Item | Value |
---|---|
geneid | 153396 |
ensemblid | ENSG00000164180.14 |
hgncid | 28483 |
symbol | TMEM161B |
name | transmembrane protein 161B |
refseq_nuc | NM_153354.5 |
refseq_prot | NP_699185.1 |
ensembl_nuc | ENST00000296595.11 |
ensembl_prot | ENSP00000296595.6 |
mane_status | MANE Select |
chr | chr5 |
start | 88195047 |
end | 88268845 |
strand | - |
ver | v1.2 |
region | chr5:88195047-88268845 |
region5000 | chr5:88190047-88273845 |
regionname0 | TMEM161B_chr5_88195047_88268845 |
regionname5000 | TMEM161B_chr5_88190047_88273845 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 487 | 240 | 78 | 53 | 68 | 12 | 27 | 49 | TMEM161B_chr5_88190047_88273845 | TMEM161B | MGVIG others(482): Show |
chr5 | 88190047 | 88273845 |
a0002 | 0/0 | 487 | 41 | 0 | 1 | 38 | 0 | 2 | 35 | TMEM161B_chr5_88190047_88273845 | TMEM161B | MGVIG others(482): Show |
chr5 | 88190047 | 88273845 |
a0003 | 0/0 | 487 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | MGVIG others(482): Show |
chr5 | 88190047 | 88273845 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1461 | 128 | 68 | 25 | 12 | 3 | 18 | TMEM161B_chr5_88190047_88273845 | TMEM161B | ATGGG others(1456): Show |
chr5 | 88190047 | 88273845 | ||
a0001c0002 | 0/0 | 1461 | 111 | 9 | 28 | 56 | 9 | 9 | TMEM161B_chr5_88190047_88273845 | TMEM161B | ATGGG others(1456): Show |
chr5 | 88190047 | 88273845 | ||
a0001c0005 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | ATGGG others(1456): Show |
chr5 | 88190047 | 88273845 | ||
a0002c0003 | 0/0 | 1461 | 41 | 0 | 1 | 38 | 0 | 2 | TMEM161B_chr5_88190047_88273845 | TMEM161B | ATGGG others(1456): Show |
chr5 | 88190047 | 88273845 | ||
a0003c0004 | 0/0 | 1461 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | ATGGG others(1456): Show |
chr5 | 88190047 | 88273845 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2750 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0001t0002 | 1/0 | 2750 | 40 | 26 | 6 | 6 | 1 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0001t0003 | 0/1 | 2750 | 59 | 29 | 13 | 1 | 2 | 13 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0001t0004 | 0/0 | 2750 | 13 | 11 | 2 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0001t0005 | 0/0 | 2750 | 12 | 0 | 4 | 5 | 0 | 3 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0001t0007 | 0/0 | 2750 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0002t0001 | 0/0 | 2750 | 102 | 9 | 23 | 55 | 9 | 6 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0002t0006 | 0/0 | 2750 | 4 | 0 | 0 | 1 | 0 | 3 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0002t0008 | 0/0 | 2750 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0002t0009 | 0/0 | 2750 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0002t0010 | 0/0 | 2750 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0002t0011 | 0/0 | 2750 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0002t0012 | 0/0 | 2750 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0001c0005t0003 | 0/0 | 2750 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0002c0003t0002 | 0/0 | 2750 | 40 | 0 | 1 | 37 | 0 | 2 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0002c0003t0013 | 0/0 | 2750 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
a0003c0004t0003 | 0/0 | 2750 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | AGAGC others(2745): Show |
chr5 | 88190047 | 88273845 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0018 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0004g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0004g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0004g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0007g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0001t0007g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0002 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0006g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0006g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0008g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0010g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0011g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0002t0012g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0001c0005t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0002c0003t0013g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
a0003c0004t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0128 | EUR | GBR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0179 | EUR | GBR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0005 | EUR | GBR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0150 | EUR | GBR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0056 | EUR | FIN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0105 | EUR | FIN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | CHS | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | CHS | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | CHS | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00733 | hp2 | a0001 | c0002 | t0010 | g0057 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01070 | hp1 | a0001 | c0002 | t0012 | g0029 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01258 | hp1 | a0001 | c0002 | t0008 | g0080 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0244 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0098 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01358 | hp2 | a0001 | c0002 | t0009 | g0228 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0177 | EUR | IBS | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | IBS | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0005 | EUR | IBS | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01928 | hp1 | a0001 | c0002 | t0011 | g0044 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0170 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01978 | hp2 | a0002 | c0003 | t0002 | g0021 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0050 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02027 | hp1 | a0002 | c0003 | t0002 | g0231 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02040 | hp1 | a0001 | c0002 | t0006 | g0086 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02080 | hp2 | a0002 | c0003 | t0002 | g0213 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02132 | hp1 | a0002 | c0003 | t0002 | g0240 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | KHV | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0126 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0211 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0204 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | MSL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | MSL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | MSL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | MSL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0185 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | MSL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | MSL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03492 | hp2 | a0002 | c0003 | t0002 | g0217 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | MSL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | MSL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0186 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0246 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0088 | SAS | PJL | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03831 | hp1 | a0003 | c0004 | t0003 | g0127 | SAS | BEB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03831 | hp2 | a0001 | c0002 | t0006 | g0085 | SAS | BEB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03942 | hp1 | a0001 | c0002 | t0006 | g0083 | SAS | BEB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG03942 | hp2 | a0001 | c0001 | t0007 | g0245 | SAS | BEB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0089 | SAS | STU | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | STU | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0132 | SAS | STU | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | STU | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | STU | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG04228 | hp2 | a0002 | c0003 | t0002 | g0038 | SAS | STU | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | YRI | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | YRI | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | CHB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | YRI | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | YRI | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18939 | hp1 | a0002 | c0003 | t0002 | g0003 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18940 | hp2 | a0002 | c0003 | t0002 | g0242 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18943 | hp2 | a0002 | c0003 | t0002 | g0218 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18945 | hp2 | a0002 | c0003 | t0002 | g0236 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18952 | hp1 | a0002 | c0003 | t0002 | g0020 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18953 | hp2 | a0002 | c0003 | t0002 | g0235 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18960 | hp1 | a0002 | c0003 | t0002 | g0222 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18961 | hp1 | a0002 | c0003 | t0002 | g0232 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18962 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18963 | hp1 | a0002 | c0003 | t0013 | g0226 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18965 | hp2 | a0002 | c0003 | t0002 | g0239 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18967 | hp2 | a0002 | c0003 | t0002 | g0021 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18971 | hp1 | a0002 | c0003 | t0002 | g0237 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18972 | hp1 | a0002 | c0003 | t0002 | g0227 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18973 | hp2 | a0002 | c0003 | t0002 | g0233 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18979 | hp1 | a0002 | c0003 | t0002 | g0219 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18980 | hp2 | a0002 | c0003 | t0002 | g0020 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18988 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18992 | hp2 | a0002 | c0003 | t0002 | g0230 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18994 | hp2 | a0002 | c0003 | t0002 | g0216 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA18998 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19001 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19009 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19010 | hp2 | a0002 | c0003 | t0002 | g0023 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | LWK | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | LWK | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19043 | hp1 | a0001 | c0005 | t0003 | g0119 | AFR | LWK | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | LWK | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19054 | hp2 | a0002 | c0003 | t0002 | g0215 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19056 | hp1 | a0002 | c0003 | t0002 | g0003 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19060 | hp2 | a0002 | c0003 | t0002 | g0224 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19062 | hp2 | a0002 | c0003 | t0002 | g0220 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19065 | hp2 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19067 | hp2 | a0002 | c0003 | t0002 | g0243 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19074 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19074 | hp2 | a0002 | c0003 | t0002 | g0223 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19079 | hp2 | a0002 | c0003 | t0002 | g0225 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19080 | hp1 | a0002 | c0003 | t0002 | g0221 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19085 | hp1 | a0002 | c0003 | t0002 | g0023 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19089 | hp1 | a0002 | c0003 | t0002 | g0229 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19091 | hp1 | a0002 | c0003 | t0002 | g0214 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | ASW | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ASW | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0064 | EUR | TSI | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0024 | EUR | TSI | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0102 | SAS | GIH | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA20905 | hp2 | a0001 | c0002 | t0006 | g0084 | SAS | GIH | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | CLM | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | USA | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0147 | AFR | USA | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | USA | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | USA | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | LWK | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | LWK | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0093 | REF | REF | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0018 | REF | REF | TMEM161B_chr5_88190047_88273845 | TMEM161B | chr5 | 88190047 | 88273845 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:88197708 | C | T | 1 | a0002 | 41 | HG01978.hp2 HG02027.hp1 HG02080.hp2 others(38): Show |
missense_variant | MODERATE | c.1147G>A | p.Val383Ile | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 11/12 | 1269/2750 | 1147/1464 | 383/487 | chr5 | 88197708 | |||
chr5:88206475 | G | A | 1 | a0003 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.623C>T | p.Ala208Val | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 7/12 | 745/2750 | 623/1464 | 208/487 | chr5 | 88206475 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:88203032 | G | A | 1 | a0001c0002 | 111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
synonymous_variant | LOW | c.844C>T | p.Leu282Leu | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/12 | 966/2750 | 844/1464 | 282/487 | chr5 | 88203032 | |||
chr5:88206498 | C | A | 1 | a0001c0005 | 1 | NA19043.hp1 | splice_region_variant&synonymous_variant | LOW | c.600G>T | p.Gly200Gly | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 7/12 | 722/2750 | 600/1464 | 200/487 | chr5 | 88206498 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:88195091 | T | C | 4 | a0001c0001t0003 a0001c0001t0007 a0001c0005t0003 others(1): Show |
62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1120A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 1120 | chr5 | 88195091 | ||||||
chr5:88195118 | G | T | 1 | a0001c0002t0011 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1093C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 1093 | chr5 | 88195118 | ||||||
chr5:88195146 | C | T | 1 | a0001c0002t0010 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1065G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 1065 | chr5 | 88195146 | ||||||
chr5:88195331 | T | C | 1 | a0001c0001t0007 | 2 | HG03669.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*880A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 880 | chr5 | 88195331 | ||||||
chr5:88195344 | T | C | 1 | a0001c0002t0012 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*867A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 867 | chr5 | 88195344 | ||||||
chr5:88195438 | A | G | 1 | a0001c0002t0009 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*773T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 773 | chr5 | 88195438 | ||||||
chr5:88195549 | A | G | 1 | a0001c0002t0008 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*662T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 662 | chr5 | 88195549 | ||||||
chr5:88195728 | T | C | 8 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0006 others(5): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*483A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 483 | chr5 | 88195728 | ||||||
chr5:88195980 | G | C | 1 | a0001c0001t0005 | 12 | HG00408.hp1 HG01258.hp2 HG01975.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*231C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 231 | chr5 | 88195980 | ||||||
chr5:88196091 | T | C | 1 | a0001c0002t0006 | 4 | HG02040.hp1 HG03831.hp2 HG03942.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*120A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 120 | chr5 | 88196091 | ||||||
chr5:88196101 | T | G | 1 | a0002c0003t0013 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*110A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 110 | chr5 | 88196101 | ||||||
chr5:88196147 | C | T | 1 | a0001c0001t0004 | 13 | HG01074.hp2 HG01109.hp2 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*64G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 12/12 | 64 | chr5 | 88196147 | ||||||
