Item | Value |
---|---|
geneid | 9524 |
ensemblid | ENSG00000099797.15 |
hgncid | 4551 |
symbol | TECR |
name | trans-2,3-enoyl-CoA reductase |
refseq_nuc | NM_138501.6 |
refseq_prot | NP_612510.1 |
ensembl_nuc | ENST00000215567.10 |
ensembl_prot | ENSP00000215567.4 |
mane_status | MANE Select |
chr | chr19 |
start | 14529594 |
end | 14565980 |
strand | + |
ver | v1.2 |
region | chr19:14529594-14565980 |
region5000 | chr19:14524594-14570980 |
regionname0 | TECR_chr19_14529594_14565980 |
regionname5000 | TECR_chr19_14524594_14570980 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 308 | 323 | 92 | 79 | 97 | 15 | 38 | 73 | TECR_chr19_14524594_14570980 | TECR | MKHYE others(303): Show |
chr19 | 14524594 | 14570980 |
a0002 | 0/0 | 61 | 9 | 0 | 3 | 3 | 1 | 2 | 1 | TECR_chr19_14524594_14570980 | TECR | MKHYE others(56): Show |
chr19 | 14524594 | 14570980 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 924 | 271 | 49 | 78 | 94 | 14 | 34 | TECR_chr19_14524594_14570980 | TECR | ATGAA others(919): Show |
chr19 | 14524594 | 14570980 | ||
a0001c0002 | 0/0 | 924 | 30 | 22 | 1 | 2 | 1 | 4 | TECR_chr19_14524594_14570980 | TECR | ATGAA others(919): Show |
chr19 | 14524594 | 14570980 | ||
a0001c0003 | 0/0 | 924 | 15 | 15 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | ATGAA others(919): Show |
chr19 | 14524594 | 14570980 | ||
a0001c0005 | 0/0 | 924 | 6 | 6 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | ATGAA others(919): Show |
chr19 | 14524594 | 14570980 | ||
a0001c0007 | 0/0 | 924 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | ATGAA others(919): Show |
chr19 | 14524594 | 14570980 | ||
a0002c0004 | 0/0 | 925 | 6 | 0 | 2 | 3 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | ATGAA others(920): Show |
chr19 | 14524594 | 14570980 | ||
a0002c0006 | 0/0 | 925 | 3 | 0 | 1 | 0 | 1 | 1 | TECR_chr19_14524594_14570980 | TECR | ATGAA others(920): Show |
chr19 | 14524594 | 14570980 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1139 | 264 | 49 | 78 | 92 | 14 | 29 | TECR_chr19_14524594_14570980 | TECR | GTTTA others(1134): Show |
chr19 | 14524594 | 14570980 |
a0001c0001t0002 | 0/0 | 1139 | 5 | 0 | 0 | 0 | 0 | 5 | TECR_chr19_14524594_14570980 | TECR | GTTTA others(1134): Show |
chr19 | 14524594 | 14570980 |
a0001c0001t0003 | 0/0 | 1139 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | GTTTA others(1134): Show |
chr19 | 14524594 | 14570980 |
a0001c0001t0004 | 0/0 | 1139 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | GTTTA others(1134): Show |
chr19 | 14524594 | 14570980 |
a0001c0002t0001 | 0/0 | 1139 | 30 | 22 | 1 | 2 | 1 | 4 | TECR_chr19_14524594_14570980 | TECR | GTTTA others(1134): Show |
chr19 | 14524594 | 14570980 |
a0001c0003t0001 | 0/0 | 1139 | 15 | 15 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | GTTTA others(1134): Show |
chr19 | 14524594 | 14570980 |
a0001c0005t0001 | 0/0 | 1139 | 6 | 6 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | GTTTA others(1134): Show |
chr19 | 14524594 | 14570980 |
a0001c0007t0001 | 0/0 | 1139 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | GTTTA others(1134): Show |
chr19 | 14524594 | 14570980 |
a0002c0004t0001 | 0/0 | 1140 | 6 | 0 | 2 | 3 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | GTTTA others(1135): Show |
chr19 | 14524594 | 14570980 |
a0002c0006t0001 | 0/0 | 1140 | 3 | 0 | 1 | 0 | 1 | 1 | TECR_chr19_14524594_14570980 | TECR | GTTTA others(1135): Show |
chr19 | 14524594 | 14570980 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0303 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0005t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0005t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0005t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0001c0007t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0002c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0002c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0002c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0002c0004t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0002c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0002c0004t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0002c0006t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0002c0006t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
a0002c0006t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | GBR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0301 | EUR | GBR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | GBR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | GBR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | FIN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | FIN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00673 | hp2 | a0002 | c0004 | t0001 | g0087 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0100 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0313 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01517 | hp2 | a0002 | c0006 | t0001 | g0126 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01934 | hp2 | a0002 | c0006 | t0001 | g0305 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02132 | hp2 | a0002 | c0004 | t0001 | g0084 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02148 | hp1 | a0002 | c0004 | t0001 | g0166 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02148 | hp2 | a0002 | c0004 | t0001 | g0269 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0295 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02451 | hp1 | a0001 | c0005 | t0001 | g0036 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0067 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02738 | hp2 | a0002 | c0006 | t0001 | g0194 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0032 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0029 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0287 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0312 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0242 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03195 | hp1 | a0001 | c0005 | t0001 | g0042 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0294 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0298 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0048 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0316 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0195 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03942 | hp1 | a0002 | c0004 | t0001 | g0134 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0228 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0227 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18944 | hp1 | a0001 | c0007 | t0001 | g0079 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18963 | hp1 | a0002 | c0004 | t0001 | g0206 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19240 | hp1 | a0001 | c0005 | t0001 | g0072 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0297 | AFR | ASW | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ASW | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0261 | EUR | TSI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0123 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02486 | hp2 | a0001 | c0005 | t0001 | g0041 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0070 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | USA | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | USA | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0303 | REF | REF | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0186 | REF | REF | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:14563670 | A | AC | 1 | a0002 | 9 | HG00673.hp2 HG01517.hp2 HG01934.hp2 others(6): Show |
frameshift_variant | HIGH | c.135dupC | p.Ala46fs | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 4/13 | 239/1139 | 136/927 | 46/308 | INFO_REALIGN_3_PRIME | chr19 | 14563670 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:14564260 | C | A | 1 | a0001c0003 | 15 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
synonymous_variant | LOW | c.462C>A | p.Gly154Gly | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 7/13 | 565/1139 | 462/927 | 154/308 | chr19 | 14564260 | |||
chr19:14564791 | C | T | 1 | a0001c0007 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.495C>T | p.Cys165Cys | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 8/13 | 598/1139 | 495/927 | 165/308 | chr19 | 14564791 | |||
chr19:14565077 | C | T | 2 | a0001c0003 a0001c0005 |
21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
synonymous_variant | LOW | c.618C>T | p.Leu206Leu | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 10/13 | 721/1139 | 618/927 | 206/308 | chr19 | 14565077 | |||
chr19:14565766 | C | T | 2 | a0001c0002 a0002c0006 |
33 | HG01515.hp1 HG01517.hp2 HG01934.hp2 others(30): Show |
synonymous_variant | LOW | c.822C>T | p.Gly274Gly | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 13/13 | 925/1139 | 822/927 | 274/308 | chr19 | 14565766 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:14529601 | C | T | 1 | a0001c0001t0004 | 1 | NA19066.hp2 | 5_prime_UTR_variant | MODIFIER | c.-96C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/13 | 96 | chr19 | 14529601 | ||||||
chr19:14529623 | T | C | 1 | a0001c0001t0002 | 5 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-74T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/13 | 74 | chr19 | 14529623 | ||||||
chr19:14529672 | G | A | 1 | a0001c0001t0003 | 1 | HG00558.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/13 | 25 | chr19 | 14529672 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:14529876 | A | G | 1 | a0001c0001t0001g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+165A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14529876 | |||||||
chr19:14529965 | C | T | 1 | a0001c0001t0001g0322 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+254C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14529965 | |||||||
chr19:14529986 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(3): Show |
6 | HG02055.hp1 HG03710.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+275T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14529986 | |||||||
chr19:14530225 | A | G | 34 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0289 others(31): Show |
36 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.15+514A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530225 | |||||||
chr19:14530242 | T | C | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(43): Show |
48 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.15+531T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530242 | |||||||
chr19:14530484 | T | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+773T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530484 | |||||||
chr19:14530656 | G | C | 1 | a0001c0001t0001g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+945G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530656 | |||||||
chr19:14530828 | A | G | 5 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(2): Show |
5 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+1117A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530828 | |||||||
chr19:14530855 | G | T | 1 | a0001c0001t0001g0288 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.15+1144G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530855 | |||||||
chr19:14531056 | CAG | C | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG01070.hp2 HG01071.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.15+1348_15+1349del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14531056 | ||||||
chr19:14531097 | C | T | 1 | a0001c0002t0001g0287 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.15+1386C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531097 | |||||||
chr19:14531240 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.15+1529T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531240 | |||||||
chr19:14531284 | T | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(13): Show |
16 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+1573T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531284 | |||||||
chr19:14531288 | C | G | 1 | a0001c0001t0001g0286 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.15+1577C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531288 | |||||||
chr19:14531326 | T | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(180): Show |
188 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.15+1615T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531326 | |||||||
chr19:14531327 | G | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(3): Show |
6 | HG01123.hp1 HG02109.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+1616G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531327 | |||||||
chr19:14531329 | G | A | 1 | a0001c0002t0001g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.15+1618G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531329 | |||||||
chr19:14531332 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(3): Show |
6 | HG02109.hp1 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+1621C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531332 | |||||||
chr19:14531350 | G | C | 21 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(18): Show |
21 | HG02145.hp2 HG02451.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.15+1639G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531350 | |||||||
chr19:14531382 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+1671C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531382 | |||||||
chr19:14531399 | A | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG02083.hp2 HG03831.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.15+1688A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531399 | |||||||
chr19:14531453 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG01934.hp1 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.15+1742G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531453 | |||||||
chr19:14531679 | C | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0292 a0001c0001t0001g0293 others(2): Show |
6 | HG01109.hp2 HG02257.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+1968C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531679 | |||||||
chr19:14531869 | C | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+2158C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531869 | |||||||
chr19:14532009 | G | GA | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0043 others(15): Show |
18 | HG01123.hp1 HG01243.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.15+2320dupA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532009 | ||||||
chr19:14532009 | GA | G | 14 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0146 others(11): Show |
14 | HG00140.hp2 HG01070.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+2320delA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532009 | ||||||
chr19:14532009 | GAAAA | G | 14 | a0001c0001t0001g0027 a0001c0001t0001g0149 a0001c0001t0001g0150 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+2317_15+2320del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532009 | ||||||
chr19:14532010 | A | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.15+2299A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532010 | |||||||
chr19:14532032 | G | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+2321G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532032 | |||||||
chr19:14532033 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(49): Show |
54 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.15+2322C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532033 | |||||||
chr19:14532283 | C | T | 14 | a0001c0001t0001g0027 a0001c0001t0001g0149 a0001c0001t0001g0150 others(11): Show |
14 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+2572C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532283 | |||||||
chr19:14532344 | A | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(219): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.15+2633A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532344 | |||||||
chr19:14532420 | C | T | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.15+2709C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532420 | |||||||
chr19:14532456 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.15+2745T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532456 | |||||||
chr19:14532512 | C | CA | 22 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0045 others(19): Show |
22 | HG01074.hp2 HG01175.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.15+2824dupA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532512 | ||||||
chr19:14532512 | CA | C | 70 | a0001c0001t0001g0044 a0001c0001t0001g0074 a0001c0001t0001g0075 others(67): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.15+2824delA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532512 | ||||||
chr19:14532512 | CAA | C | 11 | a0001c0001t0001g0150 a0001c0001t0001g0280 a0001c0001t0001g0284 others(8): Show |
11 | HG00323.hp1 HG01975.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.15+2823_15+2824del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532512 | ||||||
chr19:14532527 | A | T | 1 | a0001c0001t0001g0240 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.15+2816A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532527 | |||||||
chr19:14532542 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.15+2831C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532542 | |||||||
chr19:14532613 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0005t0001g0029 others(1): Show |
4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+2902C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532613 | |||||||
chr19:14532687 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(64): Show |
69 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.15+2976C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532687 | |||||||
chr19:14532696 | G | A | 18 | a0001c0001t0001g0027 a0001c0001t0001g0149 a0001c0001t0001g0150 others(15): Show |
18 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.15+2985G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532696 | |||||||
chr19:14532799 | G | A | 8 | a0001c0001t0001g0027 a0001c0002t0001g0020 a0001c0002t0001g0023 others(5): Show |
8 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+3088G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532799 | |||||||
chr19:14532831 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.15+3120C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532831 | |||||||
chr19:14532907 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3196C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532907 | |||||||
chr19:14532908 | G | C | 2 | a0001c0002t0001g0297 a0001c0002t0001g0298 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.15+3197G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532908 | |||||||
chr19:14533044 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(58): Show |
63 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.15+3333C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533044 | |||||||
chr19:14533216 | T | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3505T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533216 | |||||||
chr19:14533350 | G | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3639G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533350 | |||||||
chr19:14533397 | G | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3686G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533397 | |||||||
chr19:14533407 | C | T | 82 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(79): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.15+3696C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533407 | |||||||
chr19:14533548 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3837A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533548 | |||||||
chr19:14533595 | C | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3884C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533595 | |||||||
chr19:14533595 | C | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3884C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533595 | |||||||
chr19:14533680 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15+3969T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533680 | |||||||
chr19:14533797 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4086C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533797 | |||||||
chr19:14533849 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.15+4138A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533849 | |||||||
chr19:14533992 | T | A | 88 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(85): Show |
88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.15+4281T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533992 | |||||||
chr19:14533997 | C | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.15+4286C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533997 | |||||||
chr19:14534003 | A | G | 8 | a0001c0001t0001g0027 a0001c0002t0001g0020 a0001c0002t0001g0023 others(5): Show |
8 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+4292A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534003 | |||||||
chr19:14534009 | T | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4298T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534009 | |||||||
chr19:14534063 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4352C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534063 | |||||||
chr19:14534089 | T | G | 1 | a0001c0001t0001g0322 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+4378T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534089 | |||||||
chr19:14534116 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.15+4405A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534116 | |||||||
chr19:14534126 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.15+4415C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534126 | |||||||
chr19:14534164 | G | A | 84 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.15+4453G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534164 | |||||||
chr19:14534193 | T | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0052 others(45): Show |
50 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.15+4482T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534193 | |||||||
chr19:14534239 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.15+4528C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534239 | |||||||
chr19:14534273 | T | C | 92 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0031 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.15+4562T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534273 | |||||||
chr19:14534300 | AT | A | 84 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.15+4594delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534300 | ||||||
