Item | Value |
---|---|
geneid | 202018 |
ensemblid | ENSG00000169762.17 |
hgncid | 26887 |
symbol | TAPT1 |
name | transmembrane anterior posterior transformation 1 |
refseq_nuc | NM_153365.3 |
refseq_prot | NP_699196.2 |
ensembl_nuc | ENST00000405303.7 |
ensembl_prot | ENSP00000385347.2 |
mane_status | MANE Select |
chr | chr4 |
start | 16160505 |
end | 16226471 |
strand | - |
ver | v1.2 |
region | chr4:16160505-16226471 |
region5000 | chr4:16155505-16231471 |
regionname0 | TAPT1_chr4_16160505_16226471 |
regionname5000 | TAPT1_chr4_16155505_16231471 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 567 | 368 | 81 | 59 | 170 | 9 | 47 | 132 | TAPT1_chr4_16155505_16231471 | TAPT1 | MAGVG others(562): Show |
chr4 | 16155505 | 16231471 |
a0002 | 0/0 | 567 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | MAGVG others(562): Show |
chr4 | 16155505 | 16231471 |
a0003 | 0/0 | 567 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | MAGVG others(562): Show |
chr4 | 16155505 | 16231471 |
a0004 | 0/0 | 567 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | MAGVG others(562): Show |
chr4 | 16155505 | 16231471 |
a0005 | 0/0 | 567 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | MAGVG others(562): Show |
chr4 | 16155505 | 16231471 |
a0006 | 0/0 | 567 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | MAGVG others(562): Show |
chr4 | 16155505 | 16231471 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1701 | 311 | 38 | 58 | 159 | 9 | 45 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 | ||
a0001c0002 | 0/0 | 1701 | 37 | 27 | 1 | 9 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 | ||
a0001c0003 | 0/0 | 1701 | 15 | 15 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 | ||
a0001c0007 | 0/0 | 1701 | 2 | 0 | 0 | 0 | 0 | 2 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 | ||
a0001c0009 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 | ||
a0001c0010 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 | ||
a0001c0011 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 | ||
a0002c0004 | 0/0 | 1701 | 5 | 5 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 | ||
a0003c0005 | 0/0 | 1701 | 4 | 4 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 | ||
a0004c0006 | 0/0 | 1701 | 3 | 2 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 | ||
a0005c0012 | 0/0 | 1701 | 1 | 0 | 0 | 0 | 1 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 | ||
a0006c0008 | 0/0 | 1701 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | ATGGC others(1696): Show |
chr4 | 16155505 | 16231471 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4522 | 76 | 1 | 14 | 52 | 2 | 7 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4517): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0002 | 1/0 | 4521 | 72 | 0 | 16 | 47 | 3 | 5 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4516): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0003 | 0/1 | 4524 | 68 | 5 | 5 | 45 | 2 | 10 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0004 | 0/0 | 4521 | 32 | 19 | 5 | 2 | 1 | 5 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4516): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0005 | 0/0 | 4524 | 14 | 2 | 7 | 0 | 0 | 5 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0007 | 0/0 | 4523 | 20 | 3 | 6 | 1 | 0 | 10 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4518): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0009 | 0/0 | 4520 | 13 | 7 | 1 | 4 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4515): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0012 | 0/0 | 4520 | 2 | 0 | 2 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4515): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0013 | 0/0 | 4524 | 2 | 0 | 0 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0014 | 0/0 | 4521 | 2 | 0 | 2 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4516): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0016 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0017 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0018 | 0/0 | 4522 | 1 | 0 | 0 | 0 | 1 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4517): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0019 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4517): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0020 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4517): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0021 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4517): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0022 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4517): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0024 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4517): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0025 | 0/0 | 4521 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4516): Show |
chr4 | 16155505 | 16231471 |
a0001c0001t0026 | 0/0 | 4521 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4516): Show |
chr4 | 16155505 | 16231471 |
a0001c0002t0005 | 0/0 | 4524 | 14 | 13 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0002t0006 | 0/0 | 4524 | 20 | 11 | 0 | 9 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0002t0010 | 0/0 | 4524 | 3 | 3 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0003t0008 | 0/0 | 4524 | 14 | 14 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0003t0023 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0007t0005 | 0/0 | 4524 | 2 | 0 | 0 | 0 | 0 | 2 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0009t0006 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0010t0005 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0001c0011t0003 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0002c0004t0004 | 0/0 | 4521 | 5 | 5 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4516): Show |
chr4 | 16155505 | 16231471 |
a0003c0005t0005 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0003c0005t0011 | 0/0 | 4524 | 3 | 3 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0004c0006t0015 | 0/0 | 4524 | 2 | 1 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0004c0006t0027 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
a0005c0012t0007 | 0/0 | 4523 | 1 | 0 | 0 | 0 | 1 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4518): Show |
chr4 | 16155505 | 16231471 |
a0006c0008t0003 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | GTTGT others(4519): Show |
chr4 | 16155505 | 16231471 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0001 | 1/0 | 13 | 0 | 10 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0010 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0004 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0016 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0017 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0009 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0005g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0005g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0014 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0009g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0009g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0009g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0009g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0009g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0012g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0012g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0013g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0013g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0014g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0016g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0017g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0018g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0019g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0020g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0021g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0022g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0024g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0025g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0001t0026g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0006g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0002t0010g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0003t0008g0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0003t0008g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0003t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0003t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0003t0023g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0007t0005g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0009t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0010t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0001c0011t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0002c0004t0004g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0002c0004t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0002c0004t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0003c0005t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0003c0005t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0003c0005t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0003c0005t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0004c0006t0015g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0004c0006t0015g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0004c0006t0027g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0005c0012t0007g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
a0006c0008t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0053 | EUR | GBR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00099 | hp2 | a0001 | c0001 | t0018 | g0283 | EUR | GBR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0017 | EUR | GBR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00323 | hp1 | a0005 | c0012 | t0007 | g0070 | EUR | FIN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | FIN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | CHS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | CHS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | CHS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | CHS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0133 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0134 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0136 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01074 | hp1 | a0001 | c0001 | t0007 | g0079 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01081 | hp1 | a0001 | c0001 | t0007 | g0014 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0175 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01099 | hp2 | a0001 | c0001 | t0012 | g0064 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01106 | hp1 | a0001 | c0001 | t0012 | g0063 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01109 | hp2 | a0004 | c0006 | t0015 | g0141 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01167 | hp2 | a0001 | c0001 | t0007 | g0024 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01169 | hp1 | a0001 | c0001 | t0007 | g0081 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01243 | hp1 | a0001 | c0002 | t0005 | g0067 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01258 | hp2 | a0001 | c0001 | t0014 | g0043 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01346 | hp1 | a0001 | c0001 | t0007 | g0075 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01358 | hp2 | a0001 | c0001 | t0007 | g0024 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0178 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01496 | hp1 | a0001 | c0001 | t0014 | g0043 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0211 | EUR | IBS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01884 | hp1 | a0001 | c0002 | t0005 | g0160 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01884 | hp2 | a0003 | c0005 | t0011 | g0049 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG01993 | hp2 | a0001 | c0001 | t0009 | g0022 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02015 | hp1 | a0001 | c0001 | t0013 | g0123 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02015 | hp2 | a0001 | c0002 | t0006 | g0147 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02056 | hp1 | a0001 | c0001 | t0013 | g0122 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02071 | hp2 | a0001 | c0001 | t0025 | g0195 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02083 | hp1 | a0001 | c0001 | t0024 | g0264 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02145 | hp2 | a0001 | c0002 | t0006 | g0272 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | CDX | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CDX | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CDX | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02257 | hp1 | a0001 | c0003 | t0008 | g0005 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02257 | hp2 | a0001 | c0002 | t0005 | g0153 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02258 | hp1 | a0004 | c0006 | t0015 | g0165 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02280 | hp1 | a0001 | c0003 | t0008 | g0031 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0029 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02451 | hp2 | a0001 | c0002 | t0005 | g0156 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02523 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | KHV | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02572 | hp1 | a0001 | c0002 | t0005 | g0157 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02572 | hp2 | a0001 | c0002 | t0005 | g0086 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02602 | hp2 | a0001 | c0001 | t0007 | g0083 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0066 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02615 | hp2 | a0002 | c0004 | t0004 | g0020 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02622 | hp1 | a0001 | c0002 | t0005 | g0154 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02630 | hp1 | a0001 | c0002 | t0005 | g0163 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02630 | hp2 | a0002 | c0004 | t0004 | g0183 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02647 | hp1 | a0001 | c0003 | t0008 | g0003 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0188 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02683 | hp2 | a0001 | c0001 | t0007 | g0082 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02698 | hp2 | a0001 | c0001 | t0007 | g0014 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0041 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02723 | hp1 | a0001 | c0002 | t0006 | g0143 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02723 | hp2 | a0001 | c0003 | t0008 | g0005 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0127 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02809 | hp1 | a0002 | c0004 | t0004 | g0020 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02809 | hp2 | a0001 | c0002 | t0006 | g0275 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0071 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0125 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0041 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02895 | hp1 | a0001 | c0002 | t0006 | g0013 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02896 | hp1 | a0001 | c0002 | t0006 | g0013 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02896 | hp2 | a0001 | c0003 | t0008 | g0005 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02897 | hp1 | a0001 | c0002 | t0006 | g0013 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02897 | hp2 | a0001 | c0003 | t0008 | g0005 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02922 | hp2 | a0003 | c0005 | t0011 | g0052 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02970 | hp1 | a0001 | c0002 | t0005 | g0068 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02970 | hp2 | a0001 | c0002 | t0006 | g0047 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02976 | hp1 | a0001 | c0003 | t0008 | g0005 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03041 | hp2 | a0001 | c0003 | t0008 | g0003 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03098 | hp1 | a0001 | c0002 | t0005 | g0159 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0167 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03130 | hp1 | a0001 | c0002 | t0005 | g0155 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03130 | hp2 | a0001 | c0003 | t0008 | g0003 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03139 | hp1 | a0001 | c0002 | t0006 | g0047 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03139 | hp2 | a0001 | c0003 | t0008 | g0003 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03195 | hp1 | a0001 | c0003 | t0008 | g0003 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03195 | hp2 | a0001 | c0010 | t0005 | g0054 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03209 | hp1 | a0001 | c0003 | t0008 | g0003 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03209 | hp2 | a0001 | c0002 | t0005 | g0085 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03225 | hp1 | a0003 | c0005 | t0005 | g0051 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03225 | hp2 | a0002 | c0004 | t0004 | g0020 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0078 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03453 | hp1 | a0001 | c0003 | t0008 | g0139 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0193 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0126 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03490 | hp2 | a0001 | c0007 | t0005 | g0030 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03491 | hp2 | a0001 | c0001 | t0007 | g0023 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0023 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03492 | hp2 | a0001 | c0007 | t0005 | g0030 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03516 | hp1 | a0003 | c0005 | t0011 | g0050 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03516 | hp2 | a0001 | c0002 | t0010 | g0144 | AFR | ESN | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03540 | hp2 | a0001 | c0003 | t0023 | g0140 | AFR | GWD | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03579 | hp1 | a0002 | c0004 | t0004 | g0185 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0059 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0132 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03669 | hp2 | a0001 | c0001 | t0007 | g0072 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03688 | hp1 | a0006 | c0008 | t0003 | g0048 | SAS | STU | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0131 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0174 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03710 | hp2 | a0001 | c0001 | t0007 | g0080 | SAS | PJL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03831 | hp1 | a0001 | c0001 | t0007 | g0073 | SAS | BEB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0130 | SAS | BEB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | BEB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | BEB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0103 | SAS | BEB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | BEB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0107 | SAS | STU | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG04184 | hp1 | a0001 | c0001 | t0017 | g0135 | SAS | BEB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG04199 | hp2 | a0001 | c0001 | t0009 | g0065 | SAS | STU | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | STU | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | STU | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG04228 | hp1 | a0001 | c0001 | t0026 | g0179 | SAS | STU | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | STU | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18522 | hp1 | a0001 | c0003 | t0008 | g0031 | AFR | YRI | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | YRI | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CHB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18906 | hp1 | a0001 | c0002 | t0010 | g0056 | AFR | YRI | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0074 | AFR | YRI | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18945 | hp2 | a0001 | c0001 | t0019 | g0220 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18948 | hp2 | a0001 | c0002 | t0006 | g0019 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18949 | hp2 | a0001 | c0001 | t0020 | g0248 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18962 | hp1 | a0001 | c0002 | t0006 | g0148 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18967 | hp1 | a0001 | c0001 | t0022 | g0269 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18970 | hp1 | a0001 | c0002 | t0006 | g0019 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18981 | hp1 | a0001 | c0001 | t0009 | g0062 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18984 | hp2 | a0001 | c0002 | t0006 | g0146 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18995 | hp2 | a0001 | c0001 | t0009 | g0057 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18997 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19005 | hp2 | a0001 | c0011 | t0003 | g0091 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19010 | hp1 | a0001 | c0009 | t0006 | g0149 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | LWK | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0164 | AFR | LWK | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0061 | AFR | LWK | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19043 | hp2 | a0004 | c0006 | t0027 | g0151 | AFR | LWK | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19064 | hp2 | a0001 | c0002 | t0006 | g0150 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19065 | hp1 | a0001 | c0001 | t0009 | g0022 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19066 | hp1 | a0001 | c0002 | t0006 | g0142 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19068 | hp2 | a0001 | c0001 | t0021 | g0255 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19070 | hp1 | a0001 | c0002 | t0006 | g0019 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19081 | hp2 | a0001 | c0001 | t0009 | g0058 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19085 | hp2 | a0001 | c0002 | t0006 | g0145 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | YRI | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | YRI | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA20129 | hp1 | a0001 | c0002 | t0006 | g0138 | AFR | ASW | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA20129 | hp2 | a0001 | c0002 | t0010 | g0055 | AFR | ASW | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0227 | EUR | TSI | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0192 | EUR | TSI | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0173 | SAS | GIH | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0077 | SAS | GIH | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02109 | hp2 | a0001 | c0001 | t0016 | g0076 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02559 | hp1 | a0001 | c0002 | t0005 | g0152 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03471 | hp1 | a0001 | c0002 | t0006 | g0158 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG03471 | hp2 | a0001 | c0002 | t0006 | g0013 | AFR | MSL | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | USA | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | USA | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA21309 | hp1 | a0001 | c0002 | t0005 | g0084 | AFR | LWK | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | LWK | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0089 | REF | REF | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | TAPT1_chr4_16155505_16231471 | TAPT1 | chr4 | 16155505 | 16231471 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:16163447 | T | C | 1 | a0005 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.1565A>G | p.Asn522Ser | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1579/4521 | 1565/1704 | 522/567 | chr4 | 16163447 | |||
