Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 132671 |
| ensemblid | ENSG00000163071.11 |
| hgncid | 29579 |
| symbol | SPATA18 |
| name | spermatogenesis associated 18 |
| refseq_nuc | NM_145263.4 |
| refseq_prot | NP_660306.1 |
| ensembl_nuc | ENST00000295213.9 |
| ensembl_prot | ENSP00000295213.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 52051304 |
| end | 52097299 |
| strand | + |
| ver | v1.2 |
| region | chr4:52051304-52097299 |
| region5000 | chr4:52046304-52102299 |
| regionname0 | SPATA18_chr4_52051304_52097299 |
| regionname5000 | SPATA18_chr4_52046304_52102299 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 538 | 196 | 61 | 22 | 84 | 7 | 20 | 65 | SPATA18_chr4_52046304_52102299 | SPATA18 | MAENL others(533): Show |
chr4 | 52046304 | 52102299 |
| a0002 | 0/0 | 538 | 98 | 8 | 22 | 50 | 9 | 9 | 39 | SPATA18_chr4_52046304_52102299 | SPATA18 | MAENL others(533): Show |
chr4 | 52046304 | 52102299 |
| a0003 | 0/0 | 538 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | MAENL others(533): Show |
chr4 | 52046304 | 52102299 |
| a0004 | 0/0 | 538 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SPATA18_chr4_52046304_52102299 | SPATA18 | MAENL others(533): Show |
chr4 | 52046304 | 52102299 |
| a0005 | 0/0 | 538 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | MAENL others(533): Show |
chr4 | 52046304 | 52102299 |
| a0006 | 0/0 | 538 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | MAENL others(533): Show |
chr4 | 52046304 | 52102299 |
| a0007 | 0/0 | 538 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | MAENL others(533): Show |
chr4 | 52046304 | 52102299 |
| a0008 | 0/0 | 538 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | MAENL others(533): Show |
chr4 | 52046304 | 52102299 |
| a0009 | 0/0 | 497 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | MAENL others(492): Show |
chr4 | 52046304 | 52102299 |
| a0010 | 0/0 | 538 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | MAENL others(533): Show |
chr4 | 52046304 | 52102299 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1614 | 190 | 60 | 22 | 79 | 7 | 20 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 | ||
| a0001c0003 | 0/0 | 1614 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 | ||
| a0001c0011 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 | ||
| a0002c0002 | 0/0 | 1614 | 98 | 8 | 22 | 50 | 9 | 9 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 | ||
| a0003c0005 | 0/0 | 1614 | 3 | 2 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 | ||
| a0004c0004 | 0/0 | 1614 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 | ||
| a0005c0007 | 0/0 | 1614 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 | ||
| a0006c0006 | 0/0 | 1614 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 | ||
| a0007c0009 | 0/0 | 1614 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 | ||
| a0008c0008 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 | ||
| a0009c0010 | 0/0 | 1614 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 | ||
| a0010c0012 | 0/0 | 1614 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | ATGGC others(1609): Show |
chr4 | 52046304 | 52102299 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4429 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0002 | 0/1 | 4430 | 73 | 5 | 11 | 50 | 0 | 6 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0003 | 0/0 | 4429 | 54 | 5 | 7 | 27 | 6 | 9 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0004 | 1/0 | 4430 | 42 | 38 | 3 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0005 | 0/0 | 4431 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4426): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0006 | 0/0 | 4431 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4426): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0007 | 0/0 | 4429 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0009 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0010 | 0/0 | 4430 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0011 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0012 | 0/0 | 4429 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0013 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0015 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0016 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0018 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0019 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0020 | 0/0 | 4431 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4426): Show |
chr4 | 52046304 | 52102299 |
| a0001c0001t0021 | 0/0 | 4431 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4426): Show |
chr4 | 52046304 | 52102299 |
| a0001c0003t0003 | 0/0 | 4429 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0001c0011t0004 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0002c0002t0001 | 0/0 | 4429 | 95 | 8 | 21 | 49 | 9 | 8 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0002c0002t0002 | 0/0 | 4430 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0002c0002t0004 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0002c0002t0008 | 0/0 | 4429 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0003c0005t0001 | 0/0 | 4429 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0003c0005t0004 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0003c0005t0017 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0004c0004t0001 | 0/0 | 4429 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0005c0007t0002 | 0/0 | 4430 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| a0006c0006t0003 | 0/0 | 4429 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0007c0009t0001 | 0/0 | 4429 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0008c0008t0014 | 0/0 | 4429 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0009c0010t0001 | 0/0 | 4429 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4424): Show |
chr4 | 52046304 | 52102299 |
| a0010c0012t0002 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | AGTCC others(4425): Show |
chr4 | 52046304 | 52102299 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0006 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0005g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0006g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0010g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0011g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0012g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0015g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0018g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0019g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0020g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0001t0021g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0003t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0001c0011t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0001 | 0/0 | 12 | 0 | 7 | 4 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0002c0002t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0003c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0003c0005t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0003c0005t0017g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0004c0004t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0004c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0005c0007t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0006c0006t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0006c0006t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0007c0009t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0008c0008t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0009c0010t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| a0010c0012t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0169 | EUR | GBR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0217 | EUR | GBR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0170 | EUR | FIN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0154 | EUR | FIN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0131 | EUR | FIN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0160 | EUR | FIN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0168 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01168 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0210 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0149 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0126 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0034 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0034 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01884 | hp2 | a0001 | c0001 | t0021 | g0218 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0156 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0204 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0172 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0214 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02027 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0162 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02132 | hp1 | a0005 | c0007 | t0002 | g0003 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02132 | hp2 | a0007 | c0009 | t0001 | g0032 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02258 | hp1 | a0008 | c0008 | t0014 | g0036 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0221 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0191 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0166 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0094 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0122 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0157 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0088 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03225 | hp1 | a0001 | c0001 | t0016 | g0005 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0181 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0040 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0219 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03540 | hp2 | a0003 | c0005 | t0001 | g0119 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0158 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03669 | hp1 | a0003 | c0005 | t0017 | g0120 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0171 | SAS | STU | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0207 | SAS | STU | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0082 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03710 | hp2 | a0001 | c0001 | t0009 | g0076 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0177 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0043 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03927 | hp1 | a0002 | c0002 | t0004 | g0208 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0081 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0087 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0139 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG04228 | hp1 | a0001 | c0001 | t0018 | g0003 | SAS | STU | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | STU | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18522 | hp2 | a0006 | c0006 | t0003 | g0133 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | CHB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | CHB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | CHB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18940 | hp2 | a0005 | c0007 | t0002 | g0003 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18943 | hp2 | a0004 | c0004 | t0001 | g0015 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18957 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18959 | hp1 | a0001 | c0003 | t0003 | g0111 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18959 | hp2 | a0001 | c0001 | t0012 | g0145 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18967 | hp2 | a0009 | c0010 | t0001 | g0211 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18969 | hp2 | a0002 | c0002 | t0008 | g0188 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18984 | hp2 | a0001 | c0003 | t0003 | g0090 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18995 | hp2 | a0004 | c0004 | t0001 | g0196 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19010 | hp2 | a0001 | c0003 | t0003 | g0050 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | LWK | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19030 | hp2 | a0001 | c0011 | t0004 | g0113 | AFR | LWK | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19043 | hp1 | a0003 | c0005 | t0004 | g0121 | AFR | LWK | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | LWK | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19083 | hp2 | a0010 | c0012 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19085 | hp1 | a0004 | c0004 | t0001 | g0015 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19085 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA20129 | hp1 | a0001 | c0001 | t0020 | g0222 | AFR | ASW | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | ASW | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0042 | EUR | TSI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0159 | EUR | TSI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0041 | EUR | TSI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA20805 | hp2 | a0001 | c0001 | t0011 | g0118 | EUR | TSI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | USA | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| HG06807 | hp2 | a0006 | c0006 | t0003 | g0134 | AFR | USA | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | USA | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | USA | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0109 | REF | REF | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0114 | REF | REF | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:52069832 | C | T | 1 | a0003 | 3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.434C>T | p.Thr145Ile | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/13 | 835/4430 | 434/1617 | 145/538 | chr4 | 52069832 | |||