chr19:14534306 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4595A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534306 | |||||||
chr19:14534366 | C | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4655C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534366 | |||||||
chr19:14534371 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.15+4660G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534371 | |||||||
chr19:14534408 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.15+4697G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534408 | |||||||
chr19:14534423 | C | CT | 80 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
83 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+4742dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | C | CTT | 32 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0058 others(29): Show |
33 | HG00735.hp2 HG01081.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.15+4741_15+4742dup others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | C | CTTT | 14 | a0001c0001t0001g0008 a0001c0001t0001g0152 a0001c0001t0001g0292 others(11): Show |
16 | HG01109.hp2 HG01192.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+4740_15+4742dup others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | CT | C | 39 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0050 others(36): Show |
39 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.15+4742delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | CTT | C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0101 others(16): Show |
21 | HG00558.hp2 HG01081.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.15+4741_15+4742del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | CTTTT | C | 29 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0090 others(26): Show |
29 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.15+4739_15+4742del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | CTTTTT | C | 35 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(32): Show |
35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.15+4738_15+4742del others(5): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | CTTTTTT | C | 7 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0149 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+4737_15+4742del others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | CTTTTTTT | C | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02622.hp1 HG02630.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+4736_15+4742del others(7): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0150 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+4735_15+4742del others(8): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15+4732_15+4742del others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0164 a0001c0001t0001g0174 a0001c0001t0001g0175 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.15+4731_15+4742del others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534423 | CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
7 | HG01070.hp1 HG01358.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.15+4730_15+4742del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | ||||||
chr19:14534479 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.15+4768A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534479 | |||||||
chr19:14534491 | A | C | 1 | a0001c0001t0001g0160 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.15+4780A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534491 | |||||||
chr19:14534528 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0278 |
2 | HG00738.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.15+4817C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534528 | |||||||
chr19:14534549 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4838C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534549 | |||||||
chr19:14534648 | G | C | 1 | a0001c0001t0001g0044 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.15+4937G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534648 | |||||||
chr19:14534804 | G | A | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG01070.hp2 HG01071.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.15+5093G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534804 | |||||||
chr19:14534995 | G | A | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5284G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534995 | |||||||
chr19:14535198 | C | A | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0051 others(61): Show |
67 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.15+5487C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535198 | |||||||
chr19:14535245 | T | C | 92 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0031 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.15+5534T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535245 | |||||||
chr19:14535391 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5680C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535391 | |||||||
chr19:14535438 | C | T | 2 | a0001c0002t0001g0232 a0001c0002t0001g0239 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.15+5727C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535438 | |||||||
chr19:14535455 | CGAGATCG others(242): Show |
C | 2 | a0001c0002t0001g0037 a0001c0005t0001g0036 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.15+5753_15+6001del | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535455 | ||||||
chr19:14535456 | G | A | 48 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0052 others(45): Show |
50 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.15+5745G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535456 | |||||||
chr19:14535475 | C | G | 4 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0200 others(1): Show |
4 | HG01261.hp2 HG01943.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5764C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535475 | |||||||
chr19:14535493 | C | T | 1 | a0002c0006t0001g0305 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.15+5782C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535493 | |||||||
chr19:14535494 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.15+5783G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535494 | |||||||
chr19:14535506 | CA | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0053 others(8): Show |
11 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+5833delA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | ||||||
chr19:14535506 | CAA | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0160 a0001c0001t0001g0185 others(5): Show |
8 | HG01099.hp2 HG01169.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5832_15+5833del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | ||||||
chr19:14535506 | CAAA | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0151 a0001c0001t0001g0224 others(11): Show |
14 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.15+5831_15+5833del others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | ||||||
chr19:14535506 | CAAAA | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0073 a0001c0001t0001g0164 others(4): Show |
7 | HG01109.hp2 HG01358.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.15+5830_15+5833del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | ||||||
chr19:14535506 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0311 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.15+5824_15+5833del others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | ||||||
chr19:14535506 | CAAAAAAA others(5): Show |
C | 1 | a0001c0003t0001g0227 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.15+5822_15+5833del others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | ||||||
chr19:14535506 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0218 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.15+5821_15+5833del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | ||||||
chr19:14535517 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0001g0213 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.15+5808_15+5835del others(28): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535517 | ||||||
chr19:14535521 | AAAAAAAA others(35): Show |
A | 2 | a0001c0001t0001g0147 a0001c0003t0001g0145 |
2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.15+5812_15+5853del others(42): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535521 | ||||||
chr19:14535523 | AAAAAAAA others(35): Show |
A | 1 | a0001c0001t0001g0148 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.15+5814_15+5855del others(42): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535523 | ||||||
chr19:14535523 | AAAAAAAA others(37): Show |
A | 1 | a0001c0001t0001g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.15+5814_15+5857del others(44): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535523 | ||||||
chr19:14535525 | AAAAAAAA others(19): Show |
A | 1 | a0001c0001t0001g0140 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.15+5816_15+5841del others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535525 | ||||||
chr19:14535528 | AAAAAAAA others(28): Show |
A | 3 | a0001c0001t0001g0031 a0001c0005t0001g0029 a0001c0005t0001g0032 |
3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.15+5819_15+5853del others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535528 | ||||||
chr19:14535529 | AAAAAAAA others(29): Show |
A | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.15+5820_15+5855del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535529 | ||||||
chr19:14535530 | AAAAAAAA others(24): Show |
A | 1 | a0001c0003t0001g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.15+5821_15+5851del others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535530 | ||||||
chr19:14535530 | AAAAAAAA others(28): Show |
A | 1 | a0001c0001t0001g0030 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.15+5821_15+5855del others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535530 | ||||||
chr19:14535531 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0001g0313 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.15+5822_15+5849del others(28): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535531 | ||||||
chr19:14535531 | AAAAAAAA others(23): Show |
A | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.15+5822_15+5851del others(30): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535531 | ||||||
chr19:14535531 | AAAAAAAA others(33): Show |
A | 1 | a0001c0005t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+5822_15+5861del others(40): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535531 | ||||||
chr19:14535532 | AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0001g0310 a0001c0005t0001g0042 |
2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.15+5823_15+5835del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535532 | ||||||
chr19:14535532 | AAAAAAAA others(30): Show |
A | 1 | a0001c0001t0001g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.15+5823_15+5859del others(37): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535532 | ||||||
chr19:14535533 | AAAAAAAA others(19): Show |
A | 1 | a0001c0002t0001g0316 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.15+5824_15+5849del others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535533 | ||||||
chr19:14535533 | AAAAAAAA others(23): Show |
A | 6 | a0001c0001t0001g0124 a0001c0001t0001g0299 a0001c0001t0001g0317 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+5824_15+5853del others(30): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535533 | ||||||
chr19:14535533 | AAAAAAAA others(25): Show |
A | 1 | a0001c0001t0001g0090 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.15+5824_15+5855del others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535533 | ||||||
chr19:14535533 | AAAAAAAA others(29): Show |
A | 3 | a0001c0001t0001g0247 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG01891.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.15+5824_15+5859del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535533 | ||||||
chr19:14535533 | AAAAAAAA others(31): Show |
A | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.15+5824_15+5861del others(38): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535533 | ||||||
chr19:14535534 | AAAAAAAA others(18): Show |
A | 3 | a0001c0001t0001g0033 a0001c0001t0002g0011 a0001c0002t0001g0034 |
3 | HG02109.hp1 HG02723.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.15+5825_15+5849del others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | ||||||
chr19:14535534 | AAAAAAAA others(24): Show |
A | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+5825_15+5855del others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | ||||||
chr19:14535534 | AAAAAAAA others(26): Show |
A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0323 |
2 | HG01257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.15+5825_15+5857del others(33): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | ||||||
chr19:14535534 | AAAAAAAA others(28): Show |
A | 1 | a0001c0001t0001g0263 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.15+5825_15+5859del others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | ||||||
chr19:14535534 | AAAAAAAA others(30): Show |
A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0277 |
3 | HG01243.hp1 HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.15+5825_15+5861del others(37): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | ||||||
chr19:14535534 | AAAAAAAA others(32): Show |
A | 3 | a0001c0001t0001g0045 a0001c0003t0001g0123 a0001c0003t0001g0242 |
3 | HG02055.hp2 HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.15+5825_15+5863del others(39): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | ||||||
chr19:14535535 | AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.15+5826_15+5845del others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | ||||||
chr19:14535535 | AAAAAAAA others(23): Show |
A | 2 | a0001c0001t0001g0116 a0001c0001t0002g0015 |
2 | HG01081.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.15+5826_15+5855del others(30): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | ||||||
chr19:14535535 | AAAAAAAA others(25): Show |
A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0104 a0001c0001t0001g0109 others(2): Show |
5 | HG00280.hp2 HG01243.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+5826_15+5857del others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | ||||||
chr19:14535535 | AAAAAAAA others(27): Show |
A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0291 |
2 | HG03834.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.15+5826_15+5859del others(34): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | ||||||
chr19:14535535 | AAAAAAAA others(29): Show |
A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0153 |
2 | HG03831.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.15+5826_15+5861del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | ||||||
chr19:14535535 | AAAAAAAA others(31): Show |
A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0245 a0001c0001t0001g0271 others(1): Show |
4 | HG00323.hp1 HG01433.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5826_15+5863del others(38): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | ||||||
chr19:14535536 | AAAAAAAA others(4): Show |
A | 1 | a0001c0002t0001g0239 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.15+5827_15+5837del others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | ||||||
chr19:14535536 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0051 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.15+5827_15+5839del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | ||||||
chr19:14535536 | AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0001g0308 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.15+5827_15+5845del others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | ||||||
chr19:14535536 | AAAAAAAA others(14): Show |
A | 1 | a0001c0001t0001g0215 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.15+5827_15+5847del others(21): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | ||||||
chr19:14535536 | AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0002g0013 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.15+5827_15+5849del others(23): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | ||||||
chr19:14535536 | AAAAAAAA others(18): Show |
A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0103 |
3 | HG02735.hp2 HG03017.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.15+5827_15+5851del others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | ||||||
chr19:14535536 | AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0137 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.15+5827_15+5855del others(29): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | ||||||
chr19:14535536 | AAAAAAAA others(24): Show |
A | 8 | a0001c0001t0001g0101 a0001c0001t0001g0106 a0001c0001t0001g0115 others(5): Show |
8 | HG00735.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+5827_15+5857del others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | ||||||
chr19:14535536 | AAAAAAAA others(26): Show |
A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0111 others(7): Show |
11 | HG00558.hp2 HG01074.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+5827_15+5859del others(33): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | ||||||
chr19:14535536 | AAAAAAAA others(28): Show |
A | 4 | a0001c0001t0001g0081 a0001c0001t0001g0133 a0001c0001t0001g0217 others(1): Show |
4 | HG00642.hp1 HG01515.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5827_15+5861del others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | ||||||
chr19:14535536 | AAAAAAAA others(30): Show |
A | 5 | a0001c0001t0001g0162 a0001c0001t0001g0248 a0001c0001t0001g0265 others(2): Show |
5 | HG01346.hp2 HG01928.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+5827_15+5863del others(37): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | ||||||
chr19:14535537 | A | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0172 a0001c0001t0001g0177 |
3 | HG03486.hp1 NA18946.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.15+5826A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535537 | |||||||
chr19:14535537 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0309 a0001c0002t0001g0057 |
2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.15+5828_15+5837del others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | ||||||
chr19:14535537 | AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0238 |
2 | HG02630.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.15+5828_15+5845del others(18): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | ||||||
chr19:14535537 | AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0001g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.15+5828_15+5847del others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | ||||||
chr19:14535537 | AAAAAAAA others(23): Show |
A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0110 |
2 | HG02074.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.15+5828_15+5857del others(30): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | ||||||
chr19:14535537 | AAAAAAAA others(25): Show |
A | 6 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0136 others(3): Show |
6 | HG01952.hp1 HG02683.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+5828_15+5859del others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | ||||||
chr19:14535537 | AAAAAAAA others(27): Show |
A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0223 others(1): Show |
4 | HG00673.hp2 HG02602.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5828_15+5861del others(34): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | ||||||
chr19:14535537 | AAAAAAAA others(29): Show |
A | 11 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0001g0099 others(8): Show |
11 | HG00639.hp2 HG01069.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+5828_15+5863del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | ||||||
chr19:14535537 | AAAAAAAA others(31): Show |
A | 1 | a0001c0001t0001g0050 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.15+5828_15+5865del others(38): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | ||||||
chr19:14535537 | AAAAAAAA others(35): Show |
A | 1 | a0001c0001t0002g0012 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.15+5828_15+5869del others(42): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | ||||||
chr19:14535538 | AAAAAAAT others(20): Show |
A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0001g0078 others(1): Show |
4 | HG00558.hp1 HG01993.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5829_15+5855del others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535538 | ||||||
chr19:14535538 | AAAAAAAT others(24): Show |
A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0130 |
2 | HG01175.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.15+5829_15+5859del others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535538 | ||||||
chr19:14535538 | AAAAAAAT others(26): Show |
A | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.15+5829_15+5861del others(33): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535538 | ||||||
chr19:14535538 | AAAAAAAT others(28): Show |
A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0080 a0001c0001t0001g0086 others(2): Show |
5 | HG02074.hp1 HG02132.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+5829_15+5863del others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535538 | ||||||
chr19:14535538 | AAAAAAAT others(30): Show |
A | 2 | a0001c0001t0001g0273 a0002c0004t0001g0269 |
2 | HG01074.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.15+5829_15+5865del others(37): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535538 | ||||||
chr19:14535539 | A | T | 13 | a0001c0001t0001g0058 a0001c0001t0001g0152 a0001c0001t0001g0171 others(10): Show |
14 | HG01070.hp1 HG01261.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.15+5828A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535539 | |||||||
chr19:14535539 | AAAAAATA others(3): Show |
A | 2 | a0001c0002t0001g0232 a0001c0005t0001g0041 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.15+5830_15+5839del others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | ||||||
chr19:14535539 | AAAAAATA others(5): Show |
A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0304 |
2 | HG01358.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.15+5830_15+5841del others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | ||||||
chr19:14535539 | AAAAAATA others(15): Show |
A | 1 | a0001c0001t0002g0014 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.15+5830_15+5851del others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | ||||||