chr4:16166714 | C | T | 1 | a0002 | 5 | HG02615.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
missense_variant | MODERATE | c.1393G>A | p.Glu465Lys | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/14 | 1407/4521 | 1393/1704 | 465/567 | chr4 | 16166714 | |||
chr4:16191477 | C | A | 1 | a0004 | 3 | HG01109.hp2 HG02258.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.496G>T | p.Gly166Cys | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/14 | 510/4521 | 496/1704 | 166/567 | chr4 | 16191477 | |||
chr4:16226321 | A | C | 1 | a0003 | 4 | HG01884.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.137T>G | p.Leu46Arg | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/14 | 151/4521 | 137/1704 | 46/567 | chr4 | 16226321 | |||
chr4:16226370 | C | T | 1 | a0006 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.88G>A | p.Glu30Lys | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/14 | 102/4521 | 88/1704 | 30/567 | chr4 | 16226370 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:16163413 | G | A | 1 | a0001c0007 | 2 | HG03490.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.1599C>T | p.Asp533Asp | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1613/4521 | 1599/1704 | 533/567 | chr4 | 16163413 | |||
chr4:16166670 | C | T | 1 | a0001c0010 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1437G>A | p.Pro479Pro | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/14 | 1451/4521 | 1437/1704 | 479/567 | chr4 | 16166670 | |||
chr4:16179632 | A | G | 1 | a0001c0009 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.942T>C | p.Tyr314Tyr | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/14 | 956/4521 | 942/1704 | 314/567 | chr4 | 16179632 | |||
chr4:16213774 | C | T | 1 | a0001c0011 | 1 | NA19005.hp2 | synonymous_variant | LOW | c.324G>A | p.Leu108Leu | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/14 | 338/4521 | 324/1704 | 108/567 | chr4 | 16213774 | |||
chr4:16213792 | C | T | 1 | a0001c0003 | 15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
synonymous_variant | LOW | c.306G>A | p.Leu102Leu | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/14 | 320/4521 | 306/1704 | 102/567 | chr4 | 16213792 | |||
chr4:16213828 | C | T | 5 | a0001c0002 a0001c0003 a0001c0009 others(2): Show |
57 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(54): Show |
synonymous_variant | LOW | c.270G>A | p.Lys90Lys | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/14 | 284/4521 | 270/1704 | 90/567 | chr4 | 16213828 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:16160595 | T | C | 1 | a0001c0003t0023 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2713A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 2713 | chr4 | 16160595 | ||||||
chr4:16160654 | T | C | 1 | a0001c0001t0020 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2654A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 2654 | chr4 | 16160654 | ||||||
chr4:16160851 | C | A | 23 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(20): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*2457G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 2457 | chr4 | 16160851 | ||||||
chr4:16161144 | T | C | 4 | a0001c0001t0009 a0001c0001t0012 a0001c0002t0010 others(1): Show |
21 | HG01099.hp2 HG01106.hp1 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2164A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 2164 | chr4 | 16161144 | ||||||
chr4:16161405 | C | A | 1 | a0001c0001t0021 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1903G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1903 | chr4 | 16161405 | ||||||
chr4:16161461 | T | C | 1 | a0001c0001t0013 | 2 | HG02015.hp1 HG02056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1847A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1847 | chr4 | 16161461 | ||||||
chr4:16161519 | T | G | 1 | a0004c0006t0015 | 2 | HG01109.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1789A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1789 | chr4 | 16161519 | ||||||
chr4:16161553 | G | A | 1 | a0004c0006t0027 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1755C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1755 | chr4 | 16161553 | ||||||
chr4:16161586 | T | C | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(27): Show |
269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*1722A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1722 | chr4 | 16161586 | ||||||
chr4:16161598 | T | C | 13 | a0001c0001t0005 a0001c0001t0016 a0001c0001t0017 others(10): Show |
73 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1710A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1710 | chr4 | 16161598 | ||||||
chr4:16161642 | C | G | 23 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(20): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1666G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1666 | chr4 | 16161642 | ||||||
chr4:16161708 | C | T | 1 | a0001c0001t0018 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1600G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1600 | chr4 | 16161708 | ||||||
chr4:16161863 | C | T | 21 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(18): Show |
165 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1445G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1445 | chr4 | 16161863 | ||||||
chr4:16161890 | A | C | 1 | a0001c0002t0010 | 3 | HG03516.hp2 NA18906.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1418T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1418 | chr4 | 16161890 | ||||||
chr4:16162057 | G | A | 1 | a0001c0001t0022 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1251C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1251 | chr4 | 16162057 | ||||||
chr4:16162071 | C | G | 31 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(28): Show |
270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*1237G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1237 | chr4 | 16162071 | ||||||
chr4:16162086 | C | A | 2 | a0001c0001t0009 a0001c0001t0012 |
15 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1222G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 1222 | chr4 | 16162086 | ||||||
chr4:16162343 | C | G | 1 | a0001c0001t0012 | 2 | HG01099.hp2 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*965G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 965 | chr4 | 16162343 | ||||||
chr4:16162565 | G | A | 1 | a0001c0001t0026 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*743C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 743 | chr4 | 16162565 | ||||||
chr4:16162570 | T | TTA | 23 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(20): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*737_*738insTA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 737 | chr4 | 16162570 | ||||||
chr4:16162596 | T | C | 1 | a0001c0001t0024 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*712A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 712 | chr4 | 16162596 | ||||||
chr4:16162607 | T | C | 4 | a0001c0001t0003 a0001c0001t0013 a0001c0011t0003 others(1): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*701A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 701 | chr4 | 16162607 | ||||||
chr4:16162665 | CTTCA | C | 2 | a0001c0001t0009 a0001c0001t0012 |
15 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*639_*642delTGAA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 639 | chr4 | 16162665 | ||||||
chr4:16162695 | T | C | 4 | a0001c0002t0006 a0001c0009t0006 a0004c0006t0015 others(1): Show |
24 | HG01109.hp2 HG02015.hp2 HG02145.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*613A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 613 | chr4 | 16162695 | ||||||
chr4:16162704 | A | AT | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(25): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*603dupA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 603 | chr4 | 16162704 | ||||||
chr4:16162829 | T | C | 1 | a0001c0001t0025 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*479A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 479 | chr4 | 16162829 | ||||||
chr4:16162830 | G | C | 3 | a0001c0001t0004 a0001c0001t0026 a0002c0004t0004 |
38 | HG01081.hp2 HG01192.hp1 HG01256.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*478C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 478 | chr4 | 16162830 | ||||||
chr4:16162866 | G | A | 13 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0016 others(10): Show |
79 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*442C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 442 | chr4 | 16162866 | ||||||
chr4:16163112 | C | T | 1 | a0001c0001t0017 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 196 | chr4 | 16163112 | ||||||
chr4:16163167 | A | C | 1 | a0001c0001t0016 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*141T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 141 | chr4 | 16163167 | ||||||
chr4:16163294 | A | G | 1 | a0001c0001t0016 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 14/14 | 14 | chr4 | 16163294 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:16163565 | G | A | 2 | a0001c0002t0010g0055 a0001c0002t0010g0056 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1475-28C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16163565 | |||||||
chr4:16163821 | C | T | 1 | a0001c0001t0016g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1475-284G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16163821 | |||||||
chr4:16163913 | C | T | 1 | a0001c0001t0009g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1475-376G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16163913 | |||||||
chr4:16163959 | C | T | 1 | a0001c0001t0003g0025 | 2 | HG02698.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1475-422G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16163959 | |||||||
chr4:16164028 | A | T | 70 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(67): Show |
94 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1475-491T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164028 | |||||||
chr4:16164411 | G | C | 3 | a0001c0002t0010g0055 a0001c0002t0010g0056 a0001c0002t0010g0144 |
3 | HG03516.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1475-874C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164411 | |||||||
chr4:16164435 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1475-898G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164435 | |||||||
chr4:16164473 | C | A | 1 | a0001c0001t0003g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1475-936G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164473 | |||||||
chr4:16164481 | A | C | 6 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0265 others(3): Show |
6 | HG00408.hp1 HG02165.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1475-944T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164481 | |||||||
chr4:16164512 | C | A | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1475-975G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164512 | |||||||
chr4:16164550 | T | C | 1 | a0001c0001t0003g0028 | 2 | NA19077.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1475-1013A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164550 | |||||||
chr4:16164583 | G | A | 13 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(10): Show |
17 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1475-1046C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164583 | |||||||
chr4:16164619 | A | G | 1 | a0001c0002t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1475-1082T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164619 | |||||||
chr4:16164630 | T | C | 1 | a0001c0002t0010g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1475-1093A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164630 | |||||||
chr4:16164711 | G | A | 1 | a0001c0001t0005g0132 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1475-1174C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164711 | |||||||
chr4:16164751 | T | C | 1 | a0001c0001t0005g0134 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1475-1214A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164751 | |||||||
chr4:16164781 | C | T | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(61): Show |
83 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1475-1244G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164781 | |||||||
chr4:16164897 | T | C | 1 | a0001c0001t0004g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1475-1360A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16164897 | |||||||
chr4:16165020 | C | T | 69 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(66): Show |
93 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1475-1483G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165020 | |||||||
chr4:16165116 | A | G | 3 | a0001c0002t0010g0055 a0001c0002t0010g0056 a0001c0002t0010g0144 |
3 | HG03516.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1474+1517T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165116 | |||||||
chr4:16165160 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1474+1473G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165160 | |||||||
chr4:16165308 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1474+1325A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165308 | |||||||
chr4:16165346 | G | A | 1 | a0001c0002t0010g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1474+1287C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165346 | |||||||
chr4:16165430 | C | T | 3 | a0001c0001t0005g0131 a0001c0001t0005g0132 a0001c0001t0017g0135 |
3 | HG03654.hp1 HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1474+1203G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165430 | |||||||
chr4:16165456 | G | T | 2 | a0001c0001t0003g0088 a0001c0001t0003g0110 |
2 | HG00597.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1474+1177C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165456 | |||||||
chr4:16165478 | G | A | 52 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(49): Show |
72 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.1474+1155C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165478 | |||||||
chr4:16165484 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1474+1149C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165484 | |||||||
chr4:16165542 | C | T | 5 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0121 others(2): Show |
7 | HG02015.hp1 HG02056.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1474+1091G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165542 | |||||||
chr4:16165544 | T | C | 1 | a0001c0001t0002g0232 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1474+1089A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165544 | |||||||
chr4:16165548 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1474+1085G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165548 | |||||||
chr4:16165565 | G | A | 2 | a0001c0001t0005g0029 a0001c0007t0005g0030 |
4 | HG02300.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1474+1068C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165565 | |||||||
chr4:16165569 | C | CA | 8 | a0001c0001t0001g0200 a0001c0001t0001g0263 a0001c0001t0001g0277 others(5): Show |
8 | HG01169.hp1 HG01978.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1474+1063dupT | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165569 | |||||||
chr4:16165569 | CA | C | 74 | a0001c0001t0001g0246 a0001c0001t0003g0002 a0001c0001t0003g0004 others(71): Show |
108 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1474+1063delT | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165569 | |||||||
chr4:16165643 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1474+990G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165643 | |||||||
chr4:16165847 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1474+786A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165847 | |||||||
chr4:16165859 | T | C | 16 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(13): Show |
20 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1474+774A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165859 | |||||||
chr4:16165937 | G | A | 1 | a0001c0001t0004g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1474+696C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16165937 | |||||||
chr4:16166032 | C | A | 2 | a0004c0006t0015g0141 a0004c0006t0015g0165 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1474+601G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166032 | |||||||
chr4:16166062 | C | T | 68 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(65): Show |
92 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1474+571G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166062 | |||||||
chr4:16166096 | T | G | 1 | a0001c0001t0009g0041 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1474+537A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166096 | |||||||
chr4:16166137 | G | A | 1 | a0001c0002t0010g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1474+496C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166137 | |||||||
chr4:16166142 | G | T | 1 | a0001c0001t0001g0240 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1474+491C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166142 | |||||||
chr4:16166265 | G | A | 2 | a0001c0002t0005g0153 a0001c0010t0005g0054 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1474+368C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166265 | |||||||
chr4:16166331 | C | T | 13 | a0001c0001t0009g0022 a0001c0001t0009g0041 a0001c0001t0009g0057 others(10): Show |
15 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.1474+302G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166331 | |||||||
chr4:16166338 | C | T | 6 | a0001c0002t0006g0013 a0001c0002t0006g0047 a0001c0002t0006g0143 others(3): Show |
10 | HG02145.hp2 HG02723.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474+295G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166338 | |||||||
chr4:16166385 | C | G | 1 | a0001c0002t0006g0148 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1474+248G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166385 | |||||||
chr4:16166470 | TG | T | 3 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0001g0186 |
3 | HG01952.hp1 HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1474+162delC | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166470 | |||||||
chr4:16166493 | A | G | 1 | a0004c0006t0015g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1474+140T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166493 | |||||||
chr4:16166534 | A | G | 1 | a0001c0001t0004g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1474+99T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166534 | |||||||
chr4:16166621 | G | C | 1 | a0001c0001t0007g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1474+12C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166621 | |||||||
chr4:16166623 | C | T | 8 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(5): Show |
9 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1474+10G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 13/13 | chr4 | 16166623 | |||||||
chr4:16166866 | T | C | 17 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(14): Show |
21 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.1314-73A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166866 | |||||||
chr4:16166882 | G | T | 3 | a0001c0001t0001g0281 a0001c0001t0004g0173 a0001c0001t0004g0174 |
3 | HG03704.hp2 NA18946.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1314-89C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166882 | |||||||
chr4:16166889 | C | A | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1314-96G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166889 | |||||||
chr4:16166949 | G | T | 14 | a0001c0002t0006g0013 a0001c0002t0006g0019 a0001c0002t0006g0047 others(11): Show |
20 | HG02015.hp2 HG02145.hp2 HG02723.hp1 others(17): Show |
intron_variant | MODIFIER | c.1314-156C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166949 | |||||||
chr4:16166958 | T | C | 138 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(135): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1314-165A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166958 | |||||||
chr4:16166974 | C | T | 1 | a0001c0001t0004g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1314-181G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166974 | |||||||
chr4:16166975 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1314-182C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166975 | |||||||
chr4:16166991 | C | CT | 56 | a0001c0001t0001g0240 a0001c0001t0002g0209 a0001c0001t0002g0210 others(53): Show |
77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1314-199dupA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166991 | |||||||
chr4:16166991 | C | CTT | 54 | a0001c0001t0003g0026 a0001c0001t0003g0104 a0001c0001t0003g0116 others(51): Show |
77 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(74): Show |
intron_variant | MODIFIER | c.1314-200_1314-199d others(4): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166991 | |||||||
chr4:16166991 | C | CTTT | 13 | a0001c0001t0005g0127 a0001c0001t0005g0129 a0001c0001t0005g0132 others(10): Show |
13 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1314-201_1314-199d others(5): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166991 | |||||||
chr4:16166991 | C | CTTTTTTT | 14 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(11): Show |
18 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.1314-205_1314-199d others(9): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166991 | |||||||
chr4:16166991 | CT | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0040 others(30): Show |
43 | HG00408.hp1 HG00621.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1314-199delA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16166991 | |||||||
chr4:16167041 | C | T | 138 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(135): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1314-248G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167041 | |||||||
