Show |
6 | HG00733.hp1 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-2661_83-2659del others(3): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 104089947 | ||||||
chr14:104090126 | T | A | 3 | a0002c0002t0002g0018 a0002c0002t0002g0182 a0002c0002t0002g0194 |
5 | HG02015.hp1 NA18962.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-2507T>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090126 | |||||||
chr14:104090394 | C | T | 1 | a0002c0002t0022g0041 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.83-2239C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090394 | |||||||
chr14:104090431 | C | T | 1 | a0001c0001t0005g0065 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.83-2202C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090431 | |||||||
chr14:104090519 | G | T | 2 | a0002c0003t0002g0171 a0002c0003t0018g0170 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.83-2114G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090519 | |||||||
chr14:104090539 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.83-2094G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090539 | |||||||
chr14:104090553 | C | T | 10 | a0002c0003t0011g0159 a0002c0003t0016g0158 a0002c0003t0016g0160 others(7): Show |
10 | HG01074.hp1 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.83-2080C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090553 | |||||||
chr14:104090567 | C | T | 2 | a0002c0003t0009g0175 a0002c0003t0009g0176 |
2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.83-2066C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090567 | |||||||
chr14:104090695 | C | T | 8 | a0002c0003t0005g0177 a0002c0003t0009g0046 a0002c0003t0009g0172 others(5): Show |
9 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.83-1938C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090695 | |||||||
chr14:104090773 | A | C | 2 | a0002c0003t0002g0171 a0002c0003t0018g0170 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.83-1860A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090773 | |||||||
chr14:104090935 | G | C | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-1698G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090935 | |||||||
chr14:104090969 | G | T | 1 | a0002c0003t0007g0229 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.83-1664G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090969 | |||||||
chr14:104090970 | A | C | 74 | a0001c0001t0001g0226 a0002c0002t0002g0003 a0002c0002t0002g0004 others(71): Show |
117 | HG00558.hp2 HG00609.hp2 HG00738.hp2 others(114): Show |
intron_variant | MODIFIER | c.83-1663A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104090970 | |||||||
chr14:104091105 | A | G | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-1528A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091105 | |||||||
chr14:104091323 | G | C | 5 | a0002c0003t0005g0022 a0002c0003t0005g0059 a0002c0003t0005g0060 others(2): Show |
6 | HG00733.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-1310G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091323 | |||||||
chr14:104091388 | G | C | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-1245G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091388 | |||||||
chr14:104091458 | C | G | 1 | a0001c0001t0001g0141 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.83-1175C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091458 | |||||||
chr14:104091458 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.83-1175C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091458 | |||||||
chr14:104091574 | C | T | 7 | a0001c0001t0001g0105 a0001c0006t0002g0034 a0002c0003t0002g0171 others(4): Show |
8 | HG02055.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-1059C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091574 | |||||||
chr14:104091575 | G | A | 1 | a0002c0003t0007g0229 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.83-1058G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091575 | |||||||
chr14:104091599 | G | A | 1 | a0010c0011t0023g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.83-1034G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091599 | |||||||
chr14:104091603 | T | C | 1 | a0002c0003t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.83-1030T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091603 | |||||||
chr14:104091652 | C | T | 3 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0001c0019t0010g0238 |
3 | HG02451.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.83-981C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091652 | |||||||
chr14:104091695 | T | C | 1 | a0001c0001t0004g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.83-938T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091695 | |||||||
chr14:104091749 | G | A | 1 | a0002c0003t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.83-884G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091749 | |||||||
chr14:104091826 | C | T | 1 | a0002c0002t0002g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.83-807C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091826 | |||||||
chr14:104091982 | T | C | 106 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0006 others(103): Show |
154 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.83-651T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104091982 | |||||||
chr14:104092002 | C | A | 1 | a0002c0003t0010g0231 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.83-631C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104092002 | |||||||
chr14:104092390 | C | T | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-243C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104092390 | |||||||
chr14:104092400 | C | T | 1 | a0002c0003t0016g0163 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83-233C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104092400 | |||||||
chr14:104092451 | C | T | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-182C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 1/15 | chr14 | 104092451 | |||||||
chr14:104093012 | C | T | 15 | a0002c0003t0005g0177 a0002c0003t0006g0053 a0002c0003t0006g0054 others(12): Show |
19 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.191+271C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093012 | |||||||
chr14:104093015 | C | T | 1 | a0002c0003t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.191+274C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093015 | |||||||
chr14:104093026 | C | A | 6 | a0002c0003t0006g0053 a0002c0003t0006g0054 a0002c0003t0006g0055 others(3): Show |
9 | HG00735.hp1 HG01099.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.191+285C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093026 | |||||||
chr14:104093142 | A | C | 1 | a0002c0002t0002g0192 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.192-349A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093142 | |||||||
chr14:104093169 | C | T | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0006 others(106): Show |
157 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(154): Show |
intron_variant | MODIFIER | c.192-322C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093169 | |||||||
chr14:104093183 | G | A | 2 | a0002c0002t0002g0195 a0002c0002t0002g0196 |
2 | HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.192-308G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093183 | |||||||
chr14:104093215 | G | C | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0006 others(106): Show |
157 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(154): Show |
intron_variant | MODIFIER | c.192-276G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093215 | |||||||
chr14:104093286 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(198): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.192-205T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093286 | |||||||
chr14:104093311 | C | T | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.192-180C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093311 | |||||||
chr14:104093328 | C | T | 1 | a0004c0008t0004g0021 | 3 | HG00639.hp1 HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.192-163C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093328 | |||||||
chr14:104093335 | C | T | 1 | a0010c0011t0023g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.192-156C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 2/15 | chr14 | 104093335 | |||||||
chr14:104093622 | CTGGGTGG others(31): Show |
C | 106 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0006 others(103): Show |
154 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.303+52_303+89delAG others(36): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 104093622 | ||||||
chr14:104093654 | A | T | 3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.303+52A>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104093654 | |||||||
chr14:104093660 | G | GTGGGTGG others(13): Show |
3 | a0002c0003t0007g0229 a0006c0012t0023g0230 a0010c0011t0023g0149 |
3 | HG01168.hp1 HG02818.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.303+70_303+71insGG others(18): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 104093660 | ||||||
chr14:104093806 | G | A | 1 | a0003c0004t0003g0090 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.303+204G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104093806 | |||||||
