Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9747 |
| ensemblid | ENSG00000198420.10 |
| hgncid | 22201 |
| symbol | TCAF1 |
| name | TRPM8 channel associated factor 1 |
| refseq_nuc | NM_014719.3 |
| refseq_prot | NP_055534.2 |
| ensembl_nuc | ENST00000479870.6 |
| ensembl_prot | ENSP00000419235.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 143851375 |
| end | 143902176 |
| strand | - |
| ver | v1.2 |
| region | chr7:143851375-143902176 |
| region5000 | chr7:143846375-143907176 |
| regionname0 | TCAF1_chr7_143851375_143902176 |
| regionname5000 | TCAF1_chr7_143846375_143907176 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 921 | 240 | 59 | 43 | 118 | 9 | 10 | 94 | TCAF1_chr7_143846375_143907176 | TCAF1 | MATPS others(916): Show |
chr7 | 143846375 | 143907176 |
| a0002 | 1/0 | 921 | 7 | 5 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | MATPS others(916): Show |
chr7 | 143846375 | 143907176 |
| a0003 | 0/0 | 921 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | MATPS others(916): Show |
chr7 | 143846375 | 143907176 |
| a0004 | 0/0 | 921 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | MATPS others(916): Show |
chr7 | 143846375 | 143907176 |
| a0005 | 0/0 | 921 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | MATPS others(916): Show |
chr7 | 143846375 | 143907176 |
| a0006 | 0/0 | 921 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | MATPS others(916): Show |
chr7 | 143846375 | 143907176 |
| a0007 | 0/0 | 921 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | MATPS others(916): Show |
chr7 | 143846375 | 143907176 |
| a0008 | 0/0 | 921 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | MATPS others(916): Show |
chr7 | 143846375 | 143907176 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2763 | 131 | 36 | 33 | 48 | 7 | 6 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0001c0002 | 0/0 | 2763 | 40 | 14 | 4 | 19 | 1 | 2 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0001c0003 | 0/0 | 2763 | 33 | 4 | 3 | 26 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0001c0004 | 0/0 | 2763 | 32 | 3 | 3 | 23 | 1 | 2 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0001c0006 | 0/0 | 2763 | 3 | 2 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0001c0014 | 0/0 | 2763 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0002c0007 | 1/0 | 2763 | 3 | 2 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0002c0008 | 0/0 | 2763 | 2 | 2 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0002c0015 | 0/0 | 2763 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0002c0016 | 0/0 | 2763 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0003c0005 | 0/0 | 2763 | 4 | 4 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0004c0012 | 0/0 | 2763 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0005c0011 | 0/0 | 2763 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0006c0013 | 0/0 | 2763 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0007c0009 | 0/0 | 2763 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 | ||
| a0008c0010 | 0/0 | 2763 | 1 | 0 | 0 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | ATGGC others(2758): Show |
chr7 | 143846375 | 143907176 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5754 | 58 | 9 | 18 | 26 | 2 | 3 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0003 | 0/0 | 5754 | 17 | 15 | 2 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0004 | 0/1 | 5754 | 12 | 1 | 2 | 6 | 0 | 2 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0005 | 0/0 | 5754 | 11 | 0 | 3 | 7 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0007 | 0/0 | 5754 | 3 | 0 | 2 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0008 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0009 | 0/0 | 5754 | 7 | 1 | 1 | 4 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0011 | 0/0 | 5754 | 6 | 0 | 2 | 3 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0012 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0014 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0018 | 0/0 | 5754 | 2 | 1 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0022 | 0/0 | 5754 | 2 | 0 | 0 | 0 | 2 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0025 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0026 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0027 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0028 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0030 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0032 | 0/0 | 5754 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0035 | 0/0 | 5754 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0036 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0038 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0001t0040 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0002 | 0/0 | 5754 | 13 | 0 | 0 | 13 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0006 | 0/0 | 5754 | 7 | 5 | 1 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0007 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0008 | 0/0 | 5754 | 2 | 1 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0009 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0010 | 0/0 | 5754 | 4 | 0 | 3 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0013 | 0/0 | 5754 | 3 | 3 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0014 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0015 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0017 | 0/0 | 5754 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0019 | 0/0 | 5754 | 2 | 2 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0021 | 0/0 | 5754 | 2 | 0 | 0 | 2 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0024 | 0/0 | 5754 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0002t0039 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0003t0002 | 0/0 | 5754 | 13 | 0 | 0 | 13 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0003t0006 | 0/0 | 5754 | 3 | 2 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0003t0007 | 0/0 | 5754 | 7 | 0 | 0 | 7 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0003t0008 | 0/0 | 5754 | 3 | 0 | 0 | 3 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0003t0010 | 0/0 | 5754 | 2 | 0 | 1 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0003t0013 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0003t0015 | 0/0 | 5754 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0003t0017 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0003t0020 | 0/0 | 5754 | 2 | 1 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0001 | 0/0 | 5754 | 6 | 0 | 0 | 6 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0002 | 0/0 | 5754 | 2 | 0 | 0 | 2 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0003 | 0/0 | 5754 | 4 | 3 | 0 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0004 | 0/0 | 5754 | 9 | 0 | 0 | 8 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0005 | 0/0 | 5754 | 2 | 0 | 1 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0007 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0009 | 0/0 | 5754 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0012 | 0/0 | 5754 | 3 | 0 | 1 | 2 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0023 | 0/0 | 5754 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0031 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0033 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0004t0034 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0006t0003 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0006t0008 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0006t0016 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0001c0014t0029 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0002c0007t0003 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0002c0007t0037 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0002c0007t0041 | 1/0 | 5754 | 1 | 0 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0002c0008t0006 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0002c0008t0014 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0002c0015t0006 | 0/0 | 5754 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0002c0016t0003 | 0/0 | 5754 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0003c0005t0008 | 0/0 | 5754 | 4 | 4 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0004c0012t0001 | 0/0 | 5754 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0005c0011t0001 | 0/0 | 5754 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0006c0013t0016 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0007c0009t0005 | 0/0 | 5754 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| a0008c0010t0001 | 0/0 | 5754 | 1 | 0 | 0 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | GCCTA others(5749): Show |
chr7 | 143846375 | 143907176 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0004g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0005g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0007g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0008g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0009g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0009g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0009g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0011g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0011g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0011g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0011g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0011g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0012g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0018g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0022g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0025g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0026g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0027g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0028g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0030g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0032g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0035g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0036g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0038g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0001t0040g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0006g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0010g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0010g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0010g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0013g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0015g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0017g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0019g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0019g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0021g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0021g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0024g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0002t0039g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0006g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0007g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0008g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0010g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0013g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0015g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0017g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0020g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0003t0020g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0007g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0009g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0012g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0012g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0012g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0023g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0031g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0033g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0004t0034g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0006t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0006t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0006t0016g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0001c0014t0029g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0002c0007t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0002c0007t0037g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0002c0007t0041g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0002c0008t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0002c0008t0014g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0002c0015t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0002c0016t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0003c0005t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0003c0005t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0003c0005t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0003c0005t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0004c0012t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0005c0011t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0006c0013t0016g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0007c0009t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| a0008c0010t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00140 | hp2 | a0001 | c0004 | t0003 | g0074 | EUR | GBR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | CHS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | CHS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0088 | EAS | CHS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00438 | hp2 | a0001 | c0003 | t0002 | g0039 | EAS | CHS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00544 | hp1 | a0001 | c0004 | t0004 | g0151 | EAS | CHS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | CHS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00597 | hp1 | a0001 | c0004 | t0031 | g0087 | EAS | CHS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0178 | EAS | CHS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00609 | hp2 | a0001 | c0002 | t0010 | g0042 | EAS | CHS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00642 | hp1 | a0001 | c0004 | t0012 | g0047 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00642 | hp2 | a0004 | c0012 | t0001 | g0240 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00733 | hp1 | a0001 | c0001 | t0011 | g0092 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00735 | hp1 | a0001 | c0004 | t0005 | g0085 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00735 | hp2 | a0001 | c0001 | t0018 | g0004 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00741 | hp1 | a0001 | c0002 | t0006 | g0096 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01071 | hp1 | a0001 | c0002 | t0010 | g0002 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01081 | hp1 | a0001 | c0002 | t0010 | g0002 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01081 | hp2 | a0005 | c0011 | t0001 | g0233 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01109 | hp1 | a0001 | c0002 | t0010 | g0025 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01109 | hp2 | a0002 | c0016 | t0003 | g0055 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0134 | AMR | PUR | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01255 | hp1 | a0001 | c0001 | t0035 | g0140 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01255 | hp2 | a0001 | c0001 | t0011 | g0093 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0127 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01358 | hp1 | a0001 | c0003 | t0010 | g0024 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01358 | hp2 | a0001 | c0001 | t0032 | g0091 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01433 | hp1 | a0001 | c0003 | t0006 | g0101 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01496 | hp2 | a0001 | c0004 | t0009 | g0141 | AMR | CLM | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0232 | EUR | IBS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01515 | hp2 | a0001 | c0001 | t0022 | g0012 | EUR | IBS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01517 | hp1 | a0001 | c0001 | t0022 | g0012 | EUR | IBS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01884 | hp2 | a0001 | c0002 | t0013 | g0003 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0225 | AMR | PEL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0090 | AMR | PEL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG01952 | hp2 | a0001 | c0003 | t0015 | g0105 | AMR | PEL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0203 | AMR | PEL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02071 | hp1 | a0001 | c0003 | t0017 | g0064 | EAS | KHV | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | KHV | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0089 | EAS | KHV | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | KHV | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | KHV | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02132 | hp1 | a0001 | c0003 | t0020 | g0126 | EAS | KHV | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02132 | hp2 | a0001 | c0004 | t0001 | g0186 | EAS | KHV | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02135 | hp1 | a0001 | c0004 | t0001 | g0184 | EAS | KHV | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02135 | hp2 | a0001 | c0001 | t0012 | g0027 | EAS | KHV | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02145 | hp1 | a0001 | c0001 | t0036 | g0153 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0036 | EAS | CDX | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02155 | hp2 | a0001 | c0004 | t0004 | g0150 | EAS | CDX | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0086 | EAS | CDX | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02165 | hp2 | a0001 | c0004 | t0012 | g0048 | EAS | CDX | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02257 | hp1 | a0001 | c0002 | t0006 | g0112 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02280 | hp2 | a0001 | c0001 | t0040 | g0229 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02615 | hp2 | a0002 | c0015 | t0006 | g0099 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02647 | hp1 | a0001 | c0001 | t0027 | g0050 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02647 | hp2 | a0001 | c0003 | t0013 | g0098 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0109 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02886 | hp1 | a0001 | c0002 | t0019 | g0129 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02886 | hp2 | a0001 | c0002 | t0006 | g0116 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02895 | hp1 | a0001 | c0001 | t0038 | g0217 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02895 | hp2 | a0001 | c0004 | t0003 | g0008 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02897 | hp1 | a0001 | c0004 | t0003 | g0008 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02922 | hp1 | a0001 | c0002 | t0008 | g0120 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02970 | hp2 | a0001 | c0002 | t0019 | g0161 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02976 | hp1 | a0001 | c0001 | t0028 | g0060 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03041 | hp2 | a0001 | c0004 | t0003 | g0110 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03098 | hp1 | a0001 | c0002 | t0006 | g0114 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03098 | hp2 | a0002 | c0007 | t0037 | g0181 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03130 | hp1 | a0001 | c0002 | t0014 | g0149 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03139 | hp2 | a0003 | c0005 | t0008 | g0052 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03195 | hp2 | a0003 | c0005 | t0008 | g0053 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03209 | hp2 | a0001 | c0002 | t0013 | g0003 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03225 | hp1 | a0003 | c0005 | t0008 | g0056 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03225 | hp2 | a0001 | c0002 | t0013 | g0113 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03486 | hp1 | a0001 | c0001 | t0030 | g0115 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03486 | hp2 | a0003 | c0005 | t0008 | g0054 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0154 | SAS | PJL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0143 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03540 | hp1 | a0001 | c0002 | t0006 | g0094 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03688 | hp1 | a0001 | c0002 | t0024 | g0084 | SAS | STU | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0078 | SAS | BEB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0148 | SAS | BEB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03942 | hp1 | a0001 | c0004 | t0004 | g0130 | SAS | BEB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03942 | hp2 | a0001 | c0004 | t0023 | g0049 | SAS | BEB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG04115 | hp2 | a0001 | c0002 | t0017 | g0077 | SAS | STU | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0032 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18943 | hp2 | a0001 | c0004 | t0004 | g0131 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0021 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18952 | hp1 | a0001 | c0004 | t0002 | g0031 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18957 | hp1 | a0001 | c0004 | t0001 | g0197 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18960 | hp1 | a0001 | c0003 | t0002 | g0030 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18960 | hp2 | a0001 | c0004 | t0012 | g0046 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18961 | hp1 | a0001 | c0003 | t0008 | g0121 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18966 | hp1 | a0001 | c0001 | t0009 | g0138 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18966 | hp2 | a0001 | c0001 | t0011 | g0069 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18968 | hp1 | a0001 | c0003 | t0007 | g0195 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18968 | hp2 | a0001 | c0004 | t0004 | g0163 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18979 | hp1 | a0001 | c0003 | t0007 | g0177 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18980 | hp1 | a0001 | c0001 | t0009 | g0144 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18980 | hp2 | a0006 | c0013 | t0016 | g0081 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18983 | hp1 | a0001 | c0003 | t0007 | g0239 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18985 | hp1 | a0001 | c0003 | t0002 | g0015 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18986 | hp1 | a0001 | c0003 | t0010 | g0043 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18986 | hp2 | a0001 | c0003 | t0008 | g0066 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18987 | hp2 | a0001 | c0006 | t0016 | g0122 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18988 | hp1 | a0001 | c0003 | t0002 | g0044 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18988 | hp2 | a0001 | c0003 | t0002 | g0045 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18989 | hp1 | a0001 | c0002 | t0008 | g0067 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18990 | hp1 | a0001 | c0001 | t0011 | g0070 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18990 | hp2 | a0001 | c0003 | t0002 | g0033 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18991 | hp2 | a0001 | c0001 | t0009 | g0158 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18993 | hp1 | a0001 | c0003 | t0007 | g0205 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18993 | hp2 | a0001 | c0004 | t0004 | g0147 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18995 | hp1 | a0001 | c0003 | t0002 | g0029 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0037 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19000 | hp1 | a0001 | c0002 | t0021 | g0173 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19000 | hp2 | a0001 | c0004 | t0004 | g0136 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19001 | hp1 | a0001 | c0003 | t0007 | g0202 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19001 | hp2 | a0001 | c0014 | t0029 | g0082 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19002 | hp1 | a0001 | c0002 | t0021 | g0193 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19002 | hp2 | a0001 | c0001 | t0009 | g0159 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19006 | hp1 | a0001 | c0002 | t0007 | g0190 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19006 | hp2 | a0001 | c0001 | t0011 | g0119 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19007 | hp2 | a0001 | c0004 | t0034 | g0142 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19009 | hp1 | a0001 | c0003 | t0008 | g0068 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19030 | hp1 | a0001 | c0006 | t0003 | g0057 | AFR | LWK | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | LWK | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19056 | hp1 | a0001 | c0004 | t0004 | g0155 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19056 | hp2 | a0001 | c0004 | t0001 | g0169 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19057 | hp1 | a0001 | c0003 | t0007 | g0182 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19057 | hp2 | a0001 | c0004 | t0004 | g0157 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19060 | hp1 | a0001 | c0001 | t0026 | g0079 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19064 | hp1 | a0001 | c0003 | t0002 | g0035 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19064 | hp2 | a0001 | c0004 | t0007 | g0191 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19068 | hp1 | a0001 | c0004 | t0005 | g0073 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19080 | hp1 | a0001 | c0004 | t0002 | g0014 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19080 | hp2 | a0001 | c0003 | t0007 | g0174 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19081 | hp1 | a0001 | c0002 | t0009 | g0132 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19083 | hp1 | a0007 | c0009 | t0005 | g0104 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19085 | hp2 | a0001 | c0004 | t0033 | g0146 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19086 | hp1 | a0001 | c0004 | t0001 | g0222 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19086 | hp2 | a0001 | c0003 | t0002 | g0034 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA20129 | hp1 | a0002 | c0008 | t0006 | g0095 | AFR | ASW | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA20129 | hp2 | a0001 | c0006 | t0008 | g0051 | AFR | ASW | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA20752 | hp1 | a0008 | c0010 | t0001 | g0241 | EUR | TSI | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA20752 | hp2 | a0001 | c0001 | t0009 | g0162 | EUR | TSI | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA20805 | hp1 | a0001 | c0001 | t0011 | g0100 | EUR | TSI | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA20805 | hp2 | a0001 | c0002 | t0006 | g0097 | EUR | TSI | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02109 | hp1 | a0001 | c0003 | t0006 | g0007 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02109 | hp2 | a0001 | c0001 | t0018 | g0004 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG02486 | hp2 | a0001 | c0001 | t0025 | g0124 | AFR | ACB | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03471 | hp1 | a0002 | c0007 | t0003 | g0102 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG03471 | hp2 | a0001 | c0002 | t0039 | g0242 | AFR | MSL | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG06807 | hp1 | a0002 | c0008 | t0014 | g0166 | AFR | USA | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| HG06807 | hp2 | a0001 | c0003 | t0006 | g0007 | AFR | USA | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA20300 | hp1 | a0001 | c0002 | t0015 | g0106 | AFR | USA | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | USA | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA21309 | hp1 | a0001 | c0003 | t0020 | g0165 | AFR | LWK | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| NA21309 | hp2 | a0001 | c0002 | t0006 | g0072 | AFR | LWK | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0164 | REF | REF | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| homoSapiens | grch38p0 | a0002 | c0007 | t0041 | g0221 | REF | REF | TCAF1_chr7_143846375_143907176 | TCAF1 | chr7 | 143846375 | 143907176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:143861125 | C | T | 1 | a0006 | 1 | NA18980.hp2 | missense_variant | MODERATE | c.1897G>A | p.Gly633Arg | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 5/9 | 2127/5754 | 1897/2766 | 633/921 | chr7 | 143861125 | |||
| chr7:143862804 | G | A | 1 | a0003 | 4 | HG03139.hp2 HG03195.hp2 HG03225.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1613C>T | p.Pro538Leu | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 3/9 | 1843/5754 | 1613/2766 | 538/921 | chr7 | 143862804 | |||
| chr7:143862823 | C | T | 1 | a0004 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.1594G>A | p.Glu532Lys | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 3/9 | 1824/5754 | 1594/2766 | 532/921 | chr7 | 143862823 | |||
| chr7:143863516 | C | T | 7 | a0001 a0003 a0004 others(4): Show |
248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
missense_variant | MODERATE | c.901G>A | p.Val301Ile | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 3/9 | 1131/5754 | 901/2766 | 301/921 | chr7 | 143863516 | |||
| chr7:143863527 | C | T | 1 | a0005 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.890G>A | p.Arg297His | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 3/9 | 1120/5754 | 890/2766 | 297/921 | chr7 | 143863527 | |||
| chr7:143863716 | A | T | 1 | a0008 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.701T>A | p.Phe234Tyr | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 3/9 | 931/5754 | 701/2766 | 234/921 | chr7 | 143863716 | |||
| chr7:143876170 | C | T | 1 | a0007 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.439G>A | p.Gly147Ser | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/9 | 669/5754 | 439/2766 | 147/921 | chr7 | 143876170 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:143859109 | C | T | 4 | a0001c0002 a0001c0003 a0002c0008 others(1): Show |
76 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(73): Show |
synonymous_variant | LOW | c.2220G>A | p.Glu740Glu | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/9 | 2450/5754 | 2220/2766 | 740/921 | chr7 | 143859109 | |||
| chr7:143861285 | A | G | 4 | a0001c0006 a0001c0014 a0006c0013 others(1): Show |
6 | NA18980.hp2 NA18987.hp2 NA19001.hp2 others(3): Show |
synonymous_variant | LOW | c.1737T>C | p.Asp579Asp | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 5/9 | 1967/5754 | 1737/2766 | 579/921 | chr7 | 143861285 | |||
| chr7:143863472 | T | G | 5 | a0001c0003 a0001c0004 a0001c0014 others(2): Show |
68 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(65): Show |
synonymous_variant | LOW | c.945A>C | p.Ala315Ala | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 3/9 | 1175/5754 | 945/2766 | 315/921 | chr7 | 143863472 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:143851481 | C | T | 1 | a0001c0001t0032 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2652G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 2652 | chr7 | 143851481 | ||||||
| chr7:143851483 | C | T | 1 | a0001c0001t0038 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2650G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 2650 | chr7 | 143851483 | ||||||
| chr7:143851759 | C | T | 3 | a0001c0001t0014 a0001c0002t0014 a0002c0008t0014 |
3 | HG03130.hp1 HG03516.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2374G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 2374 | chr7 | 143851759 | ||||||
| chr7:143851809 | C | T | 3 | a0001c0001t0014 a0001c0002t0014 a0002c0008t0014 |
3 | HG03130.hp1 HG03516.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2324G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 2324 | chr7 | 143851809 | ||||||
| chr7:143851819 | A | G | 1 | a0002c0007t0037 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2314T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 2314 | chr7 | 143851819 | ||||||
| chr7:143851970 | T | C | 1 | a0001c0001t0027 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2163A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 2163 | chr7 | 143851970 | ||||||
| chr7:143852110 | C | G | 15 | a0001c0002t0006 a0001c0002t0010 a0001c0002t0013 others(12): Show |
32 | HG00609.hp2 HG00741.hp1 HG01071.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2023G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 2023 | chr7 | 143852110 | ||||||
| chr7:143852257 | A | G | 8 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0032 others(5): Show |
19 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1876T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 1876 | chr7 | 143852257 | ||||||
| chr7:143852425 | C | T | 1 | a0001c0001t0025 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1708G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 1708 | chr7 | 143852425 | ||||||
| chr7:143852564 | G | C | 2 | a0001c0002t0015 a0001c0003t0015 |
2 | HG01952.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1569C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 1569 | chr7 | 143852564 | ||||||
| chr7:143852603 | T | A | 1 | a0001c0001t0030 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1530A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 1530 | chr7 | 143852603 | ||||||
| chr7:143852688 | T | G | 1 | a0001c0001t0028 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1445A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 1445 | chr7 | 143852688 | ||||||
| chr7:143852748 | T | C | 1 | a0001c0004t0033 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1385A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 1385 | chr7 | 143852748 | ||||||
| chr7:143852910 | C | G | 5 | a0001c0001t0030 a0001c0004t0031 a0001c0006t0016 others(2): Show |
5 | HG00597.hp1 HG03486.hp1 NA18980.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1223G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 1223 | chr7 | 143852910 | ||||||
| chr7:143853155 | T | C | 5 | a0001c0001t0030 a0001c0001t0040 a0001c0006t0016 others(2): Show |
5 | HG02280.hp2 HG03486.hp1 NA18980.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*978A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 978 | chr7 | 143853155 | ||||||
| chr7:143853232 | G | T | 2 | a0001c0002t0013 a0001c0003t0013 |
4 | HG01884.hp2 HG02647.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*901C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 901 | chr7 | 143853232 | ||||||
| chr7:143853305 | C | T | 16 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(13): Show |
104 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*828G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 828 | chr7 | 143853305 | ||||||
| chr7:143853399 | T | C | 1 | a0001c0004t0034 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*734A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 734 | chr7 | 143853399 | ||||||
| chr7:143853464 | G | A | 1 | a0001c0001t0018 | 2 | HG00735.hp2 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*669C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 669 | chr7 | 143853464 | ||||||
| chr7:143853536 | A | G | 60 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(57): Show |
210 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*597T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 597 | chr7 | 143853536 | ||||||
| chr7:143853539 | T | A | 6 | a0001c0002t0010 a0001c0002t0017 a0001c0002t0021 others(3): Show |
12 | HG00609.hp2 HG01071.hp1 HG01081.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*594A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 594 | chr7 | 143853539 | ||||||
| chr7:143853950 | G | C | 1 | a0001c0001t0018 | 2 | HG00735.hp2 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*183C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 183 | chr7 | 143853950 | ||||||
| chr7:143854001 | C | G | 1 | a0001c0002t0024 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 9/9 | 132 | chr7 | 143854001 | ||||||
| chr7:143902101 | C | T | 1 | a0001c0004t0023 | 1 | HG03942.hp2 | 5_prime_UTR_variant | MODIFIER | c.-155G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/9 | 25493 | chr7 | 143902101 | ||||||
| chr7:143902104 | G | A | 14 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0014 others(11): Show |
40 | HG00544.hp1 HG00733.hp2 HG01175.hp2 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-158C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/9 | 25496 | chr7 | 143902104 | ||||||
| chr7:143902118 | T | C | 1 | a0001c0001t0022 | 2 | HG01515.hp2 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-172A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/9 | 25510 | chr7 | 143902118 | ||||||
| chr7:143902138 | C | G | 7 | a0001c0001t0012 a0001c0002t0002 a0001c0002t0010 others(4): Show |
38 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-192G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/9 | 25530 | chr7 | 143902138 | ||||||
| chr7:143902154 | A | G | 58 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(55): Show |
167 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(164): Show |
5_prime_UTR_variant | MODIFIER | c.-208T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/9 | 25546 | chr7 | 143902154 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:143854242 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2757-100A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143854242 | |||||||
| chr7:143854296 | G | A | 1 | a0001c0001t0018g0004 | 2 | HG00735.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2757-154C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143854296 | |||||||
| chr7:143854379 | A | G | 1 | a0001c0001t0004g0160 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2757-237T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143854379 | |||||||