chr4:16167080 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1314-287G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167080 | |||||||
chr4:16167084 | T | A | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1314-291A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167084 | |||||||
chr4:16167101 | T | A | 69 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(66): Show |
93 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.1314-308A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167101 | |||||||
chr4:16167107 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1314-314G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167107 | |||||||
chr4:16167239 | C | A | 20 | a0001c0001t0009g0022 a0001c0001t0009g0041 a0001c0001t0009g0057 others(17): Show |
22 | HG01099.hp2 HG01106.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1314-446G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167239 | |||||||
chr4:16167350 | A | G | 14 | a0001c0002t0006g0013 a0001c0002t0006g0019 a0001c0002t0006g0047 others(11): Show |
20 | HG02015.hp2 HG02145.hp2 HG02723.hp1 others(17): Show |
intron_variant | MODIFIER | c.1314-557T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167350 | |||||||
chr4:16167386 | T | C | 1 | a0001c0002t0005g0156 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1314-593A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167386 | |||||||
chr4:16167398 | T | A | 138 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(135): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1314-605A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167398 | |||||||
chr4:16167596 | G | C | 13 | a0001c0001t0009g0022 a0001c0001t0009g0041 a0001c0001t0009g0057 others(10): Show |
15 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.1314-803C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167596 | |||||||
chr4:16167683 | A | G | 69 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(66): Show |
93 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.1314-890T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167683 | |||||||
chr4:16167748 | G | A | 4 | a0001c0002t0006g0013 a0001c0002t0006g0047 a0001c0002t0006g0272 others(1): Show |
8 | HG02145.hp2 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1314-955C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167748 | |||||||
chr4:16167871 | T | C | 1 | a0001c0002t0005g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1314-1078A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167871 | |||||||
chr4:16167942 | A | G | 138 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(135): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1314-1149T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167942 | |||||||
chr4:16167943 | T | C | 1 | a0001c0001t0004g0192 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1314-1150A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16167943 | |||||||
chr4:16168055 | T | G | 74 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(71): Show |
108 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1314-1262A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168055 | |||||||
chr4:16168120 | C | CT | 137 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(134): Show |
185 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1314-1328dupA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168120 | |||||||
chr4:16168136 | A | G | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(201): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1314-1343T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168136 | |||||||
chr4:16168153 | G | A | 13 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(10): Show |
17 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1314-1360C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168153 | |||||||
chr4:16168190 | T | C | 69 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(66): Show |
93 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.1314-1397A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168190 | |||||||
chr4:16168206 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1314-1413A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168206 | |||||||
chr4:16168405 | T | C | 1 | a0001c0001t0004g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1314-1612A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168405 | |||||||
chr4:16168521 | A | G | 138 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(135): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1314-1728T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168521 | |||||||
chr4:16168541 | C | T | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1314-1748G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168541 | |||||||
chr4:16168579 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1314-1786C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168579 | |||||||
chr4:16168587 | A | C | 66 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(63): Show |
85 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1314-1794T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168587 | |||||||
chr4:16168869 | C | A | 56 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(53): Show |
88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1313+1784G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168869 | |||||||
chr4:16168869 | C | T | 18 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(15): Show |
22 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1313+1784G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168869 | |||||||
chr4:16168936 | C | T | 64 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(61): Show |
78 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.1313+1717G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168936 | |||||||
chr4:16168937 | G | A | 1 | a0001c0001t0018g0283 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1313+1716C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168937 | |||||||
chr4:16168946 | G | A | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1313+1707C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16168946 | |||||||
chr4:16169111 | T | C | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(201): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1313+1542A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16169111 | |||||||
chr4:16169175 | G | A | 1 | a0001c0002t0006g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1313+1478C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16169175 | |||||||
chr4:16169442 | T | C | 2 | a0001c0001t0003g0105 a0001c0001t0003g0116 |
2 | HG00609.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1313+1211A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16169442 | |||||||
chr4:16169453 | T | G | 15 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(12): Show |
19 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1313+1200A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16169453 | |||||||
chr4:16169572 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1313+1081A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16169572 | |||||||
chr4:16169597 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1313+1056G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16169597 | |||||||
chr4:16169659 | T | G | 1 | a0001c0002t0006g0147 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1313+994A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16169659 | |||||||
chr4:16169690 | G | T | 4 | a0001c0003t0008g0003 a0001c0003t0008g0031 a0001c0003t0008g0139 others(1): Show |
10 | HG02280.hp1 HG02647.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1313+963C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16169690 | |||||||
chr4:16169843 | T | C | 4 | a0001c0002t0006g0013 a0001c0002t0006g0047 a0001c0002t0006g0272 others(1): Show |
8 | HG02145.hp2 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1313+810A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16169843 | |||||||
chr4:16170401 | A | T | 51 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(48): Show |
71 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.1313+252T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16170401 | |||||||
chr4:16170548 | C | T | 8 | a0001c0002t0005g0067 a0001c0002t0005g0154 a0001c0002t0005g0155 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1313+105G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16170548 | |||||||
chr4:16170558 | C | T | 138 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(135): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1313+95G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 12/13 | chr4 | 16170558 | |||||||
chr4:16171081 | T | C | 69 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(66): Show |
93 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.1237-352A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171081 | |||||||
chr4:16171122 | C | G | 4 | a0001c0001t0009g0041 a0001c0001t0009g0059 a0001c0001t0009g0060 others(1): Show |
5 | HG02717.hp2 HG02886.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1237-393G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171122 | |||||||
chr4:16171176 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1237-447G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171176 | |||||||
chr4:16171263 | T | C | 1 | a0001c0001t0005g0132 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1237-534A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171263 | |||||||
chr4:16171313 | C | T | 18 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(15): Show |
22 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1237-584G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171313 | |||||||
chr4:16171497 | C | T | 2 | a0001c0002t0005g0153 a0001c0010t0005g0054 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1237-768G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171497 | |||||||
chr4:16171557 | T | C | 10 | a0001c0002t0005g0067 a0001c0002t0005g0153 a0001c0002t0005g0154 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1237-828A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171557 | |||||||
chr4:16171882 | C | T | 1 | a0001c0001t0009g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1237-1153G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171882 | |||||||
chr4:16171901 | C | T | 20 | a0001c0001t0009g0022 a0001c0001t0009g0041 a0001c0001t0009g0057 others(17): Show |
22 | HG01099.hp2 HG01106.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1237-1172G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171901 | |||||||
chr4:16171929 | G | C | 13 | a0001c0001t0009g0022 a0001c0001t0009g0041 a0001c0001t0009g0057 others(10): Show |
15 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.1237-1200C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171929 | |||||||
chr4:16171933 | C | T | 1 | a0001c0001t0009g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1237-1204G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171933 | |||||||
chr4:16171982 | T | C | 1 | a0001c0001t0003g0112 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1237-1253A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16171982 | |||||||
chr4:16172244 | T | A | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(202): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.1237-1515A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172244 | |||||||
chr4:16172245 | T | A | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(202): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.1237-1516A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172245 | |||||||
chr4:16172248 | A | C | 1 | a0001c0001t0009g0065 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1237-1519T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172248 | |||||||
chr4:16172250 | A | C | 1 | a0001c0001t0001g0241 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1237-1521T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172250 | |||||||
chr4:16172312 | C | T | 2 | a0004c0006t0015g0141 a0004c0006t0015g0165 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1237-1583G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172312 | |||||||
chr4:16172356 | CA | C | 7 | a0001c0001t0001g0237 a0001c0001t0001g0245 a0001c0001t0001g0278 others(4): Show |
7 | HG03516.hp2 NA18906.hp1 NA19003.hp1 others(4): Show |
intron_variant | MODIFIER | c.1237-1628delT | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172356 | |||||||
chr4:16172495 | T | A | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1236+1709A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172495 | |||||||
chr4:16172521 | TC | T | 30 | a0001c0001t0004g0009 a0001c0001t0004g0032 a0001c0001t0004g0033 others(27): Show |
38 | HG01081.hp2 HG01192.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.1236+1682delG | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172521 | |||||||
chr4:16172562 | G | C | 6 | a0001c0001t0002g0224 a0001c0003t0008g0003 a0001c0003t0008g0005 others(3): Show |
16 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.1236+1642C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172562 | |||||||
chr4:16172785 | C | G | 136 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(133): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1236+1419G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172785 | |||||||
chr4:16172807 | GTTTGT | G | 2 | a0001c0001t0001g0243 a0001c0001t0003g0017 |
4 | HG00140.hp1 HG00323.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236+1392_1236+139 others(9): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172807 | |||||||
chr4:16172844 | G | C | 1 | a0001c0001t0007g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1236+1360C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16172844 | |||||||
chr4:16173138 | T | C | 18 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(15): Show |
22 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1236+1066A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16173138 | |||||||
chr4:16173405 | A | C | 3 | a0001c0001t0005g0018 a0001c0001t0005g0133 a0001c0001t0005g0134 |
5 | HG00642.hp1 HG00733.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1236+799T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16173405 | |||||||
chr4:16173487 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1236+717G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16173487 | |||||||
chr4:16173547 | T | TA | 12 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(9): Show |
16 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1236+656dupT | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16173547 | |||||||
chr4:16173568 | T | C | 1 | a0001c0001t0003g0106 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1236+636A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16173568 | |||||||
chr4:16173649 | G | A | 1 | a0001c0002t0010g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1236+555C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16173649 | |||||||
chr4:16173657 | T | C | 7 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0265 others(4): Show |
7 | HG00408.hp1 HG02165.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.1236+547A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16173657 | |||||||
chr4:16173750 | A | C | 2 | a0001c0002t0005g0153 a0001c0010t0005g0054 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1236+454T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16173750 | |||||||
chr4:16173783 | A | C | 1 | a0001c0001t0002g0194 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1236+421T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16173783 | |||||||
chr4:16173998 | C | T | 4 | a0001c0002t0005g0068 a0001c0002t0005g0084 a0001c0002t0005g0085 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+206G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16173998 | |||||||
chr4:16174112 | C | A | 2 | a0001c0001t0001g0046 a0001c0001t0022g0269 |
3 | NA18945.hp1 NA18955.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1236+92G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 11/13 | chr4 | 16174112 | |||||||
chr4:16174430 | C | G | 1 | a0001c0002t0010g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1168-158G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 10/13 | chr4 | 16174430 | |||||||
chr4:16174435 | G | A | 1 | a0001c0001t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1168-163C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 10/13 | chr4 | 16174435 | |||||||
chr4:16174443 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1168-171A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 10/13 | chr4 | 16174443 | |||||||
chr4:16174883 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0278 |
2 | NA19056.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1108-154G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 9/13 | chr4 | 16174883 | |||||||
chr4:16174990 | T | C | 1 | a0001c0001t0003g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1108-261A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 9/13 | chr4 | 16174990 | |||||||
chr4:16175012 | A | G | 138 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(135): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1108-283T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 9/13 | chr4 | 16175012 | |||||||
chr4:16175165 | T | C | 1 | a0001c0002t0010g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1108-436A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 9/13 | chr4 | 16175165 | |||||||
chr4:16175607 | A | G | 1 | a0001c0002t0006g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1107+512T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 9/13 | chr4 | 16175607 | |||||||
chr4:16175861 | G | A | 4 | a0001c0003t0008g0003 a0001c0003t0008g0031 a0001c0003t0008g0139 others(1): Show |
10 | HG02280.hp1 HG02647.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1107+258C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 9/13 | chr4 | 16175861 | |||||||
chr4:16175894 | A | G | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1107+225T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 9/13 | chr4 | 16175894 | |||||||
chr4:16176040 | C | T | 3 | a0004c0006t0015g0141 a0004c0006t0015g0165 a0004c0006t0027g0151 |
3 | HG01109.hp2 HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1107+79G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 9/13 | chr4 | 16176040 | |||||||
chr4:16176062 | A | G | 2 | a0001c0002t0006g0047 a0001c0002t0006g0272 |
3 | HG02145.hp2 HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1107+57T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 9/13 | chr4 | 16176062 | |||||||
chr4:16176094 | T | C | 1 | a0001c0002t0006g0148 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1107+25A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 9/13 | chr4 | 16176094 | |||||||
chr4:16176253 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.998-25T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16176253 | |||||||
chr4:16176255 | G | A | 4 | a0001c0001t0009g0041 a0001c0001t0009g0059 a0001c0001t0009g0060 others(1): Show |
5 | HG02717.hp2 HG02886.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.998-27C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16176255 | |||||||
chr4:16176293 | A | G | 1 | a0001c0001t0004g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.998-65T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16176293 | |||||||
chr4:16176440 | C | A | 1 | a0001c0001t0013g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.998-212G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16176440 | |||||||
chr4:16176728 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.998-500G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16176728 | |||||||
chr4:16176763 | T | C | 138 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(135): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.998-535A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16176763 | |||||||
chr4:16176807 | T | A | 1 | a0001c0001t0009g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.998-579A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16176807 | |||||||
chr4:16176915 | G | A | 1 | a0004c0006t0015g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.998-687C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16176915 | |||||||
chr4:16177063 | A | G | 1 | a0001c0001t0004g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.998-835T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16177063 | |||||||
chr4:16177067 | A | T | 138 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(135): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.998-839T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16177067 | |||||||
chr4:16177243 | C | T | 42 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(39): Show |
52 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.998-1015G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16177243 | |||||||
chr4:16177293 | C | G | 1 | a0001c0001t0009g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.998-1065G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16177293 | |||||||
chr4:16177365 | G | T | 4 | a0003c0005t0005g0051 a0003c0005t0011g0049 a0003c0005t0011g0050 others(1): Show |
4 | HG01884.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.998-1137C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16177365 | |||||||
chr4:16177446 | G | A | 4 | a0003c0005t0005g0051 a0003c0005t0011g0049 a0003c0005t0011g0050 others(1): Show |
4 | HG01884.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.998-1218C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16177446 | |||||||
chr4:16177819 | GT | G | 137 | a0001c0001t0002g0205 a0001c0001t0003g0002 a0001c0001t0003g0004 others(134): Show |
185 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.998-1592delA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16177819 | |||||||
chr4:16178118 | C | A | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.997+1459G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178118 | |||||||
chr4:16178223 | G | A | 28 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0015 others(25): Show |
41 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.997+1354C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178223 | |||||||
chr4:16178306 | C | A | 1 | a0001c0001t0007g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.997+1271G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178306 | |||||||
chr4:16178335 | C | T | 1 | a0001c0001t0003g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.997+1242G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178335 | |||||||
chr4:16178355 | G | T | 1 | a0001c0001t0007g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.997+1222C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178355 | |||||||
chr4:16178708 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.997+869A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178708 | |||||||
chr4:16178768 | C | A | 46 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(43): Show |
56 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.997+809G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178768 | |||||||