chr14:104093857 | G | A | 1 | a0002c0003t0010g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.303+255G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104093857 | |||||||
chr14:104093889 | GGTGGGGC others(10): Show |
G | 1 | a0002c0002t0002g0165 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.303+298_303+314del others(17): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 104093889 | ||||||
chr14:104093964 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.303+362G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104093964 | |||||||
chr14:104094140 | C | T | 1 | a0002c0003t0017g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.303+538C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094140 | |||||||
chr14:104094149 | A | G | 1 | a0002c0003t0017g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.303+547A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094149 | |||||||
chr14:104094163 | G | A | 1 | a0002c0002t0002g0210 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.303+561G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094163 | |||||||
chr14:104094193 | G | A | 1 | a0001c0001t0031g0143 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.303+591G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094193 | |||||||
chr14:104094201 | G | A | 1 | a0001c0007t0002g0241 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.303+599G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094201 | |||||||
chr14:104094252 | G | A | 1 | a0002c0002t0002g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.303+650G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094252 | |||||||
chr14:104094374 | T | G | 1 | a0002c0002t0002g0212 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.303+772T>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094374 | |||||||
chr14:104094487 | C | T | 1 | a0002c0002t0019g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.303+885C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094487 | |||||||
chr14:104094512 | C | T | 1 | a0002c0003t0037g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.303+910C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094512 | |||||||
chr14:104094533 | G | A | 67 | a0001c0001t0004g0092 a0001c0006t0002g0034 a0002c0002t0002g0003 others(64): Show |
107 | HG00558.hp2 HG00609.hp2 HG00738.hp2 others(104): Show |
intron_variant | MODIFIER | c.303+931G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094533 | |||||||
chr14:104094558 | A | G | 1 | a0002c0013t0039g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.303+956A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094558 | |||||||
chr14:104094675 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(208): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.304-856A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094675 | |||||||
chr14:104094881 | C | T | 4 | a0002c0002t0002g0049 a0002c0002t0013g0181 a0002c0002t0013g0190 others(1): Show |
5 | HG02040.hp2 HG02071.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-650C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104094881 | |||||||
chr14:104095148 | C | T | 1 | a0003c0004t0003g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.304-383C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095148 | |||||||
chr14:104095260 | T | C | 3 | a0002c0003t0009g0046 a0006c0012t0023g0230 a0010c0011t0023g0149 |
4 | HG01168.hp1 HG02735.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-271T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095260 | |||||||
chr14:104095302 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.304-229G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095302 | |||||||
chr14:104095348 | C | T | 2 | a0002c0002t0002g0212 a0002c0002t0002g0219 |
2 | HG00558.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.304-183C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095348 | |||||||
chr14:104095354 | A | G | 1 | a0003c0004t0003g0107 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.304-177A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095354 | |||||||
chr14:104095375 | G | A | 14 | a0001c0001t0001g0085 a0001c0001t0007g0025 a0001c0001t0007g0080 others(11): Show |
16 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.304-156G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095375 | |||||||
chr14:104095514 | A | C | 3 | a0002c0003t0018g0174 a0002c0003t0021g0173 a0002c0003t0021g0178 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.304-17A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 3/15 | chr14 | 104095514 | |||||||
chr14:104095661 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(204): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
splice_region_variant&intron_variant | LOW | c.429+5T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095661 | |||||||
chr14:104095716 | C | T | 1 | a0001c0001t0004g0033 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.429+60C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095716 | |||||||
chr14:104095723 | G | A | 11 | a0001c0001t0007g0025 a0001c0001t0007g0080 a0002c0003t0005g0177 others(8): Show |
13 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+67G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095723 | |||||||
chr14:104095746 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0122 |
2 | NA18949.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.429+90G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095746 | |||||||
chr14:104095852 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(246): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.429+196A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095852 | |||||||
chr14:104095925 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.429+269C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095925 | |||||||
chr14:104095963 | G | GATGCTTC others(19): Show |
1 | a0002c0003t0005g0060 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.429+308_429+333dup others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 104095963 | ||||||
chr14:104095975 | C | T | 3 | a0001c0001t0004g0235 a0001c0019t0010g0238 a0004c0008t0004g0021 |
5 | HG00639.hp1 HG01884.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+319C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104095975 | |||||||
chr14:104096017 | C | T | 1 | a0002c0002t0002g0207 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.429+361C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096017 | |||||||
chr14:104096027 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.429+371C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096027 | |||||||
chr14:104096139 | C | A | 1 | a0001c0019t0010g0238 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.429+483C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096139 | |||||||
chr14:104096244 | G | A | 9 | a0002c0003t0002g0171 a0002c0003t0006g0053 a0002c0003t0006g0054 others(6): Show |
12 | HG00735.hp1 HG01099.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.429+588G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096244 | |||||||
chr14:104096261 | G | A | 5 | a0002c0003t0005g0022 a0002c0003t0005g0059 a0002c0003t0005g0060 others(2): Show |
6 | HG00733.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+605G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096261 | |||||||
chr14:104096475 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(96): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.429+819A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096475 | |||||||
chr14:104096499 | C | A | 3 | a0002c0003t0005g0022 a0002c0003t0005g0060 a0002c0003t0005g0061 |
4 | HG00733.hp1 HG01884.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+843C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096499 | |||||||
chr14:104096501 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.429+845C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096501 | |||||||
chr14:104096549 | G | C | 7 | a0001c0007t0002g0241 a0001c0007t0008g0071 a0001c0007t0008g0081 others(4): Show |
8 | HG02615.hp2 HG02976.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+893G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096549 | |||||||
chr14:104096681 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(206): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.430-873A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096681 | |||||||
chr14:104096769 | C | A | 3 | a0002c0003t0006g0053 a0002c0003t0006g0232 a0002c0026t0006g0213 |
4 | HG02055.hp1 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-785C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096769 | |||||||
chr14:104096778 | A | C | 4 | a0002c0003t0006g0054 a0002c0003t0006g0055 a0002c0003t0006g0233 others(1): Show |
6 | HG00735.hp1 HG01099.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-776A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096778 | |||||||
chr14:104096832 | A | G | 2 | a0001c0001t0001g0139 a0002c0003t0001g0209 |
2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.430-722A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096832 | |||||||
chr14:104096865 | C | T | 2 | a0006c0012t0023g0230 a0010c0011t0023g0149 |
2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.430-689C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096865 | |||||||
chr14:104096994 | G | A | 1 | a0002c0002t0022g0041 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.430-560G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104096994 | |||||||
