Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 256714 |
| ensemblid | ENSG00000184368.16 |
| hgncid | 25899 |
| symbol | MAP7D2 |
| name | MAP7 domain containing 2 |
| refseq_nuc | NM_001168465.2 |
| refseq_prot | NP_001161937.1 |
| ensembl_nuc | ENST00000379643.10 |
| ensembl_prot | ENSP00000368964.5 |
| mane_status | MANE Select |
| chr | chrX |
| start | 20006713 |
| end | 20116907 |
| strand | - |
| ver | v1.2 |
| region | chrX:20006713-20116907 |
| region5000 | chrX:20001713-20121907 |
| regionname0 | MAP7D2_chrX_20006713_20116907 |
| regionname5000 | MAP7D2_chrX_20001713_20121907 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 773 | 107 | 2 | 23 | 63 | 4 | 13 | 48 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | MERGG others(768): Show |
chrX | 20001713 | 20121907 |
| a0002 | 0/0 | 773 | 97 | 62 | 19 | 8 | 3 | 5 | 7 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | MERGG others(768): Show |
chrX | 20001713 | 20121907 |
| a0003 | 0/0 | 773 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | MERGG others(768): Show |
chrX | 20001713 | 20121907 |
| a0004 | 0/0 | 773 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | MERGG others(768): Show |
chrX | 20001713 | 20121907 |
| a0005 | 0/0 | 773 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | MERGG others(768): Show |
chrX | 20001713 | 20121907 |
| a0006 | 0/0 | 773 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | MERGG others(768): Show |
chrX | 20001713 | 20121907 |
| a0007 | 0/0 | 773 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | MERGG others(768): Show |
chrX | 20001713 | 20121907 |
| a0008 | 0/0 | 773 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | MERGG others(768): Show |
chrX | 20001713 | 20121907 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2319 | 106 | 1 | 23 | 63 | 4 | 13 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0001c0010 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0002c0002 | 0/0 | 2319 | 79 | 51 | 15 | 7 | 3 | 3 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0002c0003 | 0/0 | 2319 | 9 | 6 | 0 | 1 | 0 | 2 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0002c0004 | 0/0 | 2319 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0002c0005 | 0/0 | 2319 | 3 | 1 | 2 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0002c0011 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0003c0009 | 0/0 | 2319 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0004c0008 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0005c0006 | 0/0 | 2319 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0006c0013 | 0/0 | 2319 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0007c0007 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 | ||
| a0008c0012 | 0/0 | 2319 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | ATGGA others(2314): Show |
chrX | 20001713 | 20121907 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4062 | 105 | 1 | 22 | 63 | 4 | 13 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0001c0001t0004 | 0/0 | 4062 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0001c0010t0001 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0002c0002t0001 | 0/0 | 4062 | 72 | 46 | 14 | 7 | 3 | 2 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0002c0002t0002 | 0/0 | 4062 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0002c0002t0003 | 0/0 | 4062 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0002c0002t0007 | 0/0 | 4085 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4080): Show |
chrX | 20001713 | 20121907 |
| a0002c0003t0001 | 0/0 | 4062 | 5 | 5 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0002c0003t0003 | 0/0 | 4062 | 3 | 0 | 0 | 1 | 0 | 2 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0002c0003t0005 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0002c0004t0001 | 0/0 | 4062 | 5 | 4 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0002c0005t0001 | 0/0 | 4062 | 3 | 1 | 2 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0002c0011t0001 | 0/0 | 4062 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0003c0009t0001 | 0/0 | 4062 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0004c0008t0001 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0005c0006t0001 | 0/0 | 4062 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0006c0013t0006 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0007c0007t0001 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| a0008c0012t0001 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | AGTGC others(4057): Show |
chrX | 20001713 | 20121907 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0022 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0001c0010t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0002t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0003t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0004t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0004t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0005t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0005t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0002c0011t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0003c0009t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0004c0008t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0005c0006t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0006c0013t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0007c0007t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| a0008c0012t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG00735 | hp1 | a0003 | c0009 | t0001 | g0119 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0137 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01106 | hp1 | a0002 | c0004 | t0001 | g0167 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0196 | AMR | PUR | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01256 | hp1 | a0002 | c0005 | t0001 | g0120 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01346 | hp2 | a0002 | c0011 | t0001 | g0151 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0179 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01496 | hp2 | a0002 | c0005 | t0001 | g0121 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0152 | EUR | IBS | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0153 | EUR | IBS | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0130 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02015 | hp1 | a0002 | c0003 | t0003 | g0096 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02145 | hp1 | a0002 | c0003 | t0005 | g0105 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02257 | hp1 | a0001 | c0010 | t0001 | g0190 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0187 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0147 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0132 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0170 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0140 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0205 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0133 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0181 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0144 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02897 | hp1 | a0002 | c0003 | t0001 | g0018 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0169 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0016 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0201 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0173 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0186 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03017 | hp1 | a0002 | c0003 | t0003 | g0095 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0123 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0203 | AFR | GWD | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03195 | hp2 | a0002 | c0004 | t0001 | g0168 | AFR | ESN | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0166 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03486 | hp1 | a0004 | c0008 | t0001 | g0109 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03490 | hp1 | a0002 | c0003 | t0003 | g0097 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03654 | hp1 | a0005 | c0006 | t0001 | g0061 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0163 | SAS | BEB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0148 | SAS | STU | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0164 | AFR | YRI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | YRI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0165 | AFR | YRI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18989 | hp1 | a0007 | c0007 | t0001 | g0034 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0177 | AFR | LWK | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19030 | hp2 | a0002 | c0002 | t0007 | g0208 | AFR | LWK | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | LWK | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19067 | hp1 | a0008 | c0012 | t0001 | g0158 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0182 | AFR | YRI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0129 | AFR | YRI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0134 | AFR | ASW | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | ASW | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0149 | EUR | TSI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | GIH | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0066 | AMR | CLM | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02109 | hp1 | a0002 | c0005 | t0001 | g0122 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0183 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | ACB | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0199 | AFR | MSL | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | USA | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| HG06807 | hp2 | a0006 | c0013 | t0006 | g0207 | AFR | USA | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | USA | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | USA | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0005 | REF | REF | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0022 | REF | REF | MAP7D2_chrX_20001713_20121907 | MAP7D2 | chrX | 20001713 | 20121907 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:20012488 | C | T | 1 | a0005 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.1933G>A | p.Ala645Thr | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/17 | 1961/4062 | 1933/2322 | 645/773 | chrX | 20012488 | |||
| chrX:20016221 | T | C | 1 | a0007 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.1517A>G | p.Lys506Arg | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/17 | 1545/4062 | 1517/2322 | 506/773 | chrX | 20016221 | |||
| chrX:20025950 | G | A | 1 | a0004 | 1 | HG03486.hp1 | missense_variant&splice_region_variant | MODERATE | c.1010C>T | p.Thr337Ile | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/17 | 1038/4062 | 1010/2322 | 337/773 | chrX | 20025950 | |||
| chrX:20042517 | G | A | 1 | a0008 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.992C>T | p.Ser331Phe | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/17 | 1020/4062 | 992/2322 | 331/773 | chrX | 20042517 | |||
| chrX:20052928 | T | C | 3 | a0002 a0006 a0008 |
99 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(96): Show |
missense_variant | MODERATE | c.545A>G | p.Asn182Ser | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 5/17 | 573/4062 | 545/2322 | 182/773 | chrX | 20052928 | |||
| chrX:20116759 | G | A | 1 | a0003 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.121C>T | p.Arg41Trp | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | 149/4062 | 121/2322 | 41/773 | chrX | 20116759 | |||
| chrX:20116839 | G | A | 1 | a0006 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.41C>T | p.Pro14Leu | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | 69/4062 | 41/2322 | 14/773 | chrX | 20116839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:20016220 | C | T | 1 | a0007c0007 | 1 | NA18989.hp1 | synonymous_variant | LOW | c.1518G>A | p.Lys506Lys | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/17 | 1546/4062 | 1518/2322 | 506/773 | chrX | 20016220 | |||
| chrX:20044412 | A | T | 1 | a0002c0011 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.831T>A | p.Gly277Gly | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/17 | 859/4062 | 831/2322 | 277/773 | chrX | 20044412 | |||
| chrX:20056693 | G | A | 2 | a0002c0004 a0006c0013 |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
synonymous_variant | LOW | c.471C>T | p.Pro157Pro | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/17 | 499/4062 | 471/2322 | 157/773 | chrX | 20056693 | |||
| chrX:20116784 | C | G | 1 | a0002c0005 | 3 | HG01256.hp1 HG01496.hp2 HG02109.hp1 |
synonymous_variant | LOW | c.96G>C | p.Ala32Ala | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | 124/4062 | 96/2322 | 32/773 | chrX | 20116784 | |||
| chrX:20116862 | G | A | 7 | a0001c0010 a0002c0002 a0002c0004 others(4): Show |
91 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(88): Show |
synonymous_variant | LOW | c.18C>T | p.Gly6Gly | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | 46/4062 | 18/2322 | 6/773 | chrX | 20116862 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:20006778 | T | C | 1 | a0001c0001t0004 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1647A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 4025 | chrX | 20006778 | ||||||
| chrX:20007987 | T | C | 1 | a0002c0003t0005 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 2816 | chrX | 20007987 | ||||||
| chrX:20008153 | C | G | 1 | a0002c0002t0002 | 5 | HG01070.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*272G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 2650 | chrX | 20008153 | ||||||
| chrX:20008166 | A | G | 2 | a0002c0002t0003 a0002c0003t0003 |
4 | HG02015.hp1 HG03017.hp1 HG03490.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*259T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 17/17 | 2637 | chrX | 20008166 | ||||||
| chrX:20116881 | G | A | 1 | a0006c0013t0006 | 1 | HG06807.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-2C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | chrX | 20116881 | |||||||
| chrX:20116886 | G | GCGCCGGC others(16): Show |
1 | a0002c0002t0007 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8_-7insGCAGTGCGCC others(13): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/17 | 8 | chrX | 20116886 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:20009174 | T | C | 1 | a0002c0003t0005g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*27-776A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009174 | |||||||
| chrX:20009221 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.*27-823A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009221 | |||||||
| chrX:20009287 | T | C | 6 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.*27-889A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009287 | |||||||
| chrX:20009663 | C | CA | 22 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0023 others(19): Show |
23 | HG01071.hp1 HG01256.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.*26+1113dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009663 | |||||||
| chrX:20009663 | CA | C | 42 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0002c0002t0001g0124 others(39): Show |
42 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.*26+1113delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009663 | |||||||
| chrX:20009663 | CAAAAAAA others(5): Show |
C | 1 | a0002c0003t0005g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*26+1102_*26+1113d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009663 | |||||||
| chrX:20009989 | C | T | 1 | a0002c0002t0001g0171 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.*26+788G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20009989 | |||||||
| chrX:20010043 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.*26+734T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20010043 | |||||||
| chrX:20010166 | A | G | 1 | a0002c0002t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.*26+611T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20010166 | |||||||
| chrX:20010475 | GC | G | 85 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(82): Show |
86 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.*26+301delG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 16/16 | chrX | 20010475 | |||||||
| chrX:20011067 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2073-15G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20011067 | |||||||
| chrX:20011275 | GA | G | 11 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0134 others(8): Show |
11 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2073-224delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20011275 | |||||||
| chrX:20011783 | C | G | 11 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0134 others(8): Show |
11 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2072+566G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20011783 | |||||||
| chrX:20012021 | C | A | 5 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(2): Show |
5 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2072+328G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012021 | |||||||
| chrX:20012073 | T | A | 57 | a0002c0002t0001g0124 a0002c0002t0001g0126 a0002c0002t0001g0132 others(54): Show |
57 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.2072+276A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012073 | |||||||
| chrX:20012202 | G | C | 1 | a0002c0002t0001g0199 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2072+147C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 15/16 | chrX | 20012202 | |||||||
| chrX:20012558 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1886-23A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 14/16 | chrX | 20012558 | |||||||
| chrX:20012860 | A | C | 1 | a0001c0001t0001g0106 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1885+194T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 14/16 | chrX | 20012860 | |||||||
| chrX:20013739 | A | C | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1750-114T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20013739 | |||||||
| chrX:20013825 | C | T | 10 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0173 others(7): Show |
10 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.1750-200G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20013825 | |||||||
| chrX:20013839 | T | C | 1 | a0002c0002t0001g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1750-214A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20013839 | |||||||
| chrX:20013863 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1750-238G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20013863 | |||||||
| chrX:20014013 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1750-388A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20014013 | |||||||
| chrX:20014253 | G | A | 2 | a0002c0002t0001g0146 a0002c0002t0001g0169 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1750-628C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20014253 | |||||||
| chrX:20014523 | A | G | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1749+700T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20014523 | |||||||
| chrX:20014843 | C | T | 1 | a0002c0002t0001g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1749+380G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20014843 | |||||||
| chrX:20015013 | C | G | 94 | a0001c0001t0001g0088 a0002c0002t0001g0002 a0002c0002t0001g0124 others(91): Show |
