Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10407 |
| ensemblid | ENSG00000164871.18 |
| hgncid | 14534 |
| symbol | SPAG11B |
| name | sperm associated antigen 11B |
| refseq_nuc | NM_058201.4 |
| refseq_prot | NP_478108.2 |
| ensembl_nuc | ENST00000398462.7 |
| ensembl_prot | ENSP00000381480.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 7450603 |
| end | 7463542 |
| strand | - |
| ver | v1.2 |
| region | chr8:7450603-7463542 |
| region5000 | chr8:7445603-7468542 |
| regionname0 | SPAG11B_chr8_7450603_7463542 |
| regionname5000 | SPAG11B_chr8_7445603_7468542 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 133 | 97 | 12 | 16 | 54 | 6 | 9 | 37 | SPAG11B_chr8_7445603_7468542 | SPAG11B | MRQRL others(128): Show |
chr8 | 7445603 | 7468542 |
| a0002 | 0/1 | 133 | 82 | 17 | 11 | 39 | 2 | 12 | 33 | SPAG11B_chr8_7445603_7468542 | SPAG11B | MRQRL others(128): Show |
chr8 | 7445603 | 7468542 |
| a0003 | 0/0 | 133 | 13 | 2 | 3 | 8 | 0 | 0 | 5 | SPAG11B_chr8_7445603_7468542 | SPAG11B | MRQRL others(128): Show |
chr8 | 7445603 | 7468542 |
| a0004 | 0/0 | 133 | 5 | 0 | 2 | 2 | 0 | 1 | 2 | SPAG11B_chr8_7445603_7468542 | SPAG11B | MRQRL others(128): Show |
chr8 | 7445603 | 7468542 |
| a0005 | 0/0 | 133 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | MRQRL others(128): Show |
chr8 | 7445603 | 7468542 |
| a0006 | 0/0 | 133 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | MRQRL others(128): Show |
chr8 | 7445603 | 7468542 |
| a0007 | 0/0 | 133 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | MRQRL others(128): Show |
chr8 | 7445603 | 7468542 |
| a0008 | 0/0 | 133 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | MRQQL others(128): Show |
chr8 | 7445603 | 7468542 |
| a0009 | 0/0 | 133 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | MRQRL others(128): Show |
chr8 | 7445603 | 7468542 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 399 | 95 | 12 | 16 | 52 | 6 | 9 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ATGAG others(394): Show |
chr8 | 7445603 | 7468542 | ||
| a0001c0005 | 0/0 | 399 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ATGAG others(394): Show |
chr8 | 7445603 | 7468542 | ||
| a0002c0002 | 0/1 | 399 | 82 | 17 | 11 | 39 | 2 | 12 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ATGAG others(394): Show |
chr8 | 7445603 | 7468542 | ||
| a0003c0003 | 0/0 | 399 | 13 | 2 | 3 | 8 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ATGAG others(394): Show |
chr8 | 7445603 | 7468542 | ||
| a0004c0004 | 0/0 | 399 | 5 | 0 | 2 | 2 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ATGAG others(394): Show |
chr8 | 7445603 | 7468542 | ||
| a0005c0006 | 0/0 | 399 | 2 | 1 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ATGAG others(394): Show |
chr8 | 7445603 | 7468542 | ||
| a0006c0008 | 0/0 | 399 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ATGAG others(394): Show |
chr8 | 7445603 | 7468542 | ||
| a0007c0007 | 0/0 | 399 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ATGAG others(394): Show |
chr8 | 7445603 | 7468542 | ||
| a0008c0009 | 0/0 | 399 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ATGAG others(394): Show |
chr8 | 7445603 | 7468542 | ||
| a0009c0010 | 0/0 | 399 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ATGAG others(394): Show |
chr8 | 7445603 | 7468542 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 551 | 91 | 11 | 15 | 50 | 6 | 9 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0001c0001t0002 | 0/0 | 551 | 4 | 1 | 1 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0001c0005t0001 | 0/0 | 551 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0002c0002t0001 | 0/1 | 551 | 73 | 17 | 9 | 36 | 2 | 8 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0002c0002t0002 | 0/0 | 551 | 5 | 0 | 2 | 3 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0002c0002t0003 | 0/0 | 551 | 4 | 0 | 0 | 0 | 0 | 4 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0003c0003t0001 | 0/0 | 551 | 12 | 1 | 3 | 8 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0003c0003t0002 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0004c0004t0001 | 0/0 | 551 | 5 | 0 | 2 | 2 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0005c0006t0001 | 0/0 | 551 | 2 | 1 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0006c0008t0001 | 0/0 | 551 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0007c0007t0001 | 0/0 | 551 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0008c0009t0002 | 0/0 | 551 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| a0009c0010t0001 | 0/0 | 551 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | ACCCT others(546): Show |
chr8 | 7445603 | 7468542 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 1 | 4 | 1 | 3 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0001c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0001 | 0/0 | 13 | 1 | 1 | 11 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0005 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0003g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0003c0003t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0003c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0003c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0003c0003t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0004c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0004c0004t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0004c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0004c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0004c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0005c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0005c0006t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0006c0008t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0006c0008t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0007c0007t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0007c0007t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0008c0009t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| a0009c0010t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00544 | hp2 | a0003 | c0003 | t0001 | g0041 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00639 | hp2 | a0004 | c0004 | t0001 | g0065 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0062 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01169 | hp2 | a0004 | c0004 | t0001 | g0063 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01243 | hp2 | a0008 | c0009 | t0002 | g0025 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01496 | hp2 | a0009 | c0010 | t0001 | g0132 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0124 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02040 | hp1 | a0005 | c0006 | t0001 | g0064 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02293 | hp2 | a0003 | c0003 | t0001 | g0014 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0051 