Item | Value |
---|---|
geneid | 10491 |
ensemblid | ENSG00000170275.15 |
hgncid | 2379 |
symbol | CRTAP |
name | cartilage associated protein |
refseq_nuc | NM_006371.5 |
refseq_prot | NP_006362.1 |
ensembl_nuc | ENST00000320954.11 |
ensembl_prot | ENSP00000323696.5 |
mane_status | MANE Select |
chr | chr3 |
start | 33114014 |
end | 33147773 |
strand | + |
ver | v1.2 |
region | chr3:33114014-33147773 |
region5000 | chr3:33109014-33152773 |
regionname0 | CRTAP_chr3_33114014_33147773 |
regionname5000 | CRTAP_chr3_33109014_33152773 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 401 | 401 | 87 | 78 | 177 | 12 | 45 | 135 | CRTAP_chr3_33109014_33152773 | CRTAP | MEPGR others(396): Show |
chr3 | 33109014 | 33152773 |
a0002 | 0/0 | 401 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | MEPGR others(396): Show |
chr3 | 33109014 | 33152773 |
a0003 | 0/0 | 401 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | MEPGR others(396): Show |
chr3 | 33109014 | 33152773 |
a0004 | 0/0 | 401 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | MEPGR others(396): Show |
chr3 | 33109014 | 33152773 |
a0005 | 0/0 | 401 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | MEPGR others(396): Show |
chr3 | 33109014 | 33152773 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1203 | 155 | 23 | 46 | 57 | 7 | 20 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0001c0002 | 0/0 | 1203 | 107 | 12 | 5 | 81 | 1 | 8 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0001c0003 | 0/0 | 1203 | 84 | 17 | 21 | 26 | 4 | 16 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0001c0004 | 0/0 | 1203 | 24 | 12 | 2 | 9 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0001c0005 | 0/0 | 1203 | 11 | 11 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0001c0006 | 0/0 | 1203 | 11 | 6 | 1 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0001c0007 | 0/0 | 1203 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0001c0010 | 0/0 | 1203 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0001c0011 | 0/0 | 1203 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0001c0012 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0001c0013 | 0/0 | 1203 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0001c0014 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0002c0008 | 0/0 | 1203 | 3 | 0 | 0 | 0 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0003c0009 | 0/0 | 1203 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0004c0016 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 | ||
a0005c0015 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | ATGGA others(1198): Show |
chr3 | 33109014 | 33152773 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6595 | 11 | 1 | 5 | 2 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0002 | 0/0 | 6601 | 12 | 0 | 10 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0003 | 0/0 | 6595 | 55 | 3 | 10 | 33 | 1 | 8 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0004 | 0/0 | 6595 | 17 | 0 | 8 | 9 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0006 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0007 | 0/0 | 6595 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0008 | 0/0 | 6596 | 4 | 2 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6591): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0010 | 0/0 | 6595 | 6 | 0 | 3 | 0 | 2 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0011 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0012 | 0/0 | 6596 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6591): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0013 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0017 | 0/0 | 6594 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0019 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0020 | 0/0 | 6601 | 2 | 1 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0022 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0025 | 0/0 | 6594 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0027 | 0/0 | 6595 | 2 | 0 | 0 | 1 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0028 | 0/0 | 6594 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0029 | 0/1 | 6595 | 2 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0030 | 0/0 | 6595 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0031 | 0/0 | 6595 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0033 | 0/0 | 6595 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0034 | 0/0 | 6595 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0041 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0043 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0045 | 0/0 | 6595 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0046 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0054 | 0/0 | 6595 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0056 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0057 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0058 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0059 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0060 | 0/0 | 6595 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0061 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0062 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0064 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0065 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0066 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0069 | 0/0 | 6595 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0071 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0078 | 1/0 | 6595 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0080 | 0/0 | 6612 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6607): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0085 | 0/0 | 6595 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0001t0086 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0001 | 0/0 | 6595 | 70 | 3 | 5 | 54 | 0 | 8 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0003 | 0/0 | 6595 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0004 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0005 | 0/0 | 6594 | 2 | 1 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0007 | 0/0 | 6595 | 4 | 4 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0008 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6591): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0009 | 0/0 | 6595 | 8 | 0 | 0 | 7 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0011 | 0/0 | 6595 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0012 | 0/0 | 6596 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6591): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0037 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0047 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0048 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0049 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0050 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0051 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0052 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0053 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0063 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0068 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0002t0081 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0002 | 0/0 | 6601 | 57 | 10 | 15 | 19 | 4 | 9 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0003 | 0/0 | 6595 | 6 | 0 | 1 | 2 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0014 | 0/0 | 6601 | 3 | 0 | 1 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0015 | 0/0 | 6601 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0016 | 0/0 | 6601 | 3 | 0 | 0 | 2 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0021 | 0/0 | 6602 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6597): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0022 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0023 | 0/0 | 6600 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6595): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0024 | 0/0 | 6601 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0038 | 0/0 | 6600 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6595): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0039 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0040 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0044 | 0/0 | 6601 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0003t0055 | 0/0 | 6595 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0004t0001 | 0/0 | 6595 | 3 | 0 | 0 | 2 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0004t0005 | 0/0 | 6594 | 13 | 8 | 1 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0004t0019 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0004t0070 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0004t0072 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0004t0073 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0004t0074 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0004t0075 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0004t0076 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0004t0077 | 0/0 | 6594 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0005t0007 | 0/0 | 6595 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0005t0008 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6591): Show |
chr3 | 33109014 | 33152773 |
a0001c0005t0019 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0005t0026 | 0/0 | 6595 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0005t0035 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0005t0036 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0005t0082 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6591): Show |
chr3 | 33109014 | 33152773 |
a0001c0005t0083 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0001c0005t0084 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0006t0006 | 0/0 | 6595 | 8 | 4 | 0 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0006t0008 | 0/0 | 6596 | 2 | 1 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6591): Show |
chr3 | 33109014 | 33152773 |
a0001c0006t0079 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0007t0018 | 0/0 | 6595 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0010t0002 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0010t0042 | 0/0 | 6600 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6595): Show |
chr3 | 33109014 | 33152773 |
a0001c0011t0002 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0012t0067 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0001c0013t0002 | 0/0 | 6601 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0001c0014t0002 | 0/0 | 6601 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6596): Show |
chr3 | 33109014 | 33152773 |
a0002c0008t0013 | 0/0 | 6595 | 3 | 0 | 0 | 0 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0003c0009t0032 | 0/0 | 6595 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6590): Show |
chr3 | 33109014 | 33152773 |
a0004c0016t0005 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
a0005c0015t0005 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | CCTTT others(6589): Show |
chr3 | 33109014 | 33152773 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0001 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0008g0008 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0010g0003 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0010g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0012g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0013g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0017g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0017g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0019g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0020g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0020g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0022g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0025g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0027g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0027g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0028g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0028g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0029g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0029g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0030g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0030g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0031g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0033g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0033g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0034g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0041g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0043g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0045g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0046g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0054g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0056g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0057g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0058g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0059g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0060g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0061g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0062g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0064g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0065g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0066g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0069g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0071g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0078g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0080g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0085g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0001t0086g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0004 | 0/0 | 6 | 2 | 2 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0007g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0009g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0011g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0011g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0011g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0012g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0012g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0037g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0047g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0048g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0049g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0050g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0051g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0052g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0053g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0063g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0068g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0002t0081g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0002 | 0/0 | 11 | 1 | 2 | 4 | 2 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0003g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0014g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0014g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0014g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0015g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0015g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0015g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0016g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0016g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0016g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0021g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0021g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0022g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0023g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0023g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0024g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0038g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0039g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0040g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0044g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0003t0055g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0019g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0070g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0072g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0073g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0074g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0075g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0076g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0004t0077g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0007g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0019g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0026g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0026g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0035g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0036g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0082g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0083g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0005t0084g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0008g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0006t0079g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0007t0018g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0007t0018g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0010t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0010t0042g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0011t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0012t0067g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0013t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0001c0014t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0002c0008t0013g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0002c0008t0013g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0002c0008t0013g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0003c0009t0032g0048 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0004c0016t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