| chr7:143854399 | C | T | 1 | a0001c0004t0005g0073 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2757-257G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143854399 | |||||||
| chr7:143854459 | C | T | 15 | a0001c0001t0003g0058 a0001c0001t0005g0061 a0001c0001t0005g0078 others(12): Show |
15 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.2757-317G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143854459 | |||||||
| chr7:143855053 | G | C | 1 | a0001c0001t0003g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2757-911C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143855053 | |||||||
| chr7:143855089 | G | A | 1 | a0001c0002t0019g0129 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2757-947C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143855089 | |||||||
| chr7:143855311 | G | A | 1 | a0001c0004t0004g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2757-1169C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143855311 | |||||||
| chr7:143855331 | C | A | 1 | a0001c0002t0002g0018 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2757-1189G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143855331 | |||||||
| chr7:143855333 | A | C | 1 | a0001c0002t0002g0018 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2757-1191T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143855333 | |||||||
| chr7:143855573 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(101): Show |
111 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.2757-1431A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143855573 | |||||||
| chr7:143855617 | C | G | 1 | a0001c0001t0028g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2757-1475G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143855617 | |||||||
| chr7:143855676 | T | G | 2 | a0001c0002t0006g0097 a0001c0002t0024g0084 |
2 | HG03688.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2756+1424A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143855676 | |||||||
| chr7:143855892 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2756+1208T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143855892 | |||||||
| chr7:143855994 | G | A | 7 | a0001c0002t0010g0002 a0001c0002t0010g0025 a0001c0002t0010g0042 others(4): Show |
8 | HG00609.hp2 HG01071.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2756+1106C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143855994 | |||||||
| chr7:143856207 | T | C | 1 | a0001c0001t0027g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2756+893A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143856207 | |||||||
| chr7:143856272 | A | G | 1 | a0001c0002t0002g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2756+828T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143856272 | |||||||
| chr7:143856460 | C | T | 1 | a0001c0006t0003g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2756+640G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143856460 | |||||||
| chr7:143856607 | C | T | 2 | a0001c0002t0015g0106 a0001c0003t0015g0105 |
2 | HG01952.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2756+493G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143856607 | |||||||
| chr7:143856740 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2756+360T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143856740 | |||||||
| chr7:143856761 | C | G | 1 | a0001c0002t0006g0096 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2756+339G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143856761 | |||||||
| chr7:143856964 | G | A | 113 | a0001c0001t0003g0058 a0001c0001t0004g0133 a0001c0001t0005g0006 others(110): Show |
118 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.2756+136C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 8/8 | chr7 | 143856964 | |||||||
| chr7:143857358 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(95): Show |
106 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
splice_region_variant&intron_variant | LOW | c.2506-8C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143857358 | |||||||
| chr7:143857418 | A | T | 1 | a0001c0006t0008g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2506-68T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143857418 | |||||||
| chr7:143857453 | C | T | 3 | a0001c0001t0003g0065 a0001c0001t0003g0076 a0001c0001t0003g0125 |
3 | HG03195.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2506-103G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143857453 | |||||||
| chr7:143857454 | A | G | 11 | a0001c0001t0005g0006 a0001c0001t0005g0090 a0001c0001t0028g0060 others(8): Show |
12 | HG00735.hp1 HG01074.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.2506-104T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143857454 | |||||||
| chr7:143857471 | C | T | 2 | a0001c0001t0008g0109 a0001c0001t0009g0128 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2506-121G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143857471 | |||||||
| chr7:143857580 | A | G | 1 | a0001c0002t0019g0129 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2506-230T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143857580 | |||||||
| chr7:143857654 | C | A | 1 | a0001c0001t0036g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2506-304G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143857654 | |||||||
| chr7:143857658 | C | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0216 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2506-308G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143857658 | |||||||
| chr7:143857699 | A | G | 16 | a0001c0001t0007g0203 a0001c0001t0007g0225 a0001c0001t0007g0232 others(13): Show |
16 | HG00733.hp1 HG01175.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.2506-349T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143857699 | |||||||
| chr7:143858047 | A | G | 1 | a0001c0001t0027g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2506-697T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143858047 | |||||||
| chr7:143858201 | TCTCCAGT others(22): Show |
T | 4 | a0003c0005t0008g0052 a0003c0005t0008g0053 a0003c0005t0008g0054 others(1): Show |
4 | HG03139.hp2 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2505+594_2505+622d others(31): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143858201 | |||||||
| chr7:143858209 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(111): Show |
121 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.2505+615A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143858209 | |||||||
| chr7:143858213 | T | C | 1 | a0001c0006t0008g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2505+611A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143858213 | |||||||
| chr7:143858330 | G | T | 2 | a0001c0001t0003g0065 a0001c0001t0003g0076 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2505+494C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143858330 | |||||||
| chr7:143858624 | T | C | 5 | a0001c0001t0018g0004 a0001c0001t0028g0060 a0001c0002t0015g0106 others(2): Show |
6 | HG00735.hp2 HG01952.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2505+200A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143858624 | |||||||
| chr7:143858678 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2505+146C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143858678 | |||||||
| chr7:143858741 | G | A | 17 | a0001c0002t0006g0072 a0001c0002t0006g0094 a0001c0002t0006g0096 others(14): Show |
19 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2505+83C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 7/8 | chr7 | 143858741 | |||||||
| chr7:143859187 | G | C | 2 | a0001c0001t0014g0143 a0001c0001t0028g0060 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2168-26C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859187 | |||||||
| chr7:143859579 | A | G | 2 | a0001c0001t0003g0059 a0001c0001t0003g0107 |
2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2168-418T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859579 | |||||||
| chr7:143859708 | T | TA | 6 | a0001c0001t0028g0060 a0001c0006t0008g0051 a0003c0005t0008g0052 others(3): Show |
6 | HG02976.hp1 HG03139.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2167+499dupT | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859708 | |||||||
| chr7:143859771 | T | C | 72 | a0001c0001t0028g0060 a0001c0002t0002g0013 a0001c0002t0002g0016 others(69): Show |
75 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.2167+437A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859771 | |||||||
| chr7:143859857 | T | TTATATAC others(11): Show |
4 | a0003c0005t0008g0052 a0003c0005t0008g0053 a0003c0005t0008g0054 others(1): Show |
4 | HG03139.hp2 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2167+350_2167+351i others(20): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859857 | |||||||
| chr7:143859857 | T | TTATATAC others(13): Show |
1 | a0001c0001t0014g0143 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2167+350_2167+351i others(22): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859857 | |||||||
| chr7:143859862 | T | TACATATA others(9): Show |
92 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(89): Show |
99 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.2167+345_2167+346i others(18): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859862 | |||||||
| chr7:143859862 | T | TACATATA others(13): Show |
1 | a0001c0006t0003g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2167+345_2167+346i others(22): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859862 | |||||||
| chr7:143859864 | C | CATATATA others(3): Show |
1 | a0001c0006t0008g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2167+343_2167+344i others(12): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859864 | |||||||
| chr7:143859866 | C | T | 27 | a0001c0001t0001g0170 a0001c0001t0001g0188 a0001c0001t0001g0198 others(24): Show |
28 | HG00733.hp1 HG00735.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.2167+342G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859866 | |||||||
| chr7:143859872 | C | T | 26 | a0001c0001t0001g0170 a0001c0001t0001g0188 a0001c0001t0001g0198 others(23): Show |
27 | HG00733.hp1 HG00735.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.2167+336G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859872 | |||||||
| chr7:143859874 | T | C | 1 | a0001c0006t0008g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2167+334A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859874 | |||||||
| chr7:143859878 | T | C | 23 | a0001c0001t0001g0170 a0001c0001t0001g0188 a0001c0001t0001g0198 others(20): Show |
23 | HG00733.hp1 HG01175.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.2167+330A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859878 | |||||||
| chr7:143859878 | TACATATA others(146): Show |
T | 74 | a0001c0001t0001g0207 a0001c0002t0002g0013 a0001c0002t0002g0016 others(71): Show |
77 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.2167+177_2167+329d others(2): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859878 | |||||||
| chr7:143859880 | C | T | 1 | a0001c0001t0018g0004 | 2 | HG00735.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2167+328G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859880 | |||||||
| chr7:143859882 | T | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
65 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2167+326A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859882 | |||||||
| chr7:143859882 | T | C | 26 | a0001c0001t0001g0170 a0001c0001t0001g0188 a0001c0001t0001g0198 others(23): Show |
27 | HG00733.hp1 HG00735.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.2167+326A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859882 | |||||||
| chr7:143859884 | T | C | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2167+324A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859884 | |||||||
| chr7:143859886 | T | C | 1 | a0001c0006t0003g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2167+322A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859886 | |||||||
| chr7:143859887 | AT | A | 14 | a0001c0001t0001g0188 a0001c0001t0007g0232 a0001c0001t0009g0134 others(11): Show |
14 | HG00733.hp1 HG01175.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.2167+320delA | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859887 | |||||||
| chr7:143859888 | T | C | 10 | a0001c0001t0001g0170 a0001c0001t0001g0198 a0001c0001t0001g0206 others(7): Show |
10 | HG02258.hp2 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2167+320A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859888 | |||||||
| chr7:143859888 | T | TAATATAT others(35): Show |
3 | a0001c0006t0016g0122 a0001c0014t0029g0082 a0006c0013t0016g0081 |
3 | NA18980.hp2 NA18987.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2167+319_2167+320i others(44): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859888 | |||||||
| chr7:143859889 | A | AC | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2167+318_2167+319i others(3): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859889 | |||||||
| chr7:143859889 | A | AT | 9 | a0001c0001t0001g0170 a0001c0001t0001g0198 a0001c0001t0001g0206 others(6): Show |
9 | HG02258.hp2 HG02615.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.2167+318_2167+319i others(3): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859889 | |||||||
| chr7:143859889 | A | C | 14 | a0001c0001t0001g0188 a0001c0001t0007g0232 a0001c0001t0009g0134 others(11): Show |
14 | HG00733.hp1 HG01175.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.2167+319T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859889 | |||||||
| chr7:143859889 | AATATATA others(71): Show |
A | 1 | a0001c0001t0027g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2167+241_2167+318d others(80): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859889 | |||||||
| chr7:143859894 | A | AC | 3 | a0001c0001t0001g0198 a0001c0001t0001g0206 a0001c0004t0001g0169 |
3 | NA18998.hp2 NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2167+313_2167+314i others(3): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859894 | |||||||
| chr7:143859895 | T | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0206 a0001c0004t0001g0169 |
3 | NA18998.hp2 NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2167+313A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859895 | |||||||
| chr7:143859895 | T | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0211 a0001c0001t0001g0216 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2167+313A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859895 | |||||||
| chr7:143859896 | ATTATAT | A | 16 | a0001c0001t0001g0188 a0001c0001t0007g0232 a0001c0001t0009g0134 others(13): Show |
17 | HG00733.hp1 HG00735.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2167+306_2167+311d others(8): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859896 | |||||||
| chr7:143859897 | T | A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0206 a0001c0004t0001g0169 |
3 | NA18998.hp2 NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2167+311A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859897 | |||||||
| chr7:143859897 | T | TA | 6 | a0001c0001t0001g0170 a0001c0001t0001g0211 a0001c0001t0001g0216 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2167+310_2167+311i others(3): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859897 | |||||||
| chr7:143859903 | A | C | 16 | a0001c0001t0001g0188 a0001c0001t0007g0232 a0001c0001t0009g0134 others(13): Show |
17 | HG00733.hp1 HG00735.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2167+305T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859903 | |||||||
| chr7:143859905 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2167+303A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859905 | |||||||
| chr7:143859911 | TTACGG | T | 15 | a0001c0001t0001g0188 a0001c0001t0007g0232 a0001c0001t0009g0134 others(12): Show |
15 | HG00733.hp1 HG01175.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.2167+292_2167+296d others(7): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859911 | |||||||
| chr7:143859911 | TTACGGAA others(113): Show |
T | 1 | a0001c0001t0018g0004 | 2 | HG00735.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2167+177_2167+296d others(2): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859911 | |||||||
| chr7:143859914 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(106): Show |
116 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.2167+294G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859914 | |||||||
| chr7:143859915 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(101): Show |
111 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.2167+293C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859915 | |||||||
| chr7:143859916 | G | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
115 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.2167+292C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859916 | |||||||
| chr7:143859917 | A | C | 2 | a0001c0004t0004g0130 a0001c0004t0023g0049 |
2 | HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2167+291T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859917 | |||||||
| chr7:143859929 | A | G | 6 | a0001c0001t0003g0065 a0001c0001t0003g0076 a0001c0001t0014g0143 others(3): Show |
6 | HG03195.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2167+279T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859929 | |||||||
| chr7:143859930 | T | G | 2 | a0001c0001t0014g0143 a0001c0006t0003g0057 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2167+278A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859930 | |||||||
| chr7:143859946 | A | T | 4 | a0001c0001t0001g0198 a0001c0001t0001g0206 a0001c0004t0001g0169 others(1): Show |
4 | HG03139.hp2 NA18998.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+262T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859946 | |||||||
| chr7:143859948 | A | G | 1 | a0001c0001t0025g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2167+260T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859948 | |||||||
| chr7:143859952 | ATTACGGA others(44): Show |
A | 3 | a0001c0001t0001g0198 a0001c0001t0001g0206 a0001c0004t0001g0169 |
3 | NA18998.hp2 NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2167+205_2167+255d others(53): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859952 | |||||||
| chr7:143859953 | TTACGGAA | T | 2 | a0001c0001t0003g0065 a0001c0001t0003g0076 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2167+248_2167+254d others(9): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859953 | |||||||
| chr7:143859956 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
148 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.2167+252G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859956 | |||||||
| chr7:143859957 | G | A | 37 | a0001c0001t0001g0211 a0001c0001t0001g0216 a0001c0001t0004g0127 others(34): Show |
