Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100505741 |
| ensemblid | ENSG00000122432.19 |
| hgncid | 14682 |
| symbol | SPATA1 |
| name | spermatogenesis associated 1 |
| refseq_nuc | NM_001397487.1 |
| refseq_prot | NP_001384416.1 |
| ensembl_nuc | ENST00000699524.1 |
| ensembl_prot | ENSP00000514414.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 84506386 |
| end | 84567379 |
| strand | + |
| ver | v1.2 |
| region | chr1:84506386-84567379 |
| region5000 | chr1:84501386-84572379 |
| regionname0 | SPATA1_chr1_84506386_84567379 |
| regionname5000 | SPATA1_chr1_84501386_84572379 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 440 | 185 | 39 | 34 | 87 | 8 | 15 | 69 | SPATA1_chr1_84501386_84572379 | SPATA1 | MSLNP others(435): Show |
chr1 | 84501386 | 84572379 |
| a0002 | 0/0 | 440 | 84 | 17 | 12 | 45 | 1 | 9 | 33 | SPATA1_chr1_84501386_84572379 | SPATA1 | MSLNP others(435): Show |
chr1 | 84501386 | 84572379 |
| a0003 | 0/0 | 440 | 21 | 11 | 6 | 0 | 1 | 3 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | MSLNP others(435): Show |
chr1 | 84501386 | 84572379 |
| a0004 | 0/0 | 440 | 19 | 19 | 0 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | MSLNP others(435): Show |
chr1 | 84501386 | 84572379 |
| a0005 | 0/0 | 440 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | MSLNP others(435): Show |
chr1 | 84501386 | 84572379 |
| a0006 | 0/0 | 440 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | MSLNP others(435): Show |
chr1 | 84501386 | 84572379 |
| a0007 | 0/0 | 440 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | MSLNP others(435): Show |
chr1 | 84501386 | 84572379 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1320 | 136 | 19 | 26 | 71 | 5 | 13 | SPATA1_chr1_84501386_84572379 | SPATA1 | ATGTC others(1315): Show |
chr1 | 84501386 | 84572379 | ||
| a0001c0003 | 0/0 | 1320 | 44 | 15 | 8 | 16 | 3 | 2 | SPATA1_chr1_84501386_84572379 | SPATA1 | ATGTC others(1315): Show |
chr1 | 84501386 | 84572379 | ||
| a0001c0006 | 0/0 | 1320 | 5 | 5 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | ATGTC others(1315): Show |
chr1 | 84501386 | 84572379 | ||
| a0002c0002 | 0/0 | 1320 | 84 | 17 | 12 | 45 | 1 | 9 | SPATA1_chr1_84501386_84572379 | SPATA1 | ATGTC others(1315): Show |
chr1 | 84501386 | 84572379 | ||
| a0003c0004 | 0/0 | 1320 | 21 | 11 | 6 | 0 | 1 | 3 | SPATA1_chr1_84501386_84572379 | SPATA1 | ATGTC others(1315): Show |
chr1 | 84501386 | 84572379 | ||
| a0004c0005 | 0/0 | 1320 | 19 | 19 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | ATGTC others(1315): Show |
chr1 | 84501386 | 84572379 | ||
| a0005c0007 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | ATGTC others(1315): Show |
chr1 | 84501386 | 84572379 | ||
| a0006c0008 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | ATGTC others(1315): Show |
chr1 | 84501386 | 84572379 | ||
| a0007c0009 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | ATGTC others(1315): Show |
chr1 | 84501386 | 84572379 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2983 | 130 | 17 | 23 | 70 | 5 | 13 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0001c0001t0007 | 0/0 | 2983 | 4 | 1 | 3 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0001c0001t0009 | 0/0 | 2984 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2979): Show |
chr1 | 84501386 | 84572379 |
| a0001c0001t0013 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0001c0003t0001 | 0/0 | 2983 | 7 | 1 | 2 | 1 | 2 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0001c0003t0003 | 0/0 | 2983 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0001c0003t0004 | 0/0 | 2984 | 25 | 6 | 6 | 11 | 1 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2979): Show |
chr1 | 84501386 | 84572379 |
| a0001c0003t0006 | 0/0 | 2983 | 5 | 5 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0001c0003t0009 | 0/0 | 2984 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2979): Show |
chr1 | 84501386 | 84572379 |
| a0001c0003t0011 | 0/0 | 2983 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0001c0006t0008 | 0/0 | 2983 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0001c0006t0014 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0002c0002t0002 | 0/0 | 2983 | 34 | 0 | 0 | 32 | 0 | 2 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0002c0002t0003 | 0/0 | 2983 | 27 | 7 | 6 | 7 | 1 | 6 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0002c0002t0005 | 0/0 | 2983 | 12 | 6 | 6 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0002c0002t0006 | 0/0 | 2983 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0002c0002t0007 | 0/0 | 2983 | 5 | 1 | 0 | 4 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0002c0002t0010 | 0/0 | 2983 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0002c0002t0012 | 0/0 | 2983 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0003c0004t0001 | 0/0 | 2983 | 20 | 10 | 6 | 0 | 1 | 3 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0003c0004t0006 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0004c0005t0001 | 0/0 | 2983 | 19 | 19 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0005c0007t0001 | 0/0 | 2983 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0006c0008t0001 | 0/0 | 2983 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| a0007c0009t0012 | 0/0 | 2983 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | CTTTT others(2978): Show |
chr1 | 84501386 | 84572379 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0247 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0007g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0007g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0009g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0001t0013g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0006g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0009g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0011g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0003t0011g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0006t0008g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0006t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0006t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0001c0006t0014g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0005g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0005g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0007g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0010g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0002c0002t0012g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0003c0004t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0004c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0005c0007t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0006c0008t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| a0007c0009t0012g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0004 | g0050 | EUR | GBR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0132 | EUR | FIN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0128 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00597 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00609 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00621 | hp1 | a0001 | c0003 | t0004 | g0002 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00621 | hp2 | a0002 | c0002 | t0003 | g0137 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00639 | hp1 | a0001 | c0003 | t0004 | g0002 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00639 | hp2 | a0005 | c0007 | t0001 | g0040 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00735 | hp1 | a0002 | c0002 | t0003 | g0135 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG00741 | hp2 | a0003 | c0004 | t0001 | g0074 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01070 | hp1 | a0002 | c0002 | t0005 | g0024 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01071 | hp1 | a0002 | c0002 | t0005 | g0025 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01081 | hp1 | a0002 | c0002 | t0005 | g0025 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01099 | hp1 | a0002 | c0002 | t0005 | g0149 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01106 | hp1 | a0002 | c0002 | t0003 | g0131 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0091 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01109 | hp2 | a0002 | c0002 | t0003 | g0145 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01167 | hp1 | a0002 | c0002 | t0005 | g0024 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01168 | hp1 | a0002 | c0002 | t0003 | g0254 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01168 | hp2 | a0003 | c0004 | t0001 | g0015 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01169 | hp1 | a0002 | c0002 | t0005 | g0152 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01169 | hp2 | a0003 | c0004 | t0001 | g0015 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01175 | hp1 | a0006 | c0008 | t0001 | g0235 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01192 | hp2 | a0001 | c0003 | t0004 | g0002 | AMR | PUR | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0018 | AMR | CLM | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0094 | AMR | CLM | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01346 | hp1 | a0001 | c0003 | t0004 | g0044 | AMR | CLM | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01361 | hp2 | a0003 | c0004 | t0001 | g0067 | AMR | CLM | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01496 | hp2 | a0003 | c0004 | t0001 | g0068 | AMR | CLM | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0095 | EUR | IBS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0092 | EUR | IBS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01891 | hp1 | a0003 | c0004 | t0001 | g0079 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01891 | hp2 | a0004 | c0005 | t0001 | g0007 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01943 | hp1 | a0001 | c0003 | t0004 | g0045 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0018 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01975 | hp1 | a0003 | c0004 | t0001 | g0078 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01993 | hp1 | a0002 | c0002 | t0003 | g0253 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0090 | EAS | KHV | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02055 | hp1 | a0004 | c0005 | t0001 | g0011 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02055 | hp2 | a0001 | c0003 | t0004 | g0043 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | KHV | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | KHV | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | KHV | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02145 | hp1 | a0001 | c0003 | t0004 | g0060 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02145 | hp2 | a0002 | c0002 | t0005 | g0153 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02148 | hp2 | a0001 | c0003 | t0004 | g0056 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CDX | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CDX | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02257 | hp2 | a0004 | c0005 | t0001 | g0036 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02258 | hp1 | a0001 | c0003 | t0006 | g0005 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02258 | hp2 | a0002 | c0002 | t0005 | g0154 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02280 | hp1 | a0002 | c0002 | t0005 | g0026 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02293 | hp1 | a0001 | c0001 | t0007 | g0127 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02293 | hp2 | a0001 | c0003 | t0004 | g0046 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0022 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02451 | hp1 | a0002 | c0002 | t0003 | g0110 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02451 | hp2 | a0004 | c0005 | t0001 | g0039 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02572 | hp1 | a0002 | c0002 | t0005 | g0150 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02572 | hp2 | a0001 | c0003 | t0004 | g0061 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02622 | hp1 | a0001 | c0003 | t0004 | g0059 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02622 | hp2 | a0004 | c0005 | t0001 | g0037 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02630 | hp1 | a0002 | c0002 | t0006 | g0086 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02630 | hp2 | a0001 | c0003 | t0006 | g0033 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02647 | hp1 | a0004 | c0005 | t0001 | g0013 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02698 | hp1 | a0003 | c0004 | t0001 | g0071 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02717 | hp2 | a0001 | c0003 | t0004 | g0058 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02723 | hp1 | a0004 | c0005 | t0001 | g0012 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02723 | hp2 | a0001 | c0006 | t0014 | g0063 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02735 | hp2 | a0002 | c0002 | t0003 | g0138 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02738 | hp1 | a0002 | c0002 | t0003 | g0139 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02809 | hp1 | a0001 | c0003 | t0003 | g0106 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02809 | hp2 | a0001 | c0006 | t0008 | g0017 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02818 | hp1 | a0004 | c0005 | t0001 | g0007 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02818 | hp2 | a0003 | c0004 | t0006 | g0070 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02886 | hp2 | a0002 | c0002 | t0003 | g0109 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02895 | hp1 | a0001 | c0003 | t0006 | g0034 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02895 | hp2 | a0003 | c0004 | t0001 | g0016 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02897 | hp2 | a0003 | c0004 | t0001 | g0016 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02922 | hp1 | a0004 | c0005 | t0001 | g0006 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0082 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02965 | hp2 | a0001 | c0003 | t0006 | g0005 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02970 | hp1 | a0003 | c0004 | t0001 | g0083 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02976 | hp1 | a0004 | c0005 | t0001 | g0041 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02976 | hp2 | a0002 | c0002 | t0003 | g0142 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0093 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03041 | hp1 | a0002 | c0002 | t0005 | g0026 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03041 | hp2 | a0004 | c0005 | t0001 | g0038 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03130 | hp1 | a0001 | c0006 | t0008 | g0089 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03139 | hp1 | a0002 | c0002 | t0003 | g0105 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03195 | hp1 | a0004 | c0005 | t0001 | g0006 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0103 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03209 | hp1 | a0003 | c0004 | t0001 | g0075 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03209 | hp2 | a0004 | c0005 | t0001 | g0007 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03225 | hp1 | a0001 | c0003 | t0006 | g0005 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03225 | hp2 | a0004 | c0005 | t0001 | g0013 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03453 | hp1 | a0001 | c0001 | t0013 | g0162 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03486 | hp1 | a0004 | c0005 | t0001 | g0012 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0108 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03491 | hp1 | a0002 | c0002 | t0012 | g0084 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0098 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03516 | hp1 | a0002 | c0002 | t0006 | g0064 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03516 | hp2 | a0003 | c0004 | t0001 | g0080 | AFR | ESN | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03540 | hp1 | a0003 | c0004 | t0001 | g0081 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03579 | hp2 | a0002 | c0002 | t0003 | g0104 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03669 | hp1 | a0007 | c0009 | t0012 | g0085 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0148 | SAS | PJL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03834 | hp1 | a0001 | c0003 | t0004 | g0047 | SAS | BEB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0100 | SAS | STU | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG04184 | hp1 | a0003 | c0004 | t0001 | g0076 | SAS | BEB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG04199 | hp1 | a0003 | c0004 | t0001 | g0066 | SAS | STU | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0125 | SAS | STU | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0113 | SAS | STU | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG04228 | hp1 | a0002 | c0002 | t0003 | g0099 | SAS | STU | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18522 | hp2 | a0004 | c0005 | t0001 | g0006 | AFR | YRI | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18612 | hp2 | a0001 | c0003 | t0004 | g0051 | EAS | CHB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | CHB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18940 | hp1 | a0001 | c0001 | t0009 | g0222 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18940 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18942 | hp1 | a0001 | c0003 | t0004 | g0055 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18945 | hp1 | a0001 | c0003 | t0009 | g0014 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18952 | hp1 | a0002 | c0002 | t0010 | g0146 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18954 | hp2 | a0002 | c0002 | t0007 | g0129 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18962 | hp1 | a0002 | c0002 | t0007 | g0021 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18968 | hp1 | a0001 | c0003 | t0004 | g0054 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18980 | hp1 | a0002 | c0002 | t0003 | g0140 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18986 | hp2 | a0002 | c0002 | t0007 | g0021 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18988 | hp2 | a0001 | c0003 | t0011 | g0251 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18989 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18994 | hp1 | a0002 | c0002 | t0003 | g0141 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19004 | hp2 | a0001 | c0003 | t0009 | g0014 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19030 | hp1 | a0002 | c0002 | t0005 | g0151 | AFR | LWK | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19043 | hp1 | a0001 | c0006 | t0008 | g0088 | AFR | LWK | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19043 | hp2 | a0001 | c0003 | t0004 | g0057 | AFR | LWK | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19054 | hp1 | a0001 | c0003 | t0004 | g0049 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19056 | hp2 | a0002 | c0002 | t0007 | g0130 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19057 | hp2 | a0001 | c0003 | t0004 | g0052 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19058 | hp2 | a0001 | c0003 | t0004 | g0053 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19063 | hp1 | a0001 | c0003 | t0011 | g0252 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19072 | hp2 | a0002 | c0002 | t0010 | g0147 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19077 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19089 | hp2 | a0001 | c0003 | t0004 | g0048 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19090 | hp1 | a0002 | c0002 | t0003 | g0136 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19240 | hp1 | a0004 | c0005 | t0001 | g0042 | AFR | YRI | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA19240 | hp2 | a0001 | c0006 | t0008 | g0017 | AFR | YRI | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA20805 | hp1 | a0003 | c0004 | t0001 | g0073 | EUR | TSI | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02109 | hp1 | a0002 | c0002 | t0007 | g0107 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02486 | hp1 | a0004 | c0005 | t0001 | g0011 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03471 | hp1 | a0002 | c0002 | t0006 | g0065 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0097 | AFR | MSL | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG06807 | hp1 | a0003 | c0004 | t0001 | g0069 | AFR | USA | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| HG06807 | hp2 | a0004 | c0005 | t0001 | g0035 | AFR | USA | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | USA | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA20300 | hp2 | a0001 | c0003 | t0003 | g0111 | AFR | USA | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA21309 | hp1 | a0003 | c0004 | t0001 | g0072 | AFR | LWK | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| NA21309 | hp2 | a0002 | c0002 | t0003 | g0022 | AFR | LWK | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0247 | REF | REF | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0246 | REF | REF | SPATA1_chr1_84501386_84572379 | SPATA1 | chr1 | 84501386 | 84572379 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:84506416 | G | T | 2 | a0001 a0002 |