a0005c0015t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0002 | g0137 | EUR | GBR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00099 | hp2 | a0001 | c0001 | t0085 | g0003 | EUR | GBR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00140 | hp1 | a0001 | c0001 | t0027 | g0178 | EUR | GBR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0046 | EUR | GBR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00280 | hp1 | a0001 | c0002 | t0009 | g0213 | EUR | FIN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0095 | EUR | FIN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00323 | hp1 | a0001 | c0003 | t0002 | g0138 | EUR | FIN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0177 | EUR | FIN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00408 | hp2 | a0001 | c0003 | t0002 | g0112 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00438 | hp1 | a0001 | c0004 | t0072 | g0077 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00544 | hp1 | a0001 | c0001 | t0064 | g0097 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00544 | hp2 | a0001 | c0006 | t0006 | g0057 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00558 | hp1 | a0001 | c0003 | t0021 | g0161 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00558 | hp2 | a0001 | c0002 | t0009 | g0226 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00609 | hp1 | a0001 | c0001 | t0058 | g0087 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00639 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00639 | hp2 | a0001 | c0007 | t0018 | g0032 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00642 | hp1 | a0001 | c0003 | t0002 | g0132 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00673 | hp1 | a0001 | c0002 | t0009 | g0223 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00735 | hp1 | a0001 | c0001 | t0012 | g0099 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00741 | hp1 | a0001 | c0003 | t0002 | g0007 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01069 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01069 | hp2 | a0001 | c0003 | t0040 | g0127 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01071 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01074 | hp1 | a0001 | c0003 | t0002 | g0026 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01074 | hp2 | a0001 | c0003 | t0015 | g0261 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01081 | hp1 | a0001 | c0003 | t0002 | g0146 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01081 | hp2 | a0001 | c0003 | t0002 | g0123 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01099 | hp2 | a0001 | c0003 | t0002 | g0026 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01106 | hp1 | a0001 | c0003 | t0039 | g0014 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01106 | hp2 | a0001 | c0001 | t0010 | g0003 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01109 | hp1 | a0001 | c0003 | t0055 | g0029 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01109 | hp2 | a0001 | c0004 | t0077 | g0078 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01167 | hp2 | a0001 | c0003 | t0002 | g0148 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01168 | hp2 | a0001 | c0013 | t0002 | g0204 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01175 | hp2 | a0001 | c0003 | t0002 | g0014 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0176 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01243 | hp2 | a0001 | c0004 | t0005 | g0070 | AMR | PUR | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01255 | hp2 | a0001 | c0006 | t0008 | g0174 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01256 | hp2 | a0001 | c0001 | t0010 | g0003 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01261 | hp1 | a0001 | c0003 | t0002 | g0131 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01261 | hp2 | a0001 | c0003 | t0014 | g0169 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0029 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0301 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01361 | hp2 | a0001 | c0003 | t0002 | g0007 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01433 | hp1 | a0001 | c0001 | t0033 | g0024 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01433 | hp2 | a0001 | c0001 | t0043 | g0292 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01515 | hp1 | a0003 | c0009 | t0032 | g0048 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0002 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01516 | hp1 | a0001 | c0003 | t0002 | g0002 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01516 | hp2 | a0001 | c0001 | t0010 | g0003 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01517 | hp1 | a0001 | c0001 | t0010 | g0003 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01517 | hp2 | a0003 | c0009 | t0032 | g0048 | EUR | IBS | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01891 | hp1 | a0001 | c0001 | t0031 | g0021 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01891 | hp2 | a0001 | c0004 | t0005 | g0061 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01934 | hp1 | a0001 | c0001 | t0060 | g0001 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01934 | hp2 | a0001 | c0011 | t0002 | g0242 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01978 | hp1 | a0001 | c0001 | t0054 | g0006 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01981 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01993 | hp2 | a0001 | c0003 | t0002 | g0109 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02004 | hp2 | a0001 | c0003 | t0003 | g0120 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02015 | hp2 | a0001 | c0003 | t0002 | g0136 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02055 | hp2 | a0001 | c0002 | t0005 | g0208 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02056 | hp1 | a0001 | c0002 | t0051 | g0016 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02056 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02074 | hp2 | a0001 | c0003 | t0002 | g0111 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02083 | hp1 | a0001 | c0003 | t0016 | g0007 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02129 | hp1 | a0001 | c0001 | t0028 | g0084 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02132 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02135 | hp1 | a0001 | c0002 | t0011 | g0249 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02145 | hp1 | a0001 | c0001 | t0020 | g0049 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02145 | hp2 | a0001 | c0006 | t0006 | g0173 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02148 | hp2 | a0001 | c0001 | t0029 | g0083 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | CDX | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02155 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | CDX | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02165 | hp1 | a0001 | c0003 | t0003 | g0157 | EAS | CDX | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | CDX | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02257 | hp1 | a0001 | c0003 | t0002 | g0110 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02257 | hp2 | a0001 | c0010 | t0042 | g0069 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02258 | hp1 | a0001 | c0005 | t0026 | g0270 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02258 | hp2 | a0001 | c0002 | t0007 | g0037 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0281 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02280 | hp1 | a0001 | c0003 | t0002 | g0030 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02280 | hp2 | a0001 | c0004 | t0005 | g0011 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02300 | hp1 | a0001 | c0001 | t0020 | g0293 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | PEL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02451 | hp1 | a0001 | c0003 | t0022 | g0009 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02451 | hp2 | a0001 | c0005 | t0007 | g0264 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02523 | hp1 | a0001 | c0003 | t0003 | g0158 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02523 | hp2 | a0001 | c0002 | t0004 | g0253 | EAS | KHV | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02572 | hp1 | a0001 | c0003 | t0015 | g0263 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02572 | hp2 | a0001 | c0003 | t0002 | g0168 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02615 | hp1 | a0001 | c0001 | t0065 | g0296 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02615 | hp2 | a0001 | c0001 | t0013 | g0163 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02622 | hp2 | a0001 | c0005 | t0026 | g0269 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02630 | hp1 | a0001 | c0001 | t0086 | g0260 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02630 | hp2 | a0001 | c0014 | t0002 | g0271 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02647 | hp1 | a0001 | c0002 | t0008 | g0195 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02647 | hp2 | a0001 | c0004 | t0005 | g0074 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0233 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02698 | hp1 | a0001 | c0001 | t0034 | g0040 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02717 | hp1 | a0001 | c0006 | t0006 | g0175 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0287 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02735 | hp1 | a0001 | c0001 | t0030 | g0001 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02735 | hp2 | a0001 | c0003 | t0003 | g0028 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02738 | hp1 | a0001 | c0003 | t0002 | g0027 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02809 | hp1 | a0001 | c0007 | t0018 | g0032 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02809 | hp2 | a0001 | c0004 | t0005 | g0079 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02886 | hp1 | a0001 | c0002 | t0007 | g0202 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02886 | hp2 | a0001 | c0006 | t0079 | g0059 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02895 | hp1 | a0001 | c0005 | t0019 | g0191 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02896 | hp1 | a0001 | c0006 | t0006 | g0171 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02896 | hp2 | a0001 | c0002 | t0037 | g0215 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02897 | hp1 | a0001 | c0006 | t0006 | g0170 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02897 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02922 | hp1 | a0001 | c0001 | t0019 | g0156 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02922 | hp2 | a0001 | c0004 | t0005 | g0071 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02970 | hp1 | a0001 | c0003 | t0002 | g0030 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02970 | hp2 | a0001 | c0003 | t0024 | g0039 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02976 | hp1 | a0001 | c0005 | t0035 | g0298 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03017 | hp1 | a0001 | c0003 | t0002 | g0153 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03017 | hp2 | a0002 | c0008 | t0013 | g0053 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03041 | hp1 | a0001 | c0004 | t0005 | g0072 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0290 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03098 | hp1 | a0001 | c0004 | t0070 | g0255 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03098 | hp2 | a0001 | c0001 | t0022 | g0164 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03130 | hp1 | a0001 | c0003 | t0002 | g0167 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03130 | hp2 | a0001 | c0001 | t0017 | g0019 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03139 | hp1 | a0001 | c0005 | t0083 | g0186 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0279 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03195 | hp1 | a0001 | c0002 | t0007 | g0037 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03195 | hp2 | a0001 | c0003 | t0002 | g0009 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03209 | hp1 | a0001 | c0005 | t0008 | g0187 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03209 | hp2 | a0001 | c0004 | t0005 | g0011 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03225 | hp1 | a0001 | c0002 | t0050 | g0234 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03225 | hp2 | a0001 | c0002 | t0052 | g0203 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03453 | hp2 | a0001 | c0006 | t0008 | g0172 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03490 | hp1 | a0001 | c0003 | t0002 | g0002 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03491 | hp1 | a0001 | c0003 | t0003 | g0130 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0205 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03492 | hp1 | a0001 | c0003 | t0003 | g0028 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03516 | hp1 | a0001 | c0001 | t0071 | g0182 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03516 | hp2 | a0001 | c0001 | t0066 | g0054 | AFR | ESN | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0277 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03540 | hp2 | a0004 | c0016 | t0005 | g0011 | AFR | GWD | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03579 | hp1 | a0001 | c0001 | t0046 | g0284 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03579 | hp2 | a0001 | c0001 | t0017 | g0288 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03654 | hp1 | a0001 | c0001 | t0069 | g0089 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03669 | hp1 | a0001 | c0001 | t0025 | g0031 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03669 | hp2 | a0001 | c0003 | t0002 | g0027 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03688 | hp1 | a0001 | c0003 | t0002 | g0134 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03688 | hp2 | a0001 | c0003 | t0016 | g0273 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03704 | hp1 | a0001 | c0001 | t0025 | g0031 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03710 | hp1 | a0001 | c0003 | t0002 | g0007 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0149 | SAS | PJL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03831 | hp1 | a0001 | c0001 | t0010 | g0003 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03927 | hp1 | a0001 | c0001 | t0045 | g0104 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03927 | hp2 | a0001 | c0003 | t0002 | g0119 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03942 | hp1 | a0001 | c0001 | t0030 | g0272 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03942 | hp2 | a0001 | c0001 | t0034 | g0040 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04115 | hp2 | a0001 | c0003 | t0044 | g0124 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04184 | hp1 | a0001 | c0004 | t0001 | g0289 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04184 | hp2 | a0001 | c0003 | t0014 | g0064 | SAS | BEB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04199 | hp1 | a0002 | c0008 | t0013 | g0052 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04199 | hp2 | a0001 | c0003 | t0002 | g0125 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0002 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04204 | hp2 | a0002 | c0008 | t0013 | g0185 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | STU | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18522 | hp1 | a0001 | c0004 | t0019 | g0073 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18522 | hp2 | a0001 | c0005 | t0082 | g0188 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | CHB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | CHB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18906 | hp1 | a0001 | c0003 | t0023 | g0009 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18906 | hp2 | a0001 | c0001 | t0031 | g0021 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18939 | hp1 | a0001 | c0002 | t0011 | g0251 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18943 | hp1 | a0001 | c0003 | t0016 | g0285 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18943 | hp2 | a0001 | c0004 | t0001 | g0155 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18944 | hp2 | a0001 | c0002 | t0053 | g0218 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18946 | hp1 | a0001 | c0002 | t0009 | g0051 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18946 | hp2 | a0001 | c0002 | t0011 | g0038 