chr5:88268829 | G | C | 1 | a0001c0001t0007 | 2 | HG03669.hp1 HG03942.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-106C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/12 | chr5 | 88268829 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:88196648 | G | A | 1 | a0001c0002t0001g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1187-160C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 11/11 | chr5 | 88196648 | |||||||
chr5:88196850 | C | T | 1 | a0001c0001t0003g0142 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1187-362G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 11/11 | chr5 | 88196850 | |||||||
chr5:88196926 | A | T | 1 | a0001c0002t0001g0017 | 2 | NA18946.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1187-438T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 11/11 | chr5 | 88196926 | |||||||
chr5:88196995 | A | C | 1 | a0001c0001t0003g0135 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1187-507T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 11/11 | chr5 | 88196995 | |||||||
chr5:88197073 | C | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0019 a0001c0001t0004g0022 others(3): Show |
10 | HG01109.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1187-585G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 11/11 | chr5 | 88197073 | |||||||
chr5:88197074 | T | C | 169 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(166): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1187-586A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 11/11 | chr5 | 88197074 | |||||||
chr5:88197222 | G | A | 1 | a0001c0001t0005g0167 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1186+447C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 11/11 | chr5 | 88197222 | |||||||
chr5:88197437 | T | G | 2 | a0001c0002t0001g0017 a0001c0002t0001g0035 |
3 | HG02523.hp2 NA18946.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1186+232A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 11/11 | chr5 | 88197437 | |||||||
chr5:88197482 | T | C | 7 | a0001c0001t0002g0112 a0001c0001t0002g0196 a0001c0001t0002g0197 others(4): Show |
7 | HG01884.hp2 HG03195.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186+187A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 11/11 | chr5 | 88197482 | |||||||
chr5:88197567 | A | G | 2 | a0001c0002t0001g0030 a0001c0002t0012g0029 |
2 | HG01070.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1186+102T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 11/11 | chr5 | 88197567 | |||||||
chr5:88197940 | C | G | 59 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0090 others(56): Show |
61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1090-175G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 10/11 | chr5 | 88197940 | |||||||
chr5:88198207 | T | C | 6 | a0001c0001t0004g0006 a0001c0001t0004g0019 a0001c0001t0004g0022 others(3): Show |
10 | HG01109.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1090-442A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 10/11 | chr5 | 88198207 | |||||||
chr5:88198273 | A | C | 1 | a0002c0003t0002g0225 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1090-508T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 10/11 | chr5 | 88198273 | |||||||
chr5:88198498 | G | C | 170 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(167): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1089+478C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 10/11 | chr5 | 88198498 | |||||||
chr5:88198785 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1089+191C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 10/11 | chr5 | 88198785 | |||||||
chr5:88198804 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0122 |
2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1089+172G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 10/11 | chr5 | 88198804 | |||||||
chr5:88198963 | G | T | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1089+13C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 10/11 | chr5 | 88198963 | |||||||
chr5:88199288 | G | C | 2 | a0001c0002t0001g0064 a0001c0002t0001g0179 |
2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.915-138C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88199288 | |||||||
chr5:88199292 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.915-142A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88199292 | |||||||
chr5:88199520 | C | T | 60 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0090 others(57): Show |
62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.915-370G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88199520 | |||||||
chr5:88199687 | G | A | 168 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(165): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.915-537C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88199687 | |||||||
chr5:88199812 | A | G | 3 | a0001c0002t0001g0054 a0001c0002t0001g0056 a0001c0002t0001g0147 |
3 | HG00323.hp1 HG03239.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.915-662T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88199812 | |||||||
chr5:88199897 | T | G | 7 | a0001c0001t0002g0075 a0001c0001t0002g0159 a0001c0001t0002g0160 others(4): Show |
7 | HG00558.hp1 HG00597.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.915-747A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88199897 | |||||||
chr5:88200095 | T | TA | 93 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(90): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.915-946dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88200095 | |||||||
chr5:88200112 | T | C | 93 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(90): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.915-962A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88200112 | |||||||
chr5:88200158 | C | T | 1 | a0001c0001t0004g0016 | 2 | HG01074.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.915-1008G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88200158 | |||||||
chr5:88200773 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.915-1623C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88200773 | |||||||
chr5:88201054 | C | CA | 95 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0002t0001g0001 others(92): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.915-1905dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88201054 | |||||||
chr5:88201089 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0005g0025 |
2 | HG01975.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.914+1873C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88201089 | |||||||
chr5:88201191 | A | G | 10 | a0001c0001t0003g0015 a0001c0001t0003g0097 a0001c0001t0003g0113 others(7): Show |
11 | HG01496.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.914+1771T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88201191 | |||||||
chr5:88201348 | G | C | 1 | a0002c0003t0002g0236 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.914+1614C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88201348 | |||||||
chr5:88201442 | T | C | 3 | a0002c0003t0002g0220 a0002c0003t0002g0227 a0002c0003t0002g0242 |
3 | NA18940.hp2 NA18972.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.914+1520A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88201442 | |||||||
chr5:88201795 | T | C | 19 | a0001c0001t0003g0014 a0001c0001t0003g0102 a0001c0001t0003g0103 others(16): Show |
20 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.914+1167A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88201795 | |||||||
chr5:88201805 | C | G | 7 | a0001c0001t0002g0075 a0001c0001t0002g0159 a0001c0001t0002g0160 others(4): Show |
7 | HG00558.hp1 HG00597.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.914+1157G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88201805 | |||||||
chr5:88201869 | A | G | 1 | a0001c0002t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.914+1093T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88201869 | |||||||
chr5:88201962 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.914+1000G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88201962 | |||||||
chr5:88202060 | A | C | 1 | a0001c0001t0002g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.914+902T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202060 | |||||||
chr5:88202160 | C | T | 243 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0009 others(240): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.914+802G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202160 | |||||||
chr5:88202210 | G | A | 95 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0002t0001g0001 others(92): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.914+752C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202210 | |||||||
chr5:88202252 | C | T | 95 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0002t0001g0001 others(92): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.914+710G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202252 | |||||||
chr5:88202279 | C | T | 1 | a0001c0001t0002g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.914+683G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202279 | |||||||
chr5:88202311 | T | A | 95 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0002t0001g0001 others(92): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.914+651A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202311 | |||||||
chr5:88202437 | TA | T | 66 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0090 others(63): Show |
72 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.914+524delT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202437 | |||||||
chr5:88202489 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.914+473A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202489 | |||||||
chr5:88202518 | T | C | 7 | a0001c0001t0002g0112 a0001c0001t0002g0196 a0001c0001t0002g0197 others(4): Show |
7 | HG01884.hp2 HG03195.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.914+444A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202518 | |||||||
chr5:88202535 | G | A | 1 | a0001c0001t0003g0104 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.914+427C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202535 | |||||||
chr5:88202579 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.914+383A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202579 | |||||||
chr5:88202737 | G | T | 1 | a0001c0002t0001g0149 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.914+225C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202737 | |||||||
chr5:88202762 | C | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0019 a0001c0001t0004g0022 others(3): Show |
10 | HG01109.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.914+200G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 9/11 | chr5 | 88202762 | |||||||
chr5:88203178 | A | T | 6 | a0001c0001t0003g0015 a0001c0001t0003g0134 a0001c0001t0003g0135 others(3): Show |
7 | HG01496.hp1 HG01884.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.801-103T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203178 | |||||||
chr5:88203260 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.801-185T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203260 | |||||||
chr5:88203433 | A | G | 3 | a0001c0002t0001g0054 a0001c0002t0001g0056 a0001c0002t0001g0147 |
3 | HG00323.hp1 HG03239.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.801-358T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203433 | |||||||
chr5:88203488 | A | G | 6 | a0001c0001t0002g0037 a0001c0001t0002g0206 a0001c0001t0002g0207 others(3): Show |
6 | HG01346.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.801-413T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203488 | |||||||
chr5:88203638 | C | T | 7 | a0001c0001t0002g0037 a0001c0001t0004g0006 a0001c0001t0004g0019 others(4): Show |
11 | HG01109.hp2 HG01346.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.801-563G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203638 | |||||||
chr5:88203641 | G | C | 4 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0002t0001g0081 others(1): Show |
4 | NA18962.hp1 NA18979.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.801-566C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203641 | |||||||
chr5:88203750 | CAT | C | 11 | a0001c0001t0002g0194 a0001c0001t0002g0209 a0001c0001t0003g0099 others(8): Show |
11 | HG00099.hp1 HG01081.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.801-677_801-676del others(2): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATAT | C | 8 | a0001c0001t0003g0014 a0001c0001t0003g0095 a0001c0001t0003g0110 others(5): Show |
9 | HG00639.hp2 HG00642.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.801-679_801-676del others(4): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATAT | C | 12 | a0001c0001t0002g0033 a0001c0001t0002g0154 a0001c0001t0003g0090 others(9): Show |
12 | HG00408.hp1 HG01175.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.801-681_801-676del others(6): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(1): Show |
C | 7 | a0001c0001t0002g0034 a0001c0001t0002g0191 a0001c0001t0003g0100 others(4): Show |
7 | HG01258.hp2 HG01496.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.801-683_801-676del others(8): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(3): Show |
C | 1 | a0001c0001t0003g0148 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.801-685_801-676del others(10): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(5): Show |
C | 8 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0189 others(5): Show |
8 | HG00597.hp2 HG00642.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.801-687_801-676del others(12): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(7): Show |
C | 9 | a0001c0001t0002g0075 a0001c0001t0002g0160 a0001c0001t0002g0188 others(6): Show |
9 | HG00558.hp1 HG01168.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.801-689_801-676del others(14): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(9): Show |
C | 4 | a0001c0001t0002g0164 a0001c0001t0003g0104 a0001c0001t0005g0050 others(1): Show |
4 | HG02004.hp1 HG03017.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.801-691_801-676del others(16): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(11): Show |
C | 6 | a0001c0001t0002g0163 a0001c0001t0004g0016 a0001c0001t0005g0170 others(3): Show |
7 | HG01074.hp2 HG01978.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.801-693_801-676del others(18): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(13): Show |
C | 9 | a0001c0001t0002g0206 a0001c0001t0003g0107 a0001c0001t0004g0157 others(6): Show |
9 | HG01175.hp1 HG02647.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.801-695_801-676del others(20): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(15): Show |
C | 13 | a0001c0001t0002g0112 a0001c0001t0002g0207 a0001c0001t0002g0208 others(10): Show |
15 | HG01978.hp2 HG02132.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.801-697_801-676del others(22): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(17): Show |
C | 16 | a0001c0001t0002g0153 a0001c0001t0002g0183 a0001c0001t0002g0198 others(13): Show |
22 | HG02027.hp1 HG02922.hp2 HG03041.hp1 others(19): Show |
intron_variant | MODIFIER | c.801-699_801-676del others(24): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(19): Show |
C | 4 | a0002c0003t0002g0218 a0002c0003t0002g0220 a0002c0003t0002g0227 others(1): Show |
4 | NA18940.hp2 NA18943.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.801-701_801-676del others(26): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(21): Show |
C | 5 | a0001c0001t0002g0037 a0001c0001t0002g0184 a0001c0001t0002g0201 others(2): Show |
5 | HG01099.hp1 HG01346.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.801-703_801-676del others(28): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(23): Show |
C | 2 | a0001c0001t0002g0197 a0001c0001t0002g0200 |
2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.801-705_801-676del others(30): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(25): Show |
C | 6 | a0001c0001t0001g0122 a0001c0001t0002g0133 a0001c0002t0001g0049 others(3): Show |
6 | HG01891.hp1 HG02080.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.801-707_801-676del others(32): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(27): Show |
C | 13 | a0001c0002t0001g0011 a0001c0002t0001g0031 a0001c0002t0001g0041 others(10): Show |
14 | HG00741.hp2 HG01109.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.801-709_801-676del others(34): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(29): Show |
C | 81 | a0001c0001t0001g0026 a0001c0001t0002g0009 a0001c0001t0002g0193 others(78): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.801-711_801-676del others(36): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203750 | CATATATA others(41): Show |
C | 7 | a0001c0001t0003g0103 a0001c0001t0004g0006 a0001c0001t0004g0019 others(4): Show |
11 | HG01109.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.801-723_801-676del others(48): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203750 | |||||||
