Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51809 |
| ensemblid | ENSG00000109586.12 |
| hgncid | 4129 |
| symbol | GALNT7 |
| name | polypeptide N-acetylgalactosaminyltransferase 7 |
| refseq_nuc | NM_017423.3 |
| refseq_prot | NP_059119.2 |
| ensembl_nuc | ENST00000265000.9 |
| ensembl_prot | ENSP00000265000.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 173168811 |
| end | 173323967 |
| strand | + |
| ver | v1.2 |
| region | chr4:173168811-173323967 |
| region5000 | chr4:173163811-173328967 |
| regionname0 | GALNT7_chr4_173168811_173323967 |
| regionname5000 | GALNT7_chr4_173163811_173328967 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 657 | 259 | 85 | 55 | 81 | 10 | 26 | 59 | GALNT7_chr4_173163811_173328967 | GALNT7 | MRLKI others(652): Show |
chr4 | 173163811 | 173328967 |
| a0002 | 0/0 | 657 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | MRLKI others(652): Show |
chr4 | 173163811 | 173328967 |
| a0003 | 0/0 | 657 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | MRLKI others(652): Show |
chr4 | 173163811 | 173328967 |
| a0004 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | MRLKI others(652): Show |
chr4 | 173163811 | 173328967 |
| a0005 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | MRLKI others(652): Show |
chr4 | 173163811 | 173328967 |
| a0006 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | MRLKI others(652): Show |
chr4 | 173163811 | 173328967 |
| a0007 | 0/0 | 657 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | MRLKI others(652): Show |
chr4 | 173163811 | 173328967 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1971 | 144 | 42 | 34 | 47 | 6 | 15 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0001c0002 | 1/1 | 1971 | 84 | 30 | 19 | 21 | 4 | 8 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0001c0003 | 0/0 | 1971 | 17 | 1 | 2 | 12 | 0 | 2 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0001c0004 | 0/0 | 1971 | 5 | 5 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0001c0005 | 0/0 | 1971 | 5 | 4 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0001c0006 | 0/0 | 1971 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0001c0008 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0002c0007 | 0/0 | 1971 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0003c0010 | 0/0 | 1971 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0004c0012 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0005c0013 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0006c0011 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 | ||
| a0007c0009 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | ATGAG others(1966): Show |
chr4 | 173163811 | 173328967 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4249 | 113 | 30 | 30 | 34 | 5 | 14 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0001t0002 | 0/0 | 4251 | 17 | 5 | 0 | 11 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4246): Show |
chr4 | 173163811 | 173328967 |
| a0001c0001t0003 | 0/0 | 4250 | 4 | 3 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4245): Show |
chr4 | 173163811 | 173328967 |
| a0001c0001t0004 | 0/0 | 4250 | 3 | 0 | 2 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4245): Show |
chr4 | 173163811 | 173328967 |
| a0001c0001t0005 | 0/0 | 4249 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0001t0010 | 0/0 | 4249 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0001t0011 | 0/0 | 4249 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0001t0014 | 0/0 | 4249 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0001t0015 | 0/0 | 4249 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0002t0001 | 1/1 | 4249 | 68 | 16 | 18 | 20 | 4 | 8 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0002t0002 | 0/0 | 4251 | 7 | 6 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4246): Show |
chr4 | 173163811 | 173328967 |
| a0001c0002t0003 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4245): Show |
chr4 | 173163811 | 173328967 |
| a0001c0002t0006 | 0/0 | 4250 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4245): Show |
chr4 | 173163811 | 173328967 |
| a0001c0002t0009 | 0/0 | 4249 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0002t0010 | 0/0 | 4249 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0002t0011 | 0/0 | 4249 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0002t0013 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4245): Show |
chr4 | 173163811 | 173328967 |
| a0001c0003t0002 | 0/0 | 4251 | 14 | 1 | 2 | 9 | 0 | 2 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4246): Show |
chr4 | 173163811 | 173328967 |
| a0001c0003t0008 | 0/0 | 4251 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4246): Show |
chr4 | 173163811 | 173328967 |
| a0001c0003t0012 | 0/0 | 4251 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4246): Show |
chr4 | 173163811 | 173328967 |
| a0001c0004t0001 | 0/0 | 4249 | 5 | 5 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0005t0001 | 0/0 | 4249 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0005t0003 | 0/0 | 4250 | 4 | 3 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4245): Show |
chr4 | 173163811 | 173328967 |
| a0001c0006t0001 | 0/0 | 4249 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0001c0008t0002 | 0/0 | 4251 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4246): Show |
chr4 | 173163811 | 173328967 |
| a0002c0007t0007 | 0/0 | 4249 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0003c0010t0003 | 0/0 | 4250 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4245): Show |
chr4 | 173163811 | 173328967 |
| a0004c0012t0001 | 0/0 | 4249 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0005c0013t0001 | 0/0 | 4249 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| a0006c0011t0002 | 0/0 | 4251 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4246): Show |
chr4 | 173163811 | 173328967 |
| a0007c0009t0001 | 0/0 | 4249 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | GTGAG others(4244): Show |
chr4 | 173163811 | 173328967 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0010g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0011g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0014g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0001t0015g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0010g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0002t0013g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0008g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0003t0012g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0004t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0005t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0005t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0005t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0005t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0006t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0006t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0001c0008t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0002c0007t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0002c0007t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0003c0010t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0004c0012t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0005c0013t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0006c0011t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| a0007c0009t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0016 | EUR | GBR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00140 | hp2 | a0001 | c0001 | t0010 | g0121 | EUR | GBR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | FIN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0237 | EUR | FIN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00423 | hp1 | a0001 | c0003 | t0002 | g0253 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | CHS | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00642 | hp2 | a0001 | c0002 | t0010 | g0233 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0262 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0181 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0176 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0220 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01346 | hp2 | a0003 | c0010 | t0003 | g0096 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01884 | hp2 | a0001 | c0002 | t0011 | g0222 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0232 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0006 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0021 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0085 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0075 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02273 | hp2 | a0001 | c0001 | t0014 | g0054 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0193 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0130 | AMR | PEL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02523 | hp2 | a0001 | c0008 | t0002 | g0148 | EAS | KHV | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0171 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02630 | hp1 | a0001 | c0005 | t0003 | g0097 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02647 | hp1 | a0001 | c0002 | t0006 | g0170 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02886 | hp1 | a0001 | c0005 | t0003 | g0095 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02886 | hp2 | a0001 | c0006 | t0001 | g0074 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0076 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02970 | hp2 | a0004 | c0012 | t0001 | g0194 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0104 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0215 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03098 | hp2 | a0005 | c0013 | t0001 | g0175 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03130 | hp1 | a0002 | c0007 | t0007 | g0177 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0099 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03209 | hp1 | a0001 | c0002 | t0009 | g0244 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03453 | hp1 | a0001 | c0002 | t0013 | g0207 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0073 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0077 | AFR | ESN | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0172 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0209 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0221 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03834 | hp2 | a0001 | c0003 | t0002 | g0248 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0216 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0254 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04184 | hp2 | a0001 | c0005 | t0003 | g0092 | SAS | BEB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0264 | SAS | STU | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18522 | hp2 | a0001 | c0003 | t0002 | g0169 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18906 | hp1 | a0002 | c0007 | t0007 | g0178 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0071 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18946 | hp1 | a0001 | c0001 | t0015 | g0157 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0259 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18948 | hp2 | a0007 | c0009 | t0001 | g0135 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0256 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18963 | hp2 | a0001 | c0003 | t0002 | g0249 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0234 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18975 | hp1 | a0001 | c0003 | t0008 | g0250 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18979 | hp1 | a0001 | c0003 | t0002 | g0255 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19002 | hp1 | a0001 | c0003 | t0002 | g0246 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19012 | hp1 | a0001 | c0003 | t0012 | g0251 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0240 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19043 | hp1 | a0001 | c0002 | t0009 | g0245 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19055 | hp1 | a0001 | c0003 | t0002 | g0258 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19074 | hp2 | a0001 | c0003 | t0008 | g0252 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | YRI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ASW | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ASW | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0236 | EUR | TSI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0203 | EUR | TSI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | GIH | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0214 | SAS | GIH | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02109 | hp2 | a0001 | c0006 | t0001 | g0072 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02486 | hp1 | a0001 | c0004 | t0001 | g0084 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0182 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0261 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03471 | hp1 | a0001 | c0005 | t0003 | g0098 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | MSL | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | USA | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| HG06807 | hp2 | a0006 | c0011 | t0002 | g0180 | AFR | USA | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0187 | AFR | USA | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0243 | AFR | USA | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | LWK | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0201 | REF | REF | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0190 | REF | REF | GALNT7_chr4_173163811_173328967 | GALNT7 | chr4 | 173163811 | 173328967 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:173168938 | C | T | 1 | a0003 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.103C>T | p.Pro35Ser | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/12 | 128/4249 | 103/1974 | 35/657 | chr4 | 173168938 | |||
| chr4:173248208 | A | G | 1 | a0005 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.355A>G | p.Thr119Ala | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/12 | 380/4249 | 355/1974 | 119/657 | chr4 | 173248208 | |||
| chr4:173248242 | G | A | 1 | a0006 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.389G>A | p.Gly130Glu | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/12 | 414/4249 | 389/1974 | 130/657 | chr4 | 173248242 | |||
| chr4:173295400 | C | G | 1 | a0002 | 2 | HG03130.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.759C>G | p.His253Gln | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 4/12 | 784/4249 | 759/1974 | 253/657 | chr4 | 173295400 | |||
| chr4:173295837 | A | T | 1 | a0004 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.959A>T | p.Lys320Met | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/12 | 984/4249 | 959/1974 | 320/657 | chr4 | 173295837 | |||
| chr4:173303996 | A | T | 1 | a0007 | 1 | NA18948.hp2 | missense_variant&splice_region_variant | MODERATE | c.1267A>T | p.Ile423Leu | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/12 | 1292/4249 | 1267/1974 | 423/657 | chr4 | 173303996 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:173168853 | G | A | 7 | a0001c0001 a0001c0004 a0001c0005 others(4): Show |
160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
synonymous_variant | LOW | c.18G>A | p.Gly6Gly | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/12 | 43/4249 | 18/1974 | 6/657 | chr4 | 173168853 | |||
| chr4:173298139 | A | T | 3 | a0001c0005 a0003c0010 a0006c0011 |
7 | HG01346.hp2 HG02630.hp1 HG02886.hp1 others(4): Show |
synonymous_variant | LOW | c.990A>T | p.Ile330Ile | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/12 | 1015/4249 | 990/1974 | 330/657 | chr4 | 173298139 | |||
| chr4:173302131 | T | C | 1 | a0001c0004 | 5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
synonymous_variant | LOW | c.1233T>C | p.Ile411Ile | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/12 | 1258/4249 | 1233/1974 | 411/657 | chr4 | 173302131 | |||
| chr4:173314029 | G | T | 1 | a0001c0006 | 3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.1461G>T | p.Ser487Ser | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/12 | 1486/4249 | 1461/1974 | 487/657 | chr4 | 173314029 | |||
| chr4:173318553 | C | T | 2 | a0001c0003 a0001c0008 |
18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
synonymous_variant | LOW | c.1830C>T | p.Tyr610Tyr | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/12 | 1855/4249 | 1830/1974 | 610/657 | chr4 | 173318553 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:173321836 | C | T | 2 | a0001c0001t0011 a0001c0002t0011 |
2 | HG01884.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*119C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 119 | chr4 | 173321836 | ||||||
| chr4:173321871 | A | AT | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0006 others(2): Show |
13 | HG01081.hp2 HG01346.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*158dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 159 | INFO_REALIGN_3_PRIME | chr4 | 173321871 | |||||
| chr4:173321897 | G | T | 2 | a0001c0001t0010 a0001c0002t0010 |
2 | HG00140.hp2 HG00642.hp2 |
3_prime_UTR_variant | MODIFIER | c.*180G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 180 | chr4 | 173321897 | ||||||
| chr4:173321987 | T | G | 1 | a0002c0007t0007 | 2 | HG03130.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*270T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 270 | chr4 | 173321987 | ||||||
| chr4:173322115 | A | C | 1 | a0001c0001t0015 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 398 | chr4 | 173322115 | ||||||
| chr4:173322479 | C | G | 5 | a0001c0001t0005 a0001c0001t0011 a0001c0002t0009 others(2): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*762C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 762 | chr4 | 173322479 | ||||||
| chr4:173322480 | T | C | 8 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0013 others(5): Show |
44 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*763T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 763 | chr4 | 173322480 | ||||||
| chr4:173322796 | G | A | 2 | a0001c0003t0008 a0001c0003t0012 |
3 | NA18975.hp1 NA19012.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1079G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1079 | chr4 | 173322796 | ||||||
| chr4:173322881 | T | C | 1 | a0001c0003t0012 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1164T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1164 | chr4 | 173322881 | ||||||
| chr4:173323065 | G | A | 1 | a0001c0002t0009 | 2 | HG03209.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1348G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1348 | chr4 | 173323065 | ||||||
| chr4:173323084 | A | AT | 8 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0013 others(5): Show |
44 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1368dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1369 | INFO_REALIGN_3_PRIME | chr4 | 173323084 | |||||
| chr4:173323127 | T | TA | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(5): Show |
46 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1423dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1424 | INFO_REALIGN_3_PRIME | chr4 | 173323127 | |||||
| chr4:173323224 | T | C | 1 | a0001c0002t0006 | 3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1507T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1507 | chr4 | 173323224 | ||||||
| chr4:173323362 | T | C | 5 | a0001c0001t0005 a0001c0001t0011 a0001c0002t0009 others(2): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1645T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1645 | chr4 | 173323362 | ||||||
| chr4:173323485 | T | C | 1 | a0002c0007t0007 | 2 | HG03130.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1768T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 1768 | chr4 | 173323485 | ||||||
| chr4:173323953 | T | G | 1 | a0001c0001t0014 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2236T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 12/12 | 2236 | chr4 | 173323953 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:173169044 | C | CG | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(18): Show |
21 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.126+87dupG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173169044 | ||||||
| chr4:173169138 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+177C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169138 | |||||||
| chr4:173169224 | G | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+263G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169224 | |||||||
| chr4:173169230 | G | T | 1 | a0001c0001t0001g0265 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.126+269G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169230 | |||||||
| chr4:173169267 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.126+306G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169267 | |||||||
| chr4:173169336 | C | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.126+375C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169336 | |||||||
| chr4:173169417 | A | C | 1 | a0001c0002t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.126+456A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169417 | |||||||
| chr4:173169427 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.126+466C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169427 | |||||||
| chr4:173169528 | G | A | 2 | a0001c0002t0001g0167 a0001c0002t0001g0168 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.126+567G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169528 | |||||||
| chr4:173169645 | G | C | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+684G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169645 | |||||||
| chr4:173169704 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.126+743C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169704 | |||||||
| chr4:173169731 | G | T | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+770G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169731 | |||||||
| chr4:173169781 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.126+820C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169781 | |||||||
| chr4:173169855 | G | T | 3 | a0001c0002t0001g0261 a0001c0002t0001g0262 a0001c0002t0001g0263 |
3 | HG00597.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.126+894G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169855 | |||||||
| chr4:173169928 | C | T | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+967C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169928 | |||||||
| chr4:173169969 | G | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(61): Show |
64 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.126+1008G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169969 | |||||||
| chr4:173169975 | G | T | 1 | a0001c0001t0001g0013 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.126+1014G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173169975 | |||||||
| chr4:173170065 | G | A | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.126+1104G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170065 | |||||||
| chr4:173170133 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.126+1172C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170133 | |||||||
| chr4:173170156 | A | G | 4 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1195A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170156 | |||||||
| chr4:173170360 | A | G | 3 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 |
3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.126+1399A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170360 | |||||||
| chr4:173170366 | A | G | 1 | a0001c0002t0006g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.126+1405A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170366 | |||||||
| chr4:173170843 | G | A | 17 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(14): Show |
17 | HG00423.hp1 HG01192.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+1882G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173170843 | |||||||
| chr4:173171061 | AATTAAC | A | 5 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
5 | NA18946.hp1 NA18979.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+2106_126+2111d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173171061 | ||||||
| chr4:173171179 | A | C | 7 | a0001c0002t0002g0020 a0001c0002t0002g0240 a0001c0002t0002g0241 others(4): Show |
7 | HG02809.hp2 HG03209.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+2218A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171179 | |||||||
| chr4:173171406 | T | G | 1 | a0001c0001t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.126+2445T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171406 | |||||||
| chr4:173171437 | G | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.126+2476G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171437 | |||||||
| chr4:173171492 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.126+2531G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171492 | |||||||
| chr4:173171542 | A | G | 8 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0100 others(5): Show |
8 | HG01346.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+2581A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171542 | |||||||
| chr4:173171640 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.126+2679A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171640 | |||||||
| chr4:173171662 | C | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+2701C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171662 | |||||||
| chr4:173171851 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.126+2890G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173171851 | |||||||
| chr4:173172032 | G | A | 1 | a0001c0002t0001g0179 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.126+3071G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172032 | |||||||
| chr4:173172081 | G | A | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+3120G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172081 | |||||||
| chr4:173172238 | C | T | 1 | a0001c0002t0001g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.126+3277C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172238 | |||||||
| chr4:173172381 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+3420C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172381 | |||||||
| chr4:173172437 | A | G | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+3476A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172437 | |||||||
| chr4:173172556 | CA | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
40 | HG00621.hp1 HG01192.hp1 HG01257.hp1 others(37): Show |
intron_variant | MODIFIER | c.126+3597delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173172556 | ||||||
| chr4:173172793 | T | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+3832T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172793 | |||||||
| chr4:173172841 | A | G | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+3880A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172841 | |||||||
| chr4:173172892 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
24 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.126+3931C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173172892 | |||||||
| chr4:173173045 | T | G | 24 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(21): Show |
24 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.126+4084T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173045 | |||||||
| chr4:173173090 | G | C | 1 | a0001c0001t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+4129G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173090 | |||||||
| chr4:173173131 | A | G | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+4170A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173131 | |||||||
| chr4:173173380 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(102): Show |
105 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.126+4419T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173380 | |||||||
| chr4:173173439 | A | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+4478A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173439 | |||||||
| chr4:173173516 | A | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+4555A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173516 | |||||||
| chr4:173173600 | A | C | 1 | a0001c0005t0001g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.126+4639A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173600 | |||||||
| chr4:173173623 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0002g0041 others(1): Show |
4 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+4662C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173623 | |||||||
| chr4:173173683 | C | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.126+4722C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173683 | |||||||
| chr4:173173738 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.126+4777T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173738 | |||||||
| chr4:173173789 | G | A | 3 | a0001c0002t0001g0261 a0001c0002t0001g0262 a0001c0002t0001g0263 |
3 | HG00597.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.126+4828G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173789 | |||||||
| chr4:173173791 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.126+4830T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173791 | |||||||
| chr4:173173952 | A | G | 2 | a0001c0001t0005g0085 a0001c0001t0005g0086 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.126+4991A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173173952 | |||||||
| chr4:173174618 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+5657A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173174618 | |||||||
| chr4:173174761 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
54 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.126+5800C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173174761 | |||||||
| chr4:173174918 | G | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | HG00639.hp1 HG00738.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+5957G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173174918 | |||||||
| chr4:173175038 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+6077G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175038 | |||||||
| chr4:173175116 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(3): Show |
6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+6155G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175116 | |||||||
| chr4:173175486 | C | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+6525C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175486 | |||||||
| chr4:173175527 | C | T | 24 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(21): Show |
24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+6566C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175527 | |||||||
| chr4:173175549 | C | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+6588C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175549 | |||||||
| chr4:173175623 | A | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+6662A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175623 | |||||||
| chr4:173175945 | C | T | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0004t0001g0006 others(6): Show |
9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+6984C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175945 | |||||||
| chr4:173175989 | C | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(14): Show |
17 | HG01081.hp2 HG01346.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+7028C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173175989 | |||||||
| chr4:173176030 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+7069G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176030 | |||||||
| chr4:173176056 | A | G | 9 | a0001c0002t0002g0020 a0001c0002t0002g0240 a0001c0002t0002g0241 others(6): Show |
9 | HG02809.hp2 HG03098.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+7095A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176056 | |||||||
| chr4:173176072 | CA | C | 24 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(21): Show |
24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+7123delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173176072 | ||||||
| chr4:173176188 | A | G | 1 | a0001c0004t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.126+7227A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176188 | |||||||
| chr4:173176193 | A | T | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+7232A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176193 | |||||||
| chr4:173176285 | G | C | 3 | a0001c0004t0001g0076 a0001c0004t0001g0077 a0001c0004t0001g0084 |
3 | HG02486.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.126+7324G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176285 | |||||||
| chr4:173176476 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
78 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.126+7515T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176476 | |||||||
| chr4:173176496 | T | C | 1 | a0001c0003t0002g0246 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.126+7535T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176496 | |||||||
| chr4:173176577 | G | T | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+7616G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176577 | |||||||
| chr4:173176863 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.126+7902G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176863 | |||||||
| chr4:173176866 | T | C | 31 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(28): Show |
31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+7905T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176866 | |||||||
| chr4:173176909 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(28): Show |
31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+7948G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176909 | |||||||
| chr4:173176975 | C | G | 2 | a0001c0004t0001g0076 a0001c0004t0001g0077 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.126+8014C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173176975 | |||||||
| chr4:173177075 | A | C | 50 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0018 others(47): Show |
50 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.126+8114A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177075 | |||||||
| chr4:173177124 | T | C | 1 | a0001c0002t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.126+8163T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177124 | |||||||
| chr4:173177349 | T | C | 1 | a0001c0002t0001g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.126+8388T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177349 | |||||||
| chr4:173177633 | A | C | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.126+8672A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177633 | |||||||
| chr4:173177681 | T | C | 1 | a0001c0002t0001g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126+8720T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177681 | |||||||
| chr4:173177998 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+9037T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173177998 | |||||||
| chr4:173178004 | AGTCTGTG others(122): Show |
A | 5 | a0001c0002t0002g0020 a0001c0002t0002g0240 a0001c0002t0002g0241 others(2): Show |
5 | HG02809.hp2 HG03579.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+9045_126+9173d others(2): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178004 | ||||||
| chr4:173178007 | CTG | C | 17 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0053 others(14): Show |
17 | HG00323.hp2 HG00621.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+9091_126+9092d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | ||||||
| chr4:173178007 | CTGTG | C | 41 | a0001c0001t0001g0049 a0001c0001t0001g0125 a0001c0001t0001g0163 others(38): Show |
41 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.126+9089_126+9092d others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | ||||||
| chr4:173178007 | CTGTGTG | C | 24 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0055 others(21): Show |
24 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+9087_126+9092d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | ||||||
| chr4:173178007 | CTGTGTGT others(1): Show |
C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0051 others(3): Show |
6 | HG00639.hp1 HG01257.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+9085_126+9092d others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | ||||||
| chr4:173178007 | CTGTGTGT others(3): Show |
C | 3 | a0001c0001t0001g0162 a0001c0002t0001g0202 a0001c0002t0002g0182 |
3 | HG01081.hp1 HG02135.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.126+9083_126+9092d others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | ||||||
| chr4:173178007 | CTGTGTGT others(7): Show |
C | 1 | a0001c0002t0001g0208 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.126+9079_126+9092d others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178007 | ||||||
| chr4:173178044 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.126+9083T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178044 | |||||||
| chr4:173178044 | TGTGTGTG others(3): Show |
T | 1 | a0001c0005t0003g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.126+9085_126+9094d others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178044 | ||||||
| chr4:173178046 | T | C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0107 others(10): Show |
13 | HG00323.hp2 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.126+9085T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178046 | |||||||
| chr4:173178046 | T | TGC | 8 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(5): Show |
8 | HG00423.hp2 HG00597.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+9086_126+9087i others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178046 | ||||||
| chr4:173178046 | TGTGTGTG others(9): Show |
T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(2): Show |
5 | HG01257.hp1 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+9087_126+9102d others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178046 | ||||||
| chr4:173178047 | GTGTGTGC others(5): Show |
G | 2 | a0001c0001t0002g0041 a0001c0003t0002g0169 |
2 | HG02040.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.126+9087_126+9098d others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178047 | |||||||
| chr4:173178048 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0044 others(24): Show |
27 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.126+9087T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178048 | |||||||
| chr4:173178048 | T | TGC | 7 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0069 others(4): Show |
7 | HG00280.hp1 HG01361.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+9088_126+9089i others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178048 | ||||||
| chr4:173178048 | T | TGCGC | 10 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0063 others(7): Show |
10 | HG00741.hp2 HG01884.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+9088_126+9089i others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178048 | ||||||
| chr4:173178048 | T | TGCGCGC | 5 | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0129 others(2): Show |
5 | HG00140.hp2 HG02056.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+9088_126+9089i others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178048 | ||||||
| chr4:173178048 | TGTGTGCG others(7): Show |
T | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.126+9089_126+9102d others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178048 | ||||||
| chr4:173178049 | GTGTGCGC others(3): Show |
G | 7 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0002g0022 others(4): Show |
7 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+9089_126+9098d others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178049 | |||||||
| chr4:173178050 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(54): Show |
57 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.126+9089T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178050 | |||||||
| chr4:173178050 | T | TGCGC | 5 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0067 others(2): Show |
5 | HG00741.hp1 HG01943.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+9090_126+9091i others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178050 | ||||||
| chr4:173178050 | T | TGCGCGC | 10 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0114 others(7): Show |
10 | HG00558.hp2 HG00738.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+9090_126+9091i others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178050 | ||||||
| chr4:173178050 | T | TGCGCGCG others(3): Show |
1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.126+9090_126+9091i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178050 | ||||||
| chr4:173178050 | T | TGCGTGCG others(1): Show |
3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0004t0001g0104 |
3 | HG01346.hp1 HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.126+9090_126+9091i others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178050 | ||||||
| chr4:173178050 | TGTGCGC | T | 4 | a0001c0001t0001g0266 a0001c0001t0002g0026 a0001c0004t0001g0006 others(1): Show |
4 | HG02055.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+9091_126+9096d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178050 | ||||||
| chr4:173178051 | GTGCGCGC others(1): Show |
G | 5 | a0001c0001t0002g0023 a0001c0001t0002g0036 a0001c0001t0002g0039 others(2): Show |
5 | HG02602.hp1 NA18906.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+9091_126+9098d others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178051 | |||||||
| chr4:173178052 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(90): Show |