| chr4:52071925 | C | A | 1 | a0008 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.527C>A | p.Ser176Tyr | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/13 | 928/4430 | 527/1617 | 176/538 | chr4 | 52071925 | |||
| chr4:52071973 | G | A | 1 | a0004 | 3 | NA18943.hp2 NA18995.hp2 NA19085.hp1 |
missense_variant | MODERATE | c.575G>A | p.Ser192Asn | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/13 | 976/4430 | 575/1617 | 192/538 | chr4 | 52071973 | |||
| chr4:52072077 | T | C | 4 | a0002 a0004 a0007 others(1): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
missense_variant | MODERATE | c.679T>C | p.Ser227Pro | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/13 | 1080/4430 | 679/1617 | 227/538 | chr4 | 52072077 | |||
| chr4:52076820 | G | C | 1 | a0007 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.800G>C | p.Arg267Pro | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/13 | 1201/4430 | 800/1617 | 267/538 | chr4 | 52076820 | |||
| chr4:52076858 | G | A | 1 | a0006 | 2 | HG06807.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.838G>A | p.Ala280Thr | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/13 | 1239/4430 | 838/1617 | 280/538 | chr4 | 52076858 | |||
| chr4:52079908 | T | A | 1 | a0010 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.1344T>A | p.Phe448Leu | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/13 | 1745/4430 | 1344/1617 | 448/538 | chr4 | 52079908 | |||
| chr4:52082391 | C | T | 1 | a0005 | 2 | HG02132.hp1 NA18940.hp2 |
missense_variant | MODERATE | c.1360C>T | p.Arg454Cys | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/13 | 1761/4430 | 1360/1617 | 454/538 | chr4 | 52082391 | |||
| chr4:52084928 | C | T | 1 | a0009 | 1 | NA18967.hp2 | stop_gained | HIGH | c.1492C>T | p.Arg498* | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/13 | 1893/4430 | 1492/1617 | 498/538 | chr4 | 52084928 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:52076983 | G | A | 1 | a0001c0011 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.963G>A | p.Leu321Leu | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/13 | 1364/4430 | 963/1617 | 321/538 | chr4 | 52076983 | |||
| chr4:52079857 | G | A | 1 | a0001c0003 | 5 | NA18957.hp2 NA18959.hp1 NA18984.hp2 others(2): Show |
synonymous_variant | LOW | c.1293G>A | p.Gln431Gln | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/13 | 1694/4430 | 1293/1617 | 431/538 | chr4 | 52079857 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:52051461 | G | T | 3 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0021 |
3 | HG01884.hp2 HG03516.hp2 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-244G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/13 | 244 | chr4 | 52051461 | ||||||
| chr4:52051472 | C | T | 1 | a0001c0001t0018 | 1 | HG04228.hp1 | 5_prime_UTR_variant | MODIFIER | c.-233C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/13 | 233 | chr4 | 52051472 | ||||||
| chr4:52051626 | C | T | 1 | a0003c0005t0017 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/13 | 79 | chr4 | 52051626 | ||||||
| chr4:52095199 | C | T | 1 | a0001c0001t0016 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 312 | chr4 | 52095199 | ||||||
| chr4:52095203 | C | T | 1 | a0001c0001t0015 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 316 | chr4 | 52095203 | ||||||
| chr4:52095444 | A | T | 1 | a0008c0008t0014 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*557A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 557 | chr4 | 52095444 | ||||||
| chr4:52095558 | C | T | 1 | a0001c0001t0013 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*671C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 671 | chr4 | 52095558 | ||||||
| chr4:52095609 | G | T | 1 | a0008c0008t0014 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*722G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 722 | chr4 | 52095609 | ||||||
| chr4:52095751 | C | T | 1 | a0008c0008t0014 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*864C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 864 | chr4 | 52095751 | ||||||
| chr4:52095772 | A | G | 2 | a0001c0001t0005 a0001c0001t0021 |
5 | HG01884.hp2 HG02630.hp2 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*885A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 885 | chr4 | 52095772 | ||||||
| chr4:52095964 | C | A | 1 | a0001c0001t0007 | 2 | HG03704.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1077C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1077 | chr4 | 52095964 | ||||||
| chr4:52096234 | T | G | 1 | a0002c0002t0008 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1347T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1347 | chr4 | 52096234 | ||||||
| chr4:52096299 | T | C | 9 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0013 others(6): Show |
81 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1412T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1412 | chr4 | 52096299 | ||||||
| chr4:52096363 | C | T | 8 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0010 others(5): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1476C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1476 | chr4 | 52096363 | ||||||
| chr4:52096761 | C | CA | 4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0020 others(1): Show |
9 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1887dupA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1888 | INFO_REALIGN_3_PRIME | chr4 | 52096761 | |||||
| chr4:52096761 | CA | C | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(10): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1887delA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1887 | INFO_REALIGN_3_PRIME | chr4 | 52096761 | |||||
| chr4:52096773 | A | C | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(13): Show |
147 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1886A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1886 | chr4 | 52096773 | ||||||
| chr4:52097010 | C | T | 1 | a0001c0001t0011 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2123C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 2123 | chr4 | 52097010 | ||||||
| chr4:52097165 | G | A | 8 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0010 others(5): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2278G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 2278 | chr4 | 52097165 | ||||||
| chr4:52097214 | G | A | 1 | a0001c0001t0009 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2327G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 2327 | chr4 | 52097214 | ||||||
| chr4:52097290 | A | G | 1 | a0001c0001t0012 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2403A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 2403 | chr4 | 52097290 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:52051821 | CGCCCTCC others(77): Show |
C | 5 | a0001c0001t0004g0220 a0001c0001t0004g0221 a0001c0001t0019g0219 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+33_87+116delCCT others(81): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52051821 | ||||||
| chr4:52052096 | G | A | 1 | a0008c0008t0014g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.87+305G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052096 | |||||||
| chr4:52052127 | A | C | 1 | a0008c0008t0014g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.87+336A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052127 | |||||||
| chr4:52052302 | T | C | 1 | a0001c0001t0003g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.87+511T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052302 | |||||||
| chr4:52052382 | T | C | 1 | a0001c0001t0002g0038 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.87+591T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052382 | |||||||
| chr4:52052537 | C | T | 73 | a0001c0001t0002g0031 a0001c0001t0002g0167 a0001c0001t0002g0184 others(70): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.87+746C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052537 | |||||||
| chr4:52052572 | G | A | 5 | a0002c0002t0001g0016 a0002c0002t0001g0039 a0002c0002t0001g0040 others(2): Show |
6 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.87+781G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052572 | |||||||
| chr4:52052726 | G | C | 1 | a0002c0002t0001g0043 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.87+935G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052726 | |||||||
| chr4:52053073 | A | G | 2 | a0001c0001t0003g0154 a0001c0001t0003g0155 |
2 | HG00280.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.87+1282A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52053073 | |||||||
| chr4:52053453 | C | A | 1 | a0001c0001t0002g0044 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.87+1662C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52053453 | |||||||
| chr4:52053482 | A | T | 1 | a0002c0002t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.87+1691A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52053482 | |||||||
| chr4:52053709 | C | T | 1 | a0002c0002t0001g0216 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.87+1918C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52053709 | |||||||
| chr4:52053955 | C | A | 1 | a0002c0002t0001g0045 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.87+2164C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52053955 | |||||||
| chr4:52054100 | G | T | 1 | a0001c0001t0020g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.87+2309G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054100 | |||||||
| chr4:52054172 | T | C | 1 | a0001c0001t0021g0218 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.87+2381T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054172 | |||||||
| chr4:52054320 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.87+2529A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054320 | |||||||
| chr4:52054388 | C | G | 2 | a0001c0001t0002g0044 a0001c0001t0002g0152 |
2 | NA18967.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.87+2597C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054388 | |||||||
| chr4:52054393 | G | A | 4 | a0001c0001t0004g0017 a0001c0001t0004g0046 a0001c0001t0004g0047 others(1): Show |
5 | HG02109.hp2 HG02622.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+2602G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054393 | |||||||
| chr4:52054431 | A | G | 1 | a0001c0001t0004g0151 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.87+2640A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054431 | |||||||
| chr4:52054469 | A | C | 1 | a0002c0002t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.87+2678A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054469 | |||||||
| chr4:52054897 | A | AACATGGT others(35): Show |
1 | a0002c0002t0001g0045 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.87+3107_87+3148dup others(42): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52054897 | ||||||
| chr4:52055288 | C | G | 127 | a0001c0001t0001g0130 a0001c0001t0002g0031 a0001c0001t0002g0143 others(124): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.87+3497C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52055288 | |||||||
| chr4:52055835 | G | A | 1 | a0001c0001t0011g0118 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.87+4044G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52055835 | |||||||
| chr4:52056169 | C | G | 2 | a0001c0001t0004g0026 a0001c0001t0004g0117 |
3 | HG02486.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.88-4250C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056169 | |||||||
| chr4:52056269 | T | G | 1 | a0001c0001t0002g0049 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.88-4150T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056269 | |||||||
| chr4:52056455 | A | G | 4 | a0001c0001t0004g0017 a0001c0001t0004g0046 a0001c0001t0004g0047 others(1): Show |
5 | HG02109.hp2 HG02622.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-3964A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056455 | |||||||
| chr4:52056498 | GATCAGTA | G | 2 | a0002c0002t0001g0035 a0002c0002t0001g0215 |
3 | NA18957.hp1 NA19005.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.88-3918_88-3912del others(7): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52056498 | ||||||