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02976 | hp1 | a0006 | c0008 | t0001 | g0150 | AFR | ESN | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0145 | AFR | ESN | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0015 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0010 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03041 | hp1 | a0005 | c0006 | t0001 | g0070 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0102 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03130 | hp1 | a0006 | c0008 | t0001 | g0151 | AFR | ESN | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0139 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0133 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0149 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03491 | hp2 | a0002 | c0002 | t0003 | g0010 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03492 | hp2 | a0002 | c0002 | t0003 | g0010 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0101 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0067 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0107 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0116 | SAS | STU | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0138 | SAS | STU | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | CHB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18747 | hp1 | a0007 | c0007 | t0001 | g0069 | EAS | CHB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18962 | hp1 | a0001 | c0005 | t0001 | g0085 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0077 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18965 | hp2 | a0007 | c0007 | t0001 | g0068 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18966 | hp2 | a0001 | c0005 | t0001 | g0105 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18973 | hp2 | a0004 | c0004 | t0001 | g0071 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18981 | hp1 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18988 | hp2 | a0004 | c0004 | t0001 | g0066 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19002 | hp1 | a0003 | c0003 | t0001 | g0129 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | LWK | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | LWK | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19077 | hp1 | a0003 | c0003 | t0001 | g0113 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0015 | SAS | GIH | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | GIH | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02109 | hp2 | a0003 | c0003 | t0002 | g0033 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | USA | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | LWK | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0106 | REF | REF | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:7450864 | T | C | 6 | a0001 a0003 a0004 others(3): Show |
119 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(116): Show |
missense_variant | MODERATE | c.251A>G | p.His84Arg | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 3/3 | 290/551 | 251/402 | 84/133 | chr8 | 7450864 | |||
| chr8:7450881 | A | C | 3 | a0003 a0004 a0008 |
19 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(16): Show |
missense_variant | MODERATE | c.234T>G | p.Ile78Met | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 3/3 | 273/551 | 234/402 | 78/133 | chr8 | 7450881 | |||
| chr8:7450888 | G | A | 4 | a0003 a0004 a0008 others(1): Show |
20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
missense_variant | MODERATE | c.227C>T | p.Pro76Leu | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 3/3 | 266/551 | 227/402 | 76/133 | chr8 | 7450888 | |||
| chr8:7462743 | G | A | 3 | a0004 a0005 a0007 |
9 | HG00639.hp2 HG01169.hp2 HG02040.hp1 others(6): Show |
missense_variant | MODERATE | c.178C>T | p.Arg60Trp | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/3 | 217/551 | 178/402 | 60/133 | chr8 | 7462743 | |||
| chr8:7463479 | C | A | 1 | a0006 | 2 | HG02976.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.25G>T | p.Val9Phe | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/3 | 64/551 | 25/402 | 9/133 | chr8 | 7463479 | |||
| chr8:7463493 | C | T | 1 | a0008 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.11G>A | p.Arg4Gln | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/3 | 50/551 | 11/402 | 4/133 | chr8 | 7463493 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:7450872 | G | A | 1 | a0001c0005 | 2 | NA18962.hp1 NA18966.hp2 |
synonymous_variant | LOW | c.243C>T | p.Thr81Thr | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 3/3 | 282/551 | 243/402 | 81/133 | chr8 | 7450872 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:7450609 | G | A | 1 | a0002c0002t0003 | 4 | HG03017.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*104C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 3/3 | 104 | chr8 | 7450609 | ||||||
| chr8:7463525 | C | T | 4 | a0001c0001t0002 a0002c0002t0002 a0003c0003t0002 others(1): Show |
11 | HG00639.hp1 HG01243.hp1 HG01243.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-22G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/3 | 22 | chr8 | 7463525 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:7450962 | C | A | 18 | a0003c0003t0001g0014 a0003c0003t0001g0017 a0003c0003t0001g0041 others(15): Show |
20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-62G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7450962 | |||||||
| chr8:7450971 | G | A | 18 | a0003c0003t0001g0014 a0003c0003t0001g0017 a0003c0003t0001g0041 others(15): Show |
20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-71C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7450971 | |||||||
| chr8:7451007 | C | T | 18 | a0003c0003t0001g0014 a0003c0003t0001g0017 a0003c0003t0001g0041 others(15): Show |
20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-107G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451007 | |||||||
| chr8:7451031 | C | T | 1 | a0002c0002t0001g0149 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.215-131G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451031 | |||||||
| chr8:7451148 | T | C | 18 | a0003c0003t0001g0014 a0003c0003t0001g0017 a0003c0003t0001g0041 others(15): Show |
20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-248A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451148 | |||||||
| chr8:7451153 | A | G | 18 | a0003c0003t0001g0014 a0003c0003t0001g0017 a0003c0003t0001g0041 others(15): Show |
20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-253T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451153 | |||||||
| chr8:7451160 | C | T | 18 | a0003c0003t0001g0014 a0003c0003t0001g0017 a0003c0003t0001g0041 others(15): Show |
20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-260G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451160 | |||||||
| chr8:7451184 | C | T | 17 | a0003c0003t0001g0014 a0003c0003t0001g0017 a0003c0003t0001g0041 others(14): Show |