chr14:104097020 | C | T | 1 | a0001c0001t0005g0023 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.430-534C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097020 | |||||||
chr14:104097113 | G | T | 1 | a0003c0004t0003g0068 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.430-441G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097113 | |||||||
chr14:104097126 | G | A | 5 | a0002c0003t0001g0019 a0002c0003t0001g0048 a0002c0003t0001g0058 others(2): Show |
8 | HG01074.hp2 HG01167.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-428G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097126 | |||||||
chr14:104097273 | G | A | 1 | a0002c0002t0002g0212 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.430-281G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097273 | |||||||
chr14:104097322 | G | A | 6 | a0001c0007t0002g0241 a0001c0007t0008g0071 a0001c0007t0008g0081 others(3): Show |
7 | HG02615.hp2 HG02976.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-232G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097322 | |||||||
chr14:104097323 | T | A | 1 | a0001c0019t0010g0238 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.430-231T>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097323 | |||||||
chr14:104097345 | G | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(87): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.430-209G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097345 | |||||||
chr14:104097414 | C | T | 1 | a0002c0003t0009g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.430-140C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097414 | |||||||
chr14:104097421 | C | T | 7 | a0001c0007t0002g0241 a0001c0007t0008g0071 a0001c0007t0008g0081 others(4): Show |
8 | HG02615.hp2 HG02976.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-133C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097421 | |||||||
chr14:104097537 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(98): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.430-17C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 4/15 | chr14 | 104097537 | |||||||
chr14:104097676 | T | G | 2 | a0002c0002t0002g0179 a0002c0002t0002g0183 |
2 | NA18999.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.513+39T>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097676 | |||||||
chr14:104097809 | AGTTCTAC others(45): Show |
A | 9 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0069 others(6): Show |
13 | HG01081.hp1 HG01123.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.513+217_513+268del others(52): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097809 | ||||||
chr14:104097813 | CTACGTTA others(383): Show |
C | 1 | a0001c0001t0011g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.513+202_513+591del | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097813 | ||||||
chr14:104097815 | ACGTTAGA others(97): Show |
A | 2 | a0002c0003t0002g0171 a0002c0003t0018g0170 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.513+189_513+292del | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097815 | ||||||
chr14:104097826 | A | ACGTATGG others(19): Show |
2 | a0001c0006t0002g0124 a0003c0025t0003g0086 |
2 | HG02145.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.513+191_513+216dup others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097826 | ||||||
chr14:104097826 | ACGTATGG others(71): Show |
A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0085 a0001c0001t0001g0125 others(1): Show |
4 | HG01099.hp1 HG01934.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+217_513+294del others(78): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097826 | ||||||
chr14:104097826 | ACGTATGG others(123): Show |
A | 5 | a0001c0001t0001g0126 a0002c0003t0006g0054 a0002c0003t0006g0055 others(2): Show |
7 | HG00735.hp1 HG01099.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.513+217_513+346del | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097826 | ||||||
chr14:104097846 | A | AGAGATGC others(19): Show |
1 | a0001c0006t0002g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.513+216_513+217ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097846 | ||||||
chr14:104097852 | G | GCGTATGG others(45): Show |
1 | a0002c0002t0002g0217 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.513+216_513+217ins others(52): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097852 | ||||||
chr14:104097852 | GCATATGG others(19): Show |
G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0116 a0001c0001t0001g0139 others(2): Show |
5 | HG02602.hp1 HG02738.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+217_513+242del others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097852 | ||||||
chr14:104097854 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(153): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.513+217A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097854 | |||||||
chr14:104097867 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(152): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.513+230A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097867 | |||||||
chr14:104097878 | A | ACGTATGG others(19): Show |
3 | a0001c0001t0004g0029 a0001c0001t0004g0033 a0003c0004t0003g0007 |
8 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+283_513+308dup others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097878 | ||||||
chr14:104097878 | A | G | 61 | a0001c0006t0028g0138 a0001c0019t0010g0238 a0002c0002t0002g0003 others(58): Show |
97 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(94): Show |
intron_variant | MODIFIER | c.513+241A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097878 | |||||||
chr14:104097891 | C | CTGCGTTA others(45): Show |
4 | a0002c0002t0002g0216 a0002c0005t0002g0215 a0002c0005t0008g0206 others(1): Show |
4 | HG02109.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+266_513+267ins others(52): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097891 | ||||||
chr14:104097891 | C | CTGCGTTA others(71): Show |
1 | a0002c0002t0002g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+266_513+267ins others(78): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097891 | ||||||
chr14:104097891 | C | T | 3 | a0002c0002t0002g0192 a0002c0002t0002g0202 a0002c0002t0002g0218 |
3 | HG02738.hp2 HG03834.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.513+254C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097891 | |||||||
chr14:104097894 | C | T | 5 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0069 others(2): Show |
8 | HG01081.hp1 HG01123.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+257C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097894 | |||||||
chr14:104097904 | G | A | 56 | a0001c0001t0010g0239 a0001c0006t0028g0138 a0001c0019t0010g0238 others(53): Show |
92 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.513+267G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097904 | |||||||
chr14:104097917 | C | CTGCGTTA others(97): Show |
2 | a0003c0004t0003g0076 a0003c0004t0003g0093 |
2 | HG02080.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.513+308_513+309ins others(104): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097917 | ||||||
chr14:104097917 | C | CTGCGTTA others(19): Show |
1 | a0002c0002t0002g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513+305_513+306ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097917 | ||||||
chr14:104097917 | C | T | 8 | a0001c0006t0002g0034 a0001c0006t0002g0123 a0001c0006t0002g0124 others(5): Show |
10 | HG01433.hp2 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.513+280C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097917 | |||||||
chr14:104097920 | C | T | 2 | a0003c0004t0003g0103 a0003c0004t0003g0104 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.513+283C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097920 | |||||||
chr14:104097920 | CGTTAGAG others(19): Show |
C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(60): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.513+309_513+334del others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097920 | ||||||
chr14:104097930 | G | GCGTATGG others(19): Show |
1 | a0002c0003t0010g0231 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.513+307_513+308ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097930 | ||||||
chr14:104097943 | C | T | 48 | a0001c0006t0002g0123 a0001c0006t0028g0138 a0002c0002t0002g0003 others(45): Show |
82 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.513+306C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097943 | |||||||
chr14:104097945 | G | A | 3 | a0001c0001t0010g0239 a0002c0003t0010g0154 a0002c0003t0037g0162 |
3 | HG02572.hp1 HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.513+308G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097945 | |||||||
chr14:104097946 | T | C | 153 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0001g0085 others(150): Show |
216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.513+309T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097946 | |||||||
chr14:104097956 | G | A | 38 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0001g0085 others(35): Show |
46 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.513+319G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097956 | |||||||
chr14:104097956 | G | GCATATGG others(19): Show |