| chr4:52056543 | T | C | 3 | a0003c0005t0001g0119 a0003c0005t0004g0121 a0003c0005t0017g0120 |
3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.88-3876T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056543 | |||||||
| chr4:52056560 | C | CT | 75 | a0001c0001t0002g0031 a0001c0001t0002g0167 a0001c0001t0002g0184 others(72): Show |
98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.88-3857dupT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52056560 | ||||||
| chr4:52056646 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.88-3773C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056646 | |||||||
| chr4:52056785 | C | G | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.88-3634C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056785 | |||||||
| chr4:52057026 | C | T | 3 | a0002c0002t0001g0212 a0002c0002t0001g0213 a0009c0010t0001g0211 |
3 | NA18967.hp2 NA18993.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.88-3393C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057026 | |||||||
| chr4:52057039 | C | T | 117 | a0001c0001t0001g0130 a0001c0001t0002g0031 a0001c0001t0002g0143 others(114): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.88-3380C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057039 | |||||||
| chr4:52057297 | T | G | 75 | a0001c0001t0002g0031 a0001c0001t0002g0167 a0001c0001t0002g0184 others(72): Show |
98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.88-3122T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057297 | |||||||
| chr4:52057517 | C | G | 3 | a0003c0005t0001g0119 a0003c0005t0004g0121 a0003c0005t0017g0120 |
3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.88-2902C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057517 | |||||||
| chr4:52057795 | T | C | 1 | a0002c0002t0001g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.88-2624T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057795 | |||||||
| chr4:52057882 | G | A | 2 | a0001c0001t0019g0219 a0001c0001t0020g0222 |
2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.88-2537G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057882 | |||||||
| chr4:52058099 | A | G | 1 | a0002c0002t0001g0034 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.88-2320A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058099 | |||||||
| chr4:52058239 | G | C | 1 | a0001c0003t0003g0050 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.88-2180G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058239 | |||||||
| chr4:52058270 | T | G | 127 | a0001c0001t0001g0130 a0001c0001t0002g0031 a0001c0001t0002g0143 others(124): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.88-2149T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058270 | |||||||
| chr4:52058272 | T | C | 122 | a0001c0001t0001g0130 a0001c0001t0002g0031 a0001c0001t0002g0143 others(119): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.88-2147T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058272 | |||||||
| chr4:52058298 | T | TTTTGGGA others(10): Show |
2 | a0002c0002t0001g0041 a0002c0002t0001g0042 |
2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.88-2120_88-2104dup others(17): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52058298 | ||||||
| chr4:52058331 | G | GA | 4 | a0003c0005t0001g0119 a0003c0005t0004g0121 a0003c0005t0017g0120 others(1): Show |
4 | HG02258.hp1 HG03540.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-2082dupA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52058331 | ||||||
| chr4:52058462 | G | A | 3 | a0003c0005t0001g0119 a0003c0005t0004g0121 a0003c0005t0017g0120 |
3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.88-1957G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058462 | |||||||
| chr4:52058612 | G | A | 77 | a0001c0001t0002g0031 a0001c0001t0002g0167 a0001c0001t0002g0184 others(74): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.88-1807G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058612 | |||||||
| chr4:52058774 | A | T | 1 | a0001c0001t0004g0025 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.88-1645A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058774 | |||||||
| chr4:52059210 | A | T | 1 | a0002c0002t0001g0210 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.88-1209A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52059210 | |||||||
| chr4:52059340 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.88-1079A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52059340 | |||||||
| chr4:52059343 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.88-1076C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52059343 | |||||||
| chr4:52059789 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.88-630T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52059789 | |||||||
| chr4:52060020 | A | C | 1 | a0001c0001t0019g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.88-399A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52060020 | |||||||
| chr4:52060050 | T | A | 122 | a0001c0001t0001g0130 a0001c0001t0002g0031 a0001c0001t0002g0143 others(119): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.88-369T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52060050 | |||||||
| chr4:52060099 | A | T | 4 | a0001c0001t0003g0037 a0001c0001t0003g0146 a0001c0001t0003g0147 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-320A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52060099 | |||||||
| chr4:52060234 | G | A | 2 | a0002c0002t0001g0157 a0002c0002t0001g0158 |
2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.88-185G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52060234 | |||||||
| chr4:52060947 | C | A | 82 | a0001c0001t0002g0031 a0001c0001t0002g0167 a0001c0001t0002g0184 others(79): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.309+50C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52060947 | |||||||
| chr4:52061048 | A | T | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.309+151A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061048 | |||||||
| chr4:52061063 | A | G | 122 | a0001c0001t0001g0130 a0001c0001t0002g0031 a0001c0001t0002g0143 others(119): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.309+166A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061063 | |||||||
| chr4:52061231 | C | A | 2 | a0001c0001t0004g0018 a0001c0001t0004g0052 |
3 | HG02280.hp2 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.309+334C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061231 | |||||||
| chr4:52061315 | T | G | 1 | a0002c0002t0001g0159 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.309+418T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061315 | |||||||
| chr4:52061487 | A | AAAT | 10 | a0001c0001t0002g0031 a0001c0001t0003g0027 a0001c0001t0003g0124 others(7): Show |
13 | HG00099.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.309+623_309+625dup others(3): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | ||||||
| chr4:52061487 | A | AAATAAT | 57 | a0001c0001t0002g0167 a0001c0001t0002g0184 a0001c0001t0002g0185 others(54): Show |
72 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.309+620_309+625dup others(6): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | ||||||
| chr4:52061487 | A | AAATAATA others(2): Show |
21 | a0001c0001t0001g0130 a0001c0001t0003g0028 a0001c0001t0003g0029 others(18): Show |
28 | HG01257.hp1 HG01258.hp1 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.309+617_309+625dup others(9): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | ||||||
| chr4:52061487 | A | AAATAATA others(5): Show |
22 | a0001c0001t0003g0006 a0001c0001t0003g0030 a0001c0001t0003g0131 others(19): Show |
26 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.309+614_309+625dup others(12): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | ||||||
| chr4:52061487 | A | AAATAATA others(8): Show |
11 | a0001c0001t0002g0143 a0001c0001t0003g0037 a0001c0001t0003g0144 others(8): Show |
11 | HG01978.hp1 HG01993.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.309+611_309+625dup others(15): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | ||||||
| chr4:52061487 | AAAT | A | 95 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(92): Show |
140 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.309+623_309+625del others(3): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | ||||||
| chr4:52061487 | AAATAAT | A | 4 | a0001c0001t0002g0044 a0001c0001t0002g0152 a0001c0001t0004g0220 others(1): Show |
4 | HG02258.hp2 HG03098.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.309+620_309+625del others(6): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | ||||||
| chr4:52061645 | A | G | 5 | a0002c0002t0001g0015 a0002c0002t0001g0195 a0002c0002t0001g0197 others(2): Show |
6 | HG02027.hp1 NA18943.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-575A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061645 | |||||||
| chr4:52061895 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.310-325A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061895 | |||||||
| chr4:52062186 | GT | G | 192 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(189): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.310-16delT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52062186 | ||||||
| chr4:52062186 | GTT | G | 7 | a0001c0001t0003g0126 a0001c0001t0003g0131 a0001c0001t0004g0054 others(4): Show |
7 | HG00323.hp1 HG01433.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-17_310-16delTT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52062186 | ||||||
| chr4:52062431 | G | A | 1 | a0001c0001t0003g0155 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.422+99G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062431 | |||||||
| chr4:52062469 | T | C | 1 | a0001c0001t0003g0140 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.422+137T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062469 | |||||||
| chr4:52062479 | T | A | 1 | a0001c0001t0004g0132 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.422+147T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062479 | |||||||
| chr4:52062568 | A | G | 2 | a0001c0001t0004g0123 a0001c0001t0015g0122 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.422+236A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062568 | |||||||
| chr4:52062698 | GGAAA | G | 3 | a0002c0002t0001g0159 a0002c0002t0001g0163 a0002c0002t0001g0193 |
3 | HG01433.hp1 HG02273.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.422+370_422+373del others(4): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 52062698 | ||||||
| chr4:52062724 | C | G | 1 | a0002c0002t0001g0192 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.422+392C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062724 | |||||||
| chr4:52062813 | T | A | 82 | a0001c0001t0002g0031 a0001c0001t0002g0167 a0001c0001t0002g0184 others(79): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.422+481T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062813 | |||||||
| chr4:52062986 | C | G | 2 | a0001c0001t0002g0008 a0001c0001t0002g0098 |
5 | HG00597.hp2 NA18970.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+654C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062986 | |||||||
| chr4:52063006 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.422+674G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063006 | |||||||
| chr4:52063155 | T | A | 2 | a0001c0001t0019g0219 a0001c0001t0020g0222 |
2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.422+823T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063155 | |||||||
| chr4:52063156 | A | T | 4 | a0001c0001t0003g0029 a0001c0001t0003g0155 a0002c0002t0001g0190 others(1): Show |
5 | HG02280.hp1 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+824A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063156 | |||||||
| chr4:52063317 | A | G | 1 | a0001c0001t0003g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422+985A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063317 | |||||||
| chr4:52063386 | A | G | 1 | a0001c0001t0003g0142 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.422+1054A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063386 | |||||||
| chr4:52063408 | C | G | 35 | a0001c0001t0001g0130 a0001c0001t0002g0143 a0001c0001t0003g0006 others(32): Show |
42 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.422+1076C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063408 | |||||||
| chr4:52063598 | C | T | 1 | a0001c0011t0004g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.422+1266C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063598 | |||||||
| chr4:52063655 | C | A | 1 | a0001c0001t0004g0151 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.422+1323C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063655 | |||||||
| chr4:52063819 | G | C | 1 | a0002c0002t0001g0045 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.422+1487G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063819 | |||||||
| chr4:52064183 | C | CTA | 16 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0038 others(13): Show |