95 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.1749+210G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 12/16 | chrX | 20015013 | |||||||
| chrX:20015583 | G | C | 1 | a0002c0002t0001g0178 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1645-256C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/16 | chrX | 20015583 | |||||||
| chrX:20015613 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1645-286C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/16 | chrX | 20015613 | |||||||
| chrX:20016054 | T | C | 2 | a0002c0002t0001g0159 a0002c0002t0001g0160 |
2 | NA18957.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1644+40A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 11/16 | chrX | 20016054 | |||||||
| chrX:20016553 | A | G | 15 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1413-228T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20016553 | |||||||
| chrX:20017335 | A | G | 15 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1413-1010T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017335 | |||||||
| chrX:20017502 | G | C | 6 | a0002c0002t0001g0002 a0002c0002t0001g0127 a0002c0002t0001g0128 others(3): Show |
7 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413-1177C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017502 | |||||||
| chrX:20017701 | T | C | 1 | a0002c0002t0001g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1413-1376A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017701 | |||||||
| chrX:20017843 | G | A | 72 | a0002c0002t0001g0124 a0002c0002t0001g0126 a0002c0002t0001g0132 others(69): Show |
72 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.1413-1518C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017843 | |||||||
| chrX:20017934 | T | TCTTCATC others(4): Show |
1 | a0007c0007t0001g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1413-1620_1413-161 others(15): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017934 | |||||||
| chrX:20017965 | C | CT | 5 | a0001c0001t0001g0023 a0001c0001t0001g0058 a0001c0001t0001g0085 others(2): Show |
5 | HG01981.hp1 NA18979.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1413-1641dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017965 | |||||||
| chrX:20017965 | CT | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0051 others(11): Show |
14 | HG01069.hp1 HG01256.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1413-1641delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017965 | |||||||
| chrX:20017965 | CTT | C | 65 | a0002c0002t0001g0124 a0002c0002t0001g0126 a0002c0002t0001g0132 others(62): Show |
65 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.1413-1642_1413-164 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20017965 | |||||||
| chrX:20018003 | G | C | 6 | a0002c0002t0001g0002 a0002c0002t0001g0127 a0002c0002t0001g0128 others(3): Show |
7 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413-1678C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018003 | |||||||
| chrX:20018171 | G | A | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413-1846C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018171 | |||||||
| chrX:20018440 | C | CT | 10 | a0001c0001t0001g0079 a0001c0001t0001g0117 a0002c0002t0001g0002 others(7): Show |
11 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1413-2116dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018440 | |||||||
| chrX:20018440 | CT | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(63): Show |
67 | HG00733.hp1 HG00735.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.1413-2116delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018440 | |||||||
| chrX:20018579 | A | G | 3 | a0002c0002t0001g0124 a0002c0002t0001g0164 a0002c0002t0001g0184 |
3 | HG02055.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1413-2254T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20018579 | |||||||
| chrX:20019129 | C | T | 3 | a0002c0002t0001g0170 a0002c0005t0001g0121 a0002c0005t0001g0122 |
3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1413-2804G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019129 | |||||||
| chrX:20019694 | A | G | 13 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0134 others(10): Show |
13 | HG01070.hp2 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1413-3369T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019694 | |||||||
| chrX:20019705 | T | TTGATC | 13 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0134 others(10): Show |
13 | HG01070.hp2 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1413-3385_1413-338 others(9): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019705 | |||||||
| chrX:20019818 | G | A | 2 | a0002c0002t0001g0143 a0002c0002t0001g0191 |
2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1413-3493C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20019818 | |||||||
| chrX:20020105 | G | T | 1 | a0002c0002t0001g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1413-3780C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020105 | |||||||
| chrX:20020193 | T | A | 1 | a0001c0001t0001g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1413-3868A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020193 | |||||||
| chrX:20020353 | C | G | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413-4028G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020353 | |||||||
| chrX:20020453 | T | G | 5 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0195 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1413-4128A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020453 | |||||||
| chrX:20020585 | C | A | 1 | a0002c0002t0001g0182 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1413-4260G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020585 | |||||||
| chrX:20020808 | C | G | 87 | a0001c0001t0001g0088 a0002c0002t0001g0002 a0002c0002t0001g0124 others(84): Show |
88 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.1412+4143G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020808 | |||||||
| chrX:20020812 | C | T | 6 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412+4139G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020812 | |||||||
| chrX:20020962 | T | C | 2 | a0002c0002t0001g0146 a0002c0002t0001g0169 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1412+3989A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20020962 | |||||||
| chrX:20021841 | G | A | 7 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(4): Show |
8 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412+3110C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20021841 | |||||||
| chrX:20022640 | A | G | 1 | a0002c0002t0001g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1412+2311T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20022640 | |||||||
| chrX:20022793 | A | G | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412+2158T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20022793 | |||||||
| chrX:20022914 | A | G | 1 | a0002c0003t0001g0018 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1412+2037T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20022914 | |||||||
| chrX:20023142 | C | A | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412+1809G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023142 | |||||||
| chrX:20023452 | G | A | 8 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 others(5): Show |
8 | HG01081.hp1 HG01361.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412+1499C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023452 | |||||||
| chrX:20023527 | G | A | 4 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0121 others(1): Show |
4 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412+1424C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023527 | |||||||
| chrX:20023578 | T | A | 95 | a0001c0001t0001g0088 a0002c0002t0001g0002 a0002c0002t0001g0124 others(92): Show |
96 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.1412+1373A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023578 | |||||||
| chrX:20023601 | C | G | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412+1350G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023601 | |||||||
| chrX:20023937 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0067 |
2 | NA18948.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1412+1014G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20023937 | |||||||
| chrX:20024344 | C | T | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412+607G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20024344 | |||||||
| chrX:20024367 | A | C | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412+584T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20024367 | |||||||
| chrX:20024481 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1412+470C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20024481 | |||||||
| chrX:20024842 | A | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0065 a0007c0007t0001g0034 |
3 | HG02074.hp1 NA18989.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1412+109T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 10/16 | chrX | 20024842 | |||||||
| chrX:20025295 | T | C | 5 | a0002c0002t0001g0002 a0002c0002t0001g0127 a0002c0002t0001g0128 others(2): Show |
6 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-212A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025295 | |||||||
| chrX:20025349 | T | A | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280-266A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025349 | |||||||
| chrX:20025389 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1279+292T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025389 | |||||||
| chrX:20025423 | A | G | 12 | a0002c0002t0001g0170 a0002c0002t0001g0185 a0002c0002t0001g0204 others(9): Show |
12 | HG01106.hp1 HG01256.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1279+258T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025423 | |||||||
| chrX:20025644 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1279+37G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 9/16 | chrX | 20025644 | |||||||
| chrX:20025961 | C | A | 3 | a0002c0002t0001g0170 a0002c0005t0001g0121 a0002c0005t0001g0122 |
3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1008-9G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20025961 | |||||||
| chrX:20026075 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1008-123G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026075 | |||||||
| chrX:20026186 | T | C | 1 | a0006c0013t0006g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1008-234A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026186 | |||||||
| chrX:20026689 | G | A | 26 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(23): Show |
26 | HG00609.hp1 HG00735.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1008-737C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026689 | |||||||
| chrX:20026697 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1008-745T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026697 | |||||||
| chrX:20026888 | T | C | 2 | a0002c0002t0001g0146 a0002c0002t0001g0169 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1008-936A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20026888 | |||||||
| chrX:20027058 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1008-1106A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027058 | |||||||
| chrX:20027196 | C | T | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-1244G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027196 | |||||||
| chrX:20027242 | C | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0091 |
2 | HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1008-1290G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027242 | |||||||
| chrX:20027757 | G | GGA | 12 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0032 others(9): Show |
12 | HG02615.hp1 HG02630.hp2 HG03579.hp1 others(9): Show |
intron_variant | MODIFIER | c.1008-1807_1008-180 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027757 | |||||||
| chrX:20027757 | GGA | G | 13 | a0001c0001t0001g0058 a0001c0001t0001g0085 a0001c0001t0001g0114 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.1008-1807_1008-180 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027757 | |||||||
| chrX:20027757 | GGAGA | G | 9 | a0001c0001t0001g0088 a0002c0002t0001g0124 a0002c0002t0001g0164 others(6): Show |
9 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008-1809_1008-180 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027757 | |||||||
| chrX:20027757 | GGAGAGA | G | 56 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(53): Show |
56 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1008-1811_1008-180 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027757 | |||||||
| chrX:20027763 | A | G | 4 | a0002c0002t0001g0170 a0002c0005t0001g0120 a0002c0005t0001g0121 others(1): Show |
4 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008-1811T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027763 | |||||||
| chrX:20027765 | A | G | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-1813T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027765 | |||||||
| chrX:20027786 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1008-1834C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027786 | |||||||
| chrX:20027790 | GAC | G | 4 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0201 others(1): Show |
4 | HG01106.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-1840_1008-183 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027790 | |||||||
| chrX:20027792 | C | G | 3 | a0002c0002t0001g0185 a0002c0004t0001g0168 a0002c0004t0001g0205 |
3 | HG02630.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1008-1840G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20027792 | |||||||
| chrX:20028936 | T | C | 1 | a0002c0002t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1008-2984A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20028936 | |||||||
| chrX:20029005 | C | T | 1 | a0004c0008t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1008-3053G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029005 | |||||||
| chrX:20029185 | G | C | 1 | a0002c0002t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1008-3233C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029185 | |||||||
| chrX:20029197 | A | G | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-3245T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029197 | |||||||
| chrX:20029250 | G | T | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-3298C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029250 | |||||||
| chrX:20029684 | C | T | 2 | a0001c0001t0001g0036 a0002c0002t0001g0204 |
2 | HG02886.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1008-3732G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029684 | |||||||
| chrX:20029786 | T | C | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-3834A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029786 | |||||||
| chrX:20029789 | A | AT | 102 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0052 others(99): Show |
103 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(100): Show |
intron_variant | MODIFIER | c.1008-3838dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20029789 | |||||||
| chrX:20030050 | C | T | 8 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 others(5): Show |
8 | HG01081.hp1 HG01361.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008-4098G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20030050 | |||||||
| chrX:20030829 | T | C | 90 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(87): Show |
91 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.1008-4877A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20030829 | |||||||
| chrX:20030847 | T | C | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-4895A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20030847 | |||||||
| chrX:20031062 | G | A | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008-5110C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031062 | |||||||
| chrX:20031118 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1008-5166C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031118 | |||||||
| chrX:20031214 | C | T | 1 | a0002c0002t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1008-5262G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031214 | |||||||
| chrX:20031215 | G | A | 1 | a0002c0002t0001g0196 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1008-5263C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031215 | |||||||
| chrX:20031291 | A | AAAAATAA others(3): Show |
1 | a0002c0002t0001g0132 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1008-5349_1008-534 others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | |||||||
| chrX:20031291 | A | AAAAATAA others(8): Show |
1 | a0001c0001t0001g0108 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1008-5354_1008-534 others(19): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | |||||||
| chrX:20031291 | AAAAAT | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
140 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.1008-5344_1008-534 others(9): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | |||||||
| chrX:20031291 | AAAAATAA others(3): Show |
A | 8 | a0002c0002t0001g0185 a0002c0002t0002g0181 a0002c0002t0002g0203 others(5): Show |
8 | HG01106.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008-5349_1008-534 others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | |||||||
| chrX:20031291 | AAAAATAA others(8): Show |
A | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-5354_1008-534 others(19): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | |||||||
| chrX:20031291 | AAAAATAA others(13): Show |
A | 2 | a0001c0001t0001g0077 a0002c0002t0001g0188 |
2 | HG01258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1008-5359_1008-534 others(24): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031291 | |||||||
| chrX:20031526 | A | G | 12 | a0002c0002t0001g0170 a0002c0002t0001g0185 a0002c0002t0001g0204 others(9): Show |
12 | HG01106.hp1 HG01256.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1008-5574T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031526 | |||||||
| chrX:20031533 | G | A | 84 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(81): Show |
85 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1008-5581C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20031533 | |||||||
| chrX:20032357 | G | C | 11 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0004t0001g0166 others(8): Show |
11 | HG01106.hp1 HG01256.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1008-6405C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20032357 | |||||||
| chrX:20033502 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0055 others(2): Show |
5 | HG00280.hp1 HG01496.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-7550G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20033502 | |||||||
| chrX:20033688 | C | T | 1 | a0006c0013t0006g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1008-7736G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20033688 | |||||||
| chrX:20033759 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0114 |
2 | NA18979.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1008-7807C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20033759 | |||||||
| chrX:20034068 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1008-8116A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034068 | |||||||
| chrX:20034225 | C | CA | 5 | a0001c0001t0001g0021 a0001c0001t0001g0092 a0001c0001t0001g0099 others(2): Show |
5 | HG01261.hp1 HG02257.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008-8274dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034225 | |||||||