93 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.126+9091T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178052 | |||||||
| chr4:173178052 | T | TGCGCGC | 3 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0068 |
3 | HG02572.hp1 HG02738.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.126+9092_126+9097d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGCGCGCG others(1): Show |
6 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0158 others(3): Show |
6 | HG01934.hp2 NA18946.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+9097_126+9098i others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGCGCGCG others(3): Show |
3 | a0001c0001t0001g0012 a0001c0001t0001g0136 a0001c0001t0001g0138 |
3 | HG03927.hp2 NA18945.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.126+9097_126+9098i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGCGCGCG others(5): Show |
1 | a0001c0001t0001g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.126+9097_126+9098i others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGCGTGCG others(3): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0265 |
2 | NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.126+9094_126+9095i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGTGCGCG others(3): Show |
3 | a0001c0001t0001g0124 a0001c0001t0001g0150 a0001c0008t0002g0148 |
3 | HG02080.hp2 HG02523.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.126+9092_126+9093i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGTGTGCG others(5): Show |
3 | a0001c0001t0001g0109 a0001c0001t0001g0139 a0001c0001t0001g0146 |
3 | HG01074.hp1 HG03017.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.126+9092_126+9093i others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGTGTGCG others(9): Show |
1 | a0001c0001t0001g0116 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.126+9092_126+9093i others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGTGTGTG others(3): Show |
1 | a0001c0002t0001g0257 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126+9092_126+9093i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0160 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.126+9092_126+9093i others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+9092_126+9093i others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.126+9092_126+9093i others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178052 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.126+9092_126+9093i others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178052 | ||||||
| chr4:173178053 | GCGCGCA | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0079 a0001c0001t0002g0038 others(3): Show |
6 | HG01081.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+9098_126+9103d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178053 | ||||||
| chr4:173178054 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(19): Show |
22 | HG01891.hp1 HG01993.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+9093C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178054 | |||||||
| chr4:173178055 | GCGCA | G | 11 | a0001c0001t0001g0029 a0001c0001t0001g0094 a0001c0001t0002g0030 others(8): Show |
11 | HG01891.hp1 HG02257.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+9098_126+9101d others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178055 | ||||||
| chr4:173178056 | C | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0080 others(13): Show |
16 | HG01993.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+9095C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178056 | |||||||
| chr4:173178057 | GCA | G | 5 | a0001c0001t0001g0080 a0001c0001t0002g0034 a0001c0001t0003g0081 others(2): Show |
5 | HG02258.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+9098_126+9099d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173178057 | ||||||
| chr4:173178058 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0005g0085 others(2): Show |
5 | HG01993.hp2 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+9097C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178058 | |||||||
| chr4:173178058 | CACGCGCG others(1): Show |
C | 3 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 |
3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.126+9098_126+9105d others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178058 | |||||||
| chr4:173178059 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0045 others(47): Show |
50 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.126+9098A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178059 | |||||||
| chr4:173178060 | C | T | 8 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(5): Show |
8 | HG01081.hp2 HG01891.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+9099C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178060 | |||||||
| chr4:173178062 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(3): Show |
6 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+9101C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178062 | |||||||
| chr4:173178066 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
86 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.126+9105T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178066 | |||||||
| chr4:173178069 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+9108G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178069 | |||||||
| chr4:173178071 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0028 |
2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.126+9110A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178071 | |||||||
| chr4:173178081 | A | G | 1 | a0006c0011t0002g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126+9120A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178081 | |||||||
| chr4:173178141 | A | G | 1 | a0001c0002t0001g0237 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.126+9180A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178141 | |||||||
| chr4:173178306 | A | G | 14 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(11): Show |
14 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+9345A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178306 | |||||||
| chr4:173178471 | G | A | 14 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(11): Show |
14 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+9510G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178471 | |||||||
| chr4:173178505 | T | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+9544T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178505 | |||||||
| chr4:173178800 | T | A | 2 | a0001c0002t0001g0014 a0001c0002t0001g0183 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.126+9839T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178800 | |||||||
| chr4:173178829 | G | C | 2 | a0001c0001t0001g0093 a0001c0005t0003g0092 |
2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.126+9868G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178829 | |||||||
| chr4:173178919 | A | T | 3 | a0001c0004t0001g0006 a0001c0005t0003g0097 a0001c0005t0003g0098 |
3 | HG02055.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.126+9958A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173178919 | |||||||
| chr4:173179386 | T | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0100 others(5): Show |
8 | HG01346.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+10425T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179386 | |||||||
| chr4:173179392 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.126+10431T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179392 | |||||||
| chr4:173179542 | G | T | 1 | a0001c0001t0004g0154 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.126+10581G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179542 | |||||||
| chr4:173179789 | GAAAACAA others(3): Show |
G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.126+10838_126+1084 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173179789 | ||||||
| chr4:173179899 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
78 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.126+10938C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179899 | |||||||
| chr4:173179970 | C | T | 1 | a0001c0001t0005g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126+11009C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179970 | |||||||
| chr4:173179971 | G | A | 2 | a0001c0001t0005g0085 a0001c0001t0005g0086 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.126+11010G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173179971 | |||||||
| chr4:173180004 | T | C | 1 | a0001c0001t0005g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126+11043T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180004 | |||||||
| chr4:173180081 | T | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(28): Show |
31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+11120T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180081 | |||||||
| chr4:173180294 | A | G | 1 | a0001c0002t0001g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.126+11333A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180294 | |||||||
| chr4:173180326 | C | CT | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.126+11383dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173180326 | ||||||
| chr4:173180326 | C | CTT | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
69 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.126+11382_126+1138 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173180326 | ||||||
| chr4:173180378 | A | G | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+11417A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180378 | |||||||
| chr4:173180547 | C | T | 1 | a0001c0006t0001g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.126+11586C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180547 | |||||||
| chr4:173180804 | A | G | 3 | a0001c0002t0001g0260 a0001c0003t0002g0258 a0001c0003t0002g0259 |
3 | NA18946.hp2 NA18971.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.126+11843A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180804 | |||||||
| chr4:173180951 | T | C | 1 | a0001c0002t0001g0202 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.126+11990T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173180951 | |||||||
| chr4:173181118 | C | T | 3 | a0001c0004t0001g0076 a0001c0004t0001g0077 a0001c0004t0001g0084 |
3 | HG02486.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.126+12157C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181118 | |||||||
| chr4:173181246 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.126+12285G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181246 | |||||||
| chr4:173181285 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+12324G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181285 | |||||||
| chr4:173181317 | A | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(3): Show |
6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+12356A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181317 | |||||||
| chr4:173181326 | T | A | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+12365T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181326 | |||||||
| chr4:173181539 | A | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+12578A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181539 | |||||||
| chr4:173181603 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+12642T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173181603 | |||||||
| chr4:173182200 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.126+13239G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182200 | |||||||
| chr4:173182334 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0028 |
2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.126+13373T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182334 | |||||||
| chr4:173182396 | T | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(77): Show |
80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.126+13435T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182396 | |||||||
| chr4:173182444 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+13483G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182444 | |||||||
| chr4:173182486 | C | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0100 a0001c0001t0001g0101 others(4): Show |
7 | HG01346.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+13525C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182486 | |||||||
| chr4:173182604 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
78 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.126+13643C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182604 | |||||||
| chr4:173182637 | A | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(3): Show |
6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+13676A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182637 | |||||||
| chr4:173182649 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+13688G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182649 | |||||||
| chr4:173182661 | T | TAC | 30 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0001g0061 others(27): Show |
30 | HG00140.hp1 HG00738.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+13734_126+1373 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | ||||||
| chr4:173182661 | T | TACAC | 17 | a0001c0001t0001g0109 a0001c0002t0001g0014 a0001c0002t0001g0019 others(14): Show |
17 | HG00621.hp2 HG00639.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+13732_126+1373 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | ||||||
| chr4:173182661 | T | TACACAC | 3 | a0001c0001t0002g0039 a0001c0002t0001g0184 a0005c0013t0001g0175 |
3 | HG02602.hp1 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.126+13730_126+1373 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | ||||||
| chr4:173182661 | T | TACACACA others(1): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0037 others(6): Show |
9 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+13728_126+1373 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | ||||||
| chr4:173182661 | T | TACACACA others(3): Show |
7 | a0001c0001t0002g0027 a0001c0001t0002g0030 a0001c0001t0002g0031 others(4): Show |
7 | HG02723.hp1 NA18942.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+13726_126+1373 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | ||||||
| chr4:173182661 | T | TACACACA others(5): Show |
5 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0024 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+13724_126+1373 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | ||||||
| chr4:173182661 | T | TACACACA others(9): Show |
1 | a0001c0001t0002g0023 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.126+13720_126+1373 others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | ||||||
| chr4:173182661 | TAC | T | 13 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0093 others(10): Show |
13 | HG01346.hp2 HG02055.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+13734_126+1373 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | ||||||
| chr4:173182661 | TACAC | T | 8 | a0001c0001t0001g0152 a0001c0001t0005g0075 a0001c0001t0005g0085 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+13732_126+1373 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | ||||||
| chr4:173182661 | TACACAC | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(14): Show |
17 | HG01081.hp2 HG01346.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+13730_126+1373 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182661 | ||||||
| chr4:173182699 | G | A | 1 | a0001c0002t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.126+13738G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182699 | |||||||
| chr4:173182738 | T | TAC | 45 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(42): Show |
45 | HG00323.hp2 HG01071.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.126+13803_126+1380 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182738 | ||||||
| chr4:173182738 | T | TACAC | 16 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
16 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+13801_126+1380 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182738 | ||||||
| chr4:173182738 | T | TACACACA others(1): Show |
15 | a0001c0002t0001g0247 a0001c0002t0001g0260 a0001c0003t0002g0021 others(12): Show |
15 | HG00423.hp1 HG02135.hp2 HG02965.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+13797_126+1380 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182738 | ||||||
| chr4:173182738 | TAC | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(28): Show |
31 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.126+13803_126+1380 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182738 | ||||||
| chr4:173182738 | TACAC | T | 6 | a0001c0002t0001g0237 a0001c0002t0002g0020 a0001c0002t0002g0240 others(3): Show |
6 | HG00323.hp1 HG02809.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+13801_126+1380 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182738 | ||||||
| chr4:173182752 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.126+13791C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182752 | |||||||
| chr4:173182817 | T | TAC | 109 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(106): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.126+13882_126+1388 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | ||||||
| chr4:173182817 | T | TACAC | 8 | a0001c0001t0001g0002 a0001c0001t0001g0107 a0001c0001t0001g0119 others(5): Show |
8 | HG01891.hp1 HG02602.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+13880_126+1388 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | ||||||
| chr4:173182817 | T | TACACACA others(3): Show |
1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.126+13874_126+1388 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | ||||||
| chr4:173182817 | T | TACACACA others(5): Show |
3 | a0001c0002t0009g0244 a0001c0002t0009g0245 a0006c0011t0002g0180 |
3 | HG03209.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.126+13872_126+1388 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | ||||||
| chr4:173182817 | T | TACACACA others(7): Show |
1 | a0001c0002t0002g0243 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.126+13870_126+1388 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | ||||||
| chr4:173182817 | T | TACACACA others(9): Show |
3 | a0001c0002t0002g0020 a0001c0002t0002g0241 a0001c0002t0002g0242 |
3 | HG02809.hp2 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.126+13868_126+1388 others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | ||||||
| chr4:173182817 | T | TACACACA others(13): Show |
1 | a0001c0002t0002g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.126+13864_126+1388 others(24): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | ||||||
| chr4:173182817 | TACAC | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+13880_126+1388 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | ||||||
| chr4:173182817 | TACACAC | T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(28): Show |
31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+13878_126+1388 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182817 | ||||||
| chr4:173182873 | A | T | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.126+13912A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173182873 | |||||||
| chr4:173182925 | T | TAC | 6 | a0001c0002t0001g0014 a0001c0002t0001g0183 a0001c0002t0001g0214 others(3): Show |
6 | HG00639.hp2 HG01109.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+13985_126+1398 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | ||||||
| chr4:173182925 | T | TACAC | 8 | a0001c0001t0001g0266 a0001c0002t0002g0020 a0001c0002t0002g0240 others(5): Show |
8 | HG02809.hp2 HG03209.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+13983_126+1398 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | ||||||
| chr4:173182925 | T | TACACACA others(1): Show |
15 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(12): Show |
15 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+13979_126+1398 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | ||||||
| chr4:173182925 | T | TACACACA others(3): Show |
30 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0048 others(27): Show |
30 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+13977_126+1398 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | ||||||
| chr4:173182925 | T | TACACACA others(5): Show |
36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0029 others(33): Show |
36 | HG00621.hp1 HG01192.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.126+13975_126+1398 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | ||||||
| chr4:173182925 | T | TACACACA others(7): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0094 others(10): Show |
13 | HG01993.hp2 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+13973_126+1398 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182925 | ||||||
| chr4:173182941 | C | CACACAG | 5 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+13985_126+1398 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173182941 | ||||||
| chr4:173183043 | A | AAC | 18 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0061 others(15): Show |
18 | HG00140.hp2 HG01255.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+14129_126+1413 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | A | AACAC | 6 | a0001c0002t0001g0016 a0001c0002t0001g0184 a0001c0002t0001g0185 others(3): Show |
6 | HG00140.hp1 HG01099.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+14127_126+1413 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | A | AACACACA others(5): Show |
1 | a0001c0002t0013g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.126+14119_126+1413 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | A | AACACACA others(8): Show |
1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+14094_126+1409 others(19): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | AAC | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(49): Show |
52 | HG00323.hp2 HG00558.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.126+14129_126+1413 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | AACAC | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(19): Show |
22 | HG00621.hp2 HG00741.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.126+14127_126+1413 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | AACACAC | A | 15 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(12): Show |
15 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+14125_126+1413 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | AACACACA others(1): Show |
A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0047 others(41): Show |
44 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+14123_126+1413 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | AACACACA others(3): Show |
A | 9 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0002t0002g0241 others(6): Show |
9 | HG01346.hp2 HG02738.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+14121_126+1413 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | AACACACA others(5): Show |
A | 10 | a0001c0001t0001g0094 a0001c0001t0005g0075 a0001c0001t0005g0085 others(7): Show |
10 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+14119_126+1413 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | AACACACA others(7): Show |
A | 5 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0025 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+14117_126+1413 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | AACACACA others(9): Show |
A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0100 a0001c0001t0001g0101 others(4): Show |
7 | HG01346.hp1 HG02257.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+14115_126+1413 others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183043 | AACACACA others(11): Show |
A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(26): Show |
29 | HG00621.hp1 HG01081.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+14113_126+1413 others(22): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183043 | ||||||
| chr4:173183143 | G | A | 1 | a0001c0003t0002g0249 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.126+14182G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183143 | |||||||
| chr4:173183256 | C | T | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+14295C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183256 | |||||||
| chr4:173183281 | C | CT | 5 | a0001c0001t0005g0086 a0001c0001t0011g0071 a0001c0006t0001g0072 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+14335dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183281 | ||||||
| chr4:173183281 | CT | C | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0015g0157 others(2): Show |
5 | HG01070.hp2 HG02965.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+14335delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183281 | ||||||
| chr4:173183478 | A | AT | 24 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(21): Show |
24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+14529dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183478 | ||||||
| chr4:173183518 | A | T | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+14557A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183518 | |||||||
| chr4:173183660 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(87): Show |
90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.126+14699G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183660 | |||||||
| chr4:173183684 | C | T | 24 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(21): Show |
24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+14723C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183684 | |||||||
| chr4:173183688 | C | T | 3 | a0001c0002t0001g0200 a0001c0002t0001g0211 a0001c0002t0013g0207 |
3 | HG02922.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.126+14727C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183688 | |||||||
| chr4:173183730 | G | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(21): Show |
24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+14769G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183730 | |||||||
| chr4:173183760 | G | A | 2 | a0001c0002t0001g0167 a0001c0002t0001g0168 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.126+14799G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183760 | |||||||
| chr4:173183776 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.126+14815A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183776 | |||||||
| chr4:173183781 | C | G | 1 | a0001c0008t0002g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.126+14820C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183781 | |||||||
| chr4:173183781 | C | T | 14 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(11): Show |
14 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+14820C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183781 | |||||||
| chr4:173183786 | C | G | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+14825C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183786 | |||||||
| chr4:173183795 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+14834C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183795 | |||||||
| chr4:173183800 | C | T | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+14839C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183800 | |||||||
| chr4:173183801 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.126+14840G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183801 | |||||||
| chr4:173183834 | CTCCCAGA others(33): Show |
C | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+14897_126+1493 others(44): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173183834 | ||||||
| chr4:173183851 | T | C | 20 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(17): Show |
20 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.126+14890T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183851 | |||||||
| chr4:173183858 | C | T | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+14897C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183858 | |||||||
| chr4:173183882 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(3): Show |
6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+14921C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183882 | |||||||
| chr4:173183893 | C | T | 2 | a0001c0003t0002g0021 a0001c0003t0002g0255 |
2 | HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.126+14932C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183893 | |||||||
| chr4:173183900 | G | A | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+14939G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173183900 | |||||||
| chr4:173184057 | C | T | 1 | a0001c0004t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.126+15096C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184057 | |||||||
| chr4:173184078 | G | A | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+15117G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184078 | |||||||
| chr4:173184124 | G | C | 21 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(18): Show |
21 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.126+15163G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184124 | |||||||
| chr4:173184132 | G | A | 9 | a0001c0002t0002g0020 a0001c0002t0002g0240 a0001c0002t0002g0241 others(6): Show |
9 | HG02809.hp2 HG03098.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+15171G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184132 | |||||||
| chr4:173184148 | C | T | 1 | a0001c0002t0001g0263 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.126+15187C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184148 | |||||||
| chr4:173184152 | C | T | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+15191C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184152 | |||||||
| chr4:173184191 | C | CG | 7 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(4): Show |
7 | HG01952.hp1 HG02027.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+15234dupG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173184191 | ||||||
| chr4:173184247 | C | T | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+15286C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184247 | |||||||
| chr4:173184271 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
99 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.126+15310G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184271 | |||||||
| chr4:173184386 | C | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG00280.hp2 HG01099.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.126+15425C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184386 | |||||||
| chr4:173184405 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(93): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.126+15444C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184405 | |||||||
| chr4:173184430 | C | T | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+15469C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184430 | |||||||
| chr4:173184467 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+15506G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184467 | |||||||
| chr4:173184563 | GGCTCGGC others(25): Show |
G | 1 | a0001c0002t0001g0179 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.126+15636_126+1566 others(36): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173184563 | ||||||
| chr4:173184621 | A | C | 2 | a0001c0002t0001g0014 a0001c0002t0001g0183 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.126+15660A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184621 | |||||||
| chr4:173184630 | G | A | 2 | a0001c0003t0002g0246 a0001c0003t0002g0249 |
2 | NA18963.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.126+15669G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184630 | |||||||
| chr4:173184690 | G | C | 24 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(21): Show |
24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+15729G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184690 | |||||||
| chr4:173184743 | TA | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
78 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.126+15792delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173184743 | ||||||
| chr4:173184787 | T | C | 1 | a0006c0011t0002g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126+15826T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184787 | |||||||
| chr4:173184865 | G | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+15904G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184865 | |||||||
| chr4:173184952 | C | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+15991C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173184952 | |||||||
| chr4:173185064 | A | G | 1 | a0001c0002t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.126+16103A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185064 | |||||||
| chr4:173185150 | C | G | 3 | a0001c0002t0001g0187 a0001c0002t0001g0195 a0001c0002t0001g0198 |
3 | HG01952.hp1 HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.126+16189C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185150 | |||||||
| chr4:173185264 | T | C | 31 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(28): Show |
31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+16303T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185264 | |||||||
| chr4:173185413 | C | CA | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.126+16466dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173185413 | ||||||
| chr4:173185413 | C | CAA | 9 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0191 others(6): Show |
9 | HG01952.hp1 HG02027.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+16465_126+1646 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173185413 | ||||||
| chr4:173185512 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+16551C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185512 | |||||||
| chr4:173185599 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.126+16638T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185599 | |||||||
| chr4:173185656 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.126+16695A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173185656 | |||||||
| chr4:173186083 | G | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0064 |
2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.126+17122G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186083 | |||||||
| chr4:173186148 | A | T | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+17187A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186148 | |||||||
| chr4:173186227 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.126+17266A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186227 | |||||||
| chr4:173186278 | C | A | 7 | a0001c0002t0002g0020 a0001c0002t0002g0240 a0001c0002t0002g0241 others(4): Show |
7 | HG02809.hp2 HG03209.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+17317C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186278 | |||||||
| chr4:173186278 | C | T | 1 | a0001c0003t0002g0253 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.126+17317C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186278 | |||||||
| chr4:173186279 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+17318G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186279 | |||||||
| chr4:173186386 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
100 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.126+17425T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186386 | |||||||
| chr4:173186420 | C | T | 1 | a0001c0003t0002g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.126+17459C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186420 | |||||||
| chr4:173186512 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.126+17551T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186512 | |||||||
| chr4:173186780 | C | CT | 19 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0001g0247 others(16): Show |
19 | HG00423.hp1 HG01891.hp2 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.126+17831dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173186780 | ||||||
| chr4:173186783 | T | A | 9 | a0001c0002t0002g0020 a0001c0002t0002g0240 a0001c0002t0002g0241 others(6): Show |
9 | HG02809.hp2 HG03098.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+17822T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186783 | |||||||
| chr4:173186889 | C | T | 3 | a0001c0002t0001g0187 a0001c0002t0001g0195 a0001c0002t0001g0198 |
3 | HG01952.hp1 HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.126+17928C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186889 | |||||||
| chr4:173186930 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.126+17969A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186930 | |||||||
| chr4:173186981 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+18020C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173186981 | |||||||
| chr4:173187000 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.126+18039C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187000 | |||||||
| chr4:173187096 | T | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+18135T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187096 | |||||||
| chr4:173187284 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.126+18323G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187284 | |||||||
| chr4:173187308 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
78 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.126+18347T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187308 | |||||||
| chr4:173187311 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(28): Show |
31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+18350G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187311 | |||||||
| chr4:173187383 | G | GA | 15 | a0001c0001t0001g0103 a0001c0002t0001g0260 a0001c0003t0002g0021 others(12): Show |
15 | HG00423.hp1 HG02135.hp2 HG03834.hp2 others(12): Show |
intron_variant | MODIFIER | c.126+18436dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173187383 | ||||||
| chr4:173187383 | GA | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(23): Show |
26 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.126+18436delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173187383 | ||||||
| chr4:173187450 | A | G | 1 | a0001c0002t0001g0229 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.126+18489A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187450 | |||||||
| chr4:173187603 | G | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+18642G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187603 | |||||||
| chr4:173187778 | G | T | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.126+18817G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173187778 | |||||||
| chr4:173188048 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+19087T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188048 | |||||||
| chr4:173188460 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+19499A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188460 | |||||||
| chr4:173188471 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+19510C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188471 | |||||||
| chr4:173188513 | A | C | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+19552A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188513 | |||||||
| chr4:173188552 | C | G | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+19591C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188552 | |||||||
| chr4:173188666 | C | T | 1 | a0001c0002t0001g0204 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.126+19705C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188666 | |||||||
| chr4:173188691 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.126+19730C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188691 | |||||||
| chr4:173188739 | C | T | 1 | a0001c0002t0001g0202 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.126+19778C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188739 | |||||||
| chr4:173188970 | C | G | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126+20009C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188970 | |||||||
| chr4:173188970 | C | T | 2 | a0001c0002t0001g0247 a0001c0002t0001g0257 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.126+20009C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173188970 | |||||||
| chr4:173189045 | C | T | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+20084C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189045 | |||||||
| chr4:173189165 | C | A | 1 | a0001c0005t0003g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.126+20204C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189165 | |||||||
| chr4:173189178 | A | T | 1 | a0001c0002t0001g0229 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.126+20217A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189178 | |||||||
| chr4:173189405 | A | T | 2 | a0001c0002t0001g0014 a0001c0002t0001g0183 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.126+20444A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189405 | |||||||
| chr4:173189425 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.126+20464A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189425 | |||||||
| chr4:173189492 | T | C | 2 | a0001c0002t0001g0014 a0001c0002t0001g0183 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.126+20531T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189492 | |||||||
| chr4:173189506 | T | C | 24 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(21): Show |
24 | HG01081.hp2 HG01346.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+20545T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189506 | |||||||
| chr4:173189724 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.126+20763T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189724 | |||||||