1 | a0001c0019t0010g0238 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513+320_513+321ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097956 | ||||||
chr14:104097969 | C | T | 24 | a0001c0001t0025g0236 a0002c0002t0002g0004 a0002c0002t0002g0006 others(21): Show |
41 | HG00558.hp2 HG01123.hp2 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.513+332C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097969 | |||||||
chr14:104097972 | C | CGTTAGAG others(19): Show |
2 | a0006c0012t0023g0230 a0010c0011t0023g0149 |
2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.513+360_513+361ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104097972 | ||||||
chr14:104097982 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(66): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.513+345G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097982 | |||||||
chr14:104097995 | C | T | 5 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0069 others(2): Show |
8 | HG01081.hp1 HG01123.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+358C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097995 | |||||||
chr14:104097997 | G | A | 2 | a0001c0001t0025g0236 a0002c0003t0011g0159 |
2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.513+360G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104097997 | |||||||
chr14:104098009 | C | T | 2 | a0001c0001t0010g0239 a0002c0003t0010g0154 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.513+372C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098009 | |||||||
chr14:104098021 | C | CTGCGTTA others(19): Show |
1 | a0003c0004t0003g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513+436_513+461dup others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098021 | ||||||
chr14:104098021 | C | T | 22 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0056 others(19): Show |
30 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.513+384C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098021 | |||||||
chr14:104098021 | CTGCGTTA others(19): Show |
C | 16 | a0001c0001t0001g0038 a0001c0001t0001g0085 a0001c0001t0001g0116 others(13): Show |
22 | HG00423.hp2 HG01074.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.513+436_513+461del others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098021 | ||||||
chr14:104098021 | CTGCGTTA others(45): Show |
C | 4 | a0001c0001t0001g0120 a0001c0001t0001g0137 a0001c0001t0025g0236 others(1): Show |
4 | HG01981.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+410_513+461del others(52): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098021 | ||||||
chr14:104098023 | G | A | 1 | a0001c0019t0010g0238 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513+386G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098023 | |||||||
chr14:104098024 | C | T | 2 | a0006c0012t0023g0230 a0010c0011t0023g0149 |
2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.513+387C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098024 | |||||||
chr14:104098034 | G | A | 1 | a0001c0019t0010g0238 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513+397G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098034 | |||||||
chr14:104098034 | GCGTATGG others(97): Show |
G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0089 |
2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.513+410_513+513del | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098034 | ||||||
chr14:104098047 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(157): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.513+410T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098047 | |||||||
chr14:104098049 | G | A | 16 | a0001c0001t0001g0126 a0001c0001t0004g0056 a0001c0001t0004g0235 others(13): Show |
21 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.513+412G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098049 | |||||||
chr14:104098061 | C | T | 1 | a0001c0001t0014g0037 | 2 | NA18985.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.513+424C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098061 | |||||||
chr14:104098062 | G | A | 8 | a0001c0001t0001g0126 a0001c0001t0004g0056 a0001c0001t0004g0235 others(5): Show |
10 | HG00639.hp1 HG01884.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+425G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098062 | |||||||
chr14:104098073 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(187): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.513+436T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098073 | |||||||
chr14:104098073 | TTGCGTTA others(19): Show |
C | 2 | a0001c0001t0001g0126 a0002c0003t0007g0229 |
2 | NA18943.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.513+436_513+461del others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098073 | |||||||
chr14:104098075 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(94): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.513+438G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098075 | |||||||
chr14:104098075 | G | C | 24 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0056 others(21): Show |
32 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.513+438G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098075 | |||||||
chr14:104098088 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(82): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.513+451G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098088 | |||||||
chr14:104098099 | C | A | 24 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0056 others(21): Show |
32 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.513+462C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098099 | |||||||
chr14:104098099 | C | T | 27 | a0001c0001t0004g0208 a0002c0002t0002g0004 a0002c0002t0002g0006 others(24): Show |
46 | HG00558.hp2 HG01123.hp2 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.513+462C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098099 | |||||||
chr14:104098101 | G | A | 53 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0056 others(50): Show |
68 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.513+464G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098101 | |||||||
chr14:104098101 | G | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(116): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.513+464G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098101 | |||||||
chr14:104098103 | G | C | 24 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0056 others(21): Show |
32 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.513+466G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098103 | |||||||
chr14:104098112 | G | A | 22 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0069 others(19): Show |
30 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.513+475G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098112 | |||||||
chr14:104098112 | G | GCGTATGG others(19): Show |
25 | a0001c0006t0028g0138 a0001c0007t0008g0240 a0002c0002t0002g0003 others(22): Show |
39 | HG00280.hp2 HG00609.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.513+487_513+488ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | ||||||
chr14:104098112 | G | GCGTATGG others(97): Show |
3 | a0002c0005t0002g0215 a0002c0005t0008g0206 a0002c0005t0008g0221 |
3 | HG02109.hp1 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.513+487_513+488ins others(104): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | ||||||
chr14:104098112 | G | GCGTATGG others(71): Show |
25 | a0002c0002t0002g0004 a0002c0002t0002g0006 a0002c0002t0002g0009 others(22): Show |
43 | HG00558.hp2 HG01123.hp2 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.513+489_513+490ins others(78): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | ||||||
chr14:104098112 | G | GCGTATGG others(149): Show |
3 | a0002c0002t0005g0169 a0002c0005t0002g0045 a0002c0005t0002g0168 |
4 | HG02809.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+489_513+490ins others(156): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | ||||||
chr14:104098112 | G | GCGTATGG others(97): Show |
1 | a0001c0019t0010g0238 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513+489_513+490ins others(104): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | ||||||
chr14:104098112 | G | GCGTATGG others(149): Show |
2 | a0002c0002t0008g0047 a0002c0016t0006g0205 |
3 | HG02970.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.513+489_513+490ins others(156): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | ||||||
chr14:104098112 | G | GCGTATGG others(97): Show |
2 | a0001c0001t0004g0208 a0003c0004t0003g0030 |
2 | HG02895.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.513+487_513+488ins others(104): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098112 | ||||||
chr14:104098125 | C | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(89): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.513+488C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098125 | |||||||
chr14:104098127 | C | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(172): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.513+490C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098127 | |||||||
chr14:104098127 | C | CCGTTAGA others(45): Show |
66 | a0001c0001t0004g0029 a0001c0001t0004g0032 a0001c0001t0004g0033 others(63): Show |