18 | HG00673.hp2 HG02258.hp2 HG03098.hp1 others(15): Show |
intron_variant | MODIFIER | c.422+1871_422+1872d others(4): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 52064183 | ||||||
| chr4:52064183 | C | CTATA | 88 | a0001c0001t0001g0130 a0001c0001t0002g0031 a0001c0001t0002g0143 others(85): Show |
111 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.422+1869_422+1872d others(6): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 52064183 | ||||||
| chr4:52064183 | C | CTATATA | 27 | a0001c0001t0002g0167 a0001c0001t0004g0123 a0001c0001t0015g0122 others(24): Show |
35 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.422+1867_422+1872d others(8): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 52064183 | ||||||
| chr4:52064248 | G | A | 3 | a0003c0005t0001g0119 a0003c0005t0004g0121 a0003c0005t0017g0120 |
3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.422+1916G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064248 | |||||||
| chr4:52064354 | T | C | 7 | a0001c0001t0003g0169 a0002c0002t0001g0034 a0002c0002t0001g0160 others(4): Show |
8 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.422+2022T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064354 | |||||||
| chr4:52064381 | G | A | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.422+2049G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064381 | |||||||
| chr4:52064383 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.422+2051G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064383 | |||||||
| chr4:52064476 | C | G | 3 | a0001c0001t0019g0219 a0001c0001t0020g0222 a0001c0001t0021g0218 |
3 | HG01884.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.422+2144C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064476 | |||||||
| chr4:52064504 | C | G | 1 | a0002c0002t0001g0045 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.422+2172C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064504 | |||||||
| chr4:52064507 | A | G | 75 | a0001c0001t0002g0031 a0001c0001t0002g0167 a0001c0001t0002g0184 others(72): Show |
98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.422+2175A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064507 | |||||||
| chr4:52064581 | T | C | 1 | a0001c0001t0003g0127 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.422+2249T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064581 | |||||||
| chr4:52064679 | G | T | 1 | a0001c0001t0004g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.422+2347G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064679 | |||||||
| chr4:52064696 | G | T | 1 | a0002c0002t0001g0201 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.422+2364G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064696 | |||||||
| chr4:52064822 | T | A | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.422+2490T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064822 | |||||||
| chr4:52064897 | A | G | 1 | a0002c0002t0008g0188 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.422+2565A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064897 | |||||||
| chr4:52064974 | A | G | 7 | a0001c0001t0004g0025 a0001c0001t0004g0093 a0001c0001t0004g0094 others(4): Show |
8 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.422+2642A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064974 | |||||||
| chr4:52064996 | A | T | 1 | a0001c0001t0002g0092 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.422+2664A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064996 | |||||||
| chr4:52065006 | G | C | 1 | a0002c0002t0001g0171 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.422+2674G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065006 | |||||||
| chr4:52065048 | T | C | 1 | a0002c0002t0001g0199 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.422+2716T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065048 | |||||||
| chr4:52065142 | T | G | 1 | a0001c0003t0003g0050 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.422+2810T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065142 | |||||||
| chr4:52065345 | T | G | 1 | a0001c0001t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.422+3013T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065345 | |||||||
| chr4:52065408 | C | T | 1 | a0001c0001t0012g0145 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.422+3076C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065408 | |||||||
| chr4:52065857 | A | G | 1 | a0001c0001t0003g0124 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.422+3525A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065857 | |||||||
| chr4:52065893 | T | C | 1 | a0002c0002t0002g0172 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.422+3561T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065893 | |||||||
| chr4:52066119 | A | G | 4 | a0003c0005t0001g0119 a0003c0005t0004g0121 a0003c0005t0017g0120 others(1): Show |
4 | HG02258.hp1 HG03540.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-3702A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066119 | |||||||
| chr4:52066224 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.423-3597C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066224 | |||||||
| chr4:52066300 | G | A | 1 | a0001c0001t0004g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.423-3521G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066300 | |||||||
| chr4:52066524 | G | A | 3 | a0003c0005t0001g0119 a0003c0005t0004g0121 a0003c0005t0017g0120 |
3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.423-3297G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066524 | |||||||
| chr4:52066659 | C | T | 122 | a0001c0001t0001g0130 a0001c0001t0002g0031 a0001c0001t0002g0143 others(119): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.423-3162C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066659 | |||||||
| chr4:52066813 | C | T | 127 | a0001c0001t0001g0130 a0001c0001t0002g0031 a0001c0001t0002g0143 others(124): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.423-3008C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066813 | |||||||
| chr4:52066990 | T | A | 1 | a0001c0001t0015g0122 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.423-2831T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066990 | |||||||
| chr4:52067049 | G | A | 1 | a0001c0001t0002g0010 | 3 | NA19009.hp2 NA19063.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.423-2772G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067049 | |||||||
| chr4:52067130 | G | T | 1 | a0001c0003t0003g0050 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.423-2691G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067130 | |||||||
| chr4:52067151 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.423-2670C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067151 | |||||||
| chr4:52067238 | T | A | 2 | a0002c0002t0001g0173 a0002c0002t0001g0191 |
2 | HG00738.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.423-2583T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067238 | |||||||
| chr4:52067332 | AT | A | 2 | a0001c0001t0002g0008 a0001c0001t0002g0098 |
5 | HG00597.hp2 NA18970.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.423-2483delT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 52067332 | ||||||
| chr4:52067354 | T | G | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.423-2467T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067354 | |||||||
| chr4:52067453 | C | A | 1 | a0004c0004t0001g0196 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.423-2368C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067453 | |||||||
| chr4:52067608 | C | T | 1 | a0001c0011t0004g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.423-2213C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067608 | |||||||
| chr4:52067644 | C | T | 1 | a0002c0002t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.423-2177C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067644 | |||||||
| chr4:52067701 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.423-2120T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067701 | |||||||
| chr4:52067742 | T | C | 1 | a0001c0001t0002g0064 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.423-2079T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067742 | |||||||
| chr4:52067881 | G | A | 1 | a0002c0002t0001g0202 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.423-1940G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067881 | |||||||
| chr4:52067977 | A | G | 1 | a0002c0002t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.423-1844A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067977 | |||||||
| chr4:52068396 | A | G | 1 | a0008c0008t0014g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.423-1425A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52068396 | |||||||
| chr4:52068802 | T | G | 1 | a0001c0001t0002g0065 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.423-1019T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52068802 | |||||||
| chr4:52069174 | T | A | 1 | a0001c0001t0002g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.423-647T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069174 | |||||||
| chr4:52069279 | A | T | 77 | a0001c0001t0002g0031 a0001c0001t0002g0167 a0001c0001t0002g0184 others(74): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.423-542A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069279 | |||||||
| chr4:52069289 | C | T | 3 | a0003c0005t0001g0119 a0003c0005t0004g0121 a0003c0005t0017g0120 |
3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.423-532C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069289 | |||||||
| chr4:52069349 | G | A | 1 | a0008c0008t0014g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.423-472G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069349 | |||||||
| chr4:52069481 | G | C | 1 | a0002c0002t0001g0174 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.423-340G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069481 | |||||||
| chr4:52069486 | T | A | 1 | a0002c0002t0001g0207 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.423-335T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069486 | |||||||
| chr4:52069515 | A | G | 127 | a0001c0001t0001g0130 a0001c0001t0002g0031 a0001c0001t0002g0143 others(124): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.423-306A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069515 | |||||||
| chr4:52069645 | A | G | 1 | a0001c0001t0004g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.423-176A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069645 | |||||||
| chr4:52069652 | C | G | 1 | a0002c0002t0001g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.423-169C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069652 | |||||||
| chr4:52069679 | T | C | 2 | a0001c0001t0004g0099 a0001c0001t0004g0110 |
2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.423-142T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069679 | |||||||
| chr4:52070040 | TTA | T | 60 | a0001c0001t0001g0130 a0001c0001t0002g0153 a0001c0001t0003g0002 others(57): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.518+140_518+141del others(2): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 52070040 | ||||||
| chr4:52070046 | A | G | 8 | a0001c0001t0003g0002 a0001c0001t0003g0089 a0001c0001t0003g0091 others(5): Show |
17 | HG00597.hp1 HG02074.hp1 NA18945.hp2 others(14): Show |
intron_variant | MODIFIER | c.518+130A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070046 | |||||||
| chr4:52070158 | G | A | 7 | a0001c0001t0004g0025 a0001c0001t0004g0093 a0001c0001t0004g0094 others(4): Show |
8 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.518+242G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070158 | |||||||
| chr4:52070243 | T | A | 1 | a0001c0001t0003g0107 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.518+327T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070243 | |||||||
| chr4:52070323 | G | A | 1 | a0001c0001t0007g0082 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.518+407G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070323 | |||||||
| chr4:52070397 | G | A | 1 | a0001c0001t0004g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.518+481G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070397 | |||||||
| chr4:52070419 | A | C | 122 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(119): Show |
164 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.518+503A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070419 | |||||||
| chr4:52070472 | T | A | 1 | a0001c0001t0002g0143 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.518+556T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070472 | |||||||
| chr4:52070534 | T | G | 2 | a0006c0006t0003g0133 a0006c0006t0003g0134 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.518+618T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070534 | |||||||
| chr4:52070535 | G | A | 3 | a0001c0001t0005g0011 a0001c0001t0005g0135 a0001c0001t0021g0218 |