77 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(74): Show |
splice_region_variant | LOW | c.-140G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/14 | chr1 | 84506416 | |||||||
| chr1:84525893 | A | C | 1 | a0007 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.364A>C | p.Asn122His | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/14 | 534/2983 | 364/1323 | 122/440 | chr1 | 84525893 | |||
| chr1:84525986 | G | C | 3 | a0003 a0004 a0005 |
41 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(38): Show |
missense_variant | MODERATE | c.457G>C | p.Val153Leu | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/14 | 627/2983 | 457/1323 | 153/440 | chr1 | 84525986 | |||
| chr1:84544211 | A | G | 3 | a0002 a0005 a0007 |
86 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(83): Show |
missense_variant | MODERATE | c.727A>G | p.Lys243Glu | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/14 | 897/2983 | 727/1323 | 243/440 | chr1 | 84544211 | |||
| chr1:84548864 | G | A | 1 | a0006 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.1025G>A | p.Arg342Gln | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/14 | 1195/2983 | 1025/1323 | 342/440 | chr1 | 84548864 | |||
| chr1:84555919 | G | A | 1 | a0004 | 19 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(16): Show |
missense_variant | MODERATE | c.1234G>A | p.Val412Met | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/14 | 1404/2983 | 1234/1323 | 412/440 | chr1 | 84555919 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:84532954 | T | C | 1 | a0001c0006 | 5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.639T>C | p.Asp213Asp | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 7/14 | 809/2983 | 639/1323 | 213/440 | chr1 | 84532954 | |||
| chr1:84550494 | A | G | 7 | a0001c0003 a0001c0006 a0002c0002 others(4): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
synonymous_variant | LOW | c.1188A>G | p.Leu396Leu | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/14 | 1358/2983 | 1188/1323 | 396/440 | chr1 | 84550494 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:84506406 | C | G | 2 | a0002c0002t0012 a0007c0009t0012 |
2 | HG03491.hp1 HG03669.hp1 |
5_prime_UTR_variant | MODIFIER | c.-150C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/14 | 9954 | chr1 | 84506406 | ||||||
| chr1:84516255 | C | CA | 3 | a0001c0001t0009 a0001c0003t0004 a0001c0003t0009 |
28 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-97dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/14 | 96 | INFO_REALIGN_3_PRIME | chr1 | 84516255 | |||||
| chr1:84565947 | G | A | 10 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0006 others(7): Show |
112 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*58G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 14/14 | 58 | chr1 | 84565947 | ||||||
| chr1:84566140 | T | C | 1 | a0001c0006t0008 | 4 | HG02809.hp2 HG03130.hp1 NA19043.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*251T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 14/14 | 251 | chr1 | 84566140 | ||||||
| chr1:84566260 | T | C | 1 | a0002c0002t0002 | 34 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*371T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 14/14 | 371 | chr1 | 84566260 | ||||||
| chr1:84566386 | G | T | 2 | a0001c0006t0014 a0002c0002t0005 |
13 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*497G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 14/14 | 497 | chr1 | 84566386 | ||||||
| chr1:84566545 | T | G | 1 | a0002c0002t0005 | 12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*656T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 14/14 | 656 | chr1 | 84566545 | ||||||
| chr1:84566693 | C | T | 1 | a0001c0001t0013 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*804C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 14/14 | 804 | chr1 | 84566693 | ||||||
| chr1:84566752 | C | T | 2 | a0001c0006t0008 a0001c0006t0014 |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*863C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 14/14 | 863 | chr1 | 84566752 | ||||||
| chr1:84566887 | A | G | 1 | a0001c0003t0011 | 2 | NA18988.hp2 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*998A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 14/14 | 998 | chr1 | 84566887 | ||||||
| chr1:84566888 | G | C | 1 | a0002c0002t0010 | 2 | NA18952.hp1 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*999G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 14/14 | 999 | chr1 | 84566888 | ||||||
| chr1:84566909 | C | T | 2 | a0001c0006t0008 a0001c0006t0014 |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1020C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 14/14 | 1020 | chr1 | 84566909 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:84506594 | G | C | 64 | a0001c0001t0001g0062 a0001c0003t0001g0077 a0001c0003t0004g0002 others(61): Show |
81 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.-138+176G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84506594 | |||||||
| chr1:84506617 | A | C | 1 | a0002c0002t0006g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-138+199A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84506617 | |||||||
| chr1:84506653 | C | T | 2 | a0002c0002t0012g0084 a0007c0009t0012g0085 |
2 | HG03491.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-138+235C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84506653 | |||||||
| chr1:84506658 | G | T | 4 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(1): Show |
4 | HG00609.hp2 NA18975.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-138+240G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84506658 | |||||||
| chr1:84506756 | G | A | 1 | a0002c0002t0002g0087 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-138+338G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84506756 | |||||||
| chr1:84506782 | C | A | 9 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(6): Show |
10 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.-138+364C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84506782 | |||||||
| chr1:84507134 | C | T | 64 | a0001c0001t0001g0062 a0001c0003t0001g0077 a0001c0003t0004g0002 others(61): Show |
81 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.-138+716C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84507134 | |||||||
| chr1:84507169 | A | G | 2 | a0003c0004t0001g0016 a0003c0004t0001g0083 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-138+751A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84507169 | |||||||
| chr1:84507199 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG00438.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-138+781A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84507199 | |||||||
| chr1:84507428 | C | T | 20 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(17): Show |
22 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-138+1010C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84507428 | |||||||
| chr1:84507522 | G | A | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.-138+1104G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84507522 | |||||||
| chr1:84507573 | T | C | 3 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 |
4 | HG02809.hp2 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-138+1155T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84507573 | |||||||
| chr1:84507592 | G | T | 68 | a0001c0001t0001g0062 a0001c0003t0001g0077 a0001c0003t0004g0002 others(65): Show |
85 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.-138+1174G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84507592 | |||||||
| chr1:84507751 | T | A | 148 | a0001c0001t0001g0062 a0001c0001t0007g0018 a0001c0001t0007g0097 others(145): Show |
180 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.-138+1333T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84507751 | |||||||
| chr1:84507788 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-138+1370T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84507788 | |||||||
| chr1:84507790 | C | T | 1 | a0002c0002t0003g0148 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-138+1372C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84507790 | |||||||
| chr1:84507855 | G | GA | 182 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(179): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.-138+1449dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84507855 | ||||||
| chr1:84507855 | G | GAA | 19 | a0001c0001t0001g0156 a0001c0003t0006g0005 a0001c0003t0006g0033 others(16): Show |
28 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.-138+1448_-138+144 others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84507855 | ||||||
| chr1:84507914 | G | C | 1 | a0001c0001t0001g0157 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-138+1496G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84507914 | |||||||
| chr1:84508198 | C | T | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.-138+1780C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84508198 | |||||||
| chr1:84508203 | G | A | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.-138+1785G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84508203 | |||||||
| chr1:84508243 | C | A | 1 | a0002c0002t0005g0149 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-138+1825C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84508243 | |||||||
| chr1:84508262 | G | A | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-138+1844G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84508262 | |||||||
| chr1:84508282 | C | CA | 29 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0158 others(26): Show |
40 | HG00639.hp2 HG01891.hp2 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.-138+1877dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84508282 | ||||||
| chr1:84508444 | C | T | 4 | a0001c0003t0011g0251 a0001c0003t0011g0252 a0002c0002t0003g0253 others(1): Show |
4 | HG01168.hp1 HG01993.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-138+2026C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84508444 | |||||||
| chr1:84508466 | T | C | 64 | a0001c0001t0001g0062 a0001c0003t0001g0077 a0001c0003t0004g0002 others(61): Show |
81 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.-138+2048T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84508466 | |||||||
| chr1:84508527 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-138+2109A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84508527 | |||||||
| chr1:84508546 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-138+2128A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84508546 | |||||||
| chr1:84509208 | T | TA | 19 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(16): Show |
19 | HG01071.hp2 HG01099.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.-138+2804dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84509208 | ||||||
| chr1:84509208 | T | TAA | 7 | a0001c0001t0001g0165 a0002c0002t0005g0024 a0002c0002t0005g0025 others(4): Show |
10 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-138+2803_-138+280 others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84509208 | ||||||
| chr1:84509277 | T | C | 80 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(77): Show |
95 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-138+2859T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509277 | |||||||
| chr1:84509311 | C | A | 1 | a0001c0003t0004g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-138+2893C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509311 | |||||||
| chr1:84509313 | T | C | 20 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(17): Show |
22 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-138+2895T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509313 | |||||||
| chr1:84509402 | A | G | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.-138+2984A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509402 | |||||||
| chr1:84509483 | T | G | 7 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(4): Show |
7 | HG01099.hp2 HG02257.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-138+3065T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509483 | |||||||
| chr1:84509704 | T | A | 26 | a0001c0001t0001g0062 a0001c0003t0004g0002 a0001c0003t0004g0043 others(23): Show |
32 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-138+3286T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509704 | |||||||
| chr1:84509722 | C | T | 3 | a0002c0002t0006g0064 a0002c0002t0006g0065 a0002c0002t0006g0086 |
3 | HG02630.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-138+3304C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509722 | |||||||
| chr1:84509888 | A | G | 68 | a0001c0001t0001g0062 a0001c0003t0001g0077 a0001c0003t0004g0002 others(65): Show |
85 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.-138+3470A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509888 | |||||||
| chr1:84509889 | G | T | 1 | a0003c0004t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-138+3471G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509889 | |||||||
| chr1:84509904 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-138+3486A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509904 | |||||||
| chr1:84509925 | C | T | 2 | a0004c0005t0001g0013 a0004c0005t0001g0042 |
3 | HG02647.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-138+3507C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509925 | |||||||
| chr1:84509971 | C | T | 18 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(15): Show |
27 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-138+3553C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84509971 | |||||||
| chr1:84510328 | G | A | 130 | a0001c0001t0001g0062 a0001c0001t0007g0018 a0001c0001t0007g0097 others(127): Show |
158 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.-138+3910G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84510328 | |||||||
| chr1:84510593 | A | G | 3 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 |
3 | HG00735.hp2 HG00738.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-138+4175A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84510593 | |||||||
| chr1:84510634 | G | C | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-138+4216G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84510634 | |||||||
| chr1:84510827 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-138+4409C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84510827 | |||||||
| chr1:84510831 | A | C | 2 | a0002c0002t0010g0146 a0002c0002t0010g0147 |
2 | NA18952.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-138+4413A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84510831 | |||||||
| chr1:84511004 | C | T | 4 | a0003c0004t0001g0079 a0003c0004t0001g0080 a0003c0004t0001g0081 others(1): Show |
4 | HG01891.hp1 HG02965.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-138+4586C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84511004 | |||||||
| chr1:84511123 | TTTA | T | 4 | a0001c0003t0011g0251 a0001c0003t0011g0252 a0002c0002t0003g0253 others(1): Show |
4 | HG01168.hp1 HG01993.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-138+4710_-138+471 others(7): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84511123 | ||||||
| chr1:84511127 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
128 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-138+4709T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84511127 | |||||||
| chr1:84511184 | T | C | 4 | a0001c0003t0011g0251 a0001c0003t0011g0252 a0002c0002t0003g0253 others(1): Show |
4 | HG01168.hp1 HG01993.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-138+4766T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84511184 | |||||||
| chr1:84511524 | T | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG01517.hp2 HG02738.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-137-4699T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84511524 | |||||||
| chr1:84511588 | C | A | 130 | a0001c0001t0001g0062 a0001c0001t0007g0018 a0001c0001t0007g0097 others(127): Show |
158 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.-137-4635C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84511588 | |||||||
| chr1:84511655 | C | CT | 5 | a0001c0001t0001g0226 a0001c0006t0008g0017 a0001c0006t0008g0088 others(2): Show |
6 | HG02738.hp2 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137-4553dupT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84511655 | ||||||
| chr1:84511655 | C | CTT | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137-4554_-137-455 others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84511655 | ||||||
| chr1:84511655 | CT | C | 78 | a0001c0001t0001g0062 a0001c0001t0001g0172 a0001c0001t0001g0173 others(75): Show |
98 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-137-4553delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84511655 | ||||||