chr4:16178816 | T | A | 5 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0080 others(2): Show |
7 | HG01167.hp2 HG01169.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.997+761A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178816 | |||||||
chr4:16178832 | T | C | 1 | a0001c0001t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.997+745A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178832 | |||||||
chr4:16178955 | G | A | 6 | a0001c0002t0006g0013 a0001c0002t0006g0047 a0001c0002t0006g0143 others(3): Show |
10 | HG02145.hp2 HG02723.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.997+622C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178955 | |||||||
chr4:16178972 | G | A | 1 | a0001c0001t0002g0215 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.997+605C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178972 | |||||||
chr4:16178979 | C | A | 8 | a0001c0002t0006g0019 a0001c0002t0006g0142 a0001c0002t0006g0145 others(5): Show |
10 | HG02015.hp2 NA18948.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.997+598G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178979 | |||||||
chr4:16178988 | T | C | 1 | a0001c0001t0003g0028 | 2 | NA19077.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.997+589A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16178988 | |||||||
chr4:16179065 | A | G | 1 | a0001c0002t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.997+512T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16179065 | |||||||
chr4:16179092 | G | T | 1 | a0001c0001t0001g0259 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.997+485C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16179092 | |||||||
chr4:16179127 | G | A | 2 | a0001c0002t0005g0153 a0001c0010t0005g0054 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.997+450C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16179127 | |||||||
chr4:16179161 | T | C | 1 | a0004c0006t0015g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.997+416A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16179161 | |||||||
chr4:16179498 | T | C | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.997+79A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 8/13 | chr4 | 16179498 | |||||||
chr4:16179660 | A | G | 4 | a0001c0001t0002g0011 a0001c0001t0002g0209 a0001c0001t0002g0217 others(1): Show |
7 | HG00609.hp2 NA18945.hp2 NA18977.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.917-3T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179660 | |||||||
chr4:16179678 | A | G | 4 | a0001c0002t0005g0068 a0001c0002t0005g0084 a0001c0002t0005g0085 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.917-21T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179678 | |||||||
chr4:16179758 | C | T | 1 | a0001c0001t0004g0175 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.917-101G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179758 | |||||||
chr4:16179786 | CT | C | 6 | a0001c0002t0006g0013 a0001c0002t0006g0047 a0001c0002t0006g0143 others(3): Show |
10 | HG02145.hp2 HG02723.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.917-130delA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179786 | |||||||
chr4:16179788 | T | TTATATAT others(15): Show |
1 | a0001c0001t0009g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.917-132_917-131ins others(22): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179788 | |||||||
chr4:16179788 | T | TTATATAT others(17): Show |
7 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(4): Show |
8 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.917-132_917-131ins others(24): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179788 | |||||||
chr4:16179788 | T | TTATATAT others(19): Show |
3 | a0001c0001t0009g0041 a0001c0001t0009g0059 a0001c0001t0009g0060 |
4 | HG02717.hp2 HG02886.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.917-132_917-131ins others(26): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179788 | |||||||
chr4:16179788 | T | TTATATAT others(21): Show |
1 | a0001c0001t0009g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.917-132_917-131ins others(28): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179788 | |||||||
chr4:16179788 | TTA | T | 3 | a0001c0002t0010g0055 a0001c0002t0010g0056 a0001c0002t0010g0144 |
3 | HG03516.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.917-133_917-132del others(2): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179788 | |||||||
chr4:16179802 | A | G | 6 | a0001c0001t0003g0101 a0001c0003t0008g0003 a0001c0003t0008g0005 others(3): Show |
16 | HG01255.hp2 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.917-145T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179802 | |||||||
chr4:16179802 | ATG | A | 41 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0039 others(38): Show |
53 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.917-147_917-146del others(2): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179802 | |||||||
chr4:16179802 | ATGTG | A | 28 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(25): Show |
32 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.917-149_917-146del others(4): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179802 | |||||||
chr4:16179804 | G | A | 18 | a0001c0001t0009g0022 a0001c0001t0009g0041 a0001c0001t0009g0057 others(15): Show |
24 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.917-147C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179804 | |||||||
chr4:16179804 | G | GTGTATAT others(15): Show |
1 | a0001c0001t0009g0065 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.917-148_917-147ins others(22): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179804 | |||||||
chr4:16179805 | T | A | 60 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0040 others(57): Show |
77 | HG00408.hp1 HG00621.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.917-148A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179805 | |||||||
chr4:16179826 | G | A | 11 | a0001c0001t0002g0213 a0001c0002t0005g0067 a0001c0002t0005g0153 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.917-169C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179826 | |||||||
chr4:16179826 | GTA | G | 5 | a0001c0001t0007g0069 a0003c0005t0005g0051 a0003c0005t0011g0049 others(2): Show |
5 | HG01884.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.917-171_917-170del others(2): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179826 | |||||||
chr4:16179828 | A | G | 19 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.917-171T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179828 | |||||||
chr4:16179866 | C | A | 1 | a0003c0005t0005g0051 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.917-209G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179866 | |||||||
chr4:16179947 | T | C | 138 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(135): Show |
186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.917-290A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179947 | |||||||
chr4:16179958 | G | A | 46 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(43): Show |
56 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.917-301C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179958 | |||||||
chr4:16179958 | G | C | 48 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(45): Show |
70 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.917-301C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179958 | |||||||
chr4:16179958 | G | T | 1 | a0001c0001t0003g0118 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.917-301C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179958 | |||||||
chr4:16179968 | A | G | 11 | a0001c0002t0005g0067 a0001c0002t0005g0152 a0001c0002t0005g0153 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.917-311T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179968 | |||||||
chr4:16179975 | T | C | 1 | a0001c0001t0005g0125 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.917-318A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16179975 | |||||||
chr4:16180097 | T | C | 3 | a0001c0002t0010g0055 a0001c0002t0010g0056 a0001c0002t0010g0144 |
3 | HG03516.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.917-440A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16180097 | |||||||
chr4:16180175 | T | C | 46 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(43): Show |
56 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.917-518A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16180175 | |||||||
chr4:16180202 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.917-545A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16180202 | |||||||
chr4:16180579 | G | A | 1 | a0001c0002t0006g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.917-922C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16180579 | |||||||
chr4:16180599 | C | T | 1 | a0001c0001t0001g0045 | 2 | HG02080.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.917-942G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16180599 | |||||||
chr4:16180718 | G | A | 2 | a0001c0001t0004g0173 a0001c0001t0004g0174 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.917-1061C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16180718 | |||||||
chr4:16180841 | C | T | 1 | a0001c0001t0003g0102 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.917-1184G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16180841 | |||||||
chr4:16180867 | A | G | 137 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(134): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.917-1210T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16180867 | |||||||
chr4:16180977 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.917-1320G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16180977 | |||||||
chr4:16181147 | C | T | 33 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(30): Show |
39 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.917-1490G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16181147 | |||||||
chr4:16181392 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.917-1735A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16181392 | |||||||
chr4:16181452 | T | C | 1 | a0001c0002t0006g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.917-1795A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16181452 | |||||||
chr4:16181486 | G | A | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.917-1829C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16181486 | |||||||
chr4:16181557 | A | G | 104 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(101): Show |
145 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.917-1900T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16181557 | |||||||
chr4:16181689 | TC | T | 4 | a0001c0001t0002g0035 a0001c0001t0002g0198 a0001c0001t0002g0223 others(1): Show |
5 | NA18949.hp1 NA18994.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.917-2033delG | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16181689 | |||||||
chr4:16182053 | A | G | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.917-2396T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16182053 | |||||||
chr4:16182137 | G | C | 17 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(14): Show |
21 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.917-2480C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16182137 | |||||||
chr4:16182174 | T | C | 1 | a0001c0001t0003g0107 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.917-2517A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16182174 | |||||||
chr4:16182288 | A | G | 1 | a0001c0001t0003g0112 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.917-2631T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16182288 | |||||||
chr4:16182349 | G | A | 1 | a0001c0001t0007g0074 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.917-2692C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16182349 | |||||||
chr4:16182660 | C | T | 1 | a0001c0001t0003g0118 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.917-3003G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16182660 | |||||||
chr4:16182818 | G | T | 203 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(200): Show |
270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.917-3161C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16182818 | |||||||
chr4:16183105 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.916+3430T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16183105 | |||||||
chr4:16183133 | GACTCCTG others(10): Show |
G | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.916+3385_916+3401d others(19): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16183133 | |||||||
chr4:16183151 | T | C | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.916+3384A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16183151 | |||||||
chr4:16183165 | G | T | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.916+3370C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16183165 | |||||||
chr4:16183237 | T | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.916+3298A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16183237 | |||||||
chr4:16183271 | G | A | 33 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(30): Show |
39 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.916+3264C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16183271 | |||||||
chr4:16183310 | A | AT | 6 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0009g0041 others(3): Show |
7 | HG01109.hp1 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.916+3224dupA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16183310 | |||||||
chr4:16183409 | T | C | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.916+3126A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16183409 | |||||||
chr4:16183902 | G | A | 30 | a0001c0001t0004g0009 a0001c0001t0004g0032 a0001c0001t0004g0033 others(27): Show |
38 | HG01081.hp2 HG01192.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.916+2633C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16183902 | |||||||
chr4:16184207 | ATTCCTAT others(15): Show |
A | 2 | a0001c0002t0010g0055 a0001c0002t0010g0056 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.916+2306_916+2327d others(24): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16184207 | |||||||
chr4:16184392 | T | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0277 |
3 | HG00621.hp2 NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.916+2143A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16184392 | |||||||
chr4:16184415 | G | A | 1 | a0001c0002t0005g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.916+2120C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16184415 | |||||||
chr4:16184447 | T | C | 1 | a0001c0001t0004g0175 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.916+2088A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16184447 | |||||||
chr4:16184659 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.916+1876C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16184659 | |||||||
chr4:16184663 | G | A | 1 | a0001c0001t0002g0037 | 2 | NA18951.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.916+1872C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16184663 | |||||||
chr4:16184724 | C | T | 137 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(134): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.916+1811G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16184724 | |||||||
chr4:16184797 | C | T | 2 | a0001c0001t0005g0131 a0001c0001t0005g0132 |
2 | HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.916+1738G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16184797 | |||||||
chr4:16184888 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.916+1647A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16184888 | |||||||
chr4:16185107 | G | C | 13 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(10): Show |
17 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.916+1428C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185107 | |||||||
chr4:16185122 | T | C | 1 | a0001c0001t0007g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.916+1413A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185122 | |||||||
chr4:16185349 | A | C | 1 | a0001c0010t0005g0054 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.916+1186T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185349 | |||||||
chr4:16185367 | G | A | 137 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(134): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.916+1168C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185367 | |||||||
chr4:16185370 | A | AT | 17 | a0001c0001t0004g0034 a0001c0002t0005g0067 a0001c0002t0005g0068 others(14): Show |
20 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.916+1164dupA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185370 | |||||||
chr4:16185393 | C | T | 50 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(47): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.916+1142G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185393 | |||||||
chr4:16185419 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.916+1116T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185419 | |||||||
chr4:16185421 | T | A | 2 | a0001c0002t0010g0055 a0001c0002t0010g0056 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.916+1114A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185421 | |||||||
chr4:16185483 | C | T | 17 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(14): Show |
21 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.916+1052G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185483 | |||||||
chr4:16185519 | C | T | 30 | a0001c0001t0004g0009 a0001c0001t0004g0032 a0001c0001t0004g0033 others(27): Show |
38 | HG01081.hp2 HG01192.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.916+1016G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185519 | |||||||
chr4:16185609 | T | A | 2 | a0001c0001t0002g0197 a0001c0001t0002g0228 |
2 | NA19002.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.916+926A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185609 | |||||||
chr4:16185649 | G | T | 1 | a0001c0001t0002g0037 | 2 | NA18951.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.916+886C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185649 | |||||||
chr4:16185791 | A | G | 1 | a0001c0001t0003g0101 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.916+744T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185791 | |||||||
chr4:16185861 | G | C | 1 | a0001c0001t0018g0283 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.916+674C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185861 | |||||||
chr4:16185883 | T | C | 4 | a0003c0005t0005g0051 a0003c0005t0011g0049 a0003c0005t0011g0050 others(1): Show |
4 | HG01884.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.916+652A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16185883 | |||||||
chr4:16186023 | C | A | 1 | a0001c0001t0001g0270 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.916+512G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16186023 | |||||||
chr4:16186182 | A | G | 50 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(47): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.916+353T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16186182 | |||||||
chr4:16186258 | A | G | 33 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(30): Show |
39 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.916+277T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16186258 | |||||||
chr4:16186270 | C | T | 33 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(30): Show |
39 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.916+265G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16186270 | |||||||
chr4:16186285 | A | G | 1 | a0001c0001t0004g0173 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.916+250T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16186285 | |||||||
chr4:16186466 | A | G | 1 | a0001c0001t0009g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.916+69T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16186466 | |||||||
chr4:16186512 | A | C | 2 | a0004c0006t0015g0141 a0004c0006t0015g0165 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.916+23T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 7/13 | chr4 | 16186512 | |||||||
chr4:16186759 | G | A | 2 | a0001c0002t0005g0085 a0001c0002t0005g0086 |
2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.846+22C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 6/13 | chr4 | 16186759 | |||||||
chr4:16186997 | T | C | 4 | a0001c0003t0008g0003 a0001c0003t0008g0031 a0001c0003t0008g0139 others(1): Show |
10 | HG02280.hp1 HG02647.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.749-119A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16186997 | |||||||
chr4:16187023 | T | C | 1 | a0001c0001t0004g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.749-145A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16187023 | |||||||
chr4:16187065 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.749-187G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16187065 | |||||||
chr4:16187303 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0256 |
3 | HG00741.hp2 HG01256.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.749-425G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16187303 | |||||||
chr4:16187338 | G | T | 137 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(134): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.749-460C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16187338 | |||||||
chr4:16187358 | G | A | 2 | a0001c0002t0010g0055 a0001c0002t0010g0056 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.749-480C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16187358 | |||||||
chr4:16187513 | A | C | 137 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(134): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.749-635T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16187513 | |||||||
chr4:16187600 | T | C | 1 | a0001c0001t0003g0093 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748+620A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16187600 | |||||||
chr4:16187656 | T | C | 17 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(14): Show |
21 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.748+564A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16187656 | |||||||
chr4:16187770 | C | A | 2 | a0004c0006t0015g0141 a0004c0006t0015g0165 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.748+450G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16187770 | |||||||
chr4:16187814 | T | C | 1 | a0001c0002t0006g0145 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.748+406A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16187814 | |||||||
chr4:16187987 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.748+233G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 5/13 | chr4 | 16187987 | |||||||
chr4:16188368 | A | T | 50 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(47): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.613-13T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188368 | |||||||