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18949 | hp2 | a0001 | c0006 | t0006 | g0058 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18950 | hp1 | a0001 | c0006 | t0006 | g0060 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18951 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18953 | hp1 | a0001 | c0003 | t0002 | g0128 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18960 | hp1 | a0005 | c0015 | t0005 | g0076 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18962 | hp1 | a0001 | c0004 | t0005 | g0012 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18962 | hp2 | a0001 | c0001 | t0062 | g0092 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18965 | hp2 | a0001 | c0004 | t0005 | g0268 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18966 | hp2 | a0001 | c0002 | t0081 | g0219 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18969 | hp2 | a0001 | c0002 | t0012 | g0258 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18970 | hp1 | a0001 | c0004 | t0005 | g0012 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18971 | hp1 | a0001 | c0001 | t0027 | g0159 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18974 | hp2 | a0001 | c0003 | t0002 | g0129 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18975 | hp1 | a0001 | c0003 | t0002 | g0118 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18975 | hp2 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18978 | hp2 | a0001 | c0002 | t0063 | g0231 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18981 | hp1 | a0001 | c0003 | t0002 | g0117 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18986 | hp1 | a0001 | c0002 | t0012 | g0018 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18988 | hp1 | a0001 | c0001 | t0028 | g0085 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18988 | hp2 | a0001 | c0002 | t0012 | g0018 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18989 | hp1 | a0001 | c0001 | t0059 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18990 | hp2 | a0001 | c0002 | t0005 | g0246 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18991 | hp2 | a0001 | c0001 | t0080 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18997 | hp2 | a0001 | c0002 | t0009 | g0220 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18999 | hp1 | a0001 | c0002 | t0011 | g0038 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA18999 | hp2 | a0001 | c0002 | t0003 | g0214 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19001 | hp1 | a0001 | c0001 | t0061 | g0098 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19002 | hp1 | a0001 | c0003 | t0002 | g0114 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19002 | hp2 | a0001 | c0004 | t0005 | g0012 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19005 | hp1 | a0001 | c0004 | t0076 | g0065 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19010 | hp1 | a0001 | c0003 | t0002 | g0282 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19030 | hp1 | a0001 | c0010 | t0002 | g0066 | AFR | LWK | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19030 | hp2 | a0001 | c0004 | t0074 | g0067 | AFR | LWK | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19043 | hp1 | a0001 | c0001 | t0017 | g0019 | AFR | LWK | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19043 | hp2 | a0001 | c0012 | t0067 | g0193 | AFR | LWK | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19054 | hp1 | a0001 | c0003 | t0002 | g0122 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19054 | hp2 | a0001 | c0002 | t0009 | g0227 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19055 | hp1 | a0001 | c0002 | t0009 | g0210 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19055 | hp2 | a0001 | c0003 | t0002 | g0139 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19058 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19058 | hp2 | a0001 | c0002 | t0049 | g0194 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19062 | hp1 | a0001 | c0003 | t0002 | g0108 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19063 | hp2 | a0001 | c0003 | t0038 | g0121 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19065 | hp2 | a0001 | c0001 | t0033 | g0001 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19067 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19067 | hp2 | a0001 | c0002 | t0068 | g0190 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19068 | hp1 | a0001 | c0001 | t0011 | g0081 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19075 | hp1 | a0001 | c0003 | t0002 | g0126 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19075 | hp2 | a0001 | c0002 | t0009 | g0199 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19076 | hp2 | a0001 | c0002 | t0048 | g0267 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19077 | hp1 | a0001 | c0003 | t0002 | g0014 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19080 | hp1 | a0001 | c0004 | t0073 | g0075 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19080 | hp2 | a0001 | c0004 | t0001 | g0154 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19082 | hp2 | a0001 | c0001 | t0057 | g0086 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19084 | hp2 | a0001 | c0006 | t0006 | g0056 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19085 | hp1 | a0001 | c0003 | t0021 | g0160 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19085 | hp2 | a0001 | c0002 | t0047 | g0018 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19087 | hp2 | a0001 | c0003 | t0002 | g0133 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19088 | hp2 | a0001 | c0001 | t0056 | g0147 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19240 | hp1 | a0001 | c0005 | t0084 | g0266 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA19240 | hp2 | a0001 | c0004 | t0005 | g0062 | AFR | YRI | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20129 | hp1 | a0001 | c0003 | t0023 | g0189 | AFR | ASW | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | GIH | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20905 | hp2 | a0001 | c0003 | t0014 | g0115 | SAS | GIH | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01123 | hp1 | a0001 | c0001 | t0041 | g0295 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG01123 | hp2 | a0001 | c0003 | t0002 | g0135 | AMR | CLM | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02109 | hp1 | a0001 | c0003 | t0002 | g0002 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02109 | hp2 | a0001 | c0003 | t0002 | g0166 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02486 | hp1 | a0001 | c0003 | t0024 | g0039 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02486 | hp2 | a0001 | c0003 | t0015 | g0262 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02559 | hp1 | a0001 | c0005 | t0036 | g0297 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG02559 | hp2 | a0001 | c0003 | t0002 | g0165 | AFR | ACB | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03471 | hp1 | a0001 | c0002 | t0007 | g0235 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG03471 | hp2 | a0001 | c0005 | t0007 | g0265 | AFR | MSL | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG06807 | hp1 | a0001 | c0003 | t0002 | g0009 | AFR | USA | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
HG06807 | hp2 | a0001 | c0004 | t0075 | g0068 | AFR | USA | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0184 | AFR | USA | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
NA20300 | hp2 | a0001 | c0007 | t0018 | g0256 | AFR | USA | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
homoSapiens | chm13v2 | a0001 | c0001 | t0029 | g0091 | REF | REF | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
homoSapiens | grch38p0 | a0001 | c0001 | t0078 | g0019 | REF | REF | CRTAP_chr3_33109014_33152773 | CRTAP | chr3 | 33109014 | 33152773 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:33114372 | G | T | 1 | a0004 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.295G>T | p.Gly99Cys | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/7 | 359/6595 | 295/1206 | 99/401 | chr3 | 33114372 | |||
chr3:33124427 | T | C | 1 | a0002 | 3 | HG03017.hp2 HG04199.hp1 HG04204.hp2 |
missense_variant | MODERATE | c.641T>C | p.Val214Ala | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/7 | 705/6595 | 641/1206 | 214/401 | chr3 | 33124427 | |||
chr3:33132608 | C | G | 1 | a0005 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.976C>G | p.Gln326Glu | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/7 | 1040/6595 | 976/1206 | 326/401 | chr3 | 33132608 | |||
chr3:33134242 | G | A | 1 | a0003 | 2 | HG01515.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.1129G>A | p.Glu377Lys | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/7 | 1193/6595 | 1129/1206 | 377/401 | chr3 | 33134242 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:33114290 | G | A | 6 | a0001c0002 a0001c0005 a0001c0007 others(3): Show |
124 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(121): Show |
synonymous_variant | LOW | c.213G>A | p.Leu71Leu | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/7 | 277/6595 | 213/1206 | 71/401 | chr3 | 33114290 | |||
chr3:33120406 | C | T | 7 | a0001c0002 a0001c0004 a0001c0007 others(4): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
synonymous_variant | LOW | c.534C>T | p.Asp178Asp | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/7 | 598/6595 | 534/1206 | 178/401 | chr3 | 33120406 | |||
chr3:33120430 | A | G | 3 | a0001c0006 a0001c0012 a0001c0014 |
13 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(10): Show |
synonymous_variant | LOW | c.558A>G | p.Ala186Ala | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/7 | 622/6595 | 558/1206 | 186/401 | chr3 | 33120430 | |||
chr3:33130033 | C | T | 2 | a0001c0007 a0001c0012 |
4 | HG00639.hp2 HG02809.hp1 NA19043.hp2 others(1): Show |
synonymous_variant | LOW | c.888C>T | p.Thr296Thr | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/7 | 952/6595 | 888/1206 | 296/401 | chr3 | 33130033 | |||
chr3:33132664 | T | G | 5 | a0001c0003 a0001c0010 a0001c0011 others(2): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
synonymous_variant | LOW | c.1032T>G | p.Thr344Thr | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/7 | 1096/6595 | 1032/1206 | 344/401 | chr3 | 33132664 | |||
chr3:33132676 | G | A | 5 | a0001c0003 a0001c0010 a0001c0011 others(2): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
synonymous_variant | LOW | c.1044G>A | p.Ser348Ser | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/7 | 1108/6595 | 1044/1206 | 348/401 | chr3 | 33132676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:33142479 | C | T | 1 | a0001c0001t0086 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 31 | chr3 | 33142479 | ||||||
chr3:33142717 | C | T | 2 | a0001c0001t0010 a0001c0001t0085 |
7 | HG00099.hp2 HG01106.hp2 HG01243.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*269C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 269 | chr3 | 33142717 | ||||||
chr3:33142736 | C | T | 4 | a0001c0001t0019 a0001c0004t0019 a0001c0005t0019 others(1): Show |
4 | HG02895.hp1 HG02922.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*288C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 288 | chr3 | 33142736 | ||||||
chr3:33143225 | C | A | 2 | a0001c0005t0035 a0001c0005t0036 |
2 | HG02559.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*777C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 777 | chr3 | 33143225 | ||||||
chr3:33143430 | A | G | 1 | a0001c0002t0009 | 8 | HG00280.hp1 HG00558.hp2 HG00673.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*982A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 982 | chr3 | 33143430 | ||||||
chr3:33143489 | C | T | 2 | a0001c0005t0082 a0001c0005t0083 |
2 | HG03139.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1041C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1041 | chr3 | 33143489 | ||||||
chr3:33143502 | T | C | 1 | a0001c0002t0037 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1054T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1054 | chr3 | 33143502 | ||||||
chr3:33143535 | G | GGAACTA | 22 | a0001c0001t0002 a0001c0001t0020 a0001c0001t0022 others(19): Show |
99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1090_*1095dupACTA others(2): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1096 | INFO_REALIGN_3_PRIME | chr3 | 33143535 | |||||
chr3:33143572 | C | A | 1 | a0001c0001t0025 | 2 | HG03669.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1124C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1124 | chr3 | 33143572 | ||||||
chr3:33143623 | A | C | 1 | a0001c0007t0018 | 3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1175A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1175 | chr3 | 33143623 | ||||||
chr3:33143649 | A | ATGTAGTG others(10): Show |
1 | a0001c0001t0080 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1204_*1220dupTAGT others(13): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1221 | INFO_REALIGN_3_PRIME | chr3 | 33143649 | |||||
chr3:33143651 | G | T | 1 | a0001c0002t0081 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1203G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1203 | chr3 | 33143651 | ||||||
chr3:33143656 | G | T | 1 | a0001c0002t0081 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1208G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1208 | chr3 | 33143656 | ||||||
chr3:33143809 | G | A | 1 | a0001c0001t0045 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1361G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1361 | chr3 | 33143809 | ||||||
chr3:33143915 | G | A | 29 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(26): Show |
126 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1467G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1467 | chr3 | 33143915 | ||||||
chr3:33144030 | C | A | 22 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0011 others(19): Show |
93 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1582C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1582 | chr3 | 33144030 | ||||||
chr3:33144306 | T | A | 98 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(95): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
3_prime_UTR_variant | MODIFIER | c.*1858T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1858 | chr3 | 33144306 | ||||||
chr3:33144309 | A | G | 1 | a0001c0003t0044 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1861A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1861 | chr3 | 33144309 | ||||||
chr3:33144367 | A | G | 12 | a0001c0001t0025 a0001c0001t0064 a0001c0002t0005 others(9): Show |
26 | HG00438.hp1 HG00544.hp1 HG01109.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1919A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 1919 | chr3 | 33144367 | ||||||
chr3:33144595 | A | G | 26 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0025 others(23): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2147A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2147 | chr3 | 33144595 | ||||||
chr3:33144864 | T | C | 36 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(33): Show |
153 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*2416T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2416 | chr3 | 33144864 | ||||||
chr3:33144922 | T | G | 2 | a0001c0001t0020 a0001c0001t0043 |
3 | HG01433.hp2 HG02145.hp1 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2474T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2474 | chr3 | 33144922 | ||||||
chr3:33145076 | G | A | 1 | a0001c0007t0018 | 3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2628G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2628 | chr3 | 33145076 | ||||||
chr3:33145136 | G | A | 3 | a0001c0001t0019 a0001c0004t0019 a0001c0005t0019 |
3 | HG02895.hp1 HG02922.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2688G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2688 | chr3 | 33145136 | ||||||
chr3:33145324 | C | T | 2 | a0001c0004t0077 a0001c0005t0036 |
2 | HG01109.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2876C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2876 | chr3 | 33145324 | ||||||
chr3:33145349 | G | C | 15 | a0001c0001t0025 a0001c0001t0028 a0001c0001t0031 others(12): Show |
31 | HG00438.hp1 HG00609.hp1 HG01243.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2901G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2901 | chr3 | 33145349 | ||||||
chr3:33145391 | A | G | 2 | a0001c0002t0050 a0001c0003t0055 |
2 | HG01109.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2943A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 2943 | chr3 | 33145391 | ||||||
chr3:33145453 | G | A | 5 | a0001c0001t0007 a0001c0001t0046 a0001c0002t0007 others(2): Show |
10 | HG02258.hp2 HG02451.hp2 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3005G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3005 | chr3 | 33145453 | ||||||
chr3:33145572 | G | A | 1 | a0001c0004t0072 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3124G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3124 | chr3 | 33145572 | ||||||
chr3:33145578 | A | G | 1 | a0001c0005t0035 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3130A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3130 | chr3 | 33145578 | ||||||
chr3:33145590 | G | A | 19 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0029 others(16): Show |
