Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 653423 |
| ensemblid | ENSG00000178287.18 |
| hgncid | 33342 |
| symbol | SPAG11A |
| name | sperm associated antigen 11A |
| refseq_nuc | NM_001395484.1 |
| refseq_prot | NP_001382413.1 |
| ensembl_nuc | ENST00000642566.2 |
| ensembl_prot | ENSP00000496500.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 7848008 |
| end | 7860943 |
| strand | + |
| ver | v1.2 |
| region | chr8:7848008-7860943 |
| region5000 | chr8:7843008-7865943 |
| regionname0 | SPAG11A_chr8_7848008_7860943 |
| regionname5000 | SPAG11A_chr8_7843008_7865943 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 133 | 56 | 16 | 5 | 26 | 5 | 4 | 18 | SPAG11A_chr8_7843008_7865943 | SPAG11A | MRQRL others(128): Show |
chr8 | 7843008 | 7865943 |
| a0002 | 0/0 | 133 | 42 | 2 | 12 | 23 | 2 | 3 | 17 | SPAG11A_chr8_7843008_7865943 | SPAG11A | MRQRL others(128): Show |
chr8 | 7843008 | 7865943 |
| a0003 | 0/0 | 133 | 13 | 0 | 5 | 6 | 1 | 1 | 2 | SPAG11A_chr8_7843008_7865943 | SPAG11A | MRQRL others(128): Show |
chr8 | 7843008 | 7865943 |
| a0004 | 1/0 | 133 | 7 | 6 | 0 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | MRQRL others(128): Show |
chr8 | 7843008 | 7865943 |
| a0005 | 0/0 | 133 | 7 | 1 | 4 | 1 | 1 | 0 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | MRQRL others(128): Show |
chr8 | 7843008 | 7865943 |
| a0006 | 0/0 | 133 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | MRQRL others(128): Show |
chr8 | 7843008 | 7865943 |
| a0007 | 0/0 | 133 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | MRQRL others(128): Show |
chr8 | 7843008 | 7865943 |
| a0008 | 0/0 | 133 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | MRQRL others(128): Show |
chr8 | 7843008 | 7865943 |
| a0009 | 0/0 | 133 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | MRQRL others(128): Show |
chr8 | 7843008 | 7865943 |
| a0010 | 0/0 | 133 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | MRQRL others(128): Show |
chr8 | 7843008 | 7865943 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 399 | 55 | 16 | 5 | 26 | 4 | 4 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 | ||
| a0001c0008 | 0/0 | 399 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 | ||
| a0002c0002 | 0/0 | 399 | 41 | 2 | 12 | 23 | 2 | 2 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 | ||
| a0002c0011 | 0/0 | 399 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 | ||
| a0003c0003 | 0/0 | 399 | 13 | 0 | 5 | 6 | 1 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 | ||
| a0004c0005 | 1/0 | 399 | 7 | 6 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 | ||
| a0005c0004 | 0/0 | 399 | 7 | 1 | 4 | 1 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 | ||
| a0006c0006 | 0/0 | 399 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 | ||
| a0007c0007 | 0/0 | 399 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 | ||
| a0008c0010 | 0/0 | 399 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 | ||
| a0009c0012 | 0/0 | 399 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 | ||
| a0010c0009 | 0/0 | 399 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ATGAG others(394): Show |
chr8 | 7843008 | 7865943 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 551 | 45 | 11 | 5 | 23 | 2 | 4 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0001c0001t0002 | 0/0 | 551 | 9 | 5 | 0 | 2 | 2 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0001c0001t0003 | 0/0 | 551 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0001c0008t0001 | 0/0 | 551 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0002c0002t0001 | 0/0 | 551 | 26 | 1 | 8 | 16 | 0 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0002c0002t0002 | 0/0 | 551 | 15 | 1 | 4 | 7 | 2 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0002c0011t0002 | 0/0 | 551 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0003c0003t0001 | 0/0 | 551 | 13 | 0 | 5 | 6 | 1 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0004c0005t0001 | 1/0 | 551 | 7 | 6 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0005c0004t0001 | 0/0 | 551 | 7 | 1 | 4 | 1 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0006c0006t0001 | 0/0 | 551 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0007c0007t0001 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0008c0010t0001 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0009c0012t0001 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| a0010c0009t0001 | 0/0 | 551 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | ACCCT others(546): Show |
chr8 | 7843008 | 7865943 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0001c0008t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0002g0001 | 0/0 | 7 | 0 | 2 | 2 | 2 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0002c0011t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0004c0005t0001g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0004c0005t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0004c0005t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0004c0005t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0004c0005t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0004c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0004c0005t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0005c0004t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0005c0004t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0005c0004t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0005c0004t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0005c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0005c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0006c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0006c0006t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0007c0007t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0008c0010t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0009c0012t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| a0010c0009t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | GBR | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | GBR | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | FIN | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00280 | hp2 | a0001 | c0008 | t0001 | g0017 | EUR | FIN | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0033 | EUR | FIN | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0051 | EUR | FIN | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | CHS | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | PUR | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0025 | AMR | PUR | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01258 | hp2 | a0003 | c0003 | t0001 | g0048 | AMR | CLM | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0054 | AMR | CLM | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | CLM | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | CLM | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01361 | hp2 | a0005 | c0004 | t0001 | g0072 | AMR | CLM | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | CLM | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01515 | hp1 | a0005 | c0004 | t0001 | g0085 | EUR | IBS | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01934 | hp1 | a0005 | c0004 | t0001 | g0078 | AMR | PEL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | PEL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PEL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01952 | hp1 | a0005 | c0004 | t0001 | g0067 | AMR | PEL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01952 | hp2 | a0003 | c0003 | t0001 | g0043 | AMR | PEL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0049 | AMR | PEL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01978 | hp2 | a0005 | c0004 | t0001 | g0010 | AMR | PEL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0041 | AMR | PEL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0047 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0050 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0044 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02145 | hp2 | a0006 | c0006 | t0001 | g0020 | AFR | ACB | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02451 | hp1 | a0004 | c0005 | t0001 | g0097 | AFR | ACB | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02683 | hp1 | a0002 | c0011 | t0002 | g0023 | SAS | PJL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02723 | hp2 | a0004 | c0005 | t0001 | g0096 | AFR | GWD | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | GWD | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02886 | hp1 | a0004 | c0005 | t0001 | g0092 | AFR | GWD | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02886 | hp2 | a0007 | c0007 | t0001 | g0075 | AFR | GWD | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03130 | hp1 | a0006 | c0006 | t0001 | g0021 | AFR | ESN | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03453 | hp1 | a0008 | c0010 | t0001 | g0052 | AFR | MSL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03453 | hp2 | a0004 | c0005 | t0001 | g0102 | AFR | MSL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0040 | SAS | PJL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03540 | hp1 | a0005 | c0004 | t0001 | g0036 | AFR | GWD | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03579 | hp1 | a0004 | c0005 | t0001 | g0093 | AFR | MSL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | STU | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | BEB | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18952 | hp2 | a0005 | c0004 | t0001 | g0010 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0057 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19240 | hp1 | a0004 | c0005 | t0001 | g0091 | AFR | YRI | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA20805 | hp1 | a0010 | c0009 | t0001 | g0101 | EUR | TSI | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0030 | AFR | USA | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | USA | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | USA | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| NA20300 | hp2 | a0009 | c0012 | t0001 | g0019 | AFR | USA | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| homoSapiens | grch38p0 | a0004 | c0005 | t0001 | g0089 | REF | REF | SPAG11A_chr8_7843008_7865943 | SPAG11A | chr8 | 7843008 | 7865943 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:7848071 | G | T | 2 | a0006 a0009 |
3 | HG02145.hp2 HG03130.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.25G>T | p.Val9Phe | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/3 | 64/551 | 25/402 | 9/133 | chr8 | 7848071 | |||
| chr8:7848807 | C | T | 3 | a0003 a0008 a0010 |
15 | HG00323.hp2 HG01258.hp2 HG01346.hp1 others(12): Show |
missense_variant | MODERATE | c.178C>T | p.Arg60Trp | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/3 | 217/551 | 178/402 | 60/133 | chr8 | 7848807 | |||
| chr8:7860658 | T | C | 1 | a0005 | 7 | HG01361.hp2 HG01515.hp1 HG01934.hp1 others(4): Show |
missense_variant | MODERATE | c.227T>C | p.Leu76Pro | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 3/3 | 266/551 | 227/402 | 76/133 | chr8 | 7860658 | |||
| chr8:7860665 | T | G | 2 | a0002 a0003 |
55 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(52): Show |
missense_variant | MODERATE | c.234T>G | p.Ile78Met | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 3/3 | 273/551 | 234/402 | 78/133 | chr8 | 7860665 | |||
| chr8:7860744 | A | T | 8 | a0001 a0002 a0003 others(5): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
missense_variant | MODERATE | c.313A>T | p.Ser105Cys | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 3/3 | 352/551 | 313/402 | 105/133 | chr8 | 7860744 | |||
| chr8:7860759 | A | G | 2 | a0007 a0008 |
2 | HG02886.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.328A>G | p.Asn110Asp | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 3/3 | 367/551 | 328/402 | 110/133 | chr8 | 7860759 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:7848755 | A | G | 1 | a0002c0011 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.126A>G | p.Arg42Arg | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/3 | 165/551 | 126/402 | 42/133 | chr8 | 7848755 | |||
| chr8:7848839 | C | T | 1 | a0001c0008 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.210C>T | p.Tyr70Tyr | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/3 | 249/551 | 210/402 | 70/133 | chr8 | 7848839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:7848025 | G | A | 3 | a0001c0001t0002 a0002c0002t0002 a0002c0011t0002 |
25 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-22G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/3 | 22 | chr8 | 7848025 | ||||||
| chr8:7860923 | T | C | 1 | a0001c0001t0003 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*90T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 3/3 | 90 | chr8 | 7860923 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:7848127 | C | T | 2 | a0001c0001t0001g0103 a0004c0005t0001g0102 |