chr19:14535539 | AAAAAATA others(17): Show |
A | 1 | a0001c0001t0001g0143 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.15+5830_15+5853del others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | ||||||
chr19:14535539 | AAAAAATA others(19): Show |
A | 1 | a0001c0001t0001g0074 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.15+5830_15+5855del others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | ||||||
chr19:14535539 | AAAAAATA others(25): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.15+5830_15+5861del others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | ||||||
chr19:14535539 | AAAAAATA others(27): Show |
A | 5 | a0001c0001t0001g0083 a0001c0001t0001g0096 a0001c0001t0001g0098 others(2): Show |
5 | HG02040.hp1 HG03654.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+5830_15+5863del others(34): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | ||||||
chr19:14535539 | AAAAAATA others(29): Show |
A | 5 | a0001c0001t0001g0154 a0001c0001t0001g0258 a0001c0001t0001g0279 others(2): Show |
5 | HG00140.hp1 HG00733.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+5830_15+5865del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | ||||||
chr19:14535540 | AAAAATAT others(4): Show |
A | 1 | a0001c0001t0001g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.15+5831_15+5841del others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | ||||||
chr19:14535540 | AAAAATAT others(8): Show |
A | 1 | a0001c0001t0001g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.15+5831_15+5845del others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | ||||||
chr19:14535540 | AAAAATAT others(10): Show |
A | 1 | a0001c0002t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.15+5831_15+5847del others(17): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | ||||||
chr19:14535540 | AAAAATAT others(12): Show |
A | 1 | a0001c0001t0001g0181 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.15+5831_15+5849del others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | ||||||
chr19:14535540 | AAAAATAT others(16): Show |
A | 1 | a0001c0001t0001g0055 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.15+5831_15+5853del others(23): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | ||||||
chr19:14535540 | AAAAATAT others(18): Show |
A | 1 | a0001c0001t0001g0065 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.15+5831_15+5855del others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | ||||||
chr19:14535540 | AAAAATAT others(20): Show |
A | 1 | a0001c0001t0001g0214 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.15+5831_15+5857del others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | ||||||
chr19:14535540 | AAAAATAT others(22): Show |
A | 1 | a0001c0001t0001g0006 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.15+5831_15+5859del others(29): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | ||||||
chr19:14535540 | AAAAATAT others(24): Show |
A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG01192.hp2 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.15+5831_15+5861del others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | ||||||
chr19:14535540 | AAAAATAT others(26): Show |
A | 1 | a0001c0001t0001g0175 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.15+5831_15+5863del others(33): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | ||||||
chr19:14535540 | AAAAATAT others(30): Show |
A | 1 | a0001c0001t0001g0180 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.15+5831_15+5867del others(37): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | ||||||
chr19:14535541 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0158 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.15+5831_15+5832ins others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | ||||||
chr19:14535541 | A | AATATATA others(15): Show |
1 | a0001c0001t0001g0234 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.15+5831_15+5832ins others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | ||||||
chr19:14535541 | A | AT | 4 | a0001c0001t0001g0163 a0001c0001t0001g0190 a0001c0001t0001g0233 others(1): Show |
4 | NA18940.hp2 NA18970.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5830_15+5831ins others(1): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535541 | |||||||
chr19:14535541 | A | ATAT | 5 | a0001c0001t0001g0027 a0001c0001t0001g0063 a0001c0001t0001g0167 others(2): Show |
5 | HG00408.hp1 HG00438.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+5830_15+5831ins others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535541 | |||||||
chr19:14535541 | A | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0038 others(30): Show |
35 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.15+5830A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535541 | |||||||
chr19:14535541 | AAAATATA others(5): Show |
A | 1 | a0001c0001t0001g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15+5832_15+5843del others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | ||||||
chr19:14535541 | AAAATATA others(9): Show |
A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0231 |
2 | HG03098.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.15+5832_15+5847del others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | ||||||
chr19:14535541 | AAAATATA others(11): Show |
A | 1 | a0001c0001t0001g0202 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.15+5832_15+5849del others(18): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | ||||||
chr19:14535541 | AAAATATA others(17): Show |
A | 1 | a0001c0002t0001g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.15+5832_15+5855del others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | ||||||
chr19:14535542 | AAATATAT others(26): Show |
A | 1 | a0002c0004t0001g0166 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.15+5833_15+5865del others(33): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535542 | ||||||
chr19:14535543 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0005 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.15+5833_15+5834ins others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535543 | ||||||
chr19:14535543 | A | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(74): Show |
81 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.15+5832A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535543 | |||||||
chr19:14535544 | ATAT | A | 3 | a0001c0001t0001g0179 a0001c0003t0001g0022 a0001c0003t0001g0025 |
3 | HG02896.hp1 HG02897.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.15+5834_15+5836del others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535544 | |||||||
chr19:14535544 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.15+5834_15+5846del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535544 | |||||||
chr19:14535544 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.15+5834_15+5848del others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535544 | |||||||
chr19:14535544 | ATATATAT others(18): Show |
A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0212 |
2 | NA18962.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.15+5834_15+5858del others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535544 | |||||||
chr19:14535547 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.15+5836T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535547 | |||||||
chr19:14535549 | T | A | 4 | a0001c0001t0001g0179 a0001c0001t0001g0222 a0001c0003t0001g0022 others(1): Show |
4 | HG00738.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5838T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535549 | |||||||
chr19:14535551 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.15+5840T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535551 | |||||||
chr19:14535558 | ATATATAT others(29): Show |
A | 5 | a0001c0001t0001g0091 a0001c0001t0001g0252 a0001c0001t0001g0270 others(2): Show |
5 | HG00140.hp2 HG00738.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+5856_15+5891del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535558 | ||||||
chr19:14535559 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.15+5848T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535559 | |||||||
chr19:14535560 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.15+5849A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535560 | |||||||
chr19:14535560 | ATATATAT others(27): Show |
A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0251 a0001c0001t0001g0255 others(1): Show |
4 | HG00323.hp2 HG01123.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5858_15+5891del others(34): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535560 | ||||||
chr19:14535562 | ATATATAT others(25): Show |
A | 8 | a0001c0001t0001g0092 a0001c0001t0001g0250 a0001c0001t0001g0254 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5860_15+5891del others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535562 | ||||||
chr19:14535563 | T | A | 2 | a0001c0001t0001g0033 a0001c0002t0001g0034 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.15+5852T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535563 | |||||||
chr19:14535566 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0001g0274 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.15+5864_15+5891del others(28): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535566 | ||||||
chr19:14535571 | T | A | 1 | a0001c0001t0001g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+5860T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535571 | |||||||
chr19:14535575 | T | A | 1 | a0001c0001t0001g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+5864T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535575 | |||||||
chr19:14535584 | A | ATATATG | 3 | a0001c0001t0001g0062 a0001c0002t0001g0060 a0001c0002t0001g0068 |
3 | HG02717.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.15+5877_15+5882dup others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535584 | ||||||
chr19:14535584 | A | ATATG | 3 | a0001c0001t0001g0302 a0001c0002t0001g0001 a0001c0003t0001g0070 |
3 | HG02280.hp2 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.15+5876_15+5877ins others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535584 | ||||||
chr19:14535584 | A | G | 21 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0061 others(18): Show |
21 | HG00558.hp1 HG01168.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.15+5873A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535584 | |||||||
chr19:14535586 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0225 |
2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.15+5875A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535586 | |||||||
chr19:14535590 | G | A | 70 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(67): Show |
70 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.15+5879G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535590 | |||||||
chr19:14535594 | G | A | 45 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0080 others(42): Show |
45 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.15+5883G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535594 | |||||||
chr19:14535659 | C | CAGGAGAA others(4): Show |
1 | a0001c0001t0001g0317 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.15+5949_15+5959dup others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535659 | ||||||
chr19:14535693 | C | T | 88 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(85): Show |
88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.15+5982C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535693 | |||||||
chr19:14535700 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(63): Show |
68 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.15+5989G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535700 | |||||||
chr19:14535756 | C | CA | 66 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0026 others(63): Show |
68 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.15+6066dupA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535756 | ||||||
chr19:14535756 | C | CAAAAA | 53 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(50): Show |
53 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.15+6062_15+6066dup others(5): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535756 | ||||||
chr19:14535756 | C | CAAAAAA | 19 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
19 | HG00642.hp2 HG00741.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.15+6061_15+6066dup others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535756 | ||||||
chr19:14535756 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0139 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.15+6056_15+6066del others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535756 | ||||||
chr19:14535778 | G | A | 2 | a0001c0001t0001g0033 a0001c0002t0001g0034 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.15+6067G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535778 | |||||||
chr19:14535779 | G | A | 21 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0053 others(18): Show |
22 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.15+6068G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535779 | |||||||
chr19:14535948 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.15+6237A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535948 | |||||||
chr19:14535990 | C | T | 8 | a0001c0001t0001g0027 a0001c0002t0001g0020 a0001c0002t0001g0023 others(5): Show |
8 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+6279C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535990 | |||||||
chr19:14536022 | C | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6311C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536022 | |||||||
chr19:14536023 | A | G | 84 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.15+6312A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536023 | |||||||
chr19:14536091 | C | G | 88 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(85): Show |
88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.15+6380C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536091 | |||||||
chr19:14536106 | G | A | 4 | a0001c0001t0001g0149 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+6395G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536106 | |||||||
chr19:14536161 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6450G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536161 | |||||||
chr19:14536219 | C | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0066 a0001c0001t0001g0143 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+6508C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536219 | |||||||
chr19:14536267 | G | GT | 28 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0053 others(25): Show |
30 | HG00408.hp1 HG00408.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.15+6573dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14536267 | ||||||
chr19:14536267 | GT | G | 8 | a0001c0001t0001g0092 a0001c0001t0001g0124 a0001c0001t0001g0181 others(5): Show |
8 | HG02040.hp2 HG02109.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+6573delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14536267 | ||||||
chr19:14536267 | GTT | G | 79 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(76): Show |
79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.15+6572_15+6573del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14536267 | ||||||
chr19:14536414 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6703C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536414 | |||||||
chr19:14536470 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6759A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536470 | |||||||
chr19:14536547 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.15+6836G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536547 | |||||||
chr19:14536641 | G | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG01934.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+6930G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536641 | |||||||
chr19:14536690 | C | A | 2 | a0001c0002t0001g0118 a0001c0002t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.15+6979C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536690 | |||||||
chr19:14536696 | T | A | 86 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(83): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.15+6985T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536696 | |||||||
chr19:14536820 | C | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0005t0001g0029 others(1): Show |
4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+7109C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536820 | |||||||
chr19:14536923 | C | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(65): Show |
70 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.15+7212C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536923 | |||||||
chr19:14537033 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0143 a0001c0002t0001g0056 |
3 | HG01168.hp2 HG01169.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.15+7322G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537033 | |||||||
chr19:14537252 | T | TGGGGGAG others(13): Show |
5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0005t0001g0029 others(2): Show |
5 | HG01123.hp1 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+7577_15+7596dup others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537252 | ||||||
chr19:14537252 | TGGGGGAG others(13): Show |
T | 1 | a0001c0001t0001g0051 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.15+7577_15+7596del others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537252 | ||||||
chr19:14537275 | G | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+7564G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537275 | |||||||
chr19:14537431 | G | T | 8 | a0001c0001t0001g0027 a0001c0002t0001g0020 a0001c0002t0001g0023 others(5): Show |
8 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+7720G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537431 | |||||||
chr19:14537445 | T | TGAG | 89 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.15+7735_15+7737dup others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537445 | ||||||
chr19:14537497 | C | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(57): Show |
62 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.15+7786C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537497 | |||||||
chr19:14537547 | A | T | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+7836A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537547 | |||||||
chr19:14537732 | T | G | 85 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(82): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+8021T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537732 | |||||||
chr19:14537744 | G | GT | 21 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0164 others(18): Show |
21 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.15+8052dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537744 | ||||||
chr19:14537744 | G | GTT | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(56): Show |
61 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.15+8051_15+8052dup others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537744 | ||||||
chr19:14537744 | G | GTTT | 6 | a0001c0001t0001g0050 a0001c0001t0001g0109 a0001c0001t0001g0137 others(3): Show |
6 | HG01952.hp1 HG02027.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+8050_15+8052dup others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537744 | ||||||
chr19:14537744 | GT | G | 7 | a0001c0001t0001g0073 a0001c0001t0001g0098 a0001c0001t0001g0162 others(4): Show |
7 | HG00738.hp2 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+8052delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537744 | ||||||
chr19:14537744 | GTT | G | 84 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.15+8051_15+8052del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537744 | ||||||
chr19:14537834 | C | T | 85 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(82): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+8123C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537834 | |||||||
chr19:14537849 | G | T | 1 | a0001c0001t0001g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.15+8138G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537849 | |||||||
chr19:14537907 | G | C | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+8196G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537907 | |||||||
chr19:14538172 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.15+8461C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538172 | |||||||
chr19:14538229 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.15+8518G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538229 | |||||||
chr19:14538388 | G | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+8677G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538388 | |||||||
chr19:14538398 | C | T | 64 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0080 others(61): Show |
64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.15+8687C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538398 | |||||||
chr19:14538443 | G | A | 5 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0125 others(2): Show |
5 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+8732G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538443 | |||||||
chr19:14538452 | G | A | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+8741G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538452 | |||||||
chr19:14538536 | CT | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.15+8840delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14538536 | ||||||
chr19:14538544 | T | C | 1 | a0001c0002t0001g0195 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.15+8833T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538544 | |||||||
chr19:14538546 | T | C | 1 | a0001c0002t0001g0049 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.15+8835T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538546 | |||||||
chr19:14538687 | C | A | 64 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0080 others(61): Show |
64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.15+8976C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538687 | |||||||
chr19:14538721 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+9010C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538721 | |||||||
chr19:14538744 | G | A | 6 | a0001c0001t0001g0162 a0001c0001t0001g0248 a0001c0001t0001g0249 others(3): Show |
6 | HG00323.hp1 HG00639.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+9033G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538744 | |||||||