89 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*3142G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3142 | chr3 | 33145590 | ||||||
chr3:33145593 | A | G | 5 | a0001c0001t0007 a0001c0001t0046 a0001c0002t0007 others(2): Show |
10 | HG02258.hp2 HG02451.hp2 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3145A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3145 | chr3 | 33145593 | ||||||
chr3:33145691 | A | C | 5 | a0001c0001t0007 a0001c0001t0046 a0001c0002t0007 others(2): Show |
10 | HG02258.hp2 HG02451.hp2 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3243A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3243 | chr3 | 33145691 | ||||||
chr3:33145817 | G | A | 1 | a0001c0001t0059 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3369G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3369 | chr3 | 33145817 | ||||||
chr3:33145902 | C | T | 1 | a0001c0001t0071 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3454C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3454 | chr3 | 33145902 | ||||||
chr3:33145912 | A | C | 1 | a0001c0005t0082 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3464A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3464 | chr3 | 33145912 | ||||||
chr3:33145933 | G | A | 20 | a0001c0001t0002 a0001c0001t0020 a0001c0001t0022 others(17): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*3485G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3485 | chr3 | 33145933 | ||||||
chr3:33146028 | T | TA | 5 | a0001c0001t0012 a0001c0001t0057 a0001c0002t0012 others(2): Show |
8 | HG00558.hp1 HG00735.hp1 NA18969.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3592dupA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3593 | INFO_REALIGN_3_PRIME | chr3 | 33146028 | |||||
chr3:33146035 | A | C | 1 | a0001c0001t0085 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3587A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3587 | chr3 | 33146035 | ||||||
chr3:33146040 | AC | A | 1 | a0001c0007t0018 | 3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3593delC | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3593 | chr3 | 33146040 | ||||||
chr3:33146183 | C | T | 1 | a0001c0012t0067 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3735C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3735 | chr3 | 33146183 | ||||||
chr3:33146241 | C | T | 16 | a0001c0001t0025 a0001c0001t0028 a0001c0001t0031 others(13): Show |
32 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3793C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3793 | chr3 | 33146241 | ||||||
chr3:33146320 | T | C | 1 | a0001c0004t0073 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3872T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3872 | chr3 | 33146320 | ||||||
chr3:33146339 | C | A | 2 | a0001c0001t0022 a0001c0003t0022 |
2 | HG02451.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3891C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3891 | chr3 | 33146339 | ||||||
chr3:33146339 | C | T | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(22): Show |
136 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*3891C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3891 | chr3 | 33146339 | ||||||
chr3:33146361 | C | T | 1 | a0001c0004t0074 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3913C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3913 | chr3 | 33146361 | ||||||
chr3:33146397 | C | T | 16 | a0001c0001t0025 a0001c0001t0028 a0001c0001t0031 others(13): Show |
32 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3949C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 3949 | chr3 | 33146397 | ||||||
chr3:33146572 | G | A | 1 | a0001c0003t0039 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4124G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4124 | chr3 | 33146572 | ||||||
chr3:33146577 | T | C | 1 | a0001c0001t0031 | 2 | HG01891.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4129T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4129 | chr3 | 33146577 | ||||||
chr3:33146592 | A | G | 2 | a0001c0001t0062 a0001c0001t0064 |
2 | HG00544.hp1 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4144A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4144 | chr3 | 33146592 | ||||||
chr3:33146638 | C | T | 1 | a0001c0001t0061 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4190C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4190 | chr3 | 33146638 | ||||||
chr3:33146699 | G | C | 1 | a0001c0001t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4251G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4251 | chr3 | 33146699 | ||||||
chr3:33146704 | A | G | 17 | a0001c0001t0025 a0001c0001t0028 a0001c0001t0031 others(14): Show |
33 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4256A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4256 | chr3 | 33146704 | ||||||
chr3:33146892 | T | TA | 5 | a0001c0001t0008 a0001c0002t0008 a0001c0005t0008 others(2): Show |
9 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4457dupA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4458 | INFO_REALIGN_3_PRIME | chr3 | 33146892 | |||||
chr3:33146892 | TA | T | 23 | a0001c0001t0017 a0001c0001t0025 a0001c0001t0028 others(20): Show |
41 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4457delA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4457 | INFO_REALIGN_3_PRIME | chr3 | 33146892 | |||||
chr3:33147071 | A | C | 1 | a0001c0001t0041 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4623A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4623 | chr3 | 33147071 | ||||||
chr3:33147153 | G | T | 1 | a0001c0005t0036 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4705G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4705 | chr3 | 33147153 | ||||||
chr3:33147199 | T | C | 1 | a0001c0003t0040 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4751T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4751 | chr3 | 33147199 | ||||||
chr3:33147222 | C | T | 10 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0017 others(7): Show |
26 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4774C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 4774 | chr3 | 33147222 | ||||||
chr3:33147453 | G | T | 1 | a0001c0004t0070 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5005G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5005 | chr3 | 33147453 | ||||||
chr3:33147482 | C | T | 1 | a0001c0010t0042 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5034C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5034 | chr3 | 33147482 | ||||||
chr3:33147488 | A | G | 1 | a0001c0006t0079 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5040A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5040 | chr3 | 33147488 | ||||||
chr3:33147718 | A | C | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5270A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5270 | chr3 | 33147718 | ||||||
chr3:33147719 | A | G | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5271A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5271 | chr3 | 33147719 | ||||||
chr3:33147723 | A | C | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5275A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5275 | chr3 | 33147723 | ||||||
chr3:33147724 | A | G | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5276A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5276 | chr3 | 33147724 | ||||||
chr3:33147726 | G | C | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5278G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5278 | chr3 | 33147726 | ||||||
chr3:33147728 | T | A | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5280T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5280 | chr3 | 33147728 | ||||||
chr3:33147730 | T | G | 1 | a0001c0001t0060 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5282T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 7/7 | 5282 | chr3 | 33147730 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:33114624 | G | T | 1 | a0001c0001t0003g0301 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.471+76G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114624 | |||||||
chr3:33114643 | C | T | 1 | a0001c0001t0003g0300 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.471+95C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114643 | |||||||
chr3:33114643 | CTCCAGTT others(8): Show |
C | 1 | a0001c0002t0001g0050 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.471+96_471+110delT others(14): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114643 | |||||||
chr3:33114664 | C | T | 1 | a0001c0002t0001g0299 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.471+116C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114664 | |||||||
chr3:33114675 | G | T | 2 | a0001c0005t0035g0298 a0001c0005t0036g0297 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.471+127G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114675 | |||||||
chr3:33114704 | T | C | 282 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(279): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.471+156T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114704 | |||||||
chr3:33114718 | T | C | 1 | a0001c0002t0009g0051 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.471+170T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114718 | |||||||
chr3:33114722 | C | G | 1 | a0001c0014t0002g0271 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471+174C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114722 | |||||||
chr3:33114777 | C | G | 1 | a0001c0014t0002g0271 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471+229C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114777 | |||||||
chr3:33114799 | C | A | 1 | a0001c0014t0002g0271 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.471+251C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114799 | |||||||
chr3:33114802 | C | T | 2 | a0001c0005t0026g0269 a0001c0005t0026g0270 |
2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.471+254C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114802 | |||||||
chr3:33114813 | C | T | 1 | a0001c0004t0005g0268 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.471+265C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114813 | |||||||
chr3:33114843 | A | G | 107 | a0001c0001t0086g0260 a0001c0002t0001g0004 a0001c0002t0001g0005 others(104): Show |
132 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.471+295A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114843 | |||||||
chr3:33114866 | C | T | 1 | a0002c0008t0013g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.471+318C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114866 | |||||||
chr3:33114955 | T | G | 1 | a0001c0001t0003g0020 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.471+407T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114955 | |||||||
chr3:33114974 | C | T | 11 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0049 others(8): Show |
14 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.471+426C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33114974 | |||||||
chr3:33115008 | A | G | 2 | a0001c0005t0026g0269 a0001c0005t0026g0270 |
2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.471+460A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115008 | |||||||
chr3:33115553 | C | G | 1 | a0001c0002t0048g0267 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.471+1005C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115553 | |||||||
chr3:33115656 | A | T | 1 | a0001c0001t0003g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.471+1108A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115656 | |||||||
chr3:33115661 | T | A | 2 | a0002c0008t0013g0052 a0002c0008t0013g0053 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.471+1113T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115661 | |||||||
chr3:33115758 | T | G | 1 | a0001c0001t0003g0301 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.471+1210T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115758 | |||||||
chr3:33115779 | A | G | 3 | a0001c0005t0007g0264 a0001c0005t0007g0265 a0001c0005t0084g0266 |
3 | HG02451.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.471+1231A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115779 | |||||||
chr3:33115877 | C | T | 5 | a0001c0001t0086g0260 a0001c0003t0015g0261 a0001c0003t0015g0262 others(2): Show |
6 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+1329C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115877 | |||||||
chr3:33115923 | T | TA | 16 | a0001c0001t0031g0021 a0001c0001t0066g0054 a0001c0001t0086g0260 others(13): Show |
18 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.471+1384dupA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33115923 | ||||||
chr3:33115968 | A | C | 16 | a0001c0001t0031g0021 a0001c0001t0066g0054 a0001c0001t0086g0260 others(13): Show |
18 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.471+1420A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33115968 | |||||||
chr3:33116024 | T | C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0291 |
3 | HG00140.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.471+1476T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116024 | |||||||
chr3:33116179 | A | T | 4 | a0001c0002t0001g0259 a0001c0002t0012g0018 a0001c0002t0012g0258 others(1): Show |
5 | NA18969.hp2 NA18981.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+1631A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116179 | |||||||
chr3:33116360 | A | G | 19 | a0001c0001t0001g0179 a0001c0001t0002g0177 a0001c0001t0003g0003 others(16): Show |
24 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.471+1812A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116360 | |||||||
chr3:33116384 | A | G | 1 | a0001c0002t0001g0257 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.471+1836A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116384 | |||||||
chr3:33116451 | A | G | 16 | a0001c0001t0031g0021 a0001c0001t0066g0054 a0001c0001t0086g0260 others(13): Show |
18 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.471+1903A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116451 | |||||||
chr3:33116655 | A | G | 16 | a0001c0001t0031g0021 a0001c0001t0066g0054 a0001c0001t0086g0260 others(13): Show |
18 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.471+2107A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116655 | |||||||
chr3:33116661 | G | A | 1 | a0001c0002t0001g0299 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.471+2113G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116661 | |||||||
chr3:33116727 | C | T | 1 | a0001c0007t0018g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.471+2179C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116727 | |||||||
chr3:33116791 | T | C | 17 | a0001c0001t0003g0055 a0001c0001t0031g0021 a0001c0001t0066g0054 others(14): Show |
19 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.471+2243T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116791 | |||||||
chr3:33116827 | T | C | 22 | a0001c0001t0031g0021 a0001c0001t0066g0054 a0001c0001t0086g0260 others(19): Show |
24 | HG00544.hp2 HG01074.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.471+2279T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116827 | |||||||
chr3:33116831 | C | T | 1 | a0001c0003t0014g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.471+2283C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33116831 | |||||||
chr3:33117107 | C | CA | 17 | a0001c0001t0031g0021 a0001c0001t0066g0054 a0001c0001t0086g0260 others(14): Show |
19 | HG01074.hp2 HG01891.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.471+2567dupA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33117107 | ||||||
chr3:33117127 | G | A | 23 | a0001c0001t0002g0063 a0001c0003t0014g0064 a0001c0004t0005g0011 others(20): Show |
26 | HG00438.hp1 HG00738.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.471+2579G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117127 | |||||||
chr3:33117177 | A | G | 1 | a0001c0004t0070g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.471+2629A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117177 | |||||||
chr3:33117178 | T | C | 1 | a0001c0001t0003g0080 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.471+2630T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117178 | |||||||
chr3:33117256 | T | C | 6 | a0001c0006t0006g0170 a0001c0006t0006g0171 a0001c0006t0006g0173 others(3): Show |
6 | HG01255.hp2 HG02145.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+2708T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117256 | |||||||
chr3:33117420 | G | A | 271 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(268): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.471+2872G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117420 | |||||||
chr3:33117425 | A | G | 1 | a0001c0002t0001g0254 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.471+2877A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117425 | |||||||
chr3:33117459 | C | A | 3 | a0001c0001t0086g0260 a0001c0003t0015g0261 a0001c0003t0015g0262 |
3 | HG01074.hp2 HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.472-2885C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117459 | |||||||
chr3:33117711 | C | T | 12 | a0001c0002t0001g0243 a0001c0002t0001g0244 a0001c0002t0001g0245 others(9): Show |