| chrX:20034225 | CA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
95 | HG00642.hp1 HG00673.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.1008-8274delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034225 | |||||||
| chrX:20034225 | CAA | C | 61 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(58): Show |
62 | HG00609.hp1 HG00735.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.1007+8275_1008-827 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034225 | |||||||
| chrX:20034225 | CAAA | C | 12 | a0002c0002t0001g0160 a0002c0002t0001g0162 a0002c0002t0001g0171 others(9): Show |
12 | HG00733.hp1 HG01081.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1007+8274_1008-827 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034225 | |||||||
| chrX:20034372 | G | C | 1 | a0002c0002t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1007+8130C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034372 | |||||||
| chrX:20034457 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1007+8045G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034457 | |||||||
| chrX:20034564 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1007+7938A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034564 | |||||||
| chrX:20034586 | G | A | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+7916C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034586 | |||||||
| chrX:20034934 | C | T | 1 | a0002c0002t0007g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1007+7568G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034934 | |||||||
| chrX:20034969 | A | G | 7 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(4): Show |
8 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007+7533T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20034969 | |||||||
| chrX:20035162 | G | A | 1 | a0002c0002t0001g0164 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1007+7340C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035162 | |||||||
| chrX:20035492 | A | T | 2 | a0002c0002t0001g0146 a0002c0002t0001g0169 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1007+7010T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035492 | |||||||
| chrX:20035861 | C | T | 71 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(68): Show |
71 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.1007+6641G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035861 | |||||||
| chrX:20035887 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1007+6615A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035887 | |||||||
| chrX:20035926 | A | ATG | 2 | a0002c0002t0001g0131 a0006c0013t0006g0207 |
2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1007+6574_1007+657 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035926 | |||||||
| chrX:20035926 | ATG | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
101 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.1007+6574_1007+657 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035926 | |||||||
| chrX:20035926 | ATGTG | A | 9 | a0002c0002t0001g0154 a0002c0002t0001g0172 a0002c0002t0001g0173 others(6): Show |
9 | HG01081.hp1 HG01361.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1007+6572_1007+657 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035926 | |||||||
| chrX:20035926 | ATGTGTG | A | 64 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(61): Show |
64 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1007+6570_1007+657 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035926 | |||||||
| chrX:20035928 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0054 others(2): Show |
5 | HG03486.hp1 NA18943.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+6574C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20035928 | |||||||
| chrX:20036144 | C | T | 8 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(5): Show |
8 | HG01070.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007+6358G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036144 | |||||||
| chrX:20036178 | C | T | 76 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(73): Show |
76 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.1007+6324G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036178 | |||||||
| chrX:20036306 | G | A | 6 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007+6196C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036306 | |||||||
| chrX:20036532 | G | A | 71 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(68): Show |
71 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.1007+5970C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036532 | |||||||
| chrX:20036740 | C | T | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0191 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+5762G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036740 | |||||||
| chrX:20036866 | T | G | 1 | a0001c0001t0001g0103 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1007+5636A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036866 | |||||||
| chrX:20036903 | CA | C | 76 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0045 others(73): Show |
77 | HG00609.hp1 HG00642.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.1007+5598delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20036903 | |||||||
| chrX:20037295 | G | A | 91 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(88): Show |
92 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.1007+5207C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20037295 | |||||||
| chrX:20037805 | G | A | 1 | a0002c0004t0001g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1007+4697C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20037805 | |||||||
| chrX:20037807 | C | T | 89 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(86): Show |
90 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1007+4695G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20037807 | |||||||
| chrX:20038221 | C | G | 3 | a0002c0002t0001g0150 a0002c0002t0001g0161 a0002c0002t0001g0192 |
3 | HG01123.hp1 HG01167.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1007+4281G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038221 | |||||||
| chrX:20038399 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0010t0001g0190 |
3 | HG00738.hp1 HG01346.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1007+4103A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038399 | |||||||
| chrX:20038559 | C | T | 89 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(86): Show |
90 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1007+3943G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038559 | |||||||
| chrX:20038573 | G | A | 1 | a0002c0011t0001g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1007+3929C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038573 | |||||||
| chrX:20038991 | C | T | 5 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(2): Show |
5 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+3511G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038991 | |||||||
| chrX:20038999 | G | A | 1 | a0002c0002t0007g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1007+3503C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20038999 | |||||||
| chrX:20039001 | G | T | 1 | a0002c0002t0007g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1007+3501C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039001 | |||||||
| chrX:20039204 | C | A | 92 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(89): Show |
93 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.1007+3298G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039204 | |||||||
| chrX:20039236 | A | G | 1 | a0002c0002t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1007+3266T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039236 | |||||||
| chrX:20039249 | G | A | 1 | a0002c0002t0002g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1007+3253C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039249 | |||||||
| chrX:20039979 | C | A | 1 | a0002c0002t0001g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1007+2523G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039979 | |||||||
| chrX:20039997 | C | CA | 40 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0035 others(37): Show |
40 | HG00609.hp1 HG00735.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1007+2504dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20039997 | |||||||
| chrX:20040108 | C | T | 97 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(94): Show |
98 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.1007+2394G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040108 | |||||||
| chrX:20040496 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1007+2006G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040496 | |||||||
| chrX:20040549 | C | T | 3 | a0002c0002t0001g0124 a0002c0002t0001g0164 a0002c0002t0001g0184 |
3 | HG02055.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1007+1953G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040549 | |||||||
| chrX:20040577 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG02165.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1007+1925G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040577 | |||||||
| chrX:20040641 | A | G | 99 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(96): Show |
100 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(97): Show |
intron_variant | MODIFIER | c.1007+1861T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040641 | |||||||
| chrX:20040719 | G | A | 1 | a0002c0005t0001g0120 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1007+1783C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040719 | |||||||
| chrX:20040864 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1007+1638G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040864 | |||||||
| chrX:20040949 | C | A | 1 | a0002c0003t0001g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1007+1553G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20040949 | |||||||
| chrX:20041189 | G | A | 1 | a0002c0002t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1007+1313C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20041189 | |||||||
| chrX:20041516 | A | C | 1 | a0004c0008t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1007+986T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20041516 | |||||||
| chrX:20041900 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1007+602A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20041900 | |||||||
| chrX:20042307 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0068 |
2 | NA18953.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1007+195A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20042307 | |||||||
| chrX:20042402 | G | A | 5 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(2): Show |
5 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+100C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 8/16 | chrX | 20042402 | |||||||
| chrX:20042895 | G | A | 12 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0173 others(9): Show |
12 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.880-266C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20042895 | |||||||
| chrX:20042940 | C | G | 44 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(41): Show |
44 | HG00609.hp1 HG00735.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.880-311G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20042940 | |||||||
| chrX:20042952 | A | G | 5 | a0002c0002t0001g0002 a0002c0002t0001g0127 a0002c0002t0001g0128 others(2): Show |
6 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-323T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20042952 | |||||||
| chrX:20043153 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.880-524T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043153 | |||||||
| chrX:20043263 | G | A | 1 | a0002c0002t0002g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.880-634C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043263 | |||||||
| chrX:20043376 | CCTCTT | C | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0191 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-752_880-748del others(5): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043376 | |||||||
| chrX:20043464 | T | C | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-835A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043464 | |||||||
| chrX:20043685 | T | A | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.879+679A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043685 | |||||||
| chrX:20043696 | A | C | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.879+668T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043696 | |||||||
| chrX:20043886 | T | C | 1 | a0002c0002t0001g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.879+478A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20043886 | |||||||
| chrX:20044131 | T | G | 2 | a0002c0002t0001g0188 a0002c0002t0001g0189 |
2 | HG02486.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.879+233A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 7/16 | chrX | 20044131 | |||||||
| chrX:20044757 | T | C | 1 | a0007c0007t0001g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.719-233A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20044757 | |||||||
| chrX:20045293 | G | A | 1 | a0002c0002t0001g0149 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.719-769C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045293 | |||||||
| chrX:20045526 | C | CG | 5 | a0001c0001t0001g0035 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.719-1003dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045526 | |||||||
| chrX:20045527 | G | GA | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0068 others(5): Show |
8 | HG02027.hp1 HG03098.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.719-1004dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045527 | |||||||
| chrX:20045527 | GA | G | 65 | a0001c0001t0001g0086 a0002c0002t0001g0002 a0002c0002t0001g0124 others(62): Show |
66 | HG00733.hp1 HG01070.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.719-1004delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045527 | |||||||
| chrX:20045527 | GAA | G | 10 | a0002c0002t0001g0125 a0002c0002t0001g0163 a0002c0002t0001g0173 others(7): Show |
10 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.719-1005_719-1004d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045527 | |||||||
| chrX:20045528 | A | G | 1 | a0002c0002t0001g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.719-1004T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045528 | |||||||
| chrX:20045574 | C | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0087 |
2 | HG01928.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.719-1050G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20045574 | |||||||
| chrX:20046283 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.719-1759C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20046283 | |||||||
| chrX:20046504 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.719-1980C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20046504 | |||||||
| chrX:20046539 | T | C | 1 | a0002c0005t0001g0120 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.719-2015A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20046539 | |||||||
| chrX:20047214 | T | G | 1 | a0001c0001t0001g0053 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.719-2690A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047214 | |||||||
| chrX:20047239 | A | C | 1 | a0002c0002t0001g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.719-2715T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047239 | |||||||
| chrX:20047240 | C | G | 1 | a0002c0002t0001g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.719-2716G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047240 | |||||||
| chrX:20047449 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0032 others(7): Show |
10 | HG00642.hp1 HG01261.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.719-2925A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047449 | |||||||
| chrX:20047648 | CA | C | 65 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0126 others(62): Show |
66 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.719-3125delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047648 | |||||||
| chrX:20047649 | A | C | 1 | a0001c0001t0001g0098 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.719-3125T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047649 | |||||||
| chrX:20047873 | G | A | 6 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(3): Show |
6 | HG02615.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.718+2951C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047873 | |||||||
| chrX:20047875 | GA | G | 82 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(79): Show |
83 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(80): Show |
intron_variant | MODIFIER | c.718+2948delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047875 | |||||||
| chrX:20047932 | A | G | 6 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.718+2892T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20047932 | |||||||
| chrX:20048138 | G | T | 88 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(85): Show |
89 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(86): Show |
intron_variant | MODIFIER | c.718+2686C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048138 | |||||||
| chrX:20048459 | G | A | 1 | a0002c0002t0001g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.718+2365C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048459 | |||||||
| chrX:20048521 | C | T | 1 | a0002c0002t0001g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.718+2303G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048521 | |||||||
| chrX:20048884 | T | C | 1 | a0002c0002t0001g0189 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.718+1940A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048884 | |||||||
| chrX:20048929 | ATATACAT others(15): Show |
A | 1 | a0002c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.718+1873_718+1894d others(24): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048929 | |||||||
| chrX:20048934 | CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.718+1866_718+1889d others(26): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048934 | |||||||
| chrX:20048945 | A | ATATATGT others(5): Show |
1 | a0002c0003t0005g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.718+1867_718+1878d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20048945 | |||||||
| chrX:20049270 | ATT | A | 94 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(91): Show |
95 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(92): Show |
intron_variant | MODIFIER | c.718+1552_718+1553d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049270 | |||||||
| chrX:20049640 | G | C | 1 | a0002c0002t0001g0185 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.718+1184C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049640 | |||||||
| chrX:20049761 | T | C | 95 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(92): Show |
96 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.718+1063A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049761 | |||||||
| chrX:20049871 | A | C | 5 | a0002c0002t0001g0180 a0002c0002t0002g0123 a0002c0002t0002g0137 others(2): Show |
5 | HG01070.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+953T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049871 | |||||||