chr5:88203814 | T | A | 44 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0090 others(41): Show |
46 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.801-739A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203814 | |||||||
chr5:88203814 | T | TAA | 9 | a0001c0001t0003g0092 a0001c0001t0003g0094 a0001c0001t0003g0108 others(6): Show |
9 | HG01981.hp2 HG02135.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.801-741_801-740dup others(2): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203814 | |||||||
chr5:88203814 | T | TATAA | 5 | a0001c0001t0003g0098 a0001c0001t0003g0111 a0001c0001t0003g0113 others(2): Show |
5 | HG01261.hp2 HG02451.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-740_801-739ins others(4): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88203814 | |||||||
chr5:88204702 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.800+1112G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88204702 | |||||||
chr5:88204796 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.800+1018G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88204796 | |||||||
chr5:88204849 | T | TA | 59 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0090 others(56): Show |
61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.800+964dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88204849 | |||||||
chr5:88204861 | A | G | 59 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0090 others(56): Show |
61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.800+953T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88204861 | |||||||
chr5:88204899 | G | C | 7 | a0001c0001t0002g0112 a0001c0001t0002g0196 a0001c0001t0002g0197 others(4): Show |
7 | HG01884.hp2 HG03195.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.800+915C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88204899 | |||||||
chr5:88204981 | C | A | 2 | a0001c0001t0003g0114 a0001c0001t0003g0115 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.800+833G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88204981 | |||||||
chr5:88205006 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.800+808A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88205006 | |||||||
chr5:88205063 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.800+751C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88205063 | |||||||
chr5:88205314 | T | C | 1 | a0001c0002t0001g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.800+500A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88205314 | |||||||
chr5:88205375 | C | A | 6 | a0001c0001t0004g0006 a0001c0001t0004g0019 a0001c0001t0004g0022 others(3): Show |
10 | HG01109.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.800+439G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88205375 | |||||||
chr5:88205406 | G | A | 166 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(163): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.800+408C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88205406 | |||||||
chr5:88205675 | T | C | 1 | a0002c0003t0002g0217 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.800+139A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88205675 | |||||||
chr5:88205763 | G | C | 1 | a0001c0002t0001g0176 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.800+51C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 8/11 | chr5 | 88205763 | |||||||
chr5:88206179 | A | G | 2 | a0001c0001t0007g0245 a0001c0001t0007g0246 |
2 | HG03669.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.660-225T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 7/11 | chr5 | 88206179 | |||||||
chr5:88206207 | T | A | 1 | a0001c0001t0003g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.659+232A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 7/11 | chr5 | 88206207 | |||||||
chr5:88206254 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.659+185T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 7/11 | chr5 | 88206254 | |||||||
chr5:88206400 | G | C | 33 | a0002c0003t0002g0003 a0002c0003t0002g0007 a0002c0003t0002g0020 others(30): Show |
41 | HG01978.hp2 HG02027.hp1 HG02080.hp2 others(38): Show |
intron_variant | MODIFIER | c.659+39C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 7/11 | chr5 | 88206400 | |||||||
chr5:88206508 | G | A | 164 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(161): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.599-9C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 6/11 | chr5 | 88206508 | |||||||
chr5:88206519 | A | C | 1 | a0001c0002t0001g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.599-20T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 6/11 | chr5 | 88206519 | |||||||
chr5:88206522 | C | A | 1 | a0001c0002t0001g0011 | 2 | HG00741.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.599-23G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 6/11 | chr5 | 88206522 | |||||||
chr5:88206534 | C | T | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-35G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 6/11 | chr5 | 88206534 | |||||||
chr5:88206543 | A | T | 1 | a0001c0002t0001g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.599-44T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 6/11 | chr5 | 88206543 | |||||||
chr5:88206612 | A | T | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.599-113T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 6/11 | chr5 | 88206612 | |||||||
chr5:88206632 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.599-133A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 6/11 | chr5 | 88206632 | |||||||
chr5:88206806 | C | T | 2 | a0001c0001t0002g0197 a0001c0001t0002g0198 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.598+223G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 6/11 | chr5 | 88206806 | |||||||
chr5:88206984 | C | T | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.598+45G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 6/11 | chr5 | 88206984 | |||||||
chr5:88207270 | GACT | G | 93 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0004 others(90): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.447-93_447-91delAG others(1): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88207270 | |||||||
chr5:88207290 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.447-110T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88207290 | |||||||
chr5:88207321 | A | G | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.447-141T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88207321 | |||||||
chr5:88207570 | C | T | 5 | a0001c0002t0001g0013 a0001c0002t0001g0064 a0001c0002t0001g0172 others(2): Show |
6 | HG00099.hp2 HG00733.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.447-390G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88207570 | |||||||
chr5:88207814 | T | C | 177 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(174): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.447-634A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88207814 | |||||||
chr5:88207943 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.447-763A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88207943 | |||||||
chr5:88208066 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.447-886A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208066 | |||||||
chr5:88208125 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.447-945C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208125 | |||||||
chr5:88208250 | G | T | 1 | a0001c0002t0001g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.447-1070C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208250 | |||||||
chr5:88208345 | G | C | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.447-1165C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208345 | |||||||
chr5:88208418 | C | A | 1 | a0001c0002t0001g0045 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.447-1238G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208418 | |||||||
chr5:88208422 | C | A | 1 | a0001c0002t0001g0199 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.447-1242G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208422 | |||||||
chr5:88208468 | T | C | 96 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(93): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.447-1288A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208468 | |||||||
chr5:88208479 | C | G | 1 | a0001c0002t0012g0029 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.447-1299G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208479 | |||||||
chr5:88208482 | C | CA | 8 | a0001c0001t0002g0112 a0001c0001t0002g0153 a0001c0001t0002g0196 others(5): Show |
8 | HG01884.hp2 HG02922.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.447-1303dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208482 | |||||||
chr5:88208506 | G | C | 1 | a0001c0001t0003g0144 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.447-1326C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208506 | |||||||
chr5:88208666 | G | A | 176 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(173): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.447-1486C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208666 | |||||||
chr5:88208764 | C | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.447-1584G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88208764 | |||||||
chr5:88209188 | A | C | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.447-2008T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88209188 | |||||||
chr5:88209189 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.447-2009T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88209189 | |||||||
chr5:88209190 | G | T | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.447-2010C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88209190 | |||||||
chr5:88209191 | A | C | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.447-2011T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88209191 | |||||||
chr5:88209347 | C | G | 60 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0090 others(57): Show |
62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.447-2167G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88209347 | |||||||
chr5:88209412 | G | C | 60 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0090 others(57): Show |
62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.447-2232C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88209412 | |||||||
chr5:88209608 | C | T | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.447-2428G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88209608 | |||||||
chr5:88209696 | G | T | 1 | a0001c0001t0002g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.447-2516C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88209696 | |||||||
chr5:88209837 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.447-2657A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88209837 | |||||||
chr5:88209862 | A | ACTGCC | 177 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(174): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.447-2683_447-2682i others(7): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88209862 | |||||||
chr5:88209920 | A | C | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.447-2740T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88209920 | |||||||
chr5:88210102 | A | C | 1 | a0002c0003t0002g0223 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.447-2922T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88210102 | |||||||
chr5:88210273 | C | T | 1 | a0001c0002t0001g0051 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.447-3093G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88210273 | |||||||
chr5:88210276 | G | A | 7 | a0001c0001t0002g0112 a0001c0001t0002g0196 a0001c0001t0002g0197 others(4): Show |
7 | HG01884.hp2 HG03195.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.447-3096C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88210276 | |||||||
chr5:88210293 | G | C | 1 | a0001c0002t0001g0051 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.447-3113C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88210293 | |||||||
chr5:88210313 | T | A | 1 | a0001c0001t0003g0104 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.447-3133A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88210313 | |||||||
chr5:88210480 | C | A | 1 | a0001c0002t0001g0046 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.447-3300G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88210480 | |||||||
chr5:88210553 | C | G | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.447-3373G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88210553 | |||||||
chr5:88210620 | G | T | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG01175.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.447-3440C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88210620 | |||||||
chr5:88210744 | C | T | 1 | a0001c0001t0004g0022 | 2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.447-3564G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88210744 | |||||||
chr5:88210806 | G | A | 6 | a0001c0001t0003g0105 a0001c0001t0003g0106 a0001c0001t0003g0107 others(3): Show |
6 | HG00323.hp2 HG01081.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.447-3626C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88210806 | |||||||
chr5:88210930 | G | C | 1 | a0001c0001t0004g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.447-3750C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88210930 | |||||||
chr5:88211120 | G | T | 176 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(173): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.447-3940C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211120 | |||||||
chr5:88211159 | T | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.447-3979A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211159 | |||||||
chr5:88211211 | G | T | 1 | a0001c0001t0002g0209 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.447-4031C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211211 | |||||||
chr5:88211235 | G | A | 177 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(174): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.447-4055C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211235 | |||||||
chr5:88211250 | C | T | 177 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(174): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.447-4070G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211250 | |||||||
chr5:88211320 | A | G | 60 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0090 others(57): Show |
62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.447-4140T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211320 | |||||||
chr5:88211364 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.447-4184G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211364 | |||||||
chr5:88211416 | G | GA | 96 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(93): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.447-4237dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211416 | |||||||
chr5:88211620 | T | G | 1 | a0001c0001t0003g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.447-4440A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211620 | |||||||
chr5:88211620 | TGGCGGCG others(5): Show |
T | 3 | a0001c0001t0002g0112 a0001c0001t0002g0189 a0001c0002t0001g0150 |
3 | HG00140.hp2 HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.447-4452_447-4441d others(14): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211620 | |||||||
chr5:88211623 | C | T | 60 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0090 others(57): Show |
62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.447-4443G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211623 | |||||||
chr5:88211630 | C | T | 1 | a0001c0002t0001g0073 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.447-4450G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211630 | |||||||
chr5:88211633 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.447-4453C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211633 | |||||||
chr5:88211635 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.447-4455G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211635 | |||||||
chr5:88211642 | C | T | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.447-4462G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211642 | |||||||
chr5:88211719 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.447-4539G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211719 | |||||||
chr5:88211726 | G | A | 1 | a0001c0002t0001g0177 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.447-4546C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211726 | |||||||