| chr4:173189746 | T | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+20785T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189746 | |||||||
| chr4:173189994 | G | GT | 8 | a0001c0002t0002g0020 a0001c0002t0002g0240 a0001c0002t0002g0241 others(5): Show |
8 | HG02809.hp2 HG03209.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+21046dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173189994 | ||||||
| chr4:173189994 | G | T | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0004t0001g0006 others(6): Show |
9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+21033G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173189994 | |||||||
| chr4:173189994 | GT | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
27 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.126+21046delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173189994 | ||||||
| chr4:173190037 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.126+21076G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190037 | |||||||
| chr4:173190088 | T | A | 17 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(14): Show |
17 | HG01081.hp2 HG01346.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+21127T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190088 | |||||||
| chr4:173190103 | T | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(14): Show |
17 | HG01081.hp2 HG01346.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+21142T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190103 | |||||||
| chr4:173190223 | G | A | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+21262G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190223 | |||||||
| chr4:173190312 | C | T | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+21351C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190312 | |||||||
| chr4:173190529 | G | C | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0004t0001g0006 others(6): Show |
9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+21568G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190529 | |||||||
| chr4:173190542 | A | G | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126+21581A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190542 | |||||||
| chr4:173190888 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG02027.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.126+21927C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190888 | |||||||
| chr4:173190906 | T | G | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+21945T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190906 | |||||||
| chr4:173190908 | G | T | 1 | a0001c0001t0004g0154 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.126+21947G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190908 | |||||||
| chr4:173190936 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
100 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.126+21975T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173190936 | |||||||
| chr4:173191046 | G | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+22085G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191046 | |||||||
| chr4:173191063 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.126+22102G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191063 | |||||||
| chr4:173191063 | GA | G | 8 | a0001c0001t0001g0059 a0001c0002t0001g0173 a0001c0002t0001g0174 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+22114delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173191063 | ||||||
| chr4:173191063 | GAA | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+22113_126+2211 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173191063 | ||||||
| chr4:173191124 | A | C | 1 | a0001c0001t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+22163A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191124 | |||||||
| chr4:173191209 | A | G | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126+22248A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191209 | |||||||
| chr4:173191227 | T | TG | 19 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(16): Show |
19 | HG01257.hp1 HG01346.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.126+22274dupG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173191227 | ||||||
| chr4:173191230 | G | C | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.126+22269G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191230 | |||||||
| chr4:173191359 | C | T | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+22398C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191359 | |||||||
| chr4:173191385 | G | A | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+22424G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191385 | |||||||
| chr4:173191392 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
193 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.126+22431C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191392 | |||||||
| chr4:173191439 | G | A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(22): Show |
25 | HG01081.hp2 HG01346.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.126+22478G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191439 | |||||||
| chr4:173191487 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(3): Show |
6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+22526G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191487 | |||||||
| chr4:173191577 | G | A | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+22616G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173191577 | |||||||
| chr4:173192058 | C | A | 2 | a0001c0001t0005g0085 a0001c0001t0005g0086 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.126+23097C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192058 | |||||||
| chr4:173192083 | T | C | 1 | a0001c0002t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.126+23122T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192083 | |||||||
| chr4:173192212 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | HG00280.hp2 HG01099.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+23251A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192212 | |||||||
| chr4:173192223 | C | T | 1 | a0001c0002t0001g0228 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.126+23262C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192223 | |||||||
| chr4:173192308 | C | A | 1 | a0001c0001t0004g0130 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.126+23347C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192308 | |||||||
| chr4:173192475 | A | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+23514A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192475 | |||||||
| chr4:173192614 | G | A | 4 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+23653G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192614 | |||||||
| chr4:173192938 | C | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
103 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.126+23977C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173192938 | |||||||
| chr4:173193013 | G | C | 1 | a0001c0002t0001g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.126+24052G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193013 | |||||||
| chr4:173193386 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+24425G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193386 | |||||||
| chr4:173193428 | C | T | 2 | a0001c0002t0006g0170 a0001c0002t0006g0171 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.126+24467C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193428 | |||||||
| chr4:173193493 | T | A | 1 | a0001c0001t0005g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126+24532T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193493 | |||||||
| chr4:173193504 | C | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+24543C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193504 | |||||||
| chr4:173193563 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | NA18966.hp1 NA18969.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.126+24602A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173193563 | |||||||
| chr4:173194244 | A | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.126+25283A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194244 | |||||||
| chr4:173194272 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(3): Show |
6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+25311G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194272 | |||||||
| chr4:173194308 | G | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0043 |
2 | HG01192.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.126+25347G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194308 | |||||||
| chr4:173194405 | T | C | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.126+25444T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194405 | |||||||
| chr4:173194579 | C | A | 2 | a0005c0013t0001g0175 a0006c0011t0002g0180 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.126+25618C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194579 | |||||||
| chr4:173194580 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.126+25619G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194580 | |||||||
| chr4:173194776 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(26): Show |
29 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+25815C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194776 | |||||||
| chr4:173194778 | T | A | 1 | a0001c0002t0001g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.126+25817T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194778 | |||||||
| chr4:173194793 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+25832C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173194793 | |||||||
| chr4:173195284 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+26323C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195284 | |||||||
| chr4:173195304 | A | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0062 others(11): Show |
14 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+26343A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195304 | |||||||
| chr4:173195379 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.126+26418G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195379 | |||||||
| chr4:173195405 | G | C | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+26444G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195405 | |||||||
| chr4:173195461 | G | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(27): Show |
30 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+26500G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195461 | |||||||
| chr4:173195873 | T | G | 1 | a0001c0002t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.126+26912T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173195873 | |||||||
| chr4:173196127 | A | AT | 51 | a0001c0001t0001g0070 a0001c0001t0001g0124 a0001c0001t0001g0125 others(48): Show |
51 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.126+27181dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173196127 | ||||||
| chr4:173196155 | C | T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.126+27194C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196155 | |||||||
| chr4:173196252 | G | A | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+27291G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196252 | |||||||
| chr4:173196269 | C | T | 7 | a0001c0002t0001g0214 a0001c0002t0001g0215 a0001c0002t0001g0216 others(4): Show |
7 | HG01074.hp2 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+27308C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196269 | |||||||
| chr4:173196325 | A | G | 2 | a0005c0013t0001g0175 a0006c0011t0002g0180 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.126+27364A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196325 | |||||||
| chr4:173196732 | C | T | 2 | a0001c0002t0001g0219 a0001c0002t0001g0226 |
2 | NA18948.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.126+27771C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196732 | |||||||
| chr4:173196950 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(27): Show |
30 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+27989C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173196950 | |||||||
| chr4:173197063 | C | CT | 136 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.126+28122dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | ||||||
| chr4:173197063 | C | CTT | 11 | a0001c0001t0001g0002 a0001c0001t0014g0054 a0001c0002t0002g0020 others(8): Show |
11 | HG02273.hp2 HG02809.hp2 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.126+28121_126+2812 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | ||||||
| chr4:173197063 | C | CTTT | 48 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(45): Show |
48 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.126+28120_126+2812 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | ||||||
| chr4:173197063 | CT | C | 6 | a0001c0002t0001g0014 a0001c0002t0001g0183 a0001c0002t0006g0170 others(3): Show |
6 | HG00639.hp2 HG01109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+28122delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | ||||||
| chr4:173197063 | CTTTT | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
18 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.126+28119_126+2812 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | ||||||
| chr4:173197063 | CTTTTT | C | 14 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0025 others(11): Show |
14 | HG01952.hp1 HG02027.hp2 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+28118_126+2812 others(9): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197063 | ||||||
| chr4:173197137 | A | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+28176A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197137 | |||||||
| chr4:173197298 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.126+28337G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197298 | |||||||
| chr4:173197358 | TG | T | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+28398delG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197358 | |||||||
| chr4:173197379 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.126+28418G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197379 | |||||||
| chr4:173197434 | TAATC | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+28477_126+2848 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173197434 | ||||||
| chr4:173197507 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0062 others(9): Show |
12 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+28546A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197507 | |||||||
| chr4:173197519 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.126+28558T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197519 | |||||||
| chr4:173197898 | G | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0062 others(11): Show |
14 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+28937G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173197898 | |||||||
| chr4:173198065 | CT | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(61): Show |
64 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.126+29116delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198065 | ||||||
| chr4:173198065 | CTT | C | 49 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0018 others(46): Show |
49 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.126+29115_126+2911 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198065 | ||||||
| chr4:173198069 | T | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+29108T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198069 | |||||||
| chr4:173198216 | T | C | 1 | a0001c0001t0002g0031 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.126+29255T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198216 | |||||||
| chr4:173198226 | A | AT | 22 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0079 others(19): Show |
22 | HG01081.hp2 HG01884.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+29280dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198226 | ||||||
| chr4:173198226 | A | ATT | 54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(51): Show |
54 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.126+29279_126+2928 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198226 | ||||||
| chr4:173198226 | A | ATTT | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(152): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.126+29278_126+2928 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198226 | ||||||
| chr4:173198226 | A | ATTTT | 10 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0037 others(7): Show |
10 | HG01099.hp1 HG01993.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+29277_126+2928 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173198226 | ||||||
| chr4:173198265 | T | C | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+29304T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198265 | |||||||
| chr4:173198281 | G | A | 1 | a0001c0008t0002g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.126+29320G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198281 | |||||||
| chr4:173198290 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+29329G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198290 | |||||||
| chr4:173198319 | C | T | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+29358C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198319 | |||||||
| chr4:173198330 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.126+29369G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198330 | |||||||
| chr4:173198364 | G | A | 1 | a0001c0002t0001g0193 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+29403G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198364 | |||||||
| chr4:173198370 | G | T | 1 | a0001c0002t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.126+29409G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198370 | |||||||
| chr4:173198417 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.126+29456A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198417 | |||||||
| chr4:173198458 | T | A | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+29497T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198458 | |||||||
| chr4:173198526 | A | G | 9 | a0001c0002t0002g0020 a0001c0002t0002g0240 a0001c0002t0002g0241 others(6): Show |
9 | HG02809.hp2 HG03098.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+29565A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198526 | |||||||
| chr4:173198578 | C | G | 1 | a0001c0001t0002g0026 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.126+29617C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198578 | |||||||
| chr4:173198609 | A | G | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+29648A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198609 | |||||||
| chr4:173198711 | G | C | 10 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(7): Show |
10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+29750G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198711 | |||||||
| chr4:173198773 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.126+29812G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173198773 | |||||||
| chr4:173199110 | A | T | 1 | a0001c0001t0005g0075 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126+30149A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199110 | |||||||
| chr4:173199124 | C | A | 3 | a0001c0002t0001g0261 a0001c0002t0001g0262 a0001c0002t0001g0263 |
3 | HG00597.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.126+30163C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199124 | |||||||
| chr4:173199131 | G | A | 3 | a0001c0002t0001g0261 a0001c0002t0001g0262 a0001c0002t0001g0263 |
3 | HG00597.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.126+30170G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199131 | |||||||
| chr4:173199133 | G | A | 1 | a0001c0002t0001g0261 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.126+30172G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199133 | |||||||
| chr4:173199203 | G | A | 1 | a0001c0003t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.126+30242G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199203 | |||||||
| chr4:173199352 | C | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+30391C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199352 | |||||||
| chr4:173199401 | G | A | 1 | a0001c0002t0001g0217 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.126+30440G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199401 | |||||||
| chr4:173199479 | T | C | 1 | a0001c0002t0001g0014 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.126+30518T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199479 | |||||||
| chr4:173199499 | G | A | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+30538G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199499 | |||||||
| chr4:173199755 | C | T | 49 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0018 others(46): Show |
49 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.126+30794C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199755 | |||||||
| chr4:173199925 | T | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0111 a0001c0001t0001g0145 others(1): Show |
4 | HG00741.hp2 HG01074.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+30964T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199925 | |||||||
| chr4:173199968 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.126+31007T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199968 | |||||||
| chr4:173199977 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.126+31016A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173199977 | |||||||
| chr4:173200195 | T | G | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+31234T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173200195 | |||||||
| chr4:173200450 | T | TA | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+31501dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173200450 | ||||||
| chr4:173200450 | TA | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+31501delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173200450 | ||||||
| chr4:173200599 | C | T | 15 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+31638C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173200599 | |||||||
| chr4:173200773 | C | G | 10 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(7): Show |
10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+31812C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173200773 | |||||||
| chr4:173201024 | T | A | 1 | a0001c0002t0001g0205 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.126+32063T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201024 | |||||||
| chr4:173201105 | A | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.126+32144A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201105 | |||||||
| chr4:173201148 | C | T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.126+32187C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201148 | |||||||
| chr4:173201238 | AAT | A | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+32279_126+3228 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173201238 | ||||||
| chr4:173201286 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.126+32325T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201286 | |||||||
| chr4:173201405 | A | G | 49 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0018 others(46): Show |
49 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.126+32444A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201405 | |||||||
| chr4:173201439 | T | C | 1 | a0001c0002t0001g0206 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.126+32478T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201439 | |||||||
| chr4:173201469 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+32508A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201469 | |||||||
| chr4:173201654 | A | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+32693A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201654 | |||||||
| chr4:173201994 | A | G | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+33033A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173201994 | |||||||
| chr4:173202033 | A | T | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+33072A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202033 | |||||||
| chr4:173202156 | G | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.126+33195G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202156 | |||||||
| chr4:173202293 | G | C | 2 | a0001c0002t0001g0191 a0001c0002t0002g0197 |
2 | HG02027.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.126+33332G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202293 | |||||||
| chr4:173202366 | A | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0265 |
2 | NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.126+33405A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202366 | |||||||
| chr4:173202526 | A | T | 1 | a0001c0001t0004g0110 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.126+33565A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202526 | |||||||
| chr4:173202640 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.126+33679A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202640 | |||||||
| chr4:173202821 | A | C | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.126+33860A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202821 | |||||||
| chr4:173202841 | G | T | 15 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+33880G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173202841 | |||||||
| chr4:173203016 | AT | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(32): Show |
35 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.126+34068delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173203016 | ||||||
| chr4:173203017 | T | A | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+34056T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203017 | |||||||
| chr4:173203046 | G | A | 1 | a0006c0011t0002g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126+34085G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203046 | |||||||
| chr4:173203057 | C | G | 3 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 |
3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.126+34096C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203057 | |||||||
| chr4:173203126 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0005g0085 |
3 | HG02145.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.126+34165C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203126 | |||||||
| chr4:173203239 | G | T | 1 | a0001c0001t0001g0009 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.126+34278G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203239 | |||||||
| chr4:173203243 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+34282G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203243 | |||||||
| chr4:173203283 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.126+34322C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203283 | |||||||
| chr4:173203298 | A | G | 1 | a0001c0002t0001g0261 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.126+34337A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203298 | |||||||
| chr4:173203324 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.126+34363T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203324 | |||||||
| chr4:173203327 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.126+34366G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203327 | |||||||
| chr4:173203342 | C | T | 1 | a0001c0003t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.126+34381C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203342 | |||||||
| chr4:173203456 | A | C | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.126+34495A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203456 | |||||||
| chr4:173203479 | A | C | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0004t0001g0006 others(6): Show |
9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+34518A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203479 | |||||||
| chr4:173203556 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.126+34595A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203556 | |||||||
| chr4:173203653 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+34692G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203653 | |||||||
| chr4:173203826 | TTAAA | T | 7 | a0001c0002t0002g0020 a0001c0002t0002g0240 a0001c0002t0002g0241 others(4): Show |
7 | HG02809.hp2 HG03209.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+34869_126+3487 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173203826 | ||||||
| chr4:173203964 | A | G | 4 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+35003A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203964 | |||||||
| chr4:173203979 | C | T | 3 | a0001c0002t0001g0199 a0001c0002t0001g0228 a0001c0003t0002g0234 |
3 | HG00558.hp1 NA18964.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.126+35018C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203979 | |||||||
| chr4:173203982 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.126+35021G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173203982 | |||||||
| chr4:173204282 | C | T | 1 | a0001c0002t0001g0185 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.126+35321C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204282 | |||||||
| chr4:173204524 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+35563T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204524 | |||||||
| chr4:173204749 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.126+35788G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204749 | |||||||
| chr4:173204793 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0064 |
2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.126+35832T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204793 | |||||||
| chr4:173204794 | A | G | 2 | a0001c0002t0001g0167 a0001c0002t0001g0168 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.126+35833A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204794 | |||||||
| chr4:173204832 | T | C | 1 | a0001c0002t0001g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.126+35871T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204832 | |||||||
| chr4:173204986 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.126+36025A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173204986 | |||||||
| chr4:173205097 | C | G | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.126+36136C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205097 | |||||||
| chr4:173205110 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.126+36149G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205110 | |||||||
| chr4:173205260 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.126+36299T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205260 | |||||||
| chr4:173205306 | G | A | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+36345G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205306 | |||||||
| chr4:173205676 | GGGTCTGA others(13): Show |
G | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.126+36737_126+3675 others(24): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173205676 | ||||||
| chr4:173205785 | G | C | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+36824G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205785 | |||||||
| chr4:173205813 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.126+36852C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205813 | |||||||
| chr4:173205880 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(87): Show |
90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.126+36919G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173205880 | |||||||
| chr4:173206274 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+37313G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206274 | |||||||
| chr4:173206285 | A | G | 10 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(7): Show |
10 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+37324A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206285 | |||||||
| chr4:173206326 | T | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0122 |
2 | NA18983.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.126+37365T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206326 | |||||||
| chr4:173206474 | A | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(27): Show |
30 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+37513A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206474 | |||||||
| chr4:173206556 | G | C | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+37595G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206556 | |||||||
| chr4:173206765 | T | G | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+37804T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206765 | |||||||
| chr4:173206903 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.126+37942G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173206903 | |||||||
| chr4:173207102 | G | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126+38141G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173207102 | |||||||
| chr4:173207364 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126+38403A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173207364 | |||||||
| chr4:173207514 | C | T | 20 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(17): Show |
20 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.126+38553C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173207514 | |||||||
| chr4:173207619 | T | A | 2 | a0001c0001t0004g0130 a0001c0001t0004g0154 |
2 | HG01952.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.126+38658T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173207619 | |||||||
| chr4:173207762 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.126+38801T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173207762 | |||||||
| chr4:173208320 | C | T | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.126+39359C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208320 | |||||||
| chr4:173208488 | A | G | 1 | a0001c0002t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.127-39492A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208488 | |||||||
| chr4:173208545 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.127-39435C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208545 | |||||||
| chr4:173208589 | A | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(87): Show |
90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.127-39391A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208589 | |||||||
| chr4:173208633 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.127-39347G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208633 | |||||||
| chr4:173208651 | T | G | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-39329T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208651 | |||||||
| chr4:173208770 | C | A | 1 | a0001c0001t0001g0129 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.127-39210C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208770 | |||||||
| chr4:173208807 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-39173A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173208807 | |||||||
| chr4:173209054 | A | G | 3 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 |
3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.127-38926A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209054 | |||||||
| chr4:173209114 | T | G | 1 | a0001c0002t0006g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.127-38866T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209114 | |||||||
| chr4:173209257 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.127-38723C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209257 | |||||||
| chr4:173209341 | G | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(27): Show |
30 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.127-38639G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209341 | |||||||
| chr4:173209352 | T | C | 49 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0018 others(46): Show |
49 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.127-38628T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209352 | |||||||
| chr4:173209435 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-38545G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209435 | |||||||
| chr4:173209521 | T | G | 1 | a0001c0002t0001g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-38459T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209521 | |||||||
| chr4:173209716 | C | G | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-38264C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173209716 | |||||||
| chr4:173210007 | C | T | 1 | a0001c0002t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.127-37973C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210007 | |||||||
| chr4:173210133 | CA | C | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-37840delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173210133 | ||||||
| chr4:173210141 | G | GA | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0004t0001g0006 others(6): Show |
9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-37826dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173210141 | ||||||
| chr4:173210165 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-37815T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210165 | |||||||
| chr4:173210194 | G | A | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-37786G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210194 | |||||||
| chr4:173210296 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.127-37684G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210296 | |||||||
| chr4:173210305 | G | T | 1 | a0001c0002t0001g0213 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.127-37675G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210305 | |||||||
| chr4:173210323 | G | A | 1 | a0001c0005t0003g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.127-37657G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210323 | |||||||
| chr4:173210520 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.127-37460T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210520 | |||||||
| chr4:173210630 | A | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-37350A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210630 | |||||||
| chr4:173210647 | G | A | 15 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-37333G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210647 | |||||||
| chr4:173210710 | G | T | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-37270G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210710 | |||||||
| chr4:173210720 | C | T | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-37260C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210720 | |||||||
| chr4:173210758 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(4): Show |
7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-37222T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210758 | |||||||
| chr4:173210875 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0133 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.127-37105T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210875 | |||||||
| chr4:173210993 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(4): Show |
7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-36987G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210993 | |||||||
| chr4:173210995 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.127-36985G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173210995 | |||||||
| chr4:173211026 | C | T | 1 | a0001c0003t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.127-36954C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211026 | |||||||
| chr4:173211059 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.127-36921A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211059 | |||||||
| chr4:173211259 | C | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-36721C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211259 | |||||||
| chr4:173211273 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(4): Show |
7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-36707C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211273 | |||||||
| chr4:173211288 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-36692G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211288 | |||||||
| chr4:173211299 | C | T | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-36681C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211299 | |||||||
| chr4:173211337 | G | A | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-36643G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211337 | |||||||
| chr4:173211468 | C | T | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-36512C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211468 | |||||||
| chr4:173211489 | C | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-36491C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211489 | |||||||
| chr4:173211682 | A | G | 1 | a0001c0004t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-36298A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211682 | |||||||
| chr4:173211834 | T | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.127-36146T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173211834 | |||||||
| chr4:173212486 | C | T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(29): Show |
32 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.127-35494C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212486 | |||||||
| chr4:173212628 | C | CT | 26 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(23): Show |