chr19:14538769 | G | A | 85 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(82): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+9058G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538769 | |||||||
chr19:14538778 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.15+9067G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538778 | |||||||
chr19:14538779 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.15+9068C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538779 | |||||||
chr19:14538821 | A | G | 89 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.15+9110A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538821 | |||||||
chr19:14538851 | A | G | 3 | a0001c0001t0001g0031 a0001c0005t0001g0029 a0001c0005t0001g0032 |
3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.15+9140A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538851 | |||||||
chr19:14538978 | T | A | 1 | a0001c0001t0001g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+9267T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538978 | |||||||
chr19:14539004 | C | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+9293C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539004 | |||||||
chr19:14539105 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0005t0001g0029 others(1): Show |
4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+9394C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539105 | |||||||
chr19:14539140 | A | AT | 28 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(25): Show |
29 | HG00738.hp1 HG01123.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.15+9456dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | ||||||
chr19:14539140 | AT | A | 11 | a0001c0001t0001g0016 a0001c0001t0001g0103 a0001c0001t0001g0104 others(8): Show |
11 | HG01516.hp1 HG01943.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+9456delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | ||||||
chr19:14539140 | ATT | A | 45 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(42): Show |
45 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.15+9455_15+9456del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | ||||||
chr19:14539140 | ATTT | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(134): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.15+9454_15+9456del others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | ||||||
chr19:14539140 | ATTTT | A | 10 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0105 others(7): Show |
10 | HG01069.hp2 HG01074.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+9453_15+9456del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | ||||||
chr19:14539140 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+9441_15+9456del others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | ||||||
chr19:14539346 | T | C | 13 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0150 others(10): Show |
13 | HG02109.hp1 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.15+9635T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539346 | |||||||
chr19:14539358 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.15+9647A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539358 | |||||||
chr19:14539684 | C | A | 1 | a0001c0002t0001g0195 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.15+9973C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539684 | |||||||
chr19:14539710 | C | T | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(61): Show |
66 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.15+9999C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539710 | |||||||
chr19:14539750 | C | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0051 others(46): Show |
51 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.15+10039C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539750 | |||||||
chr19:14539811 | C | T | 85 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(82): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+10100C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539811 | |||||||
chr19:14539880 | CT | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(112): Show |
119 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.15+10184delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539880 | ||||||
chr19:14539880 | CTTT | C | 88 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(85): Show |
88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.15+10182_15+10184d others(5): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539880 | ||||||
chr19:14539919 | G | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+10208G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539919 | |||||||
chr19:14539973 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.15+10262G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539973 | |||||||
chr19:14540014 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+10303G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540014 | |||||||
chr19:14540063 | A | AT | 79 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(76): Show |
79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.15+10366dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14540063 | ||||||
chr19:14540082 | C | T | 1 | a0001c0003t0001g0145 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.15+10371C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540082 | |||||||
chr19:14540090 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0223 a0001c0001t0001g0286 |
3 | HG00642.hp1 HG01515.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.15+10379C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540090 | |||||||
chr19:14540237 | A | C | 6 | a0001c0001t0001g0050 a0001c0001t0001g0243 a0001c0001t0001g0244 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+10526A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540237 | |||||||
chr19:14540244 | A | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(57): Show |
62 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.15+10533A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540244 | |||||||
chr19:14540330 | A | C | 2 | a0001c0001t0001g0115 a0001c0001t0002g0015 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.15+10619A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540330 | |||||||
chr19:14540422 | G | C | 1 | a0001c0002t0001g0316 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.15+10711G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540422 | |||||||
chr19:14540469 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.15+10758T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540469 | |||||||
chr19:14540528 | A | G | 64 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0080 others(61): Show |
64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.15+10817A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540528 | |||||||
chr19:14540592 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.15+10881G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540592 | |||||||
chr19:14540709 | A | G | 5 | a0001c0001t0001g0164 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | NA18946.hp2 NA18994.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+10998A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540709 | |||||||
chr19:14540713 | GA | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(65): Show |
70 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.15+11003delA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540713 | |||||||
chr19:14540774 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(1): Show |
4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+11063C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540774 | |||||||
chr19:14540813 | A | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0005t0001g0029 others(1): Show |
4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+11102A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540813 | |||||||
chr19:14540861 | G | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0046 others(38): Show |
43 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.15+11150G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540861 | |||||||
chr19:14540904 | G | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+11193G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540904 | |||||||
chr19:14540970 | G | A | 4 | a0001c0001t0001g0149 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+11259G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540970 | |||||||
chr19:14540976 | A | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0052 others(45): Show |
50 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.15+11265A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540976 | |||||||
chr19:14541033 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(57): Show |
62 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.15+11322C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541033 | |||||||
chr19:14541045 | C | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+11334C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541045 | |||||||
chr19:14541074 | A | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(154): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.15+11363A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541074 | |||||||
chr19:14541166 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.15+11455C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541166 | |||||||
chr19:14541306 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(57): Show |
62 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.15+11595A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541306 | |||||||
chr19:14541307 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(50): Show |
55 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.15+11596C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541307 | |||||||
chr19:14541466 | A | G | 89 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.15+11755A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541466 | |||||||
chr19:14541586 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.15+11875A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541586 | |||||||
chr19:14541783 | A | AT | 6 | a0001c0001t0001g0149 a0001c0001t0001g0164 a0001c0001t0001g0290 others(3): Show |
6 | HG02280.hp1 HG03453.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+12088dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14541783 | ||||||
chr19:14541798 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.15+12087T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541798 | |||||||
chr19:14541885 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0150 a0001c0001t0001g0318 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+12174C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541885 | |||||||
chr19:14541907 | C | T | 2 | a0001c0003t0001g0022 a0001c0003t0001g0025 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.15+12196C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541907 | |||||||
chr19:14542103 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+12392C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542103 | |||||||
chr19:14542260 | C | T | 64 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0080 others(61): Show |
64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.15+12549C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542260 | |||||||
chr19:14542282 | C | T | 1 | a0001c0002t0001g0232 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.15+12571C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542282 | |||||||
chr19:14542296 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(65): Show |
70 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.15+12585T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542296 | |||||||
chr19:14542347 | G | GGGTTTTT others(3): Show |
2 | a0001c0002t0001g0020 a0001c0003t0001g0024 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+12636_15+12637i others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542347 | |||||||
chr19:14542347 | G | GGGTTTTT others(4): Show |
1 | a0001c0002t0001g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+12636_15+12637i others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542347 | |||||||
chr19:14542347 | G | GGTTTTTT others(2): Show |
3 | a0001c0001t0001g0027 a0001c0003t0001g0022 a0001c0003t0001g0025 |
3 | HG02896.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.15+12636_15+12637i others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542347 | |||||||
chr19:14542347 | G | GGTTTTTT others(4): Show |
1 | a0001c0003t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.15+12636_15+12637i others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542347 | |||||||
chr19:14542347 | G | GT | 27 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0157 others(24): Show |
28 | HG00741.hp1 HG01070.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.15+12665dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | G | GTT | 8 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0222 others(5): Show |
9 | HG00738.hp1 HG01071.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+12664_15+12665d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | G | GTTTTTTT others(2): Show |
25 | a0001c0001t0001g0043 a0001c0001t0001g0081 a0001c0001t0001g0082 others(22): Show |
25 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.15+12657_15+12665d others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | G | GTTTTTTT others(3): Show |
22 | a0001c0001t0001g0044 a0001c0001t0001g0080 a0001c0001t0001g0085 others(19): Show |
22 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.15+12656_15+12665d others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | G | GTTTTTTT others(4): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG02083.hp1 HG02083.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.15+12655_15+12665d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | G | GTTTTTTT others(5): Show |
4 | a0001c0001t0001g0153 a0001c0001t0001g0248 a0001c0001t0001g0273 others(1): Show |
4 | HG00673.hp2 HG01074.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+12654_15+12665d others(14): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | G | GTTTTTTT others(8): Show |
3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0274 |
3 | HG01167.hp2 HG02300.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.15+12651_15+12665d others(17): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | G | GTTTTTTT others(9): Show |
1 | a0001c0002t0001g0088 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.15+12650_15+12665d others(18): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | G | GTTTTTTT others(10): Show |
1 | a0001c0002t0001g0089 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.15+12649_15+12665d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | GT | G | 37 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0053 others(34): Show |
39 | HG00099.hp2 HG00558.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.15+12665delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | GTT | G | 8 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0076 others(5): Show |
8 | HG00323.hp1 HG00639.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+12664_15+12665d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | GTTTTT | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(51): Show |
56 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.15+12661_15+12665d others(7): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | GTTTTTTT others(3): Show |
G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0005t0001g0029 others(1): Show |
4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+12656_15+12665d others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542347 | GTTTTTTT others(4): Show |
G | 4 | a0001c0001t0001g0149 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+12655_15+12665d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | ||||||
chr19:14542348 | T | G | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+12637T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542348 | |||||||
chr19:14542352 | T | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+12641T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542352 | |||||||
chr19:14542355 | T | G | 1 | a0001c0003t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.15+12644T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542355 | |||||||
chr19:14542378 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.15+12667T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542378 | |||||||
chr19:14542380 | AG | A | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+12670delG | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542380 | |||||||
chr19:14542463 | T | C | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+12752T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542463 | |||||||
chr19:14542625 | G | A | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+12914G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542625 | |||||||
chr19:14542744 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.15+13033C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542744 | |||||||
chr19:14542908 | C | T | 85 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(82): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+13197C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542908 | |||||||
chr19:14542989 | C | CT | 9 | a0001c0001t0001g0040 a0001c0001t0001g0153 a0001c0001t0001g0159 others(6): Show |
9 | HG01175.hp1 HG01192.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+13294dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542989 | ||||||
chr19:14543040 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.15+13329C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543040 | |||||||
chr19:14543272 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0197 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.15+13561G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543272 | |||||||
chr19:14543301 | GGT | G | 89 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.15+13602_15+13603d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543301 | ||||||
chr19:14543319 | T | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+13608T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543319 | |||||||
chr19:14543388 | A | AATATATA others(7): Show |
2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.15+13696_15+13709d others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543388 | ||||||
chr19:14543388 | AAT | A | 5 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0001g0173 others(2): Show |
5 | HG01070.hp1 HG01255.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13708_15+13709d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543388 | ||||||
chr19:14543388 | AATATAT | A | 8 | a0001c0001t0001g0052 a0001c0001t0001g0064 a0001c0001t0001g0076 others(5): Show |
8 | HG01081.hp1 HG01175.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+13704_15+13709d others(8): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543388 | ||||||
chr19:14543395 | A | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+13684A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543395 | |||||||
chr19:14543403 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0190 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.15+13694_15+13713d others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543403 | ||||||
chr19:14543403 | ATATATAT others(16): Show |
A | 9 | a0001c0001t0001g0062 a0001c0001t0001g0151 a0001c0001t0001g0152 others(6): Show |
10 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.15+13694_15+13716d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543403 | ||||||
chr19:14543403 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.15+13694_15+13719d others(28): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543403 | ||||||
chr19:14543405 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0075 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.15+13696_15+13715d others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | ||||||
chr19:14543405 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0074 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.15+13696_15+13716d others(23): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | ||||||
chr19:14543405 | ATATATAT others(15): Show |
A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0078 others(1): Show |
4 | HG00558.hp1 HG01993.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+13696_15+13717d others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | ||||||
chr19:14543405 | ATATATAT others(16): Show |
A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
8 | HG00280.hp2 HG01358.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+13696_15+13718d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | ||||||
chr19:14543405 | ATATATAT others(17): Show |
A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0046 others(23): Show |
27 | HG00558.hp2 HG00735.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.15+13696_15+13719d others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | ||||||
chr19:14543405 | ATATATAT others(18): Show |
A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(9): Show |
12 | HG01175.hp2 HG01515.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.15+13696_15+13720d others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | ||||||
chr19:14543405 | ATATATAT others(19): Show |
A | 1 | a0001c0002t0001g0108 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.15+13696_15+13721d others(28): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | ||||||
chr19:14543405 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0001g0058 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+13696_15+13722d others(29): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | ||||||
chr19:14543405 | ATATATAT others(32): Show |
A | 3 | a0001c0001t0001g0253 a0001c0001t0001g0260 a0001c0001t0001g0272 |
3 | HG01069.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.15+13696_15+13734d others(41): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | ||||||
chr19:14543406 | TATATATA | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0306 a0001c0002t0001g0049 others(2): Show |
5 | HG01167.hp1 HG01934.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13696_15+13702d others(9): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543406 | |||||||
chr19:14543407 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.15+13698_15+13715d others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543407 | ||||||
chr19:14543407 | ATATATAT others(15): Show |
A | 4 | a0001c0001t0001g0055 a0001c0001t0001g0066 a0001c0001t0001g0143 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+13698_15+13719d others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543407 | ||||||