93 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.513+500_513+501ins others(52): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098127 | ||||||
chr14:104098127 | C | G | 2 | a0001c0001t0004g0056 a0008c0020t0029g0056 |
2 | HG02273.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.513+490C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098127 | |||||||
chr14:104098128 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.513+491C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098128 | |||||||
chr14:104098129 | G | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(87): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.513+492G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098129 | |||||||
chr14:104098129 | G | CTTAGAGA others(19): Show |
2 | a0001c0007t0002g0241 a0001c0007t0008g0082 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.513+491_513+492ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098129 | |||||||
chr14:104098129 | G | GTTAGAGA others(19): Show |
9 | a0002c0003t0005g0022 a0002c0003t0005g0059 a0002c0003t0005g0060 others(6): Show |
12 | HG00733.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.513+500_513+501ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 104098129 | ||||||
chr14:104098153 | G | A | 11 | a0001c0001t0001g0075 a0001c0001t0001g0089 a0002c0003t0005g0022 others(8): Show |
14 | HG00140.hp1 HG00733.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.513+516G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098153 | |||||||
chr14:104098153 | G | ACGTTAGA others(19): Show |
2 | a0001c0007t0008g0071 a0001c0007t0008g0081 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.513+515_513+516ins others(26): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098153 | |||||||
chr14:104098164 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0089 |
2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.513+527A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098164 | |||||||
chr14:104098166 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0089 |
2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.513+529G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098166 | |||||||
chr14:104098179 | G | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0089 |
2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.513+542G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098179 | |||||||
chr14:104098190 | G | A | 1 | a0001c0006t0002g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.513+553G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098190 | |||||||
chr14:104098216 | A | G | 1 | a0001c0006t0002g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.513+579A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098216 | |||||||
chr14:104098233 | A | G | 1 | a0001c0006t0002g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.513+596A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098233 | |||||||
chr14:104098243 | G | C | 1 | a0001c0006t0002g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.513+606G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098243 | |||||||
chr14:104098388 | C | T | 1 | a0002c0002t0002g0187 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.514-465C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098388 | |||||||
chr14:104098642 | C | T | 1 | a0003c0004t0003g0097 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.514-211C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098642 | |||||||
chr14:104098712 | C | G | 1 | a0002c0003t0009g0176 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.514-141C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098712 | |||||||
chr14:104098721 | C | A | 8 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0001c0024t0011g0064 others(5): Show |
8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-132C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098721 | |||||||
chr14:104098753 | G | A | 2 | a0006c0012t0023g0230 a0010c0011t0023g0149 |
2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.514-100G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 5/15 | chr14 | 104098753 | |||||||
chr14:104099315 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.640+336A>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099315 | |||||||
chr14:104099385 | GC | G | 8 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0001c0024t0011g0064 others(5): Show |
8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+409delC | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 104099385 | ||||||
chr14:104099414 | G | T | 8 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0001c0024t0011g0064 others(5): Show |
8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+435G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099414 | |||||||
chr14:104099442 | G | T | 64 | a0001c0001t0002g0110 a0001c0006t0002g0034 a0001c0006t0002g0123 others(61): Show |
102 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(99): Show |
intron_variant | MODIFIER | c.640+463G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099442 | |||||||
chr14:104099534 | C | T | 4 | a0002c0002t0002g0003 a0002c0002t0002g0057 a0002c0002t0002g0242 others(1): Show |
15 | HG00738.hp2 HG01192.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.640+555C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099534 | |||||||
chr14:104099535 | G | A | 1 | a0001c0022t0001g0072 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.640+556G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099535 | |||||||
chr14:104099585 | G | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(207): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.640+606G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099585 | |||||||
chr14:104099590 | G | A | 1 | a0002c0002t0027g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.640+611G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099590 | |||||||
chr14:104099652 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(125): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.640+673T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099652 | |||||||
chr14:104099782 | C | T | 97 | a0001c0001t0002g0110 a0001c0001t0004g0013 a0001c0001t0004g0024 others(94): Show |
147 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.640+803C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099782 | |||||||
chr14:104099784 | C | T | 1 | a0001c0027t0001g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.640+805C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099784 | |||||||
chr14:104099834 | G | A | 8 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0001c0024t0011g0064 others(5): Show |
8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+855G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099834 | |||||||
chr14:104099907 | G | A | 1 | a0003c0004t0012g0012 | 3 | NA18971.hp1 NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.640+928G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099907 | |||||||
chr14:104099946 | C | T | 17 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0029 others(14): Show |
26 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.640+967C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104099946 | |||||||
chr14:104100166 | G | A | 1 | a0002c0002t0002g0195 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.640+1187G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100166 | |||||||
chr14:104100213 | T | C | 4 | a0002c0002t0002g0004 a0002c0002t0002g0180 a0002c0002t0002g0192 others(1): Show |
10 | NA18941.hp1 NA18945.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+1234T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100213 | |||||||
chr14:104100251 | G | T | 2 | a0003c0004t0003g0103 a0003c0004t0003g0104 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.640+1272G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100251 | |||||||
chr14:104100333 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
9 | HG00639.hp2 HG01928.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.640+1354G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100333 | |||||||
chr14:104100356 | C | T | 2 | a0002c0002t0002g0182 a0002c0002t0002g0194 |
2 | NA18962.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.640+1377C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100356 | |||||||
chr14:104100433 | A | G | 73 | a0001c0001t0002g0110 a0001c0006t0002g0034 a0001c0006t0002g0123 others(70): Show |
112 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(109): Show |
intron_variant | MODIFIER | c.640+1454A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100433 | |||||||
chr14:104100575 | C | T | 24 | a0003c0004t0003g0002 a0003c0004t0003g0007 a0003c0004t0003g0011 others(21): Show |
42 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.640+1596C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100575 | |||||||
chr14:104100862 | G | T | 1 | a0011c0015t0002g0228 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.640+1883G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100862 | |||||||
chr14:104100879 | C | T | 11 | a0001c0001t0007g0025 a0001c0001t0007g0080 a0002c0003t0005g0177 others(8): Show |
13 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.640+1900C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104100879 | |||||||
chr14:104101008 | G | A | 1 | a0001c0001t0010g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.640+2029G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101008 | |||||||