| chrX:20049916 | T | A | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.718+908A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20049916 | |||||||
| chrX:20050691 | G | A | 2 | a0002c0002t0001g0143 a0002c0002t0001g0191 |
2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.718+133C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 6/16 | chrX | 20050691 | |||||||
| chrX:20051556 | C | CA | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-611dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 5/16 | chrX | 20051556 | |||||||
| chrX:20051560 | C | A | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-614G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 5/16 | chrX | 20051560 | |||||||
| chrX:20052706 | G | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0010t0001g0190 |
3 | HG00738.hp1 HG01346.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.595+172C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 5/16 | chrX | 20052706 | |||||||
| chrX:20053200 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.485-212T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053200 | |||||||
| chrX:20053277 | C | T | 9 | a0002c0002t0001g0132 a0002c0002t0001g0134 a0002c0002t0001g0135 others(6): Show |
9 | HG01070.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.485-289G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053277 | |||||||
| chrX:20053309 | T | A | 18 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0173 others(15): Show |
18 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.485-321A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053309 | |||||||
| chrX:20053809 | G | A | 1 | a0006c0013t0006g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.485-821C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053809 | |||||||
| chrX:20053902 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0101 |
2 | HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.485-914C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053902 | |||||||
| chrX:20053912 | C | T | 2 | a0002c0002t0001g0146 a0002c0002t0001g0169 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.485-924G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20053912 | |||||||
| chrX:20054093 | C | T | 2 | a0002c0002t0001g0179 a0002c0003t0001g0014 |
2 | HG01361.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.485-1105G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054093 | |||||||
| chrX:20054210 | A | C | 1 | a0002c0004t0001g0167 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.485-1222T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054210 | |||||||
| chrX:20054228 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.485-1240C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054228 | |||||||
| chrX:20054281 | T | A | 95 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(92): Show |
96 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.485-1293A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054281 | |||||||
| chrX:20054286 | C | T | 78 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(75): Show |
79 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.485-1298G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054286 | |||||||
| chrX:20054325 | T | A | 2 | a0002c0002t0001g0159 a0002c0002t0001g0160 |
2 | NA18957.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.485-1337A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054325 | |||||||
| chrX:20054499 | T | C | 7 | a0002c0002t0001g0165 a0002c0002t0001g0179 a0002c0002t0001g0183 others(4): Show |
7 | HG01361.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-1511A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054499 | |||||||
| chrX:20054771 | G | A | 3 | a0002c0002t0001g0124 a0002c0002t0001g0164 a0002c0002t0001g0184 |
3 | HG02055.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.485-1783C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20054771 | |||||||
| chrX:20055076 | CT | C | 69 | a0001c0001t0001g0035 a0002c0002t0001g0124 a0002c0002t0001g0125 others(66): Show |
69 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.484+1603delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20055076 | |||||||
| chrX:20055436 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.484+1244C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20055436 | |||||||
| chrX:20055623 | G | C | 1 | a0002c0003t0001g0016 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.484+1057C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20055623 | |||||||
| chrX:20056167 | C | T | 92 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(89): Show |
93 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.484+513G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056167 | |||||||
| chrX:20056323 | C | A | 79 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(76): Show |
80 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.484+357G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056323 | |||||||
| chrX:20056343 | C | A | 1 | a0002c0002t0001g0154 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.484+337G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056343 | |||||||
| chrX:20056416 | A | T | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.484+264T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056416 | |||||||
| chrX:20056482 | A | T | 6 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.484+198T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056482 | |||||||
| chrX:20056626 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0054 |
2 | NA18960.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.484+54A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 4/16 | chrX | 20056626 | |||||||
| chrX:20057010 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.373-219G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20057010 | |||||||
| chrX:20057392 | C | T | 1 | a0006c0013t0006g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.373-601G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20057392 | |||||||
| chrX:20057500 | G | C | 3 | a0002c0002t0001g0170 a0002c0005t0001g0121 a0002c0005t0001g0122 |
3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.373-709C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20057500 | |||||||
| chrX:20057590 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.373-799C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20057590 | |||||||
| chrX:20057612 | C | T | 40 | a0002c0002t0001g0126 a0002c0002t0001g0141 a0002c0002t0001g0142 others(37): Show |
40 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.373-821G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20057612 | |||||||
| chrX:20058171 | G | A | 11 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0173 others(8): Show |
11 | HG00733.hp1 HG01081.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.373-1380C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20058171 | |||||||
| chrX:20058668 | C | A | 1 | a0002c0002t0001g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.373-1877G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20058668 | |||||||
| chrX:20058913 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.373-2122G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20058913 | |||||||
| chrX:20058953 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.373-2162T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20058953 | |||||||
| chrX:20059199 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.373-2408A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059199 | |||||||
| chrX:20059308 | T | C | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0191 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-2517A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059308 | |||||||
| chrX:20059589 | T | TGGAA | 20 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0037 others(17): Show |
20 | HG00735.hp2 HG01081.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.373-2802_373-2799d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | |||||||
| chrX:20059589 | T | TGGAAGGA others(1): Show |
5 | a0002c0002t0001g0124 a0002c0002t0001g0182 a0002c0002t0001g0184 others(2): Show |
5 | HG02055.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-2806_373-2799d others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | |||||||
| chrX:20059589 | T | TGGAAGGA others(5): Show |
29 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0134 others(26): Show |
29 | HG01123.hp1 HG01167.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.373-2810_373-2799d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | |||||||
| chrX:20059589 | T | TGGAAGGA others(9): Show |
9 | a0002c0002t0001g0126 a0002c0002t0001g0140 a0002c0002t0001g0141 others(6): Show |
9 | HG00733.hp1 HG01081.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.373-2814_373-2799d others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | |||||||
| chrX:20059589 | T | TGGAAGGA others(13): Show |
4 | a0002c0002t0001g0152 a0002c0002t0001g0153 a0002c0002t0001g0154 others(1): Show |
4 | HG01346.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-2818_373-2799d others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | |||||||
| chrX:20059589 | TGGAA | T | 6 | a0001c0001t0001g0056 a0001c0001t0001g0089 a0001c0001t0001g0117 others(3): Show |
6 | HG03041.hp1 NA18522.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-2802_373-2799d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | |||||||
| chrX:20059589 | TGGAAGGA others(1): Show |
T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0059 others(11): Show |
14 | HG00642.hp1 HG01106.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.373-2806_373-2799d others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059589 | |||||||
| chrX:20059620 | A | G | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-2829T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059620 | |||||||
| chrX:20059621 | A | T | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-2830T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059621 | |||||||
| chrX:20059625 | AGGGT | A | 4 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0121 others(1): Show |
4 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-2838_373-2835d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059625 | |||||||
| chrX:20059628 | G | A | 6 | a0002c0002t0001g0156 a0002c0002t0001g0157 a0002c0002t0001g0161 others(3): Show |
6 | HG01192.hp1 HG01256.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-2837C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059628 | |||||||
| chrX:20059629 | T | A | 6 | a0002c0002t0001g0156 a0002c0002t0001g0157 a0002c0002t0001g0161 others(3): Show |
6 | HG01192.hp1 HG01256.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-2838A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059629 | |||||||
| chrX:20059629 | TGGAAGGA others(5): Show |
T | 1 | a0001c0001t0001g0078 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.373-2850_373-2839d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059629 | |||||||
| chrX:20059637 | A | AGGGT | 4 | a0002c0002t0001g0156 a0002c0002t0001g0157 a0002c0002t0001g0162 others(1): Show |
4 | NA18965.hp1 NA18979.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-2847_373-2846i others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059637 | |||||||
| chrX:20059681 | C | T | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-2890G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059681 | |||||||
| chrX:20059736 | AGAAGGAA others(10): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.373-2962_373-2946d others(19): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059736 | |||||||
| chrX:20059950 | C | T | 1 | a0002c0003t0001g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.373-3159G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059950 | |||||||
| chrX:20059995 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0037 others(2): Show |
5 | NA18971.hp1 NA18984.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-3204A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20059995 | |||||||
| chrX:20060012 | T | C | 1 | a0002c0002t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.373-3221A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060012 | |||||||
| chrX:20060378 | G | A | 3 | a0002c0002t0001g0170 a0002c0005t0001g0121 a0002c0005t0001g0122 |
3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.372+3036C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060378 | |||||||
| chrX:20060416 | AAGAG | A | 13 | a0001c0001t0001g0114 a0002c0002t0001g0129 a0002c0002t0001g0132 others(10): Show |
13 | HG01070.hp2 HG01515.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.372+2994_372+2997d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060416 | |||||||
| chrX:20060428 | G | GAGAA | 6 | a0002c0002t0001g0134 a0002c0002t0001g0140 a0002c0002t0001g0141 others(3): Show |
6 | HG01081.hp2 HG02572.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+2985_372+2986i others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | |||||||
| chrX:20060428 | G | GAGAAAGA others(1): Show |
2 | a0002c0002t0001g0136 a0006c0013t0006g0207 |
2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.372+2985_372+2986i others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | |||||||
| chrX:20060428 | GAGAGAGA others(1): Show |
G | 24 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0126 others(21): Show |
25 | HG01070.hp1 HG01071.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.372+2978_372+2985d others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | |||||||
| chrX:20060428 | GAGAGAGA others(5): Show |
G | 11 | a0002c0002t0001g0125 a0002c0002t0001g0147 a0002c0002t0001g0150 others(8): Show |
11 | HG01167.hp1 HG01192.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.372+2974_372+2985d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | |||||||
| chrX:20060428 | GAGAGAGA others(9): Show |
G | 5 | a0002c0002t0001g0142 a0002c0002t0001g0146 a0002c0002t0001g0163 others(2): Show |
5 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+2970_372+2985d others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | |||||||
| chrX:20060428 | GAGAGAGA others(13): Show |
G | 1 | a0002c0002t0001g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.372+2966_372+2985d others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | |||||||
| chrX:20060428 | GAGAGAGA others(17): Show |
G | 5 | a0002c0002t0001g0182 a0002c0002t0001g0186 a0002c0002t0001g0187 others(2): Show |
5 | HG02257.hp2 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+2962_372+2985d others(26): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060428 | |||||||
| chrX:20060432 | G | A | 25 | a0002c0002t0001g0134 a0002c0002t0001g0135 a0002c0002t0001g0136 others(22): Show |
25 | HG00733.hp1 HG00735.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.372+2982C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | |||||||
| chrX:20060432 | G | GAGAA | 3 | a0001c0001t0001g0065 a0001c0001t0001g0077 a0002c0003t0001g0016 |
3 | HG01258.hp1 HG02074.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.372+2978_372+2981d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | |||||||
| chrX:20060432 | GAGAA | G | 34 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0021 others(31): Show |
34 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.372+2978_372+2981d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | |||||||
| chrX:20060432 | GAGAAAGA others(1): Show |
G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(46): Show |
50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.372+2974_372+2981d others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | |||||||
| chrX:20060432 | GAGAAAGA others(5): Show |
G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0026 others(17): Show |
20 | HG00609.hp1 HG00673.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.372+2970_372+2981d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | |||||||
| chrX:20060432 | GAGAAAGA others(9): Show |
G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0051 a0001c0001t0001g0115 |
3 | HG01433.hp1 HG03239.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.372+2966_372+2981d others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | |||||||
| chrX:20060432 | GAGAAAGA others(13): Show |
G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0085 |
2 | NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.372+2962_372+2981d others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | |||||||
| chrX:20060432 | GAGAAAGA others(17): Show |
G | 1 | a0001c0001t0001g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.372+2958_372+2981d others(26): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060432 | |||||||
| chrX:20060436 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.372+2978T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060436 | |||||||
| chrX:20060448 | A | G | 3 | a0002c0003t0003g0095 a0002c0003t0003g0096 a0002c0003t0003g0097 |
3 | HG02015.hp1 HG03017.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.372+2966T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20060448 | |||||||
| chrX:20061118 | C | CA | 9 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0024 others(6): Show |
9 | HG01361.hp2 HG02135.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.372+2295dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061118 | |||||||
| chrX:20061118 | CA | C | 60 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0002c0002t0001g0124 others(57): Show |
60 | HG00733.hp1 HG00735.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.372+2295delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061118 | |||||||
| chrX:20061118 | CAA | C | 26 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(23): Show |
27 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.372+2294_372+2295d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061118 | |||||||
| chrX:20061312 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.372+2102C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061312 | |||||||
| chrX:20061709 | C | A | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1705G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061709 | |||||||
| chrX:20061774 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.372+1640A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20061774 | |||||||
| chrX:20062147 | A | G | 45 | a0002c0002t0001g0124 a0002c0002t0001g0126 a0002c0002t0001g0141 others(42): Show |
45 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.372+1267T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20062147 | |||||||
| chrX:20062404 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.372+1010C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20062404 | |||||||
| chrX:20062746 | A | G | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+668T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20062746 | |||||||
| chrX:20063010 | C | T | 93 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(90): Show |
94 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(91): Show |
intron_variant | MODIFIER | c.372+404G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20063010 | |||||||
| chrX:20063111 | T | C | 1 | a0002c0003t0001g0018 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.372+303A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 3/16 | chrX | 20063111 | |||||||
| chrX:20063649 | A | C | 1 | a0002c0002t0001g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.209-72T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20063649 | |||||||
| chrX:20063809 | G | T | 1 | a0002c0002t0007g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.209-232C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20063809 | |||||||