2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.61+20C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848127 | |||||||
| chr8:7848131 | T | C | 3 | a0006c0006t0001g0020 a0006c0006t0001g0021 a0009c0012t0001g0019 |
3 | HG02145.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.61+24T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848131 | |||||||
| chr8:7848151 | T | C | 23 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0002g0008 others(20): Show |
31 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.61+44T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848151 | |||||||
| chr8:7848157 | G | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0005c0004t0001g0036 |
3 | HG00642.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.61+50G>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848157 | |||||||
| chr8:7848204 | C | T | 1 | a0010c0009t0001g0101 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61+97C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848204 | |||||||
| chr8:7848240 | G | A | 2 | a0001c0001t0001g0037 a0005c0004t0001g0036 |
2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.61+133G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848240 | |||||||
| chr8:7848318 | C | T | 16 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0031 others(13): Show |
24 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.61+211C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848318 | |||||||
| chr8:7848505 | C | G | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.62-186C>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848505 | |||||||
| chr8:7848515 | G | T | 1 | a0001c0001t0002g0008 | 2 | HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.62-176G>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848515 | |||||||
| chr8:7848526 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.62-165G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848526 | |||||||
| chr8:7848539 | T | C | 19 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0002c0002t0001g0042 others(16): Show |
19 | HG00323.hp2 HG00735.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-152T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848539 | |||||||
| chr8:7848553 | G | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0005c0004t0001g0036 |
3 | HG00642.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.62-138G>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 1/2 | chr8 | 7848553 | |||||||
| chr8:7849058 | G | A | 1 | a0004c0005t0001g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214+215G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849058 | |||||||
| chr8:7849066 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.214+223A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849066 | |||||||
| chr8:7849082 | G | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(29): Show |
47 | HG00438.hp2 HG00544.hp1 HG01361.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+239G>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849082 | |||||||
| chr8:7849101 | A | G | 13 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0094 others(10): Show |
13 | HG00642.hp2 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.214+258A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849101 | |||||||
| chr8:7849122 | C | T | 1 | a0002c0002t0001g0076 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.214+279C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849122 | |||||||
| chr8:7849205 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.214+362G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849205 | |||||||
| chr8:7849209 | C | T | 3 | a0004c0005t0001g0091 a0004c0005t0001g0092 a0004c0005t0001g0093 |
3 | HG02886.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.214+366C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849209 | |||||||
| chr8:7849305 | G | T | 1 | a0007c0007t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.214+462G>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849305 | |||||||
| chr8:7849435 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.214+592G>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849435 | |||||||
| chr8:7849747 | A | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0098 a0005c0004t0001g0036 |
3 | HG02922.hp1 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.214+904A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849747 | |||||||
| chr8:7849758 | A | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0098 a0005c0004t0001g0036 |
3 | HG02922.hp1 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.214+915A>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849758 | |||||||
| chr8:7849845 | C | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0098 others(1): Show |
4 | HG00642.hp2 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+1002C>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849845 | |||||||
| chr8:7849848 | T | C | 1 | a0003c0003t0001g0040 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.214+1005T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849848 | |||||||
| chr8:7849850 | T | C | 1 | a0005c0004t0001g0036 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.214+1007T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849850 | |||||||
| chr8:7849939 | C | T | 4 | a0001c0001t0002g0035 a0002c0002t0001g0014 a0002c0002t0001g0074 others(1): Show |
5 | HG00544.hp1 HG02135.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+1096C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7849939 | |||||||
| chr8:7850013 | C | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
117 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.214+1170C>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7850013 | |||||||
| chr8:7850122 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.214+1279A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7850122 | |||||||
| chr8:7850194 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.214+1351G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7850194 | |||||||
| chr8:7850203 | T | C | 2 | a0001c0001t0001g0060 a0002c0002t0001g0059 |
2 | NA19067.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.214+1360T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7850203 | |||||||