chr5:88211768 | CA | C | 161 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(158): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.447-4589delT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211768 | |||||||
chr5:88211953 | C | T | 1 | a0001c0001t0005g0170 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.447-4773G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88211953 | |||||||
chr5:88212302 | G | A | 1 | a0001c0001t0003g0129 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.447-5122C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88212302 | |||||||
chr5:88212437 | C | T | 1 | a0001c0002t0006g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.447-5257G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88212437 | |||||||
chr5:88212753 | C | T | 9 | a0001c0001t0002g0009 a0001c0001t0002g0133 a0001c0001t0002g0188 others(6): Show |
11 | HG00639.hp1 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.447-5573G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88212753 | |||||||
chr5:88212987 | A | G | 1 | a0002c0003t0002g0225 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.447-5807T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88212987 | |||||||
chr5:88213124 | T | A | 1 | a0001c0001t0003g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.447-5944A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88213124 | |||||||
chr5:88213150 | A | C | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.447-5970T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88213150 | |||||||
chr5:88213353 | A | C | 1 | a0001c0002t0001g0049 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.447-6173T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88213353 | |||||||
chr5:88213443 | C | T | 59 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0090 others(56): Show |
61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.447-6263G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88213443 | |||||||
chr5:88213563 | G | T | 1 | a0001c0001t0003g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.447-6383C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88213563 | |||||||
chr5:88213567 | ACTAT | A | 96 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(93): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.447-6391_447-6388d others(6): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88213567 | |||||||
chr5:88213778 | C | A | 1 | a0001c0002t0001g0060 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.447-6598G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88213778 | |||||||
chr5:88213783 | T | C | 1 | a0001c0001t0003g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.447-6603A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88213783 | |||||||
chr5:88213994 | G | A | 2 | a0001c0001t0004g0019 a0001c0001t0004g0204 |
3 | HG02723.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.446+6569C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88213994 | |||||||
chr5:88214110 | G | C | 1 | a0001c0001t0002g0164 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.446+6453C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88214110 | |||||||
chr5:88214450 | G | A | 1 | a0001c0001t0004g0016 | 2 | HG01074.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.446+6113C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88214450 | |||||||
chr5:88214593 | A | G | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.446+5970T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88214593 | |||||||
chr5:88214634 | T | A | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.446+5929A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88214634 | |||||||
chr5:88214808 | T | C | 1 | a0001c0001t0003g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.446+5755A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88214808 | |||||||
chr5:88214901 | G | C | 1 | a0001c0001t0007g0245 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.446+5662C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88214901 | |||||||
chr5:88215037 | C | A | 176 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(173): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.446+5526G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88215037 | |||||||
chr5:88215199 | A | T | 1 | a0001c0001t0002g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.446+5364T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88215199 | |||||||
chr5:88215456 | T | A | 1 | a0001c0001t0003g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.446+5107A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88215456 | |||||||
chr5:88215497 | C | CA | 167 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(164): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.446+5065dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88215497 | |||||||
chr5:88215540 | C | G | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.446+5023G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88215540 | |||||||
chr5:88215896 | C | T | 3 | a0001c0001t0004g0006 a0001c0001t0004g0151 a0001c0001t0004g0152 |
5 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+4667G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88215896 | |||||||
chr5:88216015 | T | G | 97 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(94): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.446+4548A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88216015 | |||||||
chr5:88216068 | G | T | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.446+4495C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88216068 | |||||||
chr5:88216170 | C | T | 1 | a0001c0001t0005g0167 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.446+4393G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88216170 | |||||||
chr5:88216213 | A | C | 72 | a0001c0001t0001g0026 a0001c0001t0002g0206 a0001c0001t0002g0207 others(69): Show |
78 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.446+4350T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88216213 | |||||||
chr5:88216316 | T | A | 1 | a0001c0001t0004g0152 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.446+4247A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88216316 | |||||||
chr5:88216497 | C | T | 95 | a0001c0001t0001g0122 a0001c0001t0002g0037 a0001c0002t0001g0001 others(92): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.446+4066G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88216497 | |||||||
chr5:88216656 | G | T | 13 | a0002c0003t0002g0007 a0002c0003t0002g0021 a0002c0003t0002g0219 others(10): Show |
16 | HG01978.hp2 HG02132.hp1 NA18940.hp2 others(13): Show |
intron_variant | MODIFIER | c.446+3907C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88216656 | |||||||
chr5:88216684 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.446+3879A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88216684 | |||||||
chr5:88216715 | G | A | 61 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0003g0014 others(58): Show |
63 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.446+3848C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88216715 | |||||||
chr5:88217265 | A | T | 1 | a0001c0002t0001g0040 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.446+3298T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88217265 | |||||||
chr5:88217483 | A | C | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.446+3080T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88217483 | |||||||
chr5:88217561 | G | A | 1 | a0001c0002t0001g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.446+3002C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88217561 | |||||||
chr5:88217591 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.446+2972C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88217591 | |||||||
chr5:88217905 | GA | G | 184 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(181): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.446+2657delT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88217905 | |||||||
chr5:88217958 | C | T | 132 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(129): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.446+2605G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88217958 | |||||||
chr5:88217983 | G | A | 7 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 others(4): Show |
7 | HG01884.hp2 HG03195.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.446+2580C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88217983 | |||||||
chr5:88218187 | G | T | 187 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(184): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.446+2376C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88218187 | |||||||
chr5:88218194 | T | A | 2 | a0001c0001t0003g0139 a0001c0001t0003g0140 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.446+2369A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88218194 | |||||||
chr5:88218270 | T | A | 3 | a0001c0001t0004g0006 a0001c0001t0004g0151 a0001c0001t0004g0152 |
5 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+2293A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88218270 | |||||||
chr5:88218582 | A | C | 1 | a0001c0002t0001g0177 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.446+1981T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88218582 | |||||||
chr5:88218698 | G | T | 12 | a0001c0001t0003g0014 a0001c0001t0003g0102 a0001c0001t0003g0103 others(9): Show |
13 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.446+1865C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88218698 | |||||||
chr5:88218742 | T | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.446+1821A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88218742 | |||||||
chr5:88218769 | A | C | 3 | a0001c0001t0004g0019 a0001c0001t0004g0022 a0001c0001t0004g0204 |
5 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+1794T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88218769 | |||||||
chr5:88218847 | C | T | 3 | a0001c0001t0004g0006 a0001c0001t0004g0151 a0001c0001t0004g0152 |
5 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+1716G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88218847 | |||||||
chr5:88218961 | TA | T | 71 | a0001c0001t0002g0037 a0001c0001t0002g0075 a0001c0001t0005g0025 others(68): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.446+1601delT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88218961 | |||||||
chr5:88219090 | T | C | 1 | a0001c0001t0003g0121 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.446+1473A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88219090 | |||||||
chr5:88219091 | C | T | 2 | a0001c0002t0001g0060 a0001c0002t0001g0082 |
2 | NA19060.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.446+1472G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88219091 | |||||||
chr5:88219585 | A | G | 8 | a0001c0001t0002g0154 a0001c0001t0002g0196 a0001c0001t0002g0197 others(5): Show |
8 | HG01884.hp2 HG01891.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.446+978T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88219585 | |||||||
chr5:88219821 | G | A | 1 | a0001c0001t0003g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.446+742C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88219821 | |||||||
chr5:88220002 | A | C | 138 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(135): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.446+561T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88220002 | |||||||
chr5:88220029 | G | C | 1 | a0001c0002t0001g0182 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.446+534C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88220029 | |||||||
chr5:88220249 | T | C | 1 | a0001c0001t0002g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.446+314A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88220249 | |||||||
chr5:88220338 | G | C | 1 | a0001c0001t0003g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.446+225C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88220338 | |||||||
chr5:88220500 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.446+63C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 5/11 | chr5 | 88220500 | |||||||
chr5:88220727 | G | GA | 71 | a0001c0001t0001g0122 a0001c0001t0002g0112 a0001c0001t0002g0133 others(68): Show |
73 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.290-9dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88220727 | |||||||
chr5:88220727 | G | GAA | 6 | a0001c0001t0001g0026 a0001c0001t0003g0091 a0001c0001t0003g0124 others(3): Show |
7 | HG01074.hp2 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-10_290-9dupTT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88220727 | |||||||
chr5:88220727 | GA | G | 8 | a0001c0001t0002g0207 a0001c0001t0004g0204 a0001c0001t0005g0169 others(5): Show |
8 | HG01070.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.290-9delT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88220727 | |||||||
chr5:88220755 | C | CA | 4 | a0001c0002t0001g0005 a0001c0002t0001g0024 a0001c0002t0001g0070 others(1): Show |
6 | HG00140.hp1 HG01123.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-37dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88220755 | |||||||
chr5:88220764 | C | A | 4 | a0001c0002t0001g0005 a0001c0002t0001g0024 a0001c0002t0001g0070 others(1): Show |
6 | HG00140.hp1 HG01123.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-45G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88220764 | |||||||
chr5:88220766 | G | A | 4 | a0001c0002t0001g0005 a0001c0002t0001g0024 a0001c0002t0001g0070 others(1): Show |
6 | HG00140.hp1 HG01123.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-47C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88220766 | |||||||
chr5:88220820 | C | T | 1 | a0001c0002t0001g0052 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.290-101G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88220820 | |||||||
chr5:88220821 | G | T | 3 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0176 |
3 | HG00597.hp1 HG02083.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.290-102C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88220821 | |||||||
chr5:88220849 | T | G | 1 | a0001c0002t0001g0048 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.290-130A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88220849 | |||||||
chr5:88220966 | T | G | 38 | a0001c0001t0005g0234 a0001c0002t0001g0008 a0001c0002t0001g0238 others(35): Show |
48 | HG01070.hp2 HG01358.hp2 HG01928.hp2 others(45): Show |
intron_variant | MODIFIER | c.290-247A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88220966 | |||||||
chr5:88221093 | A | T | 1 | a0001c0002t0001g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.290-374T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88221093 | |||||||
chr5:88221167 | T | A | 1 | a0001c0002t0001g0048 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.290-448A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88221167 | |||||||
chr5:88221325 | C | A | 2 | a0001c0002t0001g0041 a0001c0002t0001g0087 |
2 | NA18965.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.290-606G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88221325 | |||||||
chr5:88221328 | G | A | 1 | a0001c0002t0001g0069 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.290-609C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88221328 | |||||||
chr5:88221465 | C | T | 2 | a0001c0002t0001g0042 a0001c0002t0001g0078 |
2 | NA18940.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.290-746G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88221465 | |||||||
chr5:88221553 | A | G | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-834T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88221553 | |||||||
chr5:88222061 | T | C | 183 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(180): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.290-1342A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88222061 | |||||||
chr5:88222078 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.290-1359G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88222078 | |||||||
chr5:88222523 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.290-1804C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88222523 | |||||||
chr5:88222635 | T | C | 191 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(188): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.290-1916A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88222635 | |||||||
chr5:88223131 | A | AT | 181 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(178): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.290-2413dupA | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88223131 | |||||||
chr5:88223463 | A | T | 1 | a0001c0002t0001g0173 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.289+2306T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88223463 | |||||||
chr5:88223527 | T | G | 1 | a0001c0002t0001g0028 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.289+2242A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88223527 | |||||||