37 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.2167+251C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859957 | |||||||
| chr7:143859958 | G | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
150 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.2167+250C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859958 | |||||||
| chr7:143859958 | GAATATAT others(7): Show |
G | 1 | a0001c0001t0036g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2167+236_2167+249d others(16): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859958 | |||||||
| chr7:143859959 | A | ATTATATA others(47): Show |
1 | a0001c0001t0005g0090 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2167+248_2167+249i others(56): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859959 | |||||||
| chr7:143859960 | A | T | 2 | a0001c0001t0014g0143 a0001c0006t0003g0057 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2167+248T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859960 | |||||||
| chr7:143859967 | T | A | 1 | a0001c0001t0005g0090 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2167+241A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859967 | |||||||
| chr7:143859967 | T | TTATATAA others(32): Show |
1 | a0001c0001t0003g0058 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2167+240_2167+241i others(41): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859967 | |||||||
| chr7:143859971 | A | G | 27 | a0001c0001t0004g0127 a0001c0001t0004g0135 a0001c0001t0004g0137 others(24): Show |
27 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.2167+237T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859971 | |||||||
| chr7:143859973 | AAT | A | 3 | a0001c0006t0016g0122 a0001c0014t0029g0082 a0006c0013t0016g0081 |
3 | NA18980.hp2 NA18987.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2167+233_2167+234d others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859973 | |||||||
| chr7:143859974 | A | T | 1 | a0001c0001t0005g0090 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2167+234T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859974 | |||||||
| chr7:143859981 | T | TTATATAT others(54): Show |
9 | a0001c0001t0005g0006 a0001c0001t0005g0078 a0001c0001t0005g0080 others(6): Show |
10 | HG00735.hp1 HG01074.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.2167+226_2167+227i others(63): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859981 | |||||||
| chr7:143859981 | T | TTATATAT others(72): Show |
1 | a0001c0001t0035g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2167+226_2167+227i others(81): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859981 | |||||||
| chr7:143859981 | T | TTATATAT others(79): Show |
5 | a0001c0001t0005g0061 a0001c0001t0005g0088 a0001c0001t0005g0118 others(2): Show |
5 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(2): Show |
intron_variant | MODIFIER | c.2167+226_2167+227i others(88): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859981 | |||||||
| chr7:143859982 | T | A | 1 | a0001c0006t0008g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2167+226A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859982 | |||||||
| chr7:143859983 | A | T | 1 | a0001c0006t0008g0051 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2167+225T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859983 | |||||||
| chr7:143859985 | A | G | 6 | a0001c0001t0001g0188 a0001c0001t0001g0211 a0001c0001t0001g0216 others(3): Show |
6 | HG01884.hp1 HG02135.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2167+223T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859985 | |||||||
| chr7:143859987 | A | ATTATATA others(97): Show |
1 | a0001c0001t0032g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2167+220_2167+221i others(106): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859987 | |||||||
| chr7:143859988 | A | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
87 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.2167+220T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859988 | |||||||
| chr7:143859994 | ATTATATA others(2): Show |
A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(76): Show |
86 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.2167+205_2167+213d others(11): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859994 | |||||||
| chr7:143859995 | T | A | 3 | a0001c0001t0005g0118 a0001c0001t0032g0091 a0001c0006t0008g0051 |
3 | HG00423.hp1 HG01358.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2167+213A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859995 | |||||||
| chr7:143859999 | A | G | 2 | a0001c0001t0004g0154 a0002c0016t0003g0055 |
2 | HG01109.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2167+209T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859999 | |||||||
| chr7:143859999 | ATAATATA others(46): Show |
A | 1 | a0001c0001t0027g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2167+156_2167+208d others(55): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143859999 | |||||||
| chr7:143860001 | AAT | A | 4 | a0001c0001t0001g0211 a0001c0001t0001g0216 a0001c0001t0003g0065 others(1): Show |
4 | HG02258.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+205_2167+206d others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860001 | |||||||
| chr7:143860002 | A | T | 50 | a0001c0001t0003g0058 a0001c0001t0004g0127 a0001c0001t0004g0135 others(47): Show |
51 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.2167+206T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860002 | |||||||
| chr7:143860003 | T | TATATA | 24 | a0001c0001t0004g0127 a0001c0001t0004g0135 a0001c0001t0004g0137 others(21): Show |
24 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.2167+200_2167+204d others(7): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860003 | |||||||
| chr7:143860005 | T | TATATATA others(75): Show |
4 | a0003c0005t0008g0052 a0003c0005t0008g0053 a0003c0005t0008g0054 others(1): Show |
4 | HG03139.hp2 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2167+202_2167+203i others(84): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860005 | |||||||
| chr7:143860005 | T | TATATTAT others(51): Show |
1 | a0002c0016t0003g0055 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2167+202_2167+203i others(60): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860005 | |||||||
| chr7:143860006 | A | ATATTATA others(3): Show |
3 | a0001c0001t0009g0138 a0001c0001t0012g0027 a0001c0004t0001g0222 |
3 | HG02135.hp2 NA18966.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2167+201_2167+202i others(12): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860006 | |||||||
| chr7:143860012 | A | T | 1 | a0001c0001t0028g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2167+196T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860012 | |||||||
| chr7:143860019 | ATT | A | 3 | a0001c0006t0016g0122 a0001c0014t0029g0082 a0006c0013t0016g0081 |
3 | NA18980.hp2 NA18987.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2167+187_2167+188d others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860019 | |||||||
| chr7:143860020 | T | A | 17 | a0001c0001t0005g0006 a0001c0001t0005g0061 a0001c0001t0005g0078 others(14): Show |
18 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.2167+188A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860020 | |||||||
| chr7:143860020 | T | TAA | 3 | a0001c0001t0009g0138 a0001c0001t0012g0027 a0001c0004t0001g0222 |
3 | HG02135.hp2 NA18966.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2167+187_2167+188i others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860020 | |||||||
| chr7:143860020 | TTATATAT others(18): Show |
T | 2 | a0001c0001t0003g0111 a0001c0004t0003g0008 |
3 | HG01361.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2167+163_2167+187d others(27): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860020 | |||||||
| chr7:143860026 | ATTAT | A | 7 | a0001c0001t0007g0232 a0001c0001t0009g0134 a0001c0001t0009g0144 others(4): Show |
7 | HG00733.hp1 HG01175.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.2167+178_2167+181d others(6): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860026 | |||||||
| chr7:143860028 | T | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(101): Show |
111 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.2167+180A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860028 | |||||||
| chr7:143860029 | A | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
110 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.2167+179T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860029 | |||||||
| chr7:143860030 | T | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(101): Show |
111 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.2167+178A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860030 | |||||||
| chr7:143860030 | T | TATAATAT others(23): Show |
1 | a0001c0001t0004g0154 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2167+177_2167+178i others(32): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860030 | |||||||
| chr7:143860030 | T | TATAATAT others(53): Show |
2 | a0001c0001t0003g0065 a0001c0001t0003g0076 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2167+177_2167+178i others(62): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860030 | |||||||
| chr7:143860034 | T | C | 74 | a0001c0001t0001g0207 a0001c0002t0002g0013 a0001c0002t0002g0016 others(71): Show |
77 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.2167+174A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860034 | |||||||
| chr7:143860045 | A | ATATATAT | 8 | a0001c0001t0009g0138 a0001c0001t0012g0027 a0001c0004t0001g0222 others(5): Show |
8 | HG01109.hp2 HG02135.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.2167+156_2167+162d others(9): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860045 | |||||||
| chr7:143860045 | A | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(187): Show |
201 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.2167+163T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860045 | |||||||
| chr7:143860046 | T | A | 1 | a0001c0001t0014g0143 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2167+162A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860046 | |||||||
| chr7:143860198 | G | C | 1 | a0001c0001t0004g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2167+10C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 6/8 | chr7 | 143860198 | |||||||
| chr7:143860455 | G | A | 1 | a0001c0002t0002g0026 | 1 | HG00544.hp2 | splice_region_variant&intron_variant | LOW | c.1928-8C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 5/8 | chr7 | 143860455 | |||||||
| chr7:143860734 | C | T | 3 | a0001c0006t0016g0122 a0001c0014t0029g0082 a0006c0013t0016g0081 |
3 | NA18980.hp2 NA18987.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1928-287G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 5/8 | chr7 | 143860734 | |||||||
| chr7:143860779 | T | C | 36 | a0001c0001t0001g0170 a0001c0001t0001g0211 a0001c0001t0001g0216 others(33): Show |
36 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.1927+316A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 5/8 | chr7 | 143860779 | |||||||
| chr7:143860849 | G | C | 1 | a0001c0003t0020g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1927+246C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 5/8 | chr7 | 143860849 | |||||||
| chr7:143861328 | C | G | 1 | a0001c0001t0005g0123 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1714-20G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143861328 | |||||||
| chr7:143861601 | C | T | 1 | a0001c0001t0028g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1714-293G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143861601 | |||||||
| chr7:143861625 | C | G | 1 | a0007c0009t0005g0104 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1714-317G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143861625 | |||||||
| chr7:143861626 | G | A | 6 | a0001c0001t0003g0058 a0001c0006t0008g0051 a0003c0005t0008g0052 others(3): Show |
6 | HG02257.hp2 HG03139.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1714-318C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143861626 | |||||||
| chr7:143861626 | G | C | 1 | a0007c0009t0005g0104 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1714-318C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143861626 | |||||||
| chr7:143861635 | G | C | 1 | a0001c0001t0001g0235 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1714-327C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143861635 | |||||||
| chr7:143861751 | T | G | 1 | a0007c0009t0005g0104 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1714-443A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143861751 | |||||||
| chr7:143861752 | G | T | 1 | a0007c0009t0005g0104 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1714-444C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143861752 | |||||||
| chr7:143861765 | T | A | 3 | a0001c0001t0004g0156 a0001c0004t0004g0155 a0001c0004t0004g0157 |
3 | NA18951.hp2 NA19056.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1714-457A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143861765 | |||||||
| chr7:143862064 | G | A | 2 | a0001c0001t0030g0115 a0002c0007t0037g0181 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1713+352C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143862064 | |||||||
| chr7:143862083 | A | C | 104 | a0001c0001t0001g0207 a0001c0001t0001g0219 a0001c0001t0003g0058 others(101): Show |
109 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1713+333T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143862083 | |||||||
| chr7:143862094 | A | G | 9 | a0001c0001t0007g0232 a0001c0001t0009g0134 a0001c0001t0009g0144 others(6): Show |
9 | HG00733.hp1 HG01175.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1713+322T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143862094 | |||||||
| chr7:143862377 | G | A | 8 | a0001c0001t0007g0232 a0001c0001t0009g0134 a0001c0001t0009g0144 others(5): Show |
8 | HG00733.hp1 HG01175.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1713+39C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 4/8 | chr7 | 143862377 | |||||||
| chr7:143862686 | T | TA | 58 | a0001c0001t0005g0089 a0001c0001t0008g0109 a0001c0001t0009g0128 others(55): Show |
58 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1615+115dupT | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 3/8 | chr7 | 143862686 | |||||||
| chr7:143862748 | C | G | 4 | a0001c0003t0007g0174 a0001c0003t0007g0195 a0001c0003t0007g0202 others(1): Show |
4 | NA18968.hp1 NA18993.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615+54G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 3/8 | chr7 | 143862748 | |||||||
| chr7:143863859 | G | A | 5 | a0001c0001t0011g0092 a0001c0001t0011g0093 a0001c0001t0011g0100 others(2): Show |
5 | HG00733.hp1 HG00741.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.621-63C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143863859 | |||||||
| chr7:143863867 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.621-71A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143863867 | |||||||
| chr7:143863922 | A | G | 46 | a0001c0001t0001g0167 a0001c0001t0001g0172 a0001c0001t0001g0189 others(43): Show |
48 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.621-126T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143863922 | |||||||
| chr7:143864167 | GT | G | 4 | a0001c0001t0001g0188 a0001c0001t0001g0226 a0001c0002t0006g0072 others(1): Show |
4 | HG01168.hp2 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.621-372delA | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143864167 | |||||||
| chr7:143864170 | T | C | 36 | a0001c0001t0004g0127 a0001c0001t0004g0135 a0001c0001t0004g0137 others(33): Show |
36 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.621-374A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143864170 | |||||||
| chr7:143864394 | G | C | 1 | a0001c0001t0025g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.621-598C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143864394 | |||||||
| chr7:143864493 | T | C | 37 | a0001c0001t0004g0127 a0001c0001t0004g0135 a0001c0001t0004g0137 others(34): Show |
37 | HG00642.hp1 HG00733.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.621-697A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143864493 | |||||||
| chr7:143864603 | A | AAGTATAG others(17): Show |
1 | a0001c0001t0003g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.621-831_621-808dup others(24): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143864603 | |||||||
| chr7:143864746 | A | C | 2 | a0001c0001t0001g0238 a0001c0003t0002g0015 |
2 | NA18975.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.621-950T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143864746 | |||||||
| chr7:143864791 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0004g0154 |
3 | HG01074.hp2 HG01361.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.621-995G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143864791 | |||||||
| chr7:143864906 | A | G | 4 | a0001c0002t0006g0112 a0001c0002t0006g0114 a0001c0002t0006g0116 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.621-1110T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143864906 | |||||||
| chr7:143865006 | A | C | 1 | a0001c0001t0001g0235 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.621-1210T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865006 | |||||||
| chr7:143865041 | T | A | 1 | a0001c0001t0001g0223 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.621-1245A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865041 | |||||||
| chr7:143865067 | A | G | 14 | a0001c0001t0001g0168 a0001c0001t0001g0183 a0001c0001t0001g0215 others(11): Show |
15 | HG00735.hp2 HG01257.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.621-1271T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865067 | |||||||
| chr7:143865070 | G | A | 2 | a0001c0001t0003g0058 a0001c0002t0013g0003 |
3 | HG01884.hp2 HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.621-1274C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865070 | |||||||
| chr7:143865186 | AG | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(136): Show |
148 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.621-1391delC | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865186 | |||||||
| chr7:143865190 | G | A | 1 | a0002c0007t0003g0102 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.621-1394C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865190 | |||||||
| chr7:143865255 | G | A | 9 | a0001c0001t0003g0083 a0001c0001t0003g0103 a0001c0001t0003g0107 others(6): Show |
10 | HG00140.hp2 HG00639.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.621-1459C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865255 | |||||||
| chr7:143865339 | A | C | 2 | a0001c0001t0009g0128 a0001c0002t0019g0129 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.621-1543T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865339 | |||||||