| chr8:7850458 | T | C | 1 | a0002c0002t0001g0074 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.214+1615T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7850458 | |||||||
| chr8:7850494 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.214+1651G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7850494 | |||||||
| chr8:7850566 | TCCATCAG others(2): Show |
T | 2 | a0006c0006t0001g0020 a0006c0006t0001g0021 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.214+1730_214+1738d others(11): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7850566 | ||||||
| chr8:7850650 | C | G | 1 | a0004c0005t0001g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.214+1807C>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7850650 | |||||||
| chr8:7850693 | C | G | 1 | a0003c0003t0001g0057 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.214+1850C>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7850693 | |||||||
| chr8:7850806 | C | A | 3 | a0001c0001t0001g0103 a0004c0005t0001g0097 a0004c0005t0001g0102 |
3 | HG02451.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.214+1963C>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7850806 | |||||||
| chr8:7850910 | T | C | 1 | a0009c0012t0001g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214+2067T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7850910 | |||||||
| chr8:7850981 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0098 others(3): Show |
6 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+2138G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7850981 | |||||||
| chr8:7851000 | C | T | 3 | a0001c0001t0001g0103 a0004c0005t0001g0097 a0004c0005t0001g0102 |
3 | HG02451.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.214+2157C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851000 | |||||||
| chr8:7851140 | T | A | 1 | a0004c0005t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.214+2297T>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851140 | |||||||
| chr8:7851211 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.214+2368C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851211 | |||||||
| chr8:7851273 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.214+2430G>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851273 | |||||||
| chr8:7851445 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.214+2602T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851445 | |||||||
| chr8:7851456 | G | T | 1 | a0004c0005t0001g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214+2613G>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851456 | |||||||
| chr8:7851473 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0098 others(3): Show |
6 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+2630C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851473 | |||||||
| chr8:7851552 | C | T | 6 | a0001c0001t0001g0103 a0004c0005t0001g0091 a0004c0005t0001g0092 others(3): Show |
6 | HG02451.hp1 HG02886.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+2709C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851552 | |||||||
| chr8:7851570 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(97): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.214+2727T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851570 | |||||||
| chr8:7851603 | C | T | 1 | a0003c0003t0001g0057 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.214+2760C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851603 | |||||||
| chr8:7851942 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.214+3099G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851942 | |||||||
| chr8:7851992 | C | T | 65 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(62): Show |
78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.214+3149C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7851992 | |||||||
| chr8:7852083 | G | T | 66 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(63): Show |
79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.214+3240G>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852083 | |||||||
| chr8:7852098 | G | C | 17 | a0001c0001t0001g0053 a0002c0002t0001g0042 a0003c0003t0001g0040 others(14): Show |
17 | HG00323.hp2 HG00735.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.214+3255G>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852098 | |||||||
| chr8:7852126 | G | C | 14 | a0001c0001t0002g0008 a0001c0001t0002g0022 a0001c0001t0002g0024 others(11): Show |
22 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.214+3283G>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852126 | |||||||
| chr8:7852230 | GT | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0079 |
2 | HG00544.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.214+3389delT | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7852230 | ||||||
| chr8:7852252 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.214+3409T>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852252 | |||||||
| chr8:7852320 | CT | C | 17 | a0001c0001t0001g0077 a0001c0001t0002g0008 a0001c0001t0002g0022 others(14): Show |
25 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.214+3487delT | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7852320 | ||||||
| chr8:7852346 | C | T | 15 | a0001c0001t0001g0053 a0002c0002t0001g0042 a0003c0003t0001g0040 others(12): Show |
15 | HG00323.hp2 HG00735.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+3503C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852346 | |||||||
| chr8:7852391 | A | C | 2 | a0006c0006t0001g0020 a0006c0006t0001g0021 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.214+3548A>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852391 | |||||||
| chr8:7852393 | C | A | 2 | a0006c0006t0001g0020 a0006c0006t0001g0021 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.214+3550C>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852393 | |||||||
| chr8:7852482 | C | T | 15 | a0001c0001t0001g0053 a0002c0002t0001g0042 a0003c0003t0001g0040 others(12): Show |
15 | HG00323.hp2 HG00735.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+3639C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852482 | |||||||
| chr8:7852494 | T | C | 18 | a0001c0001t0001g0053 a0001c0001t0001g0080 a0001c0001t0001g0081 others(15): Show |
18 | HG00323.hp2 HG00735.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.214+3651T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852494 | |||||||