13 | HG02027.hp1 HG02040.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.472-2633C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117711 | |||||||
chr3:33117774 | A | G | 112 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(109): Show |
150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.472-2570A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117774 | |||||||
chr3:33117861 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.472-2483C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33117861 | |||||||
chr3:33117948 | A | ATTCC | 2 | a0001c0001t0031g0021 a0001c0001t0066g0054 |
3 | HG01891.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.472-2393_472-2390d others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33117948 | ||||||
chr3:33117951 | C | CCTTT | 9 | a0001c0001t0011g0081 a0001c0002t0068g0190 a0001c0004t0005g0061 others(6): Show |
9 | HG01891.hp2 HG02559.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.472-2372_472-2369d others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33117951 | ||||||
chr3:33118255 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.472-2089G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118255 | |||||||
chr3:33118304 | A | G | 6 | a0001c0001t0001g0162 a0001c0001t0027g0159 a0001c0003t0003g0157 others(3): Show |
6 | HG00408.hp1 HG00558.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-2040A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118304 | |||||||
chr3:33118311 | C | T | 3 | a0001c0001t0031g0021 a0001c0001t0066g0054 a0001c0004t0070g0255 |
4 | HG01891.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-2033C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118311 | |||||||
chr3:33118320 | G | A | 1 | a0001c0002t0012g0258 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.472-2024G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118320 | |||||||
chr3:33118455 | A | C | 3 | a0001c0001t0019g0156 a0001c0005t0026g0269 a0001c0005t0026g0270 |
3 | HG02258.hp1 HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.472-1889A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118455 | |||||||
chr3:33118574 | A | G | 1 | a0001c0001t0003g0082 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.472-1770A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118574 | |||||||
chr3:33118884 | G | A | 5 | a0001c0001t0086g0260 a0001c0003t0015g0261 a0001c0003t0015g0262 others(2): Show |
6 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-1460G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118884 | |||||||
chr3:33118915 | G | A | 222 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(219): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.472-1429G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118915 | |||||||
chr3:33118943 | G | A | 1 | a0001c0005t0007g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.472-1401G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118943 | |||||||
chr3:33118944 | G | A | 1 | a0001c0005t0007g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.472-1400G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33118944 | |||||||
chr3:33119062 | T | C | 2 | a0001c0002t0001g0192 a0001c0002t0001g0257 |
2 | HG00621.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.472-1282T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119062 | |||||||
chr3:33119213 | A | G | 1 | a0001c0001t0003g0151 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.472-1131A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119213 | |||||||
chr3:33119246 | A | G | 2 | a0002c0008t0013g0052 a0002c0008t0013g0053 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.472-1098A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119246 | |||||||
chr3:33119251 | T | C | 6 | a0001c0006t0006g0056 a0001c0006t0006g0057 a0001c0006t0006g0058 others(3): Show |
6 | HG00544.hp2 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-1093T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119251 | |||||||
chr3:33119311 | A | C | 1 | a0001c0001t0065g0296 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.472-1033A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119311 | |||||||
chr3:33119403 | A | G | 8 | a0001c0002t0001g0010 a0001c0002t0001g0236 a0001c0002t0001g0237 others(5): Show |
11 | HG00609.hp2 HG02027.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.472-941A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119403 | |||||||
chr3:33119498 | A | AT | 19 | a0001c0001t0007g0184 a0001c0003t0015g0261 a0001c0003t0015g0262 others(16): Show |
20 | HG00544.hp2 HG01074.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.472-837dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33119498 | ||||||
chr3:33119498 | A | ATTT | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-839_472-837dup others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33119498 | ||||||
chr3:33119520 | ATTG | A | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-821_472-819del others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 33119520 | ||||||
chr3:33119606 | T | C | 1 | a0001c0004t0076g0065 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.472-738T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119606 | |||||||
chr3:33119614 | T | C | 1 | a0001c0002t0001g0243 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.472-730T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119614 | |||||||
chr3:33119621 | T | C | 2 | a0001c0003t0023g0189 a0001c0011t0002g0242 |
2 | HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.472-723T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119621 | |||||||
chr3:33119661 | A | C | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-683A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119661 | |||||||
chr3:33119673 | G | T | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-671G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119673 | |||||||
chr3:33119766 | A | G | 6 | a0001c0006t0006g0056 a0001c0006t0006g0057 a0001c0006t0006g0058 others(3): Show |
6 | HG00544.hp2 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-578A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119766 | |||||||
chr3:33119777 | A | T | 2 | a0001c0001t0003g0149 a0001c0001t0003g0150 |
2 | HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.472-567A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119777 | |||||||
chr3:33119862 | C | T | 1 | a0001c0003t0002g0148 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.472-482C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119862 | |||||||
chr3:33119863 | G | A | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-481G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119863 | |||||||
chr3:33119882 | T | C | 2 | a0001c0001t0007g0184 a0001c0005t0007g0264 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.472-462T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119882 | |||||||
chr3:33119912 | T | C | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-432T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119912 | |||||||
chr3:33119942 | G | A | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-402G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33119942 | |||||||
chr3:33120087 | G | A | 4 | a0001c0003t0015g0261 a0001c0003t0015g0262 a0001c0003t0015g0263 others(1): Show |
5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-257G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33120087 | |||||||
chr3:33120208 | C | A | 7 | a0001c0005t0007g0265 a0001c0005t0008g0187 a0001c0005t0035g0298 others(4): Show |
7 | HG02559.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.472-136C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33120208 | |||||||
chr3:33120210 | T | G | 1 | a0001c0002t0049g0194 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.472-134T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33120210 | |||||||
chr3:33120237 | A | G | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-107A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33120237 | |||||||
chr3:33120253 | A | G | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.472-91A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 1/6 | chr3 | 33120253 | |||||||
chr3:33120591 | T | C | 2 | a0001c0001t0007g0184 a0001c0005t0007g0264 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.621+98T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120591 | |||||||
chr3:33120679 | C | T | 4 | a0001c0001t0001g0162 a0001c0001t0027g0159 a0001c0003t0021g0160 others(1): Show |
4 | HG00408.hp1 HG00558.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+186C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120679 | |||||||
chr3:33120681 | G | A | 2 | a0001c0001t0007g0184 a0001c0005t0007g0264 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.621+188G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120681 | |||||||
chr3:33120757 | A | C | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.621+264A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120757 | |||||||
chr3:33120821 | A | G | 2 | a0001c0003t0023g0189 a0001c0011t0002g0242 |
2 | HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.621+328A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120821 | |||||||
chr3:33120871 | T | A | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.621+378T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120871 | |||||||
chr3:33120884 | C | T | 1 | a0001c0001t0056g0147 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.621+391C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120884 | |||||||
chr3:33120972 | A | T | 2 | a0002c0008t0013g0052 a0002c0008t0013g0053 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.621+479A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120972 | |||||||
chr3:33120998 | G | A | 8 | a0001c0001t0001g0179 a0001c0001t0002g0177 a0001c0001t0003g0003 others(5): Show |
12 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.621+505G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33120998 | |||||||
chr3:33121040 | A | C | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.621+547A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121040 | |||||||
chr3:33121130 | T | C | 112 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(109): Show |
139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.621+637T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121130 | |||||||
chr3:33121175 | G | A | 1 | a0001c0004t0070g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.621+682G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121175 | |||||||
chr3:33121254 | C | T | 1 | a0001c0003t0002g0146 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.621+761C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121254 | |||||||
chr3:33121256 | A | G | 87 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0010 others(84): Show |
110 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.621+763A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121256 | |||||||
chr3:33121270 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(133): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.621+777G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121270 | |||||||
chr3:33121344 | A | G | 25 | a0001c0002t0008g0195 a0001c0004t0005g0011 a0001c0004t0005g0012 others(22): Show |
29 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.621+851A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121344 | |||||||
chr3:33121354 | A | G | 25 | a0001c0002t0008g0195 a0001c0004t0005g0011 a0001c0004t0005g0012 others(22): Show |
29 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.621+861A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121354 | |||||||
chr3:33121369 | G | A | 1 | a0001c0001t0028g0084 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.621+876G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121369 | |||||||
chr3:33121380 | C | T | 25 | a0001c0002t0008g0195 a0001c0004t0005g0011 a0001c0004t0005g0012 others(22): Show |
29 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.621+887C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121380 | |||||||
chr3:33121385 | C | G | 1 | a0001c0004t0005g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.621+892C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121385 | |||||||
chr3:33121410 | T | C | 4 | a0001c0001t0028g0084 a0001c0001t0028g0085 a0001c0001t0057g0086 others(1): Show |
4 | HG00609.hp1 HG02129.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+917T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121410 | |||||||
chr3:33121411 | C | CAAAAAAA others(8): Show |
20 | a0001c0002t0008g0195 a0001c0004t0005g0011 a0001c0004t0005g0012 others(17): Show |
23 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.621+926_621+927ins others(15): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33121411 | ||||||
chr3:33121411 | C | CAAAAAAA others(9): Show |
3 | a0001c0004t0070g0255 a0001c0004t0074g0067 a0001c0010t0002g0066 |
3 | HG03098.hp1 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.621+926_621+927ins others(16): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33121411 | ||||||
chr3:33121411 | C | CAAAAAAA others(10): Show |
2 | a0001c0007t0018g0032 a0001c0007t0018g0256 |
3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.621+926_621+927ins others(17): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33121411 | ||||||
chr3:33121487 | G | A | 7 | a0001c0005t0007g0265 a0001c0005t0008g0187 a0001c0005t0035g0298 others(4): Show |
7 | HG02559.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.621+994G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121487 | |||||||
chr3:33121495 | TAG | T | 25 | a0001c0002t0008g0195 a0001c0004t0005g0011 a0001c0004t0005g0012 others(22): Show |
29 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.621+1005_621+1006d others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33121495 | ||||||
chr3:33121529 | G | A | 25 | a0001c0002t0008g0195 a0001c0004t0005g0011 a0001c0004t0005g0012 others(22): Show |
29 | HG00438.hp1 HG00639.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.621+1036G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121529 | |||||||
chr3:33121602 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.621+1109C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121602 | |||||||
chr3:33121761 | T | C | 1 | a0001c0002t0001g0196 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.621+1268T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121761 | |||||||
chr3:33121791 | A | G | 1 | a0001c0001t0004g0145 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.621+1298A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121791 | |||||||
chr3:33121861 | G | A | 4 | a0001c0001t0019g0156 a0001c0005t0019g0191 a0001c0005t0026g0269 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+1368G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121861 | |||||||
chr3:33121865 | C | T | 1 | a0001c0004t0070g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.621+1372C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121865 | |||||||
chr3:33121956 | G | A | 2 | a0001c0007t0018g0032 a0001c0007t0018g0256 |
3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.621+1463G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33121956 | |||||||
chr3:33122019 | C | T | 1 | a0001c0004t0005g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.621+1526C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122019 | |||||||
chr3:33122289 | C | T | 1 | a0001c0001t0003g0150 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.621+1796C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122289 | |||||||
chr3:33122290 | C | T | 1 | a0001c0001t0003g0150 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.621+1797C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122290 | |||||||
chr3:33122292 | C | T | 4 | a0001c0002t0007g0037 a0001c0002t0007g0235 a0001c0002t0050g0234 others(1): Show |
5 | HG02258.hp2 HG02572.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+1799C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122292 | |||||||
chr3:33122310 | A | G | 1 | a0001c0005t0082g0188 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.621+1817A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122310 | |||||||
chr3:33122328 | A | G | 2 | a0001c0005t0026g0269 a0001c0005t0026g0270 |
2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.621+1835A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122328 | |||||||
chr3:33122399 | G | A | 164 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(161): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.621+1906G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122399 | |||||||
chr3:33122429 | G | A | 1 | a0001c0001t0028g0084 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.621+1936G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122429 | |||||||
chr3:33122437 | C | T | 17 | a0001c0003t0015g0261 a0001c0003t0015g0262 a0001c0003t0015g0263 others(14): Show |
18 | HG00544.hp2 HG01074.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.621+1944C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122437 | |||||||
chr3:33122490 | C | T | 1 | a0001c0005t0026g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.622-1918C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122490 | |||||||
chr3:33122545 | A | G | 1 | a0001c0002t0001g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.622-1863A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122545 | |||||||