chr4:16188450 | T | G | 104 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(101): Show |
145 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.613-95A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188450 | |||||||
chr4:16188513 | A | G | 1 | a0005c0012t0007g0070 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.613-158T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188513 | |||||||
chr4:16188593 | A | C | 1 | a0003c0005t0005g0051 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.613-238T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188593 | |||||||
chr4:16188596 | A | G | 6 | a0001c0001t0003g0025 a0001c0001t0003g0094 a0001c0001t0003g0095 others(3): Show |
7 | HG01361.hp1 HG02602.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.613-241T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188596 | |||||||
chr4:16188596 | A | T | 18 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(15): Show |
22 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.613-241T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188596 | |||||||
chr4:16188696 | G | A | 1 | a0003c0005t0011g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.613-341C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188696 | |||||||
chr4:16188702 | C | T | 50 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(47): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.613-347G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188702 | |||||||
chr4:16188753 | T | C | 4 | a0001c0001t0003g0002 a0001c0001t0003g0028 a0001c0001t0003g0099 others(1): Show |
10 | HG02080.hp2 HG02155.hp2 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-398A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188753 | |||||||
chr4:16188777 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.613-422C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188777 | |||||||
chr4:16188793 | G | A | 2 | a0001c0002t0010g0055 a0001c0002t0010g0056 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.613-438C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188793 | |||||||
chr4:16188812 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.613-457G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188812 | |||||||
chr4:16188813 | G | A | 2 | a0001c0002t0010g0055 a0001c0002t0010g0056 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.613-458C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188813 | |||||||
chr4:16188903 | G | A | 1 | a0001c0001t0009g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.613-548C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16188903 | |||||||
chr4:16189016 | T | C | 1 | a0001c0009t0006g0149 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.613-661A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189016 | |||||||
chr4:16189026 | G | C | 99 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(96): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.613-671C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189026 | |||||||
chr4:16189038 | T | G | 13 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(10): Show |
17 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.613-683A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189038 | |||||||
chr4:16189113 | A | G | 4 | a0003c0005t0005g0051 a0003c0005t0011g0049 a0003c0005t0011g0050 others(1): Show |
4 | HG01884.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-758T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189113 | |||||||
chr4:16189145 | A | G | 3 | a0001c0001t0009g0059 a0001c0001t0009g0060 a0001c0001t0009g0164 |
3 | HG03579.hp2 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.613-790T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189145 | |||||||
chr4:16189167 | A | T | 4 | a0001c0002t0005g0068 a0001c0002t0005g0084 a0001c0002t0005g0085 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-812T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189167 | |||||||
chr4:16189193 | A | G | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.613-838T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189193 | |||||||
chr4:16189312 | A | G | 1 | a0001c0010t0005g0054 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.613-957T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189312 | |||||||
chr4:16189361 | A | C | 2 | a0001c0002t0010g0055 a0001c0002t0010g0056 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.613-1006T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189361 | |||||||
chr4:16189383 | G | T | 1 | a0001c0001t0002g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.613-1028C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189383 | |||||||
chr4:16189680 | T | A | 31 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(28): Show |
36 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.613-1325A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189680 | |||||||
chr4:16189739 | G | A | 68 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(65): Show |
94 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.613-1384C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189739 | |||||||
chr4:16189824 | G | A | 29 | a0001c0002t0005g0067 a0001c0002t0005g0152 a0001c0002t0005g0153 others(26): Show |
35 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.613-1469C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189824 | |||||||
chr4:16189830 | T | C | 14 | a0001c0002t0006g0013 a0001c0002t0006g0019 a0001c0002t0006g0047 others(11): Show |
20 | HG02015.hp2 HG02145.hp2 HG02723.hp1 others(17): Show |
intron_variant | MODIFIER | c.613-1475A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189830 | |||||||
chr4:16189847 | A | T | 29 | a0001c0002t0005g0067 a0001c0002t0005g0152 a0001c0002t0005g0153 others(26): Show |
35 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.613-1492T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189847 | |||||||
chr4:16189940 | G | A | 29 | a0001c0002t0005g0067 a0001c0002t0005g0152 a0001c0002t0005g0153 others(26): Show |
35 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.612+1421C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16189940 | |||||||
chr4:16190065 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.612+1296G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190065 | |||||||
chr4:16190067 | C | T | 2 | a0001c0001t0004g0169 a0001c0001t0004g0171 |
2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.612+1294G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190067 | |||||||
chr4:16190245 | T | G | 12 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(9): Show |
13 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.612+1116A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190245 | |||||||
chr4:16190297 | T | C | 18 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(15): Show |
22 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.612+1064A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190297 | |||||||
chr4:16190322 | A | T | 2 | a0001c0002t0005g0153 a0001c0010t0005g0054 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.612+1039T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190322 | |||||||
chr4:16190352 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.612+1009A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190352 | |||||||
chr4:16190430 | T | C | 137 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(134): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.612+931A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190430 | |||||||
chr4:16190586 | C | T | 17 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(14): Show |
21 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.612+775G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190586 | |||||||
chr4:16190660 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.612+701A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190660 | |||||||
chr4:16190790 | C | T | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(202): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.612+571G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190790 | |||||||
chr4:16190855 | A | G | 8 | a0001c0002t0005g0067 a0001c0002t0005g0154 a0001c0002t0005g0155 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.612+506T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190855 | |||||||
chr4:16190923 | CAT | C | 4 | a0003c0005t0005g0051 a0003c0005t0011g0049 a0003c0005t0011g0050 others(1): Show |
4 | HG01884.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+436_612+437del others(2): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16190923 | |||||||
chr4:16191101 | G | A | 1 | a0001c0001t0002g0218 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.612+260C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 4/13 | chr4 | 16191101 | |||||||
chr4:16191617 | G | A | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.450-94C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16191617 | |||||||
chr4:16191979 | T | C | 13 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(10): Show |
17 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.450-456A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16191979 | |||||||
chr4:16192265 | G | A | 104 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(101): Show |
145 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.450-742C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16192265 | |||||||
chr4:16192332 | C | T | 33 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(30): Show |
39 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.450-809G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16192332 | |||||||
chr4:16192396 | T | C | 1 | a0001c0001t0003g0025 | 2 | HG02698.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.450-873A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16192396 | |||||||
chr4:16192652 | T | C | 202 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(199): Show |
269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.450-1129A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16192652 | |||||||
chr4:16192658 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG00733.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.450-1135A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16192658 | |||||||
chr4:16192717 | TC | T | 33 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(30): Show |
39 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.450-1195delG | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16192717 | |||||||
chr4:16192771 | C | T | 7 | a0001c0001t0004g0009 a0001c0001t0004g0126 a0001c0001t0004g0176 others(4): Show |
10 | HG01192.hp1 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.450-1248G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16192771 | |||||||
chr4:16192820 | T | C | 18 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(15): Show |
22 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.450-1297A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16192820 | |||||||
chr4:16192866 | T | C | 1 | a0001c0001t0020g0248 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.450-1343A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16192866 | |||||||
chr4:16193031 | C | T | 8 | a0001c0002t0005g0067 a0001c0002t0005g0154 a0001c0002t0005g0155 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.450-1508G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16193031 | |||||||
chr4:16193044 | G | A | 31 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(28): Show |
36 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.450-1521C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16193044 | |||||||
chr4:16193354 | T | C | 4 | a0001c0002t0006g0013 a0001c0002t0006g0047 a0001c0002t0006g0272 others(1): Show |
8 | HG02145.hp2 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.450-1831A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16193354 | |||||||
chr4:16193363 | G | A | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.450-1840C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16193363 | |||||||
chr4:16193447 | G | C | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.450-1924C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16193447 | |||||||
chr4:16193475 | G | A | 8 | a0001c0002t0006g0019 a0001c0002t0006g0142 a0001c0002t0006g0145 others(5): Show |
10 | HG02015.hp2 NA18948.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.450-1952C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16193475 | |||||||
chr4:16193708 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.450-2185A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16193708 | |||||||
chr4:16193712 | T | C | 1 | a0001c0001t0003g0115 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.450-2189A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16193712 | |||||||
chr4:16193848 | T | A | 1 | a0001c0001t0016g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.450-2325A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16193848 | |||||||
chr4:16193851 | T | C | 1 | a0001c0001t0007g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.450-2328A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16193851 | |||||||
chr4:16193926 | CTAAT | C | 4 | a0001c0001t0004g0034 a0002c0004t0004g0020 a0002c0004t0004g0183 others(1): Show |
7 | HG02451.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.450-2407_450-2404d others(6): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16193926 | |||||||
chr4:16194084 | G | A | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.450-2561C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194084 | |||||||
chr4:16194119 | T | C | 50 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(47): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.450-2596A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194119 | |||||||
chr4:16194131 | T | G | 1 | a0001c0003t0008g0005 | 5 | HG02257.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.450-2608A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194131 | |||||||
chr4:16194494 | C | T | 79 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(76): Show |
106 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.450-2971G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194494 | |||||||
chr4:16194544 | A | G | 1 | a0001c0002t0010g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.450-3021T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194544 | |||||||
chr4:16194575 | G | A | 2 | a0001c0002t0010g0055 a0001c0002t0010g0056 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.450-3052C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194575 | |||||||
chr4:16194666 | T | C | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.450-3143A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194666 | |||||||
chr4:16194680 | C | T | 1 | a0001c0001t0009g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.450-3157G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194680 | |||||||
chr4:16194704 | G | A | 2 | a0001c0002t0010g0055 a0001c0002t0010g0056 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.450-3181C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194704 | |||||||
chr4:16194736 | G | A | 1 | a0001c0003t0008g0005 | 5 | HG02257.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.450-3213C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194736 | |||||||
chr4:16194840 | A | C | 1 | a0001c0002t0005g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.450-3317T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194840 | |||||||
chr4:16194856 | T | C | 3 | a0001c0002t0005g0084 a0001c0002t0005g0085 a0001c0002t0005g0086 |
3 | HG02572.hp2 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.450-3333A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194856 | |||||||
chr4:16194857 | C | CCCCCCCC others(79): Show |
1 | a0001c0002t0005g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.450-3335_450-3334i others(88): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194857 | |||||||
chr4:16194857 | C | CCCCCTCC others(139): Show |
1 | a0001c0002t0005g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.450-3335_450-3334i others(148): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194857 | |||||||
chr4:16194857 | C | CCCCTCCT others(180): Show |
1 | a0001c0002t0005g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.450-3335_450-3334i others(189): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194857 | |||||||
chr4:16194858 | T | C | 3 | a0001c0002t0005g0084 a0001c0002t0005g0085 a0001c0002t0005g0086 |
3 | HG02572.hp2 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.450-3335A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194858 | |||||||
chr4:16194859 | G | C | 3 | a0001c0002t0005g0084 a0001c0002t0005g0085 a0001c0002t0005g0086 |
3 | HG02572.hp2 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.450-3336C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194859 | G | GTCT | 22 | a0001c0001t0002g0010 a0001c0001t0002g0035 a0001c0001t0002g0196 others(19): Show |
30 | HG00423.hp2 HG01071.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.450-3339_450-3337d others(5): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194859 | G | GTCTTCT | 5 | a0001c0001t0007g0071 a0001c0001t0007g0072 a0001c0001t0007g0077 others(2): Show |
5 | HG00323.hp1 HG02602.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.450-3342_450-3337d others(8): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194859 | G | GTCTTCTT others(2): Show |
4 | a0001c0001t0002g0222 a0001c0002t0005g0067 a0001c0002t0005g0157 others(1): Show |
4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-3345_450-3337d others(11): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194859 | G | GTCTTCTT others(5): Show |
3 | a0001c0002t0005g0155 a0001c0002t0005g0156 a0001c0002t0005g0159 |
3 | HG02451.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.450-3348_450-3337d others(14): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194859 | G | GTCTTCTT others(8): Show |
2 | a0001c0001t0007g0080 a0001c0002t0005g0153 |
2 | HG02257.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.450-3351_450-3337d others(17): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194859 | G | GTCTTCTT others(11): Show |
1 | a0001c0002t0005g0154 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.450-3354_450-3337d others(20): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194859 | G | GTCTTCTT others(14): Show |
2 | a0001c0002t0005g0160 a0001c0010t0005g0054 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.450-3357_450-3337d others(23): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194859 | GTCTTCT | G | 34 | a0001c0001t0002g0219 a0001c0001t0009g0022 a0001c0001t0009g0057 others(31): Show |
51 | HG01099.hp2 HG01106.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.450-3342_450-3337d others(8): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194859 | GTCTTCTT others(2): Show |
G | 4 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0187 others(1): Show |
4 | HG03516.hp2 HG03704.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.450-3345_450-3337d others(11): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194859 | GTCTTCTT others(5): Show |
G | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(83): Show |
110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.450-3348_450-3337d others(14): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194859 | GTCTTCTT others(8): Show |
G | 51 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(48): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.450-3351_450-3337d others(17): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194859 | |||||||
chr4:16194860 | T | TCCTCGTC others(229): Show |
1 | a0001c0002t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.450-3338_450-3337i others(238): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194860 | |||||||
chr4:16194862 | T | C | 3 | a0001c0002t0005g0084 a0001c0002t0005g0085 a0001c0002t0005g0086 |
3 | HG02572.hp2 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.450-3339A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194862 | |||||||
chr4:16194865 | T | C | 3 | a0001c0002t0005g0084 a0001c0002t0005g0085 a0001c0002t0005g0086 |
3 | HG02572.hp2 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.450-3342A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194865 | |||||||
chr4:16194868 | T | C | 3 | a0001c0002t0005g0084 a0001c0002t0005g0085 a0001c0002t0005g0086 |
3 | HG02572.hp2 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.450-3345A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194868 | |||||||
chr4:16194871 | T | C | 3 | a0001c0002t0005g0084 a0001c0002t0005g0085 a0001c0002t0005g0086 |
3 | HG02572.hp2 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.450-3348A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194871 | |||||||
chr4:16194874 | T | C | 3 | a0001c0002t0005g0084 a0001c0002t0005g0085 a0001c0002t0005g0086 |
3 | HG02572.hp2 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.450-3351A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194874 | |||||||
chr4:16194877 | T | C | 3 | a0001c0002t0005g0084 a0001c0002t0005g0085 a0001c0002t0005g0086 |
3 | HG02572.hp2 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.450-3354A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194877 | |||||||
chr4:16194880 | T | C | 2 | a0001c0002t0005g0084 a0001c0002t0005g0086 |
2 | HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.450-3357A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194880 | |||||||
chr4:16194883 | T | C | 1 | a0001c0002t0005g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.450-3360A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194883 | |||||||
chr4:16194886 | T | C | 1 | a0001c0002t0005g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.450-3363A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194886 | |||||||
chr4:16194978 | G | A | 50 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(47): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.450-3455C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16194978 | |||||||
chr4:16195028 | G | A | 13 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(10): Show |
17 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.450-3505C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16195028 | |||||||
chr4:16195059 | T | C | 58 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(55): Show |
78 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(75): Show |
intron_variant | MODIFIER | c.450-3536A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16195059 | |||||||
chr4:16195072 | G | T | 2 | a0001c0001t0001g0128 a0001c0001t0014g0043 |
3 | HG01175.hp2 HG01258.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.450-3549C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16195072 | |||||||
chr4:16195454 | A | C | 1 | a0001c0001t0002g0271 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.450-3931T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16195454 | |||||||
chr4:16195481 | T | C | 1 | a0001c0001t0003g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.450-3958A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16195481 | |||||||