chr5:88223750 | G | T | 38 | a0001c0001t0005g0234 a0001c0002t0001g0008 a0001c0002t0001g0238 others(35): Show |
48 | HG01070.hp2 HG01358.hp2 HG01928.hp2 others(45): Show |
intron_variant | MODIFIER | c.289+2019C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88223750 | |||||||
chr5:88223761 | C | T | 2 | a0001c0001t0002g0161 a0001c0001t0002g0201 |
2 | HG00597.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.289+2008G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88223761 | |||||||
chr5:88223875 | C | T | 3 | a0001c0001t0004g0006 a0001c0001t0004g0151 a0001c0001t0004g0152 |
5 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+1894G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88223875 | |||||||
chr5:88223941 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.289+1828T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88223941 | |||||||
chr5:88224030 | T | A | 1 | a0002c0003t0002g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.289+1739A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224030 | |||||||
chr5:88224147 | G | A | 12 | a0001c0001t0003g0014 a0001c0001t0003g0102 a0001c0001t0003g0103 others(9): Show |
13 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.289+1622C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224147 | |||||||
chr5:88224397 | C | T | 10 | a0002c0003t0002g0003 a0002c0003t0002g0020 a0002c0003t0002g0214 others(7): Show |
14 | HG02027.hp1 NA18939.hp1 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.289+1372G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224397 | |||||||
chr5:88224420 | A | C | 1 | a0001c0002t0001g0051 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.289+1349T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224420 | |||||||
chr5:88224426 | A | G | 1 | a0002c0003t0002g0216 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.289+1343T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224426 | |||||||
chr5:88224456 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.289+1313C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224456 | |||||||
chr5:88224705 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.289+1064A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224705 | |||||||
chr5:88224778 | C | G | 70 | a0001c0001t0002g0037 a0001c0001t0002g0075 a0001c0001t0005g0025 others(67): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.289+991G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224778 | |||||||
chr5:88224959 | G | GT | 65 | a0001c0001t0002g0037 a0001c0001t0002g0154 a0001c0001t0002g0196 others(62): Show |
68 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.289+809dupA | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224959 | |||||||
chr5:88224959 | G | GTT | 34 | a0001c0001t0002g0153 a0001c0001t0002g0198 a0001c0001t0002g0202 others(31): Show |
35 | HG01975.hp1 HG01993.hp2 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.289+808_289+809dup others(2): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224959 | |||||||
chr5:88224959 | G | GTTT | 15 | a0001c0001t0005g0234 a0001c0002t0001g0008 a0001c0002t0009g0228 others(12): Show |
19 | HG01070.hp2 HG01358.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.289+807_289+809dup others(3): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224959 | |||||||
chr5:88224964 | TG | T | 3 | a0001c0001t0001g0122 a0001c0001t0004g0016 a0001c0002t0001g0040 |
4 | HG01074.hp2 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+804delC | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224964 | |||||||
chr5:88224965 | G | GT | 5 | a0001c0001t0002g0160 a0001c0001t0002g0195 a0001c0001t0005g0186 others(2): Show |
5 | HG01168.hp2 HG01261.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+803dupA | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224965 | |||||||
chr5:88224965 | G | T | 187 | a0001c0001t0001g0026 a0001c0001t0002g0037 a0001c0001t0002g0075 others(184): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.289+804C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224965 | |||||||
chr5:88224969 | T | G | 1 | a0001c0002t0001g0068 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.289+800A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224969 | |||||||
chr5:88224974 | T | G | 1 | a0001c0001t0003g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.289+795A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224974 | |||||||
chr5:88224975 | T | G | 1 | a0001c0002t0001g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.289+794A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224975 | |||||||
chr5:88224976 | T | G | 16 | a0001c0002t0001g0017 a0001c0002t0001g0158 a0001c0002t0001g0165 others(13): Show |
17 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.289+793A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224976 | |||||||
chr5:88224977 | T | G | 2 | a0001c0001t0005g0167 a0001c0001t0005g0168 |
2 | HG00408.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.289+792A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224977 | |||||||
chr5:88224998 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.289+771G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88224998 | |||||||
chr5:88225004 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.289+765C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88225004 | |||||||
chr5:88225007 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.289+762C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88225007 | |||||||
chr5:88225031 | G | A | 1 | a0001c0001t0003g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.289+738C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88225031 | |||||||
chr5:88225037 | G | A | 1 | a0001c0001t0003g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.289+732C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88225037 | |||||||
chr5:88225079 | T | G | 1 | a0001c0002t0001g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.289+690A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88225079 | |||||||
chr5:88225162 | T | A | 1 | a0001c0001t0003g0120 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.289+607A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88225162 | |||||||
chr5:88225167 | C | T | 1 | a0002c0003t0002g0221 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.289+602G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88225167 | |||||||
chr5:88225233 | C | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.289+536G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88225233 | |||||||
chr5:88225257 | G | A | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+512C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88225257 | |||||||
chr5:88225318 | G | C | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.289+451C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88225318 | |||||||
chr5:88225358 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.289+411C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 4/11 | chr5 | 88225358 | |||||||
chr5:88226212 | C | T | 1 | a0001c0001t0007g0245 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.192-346G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88226212 | |||||||
chr5:88226290 | T | C | 2 | a0001c0001t0003g0108 a0001c0001t0003g0109 |
2 | HG02135.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.192-424A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88226290 | |||||||
chr5:88226413 | T | G | 2 | a0001c0001t0003g0130 a0001c0001t0003g0131 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.192-547A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88226413 | |||||||
chr5:88226541 | T | C | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.192-675A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88226541 | |||||||
chr5:88226600 | T | C | 16 | a0001c0002t0001g0017 a0001c0002t0001g0158 a0001c0002t0001g0165 others(13): Show |
17 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.192-734A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88226600 | |||||||
chr5:88226765 | G | T | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.192-899C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88226765 | |||||||
chr5:88227104 | A | G | 38 | a0001c0001t0005g0234 a0001c0002t0001g0008 a0001c0002t0001g0238 others(35): Show |
48 | HG01070.hp2 HG01358.hp2 HG01928.hp2 others(45): Show |
intron_variant | MODIFIER | c.192-1238T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88227104 | |||||||
chr5:88227237 | G | A | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.191+1208C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88227237 | |||||||
chr5:88227746 | G | A | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.191+699C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88227746 | |||||||
chr5:88227819 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191+626G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88227819 | |||||||
chr5:88227885 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.191+560A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88227885 | |||||||
chr5:88227891 | T | G | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.191+554A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88227891 | |||||||
chr5:88228065 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.191+380C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88228065 | |||||||
chr5:88228103 | C | G | 1 | a0001c0002t0001g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.191+342G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88228103 | |||||||
chr5:88228138 | G | A | 1 | a0001c0002t0001g0011 | 2 | HG00741.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.191+307C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 3/11 | chr5 | 88228138 | |||||||
chr5:88228561 | G | A | 14 | a0001c0001t0002g0154 a0001c0001t0002g0160 a0001c0001t0002g0196 others(11): Show |
17 | HG01074.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.108-33C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88228561 | |||||||
chr5:88228819 | T | C | 1 | a0002c0003t0002g0213 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.108-291A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88228819 | |||||||
chr5:88228901 | T | C | 1 | a0001c0002t0001g0182 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.108-373A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88228901 | |||||||
chr5:88229272 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.108-744A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88229272 | |||||||
chr5:88229383 | T | G | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-855A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88229383 | |||||||
chr5:88229489 | GT | G | 189 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(186): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.108-962delA | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88229489 | |||||||
chr5:88229696 | A | G | 6 | a0001c0001t0003g0091 a0001c0001t0003g0099 a0001c0001t0003g0100 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.108-1168T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88229696 | |||||||
chr5:88230037 | A | G | 1 | a0001c0002t0001g0048 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.108-1509T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88230037 | |||||||
chr5:88230074 | C | G | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | HG02132.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.108-1546G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88230074 | |||||||
chr5:88230079 | G | A | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-1551C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88230079 | |||||||
chr5:88230085 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.108-1557C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88230085 | |||||||
chr5:88230261 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.108-1733A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88230261 | |||||||
chr5:88230277 | A | C | 1 | a0003c0004t0003g0127 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.108-1749T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88230277 | |||||||
chr5:88230312 | A | T | 1 | a0001c0001t0002g0194 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.108-1784T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88230312 | |||||||
chr5:88230768 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.108-2240G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88230768 | |||||||
chr5:88231035 | A | C | 1 | a0001c0001t0002g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.108-2507T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88231035 | |||||||
chr5:88231081 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.108-2553A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88231081 | |||||||
chr5:88231163 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.108-2635C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88231163 | |||||||
chr5:88231533 | T | C | 154 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(151): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.108-3005A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88231533 | |||||||
chr5:88231587 | G | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.108-3059C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88231587 | |||||||
chr5:88231628 | T | C | 136 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(133): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.108-3100A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88231628 | |||||||
chr5:88231816 | G | A | 3 | a0001c0001t0003g0137 a0001c0001t0003g0138 a0001c0002t0001g0064 |
3 | HG02647.hp1 HG03579.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.108-3288C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88231816 | |||||||
chr5:88231909 | A | G | 1 | a0001c0001t0003g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-3381T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88231909 | |||||||
chr5:88232070 | A | G | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-3542T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88232070 | |||||||
chr5:88232198 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.108-3670G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88232198 | |||||||
chr5:88232323 | C | CA | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.108-3796dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88232323 | |||||||
chr5:88232579 | AT | A | 242 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0009 others(239): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.108-4052delA | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88232579 | |||||||
chr5:88232623 | G | A | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-4095C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88232623 | |||||||
chr5:88232734 | C | T | 1 | a0002c0003t0002g0220 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.108-4206G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88232734 | |||||||
chr5:88232774 | C | T | 1 | a0001c0001t0002g0009 | 3 | HG00639.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.108-4246G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88232774 | |||||||
chr5:88232810 | A | G | 193 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(190): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.108-4282T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88232810 | |||||||
chr5:88232818 | C | T | 11 | a0001c0001t0005g0167 a0001c0001t0005g0168 a0001c0001t0005g0169 others(8): Show |
11 | HG00408.hp1 HG01258.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.108-4290G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88232818 | |||||||
chr5:88232863 | C | T | 13 | a0001c0001t0002g0154 a0001c0001t0002g0196 a0001c0001t0002g0197 others(10): Show |
16 | HG01074.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.108-4335G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88232863 | |||||||
chr5:88233036 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.108-4508C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88233036 | |||||||
chr5:88233102 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.108-4574C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88233102 | |||||||
chr5:88233411 | A | T | 1 | a0001c0001t0005g0050 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.108-4883T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88233411 | |||||||
chr5:88233418 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.108-4890A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88233418 | |||||||
chr5:88233553 | A | G | 1 | a0001c0002t0001g0076 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.108-5025T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88233553 | |||||||
chr5:88233705 | G | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.108-5177C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88233705 | |||||||