| chr7:143865523 | G | A | 4 | a0001c0001t0003g0058 a0001c0001t0009g0128 a0001c0002t0013g0003 others(1): Show |
5 | HG01884.hp2 HG02257.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.621-1727C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865523 | |||||||
| chr7:143865576 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.621-1780T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865576 | |||||||
| chr7:143865632 | C | T | 1 | a0001c0001t0004g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.621-1836G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865632 | |||||||
| chr7:143865802 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.621-2006C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865802 | |||||||
| chr7:143865863 | T | C | 3 | a0001c0006t0008g0051 a0003c0005t0008g0052 a0003c0005t0008g0053 |
3 | HG03139.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.621-2067A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865863 | |||||||
| chr7:143865990 | T | C | 1 | a0001c0003t0020g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.621-2194A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143865990 | |||||||
| chr7:143866101 | T | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0167 others(170): Show |
181 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.621-2305A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143866101 | |||||||
| chr7:143866180 | A | G | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.621-2384T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143866180 | |||||||
| chr7:143866184 | T | C | 1 | a0001c0003t0006g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.621-2388A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143866184 | |||||||
| chr7:143866324 | G | T | 1 | a0001c0001t0009g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.621-2528C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143866324 | |||||||
| chr7:143866592 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.621-2796C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143866592 | |||||||
| chr7:143866629 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG01361.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.621-2833T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143866629 | |||||||
| chr7:143866644 | T | C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0183 a0001c0001t0001g0215 |
3 | HG01257.hp1 HG01517.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.621-2848A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143866644 | |||||||
| chr7:143866920 | A | G | 1 | a0001c0004t0012g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.621-3124T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143866920 | |||||||
| chr7:143866960 | T | C | 3 | a0001c0001t0001g0188 a0001c0001t0001g0226 a0001c0001t0038g0217 |
3 | HG01168.hp2 HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.621-3164A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143866960 | |||||||
| chr7:143867174 | T | TAA | 51 | a0001c0001t0001g0179 a0001c0001t0003g0125 a0001c0001t0004g0127 others(48): Show |
51 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.621-3380_621-3379d others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867174 | |||||||
| chr7:143867456 | C | G | 1 | a0001c0003t0002g0035 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.621-3660G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867456 | |||||||
| chr7:143867482 | C | T | 13 | a0001c0001t0001g0168 a0001c0001t0001g0172 a0001c0001t0001g0176 others(10): Show |
13 | HG01257.hp1 HG01517.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.621-3686G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867482 | |||||||
| chr7:143867548 | C | T | 9 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0189 others(6): Show |
9 | HG01928.hp1 HG01928.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-3752G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867548 | |||||||
| chr7:143867578 | C | T | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.621-3782G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867578 | |||||||
| chr7:143867613 | A | G | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.621-3817T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867613 | |||||||
| chr7:143867718 | T | TCA | 140 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
149 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.621-3924_621-3923d others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867718 | |||||||
| chr7:143867841 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(118): Show |
129 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.621-4045A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867841 | |||||||
| chr7:143867870 | C | T | 2 | a0001c0003t0002g0035 a0001c0004t0002g0031 |
2 | NA18952.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.621-4074G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867870 | |||||||
| chr7:143867908 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.621-4112G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867908 | |||||||
| chr7:143867926 | A | C | 2 | a0003c0005t0008g0054 a0003c0005t0008g0056 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.621-4130T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867926 | |||||||
| chr7:143867945 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
149 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.621-4149G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143867945 | |||||||
| chr7:143868002 | A | C | 1 | a0001c0002t0010g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.621-4206T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143868002 | |||||||
| chr7:143868370 | G | C | 7 | a0001c0002t0006g0094 a0001c0002t0006g0112 a0001c0002t0006g0114 others(4): Show |
8 | HG02109.hp1 HG02257.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.621-4574C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143868370 | |||||||
| chr7:143868378 | G | C | 2 | a0001c0003t0002g0021 a0001c0003t0007g0239 |
2 | NA18951.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.621-4582C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143868378 | |||||||
| chr7:143868378 | G | T | 9 | a0001c0001t0001g0168 a0001c0001t0001g0179 a0001c0001t0001g0215 others(6): Show |
9 | HG01074.hp2 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.621-4582C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143868378 | |||||||
| chr7:143868437 | C | A | 2 | a0001c0001t0003g0065 a0001c0001t0003g0076 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.621-4641G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143868437 | |||||||
| chr7:143868670 | T | C | 51 | a0001c0001t0001g0179 a0001c0001t0003g0062 a0001c0001t0003g0125 others(48): Show |
51 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.621-4874A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143868670 | |||||||
| chr7:143868681 | T | A | 19 | a0001c0001t0005g0006 a0001c0001t0005g0061 a0001c0001t0005g0078 others(16): Show |
20 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.621-4885A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143868681 | |||||||
| chr7:143868818 | CAGT | C | 10 | a0001c0001t0003g0083 a0001c0001t0003g0103 a0001c0001t0003g0107 others(7): Show |
11 | HG00140.hp2 HG00639.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.621-5025_621-5023d others(5): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143868818 | |||||||
| chr7:143868922 | A | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(118): Show |
129 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.621-5126T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143868922 | |||||||
| chr7:143868978 | T | C | 5 | a0001c0001t0001g0214 a0001c0001t0001g0226 a0001c0001t0001g0235 others(2): Show |
5 | HG00738.hp2 HG01168.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.621-5182A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143868978 | |||||||
| chr7:143869003 | G | GT | 25 | a0001c0001t0003g0083 a0001c0001t0003g0103 a0001c0001t0003g0107 others(22): Show |
26 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.621-5208dupA | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869003 | |||||||
| chr7:143869003 | GT | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
117 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.621-5208delA | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869003 | |||||||
| chr7:143869065 | C | T | 2 | a0001c0001t0003g0063 a0001c0001t0030g0115 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.621-5269G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869065 | |||||||
| chr7:143869143 | C | T | 1 | a0001c0003t0007g0239 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.621-5347G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869143 | |||||||
| chr7:143869164 | A | C | 1 | a0001c0002t0006g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.621-5368T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869164 | |||||||
| chr7:143869194 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0215 a0001c0003t0007g0239 |
3 | HG01257.hp1 HG01517.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.621-5398C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869194 | |||||||
| chr7:143869568 | G | A | 8 | a0001c0001t0001g0168 a0001c0001t0001g0215 a0001c0001t0004g0133 others(5): Show |
8 | HG01257.hp1 HG01517.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.621-5772C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869568 | |||||||
| chr7:143869600 | T | C | 3 | a0001c0006t0008g0051 a0003c0005t0008g0052 a0003c0005t0008g0053 |
3 | HG03139.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.621-5804A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869600 | |||||||
| chr7:143869703 | C | G | 19 | a0001c0001t0005g0006 a0001c0001t0005g0061 a0001c0001t0005g0078 others(16): Show |
20 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.621-5907G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869703 | |||||||
| chr7:143869740 | T | C | 1 | a0001c0001t0003g0058 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.621-5944A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869740 | |||||||
| chr7:143869743 | T | G | 1 | a0001c0004t0012g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.621-5947A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869743 | |||||||
| chr7:143869751 | C | G | 30 | a0001c0001t0004g0127 a0001c0001t0004g0135 a0001c0001t0004g0137 others(27): Show |
30 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.621-5955G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869751 | |||||||
| chr7:143869827 | A | G | 1 | a0001c0003t0002g0030 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.621-6031T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869827 | |||||||
| chr7:143869857 | G | A | 2 | a0001c0002t0015g0106 a0001c0003t0015g0105 |
2 | HG01952.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.621-6061C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869857 | |||||||
| chr7:143869865 | C | A | 3 | a0001c0001t0005g0080 a0001c0001t0026g0079 a0006c0013t0016g0081 |
3 | NA18980.hp2 NA19060.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.621-6069G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869865 | |||||||
| chr7:143869962 | A | T | 1 | a0001c0001t0009g0158 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.620+6027T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143869962 | |||||||
| chr7:143870196 | CT | C | 5 | a0001c0001t0001g0198 a0001c0001t0001g0206 a0001c0001t0001g0231 others(2): Show |
5 | NA18952.hp2 NA18991.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.620+5792delA | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143870196 | |||||||
| chr7:143870203 | T | G | 4 | a0001c0001t0001g0198 a0001c0001t0001g0206 a0001c0001t0001g0231 others(1): Show |
4 | NA18952.hp2 NA18998.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+5786A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143870203 | |||||||
| chr7:143870333 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0215 |
2 | HG01257.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.620+5656G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143870333 | |||||||
| chr7:143870607 | T | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0215 |
2 | HG01257.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.620+5382A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143870607 | |||||||
| chr7:143870626 | TGGTCTAT others(6): Show |
T | 1 | a0001c0002t0024g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.620+5350_620+5362d others(15): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143870626 | |||||||
| chr7:143870639 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(136): Show |
148 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.620+5350G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143870639 | |||||||
| chr7:143870672 | A | G | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.620+5317T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143870672 | |||||||
| chr7:143870757 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.620+5232T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143870757 | |||||||
| chr7:143870890 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
131 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.620+5099A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143870890 | |||||||
| chr7:143871077 | T | C | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.620+4912A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143871077 | |||||||
| chr7:143871170 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(136): Show |
148 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.620+4819C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143871170 | |||||||
| chr7:143871206 | C | G | 2 | a0001c0001t0009g0128 a0001c0002t0019g0129 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.620+4783G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143871206 | |||||||
| chr7:143871228 | A | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
149 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.620+4761T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143871228 | |||||||
| chr7:143871639 | T | C | 2 | a0001c0001t0011g0069 a0001c0001t0011g0070 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.620+4350A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143871639 | |||||||
| chr7:143872049 | GA | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(145): Show |
158 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.620+3939delT | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143872049 | |||||||
| chr7:143872342 | G | T | 1 | a0001c0001t0027g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.620+3647C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143872342 | |||||||
| chr7:143872383 | G | C | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.620+3606C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143872383 | |||||||
| chr7:143872476 | T | C | 1 | a0001c0001t0005g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.620+3513A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143872476 | |||||||
| chr7:143872623 | G | A | 1 | a0001c0004t0001g0197 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.620+3366C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143872623 | |||||||
| chr7:143873143 | C | T | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.620+2846G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143873143 | |||||||
| chr7:143873194 | T | C | 3 | a0001c0002t0002g0041 a0001c0003t0002g0036 a0001c0003t0002g0037 |
3 | HG00423.hp2 HG02155.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.620+2795A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143873194 | |||||||
| chr7:143873290 | G | T | 86 | a0001c0001t0003g0062 a0001c0001t0003g0065 a0001c0001t0003g0075 others(83): Show |
90 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.620+2699C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143873290 | |||||||
| chr7:143873558 | C | A | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.620+2431G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143873558 | |||||||
| chr7:143873614 | C | T | 1 | a0001c0001t0011g0119 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.620+2375G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143873614 | |||||||
| chr7:143873814 | T | C | 3 | a0001c0002t0007g0190 a0001c0003t0007g0177 a0001c0003t0007g0182 |
3 | NA18979.hp1 NA19006.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.620+2175A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143873814 | |||||||
| chr7:143873940 | G | C | 3 | a0001c0006t0008g0051 a0003c0005t0008g0052 a0003c0005t0008g0053 |
3 | HG03139.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.620+2049C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143873940 | |||||||
| chr7:143873960 | G | A | 3 | a0001c0001t0001g0226 a0001c0001t0018g0004 a0001c0001t0028g0060 |
4 | HG00735.hp2 HG01168.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+2029C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143873960 | |||||||
| chr7:143874008 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
135 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.620+1981A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143874008 | |||||||
| chr7:143874062 | A | C | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.620+1927T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143874062 | |||||||
| chr7:143874086 | G | A | 2 | a0001c0001t0009g0128 a0001c0002t0019g0129 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.620+1903C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143874086 | |||||||
| chr7:143874116 | T | C | 7 | a0001c0001t0003g0059 a0001c0001t0003g0125 a0001c0001t0025g0124 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.620+1873A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143874116 | |||||||
| chr7:143874268 | C | G | 1 | a0001c0001t0001g0175 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.620+1721G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143874268 | |||||||
| chr7:143874296 | A | G | 1 | a0002c0008t0006g0095 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.620+1693T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143874296 | |||||||
| chr7:143874550 | C | T | 1 | a0002c0008t0006g0095 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.620+1439G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143874550 | |||||||
| chr7:143874554 | G | A | 2 | a0001c0001t0009g0144 a0001c0001t0009g0159 |
2 | NA18980.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.620+1435C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143874554 | |||||||
| chr7:143875193 | T | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
87 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.620+796A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143875193 | |||||||