chr19:14543407 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.15+13698_15+13720d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543407 | ||||||
chr19:14543407 | ATATATAT others(17): Show |
A | 11 | a0001c0001t0001g0045 a0001c0001t0001g0050 a0001c0001t0001g0114 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.15+13698_15+13721d others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543407 | ||||||
chr19:14543407 | ATATATAT others(18): Show |
A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02738.hp1 NA19081.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.15+13698_15+13722d others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543407 | ||||||
chr19:14543409 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0230 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.15+13700_15+13716d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | ||||||
chr19:14543409 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0233 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.15+13700_15+13717d others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | ||||||
chr19:14543409 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.15+13700_15+13719d others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | ||||||
chr19:14543409 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0133 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.15+13700_15+13721d others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | ||||||
chr19:14543409 | ATATATAT others(16): Show |
A | 1 | a0001c0005t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+13700_15+13722d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | ||||||
chr19:14543409 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.15+13700_15+13723d others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | ||||||
chr19:14543411 | A | T | 1 | a0001c0001t0001g0234 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.15+13700A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543411 | |||||||
chr19:14543411 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15+13702_15+13712d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543411 | ||||||
chr19:14543411 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.15+13702_15+13724d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543411 | ||||||
chr19:14543411 | ATATATAT others(26): Show |
A | 1 | a0001c0001t0001g0092 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.15+13702_15+13734d others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543411 | ||||||
chr19:14543413 | A | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0076 a0001c0001t0001g0221 others(2): Show |
5 | HG01081.hp1 HG01175.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13702A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543413 | |||||||
chr19:14543413 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0200 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.15+13704_15+13716d others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543413 | ||||||
chr19:14543413 | ATATATAT others(7): Show |
A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0201 |
2 | HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.15+13704_15+13717d others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543413 | ||||||
chr19:14543413 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.15+13704_15+13720d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543413 | ||||||
chr19:14543413 | ATATATAT others(26): Show |
A | 1 | a0001c0002t0001g0287 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.15+13704_15+13736d others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543413 | ||||||
chr19:14543415 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0217 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.15+13705_15+13706i others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543415 | ||||||
chr19:14543415 | A | T | 16 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0076 others(13): Show |
17 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.15+13704A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543415 | |||||||
chr19:14543415 | ATATATTT others(10): Show |
A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0218 a0001c0002t0001g0034 |
3 | HG02109.hp1 HG02723.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.15+13706_15+13722d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543415 | ||||||
chr19:14543415 | ATATATTT others(11): Show |
A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0224 |
2 | HG02080.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.15+13706_15+13723d others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543415 | ||||||
chr19:14543415 | ATATATTT others(13): Show |
A | 3 | a0001c0001t0001g0027 a0001c0002t0001g0020 a0001c0002t0001g0023 |
3 | HG02622.hp1 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.15+13706_15+13725d others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543415 | ||||||
chr19:14543417 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0006 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.15+13707_15+13708i others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0225 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.15+13707_15+13708i others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0236 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.15+13707_15+13708i others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0163 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.15+13707_15+13708i others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0204 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.15+13707_15+13708i others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0001g0039 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+13707_15+13708i others(21): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | A | T | 21 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0076 others(18): Show |
22 | HG00099.hp2 HG01081.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.15+13706A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543417 | |||||||
chr19:14543417 | ATATTTTT others(1): Show |
A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0158 others(3): Show |
7 | HG02040.hp2 HG02080.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+13708_15+13715d others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | ATATTTTT others(4): Show |
A | 1 | a0001c0002t0001g0195 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.15+13708_15+13718d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | ATATTTTT others(6): Show |
A | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.15+13708_15+13720d others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | ATATTTTT others(9): Show |
A | 1 | a0001c0001t0001g0212 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.15+13708_15+13723d others(18): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | ATATTTTT others(12): Show |
A | 1 | a0001c0001t0001g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.15+13708_15+13726d others(21): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | ATATTTTT others(13): Show |
A | 5 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(2): Show |
5 | HG02451.hp2 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13708_15+13727d others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | ATATTTTT others(15): Show |
A | 5 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0319 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13708_15+13729d others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543417 | ATATTTTT others(18): Show |
A | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+13708_15+13732d others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | ||||||
chr19:14543419 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.15+13709_15+13710i others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0006 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.15+13709_15+13710i others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATATATAT others(7): Show |
1 | a0001c0003t0001g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.15+13709_15+13710i others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0004 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.15+13709_15+13710i others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+13709_15+13710i others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0004 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.15+13709_15+13710i others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATATATTT others(10): Show |
1 | a0001c0001t0001g0187 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.15+13709_15+13710i others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATATTTTT others(8): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0322 |
3 | HG01934.hp1 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.15+13709_15+13710i others(17): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATATTTTT others(18): Show |
1 | a0001c0001t0001g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.15+13709_15+13710i others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0156 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.15+13735_15+13745d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0202 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.15+13734_15+13745d others(14): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATTTTTTT others(6): Show |
3 | a0001c0001t0001g0183 a0001c0001t0001g0197 a0001c0001t0001g0231 |
3 | HG01069.hp1 HG01071.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.15+13733_15+13745d others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATTTTTTT others(7): Show |
1 | a0001c0003t0001g0048 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+13732_15+13745d others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | ATTTTTTT others(23): Show |
1 | a0001c0001t0001g0188 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.15+13716_15+13745d others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | A | T | 34 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0039 others(31): Show |
35 | HG00099.hp2 HG00438.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.15+13708A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543419 | |||||||
chr19:14543419 | ATT | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0146 a0001c0001t0001g0169 others(3): Show |
6 | HG01928.hp1 HG02300.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+13744_15+13745d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTT | A | 6 | a0001c0001t0001g0215 a0001c0001t0001g0222 a0001c0001t0001g0229 others(3): Show |
6 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+13740_15+13745d others(8): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(3): Show |
A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0165 a0001c0001t0001g0182 others(5): Show |
8 | HG00323.hp2 HG01361.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+13736_15+13745d others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(4): Show |
A | 13 | a0001c0001t0001g0082 a0001c0001t0001g0095 a0001c0001t0001g0096 others(10): Show |
13 | HG00741.hp2 HG01346.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.15+13735_15+13745d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0266 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.15+13734_15+13745d others(14): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(6): Show |
A | 7 | a0001c0001t0001g0043 a0001c0001t0001g0083 a0001c0001t0001g0099 others(4): Show |
7 | HG01243.hp1 HG02040.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+13733_15+13745d others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.15+13732_15+13745d others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(8): Show |
A | 21 | a0001c0001t0001g0044 a0001c0001t0001g0081 a0001c0001t0001g0085 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.15+13731_15+13745d others(17): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(9): Show |
A | 2 | a0001c0001t0001g0291 a0001c0001t0001g0323 |
2 | HG03834.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.15+13730_15+13745d others(18): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(10): Show |
A | 8 | a0001c0001t0001g0180 a0001c0001t0001g0251 a0001c0001t0001g0254 others(5): Show |
8 | HG00099.hp1 HG00733.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+13729_15+13745d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(11): Show |
A | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.15+13728_15+13745d others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(12): Show |
A | 1 | a0001c0001t0001g0090 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.15+13727_15+13745d others(21): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(15): Show |
A | 1 | a0001c0001t0001g0313 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.15+13724_15+13745d others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543419 | ATTTTTTT others(16): Show |
A | 1 | a0001c0001t0001g0279 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.15+13723_15+13745d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | ||||||
chr19:14543420 | T | TATA | 3 | a0001c0001t0001g0299 a0001c0002t0001g0216 a0001c0003t0001g0145 |
3 | HG02145.hp1 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.15+13709_15+13710i others(5): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543420 | |||||||
chr19:14543421 | T | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0207 others(1): Show |
4 | HG00280.hp1 HG02738.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+13710T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543421 | |||||||
chr19:14543422 | T | A | 5 | a0001c0001t0001g0157 a0001c0001t0001g0176 a0001c0001t0001g0185 others(2): Show |
5 | HG01099.hp2 HG01978.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13711T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543422 | |||||||
chr19:14543423 | T | A | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG03130.hp2 HG03540.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13712T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543423 | |||||||
chr19:14543424 | T | A | 2 | a0001c0001t0001g0172 a0001c0003t0001g0145 |
2 | HG02572.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.15+13713T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543424 | |||||||
chr19:14543425 | T | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG03130.hp2 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.15+13714T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543425 | |||||||
chr19:14543426 | T | A | 2 | a0001c0001t0001g0282 a0001c0003t0001g0145 |
2 | HG00140.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.15+13715T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543426 | |||||||
chr19:14543427 | T | A | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0273 others(2): Show |
5 | HG00738.hp2 HG01074.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13716T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543427 | |||||||
chr19:14543428 | T | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0282 a0001c0001t0001g0284 |
3 | HG00140.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.15+13717T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543428 | |||||||
chr19:14543429 | T | A | 5 | a0001c0001t0001g0273 a0001c0001t0001g0278 a0001c0001t0001g0289 others(2): Show |
5 | HG00738.hp2 HG01074.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13718T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543429 | |||||||
chr19:14543430 | T | A | 5 | a0001c0001t0001g0248 a0001c0001t0001g0280 a0001c0001t0001g0282 others(2): Show |
5 | HG00140.hp2 HG00323.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13719T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543430 | |||||||
chr19:14543431 | T | A | 12 | a0001c0001t0001g0047 a0001c0001t0001g0165 a0001c0001t0001g0184 others(9): Show |
12 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+13720T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543431 | |||||||
chr19:14543432 | T | A | 16 | a0001c0001t0001g0082 a0001c0001t0001g0095 a0001c0001t0001g0096 others(13): Show |
16 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.15+13721T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543432 | |||||||
chr19:14543433 | T | A | 12 | a0001c0001t0001g0047 a0001c0001t0001g0165 a0001c0001t0001g0184 others(9): Show |
12 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+13722T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543433 | |||||||
chr19:14543434 | T | A | 23 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0083 others(20): Show |
23 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+13723T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543434 | |||||||
chr19:14543435 | T | A | 8 | a0001c0001t0001g0080 a0001c0001t0001g0255 a0001c0001t0001g0266 others(5): Show |
8 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+13724T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543435 | |||||||
chr19:14543436 | T | A | 44 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0081 others(41): Show |
44 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.15+13725T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543436 | |||||||
chr19:14543437 | T | A | 10 | a0001c0001t0001g0080 a0001c0001t0001g0255 a0001c0001t0001g0266 others(7): Show |
10 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+13726T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543437 | |||||||
chr19:14543438 | T | A | 50 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0081 others(47): Show |
50 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.15+13727T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543438 | |||||||
chr19:14543439 | T | A | 9 | a0001c0001t0001g0080 a0001c0001t0001g0255 a0001c0001t0001g0266 others(6): Show |
9 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+13728T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543439 | |||||||
chr19:14543440 | T | A | 51 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0081 others(48): Show |
51 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.15+13729T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543440 | |||||||
chr19:14543441 | T | A | 5 | a0001c0001t0001g0080 a0001c0001t0001g0255 a0001c0001t0001g0266 others(2): Show |
5 | HG00323.hp2 HG00738.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13730T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543441 | |||||||
chr19:14543442 | T | A | 46 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0081 others(43): Show |
46 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.15+13731T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543442 | |||||||
chr19:14543443 | T | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0283 |
2 | HG00323.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.15+13732T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543443 | |||||||
chr19:14543444 | T | A | 29 | a0001c0001t0001g0081 a0001c0001t0001g0091 a0001c0001t0001g0094 others(26): Show |
29 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.15+13733T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543444 | |||||||
chr19:14543446 | T | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0274 |
2 | HG04115.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.15+13735T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543446 | |||||||
chr19:14543456 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.15+13745T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543456 | |||||||
chr19:14543590 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.15+13879T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543590 | |||||||
chr19:14543629 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0241 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.15+13918G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543629 | |||||||
chr19:14543645 | A | T | 2 | a0001c0001t0001g0115 a0001c0001t0002g0015 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.15+13934A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543645 | |||||||
chr19:14543680 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.15+13969C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543680 | |||||||
chr19:14543681 | T | G | 89 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(86): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.15+13970T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543681 | |||||||
chr19:14543697 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0234 |
2 | NA18992.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.15+13986C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543697 | |||||||
chr19:14543727 | C | T | 11 | a0001c0001t0001g0027 a0001c0001t0001g0252 a0001c0001t0001g0262 others(8): Show |
11 | HG00642.hp2 HG01258.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+14016C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543727 | |||||||
chr19:14543730 | G | T | 1 | a0001c0001t0001g0319 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.15+14019G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543730 | |||||||
chr19:14543874 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.15+14163T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543874 | |||||||
chr19:14544114 | A | G | 85 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(82): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+14403A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544114 | |||||||
chr19:14544136 | C | G | 4 | a0001c0001t0001g0149 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+14425C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544136 | |||||||
chr19:14544297 | C | G | 4 | a0001c0001t0001g0149 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+14586C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544297 | |||||||
chr19:14544388 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.15+14677T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544388 | |||||||
chr19:14544568 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.15+14857A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544568 | |||||||
chr19:14544576 | AG | A | 85 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(82): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+14868delG | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14544576 | ||||||
chr19:14544635 | CT | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(64): Show |
69 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.15+14940delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14544635 | ||||||
chr19:14544635 | CTT | C | 90 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.15+14939_15+14940d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14544635 | ||||||