5 | HG01884.hp2 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.518+619G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070535 | |||||||
| chr4:52070540 | A | G | 50 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(47): Show |
66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.518+624A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070540 | |||||||
| chr4:52070545 | G | T | 49 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(46): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.518+629G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070545 | |||||||
| chr4:52070561 | C | T | 1 | a0001c0001t0003g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.518+645C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070561 | |||||||
| chr4:52070562 | A | T | 49 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(46): Show |
64 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.518+646A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070562 | |||||||
| chr4:52070578 | A | T | 1 | a0003c0005t0017g0120 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.518+662A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070578 | |||||||
| chr4:52070699 | A | G | 7 | a0001c0001t0004g0025 a0001c0001t0004g0093 a0001c0001t0004g0094 others(4): Show |
8 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.518+783A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070699 | |||||||
| chr4:52070758 | T | A | 107 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(104): Show |
147 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.518+842T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070758 | |||||||
| chr4:52070880 | TG | T | 25 | a0001c0001t0002g0022 a0001c0001t0002g0055 a0001c0001t0002g0069 others(22): Show |
31 | HG00673.hp2 HG01243.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.518+975delG | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 52070880 | ||||||
| chr4:52070880 | TGG | T | 110 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(107): Show |
150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.518+974_518+975del others(2): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 52070880 | ||||||
| chr4:52070933 | C | A | 12 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0093 others(9): Show |
14 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.519-984C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070933 | |||||||
| chr4:52071006 | T | C | 3 | a0002c0002t0001g0015 a0004c0004t0001g0015 a0004c0004t0001g0196 |
4 | NA18943.hp2 NA18964.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.519-911T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071006 | |||||||
| chr4:52071010 | A | G | 1 | a0002c0002t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.519-907A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071010 | |||||||
| chr4:52071054 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.519-863A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071054 | |||||||
| chr4:52071061 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.519-856A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071061 | |||||||
| chr4:52071213 | T | G | 2 | a0001c0001t0004g0026 a0001c0001t0004g0117 |
3 | HG02486.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.519-704T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071213 | |||||||
| chr4:52071630 | A | G | 1 | a0008c0008t0014g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.519-287A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071630 | |||||||
| chr4:52071768 | T | G | 1 | a0002c0002t0001g0205 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.519-149T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071768 | |||||||
| chr4:52072216 | G | T | 2 | a0002c0002t0001g0173 a0002c0002t0001g0191 |
2 | HG00738.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.758+60G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072216 | |||||||
| chr4:52072217 | G | A | 2 | a0001c0001t0004g0026 a0001c0001t0004g0117 |
3 | HG02486.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.758+61G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072217 | |||||||
| chr4:52072445 | C | T | 3 | a0001c0001t0003g0081 a0001c0001t0003g0088 a0001c0001t0003g0106 |
3 | HG02738.hp1 HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.758+289C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072445 | |||||||
| chr4:52072596 | C | T | 1 | a0001c0001t0003g0139 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.758+440C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072596 | |||||||
| chr4:52072617 | G | C | 1 | a0002c0002t0001g0043 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.758+461G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072617 | |||||||
| chr4:52072625 | C | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0069 a0001c0001t0002g0080 |
4 | NA18961.hp2 NA18974.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+469C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072625 | |||||||
| chr4:52072802 | C | A | 1 | a0001c0001t0002g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.758+646C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072802 | |||||||
| chr4:52072889 | G | A | 1 | a0001c0001t0003g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.758+733G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072889 | |||||||
| chr4:52073298 | C | T | 1 | a0002c0002t0001g0182 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.758+1142C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073298 | |||||||
| chr4:52073374 | C | T | 1 | a0008c0008t0014g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.758+1218C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073374 | |||||||
| chr4:52073556 | G | A | 51 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(48): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.758+1400G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073556 | |||||||
| chr4:52073583 | G | A | 3 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0003g0085 |
3 | HG00558.hp2 HG00673.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.758+1427G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073583 | |||||||
| chr4:52073624 | T | G | 3 | a0001c0001t0005g0011 a0001c0001t0005g0135 a0001c0001t0021g0218 |
5 | HG01884.hp2 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.758+1468T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073624 | |||||||
| chr4:52073655 | T | G | 3 | a0001c0001t0002g0153 a0001c0001t0004g0220 a0001c0001t0004g0221 |
3 | HG02258.hp2 HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.758+1499T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073655 | |||||||
| chr4:52073816 | G | C | 16 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(13): Show |
27 | HG00597.hp2 HG00673.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.758+1660G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073816 | |||||||
| chr4:52073816 | G | T | 1 | a0001c0001t0002g0079 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.758+1660G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073816 | |||||||
| chr4:52073986 | C | T | 51 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(48): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.758+1830C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073986 | |||||||
| chr4:52074041 | C | T | 12 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0093 others(9): Show |
14 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.758+1885C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074041 | |||||||
| chr4:52074339 | T | C | 1 | a0001c0001t0004g0052 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.758+2183T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074339 | |||||||
| chr4:52074399 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.758+2243C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074399 | |||||||
| chr4:52074459 | C | T | 1 | a0001c0001t0003g0126 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.758+2303C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074459 | |||||||
| chr4:52074460 | G | A | 73 | a0001c0001t0002g0020 a0001c0001t0002g0059 a0001c0001t0002g0064 others(70): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.758+2304G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074460 | |||||||
| chr4:52074480 | A | G | 3 | a0001c0001t0005g0011 a0001c0001t0005g0135 a0001c0001t0021g0218 |
5 | HG01884.hp2 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.759-2299A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074480 | |||||||
| chr4:52074536 | T | C | 5 | a0001c0001t0004g0017 a0001c0001t0004g0046 a0001c0001t0004g0047 others(2): Show |
6 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.759-2243T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074536 | |||||||
| chr4:52074558 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.759-2221A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074558 | |||||||
| chr4:52074572 | G | C | 1 | a0001c0001t0003g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.759-2207G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074572 | |||||||
| chr4:52074607 | A | T | 46 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
62 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.759-2172A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074607 | |||||||
| chr4:52074684 | G | C | 7 | a0001c0001t0002g0004 a0001c0001t0002g0022 a0001c0001t0002g0069 others(4): Show |
14 | NA18612.hp2 NA18961.hp2 NA18968.hp2 others(11): Show |
intron_variant | MODIFIER | c.759-2095G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074684 | |||||||
| chr4:52075020 | G | A | 1 | a0001c0001t0003g0137 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.759-1759G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52075020 | |||||||
| chr4:52075101 | G | T | 1 | a0001c0001t0002g0105 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.759-1678G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52075101 | |||||||
| chr4:52075639 | C | T | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.759-1140C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52075639 | |||||||
| chr4:52075897 | A | G | 201 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(198): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.759-882A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52075897 | |||||||
| chr4:52076021 | A | G | 52 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(49): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.759-758A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076021 | |||||||
| chr4:52076100 | C | T | 55 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(52): Show |
79 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.759-679C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076100 | |||||||
| chr4:52076117 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.759-662T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076117 | |||||||
| chr4:52076208 | C | T | 201 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(198): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.759-571C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076208 | |||||||
| chr4:52076239 | A | T | 131 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(128): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.759-540A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076239 | |||||||
| chr4:52076392 | T | C | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0093 others(8): Show |
13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.759-387T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076392 | |||||||
| chr4:52076613 | G | T | 79 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0009 others(76): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.759-166G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076613 | |||||||
| chr4:52077132 | T | A | 1 | a0001c0001t0003g0140 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1020+92T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077132 | |||||||
| chr4:52077174 | T | G | 1 | a0001c0001t0003g0127 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1020+134T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077174 | |||||||
| chr4:52077244 | TTCCCTCC others(1): Show |
T | 50 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(47): Show |
66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1020+212_1020+219d others(10): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52077244 | ||||||
| chr4:52077244 | TTCCCTCC others(5): Show |
T | 1 | a0001c0001t0003g0091 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1020+212_1020+223d others(14): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52077244 | ||||||
| chr4:52077341 | T | TCTCTTTC others(5): Show |
3 | a0002c0002t0001g0168 a0002c0002t0001g0210 a0002c0002t0001g0214 |
3 | HG01081.hp1 HG01168.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1020+306_1020+317d others(14): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52077341 | ||||||
| chr4:52077348 | C | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0069 |