26 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.127-35339dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173212628 | ||||||
| chr4:173212628 | CT | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.127-35339delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173212628 | ||||||
| chr4:173212683 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(4): Show |
7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-35297G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212683 | |||||||
| chr4:173212707 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-35273A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212707 | |||||||
| chr4:173212734 | CAT | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.127-35245_127-3524 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212734 | |||||||
| chr4:173212819 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-35161C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212819 | |||||||
| chr4:173212843 | A | C | 2 | a0001c0002t0009g0244 a0001c0002t0009g0245 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-35137A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173212843 | |||||||
| chr4:173213117 | G | A | 3 | a0001c0004t0001g0006 a0001c0005t0003g0097 a0001c0005t0003g0098 |
3 | HG02055.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.127-34863G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213117 | |||||||
| chr4:173213228 | T | TG | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.127-34752_127-3475 others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213228 | |||||||
| chr4:173213241 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-34739C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213241 | |||||||
| chr4:173213277 | C | T | 1 | a0001c0002t0001g0202 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.127-34703C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213277 | |||||||
| chr4:173213381 | A | G | 3 | a0001c0002t0001g0206 a0001c0002t0001g0218 a0001c0002t0001g0223 |
3 | HG01981.hp1 HG02056.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.127-34599A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213381 | |||||||
| chr4:173213533 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.127-34447G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213533 | |||||||
| chr4:173213670 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-34310G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173213670 | |||||||
| chr4:173214136 | T | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-33844T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173214136 | |||||||
| chr4:173214143 | AT | A | 4 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-33835delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214143 | ||||||
| chr4:173214288 | T | TA | 32 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(29): Show |
32 | HG00621.hp1 HG01192.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.127-33678dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214288 | ||||||
| chr4:173214288 | T | TAA | 10 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(7): Show |
10 | HG02257.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-33679_127-3367 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214288 | ||||||
| chr4:173214288 | TA | T | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-33678delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214288 | ||||||
| chr4:173214644 | A | G | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(8): Show |
11 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.127-33336A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173214644 | |||||||
| chr4:173214656 | C | A | 1 | a0001c0001t0002g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-33324C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173214656 | |||||||
| chr4:173214802 | A | AT | 6 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(3): Show |
6 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-33163dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214802 | ||||||
| chr4:173214802 | AT | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.127-33163delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214802 | ||||||
| chr4:173214802 | ATT | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0046 a0001c0001t0001g0061 others(11): Show |
14 | HG00423.hp2 HG01256.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-33164_127-3316 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173214802 | ||||||
| chr4:173214980 | T | C | 3 | a0001c0002t0001g0200 a0001c0002t0001g0211 a0001c0002t0013g0207 |
3 | HG02922.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.127-33000T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173214980 | |||||||
| chr4:173215232 | C | CT | 58 | a0001c0001t0001g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(55): Show |
58 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.127-32732dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173215232 | ||||||
| chr4:173215235 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.127-32745T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215235 | |||||||
| chr4:173215236 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.127-32744T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215236 | |||||||
| chr4:173215299 | C | T | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127-32681C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215299 | |||||||
| chr4:173215395 | T | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0062 others(11): Show |
14 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-32585T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215395 | |||||||
| chr4:173215416 | A | G | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-32564A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215416 | |||||||
| chr4:173215482 | G | A | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127-32498G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215482 | |||||||
| chr4:173215566 | A | G | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127-32414A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215566 | |||||||
| chr4:173215570 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.127-32410G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215570 | |||||||
| chr4:173215605 | C | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-32375C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215605 | |||||||
| chr4:173215606 | G | A | 1 | a0001c0002t0001g0214 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.127-32374G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215606 | |||||||
| chr4:173215708 | A | G | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-32272A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215708 | |||||||
| chr4:173215801 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.127-32179C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215801 | |||||||
| chr4:173215848 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(82): Show |
85 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.127-32132G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215848 | |||||||
| chr4:173215966 | A | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(82): Show |
85 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.127-32014A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173215966 | |||||||
| chr4:173216032 | G | A | 4 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-31948G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216032 | |||||||
| chr4:173216109 | C | A | 1 | a0001c0001t0001g0010 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.127-31871C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216109 | |||||||
| chr4:173216147 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.127-31833G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216147 | |||||||
| chr4:173216165 | A | G | 4 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-31815A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216165 | |||||||
| chr4:173216362 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.127-31618A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216362 | |||||||
| chr4:173216372 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.127-31608G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216372 | |||||||
| chr4:173216372 | G | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(32): Show |
35 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-31608G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216372 | |||||||
| chr4:173216589 | A | G | 1 | a0001c0002t0001g0214 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.127-31391A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216589 | |||||||
| chr4:173216619 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-31361G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216619 | |||||||
| chr4:173216654 | G | A | 1 | a0001c0001t0004g0110 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.127-31326G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216654 | |||||||
| chr4:173216706 | C | CAT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.127-31253_127-3125 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | ||||||
| chr4:173216706 | C | CATAT | 4 | a0001c0001t0001g0037 a0001c0001t0002g0032 a0001c0001t0002g0033 others(1): Show |
4 | NA18964.hp1 NA18970.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-31255_127-3125 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | ||||||
| chr4:173216706 | C | CATATATA others(3): Show |
1 | a0001c0002t0001g0191 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.127-31261_127-3125 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | ||||||
| chr4:173216706 | C | CATATATA others(17): Show |
5 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0186 others(2): Show |
5 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(28): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | ||||||
| chr4:173216706 | C | CATATATA others(19): Show |
2 | a0001c0002t0001g0185 a0001c0002t0001g0192 |
2 | HG02897.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(30): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | ||||||
| chr4:173216706 | C | CATATATA others(21): Show |
1 | a0001c0002t0001g0014 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(32): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | ||||||
| chr4:173216706 | C | CATATATA others(25): Show |
1 | a0001c0002t0001g0183 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.127-31252_127-3125 others(36): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | ||||||
| chr4:173216706 | C | CATATATA others(27): Show |
1 | a0001c0002t0001g0238 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(38): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216706 | ||||||
| chr4:173216718 | T | A | 14 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(11): Show |
14 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-31262T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216718 | |||||||
| chr4:173216719 | A | ATT | 5 | a0001c0001t0005g0085 a0001c0001t0005g0086 a0001c0001t0011g0071 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-31260_127-3125 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216719 | ||||||
| chr4:173216721 | A | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-31259A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216721 | |||||||
| chr4:173216723 | A | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-31257A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216723 | |||||||
| chr4:173216725 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0004g0154 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.127-31254_127-3125 others(15): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216725 | ||||||
| chr4:173216725 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0107 a0001c0001t0001g0141 |
2 | HG02083.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.127-31254_127-3125 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216725 | ||||||
| chr4:173216725 | A | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-31255A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216725 | |||||||
| chr4:173216727 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127-31252_127-3125 others(25): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(18): Show |
3 | a0001c0001t0003g0078 a0001c0001t0003g0081 a0001c0002t0001g0189 |
3 | HG02615.hp2 NA18970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(29): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(17): Show |
1 | a0001c0002t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(28): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(15): Show |
1 | a0001c0001t0003g0082 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(26): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(16): Show |
1 | a0001c0002t0011g0222 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(27): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(20): Show |
2 | a0001c0002t0001g0184 a0001c0004t0001g0084 |
2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(31): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(26): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(12): Show |
2 | a0001c0004t0001g0076 a0001c0004t0001g0077 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(23): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(9): Show |
3 | a0001c0004t0001g0006 a0001c0005t0003g0097 a0001c0005t0003g0098 |
3 | HG02055.hp1 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(2): Show |
12 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(9): Show |
12 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(3): Show |
5 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0014g0054 others(2): Show |
5 | HG02273.hp2 HG02738.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(17): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATTT others(1): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
6 | HG01257.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATTT others(3): Show |
7 | a0001c0001t0001g0045 a0001c0001t0001g0056 a0001c0001t0001g0057 others(4): Show |
7 | HG00280.hp2 HG01099.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATTT others(4): Show |
7 | a0001c0001t0001g0055 a0001c0001t0001g0093 a0001c0001t0001g0094 others(4): Show |
7 | HG01257.hp2 HG01346.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(15): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATTT others(5): Show |
3 | a0001c0001t0001g0046 a0001c0001t0001g0106 a0001c0001t0001g0266 |
3 | HG00597.hp2 HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATTT others(6): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0134 |
2 | HG02056.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(17): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATATTT others(7): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0123 |
2 | HG00423.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATTTT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0102 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATTTTT others(1): Show |
10 | a0001c0002t0001g0199 a0001c0002t0001g0219 a0001c0002t0001g0221 others(7): Show |
10 | HG00558.hp1 HG00597.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATTTTT others(2): Show |
28 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0179 others(25): Show |
28 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATTTTT others(3): Show |
25 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(22): Show |
25 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATTTTT others(4): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0131 |
2 | HG01934.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(15): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATTTTT others(5): Show |
9 | a0001c0001t0001g0009 a0001c0001t0001g0128 a0001c0001t0001g0136 others(6): Show |
9 | HG02683.hp1 HG02717.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-31252_127-3125 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATTTTT others(6): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0162 |
2 | HG02135.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(17): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATATTTTT others(7): Show |
1 | a0001c0001t0001g0156 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.127-31252_127-3125 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATTTTTTT others(2): Show |
9 | a0001c0001t0001g0013 a0001c0001t0001g0112 a0001c0002t0001g0205 others(6): Show |
9 | HG01928.hp2 HG02080.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-31242_127-3123 others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATTTTTTT others(3): Show |
27 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0070 others(24): Show |
27 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.127-31243_127-3123 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATTTTTTT others(4): Show |
12 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0118 others(9): Show |
12 | HG01071.hp1 HG01106.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-31244_127-3123 others(15): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0155 |
2 | HG02027.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.127-31245_127-3123 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173216727 | ||||||
| chr4:173216727 | A | T | 14 | a0001c0001t0001g0107 a0001c0001t0001g0141 a0001c0001t0004g0154 others(11): Show |
14 | HG01952.hp2 HG02083.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-31253A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216727 | |||||||
| chr4:173216728 | T | TATATATA others(18): Show |
2 | a0001c0002t0001g0187 a0001c0002t0001g0198 |
2 | HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(29): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216728 | |||||||
| chr4:173216728 | T | TATATATA others(22): Show |
2 | a0001c0002t0001g0195 a0001c0002t0001g0196 |
2 | HG01952.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.127-31252_127-3125 others(33): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216728 | |||||||
| chr4:173216729 | T | A | 2 | a0001c0002t0001g0191 a0001c0002t0002g0197 |
2 | HG02027.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.127-31251T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216729 | |||||||
| chr4:173216767 | G | C | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-31213G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216767 | |||||||
| chr4:173216799 | C | T | 22 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(19): Show |
22 | HG00423.hp1 HG01891.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-31181C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216799 | |||||||
| chr4:173216800 | G | T | 3 | a0001c0002t0001g0200 a0001c0002t0001g0211 a0001c0002t0013g0207 |
3 | HG02922.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.127-31180G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216800 | |||||||
| chr4:173216843 | G | A | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-31137G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216843 | |||||||
| chr4:173216856 | G | A | 2 | a0001c0002t0009g0244 a0001c0002t0009g0245 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-31124G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173216856 | |||||||
| chr4:173217168 | A | T | 1 | a0001c0002t0001g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.127-30812A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217168 | |||||||
| chr4:173217621 | A | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(3): Show |
6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-30359A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217621 | |||||||
| chr4:173217625 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.127-30355T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217625 | |||||||
| chr4:173217630 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0087 |
3 | HG02055.hp2 HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.127-30350A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217630 | |||||||
| chr4:173217716 | T | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(77): Show |
80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.127-30264T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217716 | |||||||
| chr4:173217724 | A | G | 2 | a0001c0002t0001g0247 a0001c0002t0001g0257 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.127-30256A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217724 | |||||||
| chr4:173217871 | A | G | 2 | a0001c0002t0001g0185 a0001c0002t0001g0186 |
2 | HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127-30109A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217871 | |||||||
| chr4:173217975 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.127-30005C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173217975 | |||||||
| chr4:173218024 | G | A | 15 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-29956G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173218024 | |||||||
| chr4:173218048 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.127-29932G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173218048 | |||||||
| chr4:173218096 | C | G | 1 | a0001c0002t0002g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-29884C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173218096 | |||||||
| chr4:173218138 | A | G | 28 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(25): Show |
28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-29842A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173218138 | |||||||
| chr4:173218469 | GTTTCC | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.127-29507_127-2950 others(9): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173218469 | ||||||
| chr4:173218604 | C | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(32): Show |
35 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-29376C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173218604 | |||||||
| chr4:173218976 | TA | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(4): Show |
7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-28997delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173218976 | ||||||
| chr4:173218983 | AT | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(27): Show |
30 | HG00621.hp1 HG01192.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-28987delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173218983 | ||||||
| chr4:173219048 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-28932G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219048 | |||||||
| chr4:173219176 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.127-28804T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219176 | |||||||
| chr4:173219176 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127-28804T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219176 | |||||||
| chr4:173219301 | T | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0122 a0001c0001t0001g0137 |
3 | HG02040.hp1 NA18983.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.127-28679T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219301 | |||||||
| chr4:173219360 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.127-28620A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219360 | |||||||
| chr4:173219701 | T | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(31): Show |
34 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.127-28279T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219701 | |||||||
| chr4:173219751 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.127-28229C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219751 | |||||||
| chr4:173219764 | A | AT | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-28208dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173219764 | ||||||
| chr4:173219879 | A | C | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(8): Show |
11 | HG01081.hp2 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.127-28101A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173219879 | |||||||
| chr4:173220371 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.127-27609T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220371 | |||||||
| chr4:173220430 | C | A | 1 | a0001c0001t0015g0157 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.127-27550C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220430 | |||||||
| chr4:173220430 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG00280.hp2 HG01099.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.127-27550C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220430 | |||||||
| chr4:173220449 | G | A | 1 | a0001c0005t0003g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.127-27531G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220449 | |||||||
| chr4:173220502 | A | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.127-27478A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220502 | |||||||
| chr4:173220503 | A | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(78): Show |
81 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.127-27477A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220503 | |||||||
| chr4:173220608 | G | A | 15 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-27372G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220608 | |||||||
| chr4:173220705 | C | T | 2 | a0001c0002t0001g0192 a0001c0002t0001g0238 |
2 | NA18986.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.127-27275C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220705 | |||||||
| chr4:173220748 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-27232G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220748 | |||||||
| chr4:173220827 | G | C | 1 | a0001c0008t0002g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.127-27153G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220827 | |||||||
| chr4:173220870 | A | G | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-27110A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220870 | |||||||
| chr4:173220899 | C | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.127-27081C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220899 | |||||||
| chr4:173220916 | G | A | 1 | a0001c0002t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127-27064G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220916 | |||||||
| chr4:173220938 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-27042T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220938 | |||||||
| chr4:173220951 | G | A | 1 | a0001c0002t0002g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.127-27029G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220951 | |||||||
| chr4:173220954 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(4): Show |
7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-27026A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173220954 | |||||||
| chr4:173221302 | A | G | 1 | a0001c0002t0001g0193 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-26678A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221302 | |||||||
| chr4:173221423 | G | A | 1 | a0001c0002t0001g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127-26557G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221423 | |||||||
| chr4:173221498 | G | T | 6 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0005t0001g0099 others(3): Show |
6 | HG01346.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-26482G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221498 | |||||||
| chr4:173221723 | A | G | 50 | a0001c0001t0001g0266 a0001c0002t0001g0016 a0001c0002t0001g0017 others(47): Show |
50 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.127-26257A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221723 | |||||||
| chr4:173221816 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-26164T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221816 | |||||||
| chr4:173221891 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127-26089C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173221891 | |||||||
| chr4:173222130 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(39): Show |
42 | HG00621.hp1 HG01192.hp1 HG01257.hp1 others(39): Show |
intron_variant | MODIFIER | c.127-25850C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222130 | |||||||
| chr4:173222184 | A | G | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-25796A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222184 | |||||||
| chr4:173222329 | A | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-25651A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222329 | |||||||
| chr4:173222607 | AG | A | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-25372delG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222607 | |||||||
| chr4:173222845 | A | C | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127-25135A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222845 | |||||||
| chr4:173222849 | A | G | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127-25131A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222849 | |||||||
| chr4:173222880 | A | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(25): Show |
28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-25100A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222880 | |||||||
| chr4:173222927 | A | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-25053A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173222927 | |||||||
| chr4:173223038 | G | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(25): Show |
28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-24942G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223038 | |||||||
| chr4:173223056 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.127-24924A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223056 | |||||||
| chr4:173223478 | G | GTAATAA | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.127-24498_127-2449 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173223478 | ||||||
| chr4:173223574 | C | T | 2 | a0001c0002t0009g0244 a0001c0002t0009g0245 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-24406C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223574 | |||||||
| chr4:173223598 | G | A | 2 | a0001c0003t0002g0176 a0001c0003t0002g0181 |
2 | HG01106.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.127-24382G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223598 | |||||||
| chr4:173223636 | C | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(25): Show |
28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-24344C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223636 | |||||||
| chr4:173223878 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(4): Show |
7 | HG02257.hp2 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-24102T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223878 | |||||||
| chr4:173223898 | T | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(25): Show |
28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-24082T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223898 | |||||||
| chr4:173223972 | T | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-24008T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173223972 | |||||||
| chr4:173224007 | C | CT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
41 | HG00621.hp1 HG01192.hp1 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.127-23964dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173224007 | ||||||
| chr4:173224241 | G | A | 26 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(23): Show |
26 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.127-23739G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224241 | |||||||
| chr4:173224480 | T | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.127-23500T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224480 | |||||||
| chr4:173224734 | C | T | 44 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0002t0001g0016 others(41): Show |
44 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-23246C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224734 | |||||||
| chr4:173224738 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.127-23242C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224738 | |||||||
| chr4:173224740 | C | T | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-23240C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224740 | |||||||
| chr4:173224741 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.127-23239G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224741 | |||||||
| chr4:173224753 | C | T | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-23227C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224753 | |||||||
| chr4:173224779 | G | A | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.127-23201G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224779 | |||||||
| chr4:173224789 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.127-23191G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224789 | |||||||
| chr4:173224795 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0129 |
2 | NA19010.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.127-23185G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224795 | |||||||
| chr4:173224809 | C | G | 2 | a0001c0002t0009g0244 a0001c0002t0009g0245 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-23171C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224809 | |||||||
| chr4:173224821 | G | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-23159G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224821 | |||||||
| chr4:173224828 | C | G | 3 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0003t0002g0169 |
3 | HG02622.hp1 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.127-23152C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224828 | |||||||
| chr4:173224840 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0002g0041 |
3 | HG01192.hp1 HG01943.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.127-23140G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224840 | |||||||
| chr4:173224874 | G | T | 3 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 |
3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.127-23106G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224874 | |||||||
| chr4:173224875 | C | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0070 others(51): Show |
54 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.127-23105C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224875 | |||||||
| chr4:173224879 | G | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(22): Show |
25 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-23101G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224879 | |||||||
| chr4:173224883 | C | T | 14 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(11): Show |
14 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-23097C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224883 | |||||||
| chr4:173224884 | G | A | 2 | a0001c0002t0001g0014 a0001c0002t0001g0183 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.127-23096G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224884 | |||||||
| chr4:173224885 | C | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(22): Show |
25 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-23095C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224885 | |||||||
| chr4:173224888 | G | A | 1 | a0001c0002t0001g0235 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.127-23092G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224888 | |||||||
| chr4:173224966 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.127-23014A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224966 | |||||||
| chr4:173224979 | C | A | 49 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0018 others(46): Show |
49 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.127-23001C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224979 | |||||||
| chr4:173224984 | T | C | 2 | a0001c0003t0002g0246 a0001c0003t0002g0249 |
2 | NA18963.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.127-22996T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224984 | |||||||
| chr4:173224992 | A | G | 2 | a0001c0003t0002g0246 a0001c0003t0002g0249 |
2 | NA18963.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.127-22988A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224992 | |||||||
| chr4:173224994 | G | C | 2 | a0001c0003t0002g0246 a0001c0003t0002g0249 |
2 | NA18963.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.127-22986G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173224994 | |||||||
| chr4:173225018 | A | AAATAAT | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0081 others(4): Show |
7 | HG02615.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-22934_127-2292 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | ||||||
| chr4:173225018 | A | AAATAATA others(2): Show |
4 | a0001c0001t0003g0082 a0001c0006t0001g0072 a0001c0006t0001g0073 others(1): Show |
4 | HG01081.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-22937_127-2292 others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | ||||||
| chr4:173225018 | A | AAATAATA others(5): Show |
2 | a0001c0001t0003g0078 a0001c0001t0005g0075 |
2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.127-22940_127-2292 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | ||||||
| chr4:173225018 | A | AAATAATA others(8): Show |
2 | a0001c0001t0005g0085 a0001c0001t0005g0086 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.127-22943_127-2292 others(19): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | ||||||
| chr4:173225018 | A | AAATAATA others(11): Show |
2 | a0001c0001t0011g0071 a0001c0002t0011g0222 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-22946_127-2292 others(22): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | ||||||
| chr4:173225018 | AAAT | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(46): Show |
49 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.127-22931_127-2292 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | ||||||
| chr4:173225018 | AAATAAT | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.127-22934_127-2292 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | ||||||
| chr4:173225018 | AAATAATA others(2): Show |
A | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0004t0001g0006 others(6): Show |
9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-22937_127-2292 others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225018 | ||||||
| chr4:173225046 | AATAATT | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0025 |
3 | HG02451.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.127-22924_127-2291 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225046 | ||||||
| chr4:173225049 | A | AATT | 2 | a0001c0002t0001g0014 a0001c0002t0001g0183 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.127-22928_127-2292 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173225049 | ||||||
| chr4:173225148 | C | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.127-22832C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225148 | |||||||
| chr4:173225333 | A | G | 3 | a0001c0002t0009g0244 a0001c0002t0009g0245 a0005c0013t0001g0175 |
3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-22647A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225333 | |||||||
| chr4:173225497 | A | G | 2 | a0001c0002t0009g0244 a0001c0002t0009g0245 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-22483A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225497 | |||||||
| chr4:173225504 | G | T | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(8): Show |
11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-22476G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225504 | |||||||
| chr4:173225579 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.127-22401G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225579 | |||||||
| chr4:173225621 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.127-22359T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225621 | |||||||
| chr4:173225633 | C | T | 3 | a0001c0002t0001g0200 a0001c0002t0001g0211 a0001c0002t0013g0207 |
3 | HG02922.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.127-22347C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225633 | |||||||
| chr4:173225745 | G | A | 1 | a0003c0010t0003g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.127-22235G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173225745 | |||||||
| chr4:173226189 | C | G | 1 | a0001c0001t0002g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-21791C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226189 | |||||||
| chr4:173226208 | C | T | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.127-21772C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226208 | |||||||
| chr4:173226210 | A | T | 15 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-21770A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226210 | |||||||
| chr4:173226281 | C | G | 1 | a0001c0001t0002g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-21699C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226281 | |||||||
| chr4:173226357 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(78): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.127-21623C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226357 | |||||||
| chr4:173226392 | T | A | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-21588T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226392 | |||||||
| chr4:173226426 | C | T | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(8): Show |
11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-21554C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226426 | |||||||
| chr4:173226874 | T | C | 2 | a0001c0002t0001g0185 a0001c0002t0001g0186 |
2 | HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127-21106T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226874 | |||||||
| chr4:173226926 | A | T | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127-21054A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226926 | |||||||