chr19:14544651 | T | A | 4 | a0001c0001t0001g0149 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+14940T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544651 | |||||||
chr19:14544690 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(154): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.15+14979G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544690 | |||||||
chr19:14544749 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.15+15038C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544749 | |||||||
chr19:14544796 | C | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0052 others(46): Show |
51 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.15+15085C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544796 | |||||||
chr19:14544797 | T | A | 1 | a0001c0002t0001g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.15+15086T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544797 | |||||||
chr19:14544904 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.15+15193A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544904 | |||||||
chr19:14544979 | G | A | 2 | a0001c0001t0001g0033 a0001c0002t0001g0034 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.15+15268G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544979 | |||||||
chr19:14545000 | T | C | 64 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0080 others(61): Show |
64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.15+15289T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545000 | |||||||
chr19:14545053 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(155): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.15+15342T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545053 | |||||||
chr19:14545318 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+15607C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545318 | |||||||
chr19:14545319 | G | A | 83 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(80): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.15+15608G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545319 | |||||||
chr19:14545377 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0197 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.15+15666C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545377 | |||||||
chr19:14545392 | T | TGGCCCTC others(2): Show |
11 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(8): Show |
11 | HG02257.hp1 HG02615.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.15+15691_15+15699d others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14545392 | ||||||
chr19:14545410 | G | GCACCGCT others(10): Show |
26 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0101 others(23): Show |
27 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.15+15703_15+15719d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14545410 | ||||||
chr19:14545414 | C | CGCTGTCT others(10): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
11 | HG01192.hp2 HG01257.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+15707_15+15723d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14545414 | ||||||
chr19:14545506 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0003t0001g0145 |
3 | HG02572.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.15+15795G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545506 | |||||||
chr19:14545510 | G | A | 3 | a0001c0001t0001g0307 a0001c0002t0001g0297 a0001c0002t0001g0298 |
3 | HG01891.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.15+15799G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545510 | |||||||
chr19:14545515 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.15+15804G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545515 | |||||||
chr19:14545563 | A | C | 1 | a0001c0001t0001g0322 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+15852A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545563 | |||||||
chr19:14545591 | C | T | 1 | a0001c0003t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.15+15880C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545591 | |||||||
chr19:14545643 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.15+15932C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545643 | |||||||
chr19:14545658 | A | G | 3 | a0001c0001t0001g0307 a0001c0002t0001g0297 a0001c0002t0001g0298 |
3 | HG01891.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.15+15947A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545658 | |||||||
chr19:14545682 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0318 a0001c0002t0001g0034 |
3 | HG02109.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.15+15971C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545682 | |||||||
chr19:14545741 | A | G | 1 | a0001c0003t0001g0048 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+16030A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545741 | |||||||
chr19:14545758 | A | T | 1 | a0001c0003t0001g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.15+16047A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545758 | |||||||
chr19:14545835 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(198): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.15+16124T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545835 | |||||||
chr19:14545865 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.15+16154C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545865 | |||||||
chr19:14545926 | A | C | 1 | a0001c0001t0002g0012 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.15+16215A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545926 | |||||||
chr19:14546074 | T | G | 19 | a0001c0001t0001g0055 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
20 | HG00558.hp1 HG01168.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.15+16363T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546074 | |||||||
chr19:14546090 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.15+16379G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546090 | |||||||
chr19:14546159 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.16-16366A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546159 | |||||||
chr19:14546193 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.16-16332A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546193 | |||||||
chr19:14546208 | T | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0318 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.16-16317T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546208 | |||||||
chr19:14546233 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-16292T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546233 | |||||||
chr19:14546240 | C | T | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-16285C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546240 | |||||||
chr19:14546258 | T | A | 71 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0043 others(68): Show |
71 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.16-16267T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546258 | |||||||
chr19:14546271 | A | AT | 81 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(78): Show |
81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.16-16243dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14546271 | ||||||
chr19:14546352 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0150 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.16-16173T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546352 | |||||||
chr19:14546418 | T | G | 1 | a0001c0003t0001g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.16-16107T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546418 | |||||||
chr19:14546458 | G | A | 1 | a0001c0002t0001g0287 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.16-16067G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546458 | |||||||
chr19:14546599 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-15926C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546599 | |||||||
chr19:14546616 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0005t0001g0029 others(1): Show |
4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-15909C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546616 | |||||||
chr19:14546741 | G | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(51): Show |
56 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.16-15784G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546741 | |||||||
chr19:14546765 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.16-15760A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546765 | |||||||
chr19:14546782 | C | T | 1 | a0001c0007t0001g0079 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.16-15743C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546782 | |||||||
chr19:14546846 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0230 a0001c0001t0001g0323 |
3 | HG02738.hp1 NA18977.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.16-15679C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546846 | |||||||
chr19:14546941 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-15584C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546941 | |||||||
chr19:14546987 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0143 a0001c0002t0001g0056 |
3 | HG01168.hp2 HG01169.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.16-15538A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546987 | |||||||
chr19:14547104 | G | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0150 others(9): Show |
13 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.16-15421G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547104 | |||||||
chr19:14547115 | AAG | A | 75 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(72): Show |
76 | HG00558.hp1 HG00733.hp2 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.16-15405_16-15404d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547115 | ||||||
chr19:14547118 | A | T | 75 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(72): Show |
76 | HG00558.hp1 HG00733.hp2 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.16-15407A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547118 | |||||||
chr19:14547143 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.16-15382A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547143 | |||||||
chr19:14547192 | G | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(202): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.16-15333G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547192 | |||||||
chr19:14547262 | G | A | 5 | a0001c0001t0001g0148 a0001c0002t0001g0020 a0001c0002t0001g0023 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-15263G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547262 | |||||||
chr19:14547343 | CTATTTTA others(3): Show |
C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(35): Show |
40 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.16-15163_16-15154d others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547343 | ||||||
chr19:14547603 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.16-14922C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547603 | |||||||
chr19:14547636 | A | G | 1 | a0001c0005t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.16-14889A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547636 | |||||||
chr19:14547661 | A | AT | 121 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(118): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.16-14849dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547661 | ||||||
chr19:14547661 | A | ATT | 6 | a0001c0001t0001g0103 a0001c0001t0001g0109 a0001c0001t0001g0149 others(3): Show |
6 | HG00323.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-14850_16-14849d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547661 | ||||||
chr19:14547661 | AT | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0105 others(14): Show |
18 | HG01074.hp2 HG01109.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.16-14849delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547661 | ||||||
chr19:14547714 | A | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0077 others(11): Show |
15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.16-14811A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547714 | |||||||
chr19:14547779 | T | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(36): Show |
41 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.16-14746T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547779 | |||||||
chr19:14547827 | CT | C | 3 | a0001c0001t0001g0243 a0001c0002t0001g0034 a0001c0003t0001g0242 |
3 | HG02109.hp1 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.16-14694delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547827 | ||||||
chr19:14547963 | C | CT | 10 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0074 others(7): Show |
10 | HG00558.hp1 HG01496.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-14544dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547963 | ||||||
chr19:14547963 | CT | C | 48 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0030 others(45): Show |
49 | HG00639.hp2 HG01074.hp2 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.16-14544delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547963 | ||||||
chr19:14547985 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-14540A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547985 | |||||||
chr19:14547986 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0005t0001g0029 others(1): Show |
4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-14539C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547986 | |||||||
chr19:14548072 | T | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0137 a0001c0001t0002g0011 others(3): Show |
6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-14453T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548072 | |||||||
chr19:14548088 | AAGTAGCT others(7279): Show |
A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0137 a0001c0001t0002g0011 others(3): Show |
6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-14425_16-7140de others(1): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14548088 | ||||||
chr19:14548144 | T | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(36): Show |
41 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.16-14381T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548144 | |||||||
chr19:14548164 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0125 |
2 | HG00280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.16-14361G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548164 | |||||||
chr19:14548181 | G | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(36): Show |
41 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.16-14344G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548181 | |||||||
chr19:14548241 | G | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(35): Show |
40 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.16-14284G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548241 | |||||||
chr19:14548250 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.16-14275T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548250 | |||||||
chr19:14548268 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(35): Show |
40 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.16-14257G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548268 | |||||||
chr19:14548291 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-14234A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548291 | |||||||
chr19:14548500 | G | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0159 others(4): Show |
7 | HG02056.hp2 HG02074.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-14025G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548500 | |||||||
chr19:14548577 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0045 others(35): Show |
40 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.16-13948G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548577 | |||||||
chr19:14548600 | C | T | 1 | a0001c0005t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.16-13925C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548600 | |||||||
chr19:14548648 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(206): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.16-13877A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548648 | |||||||
chr19:14548735 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-13790G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548735 | |||||||
chr19:14548888 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-13637C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548888 | |||||||
chr19:14549016 | AT | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(87): Show |
92 | HG00323.hp1 HG00558.hp2 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.16-13499delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14549016 | ||||||
chr19:14549033 | G | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG01934.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-13492G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549033 | |||||||
chr19:14549100 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0002t0001g0019 |
3 | HG02145.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.16-13425G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549100 | |||||||
chr19:14549126 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0109 others(4): Show |
7 | HG01123.hp1 HG02486.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-13399G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549126 | |||||||
chr19:14549211 | C | CTTTT | 67 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0031 others(64): Show |
68 | HG00558.hp2 HG00642.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.16-13297_16-13294d others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14549211 | ||||||
chr19:14549211 | C | CTTTTT | 12 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0143 others(9): Show |
13 | HG01109.hp2 HG01169.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.16-13298_16-13294d others(7): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14549211 | ||||||
chr19:14549211 | CT | C | 9 | a0001c0001t0001g0093 a0001c0001t0001g0106 a0001c0001t0001g0129 others(6): Show |
9 | HG00639.hp2 HG01257.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-13294delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14549211 | ||||||
chr19:14549300 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0030 |
2 | HG01123.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.16-13225C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549300 | |||||||
chr19:14549358 | A | G | 32 | a0001c0001t0001g0027 a0001c0001t0001g0038 a0001c0001t0001g0039 others(29): Show |
32 | HG01884.hp1 HG01934.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.16-13167A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549358 | |||||||
chr19:14549390 | T | G | 1 | a0001c0001t0001g0304 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.16-13135T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549390 | |||||||
chr19:14549600 | T | C | 3 | a0001c0002t0001g0216 a0001c0002t0001g0232 a0001c0002t0001g0239 |
3 | HG02145.hp1 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.16-12925T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549600 | |||||||
chr19:14549671 | G | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0074 others(37): Show |
41 | HG00438.hp2 HG00733.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.16-12854G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549671 | |||||||
chr19:14549703 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.16-12822G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549703 | |||||||
chr19:14549772 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.16-12753A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549772 | |||||||
chr19:14549907 | C | T | 2 | a0001c0005t0001g0029 a0001c0005t0001g0032 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.16-12618C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549907 | |||||||
chr19:14549954 | T | TA | 16 | a0001c0001t0001g0008 a0001c0001t0001g0248 a0001c0003t0001g0021 others(13): Show |
16 | HG01928.hp2 HG02109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.16-12563dupA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14549954 | ||||||
chr19:14550003 | CCCTTT | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0221 a0001c0001t0001g0274 others(2): Show |
5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-12515_16-12511d others(7): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14550003 | ||||||
chr19:14550031 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0221 a0001c0001t0001g0274 others(2): Show |
5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-12494C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550031 | |||||||
chr19:14550049 | A | G | 14 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(11): Show |
14 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.16-12476A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550049 | |||||||
chr19:14550052 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-12473T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550052 | |||||||
chr19:14550111 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG03491.hp1 HG03492.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.16-12414G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550111 | |||||||
chr19:14550214 | A | T | 1 | a0001c0001t0001g0236 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.16-12311A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550214 | |||||||
chr19:14550257 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.16-12268T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550257 | |||||||
chr19:14550291 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.16-12234G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550291 | |||||||
chr19:14550310 | G | A | 2 | a0001c0001t0001g0317 a0001c0003t0001g0242 |
2 | HG01981.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.16-12215G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550310 | |||||||
chr19:14550464 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0256 |
2 | HG01099.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.16-12061C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550464 | |||||||
chr19:14550496 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.16-12029G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550496 | |||||||
chr19:14550587 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.16-11938A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550587 | |||||||
chr19:14550812 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.16-11713C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550812 | |||||||