| chr8:7852523 | G | A | 15 | a0001c0001t0001g0053 a0001c0001t0001g0080 a0002c0002t0001g0042 others(12): Show |
15 | HG00323.hp2 HG00735.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+3680G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852523 | |||||||
| chr8:7852526 | T | C | 1 | a0004c0005t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.214+3683T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852526 | |||||||
| chr8:7852570 | T | A | 12 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0081 others(9): Show |
12 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+3727T>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852570 | |||||||
| chr8:7852572 | A | T | 12 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0081 others(9): Show |
12 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+3729A>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852572 | |||||||
| chr8:7852573 | T | TTG | 12 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0081 others(9): Show |
12 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+3730_214+3731i others(4): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852573 | |||||||
| chr8:7852574 | C | A | 12 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0081 others(9): Show |
12 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+3731C>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852574 | |||||||
| chr8:7852575 | T | G | 12 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0081 others(9): Show |
12 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+3732T>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852575 | |||||||
| chr8:7852580 | G | T | 13 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0081 others(10): Show |
13 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(10): Show |
intron_variant | MODIFIER | c.214+3737G>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852580 | |||||||
| chr8:7852582 | C | G | 4 | a0001c0001t0001g0053 a0002c0002t0001g0042 a0007c0007t0001g0075 others(1): Show |
4 | HG00735.hp1 HG01361.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3739C>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852582 | |||||||
| chr8:7852601 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(65): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.214+3758G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852601 | |||||||
| chr8:7852613 | G | A | 1 | a0003c0003t0001g0045 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.214+3770G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852613 | |||||||
| chr8:7852620 | AC | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0088 a0002c0002t0001g0042 others(1): Show |
4 | HG00735.hp1 HG01361.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+3779delC | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7852620 | ||||||
| chr8:7852656 | A | G | 5 | a0001c0001t0001g0087 a0001c0001t0001g0098 a0004c0005t0001g0093 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+3813A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852656 | |||||||
| chr8:7852783 | C | T | 13 | a0001c0001t0002g0022 a0001c0001t0002g0031 a0001c0001t0002g0035 others(10): Show |
22 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.214+3940C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852783 | |||||||
| chr8:7852798 | T | A | 18 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(15): Show |
27 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.214+3955T>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852798 | |||||||
| chr8:7852839 | A | ATCAGTTT others(5): Show |
2 | a0001c0001t0001g0053 a0002c0002t0001g0042 |
2 | HG00735.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.214+3998_214+3999i others(14): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7852839 | ||||||
| chr8:7852839 | A | ATGAGTTT others(5): Show |
2 | a0006c0006t0001g0020 a0006c0006t0001g0021 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.214+3997_214+3998i others(14): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7852839 | ||||||
| chr8:7852854 | CTATTTTT | C | 19 | a0001c0001t0001g0073 a0001c0001t0002g0008 a0001c0001t0002g0022 others(16): Show |
29 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.214+4013_214+4019d others(9): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7852854 | ||||||
| chr8:7852856 | A | AT | 14 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0053 others(11): Show |
15 | HG00323.hp1 HG00544.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.214+4029dupT | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7852856 | ||||||
| chr8:7852856 | A | ATT | 37 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(34): Show |
46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.214+4028_214+4029d others(4): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7852856 | ||||||
| chr8:7852856 | A | ATTT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0055 others(5): Show |
12 | HG01496.hp1 HG01515.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+4027_214+4029d others(5): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7852856 | ||||||
| chr8:7852856 | AT | A | 10 | a0001c0001t0001g0037 a0001c0001t0001g0079 a0001c0001t0001g0081 others(7): Show |
10 | HG01346.hp2 HG01515.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+4029delT | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7852856 | ||||||
| chr8:7852889 | G | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(9): Show |
16 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.214+4046G>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852889 | |||||||
| chr8:7852947 | C | T | 5 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0008t0001g0017 others(2): Show |
5 | HG00280.hp2 HG01167.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+4104C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7852947 | |||||||
| chr8:7853135 | TA | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0039 others(9): Show |
15 | HG00544.hp2 HG00642.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.214+4293delA | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853135 | |||||||
| chr8:7853263 | A | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0001g0087 others(4): Show |
8 | HG01258.hp1 HG01496.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.214+4420A>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853263 | |||||||