19 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.215-284G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451184 | |||||||
| chr8:7451207 | G | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(53): Show |
80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.215-307C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451207 | |||||||
| chr8:7451276 | A | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(131): Show |
187 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(184): Show |
intron_variant | MODIFIER | c.215-376T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451276 | |||||||
| chr8:7451399 | T | G | 1 | a0002c0002t0001g0049 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.215-499A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451399 | |||||||
| chr8:7451475 | C | A | 1 | a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.215-575G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451475 | |||||||
| chr8:7451476 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(54): Show |
81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.215-576A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451476 | |||||||
| chr8:7451512 | G | GCAA | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(94): Show |
144 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.215-615_215-613dup others(3): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451512 | |||||||
| chr8:7451701 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215-801C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451701 | |||||||
| chr8:7451709 | AC | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(92): Show |
140 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.215-810delG | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451709 | |||||||
| chr8:7451770 | A | G | 3 | a0002c0002t0001g0011 a0002c0002t0001g0133 a0002c0002t0001g0149 |
5 | HG02895.hp1 HG02897.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-870T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451770 | |||||||
| chr8:7451809 | C | T | 1 | a0005c0006t0001g0070 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.215-909G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451809 | |||||||
| chr8:7451857 | C | T | 2 | a0002c0002t0001g0121 a0002c0002t0001g0126 |
2 | HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.215-957G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451857 | |||||||
| chr8:7451998 | C | T | 2 | a0002c0002t0003g0010 a0002c0002t0003g0116 |
4 | HG03017.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1098G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451998 | |||||||
| chr8:7452051 | C | A | 1 | a0001c0001t0001g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.215-1151G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452051 | |||||||
| chr8:7452105 | C | T | 1 | a0002c0002t0001g0050 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.215-1205G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452105 | |||||||
| chr8:7452179 | T | C | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-1279A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452179 | |||||||
| chr8:7452282 | A | G | 1 | a0002c0002t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-1382T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452282 | |||||||
| chr8:7452356 | C | A | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-1456G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452356 | |||||||
| chr8:7452357 | A | G | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-1457T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452357 | |||||||
| chr8:7452396 | G | T | 1 | a0002c0002t0001g0048 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.215-1496C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452396 | |||||||
| chr8:7452416 | T | C | 1 | a0002c0002t0001g0056 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.215-1516A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452416 | |||||||
| chr8:7452477 | G | T | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-1577C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452477 | |||||||
| chr8:7452581 | G | A | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-1681C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452581 | |||||||
| chr8:7452713 | A | T | 16 | a0003c0003t0001g0014 a0003c0003t0001g0017 a0003c0003t0001g0041 others(13): Show |
18 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.215-1813T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452713 | |||||||
| chr8:7452956 | GAA | G | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-2058_215-2057d others(4): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452956 | |||||||
| chr8:7452969 | A | T | 1 | a0002c0002t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-2069T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452969 | |||||||
| chr8:7452974 | C | T | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-2074G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452974 | |||||||
| chr8:7452978 | G | A | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-2078C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452978 | |||||||
| chr8:7453019 | A | G | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-2119T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453019 | |||||||
| chr8:7453082 | G | T | 1 | a0001c0001t0001g0020 | 2 | NA18942.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.215-2182C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453082 | |||||||
| chr8:7453095 | G | C | 2 | a0002c0002t0003g0010 a0002c0002t0003g0116 |
4 | HG03017.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-2195C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453095 | |||||||
| chr8:7453132 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215-2232C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453132 | |||||||
| chr8:7453280 | T | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(53): Show |
78 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.215-2380A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453280 | |||||||
| chr8:7453388 | A | G | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-2488T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453388 | |||||||
| chr8:7453478 | C | A | 25 | a0001c0001t0001g0093 a0002c0002t0001g0001 a0002c0002t0001g0003 others(22): Show |
46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-2578G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453478 | |||||||
| chr8:7453593 | T | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(122): Show |
177 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.215-2693A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453593 | |||||||
| chr8:7453682 | T | C | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-2782A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453682 | |||||||