chr14:104101049 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0148 |
3 | NA18997.hp1 NA19060.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.640+2070G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101049 | |||||||
chr14:104101085 | G | A | 33 | a0002c0013t0039g0161 a0003c0004t0003g0002 a0003c0004t0003g0007 others(30): Show |
52 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.640+2106G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101085 | |||||||
chr14:104101116 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.640+2137G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101116 | |||||||
chr14:104101158 | G | A | 1 | a0001c0001t0004g0070 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.640+2179G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101158 | |||||||
chr14:104101173 | A | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(246): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.640+2194A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101173 | |||||||
chr14:104101188 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(213): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.640+2209C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101188 | |||||||
chr14:104101239 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(213): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.640+2260C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101239 | |||||||
chr14:104101306 | G | C | 57 | a0001c0001t0002g0110 a0001c0006t0002g0034 a0001c0006t0002g0123 others(54): Show |
94 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.641-2257G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101306 | |||||||
chr14:104101385 | C | T | 126 | a0001c0001t0002g0110 a0001c0001t0004g0013 a0001c0001t0004g0024 others(123): Show |
179 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(176): Show |
intron_variant | MODIFIER | c.641-2178C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101385 | |||||||
chr14:104101482 | G | T | 1 | a0002c0002t0002g0051 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.641-2081G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101482 | |||||||
chr14:104101585 | C | T | 2 | a0002c0003t0006g0233 a0002c0003t0006g0234 |
2 | HG00735.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.641-1978C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101585 | |||||||
chr14:104101589 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(213): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.641-1974G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101589 | |||||||
chr14:104101595 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(213): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.641-1968A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101595 | |||||||
chr14:104101599 | C | G | 8 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0001c0024t0011g0064 others(5): Show |
8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-1964C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101599 | |||||||
chr14:104101693 | T | C | 1 | a0011c0015t0002g0228 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.641-1870T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101693 | |||||||
chr14:104101756 | ACCTC | A | 9 | a0002c0003t0002g0171 a0002c0003t0006g0053 a0002c0003t0006g0054 others(6): Show |
12 | HG00735.hp1 HG01099.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-1800_641-1797d others(6): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 104101756 | ||||||
chr14:104101804 | C | A | 1 | a0002c0002t0002g0156 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.641-1759C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101804 | |||||||
chr14:104101815 | C | A | 1 | a0001c0022t0001g0072 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.641-1748C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101815 | |||||||
chr14:104101831 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.641-1732G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104101831 | |||||||
chr14:104102130 | T | C | 1 | a0011c0015t0002g0228 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.641-1433T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102130 | |||||||
chr14:104102135 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(213): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.641-1428T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102135 | |||||||
chr14:104102279 | C | A | 1 | a0001c0001t0004g0032 | 2 | HG01255.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.641-1284C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102279 | |||||||
chr14:104102279 | C | G | 1 | a0002c0013t0039g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.641-1284C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102279 | |||||||
chr14:104102367 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.641-1196G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102367 | |||||||
chr14:104102376 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.641-1187C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102376 | |||||||
chr14:104102591 | C | A | 1 | a0011c0015t0002g0228 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.641-972C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102591 | |||||||
chr14:104102600 | C | G | 1 | a0002c0002t0019g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.641-963C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102600 | |||||||
chr14:104102692 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.641-871C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102692 | |||||||
chr14:104102743 | G | A | 1 | a0001c0019t0010g0238 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.641-820G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102743 | |||||||
chr14:104102788 | G | C | 11 | a0001c0001t0007g0025 a0001c0001t0007g0080 a0002c0003t0005g0177 others(8): Show |
13 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.641-775G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102788 | |||||||
chr14:104102819 | C | G | 1 | a0001c0001t0001g0152 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.641-744C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104102819 | |||||||
chr14:104103015 | C | T | 1 | a0001c0001t0005g0065 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.641-548C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103015 | |||||||
chr14:104103129 | T | C | 3 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0002c0003t0011g0159 |
3 | HG02647.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.641-434T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103129 | |||||||
chr14:104103148 | C | T | 1 | a0001c0001t0033g0134 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.641-415C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103148 | |||||||
chr14:104103151 | G | A | 1 | a0002c0003t0017g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.641-412G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103151 | |||||||
chr14:104103182 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0035g0133 |
2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.641-381C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103182 | |||||||
chr14:104103192 | C | T | 1 | a0002c0003t0005g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.641-371C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103192 | |||||||
chr14:104103242 | C | CG | 3 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0002c0003t0011g0159 |
3 | HG02647.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.641-321_641-320ins others(1): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103242 | |||||||
chr14:104103308 | C | T | 1 | a0001c0007t0008g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.641-255C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103308 | |||||||
chr14:104103372 | A | G | 12 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0029 others(9): Show |
18 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.641-191A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103372 | |||||||
chr14:104103376 | C | T | 1 | a0003c0004t0003g0096 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.641-187C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103376 | |||||||
chr14:104103385 | C | A | 1 | a0003c0004t0003g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.641-178C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103385 | |||||||
chr14:104103464 | C | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(130): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.641-99C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103464 | |||||||
chr14:104103541 | A | G | 1 | a0002c0002t0002g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.641-22A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 6/15 | chr14 | 104103541 | |||||||
chr14:104103685 | G | A | 1 | a0002c0003t0001g0189 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.753+10G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103685 | |||||||
chr14:104103685 | G | C | 1 | a0011c0015t0002g0228 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.753+10G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103685 | |||||||
chr14:104103739 | G | A | 1 | a0003c0004t0003g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.753+64G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103739 | |||||||