| chr7:143875482 | A | T | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.620+507T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143875482 | |||||||
| chr7:143875589 | C | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0206 |
2 | NA18998.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.620+400G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143875589 | |||||||
| chr7:143875725 | T | C | 2 | a0001c0001t0005g0089 a0001c0014t0029g0082 |
2 | HG02074.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.620+264A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143875725 | |||||||
| chr7:143875775 | A | C | 2 | a0001c0001t0003g0058 a0001c0002t0013g0003 |
3 | HG01884.hp2 HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.620+214T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143875775 | |||||||
| chr7:143875817 | G | A | 2 | a0001c0001t0011g0069 a0001c0001t0011g0070 |
2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.620+172C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143875817 | |||||||
| chr7:143875823 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.620+166C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143875823 | |||||||
| chr7:143875829 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.620+160G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143875829 | |||||||
| chr7:143875890 | T | C | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.620+99A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 2/8 | chr7 | 143875890 | |||||||
| chr7:143876933 | G | C | 1 | a0001c0002t0002g0013 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-14-311C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143876933 | |||||||
| chr7:143877398 | T | A | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-776A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143877398 | |||||||
| chr7:143877752 | G | A | 1 | a0003c0005t0008g0056 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-14-1130C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143877752 | |||||||
| chr7:143878112 | C | T | 3 | a0001c0001t0003g0125 a0001c0001t0025g0124 a0001c0004t0001g0184 |
3 | HG02135.hp1 HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-14-1490G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143878112 | |||||||
| chr7:143878184 | C | T | 19 | a0001c0001t0005g0006 a0001c0001t0005g0061 a0001c0001t0005g0078 others(16): Show |
20 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-1562G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143878184 | |||||||
| chr7:143878185 | G | A | 1 | a0001c0001t0030g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-14-1563C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143878185 | |||||||
| chr7:143878223 | T | C | 1 | a0001c0002t0021g0173 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-14-1601A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143878223 | |||||||
| chr7:143878266 | A | G | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-1644T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143878266 | |||||||
| chr7:143878463 | G | A | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-1841C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143878463 | |||||||
| chr7:143878529 | A | G | 1 | a0001c0001t0003g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-14-1907T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143878529 | |||||||
| chr7:143878884 | T | G | 2 | a0001c0001t0003g0059 a0001c0001t0027g0050 |
2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-14-2262A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143878884 | |||||||
| chr7:143878890 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
87 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-14-2268C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143878890 | |||||||
| chr7:143879183 | C | T | 1 | a0001c0004t0012g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-14-2561G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143879183 | |||||||
| chr7:143879229 | T | C | 3 | a0001c0006t0008g0051 a0003c0005t0008g0052 a0003c0005t0008g0053 |
3 | HG03139.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-14-2607A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143879229 | |||||||
| chr7:143879424 | G | A | 45 | a0001c0001t0004g0127 a0001c0001t0004g0133 a0001c0001t0004g0135 others(42): Show |
45 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-14-2802C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143879424 | |||||||
| chr7:143879646 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
87 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-14-3024C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143879646 | |||||||
| chr7:143879683 | A | C | 5 | a0001c0001t0003g0107 a0001c0001t0003g0108 a0001c0001t0003g0117 others(2): Show |
5 | HG02280.hp1 HG02809.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-3061T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143879683 | |||||||
| chr7:143879819 | T | G | 1 | a0001c0002t0017g0077 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-14-3197A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143879819 | |||||||
| chr7:143879909 | G | C | 1 | a0001c0002t0015g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-3287C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143879909 | |||||||
| chr7:143879911 | G | A | 1 | a0001c0001t0011g0093 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-14-3289C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143879911 | |||||||
| chr7:143880080 | G | A | 1 | a0001c0001t0005g0090 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-14-3458C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143880080 | |||||||
| chr7:143880187 | G | A | 1 | a0001c0001t0025g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-14-3565C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143880187 | |||||||
| chr7:143880358 | C | G | 43 | a0001c0001t0004g0127 a0001c0001t0004g0133 a0001c0001t0004g0135 others(40): Show |
43 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.-14-3736G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143880358 | |||||||
| chr7:143880583 | T | A | 2 | a0001c0003t0002g0036 a0001c0003t0002g0037 |
2 | HG02155.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-14-3961A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143880583 | |||||||
| chr7:143880979 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-14-4357G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143880979 | |||||||
| chr7:143881454 | T | C | 1 | a0001c0004t0034g0142 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-14-4832A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143881454 | |||||||
| chr7:143881900 | T | C | 1 | a0001c0001t0007g0232 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-14-5278A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143881900 | |||||||
| chr7:143881939 | G | A | 3 | a0001c0006t0008g0051 a0003c0005t0008g0052 a0003c0005t0008g0053 |
3 | HG03139.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-14-5317C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143881939 | |||||||
| chr7:143882008 | AG | A | 43 | a0001c0001t0004g0127 a0001c0001t0004g0133 a0001c0001t0004g0135 others(40): Show |
43 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.-14-5387delC | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882008 | |||||||
| chr7:143882193 | A | AAC | 15 | a0001c0001t0001g0170 a0001c0001t0001g0200 a0001c0001t0001g0211 others(12): Show |
16 | HG00738.hp1 HG00738.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-14-5573_-14-5572d others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | A | AACAC | 4 | a0001c0001t0001g0183 a0001c0001t0003g0058 a0002c0016t0003g0055 others(1): Show |
4 | HG01081.hp2 HG01109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-5575_-14-5572d others(6): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | A | AACACAC | 3 | a0001c0003t0020g0126 a0003c0005t0008g0054 a0003c0005t0008g0056 |
3 | HG02132.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-14-5577_-14-5572d others(8): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | A | AACACACA others(3): Show |
1 | a0001c0002t0019g0129 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-14-5581_-14-5572d others(12): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | A | AACACACA others(5): Show |
6 | a0001c0001t0004g0127 a0001c0001t0004g0145 a0001c0001t0009g0128 others(3): Show |
6 | HG00733.hp2 HG01255.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-5583_-14-5572d others(14): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | A | AACACACA others(7): Show |
3 | a0001c0001t0018g0004 a0001c0002t0019g0161 a0001c0003t0020g0165 |
4 | HG00735.hp2 HG02109.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-5585_-14-5572d others(16): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | A | AACACACA others(9): Show |
8 | a0001c0001t0003g0125 a0001c0001t0004g0139 a0001c0001t0004g0160 others(5): Show |
8 | HG02486.hp2 HG03139.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-5587_-14-5572d others(18): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | A | AACACACA others(11): Show |
21 | a0001c0001t0004g0135 a0001c0001t0004g0137 a0001c0001t0004g0154 others(18): Show |
22 | HG00642.hp1 HG01496.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-5589_-14-5572d others(20): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | A | AACACACA others(13): Show |
8 | a0001c0001t0004g0152 a0001c0001t0009g0134 a0001c0001t0011g0119 others(5): Show |
8 | HG00544.hp1 HG01175.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-5591_-14-5572d others(22): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | A | AACACACA others(15): Show |
2 | a0001c0001t0004g0133 a0001c0004t0004g0150 |
2 | HG02155.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-14-5593_-14-5572d others(24): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | A | AACACACA others(17): Show |
3 | a0001c0001t0004g0148 a0001c0002t0014g0149 a0001c0004t0033g0146 |
3 | HG03130.hp1 HG03927.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-14-5595_-14-5572d others(26): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | A | ACACACAC others(12): Show |
1 | a0001c0004t0004g0131 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-14-5572_-14-5571i others(21): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | AAC | A | 17 | a0001c0001t0003g0062 a0001c0001t0003g0103 a0001c0001t0011g0069 others(14): Show |
17 | HG01433.hp1 HG02155.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-5573_-14-5572d others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882193 | AACAC | A | 80 | a0001c0001t0003g0005 a0001c0001t0003g0063 a0001c0001t0003g0071 others(77): Show |
85 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-14-5575_-14-5572d others(6): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882193 | |||||||
| chr7:143882413 | G | C | 1 | a0008c0010t0001g0241 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-14-5791C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882413 | |||||||
| chr7:143882484 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-14-5862C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882484 | |||||||
| chr7:143882548 | G | A | 1 | a0001c0001t0001g0011 | 2 | NA18940.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-14-5926C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882548 | |||||||
| chr7:143882674 | G | C | 105 | a0001c0001t0003g0005 a0001c0001t0003g0062 a0001c0001t0003g0063 others(102): Show |
111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-14-6052C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882674 | |||||||
| chr7:143882799 | T | C | 1 | a0001c0002t0002g0020 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-14-6177A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143882799 | |||||||
| chr7:143883035 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-14-6413G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883035 | |||||||
| chr7:143883147 | T | C | 2 | a0001c0001t0003g0062 a0001c0002t0008g0120 |
2 | HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-14-6525A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883147 | |||||||
| chr7:143883373 | ACT | A | 5 | a0001c0001t0003g0059 a0001c0001t0027g0050 a0001c0006t0008g0051 others(2): Show |
5 | HG02258.hp1 HG02647.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-6753_-14-6752d others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883373 | |||||||
| chr7:143883495 | T | C | 1 | a0002c0007t0037g0181 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-14-6873A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883495 | |||||||
| chr7:143883500 | C | CT | 14 | a0001c0001t0001g0167 a0001c0001t0001g0170 a0001c0001t0001g0201 others(11): Show |
14 | HG01361.hp2 HG01943.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-6879dupA | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883500 | |||||||
| chr7:143883500 | C | CTT | 49 | a0001c0001t0001g0211 a0001c0001t0001g0218 a0001c0001t0003g0062 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-14-6880_-14-6879d others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883500 | |||||||
| chr7:143883500 | C | CTTT | 20 | a0001c0001t0003g0005 a0001c0001t0003g0063 a0001c0001t0003g0071 others(17): Show |
22 | HG00140.hp2 HG00639.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-14-6881_-14-6879d others(5): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883500 | |||||||
| chr7:143883500 | C | CTTTT | 18 | a0001c0001t0003g0111 a0001c0001t0027g0050 a0001c0001t0028g0060 others(15): Show |
18 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.-14-6882_-14-6879d others(6): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883500 | |||||||
| chr7:143883500 | C | CTTTTT | 18 | a0001c0001t0018g0004 a0001c0002t0002g0017 a0001c0002t0002g0018 others(15): Show |
19 | HG00423.hp2 HG01071.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-6883_-14-6879d others(7): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883500 | |||||||
| chr7:143883500 | CTTTTTTT others(4): Show |
C | 1 | a0001c0003t0006g0007 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-6889_-14-6879d others(13): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883500 | |||||||
| chr7:143883505 | T | TC | 40 | a0001c0001t0004g0133 a0001c0001t0004g0135 a0001c0001t0004g0137 others(37): Show |
40 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.-14-6884_-14-6883i others(3): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883505 | |||||||
| chr7:143883506 | T | C | 3 | a0001c0001t0004g0127 a0001c0001t0009g0128 a0001c0002t0019g0129 |
3 | HG01261.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-14-6884A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883506 | |||||||
| chr7:143883511 | T | C | 1 | a0001c0004t0004g0163 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-14-6889A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883511 | |||||||
| chr7:143883535 | T | C | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-6913A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883535 | |||||||
| chr7:143883784 | C | T | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-7162G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143883784 | |||||||
| chr7:143884192 | T | G | 4 | a0001c0001t0001g0170 a0001c0001t0001g0218 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-7570A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143884192 | |||||||
| chr7:143884344 | G | A | 2 | a0001c0002t0008g0067 a0001c0003t0008g0121 |
2 | NA18961.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-14-7722C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143884344 | |||||||
| chr7:143884414 | G | A | 105 | a0001c0001t0003g0005 a0001c0001t0003g0062 a0001c0001t0003g0063 others(102): Show |
111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-14-7792C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143884414 | |||||||
| chr7:143884932 | G | A | 17 | a0001c0001t0003g0075 a0001c0001t0011g0092 a0001c0001t0011g0093 others(14): Show |
18 | HG00733.hp1 HG00741.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-14-8310C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143884932 | |||||||
| chr7:143885034 | G | A | 1 | a0001c0001t0032g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-14-8412C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143885034 | |||||||
| chr7:143885151 | A | G | 45 | a0001c0001t0004g0127 a0001c0001t0004g0133 a0001c0001t0004g0135 others(42): Show |
45 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-14-8529T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143885151 | |||||||
| chr7:143885174 | G | C | 161 | a0001c0001t0001g0011 a0001c0001t0003g0005 a0001c0001t0003g0058 others(158): Show |
169 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.-14-8552C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143885174 | |||||||
| chr7:143885297 | G | C | 1 | a0001c0001t0003g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14-8675C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143885297 | |||||||
| chr7:143885374 | G | T | 1 | a0001c0001t0003g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-14-8752C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143885374 | |||||||
| chr7:143885382 | C | T | 36 | a0001c0001t0003g0075 a0001c0001t0005g0006 a0001c0001t0005g0061 others(33): Show |
38 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-14-8760G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143885382 | |||||||
| chr7:143885691 | A | T | 3 | a0002c0016t0003g0055 a0003c0005t0008g0054 a0003c0005t0008g0056 |
3 | HG01109.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-14-9069T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143885691 | |||||||
| chr7:143885783 | T | C | 7 | a0001c0001t0003g0059 a0001c0001t0003g0125 a0001c0001t0025g0124 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-9161A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143885783 | |||||||
| chr7:143886061 | A | G | 103 | a0001c0001t0003g0005 a0001c0001t0003g0062 a0001c0001t0003g0063 others(100): Show |
108 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-14-9439T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886061 | |||||||
| chr7:143886091 | A | C | 1 | a0001c0001t0001g0219 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-14-9469T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886091 | |||||||
| chr7:143886092 | C | T | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-9470G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886092 | |||||||
| chr7:143886099 | C | T | 2 | a0001c0002t0002g0026 a0001c0002t0002g0028 |
2 | HG00544.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.-14-9477G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886099 | |||||||
| chr7:143886216 | C | T | 1 | a0007c0009t0005g0104 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-14-9594G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886216 | |||||||