chr3:33122587 | T | C | 1 | a0001c0001t0003g0180 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.622-1821T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122587 | |||||||
chr3:33122600 | T | G | 109 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0100 others(106): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.622-1808T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122600 | |||||||
chr3:33122679 | G | C | 270 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(267): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.622-1729G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122679 | |||||||
chr3:33122709 | C | CA | 77 | a0001c0001t0004g0274 a0001c0001t0004g0275 a0001c0001t0043g0292 others(74): Show |
100 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.622-1676dupA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | ||||||
chr3:33122709 | C | CAA | 9 | a0001c0002t0001g0197 a0001c0002t0001g0200 a0001c0002t0001g0201 others(6): Show |
9 | HG02738.hp2 HG04184.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-1677_622-1676d others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | ||||||
chr3:33122709 | C | CAAAA | 13 | a0001c0003t0015g0261 a0001c0003t0015g0262 a0001c0003t0015g0263 others(10): Show |
13 | HG00544.hp2 HG01074.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.622-1679_622-1676d others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | ||||||
chr3:33122709 | CAA | C | 8 | a0001c0001t0019g0156 a0001c0004t0074g0067 a0001c0004t0075g0068 others(5): Show |
8 | HG02258.hp1 HG02622.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.622-1677_622-1676d others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | ||||||
chr3:33122709 | CAAA | C | 146 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(143): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.622-1678_622-1676d others(5): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | ||||||
chr3:33122709 | CAAAA | C | 6 | a0001c0003t0002g0136 a0001c0003t0002g0137 a0001c0003t0002g0138 others(3): Show |
7 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-1679_622-1676d others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | ||||||
chr3:33122709 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0007g0184 a0001c0005t0007g0264 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.622-1687_622-1676d others(14): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33122709 | ||||||
chr3:33122730 | A | G | 7 | a0001c0001t0001g0179 a0001c0001t0002g0177 a0001c0001t0003g0003 others(4): Show |
11 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-1678A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122730 | |||||||
chr3:33122898 | G | T | 159 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(156): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.622-1510G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122898 | |||||||
chr3:33122995 | G | C | 1 | a0001c0001t0013g0163 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.622-1413G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33122995 | |||||||
chr3:33123046 | C | T | 1 | a0001c0004t0075g0068 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.622-1362C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123046 | |||||||
chr3:33123137 | TG | T | 5 | a0001c0002t0007g0037 a0001c0002t0007g0202 a0001c0002t0007g0235 others(2): Show |
6 | HG02258.hp2 HG02886.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-1270delG | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123137 | |||||||
chr3:33123159 | G | A | 5 | a0001c0002t0001g0015 a0001c0002t0001g0197 a0001c0002t0001g0205 others(2): Show |
7 | HG01168.hp2 HG02055.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-1249G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123159 | |||||||
chr3:33123219 | G | T | 1 | a0001c0004t0005g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.622-1189G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123219 | |||||||
chr3:33123244 | C | T | 23 | a0001c0002t0008g0195 a0001c0004t0005g0011 a0001c0004t0005g0012 others(20): Show |
26 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.622-1164C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123244 | |||||||
chr3:33123335 | T | C | 161 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(158): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.622-1073T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123335 | |||||||
chr3:33123366 | G | A | 1 | a0001c0003t0002g0108 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.622-1042G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123366 | |||||||
chr3:33123457 | C | CTCTT | 161 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(158): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.622-950_622-947dup others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123457 | ||||||
chr3:33123488 | C | T | 265 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(262): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.622-920C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123488 | |||||||
chr3:33123625 | G | GT | 51 | a0001c0001t0002g0049 a0001c0001t0002g0294 a0001c0001t0003g0044 others(48): Show |
58 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.622-759dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | ||||||
chr3:33123625 | G | GTT | 10 | a0001c0002t0001g0036 a0001c0006t0006g0056 a0001c0006t0006g0057 others(7): Show |
11 | HG00544.hp2 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.622-760_622-759dup others(2): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | ||||||
chr3:33123625 | G | GTTT | 6 | a0001c0001t0007g0184 a0001c0003t0015g0262 a0001c0003t0015g0263 others(3): Show |
7 | HG01255.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-761_622-759dup others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | ||||||
chr3:33123625 | GTTTT | G | 16 | a0001c0001t0001g0179 a0001c0001t0003g0024 a0001c0001t0003g0080 others(13): Show |
16 | HG00438.hp2 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.622-762_622-759del others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | ||||||
chr3:33123625 | GTTTTT | G | 86 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0100 others(83): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.622-763_622-759del others(5): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | ||||||
chr3:33123625 | GTTTTTT | G | 50 | a0001c0001t0001g0116 a0001c0001t0001g0162 a0001c0001t0003g0113 others(47): Show |
65 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.622-764_622-759del others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | ||||||
chr3:33123625 | GTTTTTTT | G | 7 | a0001c0001t0001g0025 a0001c0001t0065g0296 a0001c0003t0002g0026 others(4): Show |
9 | HG01074.hp1 HG01099.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.622-765_622-759del others(7): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 33123625 | ||||||
chr3:33123660 | C | T | 2 | a0001c0001t0007g0184 a0001c0005t0007g0264 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.622-748C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123660 | |||||||
chr3:33123716 | G | A | 1 | a0001c0001t0034g0040 | 2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.622-692G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123716 | |||||||
chr3:33123759 | A | C | 1 | a0001c0002t0001g0224 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.622-649A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123759 | |||||||
chr3:33123811 | C | G | 161 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(158): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.622-597C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123811 | |||||||
chr3:33123830 | T | C | 2 | a0001c0007t0018g0032 a0001c0007t0018g0256 |
3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.622-578T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123830 | |||||||
chr3:33123926 | C | A | 1 | a0001c0005t0083g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.622-482C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123926 | |||||||
chr3:33123944 | T | A | 270 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(267): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.622-464T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33123944 | |||||||
chr3:33124019 | C | G | 1 | a0001c0003t0040g0127 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.622-389C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33124019 | |||||||
chr3:33124040 | A | G | 2 | a0001c0007t0018g0032 a0001c0007t0018g0256 |
3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.622-368A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33124040 | |||||||
chr3:33124128 | T | C | 2 | a0001c0001t0007g0184 a0001c0005t0007g0264 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.622-280T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33124128 | |||||||
chr3:33124327 | G | A | 2 | a0001c0010t0002g0066 a0001c0010t0042g0069 |
2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.622-81G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 2/6 | chr3 | 33124327 | |||||||
chr3:33124757 | G | A | 1 | a0001c0003t0002g0111 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.793+178G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33124757 | |||||||
chr3:33124864 | T | C | 65 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0100 others(62): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.793+285T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33124864 | |||||||
chr3:33124935 | A | G | 1 | a0001c0003t0021g0161 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.793+356A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33124935 | |||||||
chr3:33124940 | T | C | 270 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(267): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.793+361T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33124940 | |||||||
chr3:33125491 | G | GT | 82 | a0001c0001t0001g0006 a0001c0001t0001g0152 a0001c0001t0002g0049 others(79): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.793+936dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33125491 | ||||||
chr3:33125491 | G | GTT | 127 | a0001c0001t0001g0025 a0001c0001t0001g0100 a0001c0001t0001g0116 others(124): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.793+935_793+936dup others(2): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33125491 | ||||||
chr3:33125491 | G | GTTT | 36 | a0001c0001t0065g0296 a0001c0002t0001g0034 a0001c0002t0001g0035 others(33): Show |
41 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.793+934_793+936dup others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33125491 | ||||||
chr3:33125491 | GT | G | 8 | a0001c0003t0015g0261 a0001c0003t0015g0262 a0001c0003t0015g0263 others(5): Show |
9 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+936delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33125491 | ||||||
chr3:33125683 | C | T | 3 | a0001c0002t0009g0220 a0001c0002t0009g0223 a0001c0002t0009g0227 |
3 | HG00673.hp1 NA18997.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.793+1104C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33125683 | |||||||
chr3:33125764 | A | G | 57 | a0001c0001t0001g0025 a0001c0001t0001g0116 a0001c0001t0003g0113 others(54): Show |
75 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.793+1185A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33125764 | |||||||
chr3:33125973 | G | A | 1 | a0001c0001t0004g0276 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.793+1394G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33125973 | |||||||
chr3:33126008 | A | C | 23 | a0001c0002t0008g0195 a0001c0003t0002g0123 a0001c0004t0005g0011 others(20): Show |
26 | HG00438.hp1 HG01081.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.793+1429A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126008 | |||||||
chr3:33126008 | A | G | 1 | a0001c0003t0002g0131 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.793+1429A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126008 | |||||||
chr3:33126111 | C | T | 2 | a0001c0005t0007g0265 a0001c0005t0084g0266 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.793+1532C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126111 | |||||||
chr3:33126137 | C | G | 124 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(121): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.793+1558C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126137 | |||||||
chr3:33126155 | C | G | 2 | a0001c0003t0015g0261 a0001c0003t0015g0262 |
2 | HG01074.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.793+1576C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126155 | |||||||
chr3:33126217 | C | G | 1 | a0001c0002t0081g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.793+1638C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126217 | |||||||
chr3:33126309 | G | A | 88 | a0001c0001t0001g0162 a0001c0002t0001g0004 a0001c0002t0001g0005 others(85): Show |
111 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.793+1730G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126309 | |||||||
chr3:33126330 | G | A | 9 | a0001c0005t0007g0265 a0001c0005t0008g0187 a0001c0005t0035g0298 others(6): Show |
10 | HG00639.hp2 HG02559.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.793+1751G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126330 | |||||||
chr3:33126361 | T | C | 270 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(267): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.793+1782T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126361 | |||||||
chr3:33126379 | T | C | 1 | a0001c0001t0071g0182 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.793+1800T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126379 | |||||||
chr3:33126410 | T | G | 7 | a0001c0005t0007g0265 a0001c0005t0008g0187 a0001c0005t0035g0298 others(4): Show |
7 | HG02559.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.793+1831T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126410 | |||||||
chr3:33126456 | A | G | 2 | a0001c0003t0003g0028 a0001c0003t0003g0130 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.793+1877A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126456 | |||||||
chr3:33126509 | A | C | 1 | a0001c0006t0006g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.793+1930A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126509 | |||||||
chr3:33126615 | A | G | 1 | a0005c0015t0005g0076 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.793+2036A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126615 | |||||||
chr3:33126631 | A | G | 1 | a0001c0003t0002g0122 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.793+2052A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126631 | |||||||
chr3:33126651 | C | T | 1 | a0001c0002t0012g0258 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.793+2072C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126651 | |||||||
chr3:33126988 | G | A | 1 | a0001c0002t0011g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.793+2409G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33126988 | |||||||
chr3:33127099 | CT | C | 241 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(238): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.793+2537delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33127099 | ||||||
chr3:33127099 | CTT | C | 9 | a0001c0001t0003g0103 a0001c0001t0061g0098 a0001c0002t0001g0225 others(6): Show |
10 | HG01070.hp1 HG01074.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.793+2536_793+2537d others(4): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33127099 | ||||||
chr3:33127116 | T | A | 1 | a0001c0003t0024g0039 | 2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.793+2537T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127116 | |||||||
chr3:33127116 | TA | T | 4 | a0001c0002t0001g0245 a0002c0008t0013g0052 a0002c0008t0013g0053 others(1): Show |
4 | HG03017.hp2 HG04199.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+2540delA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33127116 | ||||||
chr3:33127335 | C | G | 1 | a0001c0001t0086g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.794-2604C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127335 | |||||||
chr3:33127351 | A | G | 17 | a0001c0003t0015g0261 a0001c0003t0015g0262 a0001c0003t0015g0263 others(14): Show |
18 | HG00544.hp2 HG01074.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.794-2588A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127351 | |||||||
chr3:33127377 | G | T | 17 | a0001c0003t0015g0261 a0001c0003t0015g0262 a0001c0003t0015g0263 others(14): Show |
18 | HG00544.hp2 HG01074.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.794-2562G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127377 | |||||||
chr3:33127435 | A | G | 3 | a0002c0008t0013g0052 a0002c0008t0013g0053 a0002c0008t0013g0185 |
3 | HG03017.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.794-2504A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127435 | |||||||
chr3:33127439 | TTTTATTT others(5): Show |
T | 86 | a0001c0001t0001g0162 a0001c0002t0001g0004 a0001c0002t0001g0005 others(83): Show |
109 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.794-2488_794-2477d others(14): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33127439 | ||||||