chr19:14550873 | T | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0106 |
3 | NA18960.hp2 NA18973.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.16-11652T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550873 | |||||||
chr19:14550964 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-11561A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550964 | |||||||
chr19:14551061 | G | A | 2 | a0001c0005t0001g0029 a0001c0005t0001g0032 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.16-11464G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551061 | |||||||
chr19:14551108 | G | A | 4 | a0001c0005t0001g0036 a0001c0005t0001g0041 a0001c0005t0001g0042 others(1): Show |
4 | HG02451.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-11417G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551108 | |||||||
chr19:14551311 | G | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0057 |
2 | HG02602.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.16-11214G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551311 | |||||||
chr19:14551354 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-11171C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551354 | |||||||
chr19:14551895 | T | TTC | 3 | a0001c0001t0001g0149 a0001c0005t0001g0029 a0001c0005t0001g0032 |
3 | HG02280.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.16-10615_16-10614d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14551895 | ||||||
chr19:14551913 | C | G | 15 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(12): Show |
15 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.16-10612C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551913 | |||||||
chr19:14551913 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.16-10612C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551913 | |||||||
chr19:14551931 | C | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(97): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.16-10594C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551931 | |||||||
chr19:14551946 | C | CCT | 46 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0128 others(43): Show |
47 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.16-10554_16-10553d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14551946 | ||||||
chr19:14551946 | C | CCTCT | 3 | a0001c0001t0001g0181 a0001c0001t0001g0238 a0001c0001t0001g0252 |
3 | HG01346.hp1 HG02040.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.16-10556_16-10553d others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14551946 | ||||||
chr19:14551946 | C | CCTCTCTC others(15): Show |
1 | a0001c0001t0001g0090 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.16-10568_16-10567i others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14551946 | ||||||
chr19:14551946 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.16-10579C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551946 | |||||||
chr19:14551946 | CCT | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(121): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.16-10554_16-10553d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14551946 | ||||||
chr19:14551948 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.16-10577T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551948 | |||||||
chr19:14551967 | C | T | 23 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0096 others(20): Show |
23 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-10558C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551967 | |||||||
chr19:14551973 | T | C | 24 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0096 others(21): Show |
24 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.16-10552T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551973 | |||||||
chr19:14551974 | TCTCTC | T | 23 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0096 others(20): Show |
23 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-10550_16-10546d others(7): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551974 | |||||||
chr19:14551979 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.16-10546C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551979 | |||||||
chr19:14552014 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0221 a0001c0001t0001g0274 others(2): Show |
5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-10511G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552014 | |||||||
chr19:14552044 | T | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0203 a0001c0001t0001g0219 others(1): Show |
4 | NA18982.hp2 NA18999.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-10481T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552044 | |||||||
chr19:14552131 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0148 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.16-10394G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552131 | |||||||
chr19:14552145 | T | TTTTC | 23 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0096 others(20): Show |
23 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-10360_16-10357d others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14552145 | ||||||
chr19:14552145 | TTTTC | T | 21 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(18): Show |
21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.16-10360_16-10357d others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14552145 | ||||||
chr19:14552157 | CTTTCTTT others(4): Show |
C | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-10360_16-10350d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14552157 | ||||||
chr19:14552172 | C | CT | 6 | a0001c0001t0001g0052 a0001c0001t0001g0124 a0001c0001t0001g0125 others(3): Show |
6 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-10338dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14552172 | ||||||
chr19:14552172 | CT | C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0184 others(7): Show |
10 | HG01169.hp2 HG01261.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-10338delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14552172 | ||||||
chr19:14552196 | G | A | 3 | a0001c0002t0001g0118 a0001c0002t0001g0119 a0001c0002t0001g0298 |
3 | HG02486.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.16-10329G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552196 | |||||||
chr19:14552313 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-10212C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552313 | |||||||
chr19:14552429 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.16-10096A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552429 | |||||||
chr19:14552511 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0238 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.16-10014G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552511 | |||||||
chr19:14552517 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.16-10008A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552517 | |||||||
chr19:14552526 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.16-9999T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552526 | |||||||
chr19:14552630 | G | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0245 a0001c0001t0001g0318 |
3 | HG02055.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.16-9895G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552630 | |||||||
chr19:14552638 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.16-9887C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552638 | |||||||
chr19:14552686 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0141 others(4): Show |
8 | HG01109.hp2 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-9839C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552686 | |||||||
chr19:14552757 | T | C | 228 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(225): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.16-9768T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552757 | |||||||
chr19:14552871 | G | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0221 a0001c0001t0001g0274 others(2): Show |
5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-9654G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552871 | |||||||
chr19:14552936 | C | T | 1 | a0001c0002t0001g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.16-9589C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552936 | |||||||
chr19:14552941 | G | C | 313 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(310): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.16-9584G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552941 | |||||||
chr19:14553016 | T | C | 33 | a0001c0001t0001g0063 a0001c0001t0001g0307 a0001c0002t0001g0001 others(30): Show |
34 | HG01361.hp1 HG01515.hp1 HG01517.hp2 others(31): Show |
intron_variant | MODIFIER | c.16-9509T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553016 | |||||||
chr19:14553041 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.16-9484C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553041 | |||||||
chr19:14553190 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0238 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.16-9335C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553190 | |||||||
chr19:14553190 | CGCTCGGG others(5): Show |
C | 1 | a0002c0004t0001g0166 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.16-9331_16-9320del others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14553190 | ||||||
chr19:14553224 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.16-9301C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553224 | |||||||
chr19:14553234 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0139 |
2 | HG02683.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.16-9291G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553234 | |||||||
chr19:14553256 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0221 a0001c0001t0001g0274 others(2): Show |
5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-9269C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553256 | |||||||
chr19:14553330 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.16-9195C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553330 | |||||||
chr19:14553332 | G | C | 17 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(14): Show |
17 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-9193G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553332 | |||||||
chr19:14553402 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.16-9123C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553402 | |||||||
chr19:14553507 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.16-9018T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553507 | |||||||
chr19:14553511 | G | C | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.16-9014G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553511 | |||||||
chr19:14553736 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.16-8789G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553736 | |||||||
chr19:14553835 | G | A | 1 | a0001c0007t0001g0079 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.16-8690G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553835 | |||||||
chr19:14553915 | T | C | 17 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(14): Show |
17 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-8610T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553915 | |||||||
chr19:14554015 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.16-8510C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554015 | |||||||
chr19:14554036 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16-8489G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554036 | |||||||
chr19:14554047 | G | A | 22 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0096 others(19): Show |
22 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.16-8478G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554047 | |||||||
chr19:14554121 | C | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.16-8404C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554121 | |||||||
chr19:14554367 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.16-8158G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554367 | |||||||
chr19:14554378 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.16-8147C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554378 | |||||||
chr19:14554380 | A | T | 23 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0096 others(20): Show |
23 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-8145A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554380 | |||||||
chr19:14554388 | G | C | 312 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(309): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.16-8137G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554388 | |||||||
chr19:14554598 | C | T | 8 | a0001c0001t0001g0046 a0001c0001t0001g0077 a0001c0001t0001g0148 others(5): Show |
8 | HG01243.hp2 HG02280.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-7927C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554598 | |||||||
chr19:14554610 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0221 a0001c0001t0001g0274 others(2): Show |
5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-7915G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554610 | |||||||
chr19:14554660 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.16-7865T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554660 | |||||||
chr19:14554850 | C | T | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0304 |
3 | HG01167.hp2 HG01358.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.16-7675C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554850 | |||||||
chr19:14555137 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7388T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555137 | |||||||
chr19:14555143 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0292 others(1): Show |
5 | HG01109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-7382A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555143 | |||||||
chr19:14555188 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7337T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555188 | |||||||
chr19:14555193 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.16-7332C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555193 | |||||||
chr19:14555228 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.16-7297G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555228 | |||||||
chr19:14555242 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7283A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555242 | |||||||
chr19:14555351 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.16-7174C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555351 | |||||||
chr19:14555400 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7125T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555400 | |||||||
chr19:14555411 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0238 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.16-7114G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555411 | |||||||
chr19:14555413 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7112A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555413 | |||||||
chr19:14555438 | C | CT | 27 | a0001c0001t0001g0010 a0001c0001t0001g0121 a0001c0001t0001g0124 others(24): Show |
27 | HG01071.hp1 HG01099.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.16-7061dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14555438 | ||||||
chr19:14555438 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7072_16-7061dup others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14555438 | ||||||
chr19:14555438 | CT | C | 59 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0065 others(56): Show |
59 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.16-7061delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14555438 | ||||||
chr19:14555438 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.16-7071_16-7061del others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14555438 | ||||||
chr19:14555438 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0271 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.16-7073_16-7061del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14555438 | ||||||
chr19:14555601 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.16-6924A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555601 | |||||||
chr19:14555629 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-6896C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555629 | |||||||
chr19:14555698 | C | G | 12 | a0001c0002t0001g0035 a0001c0002t0001g0049 a0001c0002t0001g0057 others(9): Show |
12 | HG01515.hp1 HG01517.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-6827C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555698 | |||||||
chr19:14555741 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-6784A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555741 | |||||||
chr19:14556048 | C | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0137 a0001c0001t0002g0011 others(3): Show |
6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-6477C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556048 | |||||||
chr19:14556072 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.16-6453C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556072 | |||||||
chr19:14556096 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-6429C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556096 | |||||||
chr19:14556142 | C | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0203 a0001c0001t0001g0219 others(2): Show |
5 | NA18982.hp2 NA18983.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-6383C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556142 | |||||||
chr19:14556391 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0221 a0001c0001t0001g0274 others(2): Show |
5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-6134C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556391 | |||||||
chr19:14556408 | C | CAAAACAA others(5): Show |
24 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0104 others(21): Show |
24 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.16-6113_16-6112ins others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14556408 | ||||||
chr19:14556413 | A | AAAAAACA others(5): Show |
161 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(158): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.16-6106_16-6095dup others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14556413 | ||||||
chr19:14556413 | A | AAAAACAA others(4): Show |
1 | a0001c0001t0001g0313 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.16-6108_16-6107ins others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14556413 | ||||||
chr19:14556413 | A | C | 25 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0104 others(22): Show |
25 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.16-6112A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556413 | |||||||
chr19:14556415 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-6107_16-6106ins others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14556415 | ||||||
chr19:14556434 | C | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(94): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.16-6091C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556434 | |||||||
chr19:14556498 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0238 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.16-6027A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556498 | |||||||
chr19:14556504 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0058 |
2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.16-6021A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556504 | |||||||
chr19:14556605 | A | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(188): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.16-5920A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556605 | |||||||
chr19:14556776 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0133 |
2 | NA18964.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.16-5749G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556776 | |||||||
chr19:14556855 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-5670C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556855 | |||||||
chr19:14556919 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-5606C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556919 | |||||||
chr19:14556926 | G | C | 2 | a0001c0002t0001g0232 a0001c0002t0001g0239 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.16-5599G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556926 | |||||||
chr19:14556987 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.16-5538C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556987 | |||||||
chr19:14557027 | C | T | 2 | a0001c0005t0001g0029 a0001c0005t0001g0032 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.16-5498C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557027 | |||||||
chr19:14557071 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-5454C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557071 | |||||||
chr19:14557114 | C | CGTATTAA others(5): Show |
1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5411_16-5410ins others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557114 | |||||||
chr19:14557114 | C | CTTAT | 129 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(126): Show |
132 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.16-5372_16-5369dup others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | ||||||
chr19:14557114 | C | CTTATTTA others(1): Show |
82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.16-5376_16-5369dup others(8): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | ||||||
chr19:14557114 | C | CTTATTTA others(5): Show |
51 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(48): Show |
52 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.16-5380_16-5369dup others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | ||||||
chr19:14557114 | C | CTTATTTA others(9): Show |
7 | a0001c0001t0001g0010 a0001c0001t0001g0052 a0001c0001t0001g0073 others(4): Show |
7 | HG01361.hp2 HG01433.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-5384_16-5369dup others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | ||||||
chr19:14557114 | C | CTTATTTA others(17): Show |
1 | a0001c0001t0001g0248 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.16-5392_16-5369dup others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | ||||||
chr19:14557114 | CTTAT | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0156 a0001c0001t0001g0262 others(1): Show |