| chr1:84511655 | CTTTTTTT others(20): Show |
C | 1 | a0002c0002t0003g0145 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-137-4552_-137-452 others(31): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84511655 | ||||||
| chr1:84511667 | T | C | 2 | a0001c0003t0004g0044 a0002c0002t0002g0101 |
2 | HG01346.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-137-4556T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84511667 | |||||||
| chr1:84511678 | TC | T | 42 | a0001c0001t0001g0062 a0001c0003t0004g0002 a0001c0003t0004g0044 others(39): Show |
55 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.-137-4544delC | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84511678 | |||||||
| chr1:84511679 | C | T | 23 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(20): Show |
25 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.-137-4544C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84511679 | |||||||
| chr1:84511679 | CT | C | 5 | a0001c0001t0001g0029 a0001c0006t0008g0017 a0001c0006t0008g0088 others(2): Show |
6 | HG02809.hp2 HG03130.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137-4525delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84511679 | ||||||
| chr1:84511679 | CTT | C | 15 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(12): Show |
18 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.-137-4526_-137-452 others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84511679 | ||||||
| chr1:84511687 | T | C | 20 | a0001c0003t0004g0002 a0001c0003t0004g0044 a0001c0003t0004g0045 others(17): Show |
26 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.-137-4536T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84511687 | |||||||
| chr1:84511718 | G | T | 6 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(3): Show |
9 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137-4505G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84511718 | |||||||
| chr1:84511973 | C | T | 4 | a0001c0003t0011g0251 a0001c0003t0011g0252 a0002c0002t0003g0253 others(1): Show |
4 | HG01168.hp1 HG01993.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137-4250C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84511973 | |||||||
| chr1:84512011 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-137-4212A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512011 | |||||||
| chr1:84512090 | A | G | 68 | a0001c0001t0001g0062 a0001c0003t0001g0077 a0001c0003t0004g0002 others(65): Show |
85 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.-137-4133A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512090 | |||||||
| chr1:84512105 | A | G | 1 | a0002c0002t0002g0143 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-137-4118A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512105 | |||||||
| chr1:84512238 | C | G | 1 | a0002c0002t0003g0142 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-137-3985C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512238 | |||||||
| chr1:84512357 | T | A | 1 | a0001c0001t0001g0174 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-137-3866T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512357 | |||||||
| chr1:84512358 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-137-3865A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512358 | |||||||
| chr1:84512359 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-137-3864G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512359 | |||||||
| chr1:84512450 | G | C | 2 | a0002c0002t0002g0008 a0002c0002t0002g0102 |
4 | NA18950.hp1 NA18955.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137-3773G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512450 | |||||||
| chr1:84512536 | C | T | 13 | a0004c0005t0001g0006 a0004c0005t0001g0007 a0004c0005t0001g0011 others(10): Show |
20 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-137-3687C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512536 | |||||||
| chr1:84512545 | T | C | 1 | a0001c0003t0003g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-137-3678T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512545 | |||||||
| chr1:84512584 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-137-3639C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512584 | |||||||
| chr1:84512648 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-137-3575G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512648 | |||||||
| chr1:84512749 | T | C | 26 | a0001c0001t0001g0062 a0001c0003t0004g0002 a0001c0003t0004g0043 others(23): Show |
32 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-137-3474T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512749 | |||||||
| chr1:84512806 | C | G | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.-137-3417C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84512806 | |||||||
| chr1:84513017 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-137-3206G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84513017 | |||||||
| chr1:84513038 | CAT | C | 68 | a0001c0001t0001g0062 a0001c0003t0001g0077 a0001c0003t0004g0002 others(65): Show |
85 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.-137-3184_-137-318 others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84513038 | |||||||
| chr1:84513163 | A | G | 1 | a0002c0002t0005g0026 | 2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-137-3060A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84513163 | |||||||
| chr1:84513169 | G | C | 13 | a0004c0005t0001g0006 a0004c0005t0001g0007 a0004c0005t0001g0011 others(10): Show |
20 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-137-3054G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84513169 | |||||||
| chr1:84513190 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-137-3033G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84513190 | |||||||
| chr1:84513769 | G | A | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-137-2454G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84513769 | |||||||
| chr1:84513777 | T | G | 7 | a0001c0003t0011g0251 a0001c0003t0011g0252 a0002c0002t0003g0253 others(4): Show |
7 | HG01099.hp1 HG01168.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-137-2446T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84513777 | |||||||
| chr1:84513842 | A | AT | 31 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0216 others(28): Show |
34 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.-137-2364dupT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84513842 | ||||||
| chr1:84513842 | A | ATT | 11 | a0001c0003t0001g0093 a0001c0003t0001g0094 a0002c0002t0003g0100 others(8): Show |
14 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.-137-2365_-137-236 others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84513842 | ||||||
| chr1:84513842 | A | ATTTTT | 12 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(9): Show |
14 | HG01168.hp1 HG01993.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-137-2368_-137-236 others(9): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84513842 | ||||||
| chr1:84513842 | A | ATTTTTT | 20 | a0001c0001t0001g0062 a0001c0003t0004g0057 a0001c0003t0004g0058 others(17): Show |
27 | HG00639.hp2 HG01496.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.-137-2369_-137-236 others(10): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84513842 | ||||||
| chr1:84513842 | A | ATTTTTTT | 19 | a0001c0003t0001g0077 a0001c0003t0004g0043 a0003c0004t0001g0015 others(16): Show |
21 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.-137-2370_-137-236 others(11): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84513842 | ||||||
| chr1:84513842 | AT | A | 9 | a0001c0003t0003g0106 a0001c0003t0003g0111 a0002c0002t0003g0104 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137-2364delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84513842 | ||||||
| chr1:84514033 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-137-2190C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514033 | |||||||
| chr1:84514186 | T | C | 68 | a0001c0001t0001g0062 a0001c0003t0001g0077 a0001c0003t0004g0002 others(65): Show |
85 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.-137-2037T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514186 | |||||||
| chr1:84514227 | T | C | 1 | a0002c0002t0005g0149 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-137-1996T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514227 | |||||||
| chr1:84514324 | C | G | 4 | a0002c0002t0003g0128 a0002c0002t0007g0021 a0002c0002t0007g0129 others(1): Show |
5 | HG00408.hp1 NA18954.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-137-1899C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514324 | |||||||
| chr1:84514380 | C | G | 1 | a0001c0001t0007g0127 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-137-1843C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514380 | |||||||
| chr1:84514427 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-137-1796T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514427 | |||||||
| chr1:84514459 | G | A | 1 | a0003c0004t0001g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-137-1764G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514459 | |||||||
| chr1:84514522 | A | G | 63 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(60): Show |
74 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-137-1701A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514522 | |||||||
| chr1:84514537 | T | C | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.-137-1686T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514537 | |||||||
| chr1:84514554 | G | C | 148 | a0001c0001t0001g0062 a0001c0001t0007g0018 a0001c0001t0007g0097 others(145): Show |
180 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.-137-1669G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514554 | |||||||
| chr1:84514560 | T | G | 20 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(17): Show |
22 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-137-1663T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514560 | |||||||
| chr1:84514745 | C | G | 1 | a0001c0001t0001g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-137-1478C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514745 | |||||||
| chr1:84514753 | TTGAGGTC others(9): Show |
T | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
5 | NA18944.hp2 NA18948.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137-1469_-137-145 others(20): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514753 | |||||||
| chr1:84514819 | A | G | 3 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 |
5 | HG02258.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-137-1404A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514819 | |||||||
| chr1:84514880 | A | G | 1 | a0001c0003t0003g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137-1343A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84514880 | |||||||
| chr1:84515183 | TA | T | 20 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(17): Show |
22 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-137-1039delA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84515183 | |||||||
| chr1:84515200 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-137-1023A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84515200 | |||||||
| chr1:84515240 | A | T | 38 | a0001c0003t0001g0077 a0001c0003t0006g0005 a0001c0003t0006g0033 others(35): Show |
49 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.-137-983A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84515240 | |||||||
| chr1:84515342 | C | T | 68 | a0001c0001t0001g0062 a0001c0003t0001g0077 a0001c0003t0004g0002 others(65): Show |
85 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.-137-881C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84515342 | |||||||
| chr1:84515382 | T | TAAAACAA others(323): Show |
1 | a0002c0002t0006g0065 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-137-828_-137-827i others(332): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84515382 | ||||||
| chr1:84515382 | T | TAAAACAA others(325): Show |
1 | a0002c0002t0006g0064 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-137-828_-137-827i others(334): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84515382 | ||||||
| chr1:84515382 | T | TAAAACAA others(340): Show |
1 | a0002c0002t0006g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-137-828_-137-827i others(349): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 84515382 | ||||||
| chr1:84515416 | G | T | 4 | a0001c0003t0011g0251 a0001c0003t0011g0252 a0002c0002t0003g0253 others(1): Show |
4 | HG01168.hp1 HG01993.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137-807G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84515416 | |||||||
| chr1:84515634 | A | G | 1 | a0001c0003t0004g0061 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-137-589A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84515634 | |||||||
| chr1:84515722 | T | A | 148 | a0001c0001t0001g0062 a0001c0001t0007g0018 a0001c0001t0007g0097 others(145): Show |
180 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.-137-501T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84515722 | |||||||
| chr1:84515812 | A | C | 63 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(60): Show |
74 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-137-411A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84515812 | |||||||
| chr1:84515986 | C | A | 18 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(15): Show |
27 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-137-237C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84515986 | |||||||
| chr1:84516129 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-137-94G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84516129 | |||||||
| chr1:84516171 | G | A | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-137-52G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 1/13 | chr1 | 84516171 | |||||||
| chr1:84516486 | A | G | 3 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 |
5 | HG02258.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.36+91A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84516486 | |||||||
| chr1:84516553 | G | A | 18 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(15): Show |
27 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.36+158G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84516553 | |||||||
| chr1:84516576 | T | C | 149 | a0001c0001t0001g0062 a0001c0001t0007g0018 a0001c0001t0007g0097 others(146): Show |
181 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.36+181T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84516576 | |||||||
| chr1:84516679 | C | T | 1 | a0002c0002t0003g0140 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.36+284C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84516679 | |||||||
| chr1:84517293 | C | A | 68 | a0001c0001t0001g0062 a0001c0003t0001g0077 a0001c0003t0004g0002 others(65): Show |
85 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.36+898C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84517293 | |||||||
| chr1:84517303 | G | C | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.36+908G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84517303 | |||||||
| chr1:84517452 | C | T | 3 | a0002c0002t0006g0064 a0002c0002t0006g0065 a0002c0002t0006g0086 |
3 | HG02630.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.36+1057C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84517452 | |||||||
| chr1:84517725 | T | TA | 4 | a0001c0003t0011g0251 a0001c0003t0011g0252 a0002c0002t0003g0253 others(1): Show |
4 | HG01168.hp1 HG01993.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+1333dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 84517725 | ||||||
| chr1:84517799 | C | T | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.36+1404C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84517799 | |||||||
| chr1:84517971 | C | A | 26 | a0001c0001t0001g0062 a0001c0003t0004g0002 a0001c0003t0004g0043 others(23): Show |
32 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.36+1576C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84517971 | |||||||
| chr1:84517972 | A | AT | 26 | a0001c0001t0001g0062 a0001c0003t0004g0002 a0001c0003t0004g0043 others(23): Show |
32 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.36+1577_36+1578ins others(1): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84517972 | |||||||
| chr1:84517973 | C | A | 26 | a0001c0001t0001g0062 a0001c0003t0004g0002 a0001c0003t0004g0043 others(23): Show |
32 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.36+1578C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84517973 | |||||||
| chr1:84517974 | T | A | 26 | a0001c0001t0001g0062 a0001c0003t0004g0002 a0001c0003t0004g0043 others(23): Show |
32 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.36+1579T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84517974 | |||||||
| chr1:84518155 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.36+1760C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84518155 | |||||||
| chr1:84518206 | A | C | 1 | a0001c0003t0004g0056 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.36+1811A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84518206 | |||||||
| chr1:84518220 | C | T | 1 | a0007c0009t0012g0085 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.36+1825C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84518220 | |||||||
| chr1:84518236 | A | G | 20 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(17): Show |
22 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.36+1841A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84518236 | |||||||
| chr1:84518349 | T | C | 2 | a0001c0001t0001g0062 a0001c0006t0014g0063 |
2 | HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.36+1954T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84518349 | |||||||
| chr1:84518355 | A | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0215 |
2 | NA18946.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.36+1960A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84518355 | |||||||
| chr1:84518524 | A | C | 3 | a0003c0004t0001g0067 a0003c0004t0001g0068 a0003c0004t0001g0078 |
3 | HG01361.hp2 HG01496.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.37-2061A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84518524 | |||||||
| chr1:84518893 | T | C | 4 | a0001c0003t0011g0251 a0001c0003t0011g0252 a0002c0002t0003g0253 others(1): Show |
4 | HG01168.hp1 HG01993.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-1692T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84518893 | |||||||
| chr1:84518988 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.37-1597A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84518988 | |||||||
| chr1:84519009 | G | A | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.37-1576G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84519009 | |||||||
| chr1:84519045 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0217 |