| chrX:20063946 | A | G | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-369T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20063946 | |||||||
| chrX:20064039 | CA | C | 15 | a0002c0002t0001g0171 a0002c0002t0001g0172 a0002c0002t0001g0173 others(12): Show |
15 | HG00733.hp1 HG01081.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.209-463delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064039 | |||||||
| chrX:20064344 | T | C | 24 | a0002c0002t0001g0165 a0002c0002t0001g0171 a0002c0002t0001g0172 others(21): Show |
24 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.208+384A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064344 | |||||||
| chrX:20064363 | C | A | 3 | a0002c0002t0001g0170 a0002c0005t0001g0121 a0002c0005t0001g0122 |
3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.208+365G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064363 | |||||||
| chrX:20064436 | G | A | 1 | a0002c0002t0007g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.208+292C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064436 | |||||||
| chrX:20064471 | T | C | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+257A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064471 | |||||||
| chrX:20064659 | G | A | 9 | a0002c0002t0001g0186 a0002c0002t0001g0187 a0002c0002t0001g0188 others(6): Show |
9 | HG01243.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.208+69C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 2/16 | chrX | 20064659 | |||||||
| chrX:20064905 | G | A | 1 | a0002c0002t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.131-100C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20064905 | |||||||
| chrX:20064993 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.131-188G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20064993 | |||||||
| chrX:20065108 | T | C | 3 | a0002c0002t0001g0170 a0002c0005t0001g0121 a0002c0005t0001g0122 |
3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.131-303A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065108 | |||||||
| chrX:20065163 | C | G | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.131-358G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065163 | |||||||
| chrX:20065264 | CT | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0071 others(2): Show |
5 | HG03017.hp1 NA18957.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-460delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065264 | |||||||
| chrX:20065264 | CTTT | C | 6 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-462_131-460del others(3): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065264 | |||||||
| chrX:20065451 | G | T | 1 | a0006c0013t0006g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.131-646C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065451 | |||||||
| chrX:20065621 | A | G | 2 | a0002c0002t0001g0185 a0002c0003t0001g0018 |
2 | HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.131-816T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065621 | |||||||
| chrX:20065720 | T | C | 1 | a0002c0005t0001g0121 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.131-915A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065720 | |||||||
| chrX:20065913 | C | A | 6 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-1108G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065913 | |||||||
| chrX:20065917 | CT | C | 86 | a0001c0001t0001g0026 a0002c0002t0001g0002 a0002c0002t0001g0124 others(83): Show |
87 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.131-1113delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20065917 | |||||||
| chrX:20066282 | G | A | 6 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-1477C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066282 | |||||||
| chrX:20066319 | T | G | 1 | a0002c0002t0001g0164 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.131-1514A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066319 | |||||||
| chrX:20066365 | G | A | 2 | a0002c0002t0001g0132 a0002c0002t0001g0140 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.131-1560C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066365 | |||||||
| chrX:20066578 | T | C | 2 | a0002c0002t0001g0185 a0002c0003t0001g0018 |
2 | HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.131-1773A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066578 | |||||||
| chrX:20066625 | G | A | 73 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(70): Show |
74 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.131-1820C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066625 | |||||||
| chrX:20066973 | C | G | 1 | a0002c0005t0001g0120 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.131-2168G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20066973 | |||||||
| chrX:20067350 | A | G | 1 | a0002c0002t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.131-2545T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067350 | |||||||
| chrX:20067397 | C | T | 3 | a0002c0002t0001g0150 a0002c0002t0001g0161 a0002c0002t0001g0192 |
3 | HG01123.hp1 HG01167.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.131-2592G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067397 | |||||||
| chrX:20067466 | A | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.131-2661T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067466 | |||||||
| chrX:20067554 | G | C | 1 | a0002c0002t0001g0154 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.131-2749C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067554 | |||||||
| chrX:20067663 | T | G | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-2858A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20067663 | |||||||
| chrX:20068264 | G | A | 86 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(83): Show |
87 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(84): Show |
intron_variant | MODIFIER | c.131-3459C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20068264 | |||||||
| chrX:20069493 | G | T | 1 | a0006c0013t0006g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.131-4688C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069493 | |||||||
| chrX:20069513 | C | G | 1 | a0002c0002t0001g0171 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.131-4708G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069513 | |||||||
| chrX:20069763 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.131-4958G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069763 | |||||||
| chrX:20069774 | AT | A | 75 | a0001c0001t0001g0115 a0002c0002t0001g0124 a0002c0002t0001g0125 others(72): Show |
75 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.131-4970delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069774 | |||||||
| chrX:20069774 | ATT | A | 6 | a0002c0002t0001g0002 a0002c0002t0001g0127 a0002c0002t0001g0128 others(3): Show |
7 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-4971_131-4970d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069774 | |||||||
| chrX:20069943 | C | A | 4 | a0002c0003t0001g0013 a0002c0003t0001g0014 a0002c0003t0001g0015 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-5138G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20069943 | |||||||
| chrX:20070105 | C | T | 1 | a0002c0002t0001g0178 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.131-5300G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070105 | |||||||
| chrX:20070261 | C | CTTAT | 10 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0002c0002t0001g0161 others(7): Show |
10 | HG01123.hp1 HG01192.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-5460_131-5457d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070261 | |||||||
| chrX:20070261 | CTTAT | C | 23 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0033 others(20): Show |
23 | HG01123.hp2 HG01256.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-5460_131-5457d others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070261 | |||||||
| chrX:20070261 | CTTATTTA others(1): Show |
C | 12 | a0001c0001t0001g0065 a0002c0002t0001g0132 a0002c0002t0001g0133 others(9): Show |
12 | HG01070.hp2 HG02074.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.131-5464_131-5457d others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070261 | |||||||
| chrX:20070261 | CTTATTTA others(5): Show |
C | 4 | a0002c0002t0001g0170 a0002c0005t0001g0121 a0002c0005t0001g0122 others(1): Show |
4 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-5468_131-5457d others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070261 | |||||||
| chrX:20070261 | CTTATTTA others(9): Show |
C | 6 | a0002c0002t0001g0002 a0002c0002t0001g0127 a0002c0002t0001g0128 others(3): Show |
7 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-5472_131-5457d others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070261 | |||||||
| chrX:20070451 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.131-5646A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070451 | |||||||
| chrX:20070491 | A | T | 2 | a0002c0002t0001g0142 a0002c0002t0002g0144 |
2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.131-5686T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070491 | |||||||
| chrX:20070870 | T | C | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0191 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-6065A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20070870 | |||||||
| chrX:20071007 | G | A | 2 | a0002c0002t0001g0143 a0002c0002t0001g0191 |
2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.131-6202C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20071007 | |||||||
| chrX:20071241 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.131-6436G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20071241 | |||||||
| chrX:20071583 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.131-6778G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20071583 | |||||||
| chrX:20071784 | GTTTGTTT others(3): Show |
G | 1 | a0001c0001t0001g0025 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.131-6989_131-6980d others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20071784 | |||||||
| chrX:20072341 | C | G | 1 | a0002c0005t0001g0120 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.131-7536G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20072341 | |||||||
| chrX:20072897 | T | C | 1 | a0002c0002t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.131-8092A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20072897 | |||||||
| chrX:20072903 | G | A | 7 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 others(4): Show |
7 | HG01081.hp1 HG02258.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-8098C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20072903 | |||||||
| chrX:20072953 | T | A | 1 | a0002c0002t0001g0182 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.131-8148A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20072953 | |||||||
| chrX:20073388 | G | A | 4 | a0002c0002t0001g0126 a0002c0002t0001g0141 a0002c0002t0001g0145 others(1): Show |
4 | HG00735.hp2 HG01081.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-8583C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20073388 | |||||||
| chrX:20073532 | C | CT | 6 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-8728dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20073532 | |||||||
| chrX:20073768 | C | T | 1 | a0002c0002t0001g0202 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.131-8963G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20073768 | |||||||
| chrX:20073863 | G | A | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-9058C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20073863 | |||||||
| chrX:20074131 | G | A | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-9326C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20074131 | |||||||
| chrX:20074135 | CA | C | 5 | a0002c0002t0001g0152 a0002c0002t0001g0169 a0002c0002t0002g0123 others(2): Show |
5 | HG01515.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-9331delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20074135 | |||||||
| chrX:20074201 | C | T | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.131-9396G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20074201 | |||||||
| chrX:20074778 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.131-9973G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20074778 | |||||||
| chrX:20074908 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.131-10103G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20074908 | |||||||
| chrX:20075195 | G | A | 12 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(9): Show |
13 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-10390C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20075195 | |||||||
| chrX:20075311 | A | G | 1 | a0002c0005t0001g0120 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.131-10506T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20075311 | |||||||
| chrX:20075701 | C | T | 92 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(89): Show |
93 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.131-10896G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20075701 | |||||||
| chrX:20075813 | T | C | 1 | a0001c0001t0004g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.131-11008A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20075813 | |||||||
| chrX:20075961 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.131-11156G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20075961 | |||||||
| chrX:20076204 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.131-11399G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20076204 | |||||||
| chrX:20076701 | CA | C | 5 | a0002c0002t0001g0154 a0002c0002t0001g0170 a0002c0002t0001g0204 others(2): Show |
5 | HG01256.hp1 HG01981.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-11897delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20076701 | |||||||
| chrX:20076814 | T | C | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-12009A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20076814 | |||||||
| chrX:20076997 | T | G | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.131-12192A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20076997 | |||||||
| chrX:20077137 | C | A | 5 | a0002c0002t0001g0132 a0002c0002t0001g0140 a0002c0002t0001g0198 others(2): Show |
5 | HG02451.hp1 HG02572.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-12332G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077137 | |||||||
| chrX:20077192 | C | T | 88 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(85): Show |
89 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(86): Show |
intron_variant | MODIFIER | c.131-12387G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077192 | |||||||
| chrX:20077523 | A | G | 1 | a0006c0013t0006g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.131-12718T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077523 | |||||||
| chrX:20077533 | G | A | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0191 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-12728C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077533 | |||||||
| chrX:20077859 | G | T | 8 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0134 others(5): Show |
8 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-13054C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077859 | |||||||
| chrX:20077868 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.131-13063T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20077868 | |||||||
| chrX:20078187 | G | A | 93 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(90): Show |
94 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(91): Show |
intron_variant | MODIFIER | c.131-13382C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20078187 | |||||||
| chrX:20078273 | T | C | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-13468A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20078273 | |||||||
| chrX:20079980 | G | A | 1 | a0002c0003t0005g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.131-15175C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20079980 | |||||||
| chrX:20080051 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.131-15246G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080051 | |||||||
| chrX:20080152 | C | G | 3 | a0002c0002t0001g0170 a0002c0005t0001g0121 a0002c0005t0001g0122 |
3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.131-15347G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080152 | |||||||
| chrX:20080187 | T | A | 6 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-15382A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080187 | |||||||
| chrX:20080268 | C | T | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-15463G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080268 | |||||||
| chrX:20080540 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.131-15735C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080540 | |||||||
| chrX:20080583 | T | A | 1 | a0002c0002t0001g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.131-15778A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080583 | |||||||
| chrX:20080647 | C | T | 1 | a0002c0002t0001g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.131-15842G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20080647 | |||||||
| chrX:20081140 | T | C | 1 | a0002c0002t0007g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.131-16335A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081140 | |||||||
| chrX:20081392 | T | C | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-16587A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081392 | |||||||
| chrX:20081639 | T | C | 20 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(17): Show |
21 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.131-16834A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081639 | |||||||
| chrX:20081654 | A | AT | 10 | a0002c0002t0001g0135 a0002c0002t0001g0138 a0002c0002t0001g0165 others(7): Show |
10 | HG02109.hp2 HG02615.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-16850dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081654 | |||||||
| chrX:20081871 | A | G | 1 | a0002c0002t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.131-17066T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20081871 | |||||||
| chrX:20082183 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.131-17378G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082183 | |||||||
| chrX:20082288 | G | A | 1 | a0002c0002t0001g0149 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.131-17483C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082288 | |||||||
| chrX:20082398 | G | A | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-17593C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082398 | |||||||
| chrX:20082445 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0055 others(2): Show |
5 | HG00280.hp1 HG01496.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-17640C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082445 | |||||||
| chrX:20082501 | C | T | 46 | a0002c0002t0001g0124 a0002c0002t0001g0126 a0002c0002t0001g0141 others(43): Show |
46 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.131-17696G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082501 | |||||||
| chrX:20082629 | T | C | 6 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-17824A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082629 | |||||||
| chrX:20082671 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.131-17866C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082671 | |||||||
| chrX:20082697 | C | T | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-17892G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082697 | |||||||