chr5:88233841 | G | C | 197 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(194): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.108-5313C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88233841 | |||||||
chr5:88234062 | G | T | 1 | a0001c0001t0003g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108-5534C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88234062 | |||||||
chr5:88234112 | G | A | 135 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(132): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.108-5584C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88234112 | |||||||
chr5:88234166 | G | C | 13 | a0001c0001t0002g0154 a0001c0001t0002g0196 a0001c0001t0002g0197 others(10): Show |
16 | HG01074.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.108-5638C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88234166 | |||||||
chr5:88234287 | C | T | 1 | a0001c0001t0002g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.108-5759G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88234287 | |||||||
chr5:88234436 | A | C | 62 | a0001c0001t0001g0122 a0001c0001t0002g0112 a0001c0001t0002g0133 others(59): Show |
64 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.108-5908T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88234436 | |||||||
chr5:88234563 | C | G | 1 | a0001c0001t0004g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108-6035G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88234563 | |||||||
chr5:88235104 | C | T | 1 | a0001c0002t0001g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.107+5709G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88235104 | |||||||
chr5:88235128 | A | C | 1 | a0001c0002t0001g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.107+5685T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88235128 | |||||||
chr5:88235171 | T | C | 1 | a0001c0002t0001g0065 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.107+5642A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88235171 | |||||||
chr5:88235462 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.107+5351G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88235462 | |||||||
chr5:88235608 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107+5205A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88235608 | |||||||
chr5:88235756 | T | C | 2 | a0001c0001t0003g0130 a0001c0001t0003g0131 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.107+5057A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88235756 | |||||||
chr5:88236023 | G | C | 2 | a0001c0002t0001g0166 a0001c0002t0001g0205 |
2 | NA18992.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.107+4790C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88236023 | |||||||
chr5:88236208 | T | C | 1 | a0001c0002t0001g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.107+4605A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88236208 | |||||||
chr5:88236230 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.107+4583A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88236230 | |||||||
chr5:88236285 | C | T | 1 | a0001c0001t0003g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107+4528G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88236285 | |||||||
chr5:88236441 | G | A | 61 | a0001c0001t0001g0122 a0001c0001t0002g0112 a0001c0001t0002g0133 others(58): Show |
63 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.107+4372C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88236441 | |||||||
chr5:88236694 | A | C | 2 | a0002c0003t0002g0219 a0002c0003t0002g0243 |
2 | NA18979.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.107+4119T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88236694 | |||||||
chr5:88237160 | T | C | 136 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(133): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.107+3653A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88237160 | |||||||
chr5:88237204 | A | G | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.107+3609T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88237204 | |||||||
chr5:88237579 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.107+3234A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88237579 | |||||||
chr5:88237622 | A | G | 1 | a0001c0001t0005g0186 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.107+3191T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88237622 | |||||||
chr5:88237717 | T | TAC | 155 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(152): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.107+3094_107+3095d others(4): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88237717 | |||||||
chr5:88237751 | A | T | 13 | a0001c0001t0002g0154 a0001c0001t0002g0196 a0001c0001t0002g0197 others(10): Show |
16 | HG01074.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.107+3062T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88237751 | |||||||
chr5:88237777 | A | G | 1 | a0002c0003t0002g0218 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.107+3036T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88237777 | |||||||
chr5:88237827 | A | G | 2 | a0001c0002t0001g0030 a0001c0002t0012g0029 |
2 | HG01070.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.107+2986T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88237827 | |||||||
chr5:88238075 | C | T | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.107+2738G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88238075 | |||||||
chr5:88238209 | T | C | 1 | a0002c0003t0002g0235 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.107+2604A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88238209 | |||||||
chr5:88238408 | T | G | 1 | a0001c0001t0003g0141 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.107+2405A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88238408 | |||||||
chr5:88238574 | A | C | 1 | a0001c0001t0004g0022 | 2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.107+2239T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88238574 | |||||||
chr5:88239458 | G | A | 1 | a0001c0002t0001g0012 | 2 | NA18939.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.107+1355C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88239458 | |||||||
chr5:88239730 | T | C | 1 | a0002c0003t0002g0231 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.107+1083A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88239730 | |||||||
chr5:88240021 | C | G | 5 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0190 others(2): Show |
5 | HG00642.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+792G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88240021 | |||||||
chr5:88240062 | A | T | 13 | a0001c0001t0003g0014 a0001c0001t0003g0102 a0001c0001t0003g0103 others(10): Show |
14 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.107+751T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88240062 | |||||||
chr5:88240136 | T | TGGAAGGA others(5): Show |
1 | a0001c0002t0001g0043 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.107+665_107+676dup others(12): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88240136 | |||||||
chr5:88240272 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.107+541A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88240272 | |||||||
chr5:88240291 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107+522C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88240291 | |||||||
chr5:88240466 | G | A | 27 | a0001c0001t0002g0112 a0001c0001t0002g0133 a0001c0001t0003g0015 others(24): Show |
28 | HG01123.hp1 HG01496.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.107+347C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88240466 | |||||||
chr5:88240468 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.107+345C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88240468 | |||||||
chr5:88240514 | T | C | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+299A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88240514 | |||||||
chr5:88240563 | C | T | 3 | a0001c0001t0002g0133 a0001c0001t0003g0015 a0001c0001t0003g0134 |
4 | HG01884.hp1 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+250G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88240563 | |||||||
chr5:88240746 | G | A | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107+67C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 2/11 | chr5 | 88240746 | |||||||
chr5:88241075 | C | T | 1 | a0001c0001t0003g0144 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4-159G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88241075 | |||||||
chr5:88241092 | G | C | 1 | a0001c0001t0003g0144 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4-176C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88241092 | |||||||
chr5:88241358 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4-442G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88241358 | |||||||
chr5:88241390 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4-474T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88241390 | |||||||
chr5:88241718 | C | T | 1 | a0001c0002t0001g0012 | 2 | NA18939.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.4-802G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88241718 | |||||||
chr5:88241799 | G | A | 1 | a0001c0002t0001g0035 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4-883C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88241799 | |||||||
chr5:88241952 | A | G | 7 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0035 others(4): Show |
13 | HG00408.hp2 HG02083.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-1036T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88241952 | |||||||
chr5:88242072 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4-1156A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88242072 | |||||||
chr5:88242073 | A | G | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.4-1157T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88242073 | |||||||
chr5:88242222 | C | G | 6 | a0001c0001t0003g0091 a0001c0001t0003g0099 a0001c0001t0003g0100 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-1306G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88242222 | |||||||
chr5:88242339 | T | C | 16 | a0001c0001t0002g0154 a0001c0001t0002g0196 a0001c0001t0002g0197 others(13): Show |
18 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.4-1423A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88242339 | |||||||
chr5:88242433 | T | TAAAGTTG others(50): Show |
38 | a0001c0001t0005g0234 a0001c0002t0001g0008 a0001c0002t0001g0238 others(35): Show |
48 | HG01070.hp2 HG01358.hp2 HG01928.hp2 others(45): Show |
intron_variant | MODIFIER | c.4-1574_4-1518dupTT others(55): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88242433 | |||||||
chr5:88242566 | G | A | 1 | a0001c0002t0001g0011 | 2 | HG00741.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4-1650C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88242566 | |||||||
chr5:88242701 | C | T | 11 | a0001c0001t0002g0154 a0001c0001t0002g0196 a0001c0001t0002g0197 others(8): Show |
13 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-1785G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88242701 | |||||||
chr5:88242886 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4-1970G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88242886 | |||||||
chr5:88242901 | T | C | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-1985A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88242901 | |||||||
chr5:88243090 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4-2174A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88243090 | |||||||
chr5:88243132 | T | C | 136 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(133): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.4-2216A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88243132 | |||||||
chr5:88243214 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4-2298A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88243214 | |||||||
chr5:88243275 | G | T | 135 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(132): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.4-2359C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88243275 | |||||||
chr5:88243332 | C | G | 1 | a0001c0001t0005g0185 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4-2416G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88243332 | |||||||
chr5:88243481 | T | C | 4 | a0001c0002t0001g0013 a0001c0002t0001g0067 a0001c0002t0001g0068 others(1): Show |
5 | HG01168.hp1 HG01169.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-2565A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88243481 | |||||||
chr5:88243666 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4-2750C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88243666 | |||||||
chr5:88243927 | C | CT | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-3012dupA | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88243927 | |||||||
chr5:88243961 | C | G | 1 | a0001c0002t0001g0047 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4-3045G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88243961 | |||||||
chr5:88243985 | T | G | 2 | a0001c0001t0003g0139 a0001c0001t0003g0140 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4-3069A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88243985 | |||||||
chr5:88243994 | G | C | 3 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0096 |
3 | HG01981.hp2 HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.4-3078C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88243994 | |||||||
chr5:88244131 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4-3215T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88244131 | |||||||
chr5:88244376 | A | G | 1 | a0001c0002t0001g0043 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.4-3460T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88244376 | |||||||
chr5:88244393 | T | C | 149 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(146): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.4-3477A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88244393 | |||||||
chr5:88244520 | C | T | 5 | a0001c0002t0001g0010 a0001c0002t0001g0043 a0001c0002t0001g0045 others(2): Show |
6 | HG00738.hp1 HG01928.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-3604G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88244520 | |||||||
chr5:88244584 | C | CT | 63 | a0001c0001t0002g0112 a0001c0001t0002g0133 a0001c0001t0002g0193 others(60): Show |
65 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.4-3669dupA | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88244584 | |||||||
chr5:88244609 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4-3693C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88244609 | |||||||
chr5:88244752 | T | A | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-3836A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88244752 | |||||||
chr5:88244764 | C | T | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-3848G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88244764 | |||||||
chr5:88244805 | T | C | 5 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG00597.hp2 HG02027.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-3889A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88244805 | |||||||
chr5:88244890 | T | C | 193 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(190): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.4-3974A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88244890 | |||||||
chr5:88244989 | T | G | 197 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(194): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.4-4073A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88244989 | |||||||
chr5:88245064 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4-4148A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88245064 | |||||||
chr5:88245199 | A | G | 1 | a0001c0001t0005g0185 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4-4283T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88245199 | |||||||
chr5:88245486 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4-4570G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88245486 | |||||||
chr5:88245531 | C | T | 1 | a0001c0002t0001g0040 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.4-4615G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88245531 | |||||||
chr5:88245591 | A | G | 1 | a0003c0004t0003g0127 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4-4675T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88245591 | |||||||
chr5:88245599 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4-4683A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88245599 | |||||||
chr5:88245670 | T | G | 38 | a0001c0001t0005g0234 a0001c0002t0001g0008 a0001c0002t0001g0238 others(35): Show |
48 | HG01070.hp2 HG01358.hp2 HG01928.hp2 others(45): Show |