chr4:16195608 | A | C | 4 | a0001c0003t0008g0003 a0001c0003t0008g0031 a0001c0003t0008g0139 others(1): Show |
10 | HG02280.hp1 HG02647.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.450-4085T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16195608 | |||||||
chr4:16195645 | C | A | 1 | a0001c0001t0016g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.450-4122G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16195645 | |||||||
chr4:16195890 | C | T | 6 | a0001c0002t0006g0013 a0001c0002t0006g0047 a0001c0002t0006g0143 others(3): Show |
10 | HG02145.hp2 HG02723.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.450-4367G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16195890 | |||||||
chr4:16195911 | T | C | 1 | a0001c0001t0003g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.450-4388A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16195911 | |||||||
chr4:16196099 | A | C | 56 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(53): Show |
76 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.450-4576T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16196099 | |||||||
chr4:16196283 | A | G | 3 | a0001c0001t0009g0059 a0001c0001t0009g0060 a0001c0001t0009g0164 |
3 | HG03579.hp2 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.450-4760T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16196283 | |||||||
chr4:16196413 | T | C | 4 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(1): Show |
4 | HG01074.hp1 HG02602.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.450-4890A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16196413 | |||||||
chr4:16196755 | A | G | 137 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(134): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.450-5232T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16196755 | |||||||
chr4:16196816 | T | C | 86 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(83): Show |
123 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.450-5293A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16196816 | |||||||
chr4:16196889 | G | T | 2 | a0001c0002t0005g0153 a0001c0010t0005g0054 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.450-5366C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16196889 | |||||||
chr4:16197068 | A | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0027 |
4 | NA18946.hp1 NA18956.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.449+5394T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197068 | |||||||
chr4:16197077 | G | A | 1 | a0001c0001t0003g0120 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.449+5385C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197077 | |||||||
chr4:16197134 | G | C | 2 | a0001c0001t0012g0063 a0001c0001t0012g0064 |
2 | HG01099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.449+5328C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197134 | |||||||
chr4:16197253 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.449+5209C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197253 | |||||||
chr4:16197274 | A | G | 2 | a0001c0001t0004g0173 a0001c0001t0004g0174 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.449+5188T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197274 | |||||||
chr4:16197321 | C | T | 1 | a0001c0002t0005g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.449+5141G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197321 | |||||||
chr4:16197322 | G | A | 1 | a0001c0001t0018g0283 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.449+5140C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197322 | |||||||
chr4:16197494 | A | G | 18 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(15): Show |
22 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.449+4968T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197494 | |||||||
chr4:16197495 | A | C | 1 | a0001c0001t0002g0222 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.449+4967T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197495 | |||||||
chr4:16197602 | T | C | 1 | a0001c0001t0002g0236 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.449+4860A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197602 | |||||||
chr4:16197607 | C | G | 12 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(9): Show |
13 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.449+4855G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197607 | |||||||
chr4:16197887 | G | A | 2 | a0004c0006t0015g0141 a0004c0006t0015g0165 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.449+4575C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16197887 | |||||||
chr4:16198114 | G | A | 18 | a0001c0001t0007g0014 a0001c0001t0007g0023 a0001c0001t0007g0024 others(15): Show |
22 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.449+4348C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198114 | |||||||
chr4:16198237 | A | G | 4 | a0001c0001t0004g0126 a0001c0001t0004g0178 a0001c0001t0004g0188 others(1): Show |
4 | HG01361.hp2 HG02683.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+4225T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198237 | |||||||
chr4:16198327 | G | A | 5 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0080 others(2): Show |
7 | HG01167.hp2 HG01169.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.449+4135C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198327 | |||||||
chr4:16198387 | T | C | 1 | a0001c0001t0003g0015 | 3 | HG02040.hp2 NA18939.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.449+4075A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198387 | |||||||
chr4:16198432 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.449+4030A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198432 | |||||||
chr4:16198515 | G | C | 1 | a0001c0001t0001g0246 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.449+3947C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198515 | |||||||
chr4:16198561 | GA | G | 7 | a0001c0001t0001g0284 a0001c0001t0002g0197 a0001c0001t0004g0033 others(4): Show |
8 | HG02071.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.449+3900delT | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198561 | |||||||
chr4:16198571 | A | AAC | 54 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(51): Show |
86 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.449+3890_449+3891i others(4): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198571 | |||||||
chr4:16198571 | A | AC | 76 | a0001c0001t0005g0018 a0001c0001t0005g0029 a0001c0001t0005g0125 others(73): Show |
87 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.449+3890_449+3891i others(3): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198571 | |||||||
chr4:16198571 | A | C | 6 | a0001c0002t0006g0013 a0001c0002t0006g0047 a0001c0002t0006g0143 others(3): Show |
10 | HG02145.hp2 HG02723.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.449+3891T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198571 | |||||||
chr4:16198576 | T | C | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(198): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.449+3886A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198576 | |||||||
chr4:16198604 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.449+3858G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198604 | |||||||
chr4:16198642 | A | G | 1 | a0001c0001t0009g0057 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.449+3820T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198642 | |||||||
chr4:16198837 | T | C | 1 | a0001c0002t0005g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.449+3625A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198837 | |||||||
chr4:16198844 | G | A | 2 | a0001c0001t0007g0024 a0001c0001t0007g0081 |
3 | HG01167.hp2 HG01169.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.449+3618C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198844 | |||||||
chr4:16198887 | T | C | 1 | a0001c0001t0002g0221 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.449+3575A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198887 | |||||||
chr4:16198978 | T | C | 1 | a0001c0002t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.449+3484A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16198978 | |||||||
chr4:16199034 | G | A | 2 | a0004c0006t0015g0141 a0004c0006t0015g0165 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.449+3428C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16199034 | |||||||
chr4:16199155 | C | G | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.449+3307G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16199155 | |||||||
chr4:16199273 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.449+3189A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16199273 | |||||||
chr4:16199340 | G | A | 1 | a0001c0001t0003g0117 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.449+3122C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16199340 | |||||||
chr4:16199369 | A | T | 137 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(134): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.449+3093T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16199369 | |||||||
chr4:16199824 | A | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0257 |
3 | HG02293.hp1 HG02735.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.449+2638T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16199824 | |||||||
chr4:16199841 | T | C | 137 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(134): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.449+2621A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16199841 | |||||||
chr4:16199897 | A | G | 1 | a0001c0001t0007g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.449+2565T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16199897 | |||||||
chr4:16200173 | G | A | 1 | a0001c0001t0004g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.449+2289C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16200173 | |||||||
chr4:16200291 | A | C | 30 | a0001c0001t0004g0009 a0001c0001t0004g0032 a0001c0001t0004g0033 others(27): Show |
38 | HG01081.hp2 HG01192.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.449+2171T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16200291 | |||||||
chr4:16200312 | C | T | 50 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(47): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.449+2150G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16200312 | |||||||
chr4:16200379 | GTGGCATA others(4): Show |
G | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.449+2072_449+2082d others(13): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16200379 | |||||||
chr4:16200432 | C | A | 6 | a0001c0001t0002g0035 a0001c0001t0002g0198 a0001c0001t0002g0222 others(3): Show |
7 | HG02165.hp2 NA18949.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.449+2030G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16200432 | |||||||
chr4:16200526 | A | G | 8 | a0001c0002t0005g0067 a0001c0002t0005g0154 a0001c0002t0005g0155 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.449+1936T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16200526 | |||||||
chr4:16200632 | G | A | 2 | a0001c0002t0005g0153 a0001c0010t0005g0054 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.449+1830C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16200632 | |||||||
chr4:16200795 | G | T | 137 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(134): Show |
184 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.449+1667C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16200795 | |||||||
chr4:16200819 | T | C | 2 | a0001c0002t0005g0152 a0003c0005t0011g0052 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.449+1643A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16200819 | |||||||
chr4:16201004 | G | GT | 8 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(5): Show |
18 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.449+1457dupA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201004 | |||||||
chr4:16201390 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.449+1072G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201390 | |||||||
chr4:16201391 | G | A | 3 | a0001c0002t0005g0084 a0001c0002t0005g0085 a0001c0002t0005g0086 |
3 | HG02572.hp2 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.449+1071C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201391 | |||||||
chr4:16201415 | A | T | 48 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(45): Show |
70 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.449+1047T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201415 | |||||||
chr4:16201437 | T | G | 1 | a0001c0001t0004g0192 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.449+1025A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201437 | |||||||
chr4:16201471 | A | C | 7 | a0001c0002t0005g0068 a0001c0002t0005g0084 a0001c0002t0005g0085 others(4): Show |
7 | HG01884.hp2 HG02572.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.449+991T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201471 | |||||||
chr4:16201573 | C | T | 1 | a0002c0004t0004g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.449+889G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201573 | |||||||
chr4:16201615 | C | T | 184 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(181): Show |
244 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.449+847G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201615 | |||||||
chr4:16201666 | T | A | 1 | a0001c0002t0006g0150 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.449+796A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201666 | |||||||
chr4:16201760 | A | AT | 23 | a0001c0001t0004g0168 a0001c0001t0004g0189 a0001c0001t0004g0190 others(20): Show |
29 | HG01109.hp2 HG02015.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.449+701dupA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201760 | |||||||
chr4:16201845 | G | T | 1 | a0001c0001t0003g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.449+617C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201845 | |||||||
chr4:16201871 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0256 |
3 | HG00741.hp2 HG01256.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.449+591G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201871 | |||||||
chr4:16201929 | CAG | C | 3 | a0001c0001t0002g0036 a0001c0001t0002g0194 a0001c0001t0002g0226 |
4 | HG02027.hp1 NA18747.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+531_449+532del others(2): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201929 | |||||||
chr4:16201930 | A | T | 18 | a0001c0001t0003g0026 a0001c0001t0004g0009 a0001c0001t0004g0184 others(15): Show |
23 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(20): Show |
intron_variant | MODIFIER | c.449+532T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201930 | |||||||
chr4:16201963 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.449+499G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201963 | |||||||
chr4:16201980 | G | C | 2 | a0001c0001t0009g0059 a0001c0002t0005g0159 |
2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.449+482C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16201980 | |||||||
chr4:16202184 | G | T | 1 | a0001c0001t0005g0127 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.449+278C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16202184 | |||||||
chr4:16202232 | G | A | 1 | a0001c0001t0007g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.449+230C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16202232 | |||||||
chr4:16202249 | G | A | 3 | a0001c0002t0005g0068 a0001c0002t0005g0085 a0001c0002t0005g0086 |
3 | HG02572.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.449+213C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16202249 | |||||||
chr4:16202312 | T | C | 41 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(38): Show |
57 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(54): Show |
intron_variant | MODIFIER | c.449+150A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16202312 | |||||||
chr4:16202331 | G | T | 1 | a0001c0001t0007g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.449+131C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16202331 | |||||||
chr4:16202334 | A | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0276 a0001c0001t0021g0255 |
4 | NA18747.hp1 NA18959.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+128T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 3/13 | chr4 | 16202334 | |||||||
chr4:16202634 | A | G | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.331-54T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16202634 | |||||||
chr4:16202726 | C | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(56): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.331-146G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16202726 | |||||||
chr4:16202733 | A | G | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(57): Show |
80 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.331-153T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16202733 | |||||||
chr4:16202770 | C | T | 40 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(37): Show |
56 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.331-190G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16202770 | |||||||
chr4:16202771 | G | A | 2 | a0001c0001t0009g0059 a0001c0001t0009g0060 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.331-191C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16202771 | |||||||
chr4:16202814 | T | C | 7 | a0001c0002t0005g0067 a0001c0002t0005g0155 a0001c0002t0005g0156 others(4): Show |
7 | HG01243.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.331-234A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16202814 | |||||||
chr4:16203051 | A | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.331-471T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16203051 | |||||||
chr4:16203206 | T | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(116): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.331-626A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16203206 | |||||||
chr4:16203345 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG01109.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.331-765G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16203345 | |||||||
chr4:16203475 | A | G | 19 | a0001c0001t0001g0128 a0001c0001t0004g0126 a0001c0001t0005g0018 others(16): Show |
23 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.331-895T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16203475 | |||||||
chr4:16203476 | T | C | 3 | a0001c0003t0008g0031 a0001c0003t0008g0139 a0001c0003t0023g0140 |
4 | HG02280.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-896A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16203476 | |||||||
chr4:16203648 | C | G | 1 | a0001c0002t0005g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.331-1068G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16203648 | |||||||
chr4:16203748 | T | C | 1 | a0001c0001t0003g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.331-1168A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16203748 | |||||||
chr4:16203804 | C | T | 1 | a0001c0001t0005g0136 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.331-1224G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16203804 | |||||||
chr4:16204122 | A | G | 12 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(9): Show |
13 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.331-1542T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16204122 | |||||||
chr4:16204124 | C | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(56): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.331-1544G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16204124 | |||||||
chr4:16204131 | G | A | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(56): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.331-1551C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16204131 | |||||||
chr4:16204248 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.331-1668G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16204248 | |||||||
chr4:16204458 | A | C | 1 | a0001c0001t0002g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.331-1878T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16204458 | |||||||
chr4:16204495 | T | C | 1 | a0001c0002t0005g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.331-1915A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16204495 | |||||||
chr4:16204647 | C | T | 41 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(38): Show |
57 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(54): Show |
intron_variant | MODIFIER | c.331-2067G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16204647 | |||||||
chr4:16204661 | G | A | 2 | a0004c0006t0015g0141 a0004c0006t0015g0165 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.331-2081C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16204661 | |||||||
chr4:16204674 | G | A | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.331-2094C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16204674 | |||||||
chr4:16204825 | T | A | 11 | a0001c0002t0005g0067 a0001c0002t0005g0153 a0001c0002t0005g0154 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.331-2245A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16204825 | |||||||
chr4:16204832 | C | T | 1 | a0001c0002t0010g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.331-2252G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16204832 | |||||||
chr4:16205010 | T | A | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.331-2430A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16205010 | |||||||
chr4:16205105 | T | TG | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.331-2526dupC | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16205105 | |||||||
chr4:16205449 | T | C | 15 | a0001c0001t0001g0128 a0001c0001t0004g0126 a0001c0001t0005g0018 others(12): Show |
19 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.331-2869A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16205449 | |||||||
chr4:16205479 | G | C | 58 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(55): Show |
78 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.331-2899C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16205479 | |||||||
chr4:16205529 | T | C | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(115): Show |
158 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.331-2949A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16205529 | |||||||
chr4:16205569 | T | C | 1 | a0001c0001t0002g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.331-2989A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16205569 | |||||||
chr4:16205959 | A | G | 1 | a0001c0001t0003g0099 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.331-3379T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16205959 | |||||||
chr4:16206049 | T | C | 5 | a0001c0001t0004g0034 a0001c0001t0004g0184 a0002c0004t0004g0020 others(2): Show |