| chr8:7453684 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.215-2784T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453684 | |||||||
| chr8:7453744 | G | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(48): Show |
73 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.215-2844C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453744 | |||||||
| chr8:7453759 | T | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(49): Show |
74 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.215-2859A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453759 | |||||||
| chr8:7453771 | C | T | 6 | a0002c0002t0001g0011 a0002c0002t0001g0101 a0002c0002t0001g0133 others(3): Show |
8 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-2871G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453771 | |||||||
| chr8:7453854 | T | C | 6 | a0002c0002t0001g0011 a0002c0002t0001g0101 a0002c0002t0001g0133 others(3): Show |
8 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-2954A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453854 | |||||||
| chr8:7453902 | C | T | 1 | a0002c0002t0001g0084 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.215-3002G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453902 | |||||||
| chr8:7454084 | A | T | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-3184T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454084 | |||||||
| chr8:7454085 | A | T | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-3185T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454085 | |||||||
| chr8:7454097 | AAAG | A | 8 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0079 others(5): Show |
9 | HG00408.hp2 HG01515.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.215-3200_215-3198d others(5): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454097 | |||||||
| chr8:7454098 | AAG | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(47): Show |
72 | HG00544.hp1 HG00558.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.215-3200_215-3199d others(4): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454098 | |||||||
| chr8:7454099 | AG | A | 26 | a0001c0001t0001g0024 a0001c0001t0001g0134 a0002c0002t0001g0001 others(23): Show |
48 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.215-3200delC | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454099 | |||||||
| chr8:7454139 | G | A | 1 | a0002c0002t0001g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.215-3239C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454139 | |||||||
| chr8:7454156 | C | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(48): Show |
73 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.215-3256G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454156 | |||||||
| chr8:7454237 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.215-3337G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454237 | |||||||
| chr8:7454250 | A | C | 1 | a0005c0006t0001g0070 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.215-3350T>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454250 | |||||||
| chr8:7454412 | T | G | 34 | a0001c0001t0001g0036 a0001c0001t0002g0034 a0002c0002t0001g0001 others(31): Show |
59 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.215-3512A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454412 | |||||||
| chr8:7454526 | C | T | 8 | a0001c0001t0001g0036 a0001c0001t0002g0034 a0002c0002t0001g0011 others(5): Show |
10 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-3626G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454526 | |||||||
| chr8:7454560 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.215-3660A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454560 | |||||||
| chr8:7454594 | A | G | 1 | a0002c0002t0001g0133 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.215-3694T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454594 | |||||||
| chr8:7454597 | T | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(69): Show |
98 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.215-3697A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454597 | |||||||
| chr8:7454785 | G | C | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-3885C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454785 | |||||||
| chr8:7454831 | GGAAAA | G | 10 | a0001c0001t0001g0036 a0001c0001t0002g0034 a0002c0002t0001g0011 others(7): Show |
14 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-3936_215-3932d others(7): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454831 | |||||||
| chr8:7454893 | T | C | 1 | a0002c0002t0001g0146 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.215-3993A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454893 | |||||||
| chr8:7454920 | A | T | 3 | a0003c0003t0001g0062 a0003c0003t0001g0124 a0008c0009t0002g0025 |
3 | HG01168.hp2 HG01243.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.215-4020T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454920 | |||||||
| chr8:7454934 | TCAA | T | 1 | a0002c0002t0001g0015 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.215-4037_215-4035d others(5): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454934 | |||||||
| chr8:7455026 | A | G | 1 | a0002c0002t0002g0029 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.215-4126T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455026 | |||||||
| chr8:7455031 | A | G | 1 | a0002c0002t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-4131T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455031 | |||||||
| chr8:7455060 | C | A | 30 | a0001c0001t0001g0036 a0001c0001t0002g0034 a0002c0002t0001g0001 others(27): Show |
55 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.215-4160G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455060 | |||||||
| chr8:7455303 | C | T | 1 | a0002c0002t0002g0027 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.215-4403G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455303 | |||||||
| chr8:7455470 | A | G | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-4570T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455470 | |||||||
| chr8:7455583 | T | C | 2 | a0002c0002t0001g0011 a0002c0002t0001g0133 |
4 | HG02895.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-4683A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455583 | |||||||
| chr8:7455588 | T | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
31 | HG00558.hp2 HG01168.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.215-4688A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455588 | |||||||
| chr8:7455651 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.215-4751C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455651 | |||||||
| chr8:7455661 | G | A | 4 | a0002c0002t0001g0015 a0002c0002t0001g0050 a0002c0002t0001g0051 others(1): Show |