| chr8:7853306 | A | T | 1 | a0001c0001t0001g0038 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.214+4463A>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853306 | |||||||
| chr8:7853310 | C | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(18): Show |
27 | HG00280.hp2 HG00544.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.214+4467C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853310 | |||||||
| chr8:7853408 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.214+4565T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853408 | |||||||
| chr8:7853582 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(97): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.214+4739G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853582 | |||||||
| chr8:7853615 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.214+4772G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853615 | |||||||
| chr8:7853662 | G | A | 1 | a0002c0002t0001g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.214+4819G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853662 | |||||||
| chr8:7853714 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(62): Show |
84 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.214+4871G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853714 | |||||||
| chr8:7853821 | A | G | 13 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0077 others(10): Show |
14 | HG00323.hp2 HG01884.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.214+4978A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853821 | |||||||
| chr8:7853842 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.214+4999T>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853842 | |||||||
| chr8:7853879 | T | C | 1 | a0004c0005t0001g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.214+5036T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7853879 | |||||||
| chr8:7853925 | C | CA | 22 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(19): Show |
31 | HG00438.hp2 HG00544.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.214+5090dupA | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7853925 | ||||||
| chr8:7854243 | A | G | 16 | a0001c0001t0001g0053 a0001c0001t0001g0062 a0001c0001t0001g0065 others(13): Show |
17 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.214+5400A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7854243 | |||||||
| chr8:7854381 | A | G | 68 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(65): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.214+5538A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7854381 | |||||||
| chr8:7854385 | C | T | 14 | a0001c0001t0001g0053 a0001c0001t0001g0065 a0001c0001t0001g0077 others(11): Show |
15 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.214+5542C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7854385 | |||||||
| chr8:7854493 | T | C | 5 | a0001c0001t0001g0062 a0001c0001t0001g0084 a0001c0001t0001g0094 others(2): Show |
5 | HG02145.hp1 HG02523.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+5650T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7854493 | |||||||
| chr8:7854519 | A | C | 1 | a0002c0002t0001g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.214+5676A>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7854519 | |||||||
| chr8:7854622 | T | C | 54 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0053 others(51): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.214+5779T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7854622 | |||||||
| chr8:7854713 | G | A | 1 | a0009c0012t0001g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214+5870G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7854713 | |||||||
| chr8:7854846 | C | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(33): Show |
48 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.215-5800C>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7854846 | |||||||
| chr8:7854993 | AGAACGCA others(21): Show |
A | 1 | a0003c0003t0001g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.215-5652_215-5625d others(30): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7854993 | |||||||
| chr8:7855069 | C | A | 14 | a0001c0001t0001g0053 a0001c0001t0001g0065 a0001c0001t0001g0077 others(11): Show |
15 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.215-5577C>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7855069 | |||||||
| chr8:7855102 | C | G | 1 | a0002c0002t0002g0029 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.215-5544C>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7855102 | |||||||
| chr8:7855197 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.215-5449A>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7855197 | |||||||
| chr8:7855209 | T | C | 9 | a0002c0002t0001g0005 a0002c0002t0001g0042 a0002c0002t0001g0069 others(6): Show |
17 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.215-5437T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7855209 | |||||||
| chr8:7855247 | C | T | 8 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0002c0002t0001g0064 others(5): Show |
9 | HG01515.hp1 HG01934.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-5399C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7855247 | |||||||
| chr8:7855322 | G | C | 35 | a0001c0001t0002g0024 a0002c0002t0001g0004 a0002c0002t0001g0005 others(32): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.215-5324G>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7855322 | |||||||
| chr8:7855522 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.215-5124G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7855522 | |||||||
| chr8:7855796 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(96): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.215-4850T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7855796 | |||||||
| chr8:7855959 | A | G | 2 | a0001c0001t0001g0088 a0005c0004t0001g0072 |
2 | HG01361.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.215-4687A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7855959 | |||||||
| chr8:7855959 | A | T | 1 | a0005c0004t0001g0078 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-4687A>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7855959 | |||||||
| chr8:7855964 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.215-4682A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7855964 | |||||||