| chrX:20082931 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
203 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(200): Show |
intron_variant | MODIFIER | c.131-18126C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20082931 | |||||||
| chrX:20083652 | A | T | 12 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(9): Show |
13 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-18847T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20083652 | |||||||
| chrX:20083724 | C | T | 68 | a0002c0002t0001g0124 a0002c0002t0001g0126 a0002c0002t0001g0132 others(65): Show |
68 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.131-18919G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20083724 | |||||||
| chrX:20083744 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.131-18939T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20083744 | |||||||
| chrX:20083833 | G | A | 4 | a0002c0002t0001g0126 a0002c0002t0001g0141 a0002c0002t0001g0145 others(1): Show |
4 | HG00735.hp2 HG01081.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-19028C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20083833 | |||||||
| chrX:20083976 | G | A | 1 | a0002c0002t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.131-19171C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20083976 | |||||||
| chrX:20084196 | CA | C | 83 | a0001c0001t0001g0026 a0001c0001t0001g0072 a0002c0002t0001g0002 others(80): Show |
84 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.131-19392delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084196 | |||||||
| chrX:20084199 | A | C | 3 | a0002c0002t0001g0125 a0002c0002t0001g0180 a0002c0002t0002g0181 |
3 | HG02717.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.131-19394T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084199 | |||||||
| chrX:20084331 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.131-19526G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084331 | |||||||
| chrX:20084545 | T | TTCCCTCC others(1): Show |
75 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(72): Show |
76 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.131-19748_131-1974 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | |||||||
| chrX:20084545 | T | TTCCCTCC others(5): Show |
12 | a0001c0001t0001g0019 a0001c0001t0001g0070 a0002c0002t0001g0170 others(9): Show |
12 | HG01106.hp1 HG01256.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.131-19752_131-1974 others(16): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | |||||||
| chrX:20084545 | T | TTCCCTCC others(18): Show |
1 | a0007c0007t0001g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.131-19741_131-1974 others(29): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | |||||||
| chrX:20084545 | T | TTCCCTCC others(9): Show |
93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
94 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.131-19756_131-1974 others(20): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | |||||||
| chrX:20084545 | T | TTCCCTCC others(13): Show |
11 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0029 others(8): Show |
11 | HG01099.hp1 HG01255.hp1 HG03492.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-19741_131-1974 others(24): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | |||||||
| chrX:20084545 | T | TTCCCTCC others(17): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0002c0003t0005g0105 |
3 | HG02135.hp1 HG02145.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.131-19741_131-1974 others(28): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084545 | |||||||
| chrX:20084550 | T | TCCCTCCC others(10): Show |
1 | a0001c0001t0001g0099 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.131-19746_131-1974 others(21): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084550 | |||||||
| chrX:20084564 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.131-19759A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084564 | |||||||
| chrX:20084788 | C | T | 40 | a0002c0002t0001g0126 a0002c0002t0001g0141 a0002c0002t0001g0142 others(37): Show |
40 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.131-19983G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084788 | |||||||
| chrX:20084895 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.131-20090A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20084895 | |||||||
| chrX:20085028 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.131-20223C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085028 | |||||||
| chrX:20085057 | C | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0074 |
2 | NA18986.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.131-20252G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085057 | |||||||
| chrX:20085641 | C | T | 87 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(84): Show |
88 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.131-20836G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085641 | |||||||
| chrX:20085660 | T | C | 15 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.131-20855A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085660 | |||||||
| chrX:20085689 | G | C | 2 | a0002c0002t0001g0002 a0002c0002t0001g0127 |
3 | HG01070.hp1 HG01071.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.131-20884C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085689 | |||||||
| chrX:20085948 | G | C | 18 | a0002c0002t0001g0134 a0002c0002t0001g0139 a0002c0002t0001g0165 others(15): Show |
18 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-21143C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20085948 | |||||||
| chrX:20086582 | A | T | 1 | a0002c0003t0005g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.131-21777T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20086582 | |||||||
| chrX:20086903 | C | T | 2 | a0002c0002t0001g0180 a0002c0002t0002g0181 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.131-22098G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20086903 | |||||||
| chrX:20087170 | C | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.131-22365G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087170 | |||||||
| chrX:20087221 | G | A | 7 | a0002c0002t0001g0185 a0002c0004t0001g0166 a0002c0004t0001g0167 others(4): Show |
7 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-22416C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087221 | |||||||
| chrX:20087240 | G | T | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-22435C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087240 | |||||||
| chrX:20087277 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0085 |
2 | NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.131-22472A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087277 | |||||||
| chrX:20087297 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0101 |
2 | HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.131-22492G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087297 | |||||||
| chrX:20087297 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.131-22492G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087297 | |||||||
| chrX:20087641 | C | T | 1 | a0002c0002t0001g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.131-22836G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087641 | |||||||
| chrX:20087879 | C | CT | 23 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0033 others(20): Show |
23 | HG01255.hp1 HG01258.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-23075dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | |||||||
| chrX:20087879 | CT | C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0069 others(10): Show |
13 | HG00733.hp1 HG01081.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-23075delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | |||||||
| chrX:20087879 | CTTT | C | 6 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0128 others(3): Show |
7 | HG01071.hp1 HG01891.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-23077_131-2307 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | |||||||
| chrX:20087879 | CTTTTTT | C | 17 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0134 others(14): Show |
17 | HG01070.hp2 HG01496.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.131-23080_131-2307 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | |||||||
| chrX:20087879 | CTTTTTTT others(1): Show |
C | 43 | a0001c0001t0001g0019 a0002c0002t0001g0124 a0002c0002t0001g0126 others(40): Show |
43 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.131-23082_131-2307 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20087879 | |||||||
| chrX:20088260 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.131-23455T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088260 | |||||||
| chrX:20088295 | CT | C | 75 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(72): Show |
76 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.131-23491delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088295 | |||||||
| chrX:20088364 | A | G | 1 | a0002c0005t0001g0120 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.131-23559T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088364 | |||||||
| chrX:20088468 | G | GT | 39 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(36): Show |
40 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.131-23664dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088468 | G | GTT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0031 others(20): Show |
23 | HG00140.hp1 HG01358.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-23665_131-2366 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088468 | G | GTTT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
10 | HG01255.hp1 HG02165.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-23666_131-2366 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088468 | G | GTTTT | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0033 others(6): Show |
9 | HG02040.hp1 HG02056.hp1 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.131-23667_131-2366 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088468 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0036 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.131-23674_131-2366 others(15): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088468 | G | GTTTTTTT others(8): Show |
1 | a0002c0002t0001g0185 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.131-23678_131-2366 others(19): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088468 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0108 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.131-23674_131-2366 others(15): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088468 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0074 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.131-23678_131-2366 others(19): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088468 | GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0001g0063 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.131-23679_131-2366 others(20): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088468 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.131-23680_131-2366 others(21): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088468 | GTTTTTTT others(11): Show |
G | 6 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(3): Show |
6 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-23681_131-2366 others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088468 | GTTTTTTT others(15): Show |
G | 75 | a0001c0001t0001g0019 a0001c0001t0001g0088 a0002c0002t0001g0124 others(72): Show |
75 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.131-23685_131-2366 others(26): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088468 | |||||||
| chrX:20088480 | T | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0084 |
2 | HG01952.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.131-23675A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088480 | |||||||
| chrX:20088588 | G | C | 1 | a0002c0002t0001g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.131-23783C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088588 | |||||||
| chrX:20088655 | T | C | 1 | a0002c0002t0001g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.131-23850A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088655 | |||||||
| chrX:20088732 | A | G | 1 | a0002c0002t0001g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.131-23927T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088732 | |||||||
| chrX:20088986 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.131-24181A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20088986 | |||||||
| chrX:20089296 | G | T | 87 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(84): Show |
88 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.131-24491C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20089296 | |||||||
| chrX:20089755 | T | A | 5 | a0002c0002t0001g0132 a0002c0002t0001g0140 a0002c0002t0001g0198 others(2): Show |
5 | HG02451.hp1 HG02572.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-24950A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20089755 | |||||||
| chrX:20089822 | C | A | 1 | a0005c0006t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.131-25017G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20089822 | |||||||
| chrX:20089931 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.131-25126A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20089931 | |||||||
| chrX:20090278 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.131-25473C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090278 | |||||||
| chrX:20090342 | C | T | 7 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(4): Show |
8 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-25537G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090342 | |||||||
| chrX:20090363 | CA | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(105): Show |
109 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.131-25559delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090363 | |||||||
| chrX:20090363 | CAA | C | 12 | a0001c0001t0001g0008 a0002c0002t0001g0140 a0002c0002t0001g0142 others(9): Show |
12 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.131-25560_131-2555 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090363 | |||||||
| chrX:20090363 | CAAA | C | 65 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(62): Show |
66 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.131-25561_131-2555 others(7): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090363 | |||||||
| chrX:20090363 | CAAAA | C | 11 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(8): Show |
11 | HG01106.hp1 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-25562_131-2555 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090363 | |||||||
| chrX:20090954 | G | A | 82 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(79): Show |
83 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(80): Show |
intron_variant | MODIFIER | c.130+25796C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20090954 | |||||||
| chrX:20091052 | C | CT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0117 others(9): Show |
13 | HG01496.hp2 HG01981.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+25697dupA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20091052 | |||||||
| chrX:20091199 | G | C | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0191 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+25551C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20091199 | |||||||
| chrX:20091919 | T | C | 14 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(11): Show |
15 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+24831A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20091919 | |||||||
| chrX:20092012 | G | T | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+24738C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20092012 | |||||||
| chrX:20092118 | T | C | 1 | a0002c0002t0001g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+24632A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20092118 | |||||||
| chrX:20092173 | C | T | 1 | a0001c0001t0004g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.130+24577G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20092173 | |||||||
| chrX:20092222 | C | T | 86 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(83): Show |
87 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(84): Show |
intron_variant | MODIFIER | c.130+24528G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20092222 | |||||||
| chrX:20092514 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.130+24236T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20092514 | |||||||
| chrX:20093419 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.130+23331C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20093419 | |||||||
| chrX:20093614 | G | A | 2 | a0002c0002t0001g0135 a0002c0002t0001g0138 |
2 | HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.130+23136C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20093614 | |||||||
| chrX:20093619 | T | C | 1 | a0002c0002t0001g0155 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.130+23131A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20093619 | |||||||
| chrX:20093667 | A | G | 4 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0121 others(1): Show |
4 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+23083T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20093667 | |||||||
| chrX:20094073 | C | A | 4 | a0002c0002t0001g0152 a0002c0002t0001g0153 a0002c0002t0001g0154 others(1): Show |
4 | HG01346.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+22677G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094073 | |||||||
| chrX:20094144 | T | G | 12 | a0002c0002t0001g0170 a0002c0002t0001g0185 a0002c0002t0001g0204 others(9): Show |
12 | HG01106.hp1 HG01256.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+22606A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094144 | |||||||
| chrX:20094269 | T | C | 4 | a0001c0001t0001g0019 a0002c0002t0001g0150 a0002c0002t0001g0161 others(1): Show |
4 | HG01123.hp1 HG01167.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22481A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094269 | |||||||
| chrX:20094483 | CATACATA others(65): Show |
C | 2 | a0002c0002t0001g0002 a0002c0002t0001g0127 |
3 | HG01070.hp1 HG01071.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.130+22195_130+2226 others(76): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094483 | |||||||
| chrX:20094487 | CAT | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(22): Show |
25 | HG00280.hp1 HG01243.hp1 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.130+22261_130+2226 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094487 | |||||||
| chrX:20094487 | CATAT | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0064 a0001c0001t0001g0077 |
3 | HG01258.hp1 HG02132.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.130+22259_130+2226 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094487 | |||||||
| chrX:20094487 | CATATATA others(23): Show |
C | 1 | a0002c0002t0001g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130+22233_130+2226 others(34): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094487 | |||||||
| chrX:20094487 | CATATATA others(87): Show |
C | 2 | a0002c0002t0001g0143 a0002c0002t0001g0191 |
2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.130+22169_130+2226 others(98): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094487 | |||||||