| chr4:173226960 | A | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0064 others(7): Show |
10 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-21020A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173226960 | |||||||
| chr4:173227234 | A | G | 1 | a0001c0002t0002g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-20746A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227234 | |||||||
| chr4:173227417 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(128): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.127-20563C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227417 | |||||||
| chr4:173227461 | A | G | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-20519A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227461 | |||||||
| chr4:173227497 | A | G | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-20483A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227497 | |||||||
| chr4:173227564 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.127-20416C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227564 | |||||||
| chr4:173227572 | C | T | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(8): Show |
11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-20408C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227572 | |||||||
| chr4:173227590 | C | G | 27 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(24): Show |
27 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.127-20390C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227590 | |||||||
| chr4:173227786 | A | G | 8 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-20194A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227786 | |||||||
| chr4:173227794 | CTG | C | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-20182_127-2018 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173227794 | ||||||
| chr4:173227812 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-20168T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227812 | |||||||
| chr4:173227813 | T | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0161 others(1): Show |
4 | NA18946.hp1 NA18979.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-20167T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227813 | |||||||
| chr4:173227822 | T | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(40): Show |
43 | HG00621.hp1 HG01192.hp1 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.127-20158T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227822 | |||||||
| chr4:173227823 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-20157C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227823 | |||||||
| chr4:173227848 | G | GT | 5 | a0001c0001t0001g0013 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG01928.hp2 HG06807.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-20126dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173227848 | ||||||
| chr4:173227858 | T | C | 1 | a0001c0002t0001g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127-20122T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227858 | |||||||
| chr4:173227895 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.127-20085C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227895 | |||||||
| chr4:173227910 | C | T | 1 | a0001c0002t0011g0222 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127-20070C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227910 | |||||||
| chr4:173227960 | A | G | 15 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-20020A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173227960 | |||||||
| chr4:173227984 | GTCATGTG others(3): Show |
G | 1 | a0001c0002t0001g0204 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.127-19993_127-1998 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173227984 | ||||||
| chr4:173228141 | G | A | 4 | a0001c0001t0005g0085 a0001c0001t0005g0086 a0001c0001t0011g0071 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-19839G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228141 | |||||||
| chr4:173228150 | A | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-19830A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228150 | |||||||
| chr4:173228212 | G | T | 40 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0018 others(37): Show |
40 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.127-19768G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228212 | |||||||
| chr4:173228289 | T | TCTTCTAG others(309): Show |
6 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0128 others(3): Show |
6 | HG00423.hp2 HG00597.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-19676_127-1967 others(320): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(310): Show |
47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.127-19676_127-1967 others(321): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(311): Show |
7 | a0001c0001t0001g0013 a0001c0001t0001g0111 a0001c0001t0001g0114 others(4): Show |
7 | HG00558.hp2 HG01243.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-19676_127-1967 others(322): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(313): Show |
1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.127-19676_127-1967 others(324): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(315): Show |
1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-19676_127-1967 others(326): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(321): Show |
1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-19676_127-1967 others(332): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(326): Show |
3 | a0001c0001t0001g0065 a0001c0001t0001g0163 a0001c0001t0001g0165 |
3 | HG00280.hp1 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.127-19676_127-1967 others(337): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(327): Show |
8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(5): Show |
8 | HG00741.hp1 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-19676_127-1967 others(338): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(327): Show |
1 | a0001c0001t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.127-19676_127-1967 others(338): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(328): Show |
2 | a0001c0001t0001g0069 a0006c0011t0002g0180 |
2 | HG01361.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.127-19676_127-1967 others(339): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(329): Show |
1 | a0001c0001t0001g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.127-19676_127-1967 others(340): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(330): Show |
1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-19676_127-1967 others(341): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(330): Show |
1 | a0001c0001t0001g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.127-19676_127-1967 others(341): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(331): Show |
1 | a0001c0001t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.127-19676_127-1967 others(342): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228289 | T | TCTTCTAG others(337): Show |
1 | a0001c0001t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-19676_127-1967 others(348): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228289 | ||||||
| chr4:173228503 | A | G | 1 | a0001c0002t0001g0208 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.127-19477A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228503 | |||||||
| chr4:173228602 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.127-19378T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228602 | |||||||
| chr4:173228683 | CA | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(25): Show |
28 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-19289delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173228683 | ||||||
| chr4:173228811 | T | G | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(8): Show |
11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-19169T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173228811 | |||||||
| chr4:173229243 | C | T | 16 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(13): Show |
16 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-18737C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229243 | |||||||
| chr4:173229325 | A | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(78): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.127-18655A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229325 | |||||||
| chr4:173229361 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-18619A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229361 | |||||||
| chr4:173229711 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.127-18269T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229711 | |||||||
| chr4:173229748 | T | C | 1 | a0001c0002t0001g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-18232T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229748 | |||||||
| chr4:173229814 | A | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(34): Show |
37 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-18166A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173229814 | |||||||
| chr4:173230295 | A | AT | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.127-17684dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173230295 | ||||||
| chr4:173230298 | T | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.127-17682T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173230298 | |||||||
| chr4:173230299 | A | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.127-17681A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173230299 | |||||||
| chr4:173230468 | T | C | 49 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0018 others(46): Show |
49 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.127-17512T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173230468 | |||||||
| chr4:173230698 | G | A | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127-17282G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173230698 | |||||||
| chr4:173230863 | T | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(3): Show |
6 | HG02257.hp2 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-17117T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173230863 | |||||||
| chr4:173231017 | C | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG01928.hp2 HG06807.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-16963C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231017 | |||||||
| chr4:173231070 | C | T | 4 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-16910C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231070 | |||||||
| chr4:173231081 | T | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.127-16899T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231081 | |||||||
| chr4:173231158 | C | T | 1 | a0006c0011t0002g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127-16822C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231158 | |||||||
| chr4:173231200 | T | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-16780T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231200 | |||||||
| chr4:173231272 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127-16708G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231272 | |||||||
| chr4:173231512 | G | A | 3 | a0001c0002t0009g0244 a0001c0002t0009g0245 a0005c0013t0001g0175 |
3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-16468G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231512 | |||||||
| chr4:173231541 | C | G | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-16439C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231541 | |||||||
| chr4:173231739 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(3): Show |
6 | HG02257.hp2 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-16241A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231739 | |||||||
| chr4:173231840 | G | A | 15 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-16140G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231840 | |||||||
| chr4:173231876 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.127-16104A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173231876 | |||||||
| chr4:173232041 | A | G | 2 | a0001c0001t0001g0093 a0001c0005t0003g0092 |
2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.127-15939A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232041 | |||||||
| chr4:173232215 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-15765G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232215 | |||||||
| chr4:173232230 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0118 |
2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.127-15750G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232230 | |||||||
| chr4:173232249 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.127-15731G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232249 | |||||||
| chr4:173232271 | T | TA | 18 | a0001c0002t0001g0247 a0001c0002t0001g0257 a0001c0002t0001g0260 others(15): Show |
18 | HG00423.hp1 HG02135.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.127-15697dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173232271 | ||||||
| chr4:173232611 | T | A | 1 | a0001c0002t0011g0222 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127-15369T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232611 | |||||||
| chr4:173232636 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(3): Show |
6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-15344A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232636 | |||||||
| chr4:173232810 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0134 |
2 | HG02056.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.127-15170G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173232810 | |||||||
| chr4:173233160 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.127-14820T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173233160 | |||||||
| chr4:173233204 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(3): Show |
6 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-14776G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173233204 | |||||||
| chr4:173233456 | G | A | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0004t0001g0006 others(6): Show |
9 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-14524G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173233456 | |||||||
| chr4:173233597 | G | A | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-14383G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173233597 | |||||||
| chr4:173233999 | G | C | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0006g0170 others(3): Show |
6 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-13981G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173233999 | |||||||
| chr4:173234019 | G | A | 1 | a0002c0007t0007g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127-13961G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234019 | |||||||
| chr4:173234077 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.127-13903A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234077 | |||||||
| chr4:173234221 | G | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(3): Show |
6 | HG02257.hp2 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-13759G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234221 | |||||||
| chr4:173234223 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(34): Show |
37 | HG00621.hp1 HG01192.hp1 HG01943.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-13757G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234223 | |||||||
| chr4:173234367 | T | C | 1 | a0001c0003t0002g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.127-13613T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234367 | |||||||
| chr4:173234503 | G | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(77): Show |
80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.127-13477G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234503 | |||||||
| chr4:173234515 | A | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(78): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.127-13465A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234515 | |||||||
| chr4:173234590 | A | T | 1 | a0001c0002t0001g0213 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.127-13390A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234590 | |||||||
| chr4:173234756 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.127-13224A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234756 | |||||||
| chr4:173234842 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.127-13138C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234842 | |||||||
| chr4:173234909 | C | T | 2 | a0001c0002t0001g0261 a0001c0002t0001g0262 |
2 | HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.127-13071C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234909 | |||||||
| chr4:173234994 | A | G | 4 | a0001c0004t0001g0076 a0001c0004t0001g0077 a0001c0004t0001g0084 others(1): Show |
4 | HG02486.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-12986A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173234994 | |||||||
| chr4:173235219 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0028 |
2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.127-12761A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235219 | |||||||
| chr4:173235232 | C | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.127-12748C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235232 | |||||||
| chr4:173235313 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(3): Show |
6 | HG02257.hp2 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-12667C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235313 | |||||||
| chr4:173235387 | A | G | 63 | a0001c0001t0001g0134 a0001c0002t0001g0016 a0001c0002t0001g0017 others(60): Show |
63 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.127-12593A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235387 | |||||||
| chr4:173235556 | C | CT | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.127-12410dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173235556 | ||||||
| chr4:173235556 | C | CTTT | 9 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0247 others(6): Show |
9 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-12412_127-1241 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173235556 | ||||||
| chr4:173235644 | C | T | 2 | a0001c0004t0001g0076 a0001c0004t0001g0077 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.127-12336C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235644 | |||||||
| chr4:173235694 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.127-12286T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235694 | |||||||
| chr4:173235855 | C | T | 1 | a0001c0002t0001g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-12125C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235855 | |||||||
| chr4:173235890 | A | G | 1 | a0001c0004t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127-12090A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173235890 | |||||||
| chr4:173236025 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | HG01257.hp1 HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.127-11955G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236025 | |||||||
| chr4:173236060 | G | A | 35 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(32): Show |
35 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-11920G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236060 | |||||||
| chr4:173236140 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-11840A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236140 | |||||||
| chr4:173236311 | A | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.127-11669A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236311 | |||||||
| chr4:173236468 | A | G | 15 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-11512A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236468 | |||||||
| chr4:173236538 | C | G | 29 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(26): Show |
29 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.127-11442C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236538 | |||||||
| chr4:173236909 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0102 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-11071A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236909 | |||||||
| chr4:173236929 | A | G | 2 | a0001c0004t0001g0076 a0001c0004t0001g0077 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.127-11051A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236929 | |||||||
| chr4:173236940 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-11040T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236940 | |||||||
| chr4:173236980 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.127-11000G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236980 | |||||||
| chr4:173236981 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
125 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.127-10999A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173236981 | |||||||
| chr4:173237012 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-10968G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237012 | |||||||
| chr4:173237025 | T | C | 1 | a0001c0001t0002g0030 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.127-10955T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237025 | |||||||
| chr4:173237308 | A | G | 5 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0025 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-10672A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237308 | |||||||
| chr4:173237340 | G | T | 2 | a0001c0003t0002g0169 a0001c0003t0002g0248 |
2 | HG03834.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.127-10640G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237340 | |||||||
| chr4:173237561 | T | C | 1 | a0001c0002t0001g0217 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.127-10419T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237561 | |||||||
| chr4:173237759 | TA | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.127-10206delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173237759 | ||||||
| chr4:173237849 | G | A | 3 | a0001c0002t0001g0215 a0001c0002t0001g0220 a0001c0002t0001g0229 |
3 | HG01255.hp2 HG01256.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.127-10131G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173237849 | |||||||
| chr4:173238115 | A | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG02559.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.127-9865A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238115 | |||||||
| chr4:173238124 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-9856A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238124 | |||||||
| chr4:173238216 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.127-9764T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238216 | |||||||
| chr4:173238300 | T | G | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-9680T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238300 | |||||||
| chr4:173238318 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-9662G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238318 | |||||||
| chr4:173238637 | G | A | 62 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0018 others(59): Show |
62 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.127-9343G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238637 | |||||||
| chr4:173238768 | A | G | 8 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-9212A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173238768 | |||||||
| chr4:173239210 | G | T | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(8): Show |
11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-8770G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239210 | |||||||
| chr4:173239211 | T | C | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(8): Show |
11 | HG01081.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-8769T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239211 | |||||||
| chr4:173239524 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-8456C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239524 | |||||||
| chr4:173239525 | G | A | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0078 others(4): Show |
7 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-8455G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239525 | |||||||
| chr4:173239579 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0045 others(21): Show |
24 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.127-8401A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239579 | |||||||
| chr4:173239694 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127-8286C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173239694 | |||||||
| chr4:173240137 | A | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-7843A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173240137 | |||||||
| chr4:173240357 | A | AT | 18 | a0001c0002t0001g0200 a0001c0002t0001g0213 a0001c0002t0001g0260 others(15): Show |
18 | HG01192.hp2 HG01346.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.127-7594dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | ||||||
| chr4:173240357 | AT | A | 21 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0003g0081 others(18): Show |
21 | HG01081.hp2 HG02027.hp2 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.127-7594delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | ||||||
| chr4:173240357 | ATT | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(8): Show |
11 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-7595_127-7594d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | ||||||
| chr4:173240357 | ATTT | A | 8 | a0001c0001t0001g0266 a0001c0001t0005g0075 a0001c0001t0005g0086 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-7596_127-7594d others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | ||||||
| chr4:173240357 | ATTTT | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0002g0032 others(4): Show |
7 | HG02055.hp2 HG02738.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-7597_127-7594d others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | ||||||
| chr4:173240357 | ATTTTT | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(56): Show |
59 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.127-7598_127-7594d others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | ||||||
| chr4:173240357 | ATTTTTT | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.127-7599_127-7594d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | ||||||
| chr4:173240357 | ATTTTTTT others(9): Show |
A | 1 | a0001c0002t0001g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127-7609_127-7594d others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173240357 | ||||||
| chr4:173240658 | C | T | 1 | a0001c0002t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.127-7322C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173240658 | |||||||
| chr4:173240748 | T | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(3): Show |
6 | HG02257.hp2 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-7232T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173240748 | |||||||
| chr4:173241110 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127-6870C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241110 | |||||||
| chr4:173241137 | G | A | 2 | a0001c0002t0006g0170 a0001c0002t0006g0171 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.127-6843G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241137 | |||||||
| chr4:173241167 | T | C | 2 | a0001c0002t0001g0247 a0001c0002t0002g0182 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.127-6813T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241167 | |||||||
| chr4:173241223 | A | AAAAG | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.127-6755_127-6754i others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173241223 | ||||||
| chr4:173241223 | A | AAAG | 44 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(41): Show |
44 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-6754_127-6752d others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173241223 | ||||||
| chr4:173241223 | A | AAG | 7 | a0001c0001t0001g0005 a0001c0001t0001g0060 a0001c0001t0001g0079 others(4): Show |
7 | HG01257.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-6756_127-6755i others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173241223 | ||||||
| chr4:173241316 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-6664G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241316 | |||||||
| chr4:173241589 | G | A | 4 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0185 others(1): Show |
4 | HG02451.hp2 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-6391G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241589 | |||||||
| chr4:173241934 | T | G | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-6046T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173241934 | |||||||
| chr4:173242018 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.127-5962T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242018 | |||||||
| chr4:173242031 | T | C | 17 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(14): Show |
17 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.127-5949T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242031 | |||||||
| chr4:173242209 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.127-5771A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242209 | |||||||
| chr4:173242247 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.127-5733G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242247 | |||||||
| chr4:173242446 | T | C | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-5534T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242446 | |||||||
| chr4:173242550 | G | A | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-5430G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242550 | |||||||
| chr4:173242861 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.127-5119T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173242861 | |||||||
| chr4:173243006 | A | C | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-4974A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243006 | |||||||
| chr4:173243221 | T | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0101 others(3): Show |
6 | HG01192.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-4759T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243221 | |||||||
| chr4:173243569 | G | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-4411G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243569 | |||||||
| chr4:173243715 | A | C | 1 | a0001c0002t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.127-4265A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243715 | |||||||
| chr4:173243784 | T | C | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.127-4196T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243784 | |||||||
| chr4:173243820 | G | T | 3 | a0001c0001t0001g0090 a0001c0002t0001g0173 a0001c0002t0001g0174 |
3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.127-4160G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243820 | |||||||
| chr4:173243879 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.127-4101A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243879 | |||||||
| chr4:173243975 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.127-4005C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173243975 | |||||||
| chr4:173244163 | G | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
7 | HG01192.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-3817G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244163 | |||||||
| chr4:173244234 | C | G | 10 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0004t0001g0006 others(7): Show |
10 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-3746C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244234 | |||||||
| chr4:173244328 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.127-3652C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244328 | |||||||
| chr4:173244391 | A | G | 1 | a0001c0002t0001g0227 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.127-3589A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244391 | |||||||
| chr4:173244397 | A | C | 1 | a0001c0001t0001g0011 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.127-3583A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244397 | |||||||
| chr4:173244984 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-2996G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173244984 | |||||||
| chr4:173245197 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127-2783G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245197 | |||||||
| chr4:173245215 | CA | C | 30 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(27): Show |
30 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-2747delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173245215 | ||||||
| chr4:173245215 | CAA | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
188 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.127-2748_127-2747d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173245215 | ||||||
| chr4:173245215 | CAAA | C | 44 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0070 others(41): Show |
44 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.127-2749_127-2747d others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 173245215 | ||||||
| chr4:173245374 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-2606T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245374 | |||||||
| chr4:173245395 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-2585T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245395 | |||||||
| chr4:173245399 | A | G | 1 | a0003c0010t0003g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.127-2581A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245399 | |||||||
| chr4:173245739 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.127-2241C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245739 | |||||||
| chr4:173245795 | G | C | 10 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0004t0001g0006 others(7): Show |
10 | HG01346.hp2 HG02055.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-2185G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245795 | |||||||
| chr4:173245823 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.127-2157A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245823 | |||||||
| chr4:173245841 | C | T | 1 | a0001c0001t0002g0023 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.127-2139C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173245841 | |||||||
| chr4:173246095 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.127-1885A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246095 | |||||||
| chr4:173246143 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.127-1837C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246143 | |||||||
| chr4:173246269 | C | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0064 |
2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.127-1711C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246269 | |||||||
| chr4:173246830 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG01928.hp2 HG06807.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-1150A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246830 | |||||||
| chr4:173246861 | T | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.127-1119T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246861 | |||||||
| chr4:173246936 | G | A | 6 | a0001c0001t0001g0091 a0001c0002t0006g0170 a0001c0002t0006g0171 others(3): Show |
6 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1044G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246936 | |||||||
| chr4:173246968 | C | T | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.127-1012C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246968 | |||||||
| chr4:173246983 | T | A | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.127-997T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173246983 | |||||||
| chr4:173247268 | G | C | 2 | a0001c0002t0009g0244 a0001c0002t0009g0245 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-712G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247268 | |||||||
| chr4:173247295 | C | T | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-685C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247295 | |||||||
| chr4:173247300 | T | C | 1 | a0001c0002t0009g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.127-680T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247300 | |||||||
| chr4:173247416 | G | C | 1 | a0001c0005t0001g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.127-564G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247416 | |||||||
| chr4:173247474 | G | A | 1 | a0001c0002t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.127-506G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247474 | |||||||
| chr4:173247480 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.127-500T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247480 | |||||||
| chr4:173247588 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.127-392C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247588 | |||||||
| chr4:173247692 | T | G | 1 | a0001c0002t0001g0205 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.127-288T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 1/11 | chr4 | 173247692 | |||||||
| chr4:173248895 | G | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(23): Show |
26 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.587+455G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173248895 | |||||||
| chr4:173249509 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.587+1069A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173249509 | |||||||
| chr4:173249584 | A | C | 1 | a0001c0002t0009g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.587+1144A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173249584 | |||||||
| chr4:173249644 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587+1204G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173249644 | |||||||
| chr4:173250001 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.587+1561A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250001 | |||||||
| chr4:173250231 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.587+1791G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250231 | |||||||
| chr4:173250458 | A | G | 3 | a0001c0001t0001g0094 a0001c0005t0001g0099 a0001c0005t0003g0095 |
3 | HG02723.hp2 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.587+2018A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250458 | |||||||
| chr4:173250460 | C | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0101 others(7): Show |
10 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+2020C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250460 | |||||||
| chr4:173250482 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(23): Show |
26 | HG01192.hp1 HG01884.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.587+2042T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250482 | |||||||
| chr4:173250487 | C | T | 1 | a0003c0010t0003g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.587+2047C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250487 | |||||||
| chr4:173250488 | T | C | 1 | a0001c0002t0002g0197 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.587+2048T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250488 | |||||||
| chr4:173250530 | T | C | 11 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0004t0001g0006 others(8): Show |
11 | HG01346.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.587+2090T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250530 | |||||||
| chr4:173250620 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.587+2180C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250620 | |||||||
| chr4:173250767 | C | T | 3 | a0001c0001t0001g0091 a0002c0007t0007g0177 a0002c0007t0007g0178 |
3 | HG03130.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.587+2327C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250767 | |||||||
| chr4:173250997 | C | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
53 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.587+2557C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173250997 | |||||||
| chr4:173251003 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+2563G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251003 | |||||||
| chr4:173251149 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+2709T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251149 | |||||||
| chr4:173251208 | C | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(22): Show |
25 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.587+2768C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251208 | |||||||
| chr4:173251613 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.587+3173G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251613 | |||||||
| chr4:173251732 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+3292G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251732 | |||||||
| chr4:173251994 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.587+3554T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173251994 | |||||||
| chr4:173252100 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.587+3660A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173252100 | |||||||
| chr4:173252150 | T | C | 1 | a0001c0002t0001g0224 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.587+3710T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173252150 | |||||||
| chr4:173252592 | G | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
92 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(89): Show |
intron_variant | MODIFIER | c.587+4152G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173252592 | |||||||