4 | HG01258.hp1 HG02056.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-5372_16-5369del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | ||||||
chr19:14557116 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5409T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557116 | |||||||
chr19:14557120 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5405T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557120 | |||||||
chr19:14557124 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5401T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557124 | |||||||
chr19:14557127 | T | G | 1 | a0001c0002t0001g0108 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.16-5398T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557127 | |||||||
chr19:14557127 | T | TTATG | 31 | a0001c0001t0001g0307 a0001c0002t0001g0001 a0001c0002t0001g0019 others(28): Show |
32 | HG01515.hp1 HG01517.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.16-5395_16-5394ins others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557127 | ||||||
chr19:14557128 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5397T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557128 | |||||||
chr19:14557131 | T | G | 32 | a0001c0001t0001g0307 a0001c0002t0001g0001 a0001c0002t0001g0019 others(29): Show |
33 | HG01515.hp1 HG01517.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.16-5394T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557131 | |||||||
chr19:14557132 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5393T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557132 | |||||||
chr19:14557135 | T | G | 1 | a0001c0002t0001g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.16-5390T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557135 | |||||||
chr19:14557157 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.16-5368T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557157 | |||||||
chr19:14557168 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0137 a0001c0001t0002g0011 others(3): Show |
6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-5357C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557168 | |||||||
chr19:14557258 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.16-5267A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557258 | |||||||
chr19:14557825 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.16-4700G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557825 | |||||||
chr19:14557830 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(95): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.16-4695A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557830 | |||||||
chr19:14557857 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.16-4668G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557857 | |||||||
chr19:14557916 | C | T | 2 | a0001c0002t0001g0118 a0001c0002t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.16-4609C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557916 | |||||||
chr19:14558001 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.16-4524C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558001 | |||||||
chr19:14558007 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.16-4518G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558007 | |||||||
chr19:14558155 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-4370A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558155 | |||||||
chr19:14558225 | T | G | 1 | a0001c0001t0001g0251 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.16-4300T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558225 | |||||||
chr19:14558240 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG01123.hp1 HG01891.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.16-4285C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558240 | |||||||
chr19:14558330 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-4195C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558330 | |||||||
chr19:14558369 | C | G | 4 | a0001c0001t0001g0080 a0001c0001t0001g0167 a0001c0001t0001g0214 others(1): Show |
4 | HG00408.hp1 HG00438.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-4156C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558369 | |||||||
chr19:14558399 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-4126C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558399 | |||||||
chr19:14558440 | G | A | 17 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(14): Show |
17 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-4085G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558440 | |||||||
chr19:14558480 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-4045G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558480 | |||||||
chr19:14558517 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.16-4008C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558517 | |||||||
chr19:14558597 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.16-3928C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558597 | |||||||
chr19:14558607 | T | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(163): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.16-3918T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558607 | |||||||
chr19:14558624 | G | A | 11 | a0001c0001t0001g0053 a0001c0001t0001g0112 a0001c0001t0001g0157 others(8): Show |
11 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.16-3901G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558624 | |||||||
chr19:14558660 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-3865A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558660 | |||||||
chr19:14558982 | C | CGT | 6 | a0001c0001t0001g0104 a0001c0001t0001g0137 a0001c0001t0002g0011 others(3): Show |
6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-3531_16-3530dup others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14558982 | ||||||
chr19:14559154 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.16-3371C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559154 | |||||||
chr19:14559266 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.16-3259A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559266 | |||||||
chr19:14559289 | T | G | 2 | a0001c0002t0001g0118 a0001c0002t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.16-3236T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559289 | |||||||
chr19:14559348 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-3177C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559348 | |||||||
chr19:14559525 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.16-3000C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559525 | |||||||
chr19:14559528 | C | CTA | 16 | a0001c0001t0001g0046 a0001c0001t0001g0077 a0001c0001t0001g0148 others(13): Show |
17 | HG01243.hp2 HG02280.hp2 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.16-2994_16-2993dup others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14559528 | ||||||
chr19:14559742 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.16-2783G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559742 | |||||||
chr19:14559777 | A | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0137 a0001c0001t0002g0011 others(3): Show |
6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-2748A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559777 | |||||||
chr19:14559786 | CA | C | 163 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(160): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.16-2724delA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14559786 | ||||||
chr19:14559857 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-2668A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559857 | |||||||
chr19:14559981 | AT | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.16-2541delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14559981 | ||||||
chr19:14560002 | C | T | 4 | a0001c0005t0001g0036 a0001c0005t0001g0041 a0001c0005t0001g0042 others(1): Show |
4 | HG02451.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-2523C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560002 | |||||||
chr19:14560006 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0221 a0001c0001t0001g0274 others(2): Show |
5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-2519G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560006 | |||||||
chr19:14560025 | G | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.16-2500G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560025 | |||||||
chr19:14560121 | A | AC | 33 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0043 others(30): Show |
34 | HG00733.hp2 HG01175.hp2 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.16-2399dupC | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14560121 | ||||||
chr19:14560141 | G | A | 25 | a0001c0001t0001g0307 a0001c0002t0001g0020 a0001c0002t0001g0023 others(22): Show |
25 | HG01515.hp1 HG01517.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.16-2384G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560141 | |||||||
chr19:14560164 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.16-2361C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560164 | |||||||
chr19:14560180 | G | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0167 a0001c0001t0001g0173 others(3): Show |
6 | HG00408.hp1 HG00438.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-2345G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560180 | |||||||
chr19:14560229 | G | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.16-2296G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560229 | |||||||
chr19:14560233 | C | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.16-2292C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560233 | |||||||
chr19:14560249 | A | G | 22 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0096 others(19): Show |
22 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.16-2276A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560249 | |||||||
chr19:14560393 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-2132C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560393 | |||||||
chr19:14560396 | G | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(115): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.16-2129G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560396 | |||||||
chr19:14560469 | G | A | 1 | a0001c0002t0001g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.16-2056G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560469 | |||||||
chr19:14560488 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.16-2037T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560488 | |||||||
chr19:14560576 | G | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.16-1949G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560576 | |||||||
chr19:14560577 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.16-1948C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560577 | |||||||
chr19:14560763 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-1762A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560763 | |||||||
chr19:14560911 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.16-1614A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560911 | |||||||
chr19:14560931 | G | A | 1 | a0001c0003t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.16-1594G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560931 | |||||||
chr19:14561075 | GCTGTCGT others(33): Show |
G | 1 | a0001c0001t0001g0208 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.16-1449_16-1410del others(40): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561075 | |||||||
chr19:14561167 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-1358C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561167 | |||||||
chr19:14561217 | C | T | 21 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(18): Show |
21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.16-1308C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561217 | |||||||
chr19:14561353 | T | C | 193 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(190): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.16-1172T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561353 | |||||||
chr19:14561354 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0176 a0001c0001t0001g0182 |
3 | NA18999.hp2 NA19074.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.16-1171G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561354 | |||||||
chr19:14561459 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.16-1066G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561459 | |||||||
chr19:14561467 | C | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0148 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.16-1058C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561467 | |||||||
chr19:14561524 | G | T | 15 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(12): Show |
15 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.16-1001G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561524 | |||||||
chr19:14561539 | G | A | 4 | a0001c0005t0001g0036 a0001c0005t0001g0041 a0001c0005t0001g0042 others(1): Show |
4 | HG02451.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-986G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561539 | |||||||
chr19:14561735 | G | A | 8 | a0001c0001t0001g0046 a0001c0001t0001g0077 a0001c0001t0001g0148 others(5): Show |
8 | HG01243.hp2 HG02280.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-790G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561735 | |||||||
chr19:14561773 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.16-752A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561773 | |||||||
chr19:14561885 | C | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(93): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.16-640C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561885 | |||||||
chr19:14561921 | T | C | 93 | a0001c0001t0001g0046 a0001c0001t0001g0077 a0001c0001t0001g0085 others(90): Show |
94 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.16-604T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561921 | |||||||
chr19:14561937 | C | T | 167 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(164): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.16-588C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561937 | |||||||
chr19:14561958 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.16-567T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561958 | |||||||
chr19:14561997 | T | C | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(316): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.16-528T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561997 | |||||||
chr19:14562109 | C | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0238 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.16-416C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562109 | |||||||
chr19:14562140 | G | A | 1 | a0001c0003t0001g0242 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.16-385G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562140 | |||||||
chr19:14562147 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.16-378G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562147 | |||||||
chr19:14562221 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.16-304C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562221 | |||||||
chr19:14562236 | C | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0301 |
2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.16-289C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562236 | |||||||
chr19:14562275 | C | T | 1 | a0002c0004t0001g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.16-250C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562275 | |||||||
chr19:14562424 | G | A | 12 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(9): Show |
12 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-101G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562424 | |||||||
chr19:14562510 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.16-15G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562510 | |||||||
chr19:14562731 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.66+156C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14562731 | |||||||
chr19:14562791 | G | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0051 a0001c0001t0001g0062 others(5): Show |
8 | HG01361.hp1 HG02258.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+216G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14562791 | |||||||
chr19:14562961 | C | T | 2 | a0001c0002t0001g0100 a0002c0006t0001g0126 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.67-245C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14562961 | |||||||
chr19:14562985 | G | C | 20 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(17): Show |
20 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.67-221G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14562985 | |||||||
chr19:14563016 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(92): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.67-190C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14563016 | |||||||
chr19:14563189 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0170 |
2 | HG01358.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.67-17G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14563189 | |||||||
chr19:14563304 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.118+47G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563304 | |||||||
chr19:14563312 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.118+55A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563312 | |||||||
chr19:14563336 | A | AGAGGGG | 21 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(18): Show |
21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+79_118+80insGA others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563336 | |||||||
chr19:14563339 | C | T | 21 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(18): Show |
21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+82C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563339 | |||||||
chr19:14563340 | C | CAGAGA | 21 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(18): Show |
21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+83_118+84insAG others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563340 | |||||||
chr19:14563342 | C | G | 21 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(18): Show |
21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+85C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563342 | |||||||
chr19:14563343 | T | C | 21 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(18): Show |
21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+86T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563343 | |||||||
chr19:14563348 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.118+91G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563348 | |||||||
chr19:14563405 | C | T | 2 | a0001c0001t0001g0291 a0001c0001t0001g0300 |
2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.118+148C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563405 | |||||||
chr19:14563414 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.118+157G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563414 | |||||||
chr19:14563423 | C | T | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.118+166C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563423 | |||||||
chr19:14563445 | T | C | 1 | a0001c0001t0002g0011 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.118+188T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563445 | |||||||
chr19:14563474 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.119-184C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563474 | |||||||
chr19:14563603 | G | A | 21 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(18): Show |
21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.119-55G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563603 | |||||||
chr19:14564341 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0137 a0001c0001t0002g0011 others(3): Show |
6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+54C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 7/12 | chr19 | 14564341 | |||||||
chr19:14564395 | A | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(94): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.489+108A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 7/12 | chr19 | 14564395 | |||||||
chr19:14564499 | GGCCT | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(92): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.489+217_489+220del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 14564499 | ||||||
chr19:14564560 | G | T | 1 | a0001c0001t0001g0279 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.490-226G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 7/12 | chr19 | 14564560 | |||||||
chr19:14564917 | C | T | 1 | a0001c0005t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.563-32C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 8/12 | chr19 | 14564917 | |||||||
chr19:14565000 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03654.hp1 | splice_region_variant&intron_variant | LOW | c.606+8G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 9/12 | chr19 | 14565000 | |||||||
chr19:14565360 | T | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.753+70T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 11/12 | chr19 | 14565360 | |||||||
chr19:14565473 | C | T | 17 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(14): Show |
17 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.754-145C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 11/12 | chr19 | 14565473 | |||||||
chr19:14565589 | C | T | 4 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0283 others(1): Show |
4 | HG01167.hp2 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-29C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 11/12 | chr19 | 14565589 | |||||||
chr19:14565669 | C | T | 20 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0024 others(17): Show |
20 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.799+6C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 12/12 | chr19 | 14565669 | |||||||
chr19:14565676 | C | G | 1 | a0002c0004t0001g0134 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.799+13C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 12/12 | chr19 | 14565676 | |||||||
chr19:14565676 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.799+13C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 12/12 | chr19 | 14565676 | |||||||
chr19:14565728 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.800-16C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 12/12 | chr19 | 14565728 |