2 | HG03834.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.37-1540A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84519045 | |||||||
| chr1:84519490 | C | T | 130 | a0001c0001t0001g0062 a0001c0001t0007g0018 a0001c0001t0007g0097 others(127): Show |
158 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.37-1095C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84519490 | |||||||
| chr1:84519623 | G | A | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.37-962G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84519623 | |||||||
| chr1:84519628 | G | A | 1 | a0007c0009t0012g0085 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.37-957G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84519628 | |||||||
| chr1:84520034 | A | G | 2 | a0002c0002t0012g0084 a0007c0009t0012g0085 |
2 | HG03491.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.37-551A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84520034 | |||||||
| chr1:84520062 | C | T | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.37-523C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84520062 | |||||||
| chr1:84520310 | A | G | 20 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(17): Show |
22 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.37-275A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84520310 | |||||||
| chr1:84520356 | C | T | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.37-229C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84520356 | |||||||
| chr1:84520406 | C | A | 1 | a0001c0003t0004g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.37-179C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84520406 | |||||||
| chr1:84520487 | T | C | 5 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0150 others(2): Show |
7 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-98T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84520487 | |||||||
| chr1:84520529 | G | C | 1 | a0001c0001t0001g0163 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.37-56G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | chr1 | 84520529 | |||||||
| chr1:84520530 | AT | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(251): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.37-45delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 84520530 | ||||||
| chr1:84520729 | G | T | 20 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(17): Show |
22 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.143+38G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84520729 | |||||||
| chr1:84520802 | C | G | 1 | a0001c0001t0001g0211 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.143+111C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84520802 | |||||||
| chr1:84521186 | C | T | 9 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(6): Show |
10 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+495C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84521186 | |||||||
| chr1:84521191 | G | A | 1 | a0002c0002t0003g0131 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.143+500G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84521191 | |||||||
| chr1:84521205 | G | C | 1 | a0002c0002t0003g0140 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.143+514G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84521205 | |||||||
| chr1:84521231 | G | A | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.143+540G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84521231 | |||||||
| chr1:84521379 | T | C | 149 | a0001c0001t0001g0062 a0001c0001t0007g0018 a0001c0001t0007g0097 others(146): Show |
181 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.143+688T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84521379 | |||||||
| chr1:84521385 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | NA18967.hp1 NA18983.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.143+694C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84521385 | |||||||
| chr1:84521458 | T | C | 18 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(15): Show |
27 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.143+767T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84521458 | |||||||
| chr1:84521522 | C | G | 1 | a0001c0001t0001g0161 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.143+831C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84521522 | |||||||
| chr1:84521778 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.144-612C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84521778 | |||||||
| chr1:84522055 | A | G | 15 | a0001c0003t0004g0002 a0001c0003t0004g0044 a0001c0003t0004g0045 others(12): Show |
21 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.144-335A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84522055 | |||||||
| chr1:84522124 | G | A | 1 | a0002c0002t0003g0148 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.144-266G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84522124 | |||||||
| chr1:84522289 | T | TCAA | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.144-99_144-97dupAA others(1): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 84522289 | ||||||
| chr1:84522329 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.144-61T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 3/13 | chr1 | 84522329 | |||||||
| chr1:84522593 | T | A | 1 | a0002c0002t0003g0104 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.261+86T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84522593 | |||||||
| chr1:84522607 | G | A | 4 | a0001c0003t0011g0251 a0001c0003t0011g0252 a0002c0002t0003g0253 others(1): Show |
4 | HG01168.hp1 HG01993.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+100G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84522607 | |||||||
| chr1:84522831 | G | A | 3 | a0002c0002t0003g0128 a0002c0002t0007g0021 a0002c0002t0007g0129 |
4 | HG00408.hp1 NA18954.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+324G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84522831 | |||||||
| chr1:84522911 | CT | C | 64 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0007g0018 others(61): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.261+419delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 84522911 | ||||||
| chr1:84522926 | T | C | 10 | a0001c0001t0001g0228 a0002c0002t0005g0024 a0002c0002t0005g0025 others(7): Show |
13 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.261+419T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84522926 | |||||||
| chr1:84523120 | G | T | 13 | a0004c0005t0001g0006 a0004c0005t0001g0007 a0004c0005t0001g0011 others(10): Show |
20 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.261+613G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84523120 | |||||||
| chr1:84523143 | G | C | 5 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(2): Show |
7 | HG02258.hp1 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.261+636G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84523143 | |||||||
| chr1:84523329 | G | T | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.261+822G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84523329 | |||||||
| chr1:84523395 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.261+888T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84523395 | |||||||
| chr1:84523442 | T | A | 1 | a0004c0005t0001g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.261+935T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84523442 | |||||||
| chr1:84523637 | C | T | 20 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(17): Show |
22 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.261+1130C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84523637 | |||||||
| chr1:84524369 | T | C | 4 | a0001c0003t0011g0251 a0001c0003t0011g0252 a0002c0002t0003g0253 others(1): Show |
4 | HG01168.hp1 HG01993.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-1327T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84524369 | |||||||
| chr1:84524476 | A | C | 20 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(17): Show |
22 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.262-1220A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84524476 | |||||||
| chr1:84524560 | T | C | 13 | a0004c0005t0001g0006 a0004c0005t0001g0007 a0004c0005t0001g0011 others(10): Show |
20 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.262-1136T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84524560 | |||||||
| chr1:84524566 | C | T | 1 | a0001c0003t0001g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.262-1130C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84524566 | |||||||
| chr1:84524690 | T | G | 2 | a0001c0001t0001g0062 a0001c0006t0014g0063 |
2 | HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.262-1006T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84524690 | |||||||
| chr1:84524967 | G | GTGTTT | 16 | a0001c0001t0001g0257 a0001c0001t0001g0260 a0001c0001t0007g0097 others(13): Show |
23 | HG00639.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.262-707_262-703dup others(5): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 84524967 | ||||||
| chr1:84525173 | G | C | 1 | a0004c0005t0001g0006 | 3 | HG02922.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.262-523G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84525173 | |||||||
| chr1:84525203 | G | A | 1 | a0002c0002t0003g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.262-493G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84525203 | |||||||
| chr1:84525227 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(253): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.262-469G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84525227 | |||||||
| chr1:84525426 | G | A | 4 | a0001c0003t0011g0251 a0001c0003t0011g0252 a0002c0002t0003g0253 others(1): Show |
4 | HG01168.hp1 HG01993.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-270G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 4/13 | chr1 | 84525426 | |||||||
| chr1:84525805 | T | G | 62 | a0001c0001t0007g0018 a0001c0001t0007g0097 a0001c0001t0007g0127 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.316-40T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 5/13 | chr1 | 84525805 | |||||||
| chr1:84526427 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.544+354G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84526427 | |||||||
| chr1:84526754 | G | A | 2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.544+681G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84526754 | |||||||
| chr1:84526797 | C | A | 4 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(1): Show |
4 | HG00609.hp2 NA18975.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.544+724C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84526797 | |||||||
| chr1:84526843 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544+770G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84526843 | |||||||
| chr1:84526867 | C | CA | 10 | a0001c0001t0001g0165 a0001c0001t0001g0174 a0001c0001t0001g0183 others(7): Show |
10 | HG00438.hp1 HG00438.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.544+815dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84526867 | ||||||
| chr1:84526867 | CA | C | 86 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0205 others(83): Show |
112 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.544+815delA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84526867 | ||||||
| chr1:84526867 | CAA | C | 24 | a0001c0003t0001g0077 a0001c0003t0004g0051 a0001c0006t0008g0017 others(21): Show |
27 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.544+814_544+815del others(2): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84526867 | ||||||
| chr1:84526968 | AG | A | 38 | a0001c0003t0003g0106 a0001c0003t0004g0057 a0001c0003t0004g0058 others(35): Show |
46 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.544+897delG | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84526968 | ||||||
| chr1:84526992 | A | T | 2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.544+919A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84526992 | |||||||
| chr1:84527146 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.544+1073G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84527146 | |||||||
| chr1:84527323 | T | G | 2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.544+1250T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84527323 | |||||||
| chr1:84527364 | T | C | 65 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(62): Show |
83 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.544+1291T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84527364 | |||||||
| chr1:84527554 | T | C | 1 | a0002c0002t0005g0149 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.544+1481T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84527554 | |||||||
| chr1:84527629 | TAATA | T | 23 | a0001c0003t0003g0106 a0001c0003t0003g0111 a0001c0003t0004g0002 others(20): Show |
29 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.544+1561_544+1564d others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84527629 | ||||||
| chr1:84527671 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.544+1598T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84527671 | |||||||
| chr1:84527714 | T | C | 61 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(58): Show |
78 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.544+1641T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84527714 | |||||||
| chr1:84527731 | C | T | 1 | a0002c0002t0002g0124 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.544+1658C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84527731 | |||||||
| chr1:84527732 | AT | A | 61 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(58): Show |
78 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.544+1668delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84527732 | ||||||
| chr1:84527863 | T | A | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.544+1790T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84527863 | |||||||
| chr1:84527909 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.544+1836T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84527909 | |||||||
| chr1:84527951 | G | A | 31 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(28): Show |
33 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.544+1878G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84527951 | |||||||
| chr1:84528021 | G | A | 2 | a0002c0002t0005g0153 a0002c0002t0005g0154 |
2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.544+1948G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84528021 | |||||||
| chr1:84528171 | T | A | 3 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 |
4 | HG02809.hp2 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.544+2098T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84528171 | |||||||
| chr1:84528339 | T | C | 1 | a0003c0004t0001g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.544+2266T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84528339 | |||||||
| chr1:84528513 | C | T | 1 | a0001c0003t0003g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.544+2440C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84528513 | |||||||
| chr1:84528579 | C | T | 144 | a0001c0003t0001g0077 a0001c0003t0001g0090 a0001c0003t0001g0091 others(141): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.544+2506C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84528579 | |||||||
| chr1:84528583 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.544+2510A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84528583 | |||||||
| chr1:84528628 | C | T | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.544+2555C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84528628 | |||||||
| chr1:84528744 | C | T | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.544+2671C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84528744 | |||||||
| chr1:84528844 | T | C | 4 | a0002c0002t0003g0022 a0002c0002t0003g0131 a0002c0002t0003g0132 others(1): Show |
5 | HG00280.hp1 HG00735.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.544+2771T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84528844 | |||||||
| chr1:84528960 | A | T | 1 | a0001c0001t0001g0174 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.544+2887A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84528960 | |||||||
| chr1:84528999 | CTA | C | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.544+2936_544+2937d others(4): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84528999 | ||||||
| chr1:84529009 | A | T | 1 | a0002c0002t0002g0115 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.544+2936A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529009 | |||||||
| chr1:84529082 | CATT | C | 19 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(16): Show |
21 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.544+3011_544+3013d others(5): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84529082 | ||||||
| chr1:84529280 | GAAAT | G | 19 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(16): Show |
21 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.544+3208_544+3211d others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529280 | |||||||
| chr1:84529294 | A | T | 1 | a0001c0001t0001g0174 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.544+3221A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529294 | |||||||
| chr1:84529352 | CA | C | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.544+3280delA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529352 | |||||||
| chr1:84529373 | G | C | 16 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(13): Show |
25 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.544+3300G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529373 | |||||||
| chr1:84529452 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.544+3379C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529452 | |||||||
| chr1:84529506 | TGAAACGT others(11): Show |
T | 1 | a0001c0001t0009g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.545-3350_545-3333d others(20): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84529506 | ||||||
| chr1:84529576 | C | A | 1 | a0001c0001t0001g0187 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.545-3284C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529576 | |||||||
| chr1:84529576 | C | CT | 53 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0161 others(50): Show |
66 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.545-3260dupT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84529576 | ||||||
| chr1:84529576 | C | CTT | 28 | a0001c0001t0001g0174 a0001c0001t0001g0201 a0001c0001t0001g0202 others(25): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.545-3261_545-3260d others(4): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84529576 | ||||||
| chr1:84529576 | C | CTTT | 54 | a0001c0003t0004g0043 a0002c0002t0002g0003 a0002c0002t0002g0008 others(51): Show |