5 | HG02735.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-4761C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455661 | |||||||
| chr8:7455765 | C | T | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-4865G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455765 | |||||||
| chr8:7455800 | G | A | 1 | a0002c0002t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-4900C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455800 | |||||||
| chr8:7455849 | A | G | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-4949T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455849 | |||||||
| chr8:7455885 | C | T | 1 | a0005c0006t0001g0070 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.215-4985G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455885 | |||||||
| chr8:7455966 | T | TG | 24 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(21): Show |
45 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.215-5067dupC | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455966 | |||||||
| chr8:7456112 | T | A | 1 | a0001c0001t0001g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.215-5212A>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456112 | |||||||
| chr8:7456129 | G | A | 2 | a0002c0002t0001g0139 a0002c0002t0001g0149 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.215-5229C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456129 | |||||||
| chr8:7456225 | C | G | 15 | a0003c0003t0001g0014 a0003c0003t0001g0017 a0003c0003t0001g0041 others(12): Show |
17 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.215-5325G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456225 | |||||||
| chr8:7456236 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.215-5336G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456236 | |||||||
| chr8:7456300 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(26): Show |
43 | HG00408.hp2 HG00544.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.215-5400C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456300 | |||||||
| chr8:7456338 | A | G | 2 | a0003c0003t0001g0062 a0008c0009t0002g0025 |
2 | HG01168.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.215-5438T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456338 | |||||||
| chr8:7456395 | G | C | 1 | a0003c0003t0002g0033 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.215-5495C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456395 | |||||||
| chr8:7456478 | G | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(48): Show |
73 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.215-5578C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456478 | |||||||
| chr8:7456541 | C | G | 2 | a0002c0002t0001g0011 a0002c0002t0001g0133 |
4 | HG02895.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-5641G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456541 | |||||||
| chr8:7456632 | GC | G | 2 | a0002c0002t0003g0010 a0002c0002t0003g0116 |
4 | HG03017.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-5733delG | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456632 | |||||||
| chr8:7456701 | G | C | 2 | a0002c0002t0001g0083 a0002c0002t0001g0087 |
2 | HG01169.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.215-5801C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456701 | |||||||
| chr8:7456865 | C | G | 3 | a0001c0001t0001g0040 a0002c0002t0001g0139 a0002c0002t0001g0149 |
3 | HG02723.hp2 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.214+5842G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456865 | |||||||
| chr8:7456925 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(94): Show |
144 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.214+5782T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456925 | |||||||
| chr8:7457028 | T | G | 25 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(22): Show |
46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.214+5679A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457028 | |||||||
| chr8:7457054 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(98): Show |
150 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.214+5653C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457054 | |||||||
| chr8:7457162 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(47): Show |
72 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.214+5545C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457162 | |||||||
| chr8:7457166 | C | T | 3 | a0002c0002t0001g0140 a0002c0002t0001g0147 a0006c0008t0001g0150 |
3 | HG02559.hp2 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.214+5541G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457166 | |||||||
| chr8:7457304 | T | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(45): Show |
69 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.214+5403A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457304 | |||||||
| chr8:7457408 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.214+5299A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457408 | |||||||
| chr8:7457556 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.214+5151G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457556 | |||||||
| chr8:7457613 | G | GT | 10 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0039 others(7): Show |
12 | HG00544.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+5093dupA | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457613 | |||||||
| chr8:7457726 | T | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(26): Show |
34 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.214+4981A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457726 | |||||||
| chr8:7457746 | T | C | 1 | a0002c0002t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.214+4961A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457746 | |||||||
| chr8:7457833 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(121): Show |
176 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.214+4874G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457833 | |||||||
| chr8:7457885 | C | T | 28 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0120 others(25): Show |
51 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+4822G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457885 | |||||||
| chr8:7457940 | C | A | 18 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0005 others(15): Show |
39 | HG00558.hp1 HG01069.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.214+4767G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457940 | |||||||
| chr8:7457987 | T | A | 1 | a0002c0002t0001g0054 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.214+4720A>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457987 | |||||||
| chr8:7458078 | A | T | 1 | a0003c0003t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.214+4629T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458078 | |||||||