3 | NA18961.hp2 NA18974.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1020+308C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077348 | |||||||
| chr4:52077415 | CCTCT | C | 80 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0009 others(77): Show |
104 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1020+381_1020+384d others(6): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52077415 | ||||||
| chr4:52077422 | CTCCT | C | 3 | a0001c0001t0002g0049 a0001c0001t0004g0220 a0001c0001t0004g0221 |
3 | HG02258.hp2 HG03098.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1020+398_1020+401d others(6): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52077422 | ||||||
| chr4:52077572 | G | A | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1020+532G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077572 | |||||||
| chr4:52077687 | G | A | 1 | a0001c0001t0004g0024 | 2 | HG01167.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1020+647G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077687 | |||||||
| chr4:52077794 | C | T | 51 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(48): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1020+754C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077794 | |||||||
| chr4:52078108 | T | TA | 85 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(82): Show |
118 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1021-614dupA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52078108 | ||||||
| chr4:52078108 | TA | T | 128 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(125): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1021-614delA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52078108 | ||||||
| chr4:52078143 | A | C | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1021-592A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078143 | |||||||
| chr4:52078173 | C | A | 2 | a0002c0002t0001g0045 a0002c0002t0001g0200 |
2 | HG02074.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1021-562C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078173 | |||||||
| chr4:52078277 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1021-458G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078277 | |||||||
| chr4:52078478 | T | A | 52 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(49): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1021-257T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078478 | |||||||
| chr4:52078554 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1021-181T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078554 | |||||||
| chr4:52078664 | C | A | 2 | a0003c0005t0004g0121 a0003c0005t0017g0120 |
2 | HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1021-71C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078664 | |||||||
| chr4:52078721 | A | G | 1 | a0001c0001t0002g0044 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1021-14A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078721 | |||||||
| chr4:52078975 | C | T | 1 | a0002c0002t0001g0206 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1179+82C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52078975 | |||||||
| chr4:52078998 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0124 |
3 | NA18954.hp2 NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1179+105G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52078998 | |||||||
| chr4:52079041 | G | A | 79 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0009 others(76): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1179+148G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079041 | |||||||
| chr4:52079084 | G | A | 2 | a0002c0002t0001g0175 a0002c0002t0001g0182 |
2 | NA18951.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1179+191G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079084 | |||||||
| chr4:52079603 | G | A | 1 | a0008c0008t0014g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1180-141G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079603 | |||||||
| chr4:52079633 | C | T | 204 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(201): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1180-111C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079633 | |||||||
| chr4:52079652 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1180-92T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079652 | |||||||
| chr4:52079732 | T | C | 1 | a0002c0002t0001g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1180-12T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079732 | |||||||
| chr4:52079995 | A | G | 201 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(198): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1355+76A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52079995 | |||||||
| chr4:52080005 | C | CAA | 7 | a0002c0002t0001g0032 a0002c0002t0001g0150 a0002c0002t0001g0164 others(4): Show |
7 | HG00438.hp2 HG00609.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1355+86_1355+87ins others(2): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080005 | |||||||
| chr4:52080007 | C | T | 7 | a0002c0002t0001g0032 a0002c0002t0001g0150 a0002c0002t0001g0164 others(4): Show |
7 | HG00438.hp2 HG00609.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1355+88C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080007 | |||||||
| chr4:52080009 | G | A | 7 | a0002c0002t0001g0032 a0002c0002t0001g0150 a0002c0002t0001g0164 others(4): Show |
7 | HG00438.hp2 HG00609.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1355+90G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080009 | |||||||
| chr4:52080109 | C | G | 6 | a0002c0002t0001g0016 a0002c0002t0001g0039 a0002c0002t0001g0040 others(3): Show |
7 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1355+190C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080109 | |||||||
| chr4:52080243 | A | G | 3 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0003g0085 |
3 | HG00558.hp2 HG00673.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1355+324A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080243 | |||||||
| chr4:52080398 | C | G | 1 | a0002c0002t0001g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1355+479C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080398 | |||||||
| chr4:52080405 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1355+486T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080405 | |||||||
| chr4:52080432 | G | A | 9 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0093 others(6): Show |
11 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1355+513G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080432 | |||||||
| chr4:52080467 | G | T | 1 | a0001c0001t0007g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1355+548G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080467 | |||||||
| chr4:52080479 | C | T | 56 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(53): Show |
80 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1355+560C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080479 | |||||||
| chr4:52080523 | G | T | 1 | a0001c0001t0002g0058 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1355+604G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080523 | |||||||
| chr4:52080593 | C | G | 1 | a0001c0001t0003g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1355+674C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080593 | |||||||
| chr4:52080679 | C | T | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1355+760C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080679 | |||||||
| chr4:52080772 | G | T | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1355+853G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080772 | |||||||
| chr4:52080990 | T | C | 4 | a0001c0001t0002g0062 a0001c0001t0002g0072 a0001c0001t0002g0078 others(1): Show |
4 | HG02071.hp1 NA18974.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1355+1071T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080990 | |||||||
| chr4:52081029 | T | A | 1 | a0002c0002t0001g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1355+1110T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081029 | |||||||
| chr4:52081325 | T | G | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1356-1062T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081325 | |||||||
| chr4:52081541 | T | C | 200 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(197): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1356-846T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081541 | |||||||
| chr4:52081542 | G | A | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1356-845G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081542 | |||||||
| chr4:52081649 | A | G | 1 | a0001c0001t0003g0144 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1356-738A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081649 | |||||||
| chr4:52081825 | A | G | 1 | a0001c0001t0009g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1356-562A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081825 | |||||||
| chr4:52081827 | C | CT | 79 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0009 others(76): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1356-550dupT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 52081827 | ||||||
| chr4:52081851 | A | G | 1 | a0001c0001t0003g0030 | 2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1356-536A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081851 | |||||||
| chr4:52081883 | C | G | 1 | a0001c0001t0003g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1356-504C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081883 | |||||||
| chr4:52081945 | G | GGTTTCTA others(141): Show |
79 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0009 others(76): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1356-436_1356-435i others(150): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 52081945 | ||||||
| chr4:52081945 | G | GGTTTCTG others(141): Show |
53 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(50): Show |
76 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1356-408_1356-407i others(150): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 52081945 | ||||||
| chr4:52081945 | G | GGTTTCTG others(141): Show |
67 | a0001c0001t0001g0130 a0001c0001t0002g0153 a0001c0001t0003g0002 others(64): Show |
85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1356-295_1356-294i others(150): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 52081945 | ||||||
| chr4:52081980 | T | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0058 a0001c0001t0002g0185 |
3 | HG02129.hp2 HG04184.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1356-407T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081980 | |||||||
| chr4:52082043 | A | ATTTTGTC others(141): Show |
3 | a0001c0001t0002g0031 a0001c0001t0002g0058 a0001c0001t0002g0185 |
3 | HG02129.hp2 HG04184.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1356-295_1356-294i others(150): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 52082043 | ||||||
| chr4:52082043 | A | G | 1 | a0001c0001t0002g0031 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1356-344A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52082043 | |||||||
| chr4:52082072 | T | G | 1 | a0002c0002t0001g0159 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1356-315T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52082072 | |||||||
| chr4:52082180 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1356-207C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52082180 | |||||||
| chr4:52082668 | C | G | 52 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(49): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1479+158C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082668 | |||||||
| chr4:52082827 | G | A | 1 | a0001c0001t0004g0102 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1479+317G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082827 | |||||||
| chr4:52082846 | A | T | 51 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(48): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1479+336A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082846 | |||||||
| chr4:52082857 | A | T | 1 | a0006c0006t0003g0134 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1479+347A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082857 | |||||||
| chr4:52082874 | G | A | 2 | a0003c0005t0004g0121 a0003c0005t0017g0120 |
2 | HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1479+364G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082874 | |||||||
| chr4:52082896 | G | A | 201 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(198): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1479+386G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082896 | |||||||
| chr4:52083083 | G | C | 1 | a0003c0005t0004g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1479+573G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083083 | |||||||