chr3:33127509 | G | A | 1 | a0001c0001t0003g0113 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.794-2430G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127509 | |||||||
chr3:33127640 | G | C | 3 | a0002c0008t0013g0052 a0002c0008t0013g0053 a0002c0008t0013g0185 |
3 | HG03017.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.794-2299G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127640 | |||||||
chr3:33127681 | C | A | 1 | a0001c0002t0001g0217 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.794-2258C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33127681 | |||||||
chr3:33128007 | C | G | 8 | a0001c0004t0005g0011 a0001c0004t0005g0061 a0001c0004t0005g0062 others(5): Show |
9 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.794-1932C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128007 | |||||||
chr3:33128345 | C | A | 2 | a0001c0003t0003g0028 a0001c0003t0003g0130 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.794-1594C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128345 | |||||||
chr3:33128543 | T | A | 1 | a0001c0002t0048g0267 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.794-1396T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128543 | |||||||
chr3:33128761 | C | T | 1 | a0001c0001t0086g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.794-1178C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128761 | |||||||
chr3:33128780 | A | C | 1 | a0001c0001t0086g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.794-1159A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128780 | |||||||
chr3:33128913 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.794-1026A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33128913 | |||||||
chr3:33129005 | T | C | 1 | a0001c0001t0086g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.794-934T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129005 | |||||||
chr3:33129040 | T | C | 4 | a0001c0002t0001g0221 a0001c0002t0001g0225 a0001c0002t0001g0232 others(1): Show |
4 | NA18959.hp2 NA18974.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-899T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129040 | |||||||
chr3:33129041 | G | A | 1 | a0001c0003t0002g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.794-898G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129041 | |||||||
chr3:33129048 | A | G | 1 | a0001c0002t0052g0203 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.794-891A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129048 | |||||||
chr3:33129385 | C | T | 1 | a0001c0001t0086g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.794-554C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129385 | |||||||
chr3:33129447 | A | G | 1 | a0001c0012t0067g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.794-492A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129447 | |||||||
chr3:33129459 | T | G | 3 | a0001c0003t0002g0135 a0001c0003t0002g0137 a0001c0003t0002g0148 |
3 | HG00099.hp1 HG01123.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.794-480T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129459 | |||||||
chr3:33129535 | C | CT | 64 | a0001c0001t0001g0025 a0001c0001t0001g0116 a0001c0001t0003g0102 others(61): Show |
82 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.794-385dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33129535 | ||||||
chr3:33129535 | CT | C | 6 | a0001c0001t0002g0046 a0001c0001t0062g0092 a0001c0002t0001g0224 others(3): Show |
7 | HG00140.hp2 HG01168.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-385delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 33129535 | ||||||
chr3:33129539 | T | C | 4 | a0001c0001t0028g0084 a0001c0001t0028g0085 a0001c0001t0057g0086 others(1): Show |
4 | HG00609.hp1 HG02129.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-400T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129539 | |||||||
chr3:33129540 | T | C | 1 | a0001c0001t0019g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.794-399T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129540 | |||||||
chr3:33129541 | T | C | 1 | a0001c0002t0001g0209 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.794-398T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129541 | |||||||
chr3:33129606 | C | T | 1 | a0001c0001t0043g0292 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.794-333C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129606 | |||||||
chr3:33129639 | G | A | 2 | a0001c0002t0001g0221 a0001c0002t0001g0232 |
2 | NA18974.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.794-300G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129639 | |||||||
chr3:33129648 | C | T | 13 | a0001c0002t0001g0254 a0001c0006t0006g0056 a0001c0006t0006g0057 others(10): Show |
13 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.794-291C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129648 | |||||||
chr3:33129676 | C | T | 6 | a0001c0003t0002g0126 a0001c0003t0002g0133 a0001c0003t0002g0139 others(3): Show |
6 | NA18943.hp1 NA19010.hp1 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-263C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129676 | |||||||
chr3:33129687 | A | G | 2 | a0001c0001t0066g0054 a0001c0004t0073g0075 |
2 | HG03516.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.794-252A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129687 | |||||||
chr3:33129691 | C | T | 2 | a0001c0002t0009g0199 a0001c0002t0009g0226 |
2 | HG00558.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.794-248C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129691 | |||||||
chr3:33129699 | A | G | 2 | a0001c0005t0082g0188 a0001c0005t0083g0186 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.794-240A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129699 | |||||||
chr3:33129744 | A | G | 3 | a0001c0001t0004g0280 a0001c0002t0001g0033 a0001c0002t0003g0033 |
3 | HG01496.hp2 NA18612.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.794-195A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129744 | |||||||
chr3:33129758 | G | A | 2 | a0001c0003t0002g0027 a0001c0003t0044g0124 |
3 | HG02738.hp1 HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.794-181G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129758 | |||||||
chr3:33129784 | G | A | 1 | a0001c0004t0073g0075 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.794-155G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129784 | |||||||
chr3:33129826 | C | A | 1 | a0001c0002t0001g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.794-113C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129826 | |||||||
chr3:33129828 | C | T | 1 | a0001c0002t0001g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.794-111C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129828 | |||||||
chr3:33129936 | C | T | 1 | a0001c0004t0019g0073 | 1 | NA18522.hp1 | splice_region_variant&intron_variant | LOW | c.794-3C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 3/6 | chr3 | 33129936 | |||||||
chr3:33130167 | A | G | 285 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(282): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.922+100A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130167 | |||||||
chr3:33130220 | T | C | 2 | a0001c0002t0001g0236 a0001c0002t0001g0240 |
2 | NA18984.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.922+153T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130220 | |||||||
chr3:33130525 | CT | C | 139 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0013 others(136): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.922+483delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 33130525 | ||||||
chr3:33130525 | CTT | C | 121 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0100 others(118): Show |
147 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.922+482_922+483del others(2): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 33130525 | ||||||
chr3:33130525 | CTTT | C | 10 | a0001c0001t0001g0162 a0001c0001t0007g0279 a0001c0001t0046g0284 others(7): Show |
11 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.922+481_922+483del others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 33130525 | ||||||
chr3:33130527 | T | C | 1 | a0001c0002t0001g0209 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.922+460T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130527 | |||||||
chr3:33130531 | T | C | 3 | a0001c0005t0019g0191 a0001c0005t0026g0269 a0001c0005t0026g0270 |
3 | HG02258.hp1 HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.922+464T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130531 | |||||||
chr3:33130532 | T | C | 5 | a0001c0001t0019g0156 a0001c0003t0002g0131 a0002c0008t0013g0052 others(2): Show |
5 | HG01261.hp1 HG02922.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.922+465T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130532 | |||||||
chr3:33130734 | A | G | 1 | a0001c0002t0037g0215 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.922+667A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130734 | |||||||
chr3:33130967 | C | T | 4 | a0001c0003t0015g0261 a0001c0003t0015g0262 a0001c0003t0015g0263 others(1): Show |
5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.922+900C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130967 | |||||||
chr3:33130968 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.922+901G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130968 | |||||||
chr3:33130971 | T | C | 5 | a0001c0006t0006g0056 a0001c0006t0006g0057 a0001c0006t0006g0058 others(2): Show |
5 | HG00544.hp2 HG02886.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.922+904T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33130971 | |||||||
chr3:33131148 | C | T | 11 | a0001c0006t0006g0056 a0001c0006t0006g0057 a0001c0006t0006g0058 others(8): Show |
11 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.922+1081C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131148 | |||||||
chr3:33131200 | G | A | 1 | a0002c0008t0013g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.922+1133G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131200 | |||||||
chr3:33131211 | G | A | 2 | a0001c0005t0035g0298 a0001c0005t0036g0297 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.922+1144G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131211 | |||||||
chr3:33131253 | G | GT | 22 | a0001c0001t0013g0163 a0001c0001t0031g0021 a0001c0001t0086g0260 others(19): Show |
23 | HG00544.hp2 HG01255.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.922+1196dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 33131253 | ||||||
chr3:33131284 | A | G | 4 | a0001c0003t0015g0261 a0001c0003t0015g0262 a0001c0003t0015g0263 others(1): Show |
5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.922+1217A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131284 | |||||||
chr3:33131308 | A | T | 22 | a0001c0001t0025g0031 a0001c0002t0005g0208 a0001c0002t0068g0190 others(19): Show |
26 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.922+1241A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131308 | |||||||
chr3:33131525 | A | G | 2 | a0001c0002t0001g0248 a0001c0002t0001g0252 |
2 | NA18947.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.923-1030A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131525 | |||||||
chr3:33131667 | G | A | 1 | a0001c0012t0067g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.923-888G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131667 | |||||||
chr3:33131695 | ATGCTAC | A | 4 | a0001c0002t0008g0195 a0001c0005t0008g0187 a0001c0005t0082g0188 others(1): Show |
4 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.923-859_923-854del others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131695 | |||||||
chr3:33131702 | A | C | 4 | a0001c0002t0008g0195 a0001c0005t0008g0187 a0001c0005t0082g0188 others(1): Show |
4 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.923-853A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131702 | |||||||
chr3:33131703 | T | C | 4 | a0001c0002t0008g0195 a0001c0005t0008g0187 a0001c0005t0082g0188 others(1): Show |
4 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.923-852T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33131703 | |||||||
chr3:33132126 | G | A | 6 | a0001c0004t0005g0012 a0001c0004t0005g0268 a0001c0004t0072g0077 others(3): Show |
8 | HG00438.hp1 NA18960.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.923-429G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33132126 | |||||||
chr3:33132370 | G | A | 1 | a0001c0001t0045g0104 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.923-185G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33132370 | |||||||
chr3:33132384 | G | A | 1 | a0001c0005t0084g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.923-171G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33132384 | |||||||
chr3:33132436 | C | A | 1 | a0001c0001t0006g0287 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.923-119C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 4/6 | chr3 | 33132436 | |||||||
chr3:33132804 | G | A | 1 | a0001c0001t0086g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1068+104G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33132804 | |||||||
chr3:33132861 | T | C | 4 | a0001c0002t0008g0195 a0001c0005t0008g0187 a0001c0005t0082g0188 others(1): Show |
4 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+161T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33132861 | |||||||
chr3:33133003 | A | G | 280 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0100 others(277): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.1068+303A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133003 | |||||||
chr3:33133005 | G | GA | 280 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0100 others(277): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.1068+305_1068+306i others(3): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133005 | |||||||
chr3:33133261 | CT | C | 212 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0100 others(209): Show |
260 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.1068+576delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 33133261 | ||||||
chr3:33133382 | C | G | 1 | a0001c0012t0067g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1068+682C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133382 | |||||||
chr3:33133384 | G | A | 8 | a0001c0001t0004g0041 a0001c0001t0004g0042 a0001c0001t0004g0043 others(5): Show |
12 | HG00735.hp2 HG01175.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1068+684G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133384 | |||||||
chr3:33133466 | T | G | 5 | a0001c0002t0008g0195 a0001c0005t0008g0187 a0001c0005t0082g0188 others(2): Show |
5 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1069-716T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133466 | |||||||
chr3:33133521 | AT | A | 280 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0100 others(277): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.1069-658delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 33133521 | ||||||
chr3:33133567 | C | A | 1 | a0001c0005t0084g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1069-615C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133567 | |||||||
chr3:33133667 | A | ACTTT | 258 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0100 others(255): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1069-514_1069-511d others(6): Show |
CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 33133667 | ||||||
chr3:33133691 | G | C | 1 | a0001c0004t0005g0268 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1069-491G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133691 | |||||||
chr3:33133936 | C | A | 9 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0049 others(6): Show |
11 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1069-246C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133936 | |||||||
chr3:33133980 | A | G | 1 | a0001c0005t0084g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1069-202A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33133980 | |||||||
chr3:33134023 | G | A | 3 | a0002c0008t0013g0052 a0002c0008t0013g0053 a0002c0008t0013g0185 |
3 | HG03017.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1069-159G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33134023 | |||||||
chr3:33134058 | A | G | 1 | a0001c0002t0053g0218 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1069-124A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 5/6 | chr3 | 33134058 | |||||||
chr3:33134301 | C | A | 285 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(282): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1152+36C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134301 | |||||||
chr3:33134362 | A | G | 70 | a0001c0003t0002g0002 a0001c0003t0002g0007 a0001c0003t0002g0009 others(67): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1152+97A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134362 | |||||||
chr3:33134440 | G | A | 2 | a0001c0001t0007g0184 a0001c0005t0007g0265 |
2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1152+175G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134440 | |||||||
chr3:33134453 | A | G | 2 | a0001c0002t0001g0243 a0001c0002t0001g0247 |