chr14:104103751 | C | T | 8 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0001c0024t0011g0064 others(5): Show |
8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.753+76C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103751 | |||||||
chr14:104103779 | C | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(104): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.753+104C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103779 | |||||||
chr14:104103782 | C | T | 1 | a0001c0001t0024g0040 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.753+107C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103782 | |||||||
chr14:104103914 | C | T | 1 | a0001c0007t0008g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.753+239C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104103914 | |||||||
chr14:104104075 | C | A | 14 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0029 others(11): Show |
22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.754-229C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104104075 | |||||||
chr14:104104115 | G | C | 1 | a0002c0002t0013g0190 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.754-189G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104104115 | |||||||
chr14:104104178 | G | A | 1 | a0001c0001t0024g0040 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.754-126G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104104178 | |||||||
chr14:104104292 | A | C | 7 | a0002c0003t0006g0053 a0002c0003t0006g0054 a0002c0003t0006g0055 others(4): Show |
10 | HG00735.hp1 HG01099.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.754-12A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 7/15 | chr14 | 104104292 | |||||||
chr14:104104534 | G | A | 1 | a0002c0005t0002g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.936+48G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/15 | chr14 | 104104534 | |||||||
chr14:104104557 | C | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0127 a0001c0001t0036g0015 |
4 | HG00423.hp1 HG02165.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-65C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/15 | chr14 | 104104557 | |||||||
chr14:104104567 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(246): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.937-55T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 8/15 | chr14 | 104104567 | |||||||
chr14:104104925 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1050+190C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/15 | chr14 | 104104925 | |||||||
chr14:104105102 | C | T | 14 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0029 others(11): Show |
22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1051-226C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/15 | chr14 | 104105102 | |||||||
chr14:104105161 | C | T | 1 | a0002c0002t0002g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1051-167C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/15 | chr14 | 104105161 | |||||||
chr14:104105184 | C | G | 1 | a0002c0002t0002g0188 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1051-144C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/15 | chr14 | 104105184 | |||||||
chr14:104105257 | G | A | 1 | a0001c0001t0005g0023 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1051-71G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 9/15 | chr14 | 104105257 | |||||||
chr14:104105457 | G | C | 2 | a0002c0002t0002g0165 a0002c0002t0002g0166 |
2 | HG02451.hp1 HG02647.hp2 |
splice_region_variant&intron_variant | LOW | c.1173+7G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105457 | |||||||
chr14:104105483 | C | G | 35 | a0002c0002t0019g0167 a0003c0004t0003g0002 a0003c0004t0003g0007 others(32): Show |
54 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1173+33C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105483 | |||||||
chr14:104105489 | A | C | 1 | a0003c0004t0003g0096 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1173+39A>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105489 | |||||||
chr14:104105489 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(245): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1173+39A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105489 | |||||||
chr14:104105536 | C | T | 1 | a0002c0002t0002g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1173+86C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105536 | |||||||
chr14:104105577 | C | T | 1 | a0002c0002t0002g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1173+127C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105577 | |||||||
chr14:104105766 | G | A | 4 | a0001c0024t0011g0064 a0002c0003t0017g0164 a0002c0003t0038g0044 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+316G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105766 | |||||||
chr14:104105824 | G | A | 1 | a0001c0001t0004g0070 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1173+374G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105824 | |||||||
chr14:104105989 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1173+539C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104105989 | |||||||
chr14:104106067 | A | T | 1 | a0001c0006t0028g0138 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1173+617A>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104106067 | |||||||
chr14:104106297 | G | A | 1 | a0002c0002t0002g0199 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1174-502G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104106297 | |||||||
chr14:104106330 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(102): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1174-469G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104106330 | |||||||
chr14:104106352 | C | T | 14 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0029 others(11): Show |
22 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1174-447C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104106352 | |||||||
chr14:104106564 | G | A | 1 | a0002c0002t0002g0009 | 4 | HG01192.hp1 HG01975.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-235G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 10/15 | chr14 | 104106564 | |||||||
chr14:104106932 | C | T | 5 | a0001c0024t0011g0064 a0002c0003t0017g0157 a0002c0003t0017g0164 others(2): Show |
5 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1269+38C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 11/15 | chr14 | 104106932 | |||||||
chr14:104107353 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(246): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
splice_region_variant&intron_variant | LOW | c.1433+8A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107353 | |||||||
chr14:104107479 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1433+134C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107479 | |||||||
chr14:104107556 | C | T | 1 | a0002c0003t0006g0055 | 2 | HG01099.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1433+211C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107556 | |||||||
chr14:104107696 | C | A | 1 | a0002c0003t0005g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1433+351C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107696 | |||||||
chr14:104107855 | C | T | 1 | a0002c0003t0010g0231 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1433+510C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107855 | |||||||
chr14:104107856 | G | A | 1 | a0002c0002t0013g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1433+511G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104107856 | |||||||
chr14:104108016 | C | T | 3 | a0001c0006t0002g0034 a0002c0003t0002g0171 a0002c0010t0002g0050 |
5 | HG02280.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1433+671C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108016 | |||||||
chr14:104108108 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1433+763C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108108 | |||||||
chr14:104108194 | C | T | 2 | a0001c0019t0010g0238 a0002c0013t0039g0161 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1433+849C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108194 | |||||||
chr14:104108241 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1433+896G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108241 | |||||||
chr14:104108424 | C | T | 1 | a0003c0004t0003g0091 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1434-805C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108424 | |||||||
chr14:104108439 | G | A | 6 | a0001c0007t0002g0241 a0001c0007t0008g0071 a0001c0007t0008g0081 others(3): Show |
7 | HG02615.hp2 HG02976.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1434-790G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108439 | |||||||
chr14:104108603 | A | G | 2 | a0001c0001t0001g0142 a0002c0003t0001g0204 |
2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1434-626A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108603 | |||||||
chr14:104108728 | C | A | 1 | a0002c0002t0019g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1434-501C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108728 | |||||||
chr14:104108793 | C | T | 32 | a0002c0002t0019g0167 a0003c0004t0003g0002 a0003c0004t0003g0007 others(29): Show |
50 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1434-436C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108793 | |||||||