| chr7:143886339 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-14-9717T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886339 | |||||||
| chr7:143886383 | C | T | 1 | a0001c0003t0002g0039 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-14-9761G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886383 | |||||||
| chr7:143886419 | A | C | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-9797T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886419 | |||||||
| chr7:143886624 | G | C | 113 | a0001c0001t0003g0005 a0001c0001t0003g0059 a0001c0001t0003g0062 others(110): Show |
119 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-14-10002C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886624 | |||||||
| chr7:143886700 | C | CT | 83 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(80): Show |
86 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-14-10079dupA | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886700 | |||||||
| chr7:143886700 | C | CTT | 49 | a0001c0001t0001g0172 a0001c0001t0001g0236 a0001c0001t0003g0065 others(46): Show |
50 | HG00544.hp1 HG00733.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.-14-10080_-14-1007 others(6): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886700 | |||||||
| chr7:143886700 | C | CTTT | 5 | a0001c0001t0004g0145 a0001c0001t0009g0128 a0001c0001t0009g0144 others(2): Show |
6 | HG00733.hp2 HG00735.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-10081_-14-1007 others(7): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886700 | |||||||
| chr7:143886700 | CTT | C | 5 | a0001c0001t0003g0059 a0001c0001t0027g0050 a0001c0006t0008g0051 others(2): Show |
5 | HG02258.hp1 HG02647.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-10080_-14-1007 others(6): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886700 | |||||||
| chr7:143886738 | T | A | 3 | a0001c0002t0002g0041 a0001c0003t0002g0036 a0001c0003t0002g0037 |
3 | HG00423.hp2 HG02155.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-14-10116A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886738 | |||||||
| chr7:143886813 | C | A | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-14-10191G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886813 | |||||||
| chr7:143886817 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0199 |
2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-14-10195C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886817 | |||||||
| chr7:143886841 | G | A | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-10219C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886841 | |||||||
| chr7:143886855 | G | C | 100 | a0001c0001t0003g0005 a0001c0001t0003g0062 a0001c0001t0003g0063 others(97): Show |
105 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-10233C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886855 | |||||||
| chr7:143886866 | AT | A | 16 | a0001c0001t0001g0215 a0001c0001t0001g0235 a0001c0001t0003g0058 others(13): Show |
17 | HG01109.hp2 HG01257.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.-14-10245delA | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886866 | |||||||
| chr7:143886866 | ATT | A | 74 | a0001c0001t0003g0005 a0001c0001t0003g0062 a0001c0001t0003g0063 others(71): Show |
77 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-14-10246_-14-1024 others(6): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886866 | |||||||
| chr7:143886866 | ATTT | A | 28 | a0001c0001t0003g0083 a0001c0001t0003g0107 a0001c0001t0003g0108 others(25): Show |
31 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.-14-10247_-14-1024 others(7): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886866 | |||||||
| chr7:143886959 | C | T | 1 | a0001c0003t0008g0066 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-14-10337G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886959 | |||||||
| chr7:143886960 | G | A | 1 | a0001c0001t0004g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-14-10338C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143886960 | |||||||
| chr7:143887266 | A | T | 1 | a0002c0016t0003g0055 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-14-10644T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143887266 | |||||||
| chr7:143887276 | C | T | 4 | a0001c0001t0005g0078 a0001c0001t0018g0004 a0001c0001t0028g0060 others(1): Show |
5 | HG00735.hp2 HG02109.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-10654G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143887276 | |||||||
| chr7:143887277 | G | A | 1 | a0001c0002t0006g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-14-10655C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143887277 | |||||||
| chr7:143887302 | C | A | 1 | a0001c0002t0010g0042 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-14-10680G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143887302 | |||||||
| chr7:143887387 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-14-10765C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143887387 | |||||||
| chr7:143887953 | G | C | 1 | a0001c0001t0022g0012 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-14-11331C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143887953 | |||||||
| chr7:143888109 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-14-11487T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143888109 | |||||||
| chr7:143888155 | C | G | 2 | a0001c0001t0001g0226 a0005c0011t0001g0233 |
2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-14-11533G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143888155 | |||||||
| chr7:143888272 | A | G | 3 | a0001c0001t0003g0058 a0001c0002t0013g0003 a0001c0006t0003g0057 |
4 | HG01884.hp2 HG02257.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-11650T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143888272 | |||||||
| chr7:143888310 | A | G | 3 | a0001c0001t0001g0226 a0004c0012t0001g0240 a0008c0010t0001g0241 |
3 | HG00642.hp2 HG01168.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-14-11688T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143888310 | |||||||
| chr7:143888419 | A | G | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-11797T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143888419 | |||||||
| chr7:143888747 | A | G | 1 | a0001c0004t0034g0142 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-14-12125T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143888747 | |||||||
| chr7:143888811 | T | A | 1 | a0001c0001t0011g0100 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-14-12189A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143888811 | |||||||
| chr7:143888993 | T | G | 103 | a0001c0001t0003g0005 a0001c0001t0003g0062 a0001c0001t0003g0063 others(100): Show |
108 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-14-12371A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143888993 | |||||||
| chr7:143889370 | TAAAG | T | 3 | a0001c0001t0003g0058 a0001c0002t0013g0003 a0001c0006t0003g0057 |
4 | HG01884.hp2 HG02257.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+12587_-15+1259 others(8): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143889370 | |||||||
| chr7:143889383 | A | G | 7 | a0001c0001t0003g0059 a0001c0001t0003g0125 a0001c0001t0025g0124 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+12578T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143889383 | |||||||
| chr7:143889384 | CA | C | 3 | a0001c0001t0003g0058 a0001c0002t0013g0003 a0001c0006t0003g0057 |
4 | HG01884.hp2 HG02257.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+12576delT | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143889384 | |||||||
| chr7:143889774 | C | T | 2 | a0001c0003t0002g0044 a0001c0003t0002g0045 |
2 | NA18988.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-15+12187G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143889774 | |||||||
| chr7:143889828 | A | G | 3 | a0001c0001t0003g0058 a0001c0002t0013g0003 a0001c0006t0003g0057 |
4 | HG01884.hp2 HG02257.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+12133T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143889828 | |||||||
| chr7:143889979 | G | A | 1 | a0001c0004t0009g0141 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-15+11982C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143889979 | |||||||
| chr7:143890151 | GTTATT | G | 44 | a0001c0001t0004g0127 a0001c0001t0004g0133 a0001c0001t0004g0135 others(41): Show |
44 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.-15+11805_-15+1180 others(9): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143890151 | |||||||
| chr7:143890176 | G | A | 17 | a0001c0001t0003g0075 a0001c0001t0011g0092 a0001c0001t0011g0093 others(14): Show |
18 | HG00733.hp1 HG00741.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+11785C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143890176 | |||||||
| chr7:143890253 | C | T | 1 | a0001c0004t0009g0141 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-15+11708G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143890253 | |||||||
| chr7:143890747 | G | C | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+11214C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143890747 | |||||||
| chr7:143890985 | A | T | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+10976T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143890985 | |||||||
| chr7:143891075 | G | A | 3 | a0001c0006t0008g0051 a0003c0005t0008g0052 a0003c0005t0008g0053 |
3 | HG03139.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-15+10886C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143891075 | |||||||
| chr7:143891569 | TACATA | T | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+10387_-15+1039 others(9): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143891569 | |||||||
| chr7:143891781 | C | T | 7 | a0001c0001t0003g0059 a0001c0001t0003g0125 a0001c0001t0025g0124 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+10180G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143891781 | |||||||
| chr7:143891795 | A | C | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+10166T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143891795 | |||||||
| chr7:143891932 | G | A | 112 | a0001c0001t0003g0005 a0001c0001t0003g0059 a0001c0001t0003g0062 others(109): Show |
118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-15+10029C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143891932 | |||||||
| chr7:143892013 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-15+9948C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892013 | |||||||
| chr7:143892082 | G | A | 1 | a0001c0003t0002g0034 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-15+9879C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892082 | |||||||
| chr7:143892093 | C | G | 52 | a0001c0001t0003g0005 a0001c0001t0003g0062 a0001c0001t0003g0063 others(49): Show |
54 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-15+9868G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892093 | |||||||
| chr7:143892133 | A | C | 1 | a0001c0004t0005g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-15+9828T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892133 | |||||||
| chr7:143892296 | A | C | 1 | a0001c0002t0002g0013 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-15+9665T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892296 | |||||||
| chr7:143892393 | T | TA | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+9567dupT | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892393 | |||||||
| chr7:143892519 | T | C | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+9442A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892519 | |||||||
| chr7:143892528 | A | AT | 5 | a0001c0001t0001g0170 a0001c0001t0003g0075 a0001c0003t0002g0037 others(2): Show |
5 | HG02976.hp2 HG03579.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+9432dupA | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892528 | |||||||
| chr7:143892590 | C | T | 7 | a0001c0001t0003g0059 a0001c0001t0003g0125 a0001c0001t0025g0124 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+9371G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892590 | |||||||
| chr7:143892607 | T | A | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+9354A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892607 | |||||||
| chr7:143892620 | T | G | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+9341A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892620 | |||||||
| chr7:143892649 | G | C | 7 | a0001c0001t0003g0059 a0001c0001t0003g0125 a0001c0001t0025g0124 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+9312C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892649 | |||||||
| chr7:143892959 | G | A | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+9002C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143892959 | |||||||
| chr7:143893068 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-15+8893C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143893068 | |||||||
| chr7:143893254 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-15+8707G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143893254 | |||||||
| chr7:143893386 | C | T | 1 | a0001c0001t0018g0004 | 2 | HG00735.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-15+8575G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143893386 | |||||||
| chr7:143893481 | G | A | 1 | a0001c0003t0017g0064 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-15+8480C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143893481 | |||||||
| chr7:143893735 | A | G | 15 | a0001c0001t0003g0005 a0001c0001t0003g0063 a0001c0001t0003g0071 others(12): Show |
16 | HG01433.hp1 HG02071.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15+8226T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143893735 | |||||||
| chr7:143893761 | ATTAC | A | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+8196_-15+8199d others(6): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143893761 | |||||||
| chr7:143893801 | T | C | 4 | a0001c0001t0001g0175 a0001c0001t0001g0180 a0001c0001t0001g0208 others(1): Show |
4 | HG01257.hp2 HG01928.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+8160A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143893801 | |||||||
| chr7:143894041 | T | C | 2 | a0001c0002t0010g0002 a0001c0002t0010g0025 |
3 | HG01071.hp1 HG01081.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.-15+7920A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894041 | |||||||
| chr7:143894116 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0003t0007g0239 |
5 | NA18940.hp1 NA18983.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+7845A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894116 | |||||||
| chr7:143894200 | A | T | 1 | a0001c0001t0001g0175 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-15+7761T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894200 | |||||||
| chr7:143894248 | C | T | 1 | a0001c0003t0002g0036 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-15+7713G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894248 | |||||||
| chr7:143894336 | T | C | 7 | a0001c0001t0003g0059 a0001c0001t0003g0125 a0001c0001t0025g0124 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+7625A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894336 | |||||||
| chr7:143894398 | T | C | 17 | a0001c0001t0003g0075 a0001c0001t0011g0092 a0001c0001t0011g0093 others(14): Show |
18 | HG00733.hp1 HG00741.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+7563A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894398 | |||||||
| chr7:143894455 | C | G | 1 | a0001c0001t0001g0210 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-15+7506G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894455 | |||||||
| chr7:143894800 | G | A | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+7161C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894800 | |||||||
| chr7:143894854 | A | C | 14 | a0001c0001t0003g0005 a0001c0001t0003g0063 a0001c0001t0003g0071 others(11): Show |
15 | HG01433.hp1 HG02071.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15+7107T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894854 | |||||||
| chr7:143894903 | C | T | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-15+7058G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894903 | |||||||
| chr7:143894912 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-15+7049T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894912 | |||||||
| chr7:143894932 | C | T | 3 | a0002c0016t0003g0055 a0003c0005t0008g0054 a0003c0005t0008g0056 |
3 | HG01109.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-15+7029G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143894932 | |||||||
| chr7:143895735 | C | T | 2 | a0001c0001t0003g0065 a0001c0001t0003g0076 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-15+6226G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143895735 | |||||||
| chr7:143895803 | T | C | 1 | a0001c0001t0007g0232 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-15+6158A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143895803 | |||||||
| chr7:143895818 | A | C | 1 | a0001c0001t0003g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-15+6143T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143895818 | |||||||
| chr7:143895828 | A | T | 99 | a0001c0001t0003g0005 a0001c0001t0003g0062 a0001c0001t0003g0063 others(96): Show |
104 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-15+6133T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143895828 | |||||||
| chr7:143895935 | T | C | 110 | a0001c0001t0003g0005 a0001c0001t0003g0059 a0001c0001t0003g0062 others(107): Show |
116 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-15+6026A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143895935 | |||||||
| chr7:143896310 | C | T | 1 | a0001c0001t0035g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-15+5651G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143896310 | |||||||
| chr7:143896482 | A | C | 45 | a0001c0001t0004g0127 a0001c0001t0004g0133 a0001c0001t0004g0135 others(42): Show |
45 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-15+5479T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143896482 | |||||||
| chr7:143896542 | A | C | 3 | a0001c0006t0008g0051 a0003c0005t0008g0052 a0003c0005t0008g0053 |
3 | HG03139.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-15+5419T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143896542 | |||||||
| chr7:143896861 | G | C | 1 | a0001c0003t0002g0035 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-15+5100C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143896861 | |||||||
| chr7:143897037 | T | C | 1 | a0001c0001t0004g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-15+4924A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897037 | |||||||
| chr7:143897131 | A | AAT | 9 | a0001c0001t0001g0009 a0001c0001t0001g0209 a0001c0001t0001g0210 others(6): Show |