63 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.545-3262_545-3260d others(5): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84529576 | ||||||
| chr1:84529576 | C | CTTTT | 12 | a0002c0002t0002g0020 a0002c0002t0002g0114 a0002c0002t0002g0123 others(9): Show |
13 | HG00544.hp1 HG00621.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.545-3263_545-3260d others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84529576 | ||||||
| chr1:84529620 | T | C | 1 | a0001c0003t0003g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.545-3240T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529620 | |||||||
| chr1:84529680 | T | C | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.545-3180T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529680 | |||||||
| chr1:84529769 | C | T | 3 | a0002c0002t0003g0104 a0002c0002t0003g0105 a0002c0002t0003g0110 |
3 | HG02451.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.545-3091C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529769 | |||||||
| chr1:84529803 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.545-3057C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529803 | |||||||
| chr1:84529858 | CT | C | 4 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(1): Show |
6 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.545-2987delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84529858 | ||||||
| chr1:84529943 | G | A | 1 | a0001c0003t0004g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.545-2917G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84529943 | |||||||
| chr1:84530189 | A | C | 96 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(93): Show |
116 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.545-2671A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84530189 | |||||||
| chr1:84530193 | T | G | 2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.545-2667T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84530193 | |||||||
| chr1:84530360 | T | G | 1 | a0001c0003t0004g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.545-2500T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84530360 | |||||||
| chr1:84530433 | C | A | 1 | a0002c0002t0003g0145 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.545-2427C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84530433 | |||||||
| chr1:84530494 | T | C | 29 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(26): Show |
31 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.545-2366T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84530494 | |||||||
| chr1:84530573 | A | T | 31 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(28): Show |
33 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.545-2287A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84530573 | |||||||
| chr1:84530823 | T | A | 144 | a0001c0003t0001g0077 a0001c0003t0001g0090 a0001c0003t0001g0091 others(141): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.545-2037T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84530823 | |||||||
| chr1:84530848 | T | C | 138 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(135): Show |
169 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.545-2012T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84530848 | |||||||
| chr1:84530883 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.545-1977C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84530883 | |||||||
| chr1:84530921 | T | C | 66 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(63): Show |
85 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.545-1939T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84530921 | |||||||
| chr1:84530982 | C | T | 2 | a0004c0005t0001g0013 a0004c0005t0001g0042 |
3 | HG02647.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.545-1878C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84530982 | |||||||
| chr1:84531033 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.545-1827A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84531033 | |||||||
| chr1:84531203 | A | C | 66 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(63): Show |
85 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.545-1657A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84531203 | |||||||
| chr1:84531288 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.545-1572G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84531288 | |||||||
| chr1:84531382 | T | C | 144 | a0001c0003t0001g0077 a0001c0003t0001g0090 a0001c0003t0001g0091 others(141): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.545-1478T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84531382 | |||||||
| chr1:84531415 | G | A | 2 | a0003c0004t0001g0016 a0003c0004t0001g0083 |
3 | HG02895.hp2 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.545-1445G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84531415 | |||||||
| chr1:84531450 | G | A | 22 | a0001c0003t0003g0106 a0001c0003t0003g0111 a0001c0003t0004g0002 others(19): Show |
28 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.545-1410G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84531450 | |||||||
| chr1:84531457 | C | A | 3 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 |
4 | HG02809.hp2 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.545-1403C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84531457 | |||||||
| chr1:84531570 | C | CT | 21 | a0001c0001t0001g0165 a0001c0001t0001g0170 a0001c0001t0001g0241 others(18): Show |
30 | HG00544.hp2 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.545-1269dupT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84531570 | ||||||
| chr1:84531570 | CT | C | 94 | a0001c0001t0001g0221 a0001c0003t0001g0090 a0001c0003t0001g0091 others(91): Show |
113 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.545-1269delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84531570 | ||||||
| chr1:84531729 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.545-1131A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84531729 | |||||||
| chr1:84532245 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(108): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.545-615C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84532245 | |||||||
| chr1:84532322 | C | G | 1 | a0001c0006t0014g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.545-538C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84532322 | |||||||
| chr1:84532357 | G | A | 61 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(58): Show |
78 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.545-503G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84532357 | |||||||
| chr1:84532373 | G | A | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.545-487G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84532373 | |||||||
| chr1:84532492 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.545-368T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84532492 | |||||||
| chr1:84532495 | CA | C | 8 | a0001c0003t0004g0048 a0003c0004t0001g0016 a0003c0004t0001g0066 others(5): Show |
9 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.545-353delA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84532495 | ||||||
| chr1:84532680 | TAAAC | T | 61 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(58): Show |
78 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.545-176_545-173del others(4): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 84532680 | ||||||
| chr1:84532762 | C | G | 96 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(93): Show |
116 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.545-98C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84532762 | |||||||
| chr1:84532797 | G | A | 1 | a0003c0004t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.545-63G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 6/13 | chr1 | 84532797 | |||||||
| chr1:84533395 | C | T | 65 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(62): Show |
83 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.660-314C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 7/13 | chr1 | 84533395 | |||||||
| chr1:84533474 | T | C | 2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.660-235T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 7/13 | chr1 | 84533474 | |||||||
| chr1:84533544 | G | C | 31 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(28): Show |
33 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.660-165G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 7/13 | chr1 | 84533544 | |||||||
| chr1:84533606 | A | G | 1 | a0001c0003t0004g0054 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.660-103A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 7/13 | chr1 | 84533606 | |||||||
| chr1:84533621 | G | T | 1 | a0001c0003t0004g0053 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.660-88G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 7/13 | chr1 | 84533621 | |||||||
| chr1:84533643 | A | G | 25 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(22): Show |
32 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.660-66A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 7/13 | chr1 | 84533643 | |||||||
| chr1:84533888 | T | C | 97 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(94): Show |
118 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.717+122T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84533888 | |||||||
| chr1:84534106 | T | C | 1 | a0001c0001t0009g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.717+340T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534106 | |||||||
| chr1:84534107 | A | T | 1 | a0001c0001t0009g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.717+341A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534107 | |||||||
| chr1:84534108 | G | A | 1 | a0001c0001t0009g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.717+342G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534108 | |||||||
| chr1:84534109 | A | T | 1 | a0001c0001t0009g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.717+343A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534109 | |||||||
| chr1:84534113 | G | T | 1 | a0001c0001t0009g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.717+347G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534113 | |||||||
| chr1:84534115 | A | G | 1 | a0001c0001t0009g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.717+349A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534115 | |||||||
| chr1:84534117 | T | G | 1 | a0001c0001t0009g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.717+351T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534117 | |||||||
| chr1:84534120 | A | G | 1 | a0001c0001t0009g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.717+354A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534120 | |||||||
| chr1:84534122 | A | T | 1 | a0001c0001t0009g0222 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.717+356A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534122 | |||||||
| chr1:84534214 | G | C | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+448G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534214 | |||||||
| chr1:84534229 | T | A | 2 | a0002c0002t0003g0253 a0002c0002t0003g0254 |
2 | HG01168.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.717+463T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534229 | |||||||
| chr1:84534584 | G | A | 61 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(58): Show |
78 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.717+818G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534584 | |||||||
| chr1:84534607 | ACTAC | A | 16 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(13): Show |
25 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.717+849_717+852del others(4): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 84534607 | ||||||
| chr1:84534701 | T | G | 25 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(22): Show |
32 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.717+935T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534701 | |||||||
| chr1:84534764 | C | T | 1 | a0002c0002t0006g0064 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.717+998C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534764 | |||||||
| chr1:84534984 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.717+1218T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84534984 | |||||||
| chr1:84535170 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0227 a0001c0001t0001g0233 others(2): Show |
8 | HG00544.hp2 NA18945.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.717+1404T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84535170 | |||||||
| chr1:84535343 | G | A | 65 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(62): Show |
83 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.717+1577G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84535343 | |||||||
| chr1:84535662 | T | C | 31 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(28): Show |
33 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.717+1896T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84535662 | |||||||
| chr1:84535743 | C | T | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+1977C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84535743 | |||||||
| chr1:84535887 | C | T | 61 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(58): Show |
78 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.717+2121C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84535887 | |||||||
| chr1:84536082 | C | A | 2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.717+2316C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84536082 | |||||||
| chr1:84536213 | C | T | 1 | a0001c0003t0004g0047 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.717+2447C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84536213 | |||||||
| chr1:84536221 | T | G | 1 | a0002c0002t0003g0145 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.717+2455T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84536221 | |||||||
| chr1:84536266 | A | G | 1 | a0004c0005t0001g0042 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.717+2500A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84536266 | |||||||
| chr1:84536529 | C | T | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+2763C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84536529 | |||||||
| chr1:84536530 | G | A | 12 | a0004c0005t0001g0006 a0004c0005t0001g0007 a0004c0005t0001g0011 others(9): Show |
19 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.717+2764G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84536530 | |||||||
| chr1:84536536 | C | T | 35 | a0001c0003t0004g0052 a0002c0002t0002g0003 a0002c0002t0002g0008 others(32): Show |
43 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.717+2770C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84536536 | |||||||
| chr1:84536645 | C | T | 24 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(21): Show |
30 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.717+2879C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84536645 | |||||||
| chr1:84536733 | C | T | 3 | a0001c0003t0004g0043 a0003c0004t0001g0016 a0003c0004t0001g0083 |
4 | HG02055.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+2967C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84536733 | |||||||
| chr1:84536876 | T | C | 42 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(39): Show |
53 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.717+3110T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84536876 | |||||||
| chr1:84536881 | CT | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(239): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.717+3131delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 84536881 | ||||||
| chr1:84536881 | CTTTTTTT others(1): Show |
C | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+3124_717+3131d others(10): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 84536881 | ||||||
| chr1:84537002 | T | C | 16 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(13): Show |
25 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.717+3236T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84537002 | |||||||
| chr1:84537060 | A | G | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+3294A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84537060 | |||||||
| chr1:84537108 | G | A | 1 | a0001c0003t0004g0056 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.717+3342G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84537108 | |||||||
| chr1:84537162 | G | A | 1 | a0003c0004t0001g0075 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.717+3396G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84537162 | |||||||
| chr1:84537528 | A | G | 24 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(21): Show |
30 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.717+3762A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84537528 | |||||||
| chr1:84537885 | T | C | 144 | a0001c0003t0001g0077 a0001c0003t0001g0090 a0001c0003t0001g0091 others(141): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.717+4119T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84537885 | |||||||
| chr1:84537940 | T | C | 8 | a0004c0005t0001g0006 a0004c0005t0001g0007 a0004c0005t0001g0012 others(5): Show |
13 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.717+4174T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84537940 | |||||||
| chr1:84538038 | T | A | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.717+4272T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84538038 | |||||||
| chr1:84538054 | A | G | 66 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(63): Show |
85 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.717+4288A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84538054 | |||||||
| chr1:84538102 | G | A | 3 | a0001c0003t0001g0090 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | HG01261.hp1 HG02040.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.717+4336G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84538102 | |||||||
| chr1:84538239 | A | G | 16 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(13): Show |
25 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.717+4473A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84538239 | |||||||
| chr1:84538335 | C | T | 2 | a0002c0002t0005g0153 a0002c0002t0005g0154 |
2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.717+4569C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84538335 | |||||||
| chr1:84538487 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.717+4721G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84538487 | |||||||
| chr1:84538859 | C | G | 144 | a0001c0003t0001g0077 a0001c0003t0001g0090 a0001c0003t0001g0091 others(141): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.717+5093C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84538859 | |||||||