| chrX:20094488 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0001g0012 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.130+22234_130+2226 others(32): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094488 | |||||||
| chrX:20094490 | A | ATATATAT others(17): Show |
1 | a0007c0007t0001g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.130+22259_130+2226 others(28): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094490 | |||||||
| chrX:20094490 | ATATATAT others(45): Show |
A | 1 | a0002c0002t0001g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130+22208_130+2225 others(56): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094490 | |||||||
| chrX:20094492 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.130+22257_130+2225 others(26): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094492 | |||||||
| chrX:20094492 | ATATATAT others(43): Show |
A | 1 | a0006c0013t0006g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130+22208_130+2225 others(54): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094492 | |||||||
| chrX:20094493 | TATATATA others(69): Show |
T | 1 | a0001c0001t0001g0046 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.130+22181_130+2225 others(80): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094493 | |||||||
| chrX:20094494 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.130+22255_130+2225 others(44): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094494 | |||||||
| chrX:20094494 | ATATATAT others(41): Show |
A | 1 | a0002c0002t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+22208_130+2225 others(52): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094494 | |||||||
| chrX:20094496 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0080 a0001c0001t0001g0087 |
2 | HG01928.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.130+22253_130+2225 others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094496 | |||||||
| chrX:20094496 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.130+22253_130+2225 others(20): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094496 | |||||||
| chrX:20094496 | ATATATAT others(39): Show |
A | 4 | a0002c0002t0001g0155 a0002c0002t0001g0160 a0002c0002t0001g0161 others(1): Show |
4 | HG01192.hp1 NA19005.hp1 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22208_130+2225 others(50): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094496 | |||||||
| chrX:20094498 | ATATATAT others(37): Show |
A | 1 | a0002c0002t0001g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.130+22208_130+2225 others(48): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094498 | |||||||
| chrX:20094500 | ATATATAT others(9): Show |
A | 2 | a0002c0002t0001g0132 a0002c0002t0001g0140 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.130+22234_130+2224 others(20): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094500 | |||||||
| chrX:20094501 | T | C | 1 | a0004c0008t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+22249A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094501 | |||||||
| chrX:20094502 | ATATATAT others(7): Show |
A | 9 | a0001c0001t0001g0011 a0002c0002t0001g0134 a0002c0002t0001g0135 others(6): Show |
9 | HG01070.hp2 HG02615.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.130+22234_130+2224 others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094502 | |||||||
| chrX:20094502 | ATATATAT others(33): Show |
A | 1 | a0002c0002t0001g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.130+22208_130+2224 others(44): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094502 | |||||||
| chrX:20094503 | T | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0098 others(3): Show |
7 | HG02165.hp1 HG02165.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+22247A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094503 | |||||||
| chrX:20094503 | TATATATA others(59): Show |
T | 1 | a0002c0002t0001g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+22181_130+2224 others(70): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094503 | |||||||
| chrX:20094504 | ATATATAT others(5): Show |
A | 1 | a0002c0002t0001g0136 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130+22234_130+2224 others(16): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094504 | |||||||
| chrX:20094504 | ATATATAT others(31): Show |
A | 7 | a0001c0001t0001g0019 a0002c0002t0001g0141 a0002c0002t0001g0149 others(4): Show |
7 | HG01081.hp2 HG01496.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+22208_130+2224 others(42): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094504 | |||||||
| chrX:20094505 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.130+22245A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094505 | |||||||
| chrX:20094505 | TATATATA others(57): Show |
T | 4 | a0002c0002t0001g0125 a0002c0002t0001g0128 a0002c0002t0001g0129 others(1): Show |
4 | HG01891.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+22181_130+2224 others(68): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094505 | |||||||
| chrX:20094506 | ATATATAT others(3): Show |
A | 2 | a0002c0002t0001g0133 a0002c0002t0002g0203 |
2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.130+22234_130+2224 others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094506 | |||||||
| chrX:20094506 | ATATATAT others(29): Show |
A | 4 | a0002c0002t0001g0150 a0002c0002t0001g0163 a0002c0002t0001g0206 others(1): Show |
4 | HG01167.hp1 HG03239.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22208_130+2224 others(40): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094506 | |||||||
| chrX:20094507 | TATATATA others(55): Show |
T | 5 | a0002c0002t0001g0124 a0002c0003t0001g0018 a0002c0004t0001g0166 others(2): Show |
5 | HG01106.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+22181_130+2224 others(66): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094507 | |||||||
| chrX:20094508 | ATATATAT others(27): Show |
A | 5 | a0002c0002t0001g0156 a0002c0002t0001g0159 a0002c0002t0001g0192 others(2): Show |
5 | HG01123.hp1 HG02015.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+22208_130+2224 others(38): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094508 | |||||||
| chrX:20094509 | T | C | 1 | a0005c0006t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.130+22241A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094509 | |||||||
| chrX:20094509 | TATATATG others(53): Show |
T | 23 | a0002c0002t0001g0147 a0002c0002t0001g0164 a0002c0002t0001g0165 others(20): Show |
23 | HG00733.hp1 HG01081.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.130+22181_130+2224 others(64): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094509 | |||||||
| chrX:20094510 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0035 |
3 | HG02165.hp1 HG02165.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.130+22240T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094510 | |||||||
| chrX:20094510 | ATATATG | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0033 others(8): Show |
11 | HG01099.hp1 HG01346.hp1 NA18971.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+22234_130+2223 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094510 | |||||||
| chrX:20094510 | ATATATGT others(25): Show |
A | 2 | a0002c0002t0007g0208 a0008c0012t0001g0158 |
2 | NA19030.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.130+22208_130+2223 others(36): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094510 | |||||||
| chrX:20094511 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0117 |
2 | NA18966.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.130+22239A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094511 | |||||||
| chrX:20094511 | TATATGTA others(51): Show |
T | 2 | a0002c0002t0001g0179 a0002c0002t0001g0183 |
2 | HG01361.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.130+22181_130+2223 others(62): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094511 | |||||||
| chrX:20094512 | A | ATG | 4 | a0001c0001t0001g0053 a0001c0001t0001g0065 a0001c0001t0001g0116 others(1): Show |
4 | HG01981.hp2 HG02074.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22237_130+2223 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094512 | |||||||
| chrX:20094512 | A | ATGTATAT others(19): Show |
1 | a0001c0010t0001g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.130+22237_130+2223 others(30): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094512 | |||||||
| chrX:20094512 | A | G | 10 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0055 others(7): Show |
10 | HG00609.hp1 HG02056.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+22238T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094512 | |||||||
| chrX:20094512 | ATATG | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
8 | HG00738.hp1 HG01981.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+22234_130+2223 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094512 | |||||||
| chrX:20094513 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0030 others(4): Show |
7 | HG01255.hp1 HG02698.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+22237A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094513 | |||||||
| chrX:20094513 | TATGTATA others(49): Show |
T | 3 | a0002c0002t0001g0170 a0002c0005t0001g0121 a0002c0005t0001g0122 |
3 | HG01496.hp2 HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.130+22181_130+2223 others(60): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094513 | |||||||
| chrX:20094514 | A | G | 29 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0026 others(26): Show |
29 | HG00642.hp1 HG00673.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.130+22236T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094514 | |||||||
| chrX:20094514 | ATG | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0043 others(7): Show |
11 | HG00609.hp1 HG01517.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+22234_130+2223 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094514 | |||||||
| chrX:20094515 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0070 others(1): Show |
4 | HG02135.hp1 NA18962.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22235A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094515 | |||||||
| chrX:20094516 | G | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0026 others(34): Show |
37 | HG00642.hp1 HG00673.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.130+22234C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094516 | |||||||
| chrX:20094516 | GTA | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0115 |
2 | NA18957.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.130+22232_130+2223 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094516 | |||||||
| chrX:20094516 | GTATA | G | 3 | a0001c0001t0001g0114 a0002c0002t0001g0202 a0004c0008t0001g0109 |
3 | HG03486.hp1 NA18979.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.130+22230_130+2223 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094516 | |||||||
| chrX:20094517 | T | C | 8 | a0002c0002t0001g0134 a0002c0002t0001g0135 a0002c0002t0001g0138 others(5): Show |
8 | HG01070.hp2 HG02615.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+22233A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094517 | |||||||
| chrX:20094518 | A | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0023 others(7): Show |
10 | HG00738.hp1 HG01981.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+22232T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094518 | |||||||
| chrX:20094518 | ATATATAT others(17): Show |
A | 3 | a0002c0002t0001g0194 a0002c0002t0001g0195 a0002c0002t0001g0196 |
3 | HG01243.hp1 HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.130+22208_130+2223 others(28): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094518 | |||||||
| chrX:20094519 | T | C | 2 | a0002c0002t0001g0132 a0002c0002t0001g0140 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.130+22231A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094519 | |||||||
| chrX:20094520 | A | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0033 others(11): Show |
14 | HG01099.hp1 HG01346.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+22230T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094520 | |||||||
| chrX:20094522 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.130+22228T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094522 | |||||||
| chrX:20094524 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.130+22226T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094524 | |||||||
| chrX:20094528 | A | G | 1 | a0001c0001t0001g0011 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.130+22222T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094528 | |||||||
| chrX:20094530 | ATATATAT others(5): Show |
A | 1 | a0002c0002t0001g0193 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130+22208_130+2221 others(16): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094530 | |||||||
| chrX:20094535 | TATATATG others(27): Show |
T | 3 | a0002c0002t0001g0187 a0002c0002t0001g0188 a0002c0002t0001g0189 |
3 | HG02257.hp2 HG02486.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.130+22181_130+2221 others(38): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094535 | |||||||
| chrX:20094538 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0082 a0001c0001t0001g0104 others(1): Show |
4 | HG02083.hp1 HG02293.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22212T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094538 | |||||||
| chrX:20094540 | A | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0001g0106 others(1): Show |
4 | HG01123.hp2 HG01934.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22210T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094540 | |||||||
| chrX:20094540 | ATG | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0101 others(1): Show |
4 | HG02135.hp1 NA18940.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22208_130+2220 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094540 | |||||||
| chrX:20094540 | ATGTATAT others(30): Show |
A | 1 | a0002c0002t0001g0186 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.130+22173_130+2220 others(41): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094540 | |||||||
| chrX:20094541 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.130+22209A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094541 | |||||||
| chrX:20094542 | G | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0053 others(12): Show |
15 | HG01346.hp2 HG01433.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+22208C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094542 | |||||||
| chrX:20094542 | G | GTA | 2 | a0001c0001t0001g0087 a0001c0001t0004g0066 |
2 | HG01123.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.130+22206_130+2220 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094542 | |||||||
| chrX:20094542 | G | GTATATAT others(17): Show |
1 | a0001c0001t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.130+22207_130+2220 others(28): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094542 | |||||||
| chrX:20094544 | A | G | 17 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0080 others(14): Show |
17 | HG01070.hp2 HG01981.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.130+22206T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094544 | |||||||
| chrX:20094546 | A | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
7 | HG01346.hp2 HG01433.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+22204T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094546 | |||||||
| chrX:20094548 | A | G | 1 | a0001c0010t0001g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.130+22202T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094548 | |||||||
| chrX:20094552 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0084 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.130+22197_130+2219 others(28): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094552 | |||||||
| chrX:20094552 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG01943.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.130+22197_130+2219 others(24): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094552 | |||||||
| chrX:20094552 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0081 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.130+22197_130+2219 others(22): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094552 | |||||||
| chrX:20094555 | TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.130+22181_130+2219 others(18): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094555 | |||||||
| chrX:20094557 | T | C | 1 | a0004c0008t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+22193A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094557 | |||||||
| chrX:20094559 | TATATATA others(3): Show |
T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0038 others(1): Show |
4 | NA18971.hp1 NA18984.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+22181_130+2219 others(14): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094559 | |||||||
| chrX:20094561 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.130+22189A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094561 | |||||||
| chrX:20094561 | TATATATA others(1): Show |
T | 5 | a0001c0001t0001g0037 a0002c0002t0001g0132 a0002c0002t0001g0198 others(2): Show |
5 | HG02451.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+22181_130+2218 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094561 | |||||||
| chrX:20094563 | TATATAC | T | 21 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0075 others(18): Show |
21 | HG01070.hp2 HG02145.hp1 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.130+22181_130+2218 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094563 | |||||||
| chrX:20094565 | TATAC | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(33): Show |
36 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.130+22181_130+2218 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094565 | |||||||
| chrX:20094567 | TAC | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(14): Show |
18 | HG00609.hp1 HG00673.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.130+22181_130+2218 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094567 | |||||||
| chrX:20094569 | C | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(72): Show |
76 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.130+22181G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094569 | |||||||
| chrX:20094577 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0064 |
2 | HG02132.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.130+22173A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094577 | |||||||
| chrX:20094592 | A | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG01981.hp1 NA18977.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+22158T>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20094592 | |||||||
| chrX:20095034 | C | T | 37 | a0001c0001t0001g0019 a0002c0002t0001g0124 a0002c0002t0001g0126 others(34): Show |
37 | HG00735.hp2 HG01081.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.130+21716G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095034 | |||||||
| chrX:20095111 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.130+21639A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095111 | |||||||
| chrX:20095124 | A | G | 1 | a0002c0002t0001g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.130+21626T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095124 | |||||||
| chrX:20095134 | C | T | 1 | a0004c0008t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+21616G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095134 | |||||||