| chr8:7856150 | G | A | 1 | a0002c0002t0001g0068 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.215-4496G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7856150 | |||||||
| chr8:7856203 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.215-4443C>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7856203 | |||||||
| chr8:7856288 | A | G | 2 | a0007c0007t0001g0075 a0008c0010t0001g0052 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.215-4358A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7856288 | |||||||
| chr8:7856372 | T | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.215-4274T>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7856372 | |||||||
| chr8:7856416 | T | G | 1 | a0001c0001t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215-4230T>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7856416 | |||||||
| chr8:7856484 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215-4162C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7856484 | |||||||
| chr8:7856487 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215-4159G>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7856487 | |||||||
| chr8:7856519 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215-4127C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7856519 | |||||||
| chr8:7856627 | T | A | 17 | a0002c0002t0001g0005 a0002c0002t0001g0009 a0002c0002t0001g0042 others(14): Show |
26 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.215-4019T>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7856627 | |||||||
| chr8:7856950 | G | A | 2 | a0001c0001t0001g0037 a0003c0003t0001g0051 |
2 | HG00323.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.215-3696G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7856950 | |||||||
| chr8:7857135 | A | C | 1 | a0001c0001t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215-3511A>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857135 | |||||||
| chr8:7857282 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.215-3364G>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857282 | |||||||
| chr8:7857391 | G | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0002c0002t0001g0064 others(6): Show |
10 | HG01361.hp2 HG01515.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-3255G>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857391 | |||||||
| chr8:7857443 | C | CTT | 5 | a0001c0001t0001g0037 a0001c0001t0001g0084 a0001c0001t0001g0087 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-3184_215-3183d others(4): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7857443 | ||||||
| chr8:7857443 | CT | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(46): Show |
61 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.215-3183delT | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7857443 | ||||||
| chr8:7857446 | T | TC | 28 | a0001c0001t0001g0018 a0001c0001t0001g0077 a0001c0001t0001g0082 others(25): Show |
41 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.215-3200_215-3199i others(3): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857446 | |||||||
| chr8:7857447 | T | C | 12 | a0002c0002t0001g0061 a0002c0002t0001g0069 a0002c0002t0001g0095 others(9): Show |
12 | HG00323.hp2 HG01167.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-3199T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857447 | |||||||
| chr8:7857574 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215-3072T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857574 | |||||||
| chr8:7857627 | C | CT | 5 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0053 others(2): Show |
8 | HG00735.hp1 HG01496.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-3010dupT | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7857627 | ||||||
| chr8:7857638 | A | G | 55 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0063 others(52): Show |
69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.215-3008A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857638 | |||||||
| chr8:7857653 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.215-2993C>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857653 | |||||||
| chr8:7857692 | G | A | 54 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0063 others(51): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.215-2954G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857692 | |||||||
| chr8:7857787 | A | C | 11 | a0001c0001t0001g0037 a0001c0001t0001g0063 a0001c0001t0001g0079 others(8): Show |
12 | HG01361.hp2 HG01515.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-2859A>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857787 | |||||||
| chr8:7857802 | C | A | 11 | a0001c0001t0001g0037 a0001c0001t0001g0063 a0001c0001t0001g0079 others(8): Show |
12 | HG01361.hp2 HG01515.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.215-2844C>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857802 | |||||||
| chr8:7857920 | G | GT | 54 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0077 others(51): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.215-2726_215-2725i others(3): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857920 | |||||||
| chr8:7857923 | G | A | 54 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0077 others(51): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.215-2723G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7857923 | |||||||
| chr8:7858107 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215-2539T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7858107 | |||||||
| chr8:7858179 | T | A | 54 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0077 others(51): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.215-2467T>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7858179 | |||||||
| chr8:7858265 | C | A | 42 | a0001c0001t0001g0018 a0001c0001t0001g0077 a0001c0001t0001g0082 others(39): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.215-2381C>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7858265 | |||||||
| chr8:7858509 | A | C | 4 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0094 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-2137A>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7858509 | |||||||
| chr8:7858577 | G | GT | 44 | a0001c0001t0001g0037 a0001c0001t0001g0079 a0001c0001t0001g0084 others(41): Show |
57 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.215-2059dupT | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7858577 | ||||||