| chr8:7458237 | G | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(13): Show |
23 | HG00558.hp2 HG01169.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.214+4470C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458237 | |||||||
| chr8:7458284 | T | G | 13 | a0001c0001t0001g0076 a0001c0001t0001g0103 a0002c0002t0001g0012 others(10): Show |
15 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+4423A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458284 | |||||||
| chr8:7458379 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0094 |
3 | HG02895.hp2 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.214+4328C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458379 | |||||||
| chr8:7458410 | CT | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(29): Show |
44 | HG00544.hp2 HG00738.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.214+4296delA | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458410 | |||||||
| chr8:7458599 | G | A | 3 | a0001c0001t0001g0134 a0002c0002t0001g0133 a0002c0002t0001g0149 |
3 | HG02145.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.214+4108C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458599 | |||||||
| chr8:7458600 | G | A | 5 | a0001c0001t0001g0036 a0002c0002t0001g0146 a0002c0002t0001g0147 others(2): Show |
5 | HG00639.hp1 HG02109.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+4107C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458600 | |||||||
| chr8:7458658 | C | G | 34 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0122 others(31): Show |
56 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.214+4049G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458658 | |||||||
| chr8:7458674 | TA | T | 41 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0057 others(38): Show |
67 | HG00408.hp1 HG00558.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.214+4032delT | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458674 | |||||||
| chr8:7458674 | TAAA | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(24): Show |
39 | HG00408.hp2 HG00738.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.214+4030_214+4032d others(5): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458674 | |||||||
| chr8:7458684 | AAAAAAAA others(2): Show |
A | 10 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0103 others(7): Show |
10 | HG01074.hp2 HG01243.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+4014_214+4022d others(11): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458684 | |||||||
| chr8:7458693 | T | A | 1 | a0002c0002t0001g0140 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214+4014A>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458693 | |||||||
| chr8:7458694 | A | T | 1 | a0002c0002t0001g0140 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214+4013T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458694 | |||||||
| chr8:7458695 | G | A | 1 | a0002c0002t0001g0140 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214+4012C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458695 | |||||||
| chr8:7458707 | A | AGAAAGAG others(5): Show |
22 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0001g0001 others(19): Show |
43 | HG00558.hp1 HG00639.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.214+3999_214+4000i others(14): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458707 | |||||||
| chr8:7458708 | G | GAAAGAGA others(5): Show |
1 | a0006c0008t0001g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.214+3998_214+3999i others(14): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458708 | |||||||
| chr8:7458751 | A | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0057 others(25): Show |
37 | HG00738.hp2 HG01081.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.214+3956T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458751 | |||||||
| chr8:7458766 | G | A | 13 | a0001c0001t0001g0057 a0001c0001t0001g0072 a0001c0001t0001g0076 others(10): Show |
13 | HG00738.hp2 HG01168.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.214+3941C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458766 | |||||||
| chr8:7458858 | T | C | 1 | a0002c0002t0001g0099 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.214+3849A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458858 | |||||||
| chr8:7458860 | T | C | 1 | a0006c0008t0001g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.214+3847A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458860 | |||||||
| chr8:7458893 | T | C | 12 | a0001c0001t0001g0104 a0001c0001t0001g0131 a0001c0001t0001g0134 others(9): Show |
14 | HG00544.hp1 HG01515.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.214+3814A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458893 | |||||||
| chr8:7458904 | A | T | 1 | a0002c0002t0001g0046 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.214+3803T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458904 | |||||||
| chr8:7458926 | CG | C | 21 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0001g0001 others(18): Show |
39 | HG01069.hp2 HG01074.hp1 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.214+3780delC | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458926 | |||||||
| chr8:7458948 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
99 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.214+3759G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458948 | |||||||
| chr8:7458967 | C | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(121): Show |
156 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.214+3740G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458967 | |||||||
| chr8:7458969 | C | A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(34): Show |
50 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.214+3738G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458969 | |||||||
| chr8:7458973 | C | CCT | 34 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(31): Show |
47 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+3733_214+3734i others(4): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458973 | |||||||
| chr8:7458974 | A | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(31): Show |
47 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+3733T>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458974 | |||||||
| chr8:7458975 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(31): Show |
47 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+3732C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458975 | |||||||
| chr8:7458977 | T | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(31): Show |
47 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+3730A>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458977 | |||||||