intron_variant | MODIFIER | c.4-4754A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88245670 | |||||||
chr5:88245828 | A | G | 1 | a0001c0002t0001g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4-4912T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88245828 | |||||||
chr5:88246065 | T | A | 136 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(133): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.4-5149A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88246065 | |||||||
chr5:88246282 | G | GA | 5 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0003g0014 others(2): Show |
6 | HG00639.hp2 HG00642.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-5367dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88246282 | |||||||
chr5:88246522 | T | C | 1 | a0001c0002t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4-5606A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88246522 | |||||||
chr5:88246536 | G | A | 1 | a0001c0001t0003g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4-5620C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88246536 | |||||||
chr5:88247302 | G | A | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG01175.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.4-6386C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88247302 | |||||||
chr5:88247475 | A | C | 1 | a0001c0001t0003g0098 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4-6559T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88247475 | |||||||
chr5:88247486 | T | C | 136 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(133): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.4-6570A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88247486 | |||||||
chr5:88247690 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4-6774G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88247690 | |||||||
chr5:88247700 | A | G | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.4-6784T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88247700 | |||||||
chr5:88247755 | A | C | 38 | a0001c0001t0005g0234 a0001c0002t0001g0008 a0001c0002t0001g0238 others(35): Show |
48 | HG01070.hp2 HG01358.hp2 HG01928.hp2 others(45): Show |
intron_variant | MODIFIER | c.4-6839T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88247755 | |||||||
chr5:88247811 | A | G | 2 | a0001c0001t0005g0167 a0001c0001t0005g0168 |
2 | HG00408.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.4-6895T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88247811 | |||||||
chr5:88247888 | C | T | 3 | a0002c0003t0002g0023 a0002c0003t0002g0216 a0002c0003t0002g0239 |
4 | NA18965.hp2 NA18994.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.4-6972G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88247888 | |||||||
chr5:88248045 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4-7129A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248045 | |||||||
chr5:88248283 | G | A | 1 | a0001c0001t0004g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4-7367C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248283 | |||||||
chr5:88248289 | T | C | 3 | a0001c0001t0004g0006 a0001c0001t0004g0151 a0001c0001t0004g0152 |
5 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-7373A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248289 | |||||||
chr5:88248327 | C | T | 37 | a0001c0001t0005g0234 a0001c0002t0001g0008 a0001c0002t0001g0238 others(34): Show |
47 | HG01070.hp2 HG01358.hp2 HG01928.hp2 others(44): Show |
intron_variant | MODIFIER | c.4-7411G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248327 | |||||||
chr5:88248396 | A | G | 136 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(133): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.4-7480T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248396 | |||||||
chr5:88248486 | A | G | 5 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0190 others(2): Show |
5 | HG00642.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-7570T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248486 | |||||||
chr5:88248554 | G | C | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-7638C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248554 | |||||||
chr5:88248714 | G | GA | 8 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0003g0162 others(5): Show |
8 | HG02738.hp1 HG03017.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-7799dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248714 | |||||||
chr5:88248714 | GA | G | 138 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0037 others(135): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.4-7799delT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248714 | |||||||
chr5:88248732 | C | A | 1 | a0001c0001t0002g0197 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4-7816G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248732 | |||||||
chr5:88248874 | CTG | C | 4 | a0001c0001t0002g0154 a0001c0001t0002g0196 a0001c0001t0002g0197 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-7960_4-7959delCA | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248874 | |||||||
chr5:88248937 | T | C | 1 | a0002c0003t0002g0235 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4-8021A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88248937 | |||||||
chr5:88249031 | A | C | 1 | a0002c0003t0002g0239 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.4-8115T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88249031 | |||||||
chr5:88249057 | C | T | 1 | a0001c0001t0004g0016 | 2 | HG01074.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.4-8141G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88249057 | |||||||
chr5:88249227 | T | C | 4 | a0001c0002t0001g0005 a0001c0002t0001g0024 a0001c0002t0001g0070 others(1): Show |
6 | HG00140.hp1 HG01123.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-8311A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88249227 | |||||||
chr5:88249373 | T | A | 1 | a0001c0002t0001g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4-8457A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88249373 | |||||||
chr5:88249501 | C | T | 76 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0037 others(73): Show |
91 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.4-8585G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88249501 | |||||||
chr5:88249502 | T | A | 7 | a0001c0001t0002g0133 a0001c0001t0003g0015 a0001c0001t0003g0134 others(4): Show |
8 | HG01496.hp1 HG01884.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-8586A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88249502 | |||||||
chr5:88249502 | T | G | 150 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0033 others(147): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.4-8586A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88249502 | |||||||
chr5:88249934 | A | G | 2 | a0001c0001t0004g0019 a0001c0001t0004g0204 |
3 | HG02723.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4-9018T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88249934 | |||||||
chr5:88250166 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4-9250A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88250166 | |||||||
chr5:88250173 | GAGAGAGA others(3): Show |
G | 1 | a0001c0001t0004g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4-9267_4-9258delTT others(8): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88250173 | |||||||
chr5:88250193 | A | AAG | 3 | a0001c0001t0002g0202 a0001c0001t0004g0019 a0001c0001t0004g0204 |
4 | HG02723.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-9279_4-9278dupCT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88250193 | |||||||
chr5:88250377 | T | G | 3 | a0001c0001t0002g0155 a0001c0001t0004g0019 a0001c0001t0004g0204 |
4 | HG02615.hp2 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-9461A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88250377 | |||||||
chr5:88250829 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4-9913A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88250829 | |||||||
chr5:88250860 | G | A | 1 | a0002c0003t0002g0236 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4-9944C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88250860 | |||||||
chr5:88250962 | T | G | 2 | a0001c0001t0003g0091 a0001c0001t0003g0125 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4-10046A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88250962 | |||||||
chr5:88251009 | AGACTGAT others(7): Show |
A | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-10107_4-10094del others(14): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251009 | |||||||
chr5:88251062 | A | C | 3 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0205 |
3 | NA18992.hp1 NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.4-10146T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251062 | |||||||
chr5:88251101 | CA | C | 7 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(4): Show |
8 | HG01074.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-10186delT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251101 | |||||||
chr5:88251225 | T | C | 1 | a0001c0001t0003g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4-10309A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251225 | |||||||
chr5:88251256 | A | G | 2 | a0001c0001t0005g0185 a0001c0001t0005g0186 |
2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.4-10340T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251256 | |||||||
chr5:88251306 | G | A | 195 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0033 others(192): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.4-10390C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251306 | |||||||
chr5:88251365 | A | G | 1 | a0001c0002t0001g0077 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4-10449T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251365 | |||||||
chr5:88251449 | T | A | 1 | a0002c0003t0002g0239 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.4-10533A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251449 | |||||||
chr5:88251552 | G | A | 3 | a0001c0001t0002g0075 a0001c0002t0001g0073 a0001c0002t0001g0074 |
3 | HG00558.hp1 HG02132.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4-10636C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251552 | |||||||
chr5:88251610 | TG | T | 243 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0009 others(240): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.4-10695delC | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251610 | |||||||
chr5:88251625 | T | C | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 |
3 | HG01884.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4-10709A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251625 | |||||||
chr5:88251742 | T | C | 196 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0033 others(193): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.4-10826A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251742 | |||||||
chr5:88251745 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4-10829G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251745 | |||||||
chr5:88251885 | T | C | 1 | a0003c0004t0003g0127 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4-10969A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88251885 | |||||||
chr5:88252099 | A | G | 11 | a0001c0001t0002g0154 a0001c0001t0002g0196 a0001c0001t0002g0197 others(8): Show |
13 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.4-11183T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88252099 | |||||||
chr5:88252175 | G | A | 1 | a0001c0001t0003g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4-11259C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88252175 | |||||||
chr5:88252601 | G | T | 1 | a0001c0001t0002g0197 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4-11685C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88252601 | |||||||
chr5:88252664 | T | C | 1 | a0002c0003t0002g0237 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4-11748A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88252664 | |||||||
chr5:88252778 | T | C | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-11862A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88252778 | |||||||
chr5:88253037 | GA | G | 5 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0190 others(2): Show |
5 | HG00642.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-12122delT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88253037 | |||||||
chr5:88253048 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4-12132G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88253048 | |||||||
chr5:88253323 | A | G | 2 | a0001c0001t0004g0016 a0001c0001t0004g0157 |
3 | HG01074.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.4-12407T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88253323 | |||||||
chr5:88253337 | A | C | 1 | a0001c0001t0003g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4-12421T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88253337 | |||||||
chr5:88253489 | A | C | 1 | a0001c0002t0001g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4-12573T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88253489 | |||||||
chr5:88253893 | A | G | 195 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0033 others(192): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.4-12977T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88253893 | |||||||
chr5:88254157 | C | T | 37 | a0001c0001t0005g0234 a0001c0002t0001g0008 a0001c0002t0001g0238 others(34): Show |
47 | HG01070.hp2 HG01358.hp2 HG01928.hp2 others(44): Show |
intron_variant | MODIFIER | c.4-13241G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88254157 | |||||||
chr5:88254278 | C | G | 243 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0009 others(240): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.4-13362G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88254278 | |||||||
chr5:88254332 | G | T | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 |
3 | HG01884.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4-13416C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88254332 | |||||||
chr5:88254396 | G | T | 2 | a0001c0002t0001g0001 a0001c0002t0001g0035 |
6 | HG02523.hp2 NA18945.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-13480C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88254396 | |||||||
chr5:88254467 | A | T | 138 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0033 others(135): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.4-13551T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88254467 | |||||||
chr5:88254615 | T | G | 2 | a0001c0001t0002g0163 a0001c0001t0002g0164 |
2 | NA18974.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.4-13699A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88254615 | |||||||
chr5:88254678 | G | A | 198 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0033 others(195): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.4-13762C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88254678 | |||||||
chr5:88254860 | A | G | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+13861T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88254860 | |||||||
chr5:88254913 | G | C | 1 | a0001c0002t0001g0076 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3+13808C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88254913 | |||||||
chr5:88254963 | C | A | 1 | a0001c0002t0001g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3+13758G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88254963 | |||||||
chr5:88255102 | C | T | 9 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(6): Show |
9 | HG00597.hp2 HG01168.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.3+13619G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88255102 | |||||||
chr5:88255181 | A | G | 1 | a0001c0001t0004g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3+13540T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88255181 | |||||||
chr5:88255254 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG01175.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.3+13467T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88255254 | |||||||
chr5:88255451 | C | T | 38 | a0001c0001t0004g0022 a0001c0001t0005g0234 a0001c0002t0001g0008 others(35): Show |
49 | HG01070.hp2 HG01109.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.3+13270G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88255451 | |||||||
chr5:88255522 | A | C | 1 | a0001c0002t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3+13199T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88255522 | |||||||
chr5:88255548 | G | A | 1 | a0001c0002t0001g0238 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3+13173C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88255548 | |||||||
chr5:88255914 | T | C | 3 | a0001c0001t0003g0129 a0001c0001t0003g0130 a0001c0001t0003g0131 |