| chr8:7858577 | G | GTT | 8 | a0001c0001t0001g0018 a0001c0001t0001g0077 a0001c0001t0001g0082 others(5): Show |
9 | HG00140.hp1 HG00323.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-2060_215-2059d others(4): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7858577 | ||||||
| chr8:7858624 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215-2022T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7858624 | |||||||
| chr8:7858707 | T | C | 5 | a0001c0001t0001g0012 a0001c0001t0002g0032 a0006c0006t0001g0020 others(2): Show |
6 | HG02145.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.215-1939T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7858707 | |||||||
| chr8:7858775 | G | A | 1 | a0008c0010t0001g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.215-1871G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7858775 | |||||||
| chr8:7858831 | T | A | 35 | a0001c0001t0001g0088 a0002c0002t0001g0004 a0002c0002t0001g0005 others(32): Show |
47 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.215-1815T>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7858831 | |||||||
| chr8:7859038 | A | C | 5 | a0001c0001t0001g0037 a0001c0001t0001g0084 a0001c0001t0001g0087 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-1608A>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7859038 | |||||||
| chr8:7859201 | A | G | 1 | a0005c0004t0001g0078 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1445A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7859201 | |||||||
| chr8:7859202 | G | A | 1 | a0005c0004t0001g0078 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1444G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7859202 | |||||||
| chr8:7859262 | T | G | 1 | a0001c0001t0001g0058 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.215-1384T>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7859262 | |||||||
| chr8:7859332 | A | G | 1 | a0003c0003t0001g0047 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.215-1314A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7859332 | |||||||
| chr8:7859462 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.215-1184A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7859462 | |||||||
| chr8:7859463 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.215-1183A>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7859463 | |||||||
| chr8:7859493 | G | GGGGTATG others(7): Show |
1 | a0001c0001t0001g0079 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.215-1152_215-1139d others(16): Show |
SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7859493 | ||||||
| chr8:7859741 | A | AT | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(93): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.215-902dupT | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7859741 | ||||||
| chr8:7859800 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215-846T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7859800 | |||||||
| chr8:7859831 | AG | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(50): Show |
71 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.215-813delG | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 7859831 | ||||||
| chr8:7860070 | A | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0037 others(18): Show |
26 | HG00438.hp2 HG00544.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.215-576A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860070 | |||||||
| chr8:7860158 | T | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0094 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-488T>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860158 | |||||||
| chr8:7860224 | C | T | 1 | a0005c0004t0001g0036 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.215-422C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860224 | |||||||
| chr8:7860339 | C | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0039 others(8): Show |
16 | HG00438.hp2 HG00544.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-307C>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860339 | |||||||
| chr8:7860362 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0039 others(9): Show |
17 | HG00438.hp2 HG00544.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.215-284A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860362 | |||||||
| chr8:7860371 | G | A | 3 | a0001c0001t0001g0098 a0004c0005t0001g0096 a0004c0005t0001g0097 |
3 | HG02451.hp1 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.215-275G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860371 | |||||||
| chr8:7860386 | A | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0039 others(8): Show |
16 | HG00438.hp2 HG00544.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-260A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860386 | |||||||
| chr8:7860393 | C | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(11): Show |
21 | HG00438.hp2 HG00544.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.215-253C>T | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860393 | |||||||
| chr8:7860398 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0039 others(8): Show |
16 | HG00438.hp2 HG00544.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-248G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860398 | |||||||
| chr8:7860462 | A | G | 2 | a0004c0005t0001g0096 a0004c0005t0001g0097 |
2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.215-184A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860462 | |||||||
| chr8:7860539 | A | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0039 others(8): Show |
16 | HG00438.hp2 HG00544.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-107A>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860539 | |||||||
| chr8:7860571 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.215-75G>A | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860571 | |||||||
| chr8:7860575 | T | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0039 others(12): Show |
20 | HG00438.hp2 HG00544.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-71T>C | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860575 | |||||||
| chr8:7860584 | T | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0039 others(8): Show |
16 | HG00438.hp2 HG00544.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.215-62T>G | SPAG11A | ENSG00000178287.18 | transcript | ENST00000642566.2 | protein_coding | 2/2 | chr8 | 7860584 |