| chr4:52083093 | TAAA | T | 212 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(209): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1479+589_1479+591d others(5): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 52083093 | ||||||
| chr4:52083137 | G | A | 2 | a0003c0005t0004g0121 a0003c0005t0017g0120 |
2 | HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1479+627G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083137 | |||||||
| chr4:52083343 | A | C | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0093 others(8): Show |
13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1479+833A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083343 | |||||||
| chr4:52083489 | C | A | 2 | a0001c0001t0004g0123 a0001c0001t0015g0122 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1479+979C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083489 | |||||||
| chr4:52083515 | C | T | 1 | a0002c0002t0001g0215 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1479+1005C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083515 | |||||||
| chr4:52083572 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1479+1062T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083572 | |||||||
| chr4:52083708 | C | T | 52 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(49): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1479+1198C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083708 | |||||||
| chr4:52083739 | G | T | 1 | a0001c0001t0004g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1480-1177G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083739 | |||||||
| chr4:52083741 | C | CT | 7 | a0001c0001t0002g0057 a0001c0001t0002g0092 a0001c0001t0002g0104 others(4): Show |
9 | HG01884.hp2 HG01981.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1480-1157dupT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 52083741 | ||||||
| chr4:52083741 | CT | C | 83 | a0001c0001t0002g0023 a0001c0001t0002g0056 a0001c0001t0002g0060 others(80): Show |
108 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1480-1157delT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 52083741 | ||||||
| chr4:52083825 | C | G | 44 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(41): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1480-1091C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083825 | |||||||
| chr4:52083843 | C | T | 52 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(49): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1480-1073C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083843 | |||||||
| chr4:52084009 | G | A | 52 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(49): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1480-907G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084009 | |||||||
| chr4:52084050 | CA | C | 187 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(184): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1480-851delA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 52084050 | ||||||
| chr4:52084094 | G | A | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1480-822G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084094 | |||||||
| chr4:52084146 | C | T | 55 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(52): Show |
79 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1480-770C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084146 | |||||||
| chr4:52084153 | A | G | 1 | a0001c0001t0020g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1480-763A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084153 | |||||||
| chr4:52084243 | A | G | 1 | a0001c0001t0020g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1480-673A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084243 | |||||||
| chr4:52084494 | A | C | 79 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0009 others(76): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1480-422A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084494 | |||||||
| chr4:52084706 | G | A | 2 | a0001c0001t0007g0082 a0001c0001t0007g0087 |
2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1480-210G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084706 | |||||||
| chr4:52084801 | C | A | 1 | a0002c0002t0001g0066 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1480-115C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084801 | |||||||
| chr4:52085047 | CT | C | 87 | a0001c0001t0002g0153 a0001c0001t0004g0025 a0001c0001t0004g0026 others(84): Show |
113 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1563+62delT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 52085047 | ||||||
| chr4:52085047 | CTT | C | 110 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(107): Show |
150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1563+61_1563+62del others(2): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 52085047 | ||||||
| chr4:52085236 | A | G | 1 | a0001c0001t0004g0068 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1563+237A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085236 | |||||||
| chr4:52085525 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1563+526A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085525 | |||||||
| chr4:52085546 | A | T | 1 | a0008c0008t0014g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1563+547A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085546 | |||||||
| chr4:52085690 | T | A | 51 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(48): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1563+691T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085690 | |||||||
| chr4:52085790 | T | A | 4 | a0001c0001t0002g0019 a0001c0001t0002g0055 a0001c0001t0002g0056 others(1): Show |
5 | HG00673.hp2 NA18951.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.1563+791T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085790 | |||||||
| chr4:52085920 | G | C | 133 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(130): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1563+921G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085920 | |||||||
| chr4:52086026 | T | C | 1 | a0002c0002t0001g0053 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1563+1027T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086026 | |||||||
| chr4:52086027 | G | A | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0093 others(8): Show |
13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1563+1028G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086027 | |||||||
| chr4:52086185 | A | G | 79 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0009 others(76): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1563+1186A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086185 | |||||||
| chr4:52086312 | A | G | 1 | a0001c0001t0003g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1563+1313A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086312 | |||||||
| chr4:52086319 | T | A | 52 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(49): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1563+1320T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086319 | |||||||
| chr4:52086369 | C | T | 55 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(52): Show |
79 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1563+1370C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086369 | |||||||
| chr4:52086375 | C | T | 1 | a0001c0001t0019g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1563+1376C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086375 | |||||||
| chr4:52086520 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1563+1521G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086520 | |||||||
| chr4:52086747 | G | A | 1 | a0008c0008t0014g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1563+1748G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086747 | |||||||
| chr4:52087072 | A | G | 201 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(198): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1563+2073A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087072 | |||||||
| chr4:52087076 | C | T | 1 | a0001c0001t0004g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1563+2077C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087076 | |||||||
| chr4:52087259 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1563+2260C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087259 | |||||||
| chr4:52087326 | C | T | 1 | a0003c0005t0004g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1563+2327C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087326 | |||||||
| chr4:52087406 | C | T | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1563+2407C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087406 | |||||||
| chr4:52087451 | T | A | 1 | a0001c0001t0012g0145 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1563+2452T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087451 | |||||||
| chr4:52087588 | G | A | 1 | a0001c0001t0004g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1563+2589G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087588 | |||||||
| chr4:52087682 | A | G | 3 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0003g0085 |
3 | HG00558.hp2 HG00673.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1563+2683A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087682 | |||||||
| chr4:52087786 | G | GT | 13 | a0001c0001t0003g0002 a0001c0001t0003g0051 a0001c0001t0003g0081 others(10): Show |
22 | HG00597.hp1 HG02738.hp1 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.1563+2793dupT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 52087786 | ||||||
| chr4:52087834 | G | A | 52 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(49): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1563+2835G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087834 | |||||||
| chr4:52087900 | G | A | 1 | a0002c0002t0001g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1563+2901G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087900 | |||||||
| chr4:52087932 | T | G | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0093 others(8): Show |
13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1563+2933T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087932 | |||||||
| chr4:52087962 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1563+2963C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087962 | |||||||
| chr4:52087975 | G | A | 1 | a0002c0002t0001g0209 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1563+2976G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087975 | |||||||
| chr4:52088098 | T | C | 1 | a0001c0001t0004g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1563+3099T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088098 | |||||||
| chr4:52088183 | C | G | 131 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(128): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1563+3184C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088183 | |||||||
| chr4:52088203 | C | A | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0093 others(8): Show |
13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1563+3204C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088203 | |||||||
| chr4:52088350 | G | A | 6 | a0002c0002t0001g0016 a0002c0002t0001g0039 a0002c0002t0001g0040 others(3): Show |
7 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1563+3351G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088350 | |||||||
| chr4:52088488 | C | G | 131 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(128): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1563+3489C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088488 | |||||||
| chr4:52088493 | G | T | 131 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(128): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1563+3494G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088493 | |||||||
| chr4:52088663 | G | A | 57 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(54): Show |
81 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1563+3664G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088663 | |||||||
| chr4:52088678 | G | T | 1 | a0001c0001t0004g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1563+3679G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088678 | |||||||
| chr4:52088682 | G | A | 1 | a0002c0002t0001g0175 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1563+3683G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088682 | |||||||
| chr4:52088689 | T | G | 56 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(53): Show |
80 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1563+3690T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088689 | |||||||
| chr4:52088768 | T | A | 63 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(60): Show |
81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1563+3769T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088768 | |||||||
| chr4:52089132 | CT | C | 3 | a0001c0001t0005g0011 a0001c0001t0005g0135 a0001c0001t0021g0218 |
5 | HG01884.hp2 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1563+4134delT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089132 | |||||||