| chr8:7458979 | A | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(31): Show |
47 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+3728T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458979 | |||||||
| chr8:7459023 | A | G | 1 | a0002c0002t0001g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214+3684T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459023 | |||||||
| chr8:7459026 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(116): Show |
151 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.214+3681A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459026 | |||||||
| chr8:7459055 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): Show |
150 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.214+3652C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459055 | |||||||
| chr8:7459060 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.214+3647A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459060 | |||||||
| chr8:7459067 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(116): Show |
151 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.214+3640T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459067 | |||||||
| chr8:7459156 | G | T | 1 | a0006c0008t0001g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.214+3551C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459156 | |||||||
| chr8:7459158 | T | G | 1 | a0006c0008t0001g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.214+3549A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459158 | |||||||
| chr8:7459203 | G | A | 31 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0002c0002t0001g0001 others(28): Show |
53 | HG00558.hp1 HG00639.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.214+3504C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459203 | |||||||
| chr8:7459218 | CAA | C | 10 | a0001c0001t0001g0072 a0001c0001t0001g0103 a0001c0001t0002g0031 others(7): Show |
10 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3487_214+3488d others(4): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459218 | |||||||
| chr8:7459234 | A | T | 1 | a0003c0003t0001g0077 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.214+3473T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459234 | |||||||
| chr8:7459298 | A | C | 1 | a0002c0002t0001g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214+3409T>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459298 | |||||||
| chr8:7459317 | CA | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0108 others(6): Show |
11 | HG00544.hp2 HG02040.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.214+3389delT | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459317 | |||||||
| chr8:7459424 | C | G | 8 | a0001c0001t0001g0072 a0001c0001t0002g0031 a0002c0002t0001g0099 others(5): Show |
8 | HG01243.hp1 HG01243.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+3283G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459424 | |||||||
| chr8:7459452 | C | G | 32 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0057 others(29): Show |
54 | HG00558.hp1 HG00639.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.214+3255G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459452 | |||||||
| chr8:7459467 | A | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(37): Show |
54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.214+3240T>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459467 | |||||||
| chr8:7459558 | A | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(37): Show |
54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.214+3149T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459558 | |||||||
| chr8:7459566 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.214+3141G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459566 | |||||||
| chr8:7459691 | C | T | 1 | a0002c0002t0001g0149 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.214+3016G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459691 | |||||||
| chr8:7459776 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0141 a0001c0005t0001g0105 |
3 | HG00544.hp1 NA18966.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.214+2931G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459776 | |||||||
| chr8:7459882 | G | A | 1 | a0002c0002t0001g0011 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.214+2825C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459882 | |||||||
| chr8:7459947 | G | A | 1 | a0004c0004t0001g0071 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.214+2760C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459947 | |||||||
| chr8:7459979 | C | T | 1 | a0001c0001t0002g0026 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.214+2728G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459979 | |||||||
| chr8:7459980 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(140): Show |
195 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(192): Show |
intron_variant | MODIFIER | c.214+2727T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459980 | |||||||
| chr8:7459988 | C | T | 1 | a0002c0002t0001g0149 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.214+2719G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459988 | |||||||
| chr8:7459998 | G | A | 3 | a0001c0001t0001g0024 a0002c0002t0001g0102 a0002c0002t0001g0146 |
4 | HG02109.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+2709C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459998 | |||||||
| chr8:7460077 | G | A | 3 | a0001c0001t0001g0038 a0002c0002t0001g0012 a0002c0002t0002g0035 |
4 | HG00639.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+2630C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460077 | |||||||
| chr8:7460410 | A | T | 1 | a0002c0002t0001g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214+2297T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460410 | |||||||
| chr8:7460422 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.214+2285C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460422 | |||||||
| chr8:7460550 | G | A | 3 | a0001c0001t0001g0024 a0002c0002t0001g0102 a0002c0002t0001g0146 |
4 | HG02109.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+2157C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460550 | |||||||
| chr8:7460550 | G | GA | 3 | a0001c0001t0001g0141 a0003c0003t0001g0062 a0008c0009t0002g0025 |
3 | HG01168.hp2 HG01243.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.214+2156dupT | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460550 | |||||||
| chr8:7460569 | C | T | 3 | a0001c0001t0001g0038 a0002c0002t0001g0012 a0002c0002t0002g0035 |
4 | HG00639.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+2138G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460569 | |||||||
| chr8:7460744 | G | T | 1 | a0002c0002t0001g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214+1963C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460744 | |||||||