| chr1:84538974 | AT | A | 144 | a0001c0003t0001g0077 a0001c0003t0001g0090 a0001c0003t0001g0091 others(141): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.717+5215delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 84538974 | ||||||
| chr1:84539140 | C | T | 1 | a0001c0003t0003g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-5062C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84539140 | |||||||
| chr1:84539201 | C | T | 19 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(16): Show |
21 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.718-5001C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84539201 | |||||||
| chr1:84539202 | G | A | 13 | a0001c0001t0001g0173 a0004c0005t0001g0006 a0004c0005t0001g0007 others(10): Show |
20 | HG00673.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.718-5000G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84539202 | |||||||
| chr1:84539393 | A | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(108): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.718-4809A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84539393 | |||||||
| chr1:84539505 | C | G | 71 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(68): Show |
87 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.718-4697C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84539505 | |||||||
| chr1:84539524 | A | G | 1 | a0002c0002t0002g0124 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.718-4678A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84539524 | |||||||
| chr1:84539653 | T | G | 23 | a0001c0003t0003g0106 a0001c0003t0003g0111 a0001c0003t0004g0002 others(20): Show |
29 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.718-4549T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84539653 | |||||||
| chr1:84539899 | T | C | 22 | a0001c0003t0003g0106 a0001c0003t0003g0111 a0001c0003t0004g0002 others(19): Show |
28 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.718-4303T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84539899 | |||||||
| chr1:84539922 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.718-4280A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84539922 | |||||||
| chr1:84540088 | T | C | 4 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(1): Show |
6 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.718-4114T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540088 | |||||||
| chr1:84540224 | T | G | 1 | a0001c0001t0001g0189 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.718-3978T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540224 | |||||||
| chr1:84540380 | C | T | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(252): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.718-3822C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540380 | |||||||
| chr1:84540383 | C | T | 2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.718-3819C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540383 | |||||||
| chr1:84540393 | T | C | 1 | a0002c0002t0006g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.718-3809T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540393 | |||||||
| chr1:84540399 | T | G | 33 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(30): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.718-3803T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540399 | |||||||
| chr1:84540428 | T | A | 1 | a0001c0003t0004g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.718-3774T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540428 | |||||||
| chr1:84540561 | A | G | 2 | a0002c0002t0007g0021 a0002c0002t0007g0129 |
3 | NA18954.hp2 NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.718-3641A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540561 | |||||||
| chr1:84540565 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.718-3637T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540565 | |||||||
| chr1:84540587 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.718-3615C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540587 | |||||||
| chr1:84540669 | A | G | 138 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(135): Show |
169 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.718-3533A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540669 | |||||||
| chr1:84540898 | G | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(252): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.718-3304G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84540898 | |||||||
| chr1:84541309 | ATTGT | A | 36 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(33): Show |
49 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.718-2890_718-2887d others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 84541309 | ||||||
| chr1:84541387 | T | C | 12 | a0004c0005t0001g0006 a0004c0005t0001g0007 a0004c0005t0001g0011 others(9): Show |
19 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.718-2815T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84541387 | |||||||
| chr1:84541430 | T | TGGCTCCT others(159): Show |
1 | a0001c0003t0003g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-2756_718-2755i others(168): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 84541430 | ||||||
| chr1:84541706 | C | A | 2 | a0002c0002t0007g0107 a0005c0007t0001g0040 |
2 | HG00639.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.718-2496C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84541706 | |||||||
| chr1:84541709 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.718-2493G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84541709 | |||||||
| chr1:84541802 | G | A | 23 | a0001c0003t0001g0077 a0001c0003t0006g0005 a0001c0003t0006g0033 others(20): Show |
27 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.718-2400G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84541802 | |||||||
| chr1:84541930 | T | C | 25 | a0001c0003t0001g0077 a0001c0003t0006g0005 a0001c0003t0006g0033 others(22): Show |
29 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.718-2272T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84541930 | |||||||
| chr1:84541934 | G | GT | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-2260dupT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 84541934 | ||||||
| chr1:84541939 | TTTTG | T | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.718-2251_718-2248d others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 84541939 | ||||||
| chr1:84541955 | T | G | 6 | a0001c0001t0001g0175 a0001c0001t0001g0190 a0001c0001t0001g0191 others(3): Show |
6 | HG00639.hp2 HG01261.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-2247T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84541955 | |||||||
| chr1:84542001 | G | A | 61 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(58): Show |
78 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.718-2201G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542001 | |||||||
| chr1:84542008 | T | C | 65 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(62): Show |
83 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.718-2194T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542008 | |||||||
| chr1:84542035 | T | C | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.718-2167T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542035 | |||||||
| chr1:84542056 | A | G | 29 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(26): Show |
31 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.718-2146A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542056 | |||||||
| chr1:84542126 | A | G | 144 | a0001c0003t0001g0077 a0001c0003t0001g0090 a0001c0003t0001g0091 others(141): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.718-2076A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542126 | |||||||
| chr1:84542501 | T | C | 1 | a0001c0003t0003g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-1701T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542501 | |||||||
| chr1:84542517 | T | A | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-1685T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542517 | |||||||
| chr1:84542726 | G | A | 1 | a0001c0003t0004g0046 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.718-1476G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542726 | |||||||
| chr1:84542736 | T | C | 1 | a0002c0002t0002g0096 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.718-1466T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542736 | |||||||
| chr1:84542798 | T | C | 1 | a0001c0003t0006g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.718-1404T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542798 | |||||||
| chr1:84542879 | C | T | 33 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(30): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.718-1323C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542879 | |||||||
| chr1:84542942 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.718-1260T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542942 | |||||||
| chr1:84542955 | T | C | 1 | a0002c0002t0002g0133 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.718-1247T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542955 | |||||||
| chr1:84542971 | C | T | 1 | a0001c0003t0001g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.718-1231C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84542971 | |||||||
| chr1:84543552 | C | A | 7 | a0001c0003t0003g0106 a0001c0003t0003g0111 a0001c0003t0004g0057 others(4): Show |
7 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-650C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84543552 | |||||||
| chr1:84543774 | T | C | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | HG02486.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.718-428T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84543774 | |||||||
| chr1:84543952 | T | C | 23 | a0001c0003t0001g0077 a0001c0003t0006g0005 a0001c0003t0006g0033 others(20): Show |
27 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.718-250T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84543952 | |||||||
| chr1:84543982 | T | A | 42 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(39): Show |
53 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.718-220T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84543982 | |||||||
| chr1:84544154 | G | T | 27 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(24): Show |
35 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.718-48G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84544154 | |||||||
| chr1:84544181 | C | T | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-21C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 8/13 | chr1 | 84544181 | |||||||
| chr1:84544379 | T | A | 2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.820+75T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84544379 | |||||||
| chr1:84544476 | G | C | 2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.820+172G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84544476 | |||||||
| chr1:84544498 | A | G | 1 | a0003c0004t0001g0082 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.820+194A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84544498 | |||||||
| chr1:84544570 | TA | T | 13 | a0001c0003t0004g0056 a0004c0005t0001g0006 a0004c0005t0001g0007 others(10): Show |
20 | HG01891.hp2 HG02055.hp1 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.820+267delA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84544570 | |||||||
| chr1:84544622 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0207 a0001c0001t0001g0240 |
5 | HG00597.hp1 NA19065.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.820+318G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84544622 | |||||||
| chr1:84544664 | G | T | 1 | a0001c0003t0003g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.820+360G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84544664 | |||||||
| chr1:84544706 | G | A | 1 | a0003c0004t0001g0016 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.820+402G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84544706 | |||||||
| chr1:84545019 | G | A | 1 | a0001c0003t0004g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.821-615G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84545019 | |||||||
| chr1:84545034 | C | A | 4 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(1): Show |
6 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-600C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84545034 | |||||||
| chr1:84545052 | T | C | 33 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(30): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.821-582T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84545052 | |||||||
| chr1:84545109 | T | C | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-525T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84545109 | |||||||
| chr1:84545131 | C | T | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-503C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84545131 | |||||||
| chr1:84545222 | A | T | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-412A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84545222 | |||||||
| chr1:84545223 | AT | A | 4 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(1): Show |
6 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.821-410delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84545223 | |||||||
| chr1:84545224 | T | A | 6 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(3): Show |
9 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.821-410T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84545224 | |||||||
| chr1:84545382 | G | C | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.821-252G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84545382 | |||||||
| chr1:84545471 | C | T | 19 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(16): Show |
21 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.821-163C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 9/13 | chr1 | 84545471 | |||||||
| chr1:84545801 | T | G | 3 | a0003c0004t0001g0067 a0003c0004t0001g0068 a0003c0004t0001g0078 |
3 | HG01361.hp2 HG01496.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.946+42T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84545801 | |||||||
| chr1:84545901 | T | C | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.946+142T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84545901 | |||||||
| chr1:84545940 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.946+181G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84545940 | |||||||
| chr1:84545960 | G | T | 12 | a0004c0005t0001g0006 a0004c0005t0001g0007 a0004c0005t0001g0011 others(9): Show |
19 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.946+201G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84545960 | |||||||
| chr1:84546044 | T | C | 2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.946+285T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84546044 | |||||||
| chr1:84546179 | C | T | 31 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(28): Show |
33 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.946+420C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84546179 | |||||||
| chr1:84546251 | C | T | 1 | a0001c0006t0014g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.946+492C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84546251 | |||||||
| chr1:84546457 | C | CA | 18 | a0001c0001t0001g0156 a0001c0001t0001g0159 a0001c0001t0001g0160 others(15): Show |
18 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.946+721dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84546457 | ||||||
| chr1:84546457 | CA | C | 11 | a0001c0001t0001g0243 a0001c0003t0004g0043 a0001c0003t0004g0056 others(8): Show |
12 | HG02055.hp2 HG02148.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.946+721delA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84546457 | ||||||
| chr1:84546457 | CAA | C | 124 | a0001c0003t0001g0077 a0001c0003t0001g0090 a0001c0003t0001g0091 others(121): Show |
152 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.946+720_946+721del others(2): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84546457 | ||||||
| chr1:84546457 | CAAA | C | 10 | a0001c0003t0003g0106 a0001c0003t0003g0111 a0001c0003t0004g0057 others(7): Show |
12 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.946+719_946+721del others(3): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84546457 | ||||||
| chr1:84546633 | C | T | 3 | a0003c0004t0001g0072 a0003c0004t0001g0074 a0003c0004t0001g0075 |
3 | HG00741.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.946+874C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84546633 | |||||||
| chr1:84546981 | G | GT | 138 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(135): Show |
169 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.946+1224dupT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84546981 | ||||||
| chr1:84547012 | G | A | 15 | a0001c0003t0004g0002 a0001c0003t0004g0044 a0001c0003t0004g0045 others(12): Show |
21 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.946+1253G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84547012 | |||||||
| chr1:84547230 | T | C | 1 | a0001c0003t0003g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.946+1471T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84547230 | |||||||
| chr1:84547296 | T | C | 109 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(106): Show |
135 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.947-1490T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84547296 | |||||||
| chr1:84547314 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.947-1472T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84547314 | |||||||
| chr1:84547497 | A | G | 12 | a0004c0005t0001g0006 a0004c0005t0001g0007 a0004c0005t0001g0011 others(9): Show |
19 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.947-1289A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84547497 | |||||||
| chr1:84547718 | C | T | 101 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(98): Show |
122 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.947-1068C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84547718 | |||||||
| chr1:84547719 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG00438.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.947-1067G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84547719 | |||||||
| chr1:84548065 | C | T | 21 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(18): Show |
23 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.947-721C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84548065 | |||||||
| chr1:84548078 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.947-708T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84548078 | |||||||
| chr1:84548434 | TTA | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0001t0001g0237 others(31): Show |
38 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.947-346_947-345del others(2): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84548434 | ||||||