| chr4:173252635 | C | T | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+4195C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173252635 | |||||||
| chr4:173252809 | A | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0028 |
2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.587+4369A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173252809 | |||||||
| chr4:173253042 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587+4602A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253042 | |||||||
| chr4:173253150 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0014g0054 |
2 | HG01346.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.587+4710C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253150 | |||||||
| chr4:173253325 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(30): Show |
33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+4885C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253325 | |||||||
| chr4:173253338 | T | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(30): Show |
33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+4898T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253338 | |||||||
| chr4:173253504 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.587+5064G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253504 | |||||||
| chr4:173253538 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
78 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.587+5098T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253538 | |||||||
| chr4:173253566 | A | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(30): Show |
33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+5126A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253566 | |||||||
| chr4:173253818 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.587+5378G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253818 | |||||||
| chr4:173253837 | T | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(30): Show |
33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+5397T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253837 | |||||||
| chr4:173253852 | G | C | 2 | a0001c0003t0002g0169 a0001c0003t0002g0248 |
2 | HG03834.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.587+5412G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173253852 | |||||||
| chr4:173254001 | T | G | 1 | a0001c0002t0001g0019 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.587+5561T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254001 | |||||||
| chr4:173254089 | T | C | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+5649T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254089 | |||||||
| chr4:173254216 | A | T | 2 | a0001c0002t0001g0014 a0001c0002t0001g0183 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.587+5776A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254216 | |||||||
| chr4:173254364 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.587+5924A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254364 | |||||||
| chr4:173254374 | T | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(30): Show |
33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+5934T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254374 | |||||||
| chr4:173254653 | A | C | 3 | a0001c0001t0001g0090 a0001c0002t0001g0173 a0001c0002t0001g0174 |
3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.587+6213A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254653 | |||||||
| chr4:173254655 | A | G | 1 | a0001c0002t0001g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.587+6215A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254655 | |||||||
| chr4:173254754 | G | T | 1 | a0001c0001t0001g0265 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.587+6314G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254754 | |||||||
| chr4:173254764 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.587+6324T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254764 | |||||||
| chr4:173254932 | T | C | 5 | a0001c0002t0002g0020 a0001c0002t0002g0240 a0001c0002t0002g0241 others(2): Show |
5 | HG02809.hp2 HG03579.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+6492T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254932 | |||||||
| chr4:173254944 | T | G | 3 | a0001c0002t0001g0200 a0001c0002t0001g0211 a0001c0002t0013g0207 |
3 | HG02922.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.587+6504T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173254944 | |||||||
| chr4:173255085 | C | T | 1 | a0007c0009t0001g0135 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.587+6645C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255085 | |||||||
| chr4:173255158 | A | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
44 | HG00621.hp1 HG01257.hp1 HG01993.hp2 others(41): Show |
intron_variant | MODIFIER | c.587+6718A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255158 | |||||||
| chr4:173255177 | A | C | 5 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(2): Show |
5 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+6737A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255177 | |||||||
| chr4:173255279 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+6839G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255279 | |||||||
| chr4:173255455 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+7015G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255455 | |||||||
| chr4:173255542 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+7102G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255542 | |||||||
| chr4:173255563 | A | G | 1 | a0001c0003t0002g0256 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.587+7123A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255563 | |||||||
| chr4:173255743 | G | A | 1 | a0001c0002t0003g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.587+7303G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255743 | |||||||
| chr4:173255828 | G | A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0070 others(2): Show |
5 | HG01884.hp1 HG02717.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+7388G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255828 | |||||||
| chr4:173255836 | C | T | 1 | a0001c0002t0001g0016 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.587+7396C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173255836 | |||||||
| chr4:173256207 | A | G | 5 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(2): Show |
5 | HG02622.hp1 HG02647.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+7767A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256207 | |||||||
| chr4:173256270 | A | C | 1 | a0001c0001t0002g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.587+7830A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256270 | |||||||
| chr4:173256329 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+7889G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256329 | |||||||
| chr4:173256494 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.587+8054G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256494 | |||||||
| chr4:173256502 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
81 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.587+8062A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256502 | |||||||
| chr4:173256692 | T | C | 1 | a0001c0002t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.587+8252T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256692 | |||||||
| chr4:173256821 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.587+8381A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256821 | |||||||
| chr4:173256926 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0028 |
2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.587+8486T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173256926 | |||||||
| chr4:173257058 | C | T | 2 | a0001c0002t0001g0014 a0001c0002t0001g0183 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.587+8618C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257058 | |||||||
| chr4:173257059 | A | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(30): Show |
33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.587+8619A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257059 | |||||||
| chr4:173257102 | C | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+8662C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257102 | |||||||
| chr4:173257163 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(45): Show |
48 | HG00621.hp1 HG01257.hp1 HG01993.hp2 others(45): Show |
intron_variant | MODIFIER | c.587+8723T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257163 | |||||||
| chr4:173257211 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+8771A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257211 | |||||||
| chr4:173257777 | C | T | 2 | a0001c0002t0001g0215 a0001c0002t0001g0229 |
2 | HG01256.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.587+9337C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257777 | |||||||
| chr4:173257808 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.587+9368T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257808 | |||||||
| chr4:173257884 | G | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(30): Show |
33 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.587+9444G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257884 | |||||||
| chr4:173257906 | G | A | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.587+9466G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173257906 | |||||||
| chr4:173258031 | T | G | 1 | a0001c0002t0001g0216 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.587+9591T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258031 | |||||||
| chr4:173258053 | AAGG | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+9618_587+9620d others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173258053 | ||||||
| chr4:173258342 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(28): Show |
31 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.587+9902T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258342 | |||||||
| chr4:173258350 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0064 |
2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.587+9910C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258350 | |||||||
| chr4:173258523 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
80 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.587+10083T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258523 | |||||||
| chr4:173258560 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.587+10120C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258560 | |||||||
| chr4:173258581 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.587+10141C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258581 | |||||||
| chr4:173258637 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.587+10197C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258637 | |||||||
| chr4:173258686 | A | G | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+10246A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258686 | |||||||
| chr4:173258936 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.587+10496C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258936 | |||||||
| chr4:173258987 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+10547G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173258987 | |||||||
| chr4:173259171 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.587+10731A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259171 | |||||||
| chr4:173259188 | C | T | 1 | a0001c0002t0006g0171 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.587+10748C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259188 | |||||||
| chr4:173259410 | C | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(29): Show |
32 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.587+10970C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259410 | |||||||
| chr4:173259428 | C | CT | 16 | a0001c0003t0002g0021 a0001c0003t0002g0176 a0001c0003t0002g0181 others(13): Show |
16 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.587+11001dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173259428 | ||||||
| chr4:173259474 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.587+11034C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259474 | |||||||
| chr4:173259485 | A | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
27 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.587+11045A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259485 | |||||||
| chr4:173259677 | G | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+11237G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259677 | |||||||
| chr4:173259700 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.587+11260C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259700 | |||||||
| chr4:173259933 | C | T | 1 | a0001c0002t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.587+11493C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173259933 | |||||||
| chr4:173260054 | GTA | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0004g0110 |
3 | HG02056.hp1 NA18945.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.587+11617_587+1161 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173260054 | ||||||
| chr4:173260239 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(28): Show |
31 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.587+11799T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260239 | |||||||
| chr4:173260245 | A | G | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+11805A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260245 | |||||||
| chr4:173260374 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.587+11934G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260374 | |||||||
| chr4:173260458 | G | A | 1 | a0006c0011t0002g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.587+12018G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260458 | |||||||
| chr4:173260503 | T | TA | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+12064dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173260503 | ||||||
| chr4:173260513 | G | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+12073G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260513 | |||||||
| chr4:173260581 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+12141G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260581 | |||||||
| chr4:173260764 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.587+12324A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260764 | |||||||
| chr4:173260765 | C | T | 32 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.587+12325C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260765 | |||||||
| chr4:173260799 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+12359T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260799 | |||||||
| chr4:173260933 | C | T | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587+12493C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173260933 | |||||||
| chr4:173261028 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.587+12588C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261028 | |||||||
| chr4:173261232 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+12792G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261232 | |||||||
| chr4:173261304 | C | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+12864C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261304 | |||||||
| chr4:173261390 | G | GT | 23 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(20): Show |
23 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.587+12961dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173261390 | ||||||
| chr4:173261426 | G | C | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+12986G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261426 | |||||||
| chr4:173261459 | A | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+13019A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261459 | |||||||
| chr4:173261481 | G | A | 21 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(18): Show |
21 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.587+13041G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261481 | |||||||
| chr4:173261502 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(28): Show |
31 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.587+13062A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261502 | |||||||
| chr4:173261518 | A | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+13078A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261518 | |||||||
| chr4:173261614 | C | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+13174C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261614 | |||||||
| chr4:173261696 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.587+13256G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261696 | |||||||
| chr4:173261743 | C | T | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+13303C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173261743 | |||||||
| chr4:173262129 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+13689A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262129 | |||||||
| chr4:173262167 | A | T | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.587+13727A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262167 | |||||||
| chr4:173262305 | C | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+13865C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262305 | |||||||
| chr4:173262441 | A | T | 2 | a0001c0002t0001g0191 a0001c0002t0002g0197 |
2 | HG02027.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.587+14001A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262441 | |||||||
| chr4:173262613 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.587+14173T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262613 | |||||||
| chr4:173262680 | G | A | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+14240G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262680 | |||||||
| chr4:173262744 | C | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+14304C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262744 | |||||||
| chr4:173262753 | T | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(23): Show |
26 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.587+14313T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262753 | |||||||
| chr4:173262760 | ACCCAT | A | 21 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(18): Show |
21 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.587+14322_587+1432 others(9): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173262760 | ||||||
| chr4:173262799 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.587+14359A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173262799 | |||||||
| chr4:173263113 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
66 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.587+14673C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263113 | |||||||
| chr4:173263195 | GA | G | 32 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.587+14760delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173263195 | ||||||
| chr4:173263268 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
101 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.587+14828G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263268 | |||||||
| chr4:173263552 | A | T | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.587+15112A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263552 | |||||||
| chr4:173263697 | A | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+15257A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263697 | |||||||
| chr4:173263698 | A | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+15258A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263698 | |||||||
| chr4:173263864 | C | A | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+15424C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173263864 | |||||||
| chr4:173264036 | A | G | 1 | a0001c0002t0001g0189 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.587+15596A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264036 | |||||||
| chr4:173264070 | G | A | 3 | a0001c0001t0001g0090 a0001c0002t0001g0173 a0001c0002t0001g0174 |
3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.587+15630G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264070 | |||||||
| chr4:173264169 | A | G | 5 | a0001c0004t0001g0006 a0001c0004t0001g0076 a0001c0004t0001g0077 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+15729A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264169 | |||||||
| chr4:173264199 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.587+15759G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264199 | |||||||
| chr4:173264435 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(30): Show |
33 | HG00621.hp1 HG01884.hp2 HG01993.hp2 others(30): Show |
intron_variant | MODIFIER | c.587+15995G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264435 | |||||||
| chr4:173264692 | T | C | 5 | a0001c0004t0001g0006 a0001c0004t0001g0076 a0001c0004t0001g0077 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+16252T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264692 | |||||||
| chr4:173264732 | C | T | 3 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 |
3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.587+16292C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264732 | |||||||
| chr4:173264749 | A | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0118 |
2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.587+16309A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264749 | |||||||
| chr4:173264878 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+16438G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264878 | |||||||
| chr4:173264893 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.587+16453C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264893 | |||||||
| chr4:173264913 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.587+16473G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264913 | |||||||
| chr4:173264957 | A | G | 3 | a0001c0002t0001g0214 a0001c0002t0001g0216 a0001c0002t0001g0221 |
3 | HG03704.hp2 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.587+16517A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264957 | |||||||
| chr4:173264976 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0138 a0001c0001t0001g0160 |
3 | NA18975.hp2 NA18986.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.587+16536A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173264976 | |||||||
| chr4:173265101 | G | A | 2 | a0001c0003t0002g0021 a0001c0003t0002g0255 |
2 | HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.587+16661G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265101 | |||||||
| chr4:173265118 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.587+16678C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265118 | |||||||
| chr4:173265171 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
100 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.587+16731G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265171 | |||||||
| chr4:173265175 | G | A | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587+16735G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265175 | |||||||
| chr4:173265220 | T | C | 1 | a0001c0002t0001g0232 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.587+16780T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265220 | |||||||
| chr4:173265493 | C | A | 2 | a0001c0002t0006g0170 a0001c0002t0006g0171 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.587+17053C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265493 | |||||||
| chr4:173265568 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.587+17128C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265568 | |||||||
| chr4:173265587 | A | ATC | 7 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0059 others(4): Show |
7 | HG00738.hp2 HG01256.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+17179_587+1718 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | ||||||
| chr4:173265587 | A | ATCTC | 14 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0070 others(11): Show |
14 | HG01257.hp1 HG01891.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.587+17177_587+1718 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | ||||||
| chr4:173265587 | A | ATCTCTC | 6 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0063 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.587+17175_587+1718 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | ||||||
| chr4:173265587 | A | ATCTCTCT others(1): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0060 a0001c0001t0001g0079 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+17173_587+1718 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | ||||||
| chr4:173265587 | A | ATCTCTCT others(3): Show |
1 | a0001c0001t0001g0163 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.587+17171_587+1718 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | ||||||
| chr4:173265587 | ATC | A | 5 | a0001c0001t0001g0266 a0001c0002t0001g0193 a0001c0002t0001g0231 others(2): Show |
5 | HG02273.hp1 HG02280.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+17179_587+1718 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | ||||||
| chr4:173265587 | ATCTC | A | 61 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0065 others(58): Show |
61 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.587+17177_587+1718 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | ||||||
| chr4:173265587 | ATCTCTCT others(1): Show |
A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(11): Show |
14 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.587+17173_587+1718 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | ||||||
| chr4:173265587 | ATCTCTCT others(3): Show |
A | 12 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0002t0006g0170 others(9): Show |
12 | HG01346.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.587+17171_587+1718 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265587 | ||||||
| chr4:173265611 | CTCTCTCT others(3): Show |
C | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+17177_587+1718 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173265611 | ||||||
| chr4:173265621 | G | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+17181G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173265621 | |||||||
| chr4:173266039 | C | T | 8 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0070 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+17599C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266039 | |||||||
| chr4:173266079 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+17639G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266079 | |||||||
| chr4:173266255 | G | A | 1 | a0001c0002t0001g0193 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.587+17815G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266255 | |||||||
| chr4:173266256 | T | G | 3 | a0001c0001t0005g0075 a0001c0002t0009g0244 a0001c0002t0009g0245 |
3 | HG02257.hp1 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.587+17816T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266256 | |||||||
| chr4:173266282 | A | G | 27 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(24): Show |
27 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.587+17842A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266282 | |||||||
| chr4:173266325 | G | C | 1 | a0001c0003t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.587+17885G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266325 | |||||||
| chr4:173266337 | A | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(7): Show |
10 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+17897A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266337 | |||||||
| chr4:173266432 | T | C | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+17992T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266432 | |||||||
| chr4:173266486 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+18046A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266486 | |||||||
| chr4:173266866 | AG | A | 4 | a0001c0001t0001g0102 a0001c0001t0002g0042 a0001c0002t0001g0018 others(1): Show |
4 | HG00621.hp1 HG01934.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.587+18429delG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266866 | ||||||
| chr4:173266867 | GGGTGTGT others(10): Show |
G | 1 | a0001c0001t0001g0056 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.587+18429_587+1844 others(21): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266867 | ||||||
| chr4:173266868 | G | GGT | 38 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0045 others(35): Show |
38 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.587+18486_587+1848 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | G | GGTGT | 21 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(18): Show |
21 | HG00423.hp1 HG00558.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.587+18484_587+1848 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | G | GGTGTGT | 3 | a0001c0001t0001g0064 a0001c0001t0001g0161 a0001c0002t0001g0230 |
3 | HG01109.hp2 NA18942.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.587+18482_587+1848 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | G | GGTGTGTG others(1): Show |
8 | a0001c0001t0001g0061 a0001c0001t0001g0132 a0001c0001t0002g0041 others(5): Show |
8 | HG02040.hp2 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+18480_587+1848 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | G | GGTGTGTG others(3): Show |
1 | a0001c0004t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.587+18478_587+1848 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | G | GT | 5 | a0001c0001t0001g0001 a0001c0001t0002g0026 a0001c0003t0002g0249 others(2): Show |
5 | HG01993.hp2 HG02615.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+18428_587+1842 others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266868 | |||||||
| chr4:173266868 | G | GTGTGTGT others(4): Show |
1 | a0001c0003t0012g0251 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.587+18428_587+1842 others(15): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266868 | |||||||
| chr4:173266868 | G | T | 1 | a0001c0001t0001g0037 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.587+18428G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266868 | |||||||
| chr4:173266868 | GGT | G | 49 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0065 others(46): Show |
49 | HG00323.hp2 HG01070.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.587+18486_587+1848 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | GGTGT | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0090 others(17): Show |
20 | HG00280.hp1 HG01255.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.587+18484_587+1848 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | GGTGTGT | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0094 a0001c0001t0001g0109 others(4): Show |
7 | HG00558.hp2 HG00621.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.587+18482_587+1848 others(10): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | GGTGTGTG others(1): Show |
G | 6 | a0001c0001t0001g0111 a0001c0002t0001g0187 a0001c0002t0001g0228 others(3): Show |
6 | HG01243.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.587+18480_587+1848 others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | GGTGTGTG others(3): Show |
G | 11 | a0001c0001t0001g0266 a0001c0002t0001g0185 a0001c0002t0001g0186 others(8): Show |
11 | HG00323.hp1 HG02109.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.587+18478_587+1848 others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | GGTGTGTG others(5): Show |
G | 5 | a0001c0001t0001g0040 a0001c0002t0002g0020 a0001c0002t0002g0241 others(2): Show |
5 | HG01943.hp1 HG02809.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+18476_587+1848 others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | GGTGTGTG others(7): Show |
G | 1 | a0001c0004t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.587+18474_587+1848 others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | GGTGTGTG others(9): Show |
G | 3 | a0001c0002t0001g0017 a0001c0002t0001g0236 a0001c0005t0003g0092 |
3 | HG01978.hp1 HG04184.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.587+18472_587+1848 others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | GGTGTGTG others(11): Show |
G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0134 a0001c0001t0001g0153 others(1): Show |
4 | HG00140.hp1 HG02056.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+18470_587+1848 others(22): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | GGTGTGTG others(13): Show |
G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(6): Show |
9 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.587+18468_587+1848 others(24): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266868 | GGTGTGTG others(15): Show |
G | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.587+18466_587+1848 others(26): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173266868 | ||||||
| chr4:173266870 | T | G | 5 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG00639.hp1 HG00738.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+18430T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266870 | |||||||
| chr4:173266874 | T | G | 2 | a0001c0001t0001g0048 a0001c0002t0001g0261 |
2 | HG01255.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.587+18434T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266874 | |||||||
| chr4:173266893 | G | A | 1 | a0001c0002t0003g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.587+18453G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266893 | |||||||
| chr4:173266939 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
98 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.587+18499T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266939 | |||||||
| chr4:173266969 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
63 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.587+18529A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173266969 | |||||||
| chr4:173267063 | G | A | 8 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0070 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+18623G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173267063 | |||||||
| chr4:173267123 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.587+18683T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173267123 | |||||||
| chr4:173267128 | A | G | 3 | a0001c0001t0001g0090 a0001c0002t0001g0173 a0001c0002t0001g0174 |
3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.587+18688A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173267128 | |||||||
| chr4:173267648 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.587+19208G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173267648 | |||||||
| chr4:173267763 | T | C | 18 | a0001c0003t0002g0021 a0001c0003t0002g0169 a0001c0003t0002g0176 others(15): Show |
18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.587+19323T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173267763 | |||||||
| chr4:173267773 | TA | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(23): Show |
26 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.587+19335delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173267773 | ||||||
| chr4:173268204 | C | CA | 7 | a0001c0001t0001g0127 a0001c0002t0001g0217 a0001c0002t0001g0219 others(4): Show |
7 | HG01070.hp2 HG01257.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+19769dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268204 | ||||||
| chr4:173268209 | A | C | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.587+19769A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268209 | |||||||
| chr4:173268298 | A | T | 1 | a0001c0002t0002g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.587+19858A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268298 | |||||||
| chr4:173268328 | C | T | 1 | a0001c0002t0001g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587+19888C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268328 | |||||||
| chr4:173268355 | G | A | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+19915G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268355 | |||||||
| chr4:173268441 | T | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG01928.hp2 HG06807.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+20001T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268441 | |||||||
| chr4:173268530 | G | GT | 75 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0040 others(72): Show |
75 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.587+20117dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268530 | ||||||
| chr4:173268530 | G | GTT | 76 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.587+20116_587+2011 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268530 | ||||||
| chr4:173268530 | G | GTTT | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(23): Show |
26 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.587+20115_587+2011 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268530 | ||||||
| chr4:173268530 | GT | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0060 a0001c0001t0001g0080 others(5): Show |
8 | HG01257.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.587+20117delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268530 | ||||||
| chr4:173268530 | GTTTT | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(26): Show |
29 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.587+20114_587+2011 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268530 | ||||||
| chr4:173268655 | C | T | 4 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0185 others(1): Show |
4 | HG02451.hp2 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.587+20215C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268655 | |||||||
| chr4:173268697 | AT | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(26): Show |
29 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.587+20272delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173268697 | ||||||
| chr4:173268713 | G | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.587+20273G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268713 | |||||||
| chr4:173268715 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.587+20275A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268715 | |||||||
| chr4:173268760 | C | A | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587+20320C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268760 | |||||||
| chr4:173268781 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+20341C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268781 | |||||||
| chr4:173268958 | T | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.587+20518T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173268958 | |||||||
| chr4:173269071 | G | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0040 others(54): Show |
57 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.587+20631G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269071 | |||||||
| chr4:173269077 | A | G | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | HG00639.hp1 HG00738.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+20637A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269077 | |||||||
| chr4:173269097 | G | A | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587+20657G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269097 | |||||||
| chr4:173269159 | C | T | 35 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(32): Show |
35 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.587+20719C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269159 | |||||||
| chr4:173269302 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587+20862A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269302 | |||||||
| chr4:173269482 | G | T | 1 | a0001c0002t0001g0236 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.587+21042G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269482 | |||||||
| chr4:173269630 | A | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.587+21190A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269630 | |||||||
| chr4:173269800 | T | C | 1 | a0001c0003t0002g0248 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.587+21360T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269800 | |||||||
| chr4:173269980 | G | A | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587+21540G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173269980 | |||||||
| chr4:173270013 | G | C | 2 | a0001c0002t0001g0014 a0001c0002t0001g0183 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.587+21573G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270013 | |||||||
| chr4:173270110 | G | A | 1 | a0001c0002t0001g0235 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.587+21670G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270110 | |||||||
| chr4:173270116 | C | A | 5 | a0001c0001t0003g0078 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.587+21676C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270116 | |||||||
| chr4:173270127 | T | C | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.587+21687T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270127 | |||||||
| chr4:173270294 | G | A | 35 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(32): Show |
35 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.588-21814G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270294 | |||||||
| chr4:173270462 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
45 | HG00621.hp1 HG01257.hp1 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-21646T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270462 | |||||||
| chr4:173270544 | G | A | 7 | a0001c0001t0003g0078 a0001c0001t0003g0081 a0001c0001t0003g0082 others(4): Show |