| chr8:7460857 | G | C | 1 | a0004c0004t0001g0071 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.214+1850C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460857 | |||||||
| chr8:7460900 | G | C | 2 | a0001c0001t0001g0100 a0002c0002t0001g0101 |
2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.214+1807C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460900 | |||||||
| chr8:7460968 | ATGATGGG others(2): Show |
A | 2 | a0006c0008t0001g0150 a0006c0008t0001g0151 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.214+1730_214+1738d others(11): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460968 | |||||||
| chr8:7461092 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0026 |
3 | HG02056.hp2 NA18966.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.214+1615T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461092 | |||||||
| chr8:7461226 | G | C | 1 | a0002c0002t0001g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.214+1481C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461226 | |||||||
| chr8:7461347 | A | G | 1 | a0003c0003t0001g0073 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.214+1360T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461347 | |||||||
| chr8:7461356 | C | T | 2 | a0001c0001t0001g0100 a0002c0002t0001g0101 |
2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.214+1351G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461356 | |||||||
| chr8:7461488 | G | A | 1 | a0002c0002t0001g0005 | 3 | HG01074.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.214+1219C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461488 | |||||||
| chr8:7461537 | G | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
191 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.214+1170C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461537 | |||||||
| chr8:7461549 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.214+1158C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461549 | |||||||
| chr8:7461611 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(3): Show |
13 | HG00558.hp2 HG00597.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.214+1096C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461611 | |||||||
| chr8:7461705 | G | C | 2 | a0001c0001t0001g0038 a0002c0002t0001g0012 |
3 | HG01257.hp1 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.214+1002C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461705 | |||||||
| chr8:7461747 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.214+960A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461747 | |||||||
| chr8:7461877 | T | G | 1 | a0001c0001t0001g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.214+830A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461877 | |||||||
| chr8:7461879 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.214+828C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461879 | |||||||
| chr8:7461888 | G | A | 3 | a0001c0001t0001g0024 a0002c0002t0001g0146 a0002c0002t0001g0147 |
4 | HG02109.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+819C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461888 | |||||||
| chr8:7461935 | A | G | 2 | a0002c0002t0001g0013 a0002c0002t0001g0042 |
3 | NA18975.hp2 NA19006.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.214+772T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461935 | |||||||
| chr8:7462266 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(146): Show |
203 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.214+441A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7462266 | |||||||
| chr8:7462404 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.214+303A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7462404 | |||||||
| chr8:7462449 | T | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0038 others(6): Show |
11 | HG01257.hp1 HG01258.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.214+258A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7462449 | |||||||
| chr8:7462468 | C | G | 34 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
47 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+239G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7462468 | |||||||
| chr8:7462484 | T | C | 1 | a0002c0002t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.214+223A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7462484 | |||||||
| chr8:7462935 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.62-76G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7462935 | |||||||
| chr8:7462951 | T | C | 1 | a0002c0002t0001g0149 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.62-92A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7462951 | |||||||
| chr8:7462997 | C | G | 2 | a0001c0001t0001g0038 a0002c0002t0001g0012 |
3 | HG01257.hp1 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.62-138G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7462997 | |||||||
| chr8:7463005 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.62-146C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463005 | |||||||
| chr8:7463011 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
143 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.62-152C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463011 | |||||||
| chr8:7463024 | C | T | 1 | a0003c0003t0001g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.62-165G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463024 | |||||||
| chr8:7463081 | C | CATGT | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-223_62-222insAC others(2): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463081 | |||||||
| chr8:7463085 | A | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-226T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463085 | |||||||
| chr8:7463232 | G | A | 11 | a0001c0001t0002g0026 a0001c0001t0002g0031 a0001c0001t0002g0032 others(8): Show |
11 | HG00639.hp1 HG01243.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+211C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463232 | |||||||
| chr8:7463271 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.61+172G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463271 | |||||||
| chr8:7463393 | C | A | 2 | a0001c0001t0001g0038 a0002c0002t0001g0012 |
3 | HG01257.hp1 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.61+50G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463393 | |||||||
| chr8:7463399 | A | G | 17 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(14): Show |
18 | HG00639.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.61+44T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463399 | |||||||
| chr8:7463419 | A | G | 2 | a0006c0008t0001g0150 a0006c0008t0001g0151 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.61+24T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463419 |