8 | HG02451.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-3469A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206049 | |||||||
chr4:16206067 | C | T | 1 | a0001c0002t0010g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.331-3487G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206067 | |||||||
chr4:16206073 | T | A | 1 | a0001c0001t0003g0166 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.331-3493A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206073 | |||||||
chr4:16206182 | C | A | 60 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(57): Show |
80 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(77): Show |
intron_variant | MODIFIER | c.331-3602G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206182 | |||||||
chr4:16206343 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.331-3763C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206343 | |||||||
chr4:16206498 | G | A | 2 | a0001c0001t0009g0059 a0001c0001t0009g0060 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.331-3918C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206498 | |||||||
chr4:16206533 | T | C | 1 | a0001c0001t0001g0279 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.331-3953A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206533 | |||||||
chr4:16206556 | G | A | 1 | a0001c0001t0003g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.331-3976C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206556 | |||||||
chr4:16206663 | C | T | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.331-4083G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206663 | |||||||
chr4:16206780 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.331-4200A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206780 | |||||||
chr4:16206846 | A | G | 6 | a0001c0001t0003g0025 a0001c0001t0003g0094 a0001c0001t0003g0095 others(3): Show |
7 | HG01361.hp1 HG02602.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.331-4266T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206846 | |||||||
chr4:16206918 | C | T | 58 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(55): Show |
78 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.331-4338G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206918 | |||||||
chr4:16206943 | G | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.331-4363C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206943 | |||||||
chr4:16206948 | T | C | 13 | a0001c0002t0006g0013 a0001c0002t0006g0019 a0001c0002t0006g0047 others(10): Show |
19 | HG02015.hp2 HG02145.hp2 HG02723.hp1 others(16): Show |
intron_variant | MODIFIER | c.331-4368A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206948 | |||||||
chr4:16206960 | C | T | 12 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(9): Show |
13 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.331-4380G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16206960 | |||||||
chr4:16207018 | G | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.331-4438C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16207018 | |||||||
chr4:16207289 | T | A | 12 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(9): Show |
13 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.331-4709A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16207289 | |||||||
chr4:16207331 | A | G | 1 | a0001c0002t0006g0143 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.331-4751T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16207331 | |||||||
chr4:16207396 | G | T | 230 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(227): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.331-4816C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16207396 | |||||||
chr4:16207403 | G | A | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(109): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.331-4823C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16207403 | |||||||
chr4:16207430 | T | A | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(109): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.331-4850A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16207430 | |||||||
chr4:16207554 | T | G | 1 | a0001c0002t0005g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.331-4974A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16207554 | |||||||
chr4:16207569 | C | T | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.331-4989G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16207569 | |||||||
chr4:16207684 | T | C | 59 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(56): Show |
79 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(76): Show |
intron_variant | MODIFIER | c.331-5104A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16207684 | |||||||
chr4:16207843 | T | C | 1 | a0003c0005t0005g0051 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.331-5263A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16207843 | |||||||
chr4:16208093 | C | A | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(109): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.331-5513G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208093 | |||||||
chr4:16208222 | T | A | 1 | a0001c0002t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.330+5546A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208222 | |||||||
chr4:16208313 | C | T | 1 | a0001c0001t0001g0006 | 5 | NA18947.hp2 NA18956.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+5455G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208313 | |||||||
chr4:16208375 | A | T | 32 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0001g0186 others(29): Show |
40 | HG01081.hp2 HG01192.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.330+5393T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208375 | |||||||
chr4:16208392 | T | C | 1 | a0001c0001t0007g0082 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.330+5376A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208392 | |||||||
chr4:16208458 | C | T | 1 | a0001c0001t0004g0176 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.330+5310G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208458 | |||||||
chr4:16208459 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.330+5309C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208459 | |||||||
chr4:16208510 | T | C | 2 | a0001c0001t0002g0197 a0001c0001t0002g0228 |
2 | NA19002.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.330+5258A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208510 | |||||||
chr4:16208575 | C | T | 59 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(56): Show |
79 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(76): Show |
intron_variant | MODIFIER | c.330+5193G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208575 | |||||||
chr4:16208628 | T | C | 6 | a0001c0001t0005g0018 a0001c0001t0005g0131 a0001c0001t0005g0132 others(3): Show |
8 | HG00642.hp1 HG00733.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.330+5140A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208628 | |||||||
chr4:16208654 | G | GT | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(56): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.330+5113dupA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208654 | |||||||
chr4:16208700 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.330+5068G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208700 | |||||||
chr4:16208726 | C | T | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.330+5042G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208726 | |||||||
chr4:16208759 | C | A | 1 | a0001c0001t0024g0264 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.330+5009G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208759 | |||||||
chr4:16208770 | G | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.330+4998C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16208770 | |||||||
chr4:16209023 | C | A | 1 | a0001c0001t0002g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.330+4745G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16209023 | |||||||
chr4:16209136 | T | C | 5 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0121 others(2): Show |
7 | HG02015.hp1 HG02056.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.330+4632A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16209136 | |||||||
chr4:16209407 | T | C | 1 | a0001c0001t0002g0229 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.330+4361A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16209407 | |||||||
chr4:16209513 | C | A | 1 | a0001c0001t0004g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.330+4255G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16209513 | |||||||
chr4:16209602 | T | G | 1 | a0001c0002t0005g0153 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.330+4166A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16209602 | |||||||
chr4:16209637 | G | A | 1 | a0001c0003t0008g0005 | 5 | HG02257.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+4131C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16209637 | |||||||
chr4:16209680 | G | T | 1 | a0001c0001t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.330+4088C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16209680 | |||||||
chr4:16209709 | A | T | 169 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(166): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.330+4059T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16209709 | |||||||
chr4:16210048 | T | C | 60 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(57): Show |
80 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(77): Show |
intron_variant | MODIFIER | c.330+3720A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16210048 | |||||||
chr4:16210064 | T | C | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.330+3704A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16210064 | |||||||
chr4:16210173 | G | C | 5 | a0001c0001t0003g0015 a0001c0001t0003g0112 a0001c0001t0003g0113 others(2): Show |
7 | HG02040.hp2 NA18939.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3595C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16210173 | |||||||
chr4:16210300 | G | A | 4 | a0001c0003t0008g0003 a0001c0003t0008g0031 a0001c0003t0008g0139 others(1): Show |
10 | HG02280.hp1 HG02647.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.330+3468C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16210300 | |||||||
chr4:16210439 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.330+3329C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16210439 | |||||||
chr4:16210473 | TCTCA | T | 4 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0175 others(1): Show |
4 | HG01081.hp2 HG03704.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+3291_330+3294d others(6): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16210473 | |||||||
chr4:16210665 | G | C | 11 | a0001c0002t0005g0067 a0001c0002t0005g0153 a0001c0002t0005g0154 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.330+3103C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16210665 | |||||||
chr4:16210782 | A | C | 1 | a0001c0001t0001g0252 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.330+2986T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16210782 | |||||||
chr4:16210804 | T | C | 1 | a0001c0001t0001g0280 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.330+2964A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16210804 | |||||||
chr4:16211041 | GGTGT | G | 32 | a0001c0002t0005g0067 a0001c0002t0005g0152 a0001c0002t0005g0153 others(29): Show |
38 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.330+2723_330+2726d others(6): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211041 | |||||||
chr4:16211042 | GTGTT | G | 23 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(20): Show |
27 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.330+2722_330+2725d others(6): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211042 | |||||||
chr4:16211050 | T | C | 4 | a0003c0005t0005g0051 a0003c0005t0011g0049 a0003c0005t0011g0050 others(1): Show |
4 | HG01884.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+2718A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211050 | |||||||
chr4:16211079 | G | A | 15 | a0001c0001t0001g0128 a0001c0001t0004g0126 a0001c0001t0005g0018 others(12): Show |
19 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.330+2689C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211079 | |||||||
chr4:16211080 | A | T | 1 | a0001c0001t0001g0251 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.330+2688T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211080 | |||||||
chr4:16211098 | T | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.330+2670A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211098 | |||||||
chr4:16211228 | A | AC | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(117): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.330+2539_330+2540i others(3): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211228 | |||||||
chr4:16211263 | A | C | 11 | a0001c0002t0005g0067 a0001c0002t0005g0153 a0001c0002t0005g0154 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.330+2505T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211263 | |||||||
chr4:16211305 | G | C | 7 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0265 others(4): Show |
8 | HG00408.hp1 HG01258.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+2463C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211305 | |||||||
chr4:16211399 | T | G | 1 | a0001c0001t0009g0060 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.330+2369A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211399 | |||||||
chr4:16211454 | T | C | 1 | a0001c0002t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.330+2314A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211454 | |||||||
chr4:16211716 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0277 |
3 | HG00621.hp2 NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.330+2052C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211716 | |||||||
chr4:16211937 | C | T | 12 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(9): Show |
13 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.330+1831G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16211937 | |||||||
chr4:16212081 | C | T | 2 | a0004c0006t0015g0141 a0004c0006t0015g0165 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.330+1687G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16212081 | |||||||
chr4:16212249 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.330+1519T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16212249 | |||||||
chr4:16212382 | A | G | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(57): Show |
80 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.330+1386T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16212382 | |||||||
chr4:16212550 | G | A | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(57): Show |
80 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.330+1218C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16212550 | |||||||
chr4:16212575 | T | C | 121 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(118): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.330+1193A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16212575 | |||||||
chr4:16212582 | C | G | 2 | a0001c0001t0004g0189 a0001c0001t0004g0190 |
2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.330+1186G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16212582 | |||||||
chr4:16212630 | C | G | 41 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(38): Show |
57 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(54): Show |
intron_variant | MODIFIER | c.330+1138G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16212630 | |||||||
chr4:16212698 | C | T | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.330+1070G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16212698 | |||||||
chr4:16212843 | T | C | 1 | a0001c0001t0004g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.330+925A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16212843 | |||||||
chr4:16212858 | C | T | 1 | a0001c0001t0003g0015 | 3 | HG02040.hp2 NA18939.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.330+910G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16212858 | |||||||
chr4:16213028 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG02080.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.330+740C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16213028 | |||||||
chr4:16213041 | C | T | 1 | a0001c0002t0010g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.330+727G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16213041 | |||||||
chr4:16213164 | A | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG00408.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.330+604T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16213164 | |||||||
chr4:16213166 | C | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0239 others(11): Show |
21 | HG01978.hp2 HG02040.hp1 NA18939.hp1 others(18): Show |
intron_variant | MODIFIER | c.330+602G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16213166 | |||||||
chr4:16213331 | T | C | 60 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(57): Show |
80 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(77): Show |
intron_variant | MODIFIER | c.330+437A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16213331 | |||||||
chr4:16213345 | T | C | 1 | a0001c0002t0006g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.330+423A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16213345 | |||||||
chr4:16213359 | CAT | C | 12 | a0001c0002t0005g0067 a0001c0002t0005g0152 a0001c0002t0005g0153 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.330+407_330+408del others(2): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16213359 | |||||||
chr4:16213430 | GA | G | 12 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(9): Show |
13 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.330+337delT | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16213430 | |||||||
chr4:16213694 | G | A | 3 | a0001c0003t0008g0031 a0001c0003t0008g0139 a0001c0003t0023g0140 |
4 | HG02280.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+74C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 2/13 | chr4 | 16213694 | |||||||
chr4:16213914 | T | G | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.200-16A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16213914 | |||||||
chr4:16214142 | A | G | 1 | a0001c0001t0003g0117 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.200-244T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16214142 | |||||||
chr4:16214163 | G | C | 1 | a0001c0002t0005g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.200-265C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16214163 | |||||||
chr4:16214232 | T | C | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.200-334A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16214232 | |||||||
chr4:16214296 | A | G | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.200-398T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16214296 | |||||||
chr4:16214428 | C | G | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(57): Show |
80 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.200-530G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16214428 | |||||||
chr4:16214438 | A | C | 4 | a0003c0005t0005g0051 a0003c0005t0011g0049 a0003c0005t0011g0050 others(1): Show |
4 | HG01884.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-540T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16214438 | |||||||
chr4:16214514 | G | A | 1 | a0001c0002t0010g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.200-616C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16214514 | |||||||
chr4:16214525 | C | T | 1 | a0001c0001t0003g0090 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.200-627G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16214525 | |||||||
chr4:16214664 | C | A | 1 | a0001c0001t0005g0125 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.200-766G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16214664 | |||||||
chr4:16214993 | T | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(46): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.200-1095A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16214993 | |||||||
chr4:16215140 | A | C | 1 | a0001c0002t0006g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.200-1242T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16215140 | |||||||
chr4:16215164 | G | A | 12 | a0001c0002t0005g0067 a0001c0002t0005g0152 a0001c0002t0005g0153 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.200-1266C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16215164 | |||||||
chr4:16215206 | G | A | 2 | a0001c0002t0010g0055 a0001c0002t0010g0056 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.200-1308C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16215206 | |||||||
chr4:16215234 | T | G | 1 | a0001c0001t0012g0064 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.200-1336A>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16215234 | |||||||
chr4:16215247 | C | T | 11 | a0001c0002t0005g0067 a0001c0002t0005g0153 a0001c0002t0005g0154 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.200-1349G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16215247 | |||||||
chr4:16215308 | A | C | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.200-1410T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16215308 | |||||||
chr4:16215322 | C | A | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(111): Show |
144 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.200-1424G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16215322 | |||||||
chr4:16215486 | T | C | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.200-1588A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16215486 | |||||||
chr4:16215900 | A | G | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.200-2002T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16215900 | |||||||
chr4:16215995 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0270 a0001c0001t0002g0271 others(1): Show |
5 | NA18945.hp1 NA18955.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.200-2097C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16215995 | |||||||
chr4:16216004 | T | C | 50 | a0001c0001t0001g0281 a0001c0001t0003g0002 a0001c0001t0003g0004 others(47): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.200-2106A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16216004 | |||||||
chr4:16216519 | A | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(116): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.200-2621T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16216519 | |||||||
chr4:16216588 | T | C | 1 | a0001c0001t0003g0116 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.200-2690A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16216588 | |||||||
chr4:16216822 | C | G | 1 | a0001c0001t0005g0125 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.200-2924G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16216822 | |||||||