3 | HG01123.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3+12807A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88255914 | |||||||
chr5:88256030 | G | A | 1 | a0001c0001t0005g0244 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3+12691C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88256030 | |||||||
chr5:88256089 | C | T | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3+12632G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88256089 | |||||||
chr5:88256401 | T | A | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3+12320A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88256401 | |||||||
chr5:88256533 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3+12188A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88256533 | |||||||
chr5:88256555 | T | C | 1 | a0001c0001t0003g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3+12166A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88256555 | |||||||
chr5:88256581 | C | T | 4 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(1): Show |
4 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+12140G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88256581 | |||||||
chr5:88256596 | G | A | 11 | a0001c0001t0002g0154 a0001c0001t0002g0196 a0001c0001t0002g0197 others(8): Show |
13 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3+12125C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88256596 | |||||||
chr5:88256675 | T | C | 138 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0033 others(135): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.3+12046A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88256675 | |||||||
chr5:88256682 | C | A | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3+12039G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88256682 | |||||||
chr5:88256883 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3+11838C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88256883 | |||||||
chr5:88257015 | C | T | 1 | a0001c0002t0001g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3+11706G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88257015 | |||||||
chr5:88257143 | C | A | 1 | a0001c0001t0002g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3+11578G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88257143 | |||||||
chr5:88257306 | T | C | 1 | a0001c0002t0001g0199 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3+11415A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88257306 | |||||||
chr5:88257477 | T | C | 7 | a0001c0001t0002g0133 a0001c0001t0003g0015 a0001c0001t0003g0134 others(4): Show |
8 | HG01496.hp1 HG01884.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3+11244A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88257477 | |||||||
chr5:88257495 | T | G | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3+11226A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88257495 | |||||||
chr5:88257928 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3+10793A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88257928 | |||||||
chr5:88257940 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3+10781G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88257940 | |||||||
chr5:88258094 | T | C | 3 | a0001c0001t0005g0185 a0001c0001t0005g0186 a0001c0002t0001g0187 |
3 | HG01261.hp1 HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.3+10627A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88258094 | |||||||
chr5:88258282 | G | A | 1 | a0002c0003t0002g0213 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3+10439C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88258282 | |||||||
chr5:88258289 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3+10432A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88258289 | |||||||
chr5:88258316 | G | A | 5 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0190 others(2): Show |
5 | HG00642.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+10405C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88258316 | |||||||
chr5:88258416 | G | A | 3 | a0001c0001t0002g0009 a0001c0001t0002g0193 a0001c0001t0002g0194 |
5 | HG00639.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+10305C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88258416 | |||||||
chr5:88258871 | A | C | 1 | a0001c0001t0003g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3+9850T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88258871 | |||||||
chr5:88258909 | C | G | 3 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0096 |
3 | HG01981.hp2 HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3+9812G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88258909 | |||||||
chr5:88258952 | C | T | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+9769G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88258952 | |||||||
chr5:88259285 | T | G | 1 | a0001c0002t0001g0012 | 2 | NA18939.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.3+9436A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88259285 | |||||||
chr5:88259477 | G | A | 138 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0033 others(135): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.3+9244C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88259477 | |||||||
chr5:88259516 | C | T | 2 | a0001c0002t0001g0027 a0001c0002t0001g0028 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.3+9205G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88259516 | |||||||
chr5:88259575 | C | T | 5 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0030 others(2): Show |
5 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+9146G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88259575 | |||||||
chr5:88259653 | T | C | 1 | a0001c0001t0003g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3+9068A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88259653 | |||||||
chr5:88260191 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3+8530G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88260191 | |||||||
chr5:88260450 | T | C | 38 | a0001c0001t0004g0022 a0001c0001t0005g0234 a0001c0002t0001g0008 others(35): Show |
49 | HG01070.hp2 HG01109.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.3+8271A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88260450 | |||||||
chr5:88260522 | A | G | 151 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0033 others(148): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.3+8199T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88260522 | |||||||
chr5:88260535 | T | G | 1 | a0001c0002t0001g0077 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3+8186A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88260535 | |||||||
chr5:88260574 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3+8147G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88260574 | |||||||
chr5:88260609 | G | A | 2 | a0002c0003t0002g0023 a0002c0003t0002g0239 |
3 | NA18965.hp2 NA19010.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3+8112C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88260609 | |||||||
chr5:88260642 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3+8079C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88260642 | |||||||
chr5:88260759 | T | C | 38 | a0001c0001t0004g0022 a0001c0001t0005g0234 a0001c0002t0001g0008 others(35): Show |
49 | HG01070.hp2 HG01109.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.3+7962A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88260759 | |||||||
chr5:88260939 | G | A | 2 | a0001c0001t0003g0139 a0001c0001t0003g0140 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3+7782C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88260939 | |||||||
chr5:88261055 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3+7666C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88261055 | |||||||
chr5:88261242 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3+7479G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88261242 | |||||||
chr5:88261390 | A | G | 76 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0037 others(73): Show |
91 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.3+7331T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88261390 | |||||||
chr5:88261597 | A | C | 1 | a0001c0002t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3+7124T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88261597 | |||||||
chr5:88261726 | T | C | 1 | a0001c0002t0001g0149 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3+6995A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88261726 | |||||||
chr5:88261730 | C | CA | 91 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0037 others(88): Show |
107 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.3+6990dupT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88261730 | |||||||
chr5:88261730 | C | CAA | 10 | a0001c0001t0002g0153 a0001c0001t0002g0200 a0001c0001t0002g0201 others(7): Show |
11 | HG01168.hp1 HG01169.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3+6989_3+6990dupTT | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88261730 | |||||||
chr5:88262176 | ATCATG | A | 5 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0004g0006 others(2): Show |
7 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3+6540_3+6544delCA others(3): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88262176 | |||||||
chr5:88262228 | T | C | 4 | a0001c0002t0006g0083 a0001c0002t0006g0084 a0001c0002t0006g0085 others(1): Show |
4 | HG02040.hp1 HG03831.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+6493A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88262228 | |||||||
chr5:88262310 | T | G | 1 | a0001c0002t0001g0087 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3+6411A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88262310 | |||||||
chr5:88262424 | C | A | 3 | a0001c0001t0002g0155 a0001c0001t0004g0019 a0001c0001t0004g0204 |
4 | HG02615.hp2 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+6297G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88262424 | |||||||
chr5:88262480 | C | T | 1 | a0002c0003t0002g0215 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3+6241G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88262480 | |||||||
chr5:88262884 | A | T | 1 | a0001c0002t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3+5837T>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88262884 | |||||||
chr5:88263714 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3+5007A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88263714 | |||||||
chr5:88263919 | G | T | 1 | a0001c0001t0003g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3+4802C>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88263919 | |||||||
chr5:88264177 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3+4544G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88264177 | |||||||
chr5:88264217 | C | T | 61 | a0001c0001t0001g0122 a0001c0001t0002g0112 a0001c0001t0002g0133 others(58): Show |
63 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.3+4504G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88264217 | |||||||
chr5:88264230 | C | G | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+4491G>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88264230 | |||||||
chr5:88264460 | T | C | 5 | a0001c0001t0003g0143 a0001c0001t0003g0144 a0001c0001t0003g0145 others(2): Show |
5 | HG01346.hp2 HG01496.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+4261A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88264460 | |||||||
chr5:88264466 | C | T | 1 | a0001c0001t0003g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+4255G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88264466 | |||||||
chr5:88264778 | T | G | 1 | a0001c0002t0001g0088 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3+3943A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88264778 | |||||||
chr5:88264941 | G | A | 1 | a0001c0002t0001g0205 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3+3780C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88264941 | |||||||
chr5:88264979 | T | C | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3+3742A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88264979 | |||||||
chr5:88265141 | C | T | 2 | a0001c0001t0005g0244 a0001c0002t0001g0156 |
2 | HG01258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3+3580G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88265141 | |||||||
chr5:88265372 | G | C | 1 | a0001c0002t0001g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3+3349C>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88265372 | |||||||
chr5:88265481 | C | A | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+3240G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88265481 | |||||||
chr5:88265728 | C | T | 38 | a0001c0001t0004g0022 a0001c0001t0005g0234 a0001c0002t0001g0008 others(35): Show |
49 | HG01070.hp2 HG01109.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.3+2993G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88265728 | |||||||
chr5:88265736 | C | T | 1 | a0002c0003t0002g0214 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3+2985G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88265736 | |||||||
chr5:88265839 | T | G | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+2882A>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88265839 | |||||||
chr5:88265948 | T | C | 61 | a0001c0001t0001g0122 a0001c0001t0002g0112 a0001c0001t0002g0133 others(58): Show |
63 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.3+2773A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88265948 | |||||||
chr5:88266172 | T | C | 1 | a0001c0002t0001g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3+2549A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88266172 | |||||||
chr5:88266194 | T | C | 1 | a0001c0002t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3+2527A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88266194 | |||||||
chr5:88266372 | G | A | 1 | a0001c0001t0005g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3+2349C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88266372 | |||||||
chr5:88266518 | A | C | 1 | a0001c0001t0002g0155 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3+2203T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88266518 | |||||||
chr5:88266793 | T | C | 1 | a0001c0002t0001g0212 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3+1928A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88266793 | |||||||
chr5:88266903 | A | G | 1 | a0002c0003t0002g0213 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3+1818T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88266903 | |||||||
chr5:88266924 | A | G | 1 | a0001c0002t0001g0024 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3+1797T>C | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88266924 | |||||||
chr5:88266968 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3+1753C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88266968 | |||||||
chr5:88267495 | T | C | 1 | a0001c0002t0001g0149 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3+1226A>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88267495 | |||||||
chr5:88267571 | T | A | 138 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0033 others(135): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.3+1150A>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88267571 | |||||||
chr5:88267827 | ACCTGTC | A | 38 | a0001c0001t0004g0022 a0001c0001t0005g0234 a0001c0002t0001g0008 others(35): Show |
49 | HG01070.hp2 HG01109.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.3+888_3+893delGACA others(2): Show |
TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88267827 | |||||||
chr5:88267923 | A | C | 1 | a0001c0001t0002g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3+798T>G | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88267923 | |||||||
chr5:88268002 | C | T | 4 | a0001c0001t0002g0153 a0001c0001t0004g0006 a0001c0001t0004g0151 others(1): Show |
6 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+719G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88268002 | |||||||
chr5:88268068 | C | A | 1 | a0001c0002t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3+653G>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88268068 | |||||||
chr5:88268106 | C | T | 138 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0002g0033 others(135): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.3+615G>A | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88268106 | |||||||
chr5:88268319 | G | A | 1 | a0001c0001t0005g0244 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3+402C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88268319 | |||||||
chr5:88268353 | G | A | 1 | a0001c0001t0002g0009 | 3 | HG00639.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3+368C>T | TMEM161B | ENSG00000164180.14 | transcript | ENST00000296595.11 | protein_coding | 1/11 | chr5 | 88268353 |