chr14:104108873 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(86): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1434-356C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108873 | |||||||
chr14:104108953 | C | G | 32 | a0003c0004t0003g0002 a0003c0004t0003g0007 a0003c0004t0003g0011 others(29): Show |
51 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1434-276C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108953 | |||||||
chr14:104108989 | C | A | 32 | a0003c0004t0003g0002 a0003c0004t0003g0007 a0003c0004t0003g0011 others(29): Show |
51 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1434-240C>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104108989 | |||||||
chr14:104109000 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1434-229C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104109000 | |||||||
chr14:104109122 | C | G | 1 | a0003c0004t0003g0068 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1434-107C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104109122 | |||||||
chr14:104109129 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(243): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1434-100C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104109129 | |||||||
chr14:104109194 | C | G | 89 | a0001c0001t0001g0035 a0001c0001t0001g0105 a0001c0001t0002g0110 others(86): Show |
138 | HG00558.hp2 HG00639.hp1 HG00673.hp2 others(135): Show |
intron_variant | MODIFIER | c.1434-35C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 12/15 | chr14 | 104109194 | |||||||
chr14:104109343 | C | T | 1 | a0002c0003t0038g0044 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1520+28C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109343 | |||||||
chr14:104109532 | G | A | 75 | a0001c0001t0002g0110 a0001c0001t0004g0013 a0001c0001t0004g0024 others(72): Show |
111 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.1520+217G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109532 | |||||||
chr14:104109597 | CAT | C | 64 | a0001c0001t0002g0110 a0001c0006t0002g0034 a0001c0006t0002g0123 others(61): Show |
102 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(99): Show |
intron_variant | MODIFIER | c.1520+283_1520+284d others(4): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109597 | |||||||
chr14:104109601 | T | C | 8 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0001c0024t0011g0064 others(5): Show |
8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1520+286T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109601 | |||||||
chr14:104109668 | G | T | 1 | a0001c0007t0008g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1520+353G>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109668 | |||||||
chr14:104109888 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1520+573G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109888 | |||||||
chr14:104109897 | A | G | 3 | a0002c0003t0009g0172 a0002c0003t0009g0175 a0002c0003t0009g0176 |
3 | HG00280.hp2 HG00642.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1520+582A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104109897 | |||||||
chr14:104110111 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(93): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1520+796G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110111 | |||||||
chr14:104110128 | G | A | 1 | a0002c0002t0002g0052 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1520+813G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110128 | |||||||
chr14:104110131 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1520+816T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110131 | |||||||
chr14:104110326 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1520+1011C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110326 | |||||||
chr14:104110410 | C | G | 1 | a0003c0004t0003g0150 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1521-1092C>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110410 | |||||||
chr14:104110479 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(126): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1521-1023A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110479 | |||||||
chr14:104110547 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1521-955C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110547 | |||||||
chr14:104110607 | G | C | 1 | a0009c0021t0003g0067 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1521-895G>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110607 | |||||||
chr14:104110658 | C | T | 1 | a0002c0003t0037g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1521-844C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110658 | |||||||
chr14:104110670 | T | C | 2 | a0002c0002t0002g0195 a0002c0002t0002g0196 |
2 | HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1521-832T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110670 | |||||||
chr14:104110794 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(126): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1521-708G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110794 | |||||||
chr14:104110796 | G | A | 65 | a0001c0001t0002g0110 a0001c0006t0002g0034 a0001c0006t0002g0123 others(62): Show |
103 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(100): Show |
intron_variant | MODIFIER | c.1521-706G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110796 | |||||||
chr14:104110858 | C | T | 1 | a0003c0004t0003g0031 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1521-644C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104110858 | |||||||
chr14:104111056 | C | T | 1 | a0003c0004t0003g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1521-446C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111056 | |||||||
chr14:104111062 | G | A | 2 | a0001c0001t0007g0025 a0001c0001t0007g0080 |
3 | HG01891.hp1 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1521-440G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111062 | |||||||
chr14:104111192 | G | A | 1 | a0001c0001t0007g0117 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1521-310G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111192 | |||||||
chr14:104111223 | ATGTATGC others(5): Show |
A | 1 | a0002c0016t0006g0205 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1521-263_1521-252d others(14): Show |
ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 104111223 | ||||||
chr14:104111237 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1521-265G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111237 | |||||||
chr14:104111279 | A | G | 1 | a0003c0004t0003g0244 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1521-223A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111279 | |||||||
chr14:104111288 | C | T | 2 | a0006c0012t0023g0230 a0010c0011t0023g0149 |
2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1521-214C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111288 | |||||||
chr14:104111311 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0087 |
2 | HG01257.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1521-191A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111311 | |||||||
chr14:104111378 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1521-124T>C | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111378 | |||||||
chr14:104111480 | C | T | 4 | a0001c0007t0008g0071 a0001c0007t0008g0081 a0001c0007t0008g0082 others(1): Show |
4 | HG02976.hp2 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521-22C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111480 | |||||||
chr14:104111489 | C | T | 4 | a0001c0007t0008g0071 a0001c0007t0008g0081 a0001c0007t0008g0082 others(1): Show |
4 | HG02976.hp2 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521-13C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 13/15 | chr14 | 104111489 | |||||||
chr14:104111740 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1620+139C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 14/15 | chr14 | 104111740 | |||||||
chr14:104111741 | G | A | 1 | a0004c0008t0004g0021 | 3 | HG00639.hp1 HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1620+140G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 14/15 | chr14 | 104111741 | |||||||
chr14:104112091 | A | G | 4 | a0002c0002t0002g0057 a0002c0002t0013g0181 a0002c0002t0013g0190 others(1): Show |
5 | HG02132.hp1 NA18944.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1701+91A>G | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 15/15 | chr14 | 104112091 | |||||||
chr14:104112144 | C | T | 8 | a0001c0001t0011g0237 a0001c0001t0025g0236 a0001c0024t0011g0064 others(5): Show |
8 | HG02109.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1701+144C>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 15/15 | chr14 | 104112144 | |||||||
chr14:104112345 | A | T | 2 | a0006c0012t0023g0230 a0010c0011t0023g0149 |
2 | HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1702-179A>T | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 15/15 | chr14 | 104112345 | |||||||
chr14:104112480 | G | A | 13 | a0001c0001t0004g0013 a0001c0001t0004g0024 a0001c0001t0004g0029 others(10): Show |
20 | HG00639.hp1 HG01071.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1702-44G>A | ASPG | ENSG00000166183.16 | transcript | ENST00000551177.6 | protein_coding | 15/15 | chr14 | 104112480 |