chr4:16216873 | G | A | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(56): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.200-2975C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16216873 | |||||||
chr4:16217101 | A | G | 1 | a0001c0002t0006g0142 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.200-3203T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217101 | |||||||
chr4:16217135 | C | T | 119 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(116): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.200-3237G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217135 | |||||||
chr4:16217153 | G | T | 4 | a0001c0002t0005g0068 a0001c0002t0005g0084 a0001c0002t0005g0085 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-3255C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217153 | |||||||
chr4:16217210 | C | T | 4 | a0001c0003t0008g0003 a0001c0003t0008g0031 a0001c0003t0008g0139 others(1): Show |
10 | HG02280.hp1 HG02647.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.200-3312G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217210 | |||||||
chr4:16217386 | T | C | 9 | a0001c0002t0005g0067 a0001c0002t0005g0154 a0001c0002t0005g0155 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.200-3488A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217386 | |||||||
chr4:16217418 | T | C | 32 | a0001c0002t0005g0067 a0001c0002t0005g0152 a0001c0002t0005g0153 others(29): Show |
38 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.200-3520A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217418 | |||||||
chr4:16217429 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.200-3531G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217429 | |||||||
chr4:16217512 | A | C | 1 | a0001c0001t0002g0198 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.200-3614T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217512 | |||||||
chr4:16217539 | T | A | 12 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(9): Show |
13 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.200-3641A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217539 | |||||||
chr4:16217589 | C | T | 3 | a0004c0006t0015g0141 a0004c0006t0015g0165 a0004c0006t0027g0151 |
3 | HG01109.hp2 HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.200-3691G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217589 | |||||||
chr4:16217593 | G | A | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(56): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.200-3695C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217593 | |||||||
chr4:16217610 | G | C | 15 | a0001c0002t0006g0013 a0001c0002t0006g0019 a0001c0002t0006g0047 others(12): Show |
21 | HG02015.hp2 HG02145.hp2 HG02723.hp1 others(18): Show |
intron_variant | MODIFIER | c.200-3712C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217610 | |||||||
chr4:16217851 | A | G | 1 | a0001c0002t0005g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.200-3953T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16217851 | |||||||
chr4:16218034 | C | A | 1 | a0001c0001t0004g0188 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.200-4136G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16218034 | |||||||
chr4:16218145 | G | A | 1 | a0001c0001t0005g0136 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.200-4247C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16218145 | |||||||
chr4:16218471 | C | G | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.200-4573G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16218471 | |||||||
chr4:16218630 | G | A | 1 | a0001c0001t0007g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.200-4732C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16218630 | |||||||
chr4:16218785 | A | G | 1 | a0001c0001t0005g0018 | 3 | HG01106.hp2 HG01346.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.200-4887T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16218785 | |||||||
chr4:16218794 | T | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(56): Show |
79 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.200-4896A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16218794 | |||||||
chr4:16218857 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.200-4959T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16218857 | |||||||
chr4:16219092 | C | T | 4 | a0001c0002t0006g0013 a0001c0002t0006g0047 a0001c0002t0006g0272 others(1): Show |
8 | HG02145.hp2 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-5194G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219092 | |||||||
chr4:16219222 | A | T | 199 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(196): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.200-5324T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219222 | |||||||
chr4:16219328 | CTTT | C | 36 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(33): Show |
42 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.200-5433_200-5431d others(5): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219328 | |||||||
chr4:16219424 | G | C | 15 | a0001c0001t0001g0128 a0001c0001t0004g0126 a0001c0001t0005g0018 others(12): Show |
19 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.200-5526C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219424 | |||||||
chr4:16219447 | C | T | 3 | a0004c0006t0015g0141 a0004c0006t0015g0165 a0004c0006t0027g0151 |
3 | HG01109.hp2 HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.200-5549G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219447 | |||||||
chr4:16219495 | G | A | 36 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(33): Show |
42 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.200-5597C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219495 | |||||||
chr4:16219512 | C | T | 2 | a0004c0006t0015g0141 a0004c0006t0015g0165 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.200-5614G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219512 | |||||||
chr4:16219552 | A | G | 2 | a0001c0001t0009g0059 a0001c0001t0009g0060 |
2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.200-5654T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219552 | |||||||
chr4:16219573 | G | C | 4 | a0003c0005t0005g0051 a0003c0005t0011g0049 a0003c0005t0011g0050 others(1): Show |
4 | HG01884.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-5675C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219573 | |||||||
chr4:16219678 | A | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(76): Show |
103 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.200-5780T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219678 | |||||||
chr4:16219760 | T | C | 10 | a0001c0001t0003g0008 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
15 | HG00621.hp1 HG02015.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.200-5862A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219760 | |||||||
chr4:16219811 | G | A | 1 | a0001c0001t0009g0060 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.200-5913C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219811 | |||||||
chr4:16219889 | C | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG02040.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.200-5991G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219889 | |||||||
chr4:16219989 | G | A | 4 | a0001c0002t0005g0068 a0001c0002t0005g0084 a0001c0002t0005g0085 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-6091C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16219989 | |||||||
chr4:16220000 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.200-6102C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220000 | |||||||
chr4:16220083 | G | A | 1 | a0001c0002t0006g0275 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.199+6176C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220083 | |||||||
chr4:16220095 | C | T | 7 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0169 others(4): Show |
9 | HG02145.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.199+6164G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220095 | |||||||
chr4:16220168 | T | A | 8 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(5): Show |
9 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.199+6091A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220168 | |||||||
chr4:16220198 | G | C | 1 | a0004c0006t0027g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.199+6061C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220198 | |||||||
chr4:16220224 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.199+6035A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220224 | |||||||
chr4:16220423 | A | C | 32 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(29): Show |
34 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.199+5836T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220423 | |||||||
chr4:16220680 | C | T | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.199+5579G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220680 | |||||||
chr4:16220742 | T | C | 54 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(51): Show |
86 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.199+5517A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220742 | |||||||
chr4:16220747 | C | CA | 15 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0002t0005g0067 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.199+5511dupT | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220747 | |||||||
chr4:16220906 | G | A | 4 | a0001c0001t0004g0168 a0001c0001t0004g0189 a0001c0001t0004g0190 others(1): Show |
4 | HG02717.hp1 HG02895.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+5353C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220906 | |||||||
chr4:16220916 | T | C | 4 | a0001c0001t0002g0021 a0001c0001t0002g0037 a0001c0001t0002g0232 others(1): Show |
7 | HG00597.hp2 HG02056.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.199+5343A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220916 | |||||||
chr4:16220972 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.199+5287T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16220972 | |||||||
chr4:16221101 | C | T | 32 | a0001c0002t0005g0067 a0001c0002t0005g0068 a0001c0002t0005g0084 others(29): Show |
34 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.199+5158G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221101 | |||||||
chr4:16221120 | A | ATAC | 4 | a0001c0002t0005g0068 a0001c0002t0005g0084 a0001c0002t0005g0085 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+5138_199+5139i others(5): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221120 | |||||||
chr4:16221121 | C | CT | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(113): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.199+5137dupA | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221121 | |||||||
chr4:16221121 | C | T | 4 | a0001c0002t0005g0068 a0001c0002t0005g0084 a0001c0002t0005g0085 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+5138G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221121 | |||||||
chr4:16221184 | G | A | 1 | a0001c0002t0005g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199+5075C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221184 | |||||||
chr4:16221190 | G | A | 5 | a0001c0001t0001g0237 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | NA18946.hp2 NA18986.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+5069C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221190 | |||||||
chr4:16221204 | T | A | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(61): Show |
88 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.199+5055A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221204 | |||||||
chr4:16221329 | T | A | 1 | a0001c0001t0002g0234 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.199+4930A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221329 | |||||||
chr4:16221405 | A | C | 169 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(166): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.199+4854T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221405 | |||||||
chr4:16221463 | C | T | 1 | a0001c0001t0002g0197 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.199+4796G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221463 | |||||||
chr4:16221508 | T | C | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.199+4751A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221508 | |||||||
chr4:16221607 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.199+4652T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221607 | |||||||
chr4:16221831 | G | C | 1 | a0001c0001t0003g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.199+4428C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16221831 | |||||||
chr4:16222056 | A | T | 1 | a0001c0001t0002g0196 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.199+4203T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222056 | |||||||
chr4:16222138 | T | C | 1 | a0001c0001t0003g0028 | 2 | NA19077.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.199+4121A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222138 | |||||||
chr4:16222296 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.199+3963A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222296 | |||||||
chr4:16222473 | A | G | 5 | a0001c0003t0008g0003 a0001c0003t0008g0005 a0001c0003t0008g0031 others(2): Show |
15 | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.199+3786T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222473 | |||||||
chr4:16222571 | C | T | 1 | a0001c0002t0006g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.199+3688G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222571 | |||||||
chr4:16222619 | G | A | 200 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(197): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.199+3640C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222619 | |||||||
chr4:16222665 | C | T | 1 | a0001c0002t0005g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.199+3594G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222665 | |||||||
chr4:16222776 | T | C | 12 | a0001c0002t0005g0067 a0001c0002t0005g0152 a0001c0002t0005g0153 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.199+3483A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222776 | |||||||
chr4:16222790 | G | C | 1 | a0001c0001t0002g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.199+3469C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222790 | |||||||
chr4:16222810 | G | C | 1 | a0001c0010t0005g0054 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.199+3449C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222810 | |||||||
chr4:16222815 | GGAT | G | 15 | a0001c0001t0001g0128 a0001c0001t0004g0126 a0001c0001t0005g0018 others(12): Show |
19 | HG00642.hp1 HG00733.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.199+3441_199+3443d others(5): Show |
TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222815 | |||||||
chr4:16222835 | A | G | 1 | a0001c0001t0003g0088 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.199+3424T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16222835 | |||||||
chr4:16223008 | C | T | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.199+3251G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223008 | |||||||
chr4:16223048 | A | G | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.199+3211T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223048 | |||||||
chr4:16223103 | A | G | 1 | a0001c0001t0004g0168 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.199+3156T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223103 | |||||||
chr4:16223115 | A | G | 19 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(16): Show |
23 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.199+3144T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223115 | |||||||
chr4:16223178 | C | T | 1 | a0001c0002t0006g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.199+3081G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223178 | |||||||
chr4:16223244 | A | G | 1 | a0001c0001t0009g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.199+3015T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223244 | |||||||
chr4:16223253 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.199+3006A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223253 | |||||||
chr4:16223284 | C | G | 54 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(51): Show |
70 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.199+2975G>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223284 | |||||||
chr4:16223522 | A | C | 1 | a0001c0002t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.199+2737T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223522 | |||||||
chr4:16223574 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.199+2685G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223574 | |||||||
chr4:16223588 | G | T | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(117): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.199+2671C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223588 | |||||||
chr4:16223596 | A | G | 1 | a0001c0001t0004g0032 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.199+2663T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223596 | |||||||
chr4:16223829 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.199+2430C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223829 | |||||||
chr4:16223831 | T | C | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(61): Show |
88 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.199+2428A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223831 | |||||||
chr4:16223910 | G | A | 1 | a0001c0001t0009g0065 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.199+2349C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223910 | |||||||
chr4:16223931 | A | G | 1 | a0001c0001t0009g0058 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.199+2328T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16223931 | |||||||
chr4:16224047 | A | C | 1 | a0001c0001t0025g0195 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.199+2212T>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16224047 | |||||||
chr4:16224062 | A | G | 27 | a0001c0001t0001g0087 a0001c0001t0007g0014 a0001c0001t0007g0023 others(24): Show |
31 | HG00323.hp1 HG01074.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.199+2197T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16224062 | |||||||
chr4:16224088 | A | T | 1 | a0001c0001t0002g0194 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.199+2171T>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16224088 | |||||||
chr4:16224176 | C | T | 199 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(196): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.199+2083G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16224176 | |||||||
chr4:16224481 | G | A | 1 | a0001c0001t0004g0192 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.199+1778C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16224481 | |||||||
chr4:16224675 | A | G | 88 | a0001c0001t0001g0087 a0001c0001t0001g0128 a0001c0001t0003g0002 others(85): Show |
118 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.199+1584T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16224675 | |||||||
chr4:16224865 | C | T | 1 | a0001c0001t0004g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.199+1394G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16224865 | |||||||
chr4:16224976 | C | T | 1 | a0001c0002t0005g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.199+1283G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16224976 | |||||||
chr4:16225070 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.199+1189A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16225070 | |||||||
chr4:16225167 | T | C | 1 | a0001c0002t0005g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199+1092A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16225167 | |||||||
chr4:16225190 | C | CA | 12 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(9): Show |
13 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.199+1068dupT | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16225190 | |||||||
chr4:16225239 | G | T | 12 | a0001c0001t0009g0022 a0001c0001t0009g0057 a0001c0001t0009g0058 others(9): Show |
13 | HG01099.hp2 HG01106.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.199+1020C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16225239 | |||||||
chr4:16225256 | T | A | 1 | a0001c0001t0018g0283 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.199+1003A>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16225256 | |||||||
chr4:16225434 | T | C | 1 | a0001c0001t0009g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.199+825A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16225434 | |||||||
chr4:16225809 | T | C | 1 | a0004c0006t0015g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.199+450A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16225809 | |||||||
chr4:16225813 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.199+446C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16225813 | |||||||
chr4:16225971 | A | G | 200 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(197): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.199+288T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16225971 | |||||||
chr4:16226019 | C | T | 2 | a0001c0002t0010g0055 a0001c0002t0010g0056 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.199+240G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16226019 | |||||||
chr4:16226025 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.199+234A>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16226025 | |||||||
chr4:16226059 | G | C | 1 | a0001c0001t0004g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.199+200C>G | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16226059 | |||||||
chr4:16226059 | G | T | 1 | a0001c0010t0005g0054 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.199+200C>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16226059 | |||||||
chr4:16226156 | G | A | 1 | a0001c0001t0002g0236 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.199+103C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16226156 | |||||||
chr4:16226157 | C | A | 1 | a0001c0001t0002g0236 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.199+102G>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16226157 | |||||||
chr4:16226158 | A | G | 232 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(229): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.199+101T>C | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16226158 | |||||||
chr4:16226161 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.199+98G>A | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16226161 | |||||||
chr4:16226200 | G | A | 62 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(59): Show |
86 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.199+59C>T | TAPT1 | ENSG00000169762.17 | transcript | ENST00000405303.7 | protein_coding | 1/13 | chr4 | 16226200 |