| chr4:52089179 | C | G | 1 | a0001c0001t0011g0118 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1563+4180C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089179 | |||||||
| chr4:52089603 | T | G | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1563+4604T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089603 | |||||||
| chr4:52089813 | C | G | 201 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(198): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1564-4714C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089813 | |||||||
| chr4:52089900 | A | G | 80 | a0001c0001t0001g0130 a0002c0002t0001g0001 a0002c0002t0001g0007 others(77): Show |
104 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1564-4627A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089900 | |||||||
| chr4:52089968 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1564-4559T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089968 | |||||||
| chr4:52090058 | C | G | 1 | a0004c0004t0001g0196 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1564-4469C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090058 | |||||||
| chr4:52090274 | G | A | 1 | a0001c0001t0003g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1564-4253G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090274 | |||||||
| chr4:52090306 | T | A | 201 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(198): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1564-4221T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090306 | |||||||
| chr4:52090445 | G | A | 1 | a0001c0001t0003g0137 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1564-4082G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090445 | |||||||
| chr4:52090445 | G | T | 138 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(135): Show |
186 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1564-4082G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090445 | |||||||
| chr4:52090527 | C | CTTCCTCT others(26): Show |
1 | a0002c0002t0001g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1564-4000_1564-399 others(37): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090527 | |||||||
| chr4:52090530 | T | A | 1 | a0002c0002t0001g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1564-3997T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090530 | |||||||
| chr4:52090597 | T | C | 57 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(54): Show |
81 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1564-3930T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090597 | |||||||
| chr4:52090614 | C | T | 1 | a0001c0001t0020g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1564-3913C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090614 | |||||||
| chr4:52090753 | G | T | 1 | a0002c0002t0001g0179 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1564-3774G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090753 | |||||||
| chr4:52090808 | A | G | 1 | a0002c0002t0001g0210 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1564-3719A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090808 | |||||||
| chr4:52090849 | G | A | 79 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0009 others(76): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1564-3678G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090849 | |||||||
| chr4:52090850 | A | T | 79 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0009 others(76): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1564-3677A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090850 | |||||||
| chr4:52091159 | A | T | 52 | a0001c0001t0001g0130 a0001c0001t0003g0002 a0001c0001t0003g0006 others(49): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1564-3368A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091159 | |||||||
| chr4:52091193 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1564-3334T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091193 | |||||||
| chr4:52091270 | G | A | 7 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0049 others(4): Show |
9 | HG01943.hp2 HG02004.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.1564-3257G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091270 | |||||||
| chr4:52091292 | G | A | 56 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(53): Show |
80 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1564-3235G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091292 | |||||||
| chr4:52091548 | G | A | 55 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(52): Show |
79 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1564-2979G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091548 | |||||||
| chr4:52091580 | TGCCTGGG others(26): Show |
T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2946_1564-291 others(37): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091580 | |||||||
| chr4:52091614 | C | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2913C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091614 | |||||||
| chr4:52091616 | A | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2911A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091616 | |||||||
| chr4:52091617 | A | ATTTTTTT others(25): Show |
1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2910_1564-290 others(36): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091617 | |||||||
| chr4:52091618 | G | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2909G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091618 | |||||||
| chr4:52091622 | G | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2905G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091622 | |||||||
| chr4:52091623 | C | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2904C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091623 | |||||||
| chr4:52091625 | G | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2902G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091625 | |||||||
| chr4:52091626 | C | A | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2901C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091626 | |||||||
| chr4:52091627 | C | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2900C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091627 | |||||||
| chr4:52091629 | G | A | 6 | a0002c0002t0001g0016 a0002c0002t0001g0039 a0002c0002t0001g0040 others(3): Show |
7 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1564-2898G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091629 | |||||||
| chr4:52091629 | G | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2898G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091629 | |||||||
| chr4:52091632 | C | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2895C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091632 | |||||||
| chr4:52091636 | C | A | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2891C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091636 | |||||||
| chr4:52091637 | C | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2890C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091637 | |||||||
| chr4:52091639 | C | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2888C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091639 | |||||||
| chr4:52091641 | G | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2886G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091641 | |||||||
| chr4:52091642 | G | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2885G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091642 | |||||||
| chr4:52091644 | A | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2883A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091644 | |||||||
| chr4:52091645 | G | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2882G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091645 | |||||||
| chr4:52091646 | C | T | 1 | a0001c0001t0004g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2881C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091646 | |||||||
| chr4:52091712 | C | A | 51 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0027 others(48): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1564-2815C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091712 | |||||||
| chr4:52091770 | G | A | 7 | a0001c0001t0004g0025 a0001c0001t0004g0093 a0001c0001t0004g0094 others(4): Show |
8 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1564-2757G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091770 | |||||||
| chr4:52091772 | A | G | 1 | a0001c0011t0004g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1564-2755A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091772 | |||||||
| chr4:52091846 | G | A | 56 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(53): Show |
80 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1564-2681G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091846 | |||||||
| chr4:52091997 | A | T | 2 | a0001c0001t0002g0065 a0001c0001t0002g0074 |
2 | HG03492.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1564-2530A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091997 | |||||||
| chr4:52092144 | C | T | 1 | a0002c0002t0001g0178 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1564-2383C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092144 | |||||||
| chr4:52092243 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1564-2284G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092243 | |||||||
| chr4:52092291 | A | G | 201 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(198): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1564-2236A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092291 | |||||||
| chr4:52092307 | C | A | 2 | a0001c0001t0004g0220 a0001c0001t0004g0221 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1564-2220C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092307 | |||||||
| chr4:52092453 | G | T | 2 | a0001c0001t0003g0088 a0001c0001t0003g0106 |
2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1564-2074G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092453 | |||||||
| chr4:52092459 | G | A | 79 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0009 others(76): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1564-2068G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092459 | |||||||
| chr4:52092537 | A | C | 1 | a0003c0005t0017g0120 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1564-1990A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092537 | |||||||
| chr4:52093154 | A | G | 1 | a0002c0002t0001g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1564-1373A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52093154 | |||||||
| chr4:52093425 | A | G | 1 | a0001c0001t0004g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1564-1102A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52093425 | |||||||
| chr4:52093551 | G | A | 7 | a0001c0001t0004g0025 a0001c0001t0004g0093 a0001c0001t0004g0094 others(4): Show |
8 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1564-976G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52093551 | |||||||
| chr4:52093641 | A | G | 1 | a0001c0001t0002g0069 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1564-886A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52093641 | |||||||
| chr4:52093977 | A | G | 55 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(52): Show |
79 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1564-550A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52093977 | |||||||
| chr4:52094222 | G | A | 201 | a0001c0001t0001g0130 a0001c0001t0002g0003 a0001c0001t0002g0004 others(198): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1564-305G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52094222 | |||||||
| chr4:52094246 | G | T | 2 | a0001c0001t0006g0013 a0001c0001t0020g0222 |
4 | HG02145.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1564-281G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52094246 | |||||||
| chr4:52094407 | T | C | 1 | a0001c0001t0004g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1564-120T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52094407 | |||||||
| chr4:52094435 | G | C | 11 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0093 others(8): Show |
13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1564-92G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52094435 | |||||||
| chr4:52094625 | C | G | 1 | a0001c0001t0002g0059 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1609+53C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 12/12 | chr4 | 52094625 | |||||||
| chr4:52094742 | T | A | 79 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0009 others(76): Show |
103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1610-138T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 12/12 | chr4 | 52094742 | |||||||
| chr4:52094802 | G | A | 1 | a0001c0001t0003g0030 | 2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1610-78G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 12/12 | chr4 | 52094802 |