10 | HG00639.hp1 HG00738.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-15+4828_-15+4829d others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | A | AATAT | 9 | a0001c0001t0001g0201 a0001c0001t0001g0204 a0001c0001t0001g0206 others(6): Show |
9 | HG01257.hp2 HG01361.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+4826_-15+4829d others(6): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | A | AATATAT | 15 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0194 others(12): Show |
16 | HG00597.hp2 HG00738.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+4824_-15+4829d others(8): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | A | AATATATA others(1): Show |
8 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0187 others(5): Show |
8 | HG01884.hp1 HG01952.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+4822_-15+4829d others(10): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | A | AATATATA others(3): Show |
8 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG00609.hp1 HG01074.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+4820_-15+4829d others(12): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | A | AATATATA others(5): Show |
3 | a0001c0001t0001g0172 a0001c0002t0021g0173 a0001c0003t0007g0174 |
3 | HG01928.hp2 NA19000.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-15+4818_-15+4829d others(14): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | A | AATATATA others(7): Show |
2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01175.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-15+4816_-15+4829d others(16): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | A | AATATATA others(13): Show |
1 | a0001c0004t0001g0169 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-15+4810_-15+4829d others(22): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AAT | A | 13 | a0001c0001t0001g0168 a0001c0001t0001g0226 a0001c0001t0001g0227 others(10): Show |
13 | HG01168.hp1 HG01168.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+4828_-15+4829d others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATAT | A | 7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0003g0063 others(4): Show |
7 | HG00140.hp1 HG01081.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+4826_-15+4829d others(6): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATAT | A | 5 | a0001c0001t0003g0065 a0001c0002t0002g0022 a0001c0002t0002g0023 others(2): Show |
5 | HG01109.hp1 HG01358.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+4824_-15+4829d others(8): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATATA others(1): Show |
A | 27 | a0001c0001t0003g0005 a0001c0001t0003g0071 a0001c0001t0003g0075 others(24): Show |
29 | HG00140.hp2 HG00544.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15+4822_-15+4829d others(10): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATATA others(3): Show |
A | 21 | a0001c0001t0003g0076 a0001c0001t0003g0083 a0001c0001t0005g0061 others(18): Show |
21 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+4820_-15+4829d others(12): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATATA others(5): Show |
A | 21 | a0001c0001t0001g0236 a0001c0001t0005g0006 a0001c0001t0005g0086 others(18): Show |
23 | HG00438.hp1 HG00597.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-15+4818_-15+4829d others(14): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATATA others(7): Show |
A | 22 | a0001c0001t0003g0059 a0001c0001t0003g0103 a0001c0001t0003g0107 others(19): Show |
24 | HG01361.hp1 HG01433.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-15+4816_-15+4829d others(16): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATATA others(9): Show |
A | 4 | a0001c0001t0001g0237 a0001c0001t0003g0058 a0001c0001t0005g0118 others(1): Show |
4 | HG00423.hp1 HG02257.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+4814_-15+4829d others(18): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATATA others(11): Show |
A | 1 | a0001c0004t0004g0130 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-15+4812_-15+4829d others(20): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATATA others(13): Show |
A | 14 | a0001c0001t0001g0238 a0001c0001t0004g0133 a0001c0001t0004g0135 others(11): Show |
14 | HG00642.hp1 HG01175.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.-15+4810_-15+4829d others(22): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATATA others(15): Show |
A | 30 | a0001c0001t0004g0127 a0001c0001t0004g0145 a0001c0001t0004g0148 others(27): Show |
31 | HG00544.hp1 HG00733.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-15+4808_-15+4829d others(24): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATATA others(17): Show |
A | 1 | a0001c0003t0020g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15+4806_-15+4829d others(26): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATATA others(19): Show |
A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0003t0007g0239 |
5 | NA18940.hp1 NA18983.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+4804_-15+4829d others(28): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897131 | AATATATA others(21): Show |
A | 2 | a0004c0012t0001g0240 a0008c0010t0001g0241 |
2 | HG00642.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-15+4802_-15+4829d others(30): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897131 | |||||||
| chr7:143897147 | T | A | 1 | a0001c0004t0003g0008 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-15+4814A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897147 | |||||||
| chr7:143897194 | C | G | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+4767G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897194 | |||||||
| chr7:143897438 | T | C | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-15+4523A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897438 | |||||||
| chr7:143897707 | G | GTACTATA others(21): Show |
1 | a0001c0001t0004g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-15+4253_-15+4254i others(30): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897707 | |||||||
| chr7:143897709 | A | C | 1 | a0001c0001t0004g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-15+4252T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897709 | |||||||
| chr7:143897710 | A | T | 1 | a0001c0001t0004g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-15+4251T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897710 | |||||||
| chr7:143897712 | C | T | 1 | a0001c0001t0004g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-15+4249G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897712 | |||||||
| chr7:143897713 | C | T | 1 | a0001c0001t0004g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-15+4248G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897713 | |||||||
| chr7:143897739 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-15+4222G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897739 | |||||||
| chr7:143897869 | A | T | 1 | a0001c0003t0020g0126 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-15+4092T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897869 | |||||||
| chr7:143897871 | T | C | 1 | a0001c0001t0003g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-15+4090A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897871 | |||||||
| chr7:143897942 | G | A | 1 | a0001c0002t0008g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-15+4019C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143897942 | |||||||
| chr7:143898229 | T | C | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+3732A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143898229 | |||||||
| chr7:143898287 | C | T | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-15+3674G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143898287 | |||||||
| chr7:143898809 | T | A | 1 | a0001c0003t0008g0121 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-15+3152A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143898809 | |||||||
| chr7:143898815 | A | G | 1 | a0001c0001t0003g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-15+3146T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143898815 | |||||||
| chr7:143899111 | A | G | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+2850T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143899111 | |||||||
| chr7:143899223 | T | C | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+2738A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143899223 | |||||||
| chr7:143899347 | A | G | 1 | a0001c0004t0002g0014 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-15+2614T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143899347 | |||||||
| chr7:143899544 | G | A | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+2417C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143899544 | |||||||
| chr7:143900058 | G | A | 3 | a0002c0016t0003g0055 a0003c0005t0008g0054 a0003c0005t0008g0056 |
3 | HG01109.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-15+1903C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900058 | |||||||
| chr7:143900060 | A | AAC | 117 | a0001c0001t0003g0005 a0001c0001t0003g0059 a0001c0001t0003g0062 others(114): Show |
123 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-15+1900_-15+1901i others(4): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900060 | |||||||
| chr7:143900282 | T | C | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+1679A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900282 | |||||||
| chr7:143900344 | C | T | 1 | a0001c0001t0005g0061 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-15+1617G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900344 | |||||||
| chr7:143900494 | T | C | 1 | a0001c0001t0003g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-15+1467A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900494 | |||||||
| chr7:143900743 | T | C | 2 | a0001c0001t0005g0123 a0001c0006t0016g0122 |
2 | NA18975.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.-15+1218A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900743 | |||||||
| chr7:143900900 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1061T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900900 | |||||||
| chr7:143900901 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1060T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900901 | |||||||
| chr7:143900905 | C | A | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1056G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900905 | |||||||
| chr7:143900906 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1055T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900906 | |||||||
| chr7:143900907 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1054A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900907 | |||||||
| chr7:143900914 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1047C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900914 | |||||||
| chr7:143900915 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1046T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900915 | |||||||
| chr7:143900916 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1045C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900916 | |||||||
| chr7:143900919 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1042T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900919 | |||||||
| chr7:143900920 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1041C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900920 | |||||||
| chr7:143900921 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1040G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900921 | |||||||
| chr7:143900922 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1039G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900922 | |||||||
| chr7:143900923 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1038T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900923 | |||||||
| chr7:143900927 | C | G | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1034G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900927 | |||||||
| chr7:143900932 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1029C>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900932 | |||||||
| chr7:143900936 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1025A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900936 | |||||||
| chr7:143900938 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1023C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900938 | |||||||
| chr7:143900940 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1021T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900940 | |||||||
| chr7:143900941 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1020T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900941 | |||||||
| chr7:143900943 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1018T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900943 | |||||||
| chr7:143900945 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1016T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900945 | |||||||
| chr7:143900946 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1015G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900946 | |||||||
| chr7:143900947 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1014T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900947 | |||||||
| chr7:143900949 | A | ATTTTGTT others(5): Show |
1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1011_-15+1012i others(14): Show |
TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900949 | |||||||
| chr7:143900952 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1009T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900952 | |||||||
| chr7:143900953 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1008T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900953 | |||||||
| chr7:143900956 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+1005A>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900956 | |||||||
| chr7:143900965 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+996A>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900965 | |||||||
| chr7:143900966 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+995T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900966 | |||||||
| chr7:143900970 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+991T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900970 | |||||||
| chr7:143900972 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+989T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900972 | |||||||
| chr7:143900974 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+987T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900974 | |||||||
| chr7:143900977 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+984G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900977 | |||||||
| chr7:143900980 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+981C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900980 | |||||||
| chr7:143900981 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+980C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900981 | |||||||
| chr7:143900982 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+979C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900982 | |||||||
| chr7:143900985 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+976A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900985 | |||||||
| chr7:143900990 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+971T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900990 | |||||||
| chr7:143900991 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+970T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900991 | |||||||
| chr7:143900993 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+968A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900993 | |||||||
| chr7:143900996 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+965T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900996 | |||||||
| chr7:143900999 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+962G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143900999 | |||||||
| chr7:143901000 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+961T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901000 | |||||||
| chr7:143901001 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+960T>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901001 | |||||||
| chr7:143901003 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+958T>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901003 | |||||||
| chr7:143901007 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+954T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901007 | |||||||
| chr7:143901008 | C | G | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+953G>C | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901008 | |||||||
| chr7:143901011 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+950T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901011 | |||||||
| chr7:143901016 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+945C>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901016 | |||||||
| chr7:143901021 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+940T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901021 | |||||||
| chr7:143901026 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+935T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901026 | |||||||
| chr7:143901040 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-15+921T>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901040 | |||||||
| chr7:143901090 | C | T | 1 | a0001c0002t0002g0013 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-15+871G>A | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901090 | |||||||
| chr7:143901274 | G | A | 1 | a0001c0001t0003g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-15+687C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901274 | |||||||
| chr7:143901290 | T | C | 1 | a0002c0008t0014g0166 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-15+671A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901290 | |||||||
| chr7:143901553 | T | C | 2 | a0001c0001t0018g0004 a0001c0001t0028g0060 |
3 | HG00735.hp2 HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-15+408A>G | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901553 | |||||||
| chr7:143901555 | C | A | 68 | a0001c0001t0003g0005 a0001c0001t0003g0062 a0001c0001t0003g0063 others(65): Show |
72 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.-15+406G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901555 | |||||||
| chr7:143901627 | G | A | 1 | a0001c0002t0039g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-15+334C>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901627 | |||||||
| chr7:143901704 | C | A | 2 | a0001c0001t0003g0125 a0001c0001t0025g0124 |
2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-15+257G>T | TCAF1 | ENSG00000198420.10 | transcript | ENST00000479870.6 | protein_coding | 1/8 | chr7 | 143901704 |