2 | HG02027.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1152+188A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134453 | |||||||
chr3:33134673 | G | A | 1 | a0001c0001t0028g0085 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1152+408G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134673 | |||||||
chr3:33134743 | C | T | 5 | a0001c0002t0008g0195 a0001c0005t0008g0187 a0001c0005t0082g0188 others(2): Show |
5 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1152+478C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134743 | |||||||
chr3:33134761 | T | A | 1 | a0001c0001t0004g0276 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1152+496T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134761 | |||||||
chr3:33134803 | G | A | 2 | a0001c0007t0018g0032 a0001c0007t0018g0256 |
3 | HG00639.hp2 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1152+538G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134803 | |||||||
chr3:33134884 | G | A | 2 | a0001c0003t0015g0261 a0001c0003t0015g0262 |
2 | HG01074.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1152+619G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134884 | |||||||
chr3:33134958 | G | A | 1 | a0001c0005t0084g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1152+693G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33134958 | |||||||
chr3:33135022 | G | C | 1 | a0001c0001t0002g0047 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1152+757G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135022 | |||||||
chr3:33135332 | A | G | 285 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(282): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1152+1067A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135332 | |||||||
chr3:33135487 | G | A | 1 | a0001c0001t0065g0296 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1152+1222G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135487 | |||||||
chr3:33135505 | C | T | 62 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0013 others(59): Show |
87 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1152+1240C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135505 | |||||||
chr3:33135510 | T | C | 9 | a0001c0003t0002g0114 a0001c0003t0002g0117 a0001c0003t0002g0118 others(6): Show |
9 | NA18943.hp1 NA18975.hp1 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1152+1245T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135510 | |||||||
chr3:33135581 | C | T | 4 | a0001c0003t0015g0261 a0001c0003t0015g0262 a0001c0003t0015g0263 others(1): Show |
5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152+1316C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135581 | |||||||
chr3:33135705 | G | T | 21 | a0001c0001t0025g0031 a0001c0002t0005g0208 a0001c0002t0068g0190 others(18): Show |
25 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1152+1440G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135705 | |||||||
chr3:33135706 | T | A | 21 | a0001c0001t0025g0031 a0001c0002t0005g0208 a0001c0002t0068g0190 others(18): Show |
25 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1152+1441T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33135706 | |||||||
chr3:33136103 | T | G | 1 | a0001c0001t0002g0294 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1152+1838T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33136103 | |||||||
chr3:33136508 | T | C | 1 | a0001c0001t0086g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1152+2243T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33136508 | |||||||
chr3:33136550 | C | T | 284 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(281): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1152+2285C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33136550 | |||||||
chr3:33136856 | G | A | 2 | a0001c0001t0003g0080 a0001c0001t0003g0093 |
2 | NA18986.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1152+2591G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33136856 | |||||||
chr3:33137069 | C | CT | 65 | a0001c0003t0002g0002 a0001c0003t0002g0007 a0001c0003t0002g0009 others(62): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1152+2814dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 33137069 | ||||||
chr3:33137114 | T | C | 1 | a0001c0003t0021g0161 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1152+2849T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137114 | |||||||
chr3:33137204 | G | A | 66 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0013 others(63): Show |
91 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1152+2939G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137204 | |||||||
chr3:33137227 | G | A | 11 | a0001c0006t0006g0056 a0001c0006t0006g0057 a0001c0006t0006g0058 others(8): Show |
11 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1152+2962G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137227 | |||||||
chr3:33137262 | T | C | 284 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(281): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1152+2997T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137262 | |||||||
chr3:33137365 | T | G | 1 | a0001c0003t0002g0119 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1152+3100T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137365 | |||||||
chr3:33137388 | G | A | 1 | a0002c0008t0013g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1152+3123G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137388 | |||||||
chr3:33137416 | C | T | 65 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0013 others(62): Show |
90 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1152+3151C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137416 | |||||||
chr3:33137417 | A | G | 1 | a0001c0004t0073g0075 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1152+3152A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137417 | |||||||
chr3:33137421 | G | A | 1 | a0001c0003t0002g0131 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1152+3156G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137421 | |||||||
chr3:33137522 | A | G | 1 | a0001c0003t0014g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1152+3257A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137522 | |||||||
chr3:33137618 | T | C | 4 | a0001c0001t0028g0084 a0001c0001t0028g0085 a0001c0001t0057g0086 others(1): Show |
4 | HG00609.hp1 HG02129.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+3353T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137618 | |||||||
chr3:33137832 | C | T | 1 | a0001c0013t0002g0204 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1152+3567C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137832 | |||||||
chr3:33137982 | T | G | 3 | a0001c0007t0018g0032 a0001c0007t0018g0256 a0001c0012t0067g0193 |
4 | HG00639.hp2 HG02809.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+3717T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33137982 | |||||||
chr3:33138053 | G | T | 2 | a0001c0001t0013g0163 a0001c0001t0031g0021 |
3 | HG01891.hp1 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1152+3788G>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138053 | |||||||
chr3:33138084 | T | C | 1 | a0001c0001t0071g0182 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1152+3819T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138084 | |||||||
chr3:33138099 | C | CT | 16 | a0001c0001t0007g0184 a0001c0002t0001g0259 a0001c0002t0007g0037 others(13): Show |
19 | HG01074.hp2 HG02258.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1152+3845dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 33138099 | ||||||
chr3:33138117 | C | T | 2 | a0001c0005t0026g0269 a0001c0005t0026g0270 |
2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1152+3852C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138117 | |||||||
chr3:33138459 | C | A | 63 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0013 others(60): Show |
88 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1153-3936C>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138459 | |||||||
chr3:33138491 | A | T | 66 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0013 others(63): Show |
91 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1153-3904A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138491 | |||||||
chr3:33138712 | A | G | 1 | a0001c0001t0003g0096 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1153-3683A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138712 | |||||||
chr3:33138713 | G | A | 2 | a0001c0003t0002g0114 a0001c0003t0002g0117 |
2 | NA18981.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1153-3682G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138713 | |||||||
chr3:33138765 | G | C | 79 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0013 others(76): Show |
105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1153-3630G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138765 | |||||||
chr3:33138932 | C | T | 2 | a0001c0005t0035g0298 a0001c0005t0036g0297 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1153-3463C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33138932 | |||||||
chr3:33139059 | G | A | 4 | a0001c0006t0006g0056 a0001c0006t0006g0057 a0001c0006t0006g0058 others(1): Show |
4 | HG00544.hp2 NA18949.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-3336G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139059 | |||||||
chr3:33139093 | G | A | 1 | a0001c0007t0018g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1153-3302G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139093 | |||||||
chr3:33139152 | A | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0100 others(2): Show |
7 | HG01255.hp1 HG01358.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153-3243A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139152 | |||||||
chr3:33139349 | C | G | 1 | a0001c0001t0031g0021 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1153-3046C>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139349 | |||||||
chr3:33139378 | C | T | 4 | a0001c0002t0008g0195 a0001c0005t0008g0187 a0001c0005t0082g0188 others(1): Show |
4 | HG02647.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153-3017C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139378 | |||||||
chr3:33139414 | C | T | 1 | a0002c0008t0013g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1153-2981C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139414 | |||||||
chr3:33139475 | A | AT | 52 | a0001c0001t0003g0003 a0001c0001t0003g0094 a0001c0001t0003g0095 others(49): Show |
61 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1153-2902dupT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 33139475 | ||||||
chr3:33139475 | AT | A | 7 | a0001c0001t0003g0151 a0001c0001t0004g0281 a0001c0002t0001g0232 others(4): Show |
8 | HG01074.hp1 HG01099.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1153-2902delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 33139475 | ||||||
chr3:33139632 | A | T | 2 | a0001c0001t0013g0163 a0001c0001t0031g0021 |
3 | HG01891.hp1 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1153-2763A>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139632 | |||||||
chr3:33139639 | G | C | 2 | a0001c0001t0003g0300 a0001c0001t0061g0098 |
2 | NA19001.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1153-2756G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139639 | |||||||
chr3:33139677 | C | T | 1 | a0001c0003t0002g0125 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1153-2718C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139677 | |||||||
chr3:33139693 | G | A | 1 | a0001c0001t0031g0021 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1153-2702G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139693 | |||||||
chr3:33139705 | T | G | 84 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(81): Show |
108 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1153-2690T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139705 | |||||||
chr3:33139768 | G | A | 1 | a0001c0005t0084g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1153-2627G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139768 | |||||||
chr3:33139848 | A | G | 86 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0013 others(83): Show |
112 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1153-2547A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139848 | |||||||
chr3:33139990 | T | A | 11 | a0001c0006t0006g0056 a0001c0006t0006g0057 a0001c0006t0006g0058 others(8): Show |
11 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-2405T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33139990 | |||||||
chr3:33140328 | G | A | 1 | a0005c0015t0005g0076 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1153-2067G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140328 | |||||||
chr3:33140414 | C | T | 1 | a0001c0001t0086g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1153-1981C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140414 | |||||||
chr3:33140560 | A | C | 80 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0013 others(77): Show |
106 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1153-1835A>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140560 | |||||||
chr3:33140563 | T | C | 1 | a0001c0002t0001g0196 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1153-1832T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140563 | |||||||
chr3:33140661 | CA | C | 21 | a0001c0001t0025g0031 a0001c0002t0005g0208 a0001c0002t0068g0190 others(18): Show |
25 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1153-1733delA | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140661 | |||||||
chr3:33140677 | T | C | 1 | a0001c0002t0001g0211 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1153-1718T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140677 | |||||||
chr3:33140688 | T | G | 1 | a0001c0001t0006g0287 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1153-1707T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140688 | |||||||
chr3:33140841 | G | A | 1 | a0001c0001t0008g0008 | 4 | HG01069.hp1 HG01071.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-1554G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140841 | |||||||
chr3:33140863 | C | T | 1 | a0001c0003t0002g0136 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1153-1532C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33140863 | |||||||
chr3:33141002 | GT | G | 283 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0090 others(280): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1153-1384delT | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 33141002 | ||||||
chr3:33141037 | G | A | 2 | a0001c0001t0013g0163 a0001c0001t0031g0021 |
3 | HG01891.hp1 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1153-1358G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141037 | |||||||
chr3:33141095 | T | G | 1 | a0001c0006t0006g0175 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1153-1300T>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141095 | |||||||
chr3:33141240 | G | C | 5 | a0001c0001t0003g0013 a0001c0001t0003g0094 a0001c0001t0003g0151 others(2): Show |
7 | HG00544.hp1 HG00673.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1153-1155G>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141240 | |||||||
chr3:33141324 | T | C | 5 | a0001c0001t0019g0156 a0001c0004t0019g0073 a0001c0005t0019g0191 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1153-1071T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141324 | |||||||
chr3:33141347 | A | G | 21 | a0001c0001t0025g0031 a0001c0002t0005g0208 a0001c0002t0068g0190 others(18): Show |
25 | HG00438.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1153-1048A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141347 | |||||||
chr3:33141415 | T | C | 3 | a0002c0008t0013g0052 a0002c0008t0013g0053 a0002c0008t0013g0185 |
3 | HG03017.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1153-980T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141415 | |||||||
chr3:33141456 | T | C | 1 | a0001c0003t0002g0148 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1153-939T>C | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141456 | |||||||
chr3:33141504 | A | G | 11 | a0001c0006t0006g0056 a0001c0006t0006g0057 a0001c0006t0006g0058 others(8): Show |
11 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153-891A>G | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141504 | |||||||
chr3:33141823 | G | A | 4 | a0001c0003t0015g0261 a0001c0003t0015g0262 a0001c0003t0015g0263 others(1): Show |
5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-572G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141823 | |||||||
chr3:33141861 | C | T | 4 | a0001c0003t0015g0261 a0001c0003t0015g0262 a0001c0003t0015g0263 others(1): Show |
5 | HG01074.hp2 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-534C>T | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33141861 | |||||||
chr3:33142231 | T | A | 2 | a0002c0008t0013g0052 a0002c0008t0013g0053 |
2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1153-164T>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33142231 | |||||||
chr3:33142317 | G | A | 1 | a0002c0008t0013g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1153-78G>A | CRTAP | ENSG00000170275.15 | transcript | ENST00000320954.11 | protein_coding | 6/6 | chr3 | 33142317 |