7 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-21564G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270544 | |||||||
| chr4:173270681 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.588-21427G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270681 | |||||||
| chr4:173270749 | A | G | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-21359A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270749 | |||||||
| chr4:173270806 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.588-21302C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173270806 | |||||||
| chr4:173271386 | C | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.588-20722C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173271386 | |||||||
| chr4:173271435 | CTGTT | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(43): Show |
46 | HG00621.hp1 HG01257.hp1 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.588-20659_588-2065 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173271435 | ||||||
| chr4:173271453 | A | G | 8 | a0001c0001t0003g0078 a0001c0001t0003g0081 a0001c0001t0003g0082 others(5): Show |
8 | HG01081.hp2 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.588-20655A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173271453 | |||||||
| chr4:173272464 | G | A | 1 | a0001c0002t0001g0263 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.588-19644G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173272464 | |||||||
| chr4:173272642 | G | A | 1 | a0003c0010t0003g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.588-19466G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173272642 | |||||||
| chr4:173272927 | C | G | 18 | a0001c0003t0002g0021 a0001c0003t0002g0169 a0001c0003t0002g0176 others(15): Show |
18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-19181C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173272927 | |||||||
| chr4:173272947 | C | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
101 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.588-19161C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173272947 | |||||||
| chr4:173273018 | C | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0101 others(3): Show |
6 | HG01192.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.588-19090C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273018 | |||||||
| chr4:173273170 | T | C | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.588-18938T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273170 | |||||||
| chr4:173273302 | C | T | 85 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.588-18806C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273302 | |||||||
| chr4:173273369 | T | C | 1 | a0001c0002t0001g0224 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.588-18739T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273369 | |||||||
| chr4:173273384 | A | G | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-18724A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273384 | |||||||
| chr4:173273419 | A | G | 1 | a0001c0001t0002g0033 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.588-18689A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273419 | |||||||
| chr4:173273523 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.588-18585C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273523 | |||||||
| chr4:173273578 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.588-18530C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273578 | |||||||
| chr4:173273658 | G | A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0070 others(2): Show |
5 | HG01884.hp1 HG02717.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-18450G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273658 | |||||||
| chr4:173273660 | A | T | 2 | a0001c0001t0001g0124 a0001c0002t0001g0213 |
2 | HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.588-18448A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273660 | |||||||
| chr4:173273788 | C | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(43): Show |
46 | HG00621.hp1 HG01257.hp1 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.588-18320C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273788 | |||||||
| chr4:173273805 | T | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-18303T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173273805 | |||||||
| chr4:173274807 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.588-17301C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173274807 | |||||||
| chr4:173274822 | C | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0025 |
3 | HG02451.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.588-17286C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173274822 | |||||||
| chr4:173274890 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.588-17218G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173274890 | |||||||
| chr4:173274934 | T | G | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588-17174T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173274934 | |||||||
| chr4:173274983 | C | T | 3 | a0001c0001t0001g0090 a0001c0002t0001g0173 a0001c0002t0001g0174 |
3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.588-17125C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173274983 | |||||||
| chr4:173275117 | T | G | 5 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0025 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.588-16991T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275117 | |||||||
| chr4:173275273 | G | C | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-16835G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275273 | |||||||
| chr4:173275335 | G | T | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-16773G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275335 | |||||||
| chr4:173275445 | T | C | 5 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0070 others(2): Show |
5 | HG01884.hp1 HG02717.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-16663T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275445 | |||||||
| chr4:173275626 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(9): Show |
12 | HG01257.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.588-16482C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275626 | |||||||
| chr4:173275681 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.588-16427C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275681 | |||||||
| chr4:173275694 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.588-16414A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275694 | |||||||
| chr4:173275699 | T | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-16409T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275699 | |||||||
| chr4:173275762 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588-16346G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275762 | |||||||
| chr4:173275917 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.588-16191C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275917 | |||||||
| chr4:173275930 | C | G | 1 | a0001c0001t0001g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.588-16178C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173275930 | |||||||
| chr4:173276127 | A | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(23): Show |
26 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.588-15981A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276127 | |||||||
| chr4:173276363 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.588-15745A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276363 | |||||||
| chr4:173276606 | G | A | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.588-15502G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276606 | |||||||
| chr4:173276699 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(30): Show |
33 | HG00621.hp1 HG01884.hp2 HG01993.hp2 others(30): Show |
intron_variant | MODIFIER | c.588-15409G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276699 | |||||||
| chr4:173276731 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.588-15377C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276731 | |||||||
| chr4:173276815 | AT | A | 6 | a0001c0002t0002g0020 a0001c0002t0002g0197 a0001c0002t0002g0240 others(3): Show |
6 | HG02809.hp2 HG03579.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.588-15283delT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173276815 | ||||||
| chr4:173276916 | A | C | 18 | a0001c0003t0002g0021 a0001c0003t0002g0169 a0001c0003t0002g0176 others(15): Show |
18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-15192A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173276916 | |||||||
| chr4:173277044 | A | T | 40 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(37): Show |
40 | HG00639.hp2 HG01081.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.588-15064A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173277044 | |||||||
| chr4:173277192 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.588-14916T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173277192 | |||||||
| chr4:173277418 | C | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(23): Show |
26 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.588-14690C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173277418 | |||||||
| chr4:173277763 | G | T | 1 | a0001c0002t0001g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.588-14345G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173277763 | |||||||
| chr4:173277996 | AGAG | A | 21 | a0001c0003t0002g0021 a0001c0003t0002g0169 a0001c0003t0002g0176 others(18): Show |
21 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.588-14108_588-1410 others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173277996 | ||||||
| chr4:173278215 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.588-13893T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278215 | |||||||
| chr4:173278320 | T | C | 1 | a0001c0002t0001g0261 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.588-13788T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278320 | |||||||
| chr4:173278339 | A | G | 32 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.588-13769A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278339 | |||||||
| chr4:173278560 | A | G | 1 | a0001c0001t0001g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.588-13548A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278560 | |||||||
| chr4:173278705 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.588-13403C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278705 | |||||||
| chr4:173278788 | A | C | 3 | a0001c0002t0001g0215 a0001c0002t0001g0220 a0001c0002t0001g0229 |
3 | HG01255.hp2 HG01256.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.588-13320A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278788 | |||||||
| chr4:173278846 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.588-13262C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278846 | |||||||
| chr4:173278893 | C | A | 1 | a0001c0008t0002g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.588-13215C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278893 | |||||||
| chr4:173278982 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(32): Show |
35 | HG00621.hp1 HG01884.hp2 HG01993.hp2 others(32): Show |
intron_variant | MODIFIER | c.588-13126C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173278982 | |||||||
| chr4:173279121 | A | G | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.588-12987A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279121 | |||||||
| chr4:173279345 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.588-12763G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279345 | |||||||
| chr4:173279435 | C | T | 32 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.588-12673C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279435 | |||||||
| chr4:173279771 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.588-12337G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279771 | |||||||
| chr4:173279783 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(66): Show |
69 | HG00621.hp1 HG00639.hp2 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.588-12325A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279783 | |||||||
| chr4:173279990 | A | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-12118A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173279990 | |||||||
| chr4:173280095 | C | A | 1 | a0001c0001t0010g0121 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.588-12013C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173280095 | |||||||
| chr4:173280106 | C | CT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.588-11999dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173280106 | ||||||
| chr4:173280277 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.588-11831G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173280277 | |||||||
| chr4:173280340 | A | G | 27 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(24): Show |
27 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.588-11768A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173280340 | |||||||
| chr4:173280420 | A | ATT | 18 | a0001c0003t0002g0021 a0001c0003t0002g0169 a0001c0003t0002g0176 others(15): Show |
18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-11683_588-1168 others(6): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173280420 | ||||||
| chr4:173280815 | C | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-11293C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173280815 | |||||||
| chr4:173280947 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.588-11161C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173280947 | |||||||
| chr4:173281085 | C | T | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0005t0001g0099 others(6): Show |
9 | HG01346.hp2 HG02630.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.588-11023C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281085 | |||||||
| chr4:173281162 | G | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(11): Show |
14 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-10946G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281162 | |||||||
| chr4:173281186 | C | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-10922C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281186 | |||||||
| chr4:173281346 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.588-10762G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281346 | |||||||
| chr4:173281351 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0029 others(54): Show |
57 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.588-10757A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281351 | |||||||
| chr4:173281438 | A | G | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.588-10670A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281438 | |||||||
| chr4:173281768 | C | T | 1 | a0007c0009t0001g0135 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.588-10340C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281768 | |||||||
| chr4:173281779 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(11): Show |
14 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-10329C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173281779 | |||||||
| chr4:173282010 | T | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-10098T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282010 | |||||||
| chr4:173282134 | A | G | 20 | a0001c0003t0002g0021 a0001c0003t0002g0169 a0001c0003t0002g0176 others(17): Show |
20 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.588-9974A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282134 | |||||||
| chr4:173282218 | T | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(30): Show |
33 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.588-9890T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282218 | |||||||
| chr4:173282373 | G | C | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.588-9735G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282373 | |||||||
| chr4:173282391 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(28): Show |
31 | HG00621.hp1 HG01993.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.588-9717A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282391 | |||||||
| chr4:173282449 | T | G | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-9659T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282449 | |||||||
| chr4:173282471 | G | GT | 5 | a0001c0004t0001g0006 a0001c0004t0001g0076 a0001c0004t0001g0077 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.588-9636dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173282471 | ||||||
| chr4:173282608 | G | A | 1 | a0001c0002t0001g0227 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.588-9500G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282608 | |||||||
| chr4:173282646 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-9462G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282646 | |||||||
| chr4:173282720 | A | G | 21 | a0001c0002t0001g0215 a0001c0002t0001g0220 a0001c0002t0001g0227 others(18): Show |
21 | HG01074.hp2 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.588-9388A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173282720 | |||||||
| chr4:173283006 | T | C | 42 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(39): Show |
42 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.588-9102T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283006 | |||||||
| chr4:173283329 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.588-8779A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283329 | |||||||
| chr4:173283377 | T | C | 1 | a0001c0001t0001g0010 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.588-8731T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283377 | |||||||
| chr4:173283500 | C | T | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-8608C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283500 | |||||||
| chr4:173283524 | C | T | 36 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(33): Show |
36 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.588-8584C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283524 | |||||||
| chr4:173283548 | G | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-8560G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283548 | |||||||
| chr4:173283635 | G | C | 1 | a0001c0002t0002g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.588-8473G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283635 | |||||||
| chr4:173283635 | G | GA | 11 | a0001c0001t0001g0068 a0001c0001t0001g0116 a0001c0001t0001g0153 others(8): Show |
11 | HG02027.hp2 HG02109.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.588-8455dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173283635 | ||||||
| chr4:173283650 | A | C | 3 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 |
3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.588-8458A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283650 | |||||||
| chr4:173283703 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0064 |
2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.588-8405T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283703 | |||||||
| chr4:173283984 | C | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0094 others(12): Show |
15 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.588-8124C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173283984 | |||||||
| chr4:173284115 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.588-7993T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284115 | |||||||
| chr4:173284227 | C | T | 24 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(21): Show |
24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.588-7881C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284227 | |||||||
| chr4:173284387 | T | G | 24 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(21): Show |
24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.588-7721T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284387 | |||||||
| chr4:173284392 | A | C | 45 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(42): Show |
45 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-7716A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284392 | |||||||
| chr4:173284396 | T | G | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-7712T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284396 | |||||||
| chr4:173284426 | C | T | 1 | a0001c0006t0001g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.588-7682C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284426 | |||||||
| chr4:173284427 | A | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.588-7681A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284427 | |||||||
| chr4:173284466 | C | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-7642C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284466 | |||||||
| chr4:173284545 | T | C | 1 | a0001c0004t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.588-7563T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284545 | |||||||
| chr4:173284583 | C | T | 45 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(42): Show |
45 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-7525C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284583 | |||||||
| chr4:173284681 | A | T | 1 | a0001c0002t0001g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.588-7427A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284681 | |||||||
| chr4:173284726 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.588-7382A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284726 | |||||||
| chr4:173284729 | A | C | 43 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(40): Show |
43 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.588-7379A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284729 | |||||||
| chr4:173284791 | T | TC | 45 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(42): Show |
45 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-7317_588-7316i others(3): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284791 | |||||||
| chr4:173284856 | A | G | 45 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(42): Show |
45 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-7252A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284856 | |||||||
| chr4:173284859 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(84): Show |
87 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.588-7249C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284859 | |||||||
| chr4:173284904 | T | G | 4 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0185 others(1): Show |
4 | HG02451.hp2 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-7204T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173284904 | |||||||
| chr4:173285332 | A | G | 45 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(42): Show |
45 | HG00423.hp1 HG00639.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.588-6776A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285332 | |||||||
| chr4:173285641 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.588-6467C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285641 | |||||||
| chr4:173285645 | T | C | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.588-6463T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285645 | |||||||
| chr4:173285763 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-6345G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285763 | |||||||
| chr4:173285824 | T | A | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.588-6284T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285824 | |||||||
| chr4:173285849 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.588-6259T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285849 | |||||||
| chr4:173285852 | C | T | 1 | a0001c0003t0002g0254 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.588-6256C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285852 | |||||||
| chr4:173285895 | T | G | 42 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.588-6213T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285895 | |||||||
| chr4:173285981 | G | A | 1 | a0001c0002t0001g0235 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.588-6127G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173285981 | |||||||
| chr4:173286018 | A | C | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-6090A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173286018 | |||||||
| chr4:173286061 | T | C | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.588-6047T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173286061 | |||||||
| chr4:173286137 | T | G | 42 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(39): Show |
42 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.588-5971T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173286137 | |||||||
| chr4:173287067 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0094 others(11): Show |
14 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-5041C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287067 | |||||||
| chr4:173287165 | G | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.588-4943G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287165 | |||||||
| chr4:173287186 | A | G | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-4922A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287186 | |||||||
| chr4:173287227 | A | G | 1 | a0001c0001t0002g0036 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.588-4881A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287227 | |||||||
| chr4:173287390 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.588-4718C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287390 | |||||||
| chr4:173287391 | G | A | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.588-4717G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287391 | |||||||
| chr4:173287415 | G | A | 1 | a0001c0002t0001g0209 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.588-4693G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287415 | |||||||
| chr4:173287643 | G | A | 3 | a0001c0001t0001g0069 a0001c0002t0001g0261 a0001c0002t0001g0262 |
3 | HG01099.hp1 HG01361.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.588-4465G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287643 | |||||||
| chr4:173287907 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0142 |
2 | HG00597.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.588-4201A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173287907 | |||||||
| chr4:173288086 | A | T | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.588-4022A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288086 | |||||||
| chr4:173288140 | A | G | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-3968A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288140 | |||||||
| chr4:173288144 | C | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(100): Show |
103 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.588-3964C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288144 | |||||||
| chr4:173288231 | C | T | 2 | a0001c0002t0001g0191 a0001c0002t0002g0197 |
2 | HG02027.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.588-3877C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288231 | |||||||
| chr4:173288270 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-3838G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288270 | |||||||
| chr4:173288278 | A | G | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-3830A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288278 | |||||||
| chr4:173288282 | C | CAAAAA | 31 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(28): Show |
31 | HG01106.hp1 HG01192.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.588-3807_588-3803d others(7): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAA | 7 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0002t0002g0182 others(4): Show |
7 | HG00423.hp1 HG00621.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.588-3808_588-3803d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0005 a0001c0001t0001g0060 a0001c0001t0001g0080 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-3811_588-3803d others(11): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(3): Show |
12 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0079 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-3812_588-3803d others(12): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0090 a0001c0002t0001g0174 |
3 | HG01192.hp1 HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.588-3813_588-3803d others(13): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0103 a0001c0004t0001g0084 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.588-3814_588-3803d others(14): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0265 a0001c0005t0003g0098 a0006c0011t0002g0180 |
3 | HG03471.hp1 HG06807.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.588-3816_588-3803d others(16): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(8): Show |
2 | a0001c0004t0001g0006 a0001c0005t0003g0095 |
2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.588-3817_588-3803d others(17): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0266 a0001c0002t0006g0170 a0001c0002t0006g0171 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-3818_588-3803d others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(11): Show |
1 | a0001c0005t0003g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.588-3820_588-3803d others(20): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(12): Show |
1 | a0001c0002t0006g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.588-3821_588-3803d others(21): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.588-3824_588-3803d others(24): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.588-3803_588-3802i others(26): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(28): Show |
1 | a0001c0001t0001g0163 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.588-3803_588-3802i others(37): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | C | CAAAAAAA others(41): Show |
1 | a0001c0002t0001g0193 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.588-3803_588-3802i others(50): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | CA | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.588-3803delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288282 | CAA | C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0140 a0001c0001t0001g0155 others(3): Show |
6 | HG02922.hp1 HG03516.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.588-3804_588-3803d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288282 | ||||||
| chr4:173288301 | A | AAAAAAAA others(9): Show |
2 | a0001c0002t0001g0014 a0001c0002t0001g0183 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.588-3803_588-3802i others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173288301 | ||||||
| chr4:173288301 | A | G | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.588-3807A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288301 | |||||||
| chr4:173288306 | G | A | 3 | a0001c0001t0001g0266 a0001c0002t0001g0173 a0001c0002t0001g0174 |
3 | HG01891.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.588-3802G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288306 | |||||||
| chr4:173288466 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.588-3642A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288466 | |||||||
| chr4:173288467 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.588-3641T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288467 | |||||||
| chr4:173288573 | A | T | 1 | a0001c0002t0011g0222 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.588-3535A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288573 | |||||||
| chr4:173288756 | G | A | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-3352G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173288756 | |||||||
| chr4:173289010 | C | A | 79 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0043 others(76): Show |
79 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.588-3098C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289010 | |||||||
| chr4:173289080 | G | A | 1 | a0001c0006t0001g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.588-3028G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289080 | |||||||
| chr4:173289207 | C | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.588-2901C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289207 | |||||||
| chr4:173289247 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.588-2861T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289247 | |||||||
| chr4:173289394 | G | A | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.588-2714G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289394 | |||||||
| chr4:173289557 | G | A | 1 | a0001c0005t0003g0095 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.588-2551G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289557 | |||||||
| chr4:173289805 | G | GT | 11 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(8): Show |
11 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.588-2293dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173289805 | ||||||
| chr4:173289920 | C | A | 10 | a0001c0001t0001g0037 a0001c0002t0001g0187 a0001c0002t0001g0189 others(7): Show |
10 | HG01952.hp1 HG02027.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.588-2188C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289920 | |||||||
| chr4:173289940 | G | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-2168G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289940 | |||||||
| chr4:173289981 | A | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.588-2127A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173289981 | |||||||
| chr4:173290134 | G | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
193 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.588-1974G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173290134 | |||||||
| chr4:173290238 | GACTATGG others(9): Show |
G | 2 | a0001c0002t0001g0219 a0001c0002t0001g0226 |
2 | NA18948.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.588-1844_588-1829d others(18): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173290238 | ||||||
| chr4:173290393 | T | C | 1 | a0001c0001t0002g0031 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.588-1715T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173290393 | |||||||
| chr4:173290628 | T | C | 18 | a0001c0003t0002g0021 a0001c0003t0002g0169 a0001c0003t0002g0176 others(15): Show |
18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.588-1480T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173290628 | |||||||
| chr4:173290648 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.588-1460C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173290648 | |||||||
| chr4:173290870 | C | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0062 others(46): Show |
49 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.588-1238C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173290870 | |||||||
| chr4:173291119 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.588-989C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291119 | |||||||
| chr4:173291162 | C | T | 24 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(21): Show |
24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.588-946C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291162 | |||||||
| chr4:173291169 | C | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0094 others(11): Show |
14 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.588-939C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291169 | |||||||
| chr4:173291395 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.588-713C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291395 | |||||||
| chr4:173291783 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(14): Show |
17 | HG01257.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.588-325G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291783 | |||||||
| chr4:173291794 | G | GA | 14 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0063 others(11): Show |
14 | HG00738.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.588-298dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173291794 | ||||||
| chr4:173291794 | GA | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0094 others(9): Show |
12 | HG01256.hp2 HG02055.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.588-298delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 173291794 | ||||||
| chr4:173291836 | C | T | 1 | a0001c0002t0001g0216 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.588-272C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291836 | |||||||
| chr4:173291846 | T | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-262T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291846 | |||||||
| chr4:173291942 | G | C | 1 | a0001c0002t0001g0263 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.588-166G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291942 | |||||||
| chr4:173291962 | A | G | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.588-146A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173291962 | |||||||
| chr4:173292030 | A | C | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.588-78A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173292030 | |||||||
| chr4:173292035 | C | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588-73C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 2/11 | chr4 | 173292035 | |||||||
| chr4:173292493 | G | A | 1 | a0001c0002t0001g0016 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.754+219G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173292493 | |||||||
| chr4:173292563 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.754+289T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173292563 | |||||||
| chr4:173292577 | C | T | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.754+303C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173292577 | |||||||
| chr4:173293106 | C | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.754+832C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293106 | |||||||
| chr4:173293282 | C | CT | 10 | a0001c0001t0004g0130 a0001c0002t0001g0187 a0001c0002t0001g0189 others(7): Show |
10 | HG01952.hp1 HG02027.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.754+1018dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 173293282 | ||||||
| chr4:173293320 | T | C | 32 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(29): Show |
32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.754+1046T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293320 | |||||||
| chr4:173293347 | TTTAGAG | T | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.754+1075_754+1080d others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 173293347 | ||||||
| chr4:173293448 | A | T | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.754+1174A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293448 | |||||||
| chr4:173293532 | T | TTTAAGA | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.754+1259_754+1260i others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 173293532 | ||||||
| chr4:173293589 | A | G | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.754+1315A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293589 | |||||||
| chr4:173293728 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.754+1454C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293728 | |||||||
| chr4:173293817 | C | G | 5 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0070 others(2): Show |
5 | HG01884.hp1 HG02717.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+1543C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293817 | |||||||
| chr4:173293993 | A | G | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.755-1403A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173293993 | |||||||
| chr4:173294057 | T | C | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-1339T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173294057 | |||||||
| chr4:173294243 | C | T | 1 | a0001c0002t0001g0017 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.755-1153C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173294243 | |||||||
| chr4:173294274 | C | CT | 6 | a0001c0001t0001g0158 a0001c0002t0001g0215 a0001c0002t0001g0220 others(3): Show |
6 | HG01074.hp2 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.755-1109dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 173294274 | ||||||
| chr4:173294274 | CTT | C | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.755-1110_755-1109d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 173294274 | ||||||
| chr4:173294343 | G | A | 2 | a0001c0002t0002g0240 a0001c0002t0002g0243 |
2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.755-1053G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173294343 | |||||||
| chr4:173294345 | G | A | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.755-1051G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173294345 | |||||||
| chr4:173295053 | A | G | 54 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(51): Show |
54 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.755-343A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173295053 | |||||||
| chr4:173295259 | C | A | 1 | a0001c0006t0001g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.755-137C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173295259 | |||||||
| chr4:173295375 | T | G | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.755-21T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 3/11 | chr4 | 173295375 | |||||||
| chr4:173295596 | C | T | 24 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(21): Show |
24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.885+70C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 4/11 | chr4 | 173295596 | |||||||
| chr4:173295971 | A | G | 20 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(17): Show |