| chr1:84548606 | A | C | 19 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(16): Show |
21 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.947-180A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84548606 | |||||||
| chr1:84548647 | G | A | 25 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(22): Show |
28 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.947-139G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84548647 | |||||||
| chr1:84548750 | C | CT | 21 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0002c0002t0002g0019 others(18): Show |
24 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(21): Show |
splice_region_variant&intron_variant | LOW | c.947-5dupT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84548750 | ||||||
| chr1:84548750 | C | CTT | 7 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0115 others(4): Show |
12 | HG00408.hp1 HG02015.hp1 HG02080.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.947-6_947-5dupTT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84548750 | ||||||
| chr1:84548750 | CT | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0163 a0001c0001t0001g0164 others(36): Show |
51 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
splice_region_variant&intron_variant | LOW | c.947-5delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84548750 | ||||||
| chr1:84548750 | CTT | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
120 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
splice_region_variant&intron_variant | LOW | c.947-6_947-5delTT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84548750 | ||||||
| chr1:84548750 | CTTT | C | 20 | a0001c0001t0001g0167 a0001c0001t0001g0174 a0001c0001t0001g0191 others(17): Show |
21 | HG01517.hp2 HG01891.hp1 HG01975.hp1 others(18): Show |
splice_region_variant&intron_variant | LOW | c.947-7_947-5delTTT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84548750 | ||||||
| chr1:84548750 | CTTTT | C | 21 | a0001c0003t0001g0077 a0002c0002t0005g0025 a0002c0002t0005g0026 others(18): Show |
25 | HG00741.hp2 HG01071.hp1 HG01081.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.947-8_947-5delTTTT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84548750 | ||||||
| chr1:84548750 | CTTTTT | C | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
6 | HG01070.hp1 HG01167.hp1 HG02809.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.947-9_947-5delTTTT others(1): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84548750 | ||||||
| chr1:84548750 | CTTTTTTT others(8): Show |
C | 31 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(28): Show |
33 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(30): Show |
splice_region_variant&intron_variant | LOW | c.947-19_947-5delTTT others(12): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 84548750 | ||||||
| chr1:84548754 | T | C | 1 | a0001c0001t0001g0028 | 2 | HG00140.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.947-32T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84548754 | |||||||
| chr1:84548781 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG01099.hp2 | splice_region_variant&intron_variant | LOW | c.947-5T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 10/13 | chr1 | 84548781 | |||||||
| chr1:84548996 | G | A | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1125+32G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84548996 | |||||||
| chr1:84549162 | G | A | 3 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 |
5 | HG02258.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1125+198G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84549162 | |||||||
| chr1:84549234 | G | C | 1 | a0002c0002t0006g0065 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1125+270G>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84549234 | |||||||
| chr1:84549306 | A | G | 19 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(16): Show |
21 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1125+342A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84549306 | |||||||
| chr1:84549506 | T | C | 25 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(22): Show |
28 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1125+542T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84549506 | |||||||
| chr1:84549742 | T | A | 1 | a0001c0003t0003g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1126-690T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84549742 | |||||||
| chr1:84549767 | G | A | 4 | a0002c0002t0003g0098 a0002c0002t0003g0099 a0002c0002t0003g0100 others(1): Show |
4 | HG03492.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-665G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84549767 | |||||||
| chr1:84549872 | C | CT | 136 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(133): Show |
167 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.1126-550dupT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 84549872 | ||||||
| chr1:84550024 | T | C | 8 | a0001c0003t0001g0077 a0003c0004t0001g0016 a0003c0004t0001g0066 others(5): Show |
9 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1126-408T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84550024 | |||||||
| chr1:84550084 | ATAT | A | 32 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(29): Show |
39 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1126-342_1126-340d others(5): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 84550084 | ||||||
| chr1:84550090 | TTAAG | T | 4 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(1): Show |
6 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126-339_1126-336d others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 84550090 | ||||||
| chr1:84550117 | T | G | 25 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(22): Show |
28 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1126-315T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84550117 | |||||||
| chr1:84550123 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1126-309G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84550123 | |||||||
| chr1:84550206 | C | T | 1 | a0003c0004t0006g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1126-226C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84550206 | |||||||
| chr1:84550429 | C | T | 25 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(22): Show |
28 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
splice_region_variant&intron_variant | LOW | c.1126-3C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 11/13 | chr1 | 84550429 | |||||||
| chr1:84550720 | A | G | 144 | a0001c0003t0001g0077 a0001c0003t0001g0090 a0001c0003t0001g0091 others(141): Show |
175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1224+190A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84550720 | |||||||
| chr1:84550895 | T | C | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1224+365T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84550895 | |||||||
| chr1:84551080 | A | G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0202 |
3 | NA18942.hp2 NA18971.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1224+550A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84551080 | |||||||
| chr1:84551370 | AAAAT | A | 4 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(1): Show |
6 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1224+848_1224+851d others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 84551370 | ||||||
| chr1:84551427 | T | C | 1 | a0004c0005t0001g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1224+897T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84551427 | |||||||
| chr1:84551643 | C | T | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1224+1113C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84551643 | |||||||
| chr1:84551724 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1224+1194A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84551724 | |||||||
| chr1:84551725 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1224+1195C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84551725 | |||||||
| chr1:84551823 | C | T | 1 | a0002c0002t0002g0121 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1224+1293C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84551823 | |||||||
| chr1:84551918 | C | A | 22 | a0001c0003t0003g0106 a0001c0003t0003g0111 a0001c0003t0004g0002 others(19): Show |
28 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1224+1388C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84551918 | |||||||
| chr1:84552060 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1224+1530T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84552060 | |||||||
| chr1:84552251 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1224+1721A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84552251 | |||||||
| chr1:84552280 | G | A | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1224+1750G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84552280 | |||||||
| chr1:84552638 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1224+2108G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84552638 | |||||||
| chr1:84552663 | T | G | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1224+2133T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84552663 | |||||||
| chr1:84552965 | C | T | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1224+2435C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84552965 | |||||||
| chr1:84553030 | T | C | 1 | a0001c0003t0004g0053 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1224+2500T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84553030 | |||||||
| chr1:84553252 | G | A | 1 | a0002c0002t0003g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1225-2658G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84553252 | |||||||
| chr1:84553462 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1225-2448G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84553462 | |||||||
| chr1:84553597 | T | C | 4 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(1): Show |
6 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1225-2313T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84553597 | |||||||
| chr1:84553746 | G | A | 1 | a0002c0002t0002g0144 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1225-2164G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84553746 | |||||||
| chr1:84553866 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1225-2044G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84553866 | |||||||
| chr1:84554052 | G | A | 3 | a0002c0002t0002g0112 a0002c0002t0002g0133 a0002c0002t0002g0134 |
3 | HG02083.hp1 NA18951.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1225-1858G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84554052 | |||||||
| chr1:84554241 | T | TG | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1225-1668dupG | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 84554241 | ||||||
| chr1:84554674 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1225-1236A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84554674 | |||||||
| chr1:84554804 | C | T | 24 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(21): Show |
30 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1225-1106C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84554804 | |||||||
| chr1:84554813 | T | A | 16 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(13): Show |
25 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1225-1097T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84554813 | |||||||
| chr1:84554954 | G | T | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1225-956G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84554954 | |||||||
| chr1:84554966 | C | T | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1225-944C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84554966 | |||||||
| chr1:84555086 | G | A | 4 | a0003c0004t0001g0015 a0003c0004t0001g0071 a0003c0004t0001g0073 others(1): Show |
5 | HG01168.hp2 HG01169.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-824G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84555086 | |||||||
| chr1:84555112 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1225-798G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84555112 | |||||||
| chr1:84555546 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1225-364G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84555546 | |||||||
| chr1:84555594 | T | G | 33 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(30): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1225-316T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84555594 | |||||||
| chr1:84555674 | A | T | 6 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(3): Show |
9 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1225-236A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84555674 | |||||||
| chr1:84555874 | A | G | 29 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(26): Show |
31 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1225-36A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84555874 | |||||||
| chr1:84555906 | G | A | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1225-4G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 12/13 | chr1 | 84555906 | |||||||
| chr1:84556059 | T | C | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1294+80T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84556059 | |||||||
| chr1:84556441 | G | A | 2 | a0004c0005t0001g0013 a0004c0005t0001g0042 |
3 | HG02647.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1294+462G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84556441 | |||||||
| chr1:84556445 | T | G | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1294+466T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84556445 | |||||||
| chr1:84556544 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(252): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1294+565T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84556544 | |||||||
| chr1:84556548 | T | TA | 138 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(135): Show |
169 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1294+573dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84556548 | ||||||
| chr1:84556551 | A | C | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1294+572A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84556551 | |||||||
| chr1:84556578 | G | A | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1294+599G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84556578 | |||||||
| chr1:84556656 | A | C | 1 | a0001c0003t0004g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1294+677A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84556656 | |||||||
| chr1:84556710 | C | CA | 105 | a0001c0001t0001g0243 a0001c0001t0001g0258 a0001c0003t0001g0090 others(102): Show |
129 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1294+749dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84556710 | ||||||
| chr1:84556710 | C | CAA | 31 | a0001c0003t0001g0077 a0001c0003t0011g0252 a0002c0002t0005g0024 others(28): Show |
36 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1294+748_1294+749d others(4): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84556710 | ||||||
| chr1:84556710 | C | CAAA | 5 | a0001c0003t0011g0251 a0001c0006t0008g0017 a0001c0006t0008g0088 others(2): Show |
6 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1294+747_1294+749d others(5): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84556710 | ||||||
| chr1:84556769 | C | T | 1 | a0002c0002t0006g0064 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1294+790C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84556769 | |||||||
| chr1:84556840 | T | C | 29 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(26): Show |
31 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1294+861T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84556840 | |||||||
| chr1:84557022 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1294+1043T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557022 | |||||||
| chr1:84557073 | C | CA | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1294+1099dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84557073 | ||||||
| chr1:84557533 | C | CA | 9 | a0001c0001t0001g0177 a0001c0001t0001g0225 a0001c0001t0001g0236 others(6): Show |
9 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1294+1574dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84557533 | ||||||
| chr1:84557533 | CAAA | C | 27 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(24): Show |
29 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1294+1572_1294+157 others(7): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84557533 | ||||||
| chr1:84557544 | A | G | 19 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(16): Show |
21 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1294+1565A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557544 | |||||||
| chr1:84557550 | A | G | 3 | a0001c0003t0004g0054 a0001c0003t0011g0251 a0001c0003t0011g0252 |
3 | NA18968.hp1 NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1294+1571A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557550 | |||||||
| chr1:84557551 | A | G | 54 | a0001c0003t0001g0077 a0001c0003t0003g0103 a0001c0003t0003g0106 others(51): Show |
65 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1294+1572A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557551 | |||||||
| chr1:84557552 | A | G | 47 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(44): Show |
63 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1294+1573A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557552 | |||||||
| chr1:84557552 | AAG | A | 33 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0004g0002 others(30): Show |
42 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1294+1575_1294+157 others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84557552 | ||||||
| chr1:84557553 | AG | A | 66 | a0001c0003t0001g0077 a0001c0003t0003g0111 a0002c0002t0002g0003 others(63): Show |
83 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1294+1575delG | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557553 | |||||||
| chr1:84557554 | G | A | 8 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(5): Show |
11 | HG02258.hp1 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1294+1575G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557554 | |||||||
| chr1:84557582 | G | A | 1 | a0001c0003t0004g0054 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1294+1603G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557582 | |||||||
| chr1:84557584 | G | A | 3 | a0002c0002t0005g0149 a0002c0002t0005g0153 a0002c0002t0005g0154 |
3 | HG01099.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1294+1605G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557584 | |||||||
| chr1:84557644 | A | G | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1294+1665A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557644 | |||||||