20 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.965+128A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173295971 | |||||||
| chr4:173296131 | T | C | 24 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(21): Show |
24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.965+288T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296131 | |||||||
| chr4:173296254 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.965+411T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296254 | |||||||
| chr4:173296293 | A | C | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.965+450A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296293 | |||||||
| chr4:173296437 | C | T | 1 | a0001c0002t0001g0214 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.965+594C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296437 | |||||||
| chr4:173296483 | T | C | 42 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.965+640T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296483 | |||||||
| chr4:173296525 | A | G | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.965+682A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296525 | |||||||
| chr4:173296642 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.965+799C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296642 | |||||||
| chr4:173296647 | A | C | 24 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(21): Show |
24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.965+804A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296647 | |||||||
| chr4:173296656 | C | T | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.965+813C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296656 | |||||||
| chr4:173296927 | A | G | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.965+1084A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173296927 | |||||||
| chr4:173297172 | A | G | 1 | a0001c0003t0002g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.966-943A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297172 | |||||||
| chr4:173297213 | C | CT | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.966-891dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 173297213 | ||||||
| chr4:173297245 | T | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0044 |
3 | HG01993.hp2 HG02293.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.966-870T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297245 | |||||||
| chr4:173297248 | TG | T | 15 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(12): Show |
15 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.966-866delG | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297248 | |||||||
| chr4:173297249 | G | T | 68 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0043 others(65): Show |
68 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.966-866G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297249 | |||||||
| chr4:173297274 | T | G | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.966-841T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297274 | |||||||
| chr4:173297293 | G | A | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.966-822G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297293 | |||||||
| chr4:173297414 | A | G | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.966-701A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297414 | |||||||
| chr4:173297505 | A | G | 1 | a0001c0002t0001g0218 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.966-610A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297505 | |||||||
| chr4:173297639 | C | T | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.966-476C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297639 | |||||||
| chr4:173297751 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.966-364T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 5/11 | chr4 | 173297751 | |||||||
| chr4:173298430 | A | G | 31 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(28): Show |
31 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1148+133A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298430 | |||||||
| chr4:173298430 | A | T | 1 | a0001c0001t0001g0265 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1148+133A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298430 | |||||||
| chr4:173298439 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1148+142G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298439 | |||||||
| chr4:173298461 | G | C | 5 | a0001c0001t0003g0078 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148+164G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298461 | |||||||
| chr4:173298681 | C | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1148+384C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298681 | |||||||
| chr4:173298702 | A | T | 1 | a0001c0002t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1148+405A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173298702 | |||||||
| chr4:173299087 | T | C | 3 | a0001c0003t0008g0250 a0001c0003t0008g0252 a0001c0003t0012g0251 |
3 | NA18975.hp1 NA19012.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1148+790T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299087 | |||||||
| chr4:173299180 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1148+883T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299180 | |||||||
| chr4:173299539 | C | T | 54 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(51): Show |
54 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.1148+1242C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299539 | |||||||
| chr4:173299582 | C | T | 42 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1148+1285C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299582 | |||||||
| chr4:173299652 | A | G | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1148+1355A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299652 | |||||||
| chr4:173299838 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1148+1541T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299838 | |||||||
| chr4:173299851 | C | CA | 29 | a0001c0001t0001g0114 a0001c0001t0005g0075 a0001c0001t0005g0085 others(26): Show |
29 | HG00423.hp1 HG00558.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1148+1565dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 173299851 | ||||||
| chr4:173299857 | A | C | 1 | a0001c0002t0001g0019 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1148+1560A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299857 | |||||||
| chr4:173299877 | G | A | 1 | a0001c0002t0001g0229 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1148+1580G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173299877 | |||||||
| chr4:173300008 | A | G | 1 | a0001c0003t0002g0021 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1148+1711A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300008 | |||||||
| chr4:173300176 | G | A | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1149-1871G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300176 | |||||||
| chr4:173300335 | C | T | 5 | a0001c0004t0001g0006 a0001c0004t0001g0076 a0001c0004t0001g0077 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149-1712C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300335 | |||||||
| chr4:173300589 | G | A | 4 | a0001c0001t0001g0139 a0001c0001t0001g0147 a0001c0002t0001g0018 others(1): Show |
4 | HG01934.hp1 NA18948.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149-1458G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300589 | |||||||
| chr4:173300751 | C | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1149-1296C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300751 | |||||||
| chr4:173300778 | A | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0265 |
3 | HG01192.hp1 NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1149-1269A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300778 | |||||||
| chr4:173300937 | C | G | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1149-1110C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300937 | |||||||
| chr4:173300955 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0060 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149-1092G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173300955 | |||||||
| chr4:173301059 | C | T | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1149-988C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301059 | |||||||
| chr4:173301083 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0149 |
2 | HG00558.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1149-964C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301083 | |||||||
| chr4:173301207 | T | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1149-840T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301207 | |||||||
| chr4:173301345 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1149-702C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301345 | |||||||
| chr4:173301567 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1149-480T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301567 | |||||||
| chr4:173301693 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0118 |
2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1149-354G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301693 | |||||||
| chr4:173301830 | G | A | 95 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0043 others(92): Show |
95 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.1149-217G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301830 | |||||||
| chr4:173301834 | C | T | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1149-213C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 6/11 | chr4 | 173301834 | |||||||
| chr4:173302232 | C | T | 5 | a0001c0001t0003g0078 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1266+68C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302232 | |||||||
| chr4:173302250 | A | G | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1266+86A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302250 | |||||||
| chr4:173302504 | A | G | 1 | a0001c0002t0001g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1266+340A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302504 | |||||||
| chr4:173302518 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1266+354C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302518 | |||||||
| chr4:173302669 | C | A | 1 | a0001c0001t0001g0002 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1266+505C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302669 | |||||||
| chr4:173302839 | A | T | 1 | a0001c0002t0001g0193 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1266+675A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302839 | |||||||
| chr4:173302914 | A | C | 20 | a0001c0001t0001g0040 a0001c0001t0001g0065 a0001c0001t0001g0066 others(17): Show |
20 | HG00140.hp1 HG00323.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1266+750A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302914 | |||||||
| chr4:173302914 | A | T | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266+750A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302914 | |||||||
| chr4:173302921 | G | A | 2 | a0001c0001t0001g0124 a0001c0002t0001g0019 |
2 | HG00621.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1266+757G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173302921 | |||||||
| chr4:173303019 | A | G | 18 | a0001c0003t0002g0021 a0001c0003t0002g0169 a0001c0003t0002g0176 others(15): Show |
18 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1266+855A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303019 | |||||||
| chr4:173303031 | C | T | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266+867C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303031 | |||||||
| chr4:173303032 | T | A | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266+868T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303032 | |||||||
| chr4:173303037 | T | A | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266+873T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303037 | |||||||
| chr4:173303039 | C | A | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1266+875C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303039 | |||||||
| chr4:173303087 | C | T | 1 | a0001c0002t0001g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1267-909C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303087 | |||||||
| chr4:173303182 | G | A | 2 | a0001c0005t0003g0097 a0001c0005t0003g0098 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1267-814G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303182 | |||||||
| chr4:173303194 | C | CA | 48 | a0001c0001t0001g0029 a0001c0001t0001g0067 a0001c0001t0001g0165 others(45): Show |
48 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1267-789dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 173303194 | ||||||
| chr4:173303223 | A | G | 45 | a0001c0001t0001g0029 a0001c0001t0001g0090 a0001c0001t0001g0091 others(42): Show |
45 | HG00621.hp1 HG01884.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.1267-773A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303223 | |||||||
| chr4:173303334 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1267-662A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303334 | |||||||
| chr4:173303513 | C | T | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1267-483C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303513 | |||||||
| chr4:173303563 | C | G | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1267-433C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303563 | |||||||
| chr4:173303566 | A | G | 10 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1267-430A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303566 | |||||||
| chr4:173303586 | A | G | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1267-410A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303586 | |||||||
| chr4:173303609 | A | G | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1267-387A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303609 | |||||||
| chr4:173303612 | C | T | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1267-384C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303612 | |||||||
| chr4:173303979 | G | A | 3 | a0001c0001t0001g0090 a0001c0002t0001g0173 a0001c0002t0001g0174 |
3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1267-17G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 7/11 | chr4 | 173303979 | |||||||
| chr4:173304386 | G | A | 3 | a0001c0001t0001g0107 a0001c0001t0004g0130 a0001c0001t0004g0154 |
3 | HG01952.hp2 HG02300.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1389+268G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304386 | |||||||
| chr4:173304400 | TA | T | 6 | a0001c0001t0001g0053 a0001c0001t0001g0126 a0001c0001t0001g0131 others(3): Show |
6 | HG00642.hp1 HG01070.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1389+294delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173304400 | ||||||
| chr4:173304434 | T | C | 1 | a0001c0005t0003g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1389+316T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304434 | |||||||
| chr4:173304587 | C | T | 1 | a0001c0002t0001g0237 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1389+469C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304587 | |||||||
| chr4:173304686 | C | T | 2 | a0001c0001t0003g0081 a0001c0001t0003g0083 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1389+568C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304686 | |||||||
| chr4:173304699 | C | T | 2 | a0001c0002t0006g0170 a0001c0002t0006g0171 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1389+581C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304699 | |||||||
| chr4:173304724 | C | T | 42 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1389+606C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304724 | |||||||
| chr4:173304733 | A | C | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+615A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304733 | |||||||
| chr4:173304984 | G | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | HG00639.hp1 HG00738.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+866G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173304984 | |||||||
| chr4:173305113 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1389+995G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173305113 | |||||||
| chr4:173305584 | T | A | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1389+1466T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173305584 | |||||||
| chr4:173305711 | C | T | 1 | a0001c0002t0001g0263 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1389+1593C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173305711 | |||||||
| chr4:173306043 | A | G | 1 | a0001c0002t0001g0018 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1389+1925A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306043 | |||||||
| chr4:173306047 | A | G | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+1929A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306047 | |||||||
| chr4:173306151 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1389+2033C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306151 | |||||||
| chr4:173306180 | T | C | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+2062T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306180 | |||||||
| chr4:173306298 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1389+2180A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306298 | |||||||
| chr4:173306356 | T | TTTTC | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+2244_1389+224 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173306356 | ||||||
| chr4:173306451 | T | C | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+2333T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306451 | |||||||
| chr4:173306472 | T | G | 1 | a0001c0001t0001g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1389+2354T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306472 | |||||||
| chr4:173306640 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1389+2522G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306640 | |||||||
| chr4:173306861 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1389+2743T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173306861 | |||||||
| chr4:173307056 | T | C | 1 | a0001c0004t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1389+2938T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307056 | |||||||
| chr4:173307247 | G | T | 2 | a0001c0001t0010g0121 a0001c0002t0010g0233 |
2 | HG00140.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1389+3129G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307247 | |||||||
| chr4:173307251 | G | T | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+3133G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307251 | |||||||
| chr4:173307371 | C | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1389+3253C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307371 | |||||||
| chr4:173307394 | C | T | 1 | a0001c0003t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1389+3276C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307394 | |||||||
| chr4:173307442 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1389+3324C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307442 | |||||||
| chr4:173307492 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1389+3374G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307492 | |||||||
| chr4:173307876 | G | T | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+3758G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307876 | |||||||
| chr4:173307947 | C | T | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1389+3829C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307947 | |||||||
| chr4:173307977 | G | A | 24 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(21): Show |
24 | HG00621.hp1 HG02040.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1389+3859G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173307977 | |||||||
| chr4:173308409 | C | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+4291C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308409 | |||||||
| chr4:173308433 | G | T | 1 | a0001c0002t0006g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1389+4315G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308433 | |||||||
| chr4:173308486 | C | T | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+4368C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308486 | |||||||
| chr4:173308534 | A | G | 1 | a0001c0002t0001g0213 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1389+4416A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308534 | |||||||
| chr4:173308550 | T | C | 1 | a0001c0003t0002g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1389+4432T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308550 | |||||||
| chr4:173308611 | T | C | 42 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1389+4493T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308611 | |||||||
| chr4:173308633 | A | G | 1 | a0001c0002t0013g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1389+4515A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308633 | |||||||
| chr4:173308661 | C | T | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+4543C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308661 | |||||||
| chr4:173308662 | G | A | 5 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0002t0001g0179 others(2): Show |
5 | HG00642.hp1 HG01070.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+4544G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308662 | |||||||
| chr4:173308718 | C | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0094 a0001c0001t0001g0103 |
3 | HG02572.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1389+4600C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308718 | |||||||
| chr4:173308721 | A | G | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1389+4603A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308721 | |||||||
| chr4:173308772 | G | A | 5 | a0001c0004t0001g0006 a0001c0004t0001g0076 a0001c0004t0001g0077 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+4654G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173308772 | |||||||
| chr4:173309199 | C | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0094 a0001c0001t0001g0103 |
3 | HG02572.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1390-4759C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173309199 | |||||||
| chr4:173309217 | G | A | 12 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1390-4741G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173309217 | |||||||
| chr4:173309883 | CA | C | 13 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(10): Show |
13 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1390-4073delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173309883 | ||||||
| chr4:173310097 | A | C | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-3861A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173310097 | |||||||
| chr4:173310541 | G | A | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-3417G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173310541 | |||||||
| chr4:173310828 | C | A | 2 | a0001c0001t0001g0266 a0001c0002t0001g0193 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1390-3130C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173310828 | |||||||
| chr4:173310937 | T | C | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | HG00639.hp1 HG00738.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390-3021T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173310937 | |||||||
| chr4:173311096 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0094 a0001c0001t0001g0103 |
3 | HG02572.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1390-2862C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311096 | |||||||
| chr4:173311115 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1390-2843G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311115 | |||||||
| chr4:173311304 | A | G | 1 | a0001c0002t0001g0183 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1390-2654A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311304 | |||||||
| chr4:173311305 | T | G | 1 | a0001c0002t0001g0185 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1390-2653T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311305 | |||||||
| chr4:173311323 | G | A | 5 | a0001c0004t0001g0006 a0001c0004t0001g0076 a0001c0004t0001g0077 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390-2635G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311323 | |||||||
| chr4:173311474 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1390-2484C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311474 | |||||||
| chr4:173311515 | T | C | 87 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0043 others(84): Show |
87 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1390-2443T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311515 | |||||||
| chr4:173311719 | G | A | 42 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1390-2239G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311719 | |||||||
| chr4:173311892 | A | G | 3 | a0001c0002t0001g0018 a0002c0007t0007g0177 a0002c0007t0007g0178 |
3 | HG01934.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1390-2066A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173311892 | |||||||
| chr4:173312761 | A | G | 1 | a0001c0003t0002g0248 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1390-1197A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173312761 | |||||||
| chr4:173312788 | A | G | 55 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(52): Show |
55 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.1390-1170A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173312788 | |||||||
| chr4:173313005 | G | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1390-953G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313005 | |||||||
| chr4:173313070 | T | TA | 32 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0061 others(29): Show |
32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1390-888_1390-887i others(3): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313070 | |||||||
| chr4:173313071 | T | A | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1390-887T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313071 | |||||||
| chr4:173313086 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1390-872G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313086 | |||||||
| chr4:173313282 | T | C | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1390-676T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313282 | |||||||
| chr4:173313290 | C | G | 1 | a0005c0013t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1390-668C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313290 | |||||||
| chr4:173313296 | C | T | 42 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1390-662C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313296 | |||||||
| chr4:173313379 | G | T | 1 | a0001c0002t0001g0237 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1390-579G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313379 | |||||||
| chr4:173313405 | C | CA | 52 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0028 others(49): Show |
52 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1390-546dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313405 | ||||||
| chr4:173313458 | C | T | 4 | a0001c0002t0013g0207 a0001c0006t0001g0072 a0001c0006t0001g0073 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-500C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313458 | |||||||
| chr4:173313570 | C | CA | 11 | a0001c0001t0001g0004 a0001c0002t0001g0173 a0001c0002t0001g0174 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1390-372dupA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313570 | ||||||
| chr4:173313570 | CA | C | 7 | a0001c0001t0001g0063 a0001c0001t0001g0087 a0001c0001t0002g0038 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1390-372delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313570 | ||||||
| chr4:173313666 | A | G | 5 | a0001c0001t0003g0078 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1390-292A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313666 | |||||||
| chr4:173313820 | G | A | 6 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0025 others(3): Show |
6 | HG02451.hp1 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1390-138G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313820 | |||||||
| chr4:173313901 | A | G | 1 | a0001c0002t0013g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1390-57A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313901 | |||||||
| chr4:173313928 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1390-30G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313928 | |||||||
| chr4:173313928 | G | GATAT | 10 | a0001c0001t0001g0029 a0001c0001t0002g0023 a0001c0001t0002g0030 others(7): Show |
10 | HG00621.hp1 HG02040.hp2 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.1390-17_1390-14dup others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313928 | ||||||
| chr4:173313941 | A | AT | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1390-16dupT | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313941 | ||||||
| chr4:173313941 | A | T | 17 | a0001c0003t0002g0021 a0001c0003t0002g0176 a0001c0003t0002g0181 others(14): Show |
17 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.1390-17A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313941 | |||||||
| chr4:173313943 | A | ATAT | 13 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0025 others(10): Show |
13 | HG02451.hp1 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1390-14_1390-13ins others(3): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 173313943 | ||||||
| chr4:173313943 | A | T | 33 | a0001c0001t0001g0266 a0001c0001t0005g0075 a0001c0001t0005g0085 others(30): Show |
33 | HG00423.hp1 HG01106.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.1390-15A>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313943 | |||||||
| chr4:173313944 | T | TA | 5 | a0001c0001t0001g0090 a0001c0002t0001g0173 a0001c0002t0001g0174 others(2): Show |
5 | HG01891.hp1 HG03130.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1390-14_1390-13ins others(1): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313944 | |||||||
| chr4:173313945 | T | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0028 |
2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1390-13T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313945 | |||||||
| chr4:173313946 | T | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1390-12T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313946 | |||||||
| chr4:173313951 | T | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
splice_region_variant&intron_variant | LOW | c.1390-7T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 8/11 | chr4 | 173313951 | |||||||
| chr4:173314329 | T | C | 45 | a0001c0001t0001g0029 a0001c0001t0001g0067 a0001c0001t0001g0165 others(42): Show |
45 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1608+153T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314329 | |||||||
| chr4:173314445 | T | A | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1608+269T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314445 | |||||||
| chr4:173314473 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
93 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1608+297T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314473 | |||||||
| chr4:173314662 | G | A | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1608+486G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314662 | |||||||
| chr4:173314782 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1608+606T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314782 | |||||||
| chr4:173314852 | C | T | 1 | a0001c0002t0001g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1608+676C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314852 | |||||||
| chr4:173314869 | C | G | 1 | a0001c0002t0013g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1608+693C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173314869 | |||||||
| chr4:173315046 | GATA | G | 42 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1608+873_1608+875d others(5): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 173315046 | ||||||
| chr4:173315270 | T | G | 9 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 others(6): Show |
9 | HG01346.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1608+1094T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315270 | |||||||
| chr4:173315353 | G | A | 1 | a0001c0002t0001g0238 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1608+1177G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315353 | |||||||
| chr4:173315559 | G | A | 5 | a0001c0001t0003g0078 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1608+1383G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315559 | |||||||
| chr4:173315602 | C | G | 42 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1608+1426C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315602 | |||||||
| chr4:173315667 | C | CTTAT | 54 | a0001c0001t0001g0029 a0001c0001t0001g0101 a0001c0001t0002g0022 others(51): Show |
54 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.1608+1494_1608+149 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 173315667 | ||||||
| chr4:173315697 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1608+1521A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315697 | |||||||
| chr4:173315885 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1709A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315885 | |||||||
| chr4:173315910 | C | T | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1609-1724C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315910 | |||||||
| chr4:173315940 | C | G | 1 | a0001c0002t0013g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1609-1694C>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173315940 | |||||||
| chr4:173316038 | AGAGT | A | 9 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0002t0001g0173 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1609-1593_1609-159 others(8): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 173316038 | ||||||
| chr4:173316065 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1609-1569A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316065 | |||||||
| chr4:173316171 | GGCCTCAC others(8): Show |
G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
93 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1609-1460_1609-144 others(19): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 173316171 | ||||||
| chr4:173316221 | C | T | 1 | a0001c0005t0003g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1609-1413C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316221 | |||||||
| chr4:173316291 | G | C | 1 | a0001c0001t0002g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1609-1343G>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316291 | |||||||
| chr4:173316420 | T | C | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0002t0001g0173 others(1): Show |
4 | HG01891.hp1 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-1214T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316420 | |||||||
| chr4:173316654 | T | G | 3 | a0001c0006t0001g0072 a0001c0006t0001g0073 a0001c0006t0001g0074 |
3 | HG02109.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1609-980T>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316654 | |||||||
| chr4:173316838 | C | T | 1 | a0001c0002t0001g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1609-796C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316838 | |||||||
| chr4:173316897 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1609-737T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173316897 | |||||||
| chr4:173317005 | A | C | 1 | a0001c0001t0011g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1609-629A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173317005 | |||||||
| chr4:173317199 | C | T | 1 | a0001c0002t0013g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1609-435C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173317199 | |||||||
| chr4:173317449 | C | A | 1 | a0001c0002t0001g0236 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1609-185C>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173317449 | |||||||
| chr4:173317451 | T | A | 2 | a0001c0002t0001g0200 a0001c0002t0001g0211 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1609-183T>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 9/11 | chr4 | 173317451 | |||||||
| chr4:173317769 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0265 |
3 | HG01192.hp1 NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1707+37A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 10/11 | chr4 | 173317769 | |||||||
| chr4:173317889 | A | G | 51 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(48): Show |
51 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.1707+157A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 10/11 | chr4 | 173317889 | |||||||
| chr4:173318106 | A | G | 3 | a0001c0002t0006g0170 a0001c0002t0006g0171 a0001c0002t0006g0172 |
3 | HG02622.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1708-325A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 10/11 | chr4 | 173318106 | |||||||
| chr4:173318226 | G | T | 5 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0070 others(2): Show |
5 | HG01884.hp1 HG02897.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1708-205G>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 10/11 | chr4 | 173318226 | |||||||
| chr4:173318396 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1708-35C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 10/11 | chr4 | 173318396 | |||||||
| chr4:173318786 | G | A | 43 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(40): Show |
43 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.1836+227G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173318786 | |||||||
| chr4:173319057 | G | A | 3 | a0001c0001t0001g0090 a0001c0002t0001g0173 a0001c0002t0001g0174 |
3 | HG01891.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1836+498G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173319057 | |||||||
| chr4:173319109 | G | A | 5 | a0001c0004t0001g0006 a0001c0004t0001g0076 a0001c0004t0001g0077 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1836+550G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173319109 | |||||||
| chr4:173319275 | T | TAA | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1836+722_1836+723d others(4): Show |
GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 173319275 | ||||||
| chr4:173319526 | CA | C | 45 | a0001c0001t0001g0029 a0001c0001t0002g0022 a0001c0001t0002g0023 others(42): Show |
45 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.1836+976delA | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 173319526 | ||||||
| chr4:173319818 | A | G | 9 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1836+1259A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173319818 | |||||||
| chr4:173320383 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1837-1197A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320383 | |||||||
| chr4:173320443 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1837-1137A>G | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320443 | |||||||
| chr4:173320542 | T | C | 53 | a0001c0001t0001g0101 a0001c0001t0002g0022 a0001c0001t0002g0023 others(50): Show |
53 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.1837-1038T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320542 | |||||||
| chr4:173320614 | G | A | 7 | a0001c0001t0005g0075 a0001c0001t0005g0085 a0001c0001t0005g0086 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-966G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320614 | |||||||
| chr4:173320619 | C | T | 1 | a0001c0002t0006g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1837-961C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320619 | |||||||
| chr4:173320656 | A | C | 2 | a0001c0001t0001g0139 a0001c0002t0001g0018 |
2 | HG01934.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1837-924A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320656 | |||||||
| chr4:173320827 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1837-753C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320827 | |||||||
| chr4:173320939 | G | A | 1 | a0001c0002t0001g0210 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1837-641G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173320939 | |||||||
| chr4:173321044 | C | T | 1 | a0001c0002t0001g0192 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1837-536C>T | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321044 | |||||||
| chr4:173321075 | A | C | 1 | a0001c0002t0001g0235 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1837-505A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321075 | |||||||
| chr4:173321126 | T | C | 53 | a0001c0001t0001g0101 a0001c0001t0002g0022 a0001c0001t0002g0023 others(50): Show |
53 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.1837-454T>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321126 | |||||||
| chr4:173321147 | A | C | 43 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(40): Show |
43 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.1837-433A>C | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321147 | |||||||
| chr4:173321167 | G | A | 1 | a0001c0005t0003g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1837-413G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321167 | |||||||
| chr4:173321516 | G | A | 2 | a0002c0007t0007g0177 a0002c0007t0007g0178 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1837-64G>A | GALNT7 | ENSG00000109586.12 | transcript | ENST00000265000.9 | protein_coding | 11/11 | chr4 | 173321516 |