| chr1:84557857 | C | CA | 36 | a0001c0003t0004g0059 a0001c0003t0006g0005 a0001c0003t0006g0033 others(33): Show |
40 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1294+1892dupA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84557857 | ||||||
| chr1:84557872 | G | A | 2 | a0001c0001t0007g0018 a0001c0001t0007g0127 |
3 | HG01255.hp1 HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1294+1893G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557872 | |||||||
| chr1:84557905 | T | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(108): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1294+1926T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557905 | |||||||
| chr1:84557977 | C | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0227 a0001c0001t0001g0231 others(3): Show |
9 | HG00544.hp2 HG02040.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1294+1998C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84557977 | |||||||
| chr1:84558020 | G | A | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1294+2041G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558020 | |||||||
| chr1:84558077 | A | G | 33 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(30): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1294+2098A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558077 | |||||||
| chr1:84558221 | T | C | 1 | a0001c0003t0004g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1294+2242T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558221 | |||||||
| chr1:84558246 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1294+2267A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558246 | |||||||
| chr1:84558272 | T | C | 33 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(30): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1294+2293T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558272 | |||||||
| chr1:84558284 | G | T | 19 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(16): Show |
21 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1294+2305G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558284 | |||||||
| chr1:84558293 | C | CT | 5 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(2): Show |
7 | HG02723.hp2 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1294+2328dupT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84558293 | ||||||
| chr1:84558293 | CT | C | 30 | a0001c0001t0001g0221 a0002c0002t0003g0022 a0002c0002t0003g0023 others(27): Show |
32 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1294+2328delT | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84558293 | ||||||
| chr1:84558415 | A | G | 4 | a0002c0002t0002g0019 a0002c0002t0002g0118 a0002c0002t0002g0121 others(1): Show |
5 | NA18967.hp2 NA18992.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.1294+2436A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558415 | |||||||
| chr1:84558444 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0217 |
2 | HG03834.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1294+2465T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558444 | |||||||
| chr1:84558445 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0217 |
2 | HG03834.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1294+2466A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558445 | |||||||
| chr1:84558538 | G | A | 2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1294+2559G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558538 | |||||||
| chr1:84558579 | C | T | 111 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(108): Show |
139 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1294+2600C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558579 | |||||||
| chr1:84558604 | TA | T | 26 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(23): Show |
29 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1294+2637delA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84558604 | ||||||
| chr1:84558718 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1294+2739T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558718 | |||||||
| chr1:84558773 | C | T | 25 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(22): Show |
28 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1294+2794C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558773 | |||||||
| chr1:84558827 | A | G | 1 | a0001c0003t0001g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1294+2848A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558827 | |||||||
| chr1:84558927 | T | A | 1 | a0001c0003t0001g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1294+2948T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558927 | |||||||
| chr1:84558969 | G | A | 4 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(1): Show |
6 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1294+2990G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84558969 | |||||||
| chr1:84559007 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1294+3028C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84559007 | |||||||
| chr1:84559066 | C | G | 12 | a0004c0005t0001g0006 a0004c0005t0001g0007 a0004c0005t0001g0011 others(9): Show |
19 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1294+3087C>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84559066 | |||||||
| chr1:84559348 | C | T | 1 | a0002c0002t0003g0148 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1294+3369C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84559348 | |||||||
| chr1:84559466 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1294+3487C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84559466 | |||||||
| chr1:84559604 | G | A | 1 | a0002c0002t0006g0064 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1294+3625G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84559604 | |||||||
| chr1:84559818 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1294+3839C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84559818 | |||||||
| chr1:84559822 | T | G | 1 | a0001c0003t0003g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1294+3843T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84559822 | |||||||
| chr1:84559844 | G | A | 1 | a0005c0007t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1294+3865G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84559844 | |||||||
| chr1:84560093 | AAAAAAAA others(5): Show |
A | 1 | a0002c0002t0002g0117 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1294+4118_1294+412 others(16): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560093 | ||||||
| chr1:84560096 | AAAAAGAA others(6): Show |
A | 2 | a0001c0003t0004g0052 a0002c0002t0007g0021 |
2 | NA18962.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1294+4121_1294+413 others(17): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560096 | ||||||
| chr1:84560097 | A | AAAGAAAG others(4): Show |
2 | a0001c0003t0011g0251 a0001c0003t0011g0252 |
2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1294+4120_1294+412 others(15): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560097 | ||||||
| chr1:84560097 | AAAAG | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(101): Show |
122 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1294+4151_1294+415 others(8): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560097 | ||||||
| chr1:84560097 | AAAAGAAA others(1): Show |
A | 66 | a0001c0001t0001g0184 a0001c0003t0003g0103 a0001c0003t0004g0002 others(63): Show |
85 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1294+4147_1294+415 others(12): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560097 | ||||||
| chr1:84560097 | AAAAGAAA others(5): Show |
A | 31 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(28): Show |
37 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.1294+4143_1294+415 others(16): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560097 | ||||||
| chr1:84560098 | AAAG | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(5): Show |
8 | HG00140.hp2 HG00741.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+4122_1294+412 others(7): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560098 | ||||||
| chr1:84560098 | AAAGAAAG | A | 11 | a0001c0001t0001g0183 a0001c0003t0003g0106 a0001c0003t0004g0002 others(8): Show |
11 | HG00140.hp1 HG00621.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1294+4122_1294+412 others(11): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560098 | ||||||
| chr1:84560098 | AAAGAAAG others(4): Show |
A | 3 | a0002c0002t0002g0003 a0002c0002t0002g0118 a0003c0004t0001g0082 |
3 | HG02965.hp1 NA18967.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1294+4122_1294+413 others(15): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560098 | ||||||
| chr1:84560098 | AAAGAAAG others(8): Show |
A | 1 | a0001c0003t0003g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1294+4122_1294+413 others(19): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560098 | ||||||
| chr1:84560099 | AAGAAAGA others(3): Show |
A | 14 | a0001c0003t0001g0077 a0003c0004t0001g0015 a0003c0004t0001g0016 others(11): Show |
16 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1294+4122_1294+413 others(14): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560099 | ||||||
| chr1:84560099 | AAGAAAGA others(15): Show |
A | 1 | a0003c0004t0001g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1294+4122_1294+414 others(26): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560099 | ||||||
| chr1:84560100 | AGAAAG | A | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1294+4122_1294+412 others(9): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84560100 | |||||||
| chr1:84560100 | AGAAAGAA others(2): Show |
A | 4 | a0003c0004t0001g0072 a0003c0004t0001g0076 a0003c0004t0001g0079 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1294+4122_1294+413 others(13): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84560100 | |||||||
| chr1:84560108 | AGAAAGAA others(18): Show |
A | 1 | a0001c0001t0001g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1294+4148_1294+417 others(29): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84560108 | ||||||
| chr1:84560125 | GAAAGAAA others(5): Show |
G | 1 | a0001c0003t0004g0053 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1294+4147_1294+415 others(16): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84560125 | |||||||
| chr1:84560246 | T | C | 1 | a0003c0004t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1294+4267T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84560246 | |||||||
| chr1:84560262 | T | C | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1294+4283T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84560262 | |||||||
| chr1:84560534 | G | A | 2 | a0002c0002t0007g0107 a0005c0007t0001g0040 |
2 | HG00639.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1294+4555G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84560534 | |||||||
| chr1:84560573 | C | T | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1294+4594C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84560573 | |||||||
| chr1:84560596 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1294+4617T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84560596 | |||||||
| chr1:84560908 | T | C | 4 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(1): Show |
6 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1294+4929T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84560908 | |||||||
| chr1:84560948 | G | A | 2 | a0002c0002t0007g0107 a0005c0007t0001g0040 |
2 | HG00639.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1295-4913G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84560948 | |||||||
| chr1:84561160 | T | G | 111 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(108): Show |
139 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1295-4701T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84561160 | |||||||
| chr1:84561215 | A | T | 1 | a0004c0005t0001g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1295-4646A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84561215 | |||||||
| chr1:84561407 | G | A | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295-4454G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84561407 | |||||||
| chr1:84561418 | A | G | 1 | a0002c0002t0002g0087 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1295-4443A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84561418 | |||||||
| chr1:84561442 | C | T | 33 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0019 others(30): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1295-4419C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84561442 | |||||||
| chr1:84561577 | G | A | 16 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(13): Show |
25 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1295-4284G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84561577 | |||||||
| chr1:84561637 | G | A | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295-4224G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84561637 | |||||||
| chr1:84561769 | T | G | 5 | a0002c0002t0003g0023 a0002c0002t0003g0136 a0002c0002t0003g0137 others(2): Show |
6 | HG00609.hp1 HG00621.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1295-4092T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84561769 | |||||||
| chr1:84562102 | T | A | 111 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(108): Show |
139 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1295-3759T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84562102 | |||||||
| chr1:84562123 | T | G | 1 | a0004c0005t0001g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1295-3738T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84562123 | |||||||
| chr1:84562184 | G | A | 1 | a0001c0006t0008g0089 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1295-3677G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84562184 | |||||||
| chr1:84562307 | T | C | 27 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(24): Show |
30 | HG00639.hp2 HG00741.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1295-3554T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84562307 | |||||||
| chr1:84562558 | A | G | 1 | a0002c0002t0003g0135 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1295-3303A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84562558 | |||||||
| chr1:84562591 | T | G | 52 | a0001c0003t0001g0077 a0002c0002t0002g0003 a0002c0002t0002g0008 others(49): Show |
62 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1295-3270T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84562591 | |||||||
| chr1:84562638 | CTG | C | 4 | a0001c0003t0006g0005 a0001c0003t0006g0033 a0001c0003t0006g0034 others(1): Show |
6 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295-3221_1295-322 others(6): Show |
SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84562638 | ||||||
| chr1:84563286 | C | A | 4 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(1): Show |
4 | HG00609.hp2 NA18975.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1295-2575C>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84563286 | |||||||
| chr1:84563394 | C | T | 28 | a0002c0002t0003g0022 a0002c0002t0003g0023 a0002c0002t0003g0098 others(25): Show |
30 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1295-2467C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84563394 | |||||||
| chr1:84563548 | TA | T | 9 | a0002c0002t0005g0024 a0002c0002t0005g0025 a0002c0002t0005g0026 others(6): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1295-2309delA | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 84563548 | ||||||
| chr1:84563806 | T | A | 1 | a0001c0001t0001g0249 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1295-2055T>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84563806 | |||||||
| chr1:84563964 | A | G | 1 | a0002c0002t0003g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1295-1897A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84563964 | |||||||
| chr1:84564052 | A | G | 1 | a0001c0003t0004g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1295-1809A>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84564052 | |||||||
| chr1:84564062 | T | C | 8 | a0001c0003t0001g0077 a0003c0004t0001g0016 a0003c0004t0001g0066 others(5): Show |
9 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1295-1799T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84564062 | |||||||
| chr1:84564237 | T | G | 4 | a0001c0006t0008g0017 a0001c0006t0008g0088 a0001c0006t0008g0089 others(1): Show |
5 | HG02723.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295-1624T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84564237 | |||||||
| chr1:84564280 | A | C | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295-1581A>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84564280 | |||||||
| chr1:84564370 | C | T | 53 | a0001c0003t0001g0077 a0001c0003t0011g0251 a0001c0003t0011g0252 others(50): Show |
62 | HG00438.hp1 HG00544.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1295-1491C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84564370 | |||||||
| chr1:84564676 | G | T | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(252): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1295-1185G>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84564676 | |||||||
| chr1:84564781 | C | T | 1 | a0001c0003t0003g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1295-1080C>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84564781 | |||||||
| chr1:84565143 | G | A | 7 | a0001c0003t0003g0106 a0001c0003t0003g0111 a0001c0003t0004g0057 others(4): Show |
7 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1295-718G>A | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84565143 | |||||||
| chr1:84565213 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1295-648A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84565213 | |||||||
| chr1:84565274 | T | C | 7 | a0001c0003t0003g0106 a0001c0003t0003g0111 a0001c0003t0004g0057 others(4): Show |
7 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1295-587T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84565274 | |||||||
| chr1:84565316 | A | T | 1 | a0002c0002t0005g0149 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1295-545A>T | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84565316 | |||||||
| chr1:84565331 | T | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0250 |
2 | HG00735.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1295-530T>G | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84565331 | |||||||
| chr1:84565735 | T | C | 24 | a0001c0003t0003g0103 a0001c0003t0003g0106 a0001c0003t0003g0111 others(21): Show |
29 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.1295-126T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84565735 | |||||||
| chr1:84565809 | T | C | 6 | a0001c0003t0001g0090 a0001c0003t0001g0091 a0001c0003t0001g0092 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295-52T>C | SPATA1 | ENSG00000122432.19 | transcript | ENST00000699524.1 | protein_coding | 13/13 | chr1 | 84565809 |