| chrX:20095156 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.130+21594A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095156 | |||||||
| chrX:20095886 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.130+20864G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095886 | |||||||
| chrX:20095972 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0088 |
3 | HG00673.hp1 NA18990.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.130+20778G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20095972 | |||||||
| chrX:20096006 | C | T | 1 | a0002c0003t0005g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.130+20744G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096006 | |||||||
| chrX:20096013 | C | T | 69 | a0002c0002t0001g0124 a0002c0002t0001g0126 a0002c0002t0001g0132 others(66): Show |
69 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.130+20737G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096013 | |||||||
| chrX:20096081 | C | CA | 30 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(27): Show |
30 | HG01123.hp2 HG01255.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.130+20668dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096081 | |||||||
| chrX:20096081 | CA | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0085 others(3): Show |
6 | HG01069.hp1 HG01070.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+20668delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096081 | |||||||
| chrX:20096259 | CT | C | 6 | a0001c0001t0001g0071 a0002c0002t0001g0138 a0002c0002t0001g0150 others(3): Show |
6 | HG01167.hp1 HG02897.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+20490delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096259 | |||||||
| chrX:20096397 | T | C | 5 | a0002c0002t0001g0170 a0002c0002t0001g0204 a0002c0005t0001g0120 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+20353A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096397 | |||||||
| chrX:20096429 | C | CA | 7 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG01361.hp1 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+20320dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096429 | |||||||
| chrX:20096429 | CA | C | 40 | a0001c0001t0001g0086 a0001c0001t0001g0099 a0002c0002t0001g0124 others(37): Show |
40 | HG00735.hp2 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.130+20320delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096429 | |||||||
| chrX:20096429 | CAA | C | 7 | a0002c0002t0001g0126 a0002c0002t0001g0170 a0002c0002t0001g0204 others(4): Show |
7 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+20319_130+2032 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20096429 | |||||||
| chrX:20098036 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.130+18714T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098036 | |||||||
| chrX:20098097 | G | A | 34 | a0002c0002t0001g0126 a0002c0002t0001g0141 a0002c0002t0001g0145 others(31): Show |
34 | HG00735.hp2 HG01081.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.130+18653C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098097 | |||||||
| chrX:20098395 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.130+18355T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098395 | |||||||
| chrX:20098446 | T | G | 3 | a0002c0002t0001g0124 a0002c0002t0001g0164 a0002c0002t0001g0184 |
3 | HG02055.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.130+18304A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098446 | |||||||
| chrX:20098506 | C | G | 1 | a0002c0002t0001g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+18244G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098506 | |||||||
| chrX:20098557 | T | TG | 16 | a0001c0001t0001g0093 a0001c0001t0001g0113 a0002c0002t0001g0131 others(13): Show |
16 | HG01070.hp2 HG01261.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.130+18192dupC | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098557 | |||||||
| chrX:20098560 | G | T | 2 | a0002c0002t0001g0124 a0002c0002t0001g0164 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.130+18190C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098560 | |||||||
| chrX:20098900 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.130+17850G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098900 | |||||||
| chrX:20098948 | A | G | 1 | a0002c0003t0005g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.130+17802T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20098948 | |||||||
| chrX:20099225 | G | A | 5 | a0002c0002t0001g0132 a0002c0002t0001g0140 a0002c0002t0001g0198 others(2): Show |
5 | HG02451.hp1 HG02572.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+17525C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099225 | |||||||
| chrX:20099235 | A | ACT | 2 | a0002c0002t0001g0180 a0002c0002t0002g0181 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.130+17513_130+1751 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099235 | |||||||
| chrX:20099235 | ACT | A | 19 | a0001c0001t0001g0088 a0002c0002t0001g0146 a0002c0002t0001g0165 others(16): Show |
19 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.130+17513_130+1751 others(6): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099235 | |||||||
| chrX:20099235 | ACTCT | A | 37 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0023 others(34): Show |
37 | HG00735.hp2 HG01109.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.130+17511_130+1751 others(8): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099235 | |||||||
| chrX:20099235 | ACTCTCT | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
141 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.130+17509_130+1751 others(10): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099235 | |||||||
| chrX:20099235 | ACTCTCTC others(1): Show |
A | 8 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0002c0002t0001g0140 others(5): Show |
8 | HG01081.hp2 HG02300.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+17507_130+1751 others(12): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099235 | |||||||
| chrX:20099781 | C | A | 1 | a0003c0009t0001g0119 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.130+16969G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20099781 | |||||||
| chrX:20100067 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.130+16683G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100067 | |||||||
| chrX:20100394 | C | T | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0191 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+16356G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100394 | |||||||
| chrX:20100683 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.130+16067G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100683 | |||||||
| chrX:20100768 | T | G | 1 | a0004c0008t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+15982A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100768 | |||||||
| chrX:20100793 | A | G | 18 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(15): Show |
19 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.130+15957T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100793 | |||||||
| chrX:20100847 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.130+15903G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20100847 | |||||||
| chrX:20101021 | C | CA | 10 | a0002c0002t0001g0134 a0002c0002t0001g0159 a0002c0002t0001g0160 others(7): Show |
10 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.130+15728dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20101021 | |||||||
| chrX:20101033 | A | C | 1 | a0002c0002t0001g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+15717T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20101033 | |||||||
| chrX:20101291 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.130+15459C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20101291 | |||||||
| chrX:20101816 | T | C | 8 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+14934A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20101816 | |||||||
| chrX:20102369 | C | T | 12 | a0002c0002t0001g0170 a0002c0002t0001g0171 a0002c0002t0001g0172 others(9): Show |
12 | HG00733.hp1 HG01081.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+14381G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20102369 | |||||||
| chrX:20102411 | T | G | 26 | a0001c0001t0001g0019 a0002c0002t0001g0126 a0002c0002t0001g0141 others(23): Show |
26 | HG00735.hp2 HG01081.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.130+14339A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20102411 | |||||||
| chrX:20102447 | T | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0010t0001g0190 |
3 | HG00738.hp1 HG01346.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.130+14303A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20102447 | |||||||
| chrX:20102821 | T | C | 98 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0124 others(95): Show |
99 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.130+13929A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20102821 | |||||||
| chrX:20102935 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.130+13815A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20102935 | |||||||
| chrX:20103051 | C | T | 91 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0124 others(88): Show |
92 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(89): Show |
intron_variant | MODIFIER | c.130+13699G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103051 | |||||||
| chrX:20103122 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.130+13628A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103122 | |||||||
| chrX:20103290 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.130+13460G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103290 | |||||||
| chrX:20103343 | G | C | 1 | a0002c0002t0001g0182 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.130+13407C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103343 | |||||||
| chrX:20103408 | C | T | 1 | a0002c0002t0001g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.130+13342G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103408 | |||||||
| chrX:20103498 | T | A | 2 | a0002c0002t0001g0132 a0002c0002t0001g0140 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.130+13252A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103498 | |||||||
| chrX:20103524 | T | C | 1 | a0002c0002t0001g0182 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.130+13226A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103524 | |||||||
| chrX:20103623 | G | T | 83 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(80): Show |
84 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.130+13127C>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103623 | |||||||
| chrX:20103701 | C | T | 87 | a0002c0002t0001g0002 a0002c0002t0001g0124 a0002c0002t0001g0125 others(84): Show |
88 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.130+13049G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103701 | |||||||
| chrX:20103914 | C | G | 1 | a0006c0013t0006g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130+12836G>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20103914 | |||||||
| chrX:20104013 | A | G | 2 | a0002c0005t0001g0121 a0002c0005t0001g0122 |
2 | HG01496.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.130+12737T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104013 | |||||||
| chrX:20104332 | G | A | 1 | a0002c0002t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130+12418C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104332 | |||||||
| chrX:20104336 | T | A | 4 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
4 | HG01934.hp1 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+12414A>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104336 | |||||||
| chrX:20104445 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.130+12305G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104445 | |||||||
| chrX:20104752 | GGAAAGCT others(6): Show |
G | 1 | a0001c0001t0001g0085 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.130+11985_130+1199 others(17): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104752 | |||||||
| chrX:20104792 | C | T | 50 | a0001c0001t0001g0019 a0002c0002t0001g0126 a0002c0002t0001g0132 others(47): Show |
50 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.130+11958G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20104792 | |||||||
| chrX:20105342 | A | C | 5 | a0002c0004t0001g0166 a0002c0004t0001g0167 a0002c0004t0001g0168 others(2): Show |
5 | HG01106.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+11408T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20105342 | |||||||
| chrX:20105421 | A | G | 1 | a0002c0002t0001g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+11329T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20105421 | |||||||
| chrX:20106366 | G | A | 1 | a0002c0002t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+10384C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20106366 | |||||||
| chrX:20106494 | T | C | 1 | a0002c0002t0001g0185 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.130+10256A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20106494 | |||||||
| chrX:20106859 | T | C | 1 | a0002c0002t0002g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130+9891A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20106859 | |||||||
| chrX:20106990 | A | G | 1 | a0002c0002t0001g0193 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130+9760T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20106990 | |||||||
| chrX:20107076 | A | G | 1 | a0002c0002t0001g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130+9674T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107076 | |||||||
| chrX:20107086 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.130+9664C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107086 | |||||||
| chrX:20107495 | G | A | 1 | a0002c0002t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.130+9255C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107495 | |||||||
| chrX:20107573 | G | GC | 18 | a0001c0001t0001g0087 a0001c0001t0001g0112 a0002c0002t0001g0002 others(15): Show |
19 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.130+9176dupG | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107573 | |||||||
| chrX:20107866 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.130+8884G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20107866 | |||||||
| chrX:20108032 | G | A | 5 | a0002c0002t0001g0204 a0002c0005t0001g0120 a0002c0005t0001g0121 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+8718C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20108032 | |||||||
| chrX:20108720 | C | CA | 13 | a0001c0001t0001g0088 a0001c0001t0001g0094 a0001c0001t0001g0107 others(10): Show |
13 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+8029dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20108720 | |||||||
| chrX:20108834 | GT | G | 5 | a0002c0002t0001g0204 a0002c0005t0001g0120 a0002c0005t0001g0121 others(2): Show |
5 | HG01256.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+7915delA | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20108834 | |||||||
| chrX:20108868 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.130+7882C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20108868 | |||||||
| chrX:20109169 | A | G | 13 | a0002c0002t0001g0002 a0002c0002t0001g0125 a0002c0002t0001g0127 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+7581T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109169 | |||||||
| chrX:20109229 | T | G | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0191 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+7521A>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109229 | |||||||
| chrX:20109248 | A | G | 91 | a0001c0001t0001g0019 a0002c0002t0001g0002 a0002c0002t0001g0124 others(88): Show |
92 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(89): Show |
intron_variant | MODIFIER | c.130+7502T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109248 | |||||||
| chrX:20109420 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.130+7330A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109420 | |||||||
| chrX:20109480 | A | ACT | 7 | a0002c0002t0001g0124 a0002c0002t0001g0133 a0002c0002t0001g0134 others(4): Show |
7 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+7268_130+7269d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109480 | |||||||
| chrX:20109519 | C | CA | 10 | a0001c0001t0001g0011 a0001c0001t0001g0089 a0001c0001t0001g0090 others(7): Show |
10 | HG00733.hp2 HG02027.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+7230dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109519 | |||||||
| chrX:20109519 | CA | C | 46 | a0001c0001t0001g0017 a0001c0001t0001g0107 a0002c0002t0001g0002 others(43): Show |
47 | HG00733.hp1 HG01070.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.130+7230delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109519 | |||||||
| chrX:20109519 | CAA | C | 35 | a0002c0002t0001g0125 a0002c0002t0001g0126 a0002c0002t0001g0132 others(32): Show |
35 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.130+7229_130+7230d others(4): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109519 | |||||||
| chrX:20109811 | G | A | 3 | a0002c0003t0003g0095 a0002c0003t0003g0096 a0002c0003t0003g0097 |
3 | HG02015.hp1 HG03017.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.130+6939C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109811 | |||||||
| chrX:20109989 | T | C | 1 | a0002c0002t0001g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130+6761A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20109989 | |||||||
| chrX:20110027 | C | T | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0001g0191 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+6723G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110027 | |||||||
| chrX:20110605 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | HG02027.hp1 NA18945.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+6145C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110605 | |||||||
| chrX:20110662 | C | CA | 13 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0102 others(10): Show |
13 | HG02109.hp1 HG02135.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+6087dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110662 | |||||||
| chrX:20110780 | T | C | 1 | a0002c0002t0001g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.130+5970A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20110780 | |||||||
| chrX:20111127 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.130+5623G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111127 | |||||||
| chrX:20111265 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0114 |
2 | NA18979.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.130+5485T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111265 | |||||||
| chrX:20111371 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.130+5379G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111371 | |||||||
| chrX:20111426 | G | A | 1 | a0002c0002t0001g0130 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.130+5324C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111426 | |||||||
| chrX:20111517 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.130+5233G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111517 | |||||||
| chrX:20111582 | T | C | 1 | a0002c0002t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+5168A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111582 | |||||||
| chrX:20111629 | G | A | 1 | a0006c0013t0006g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130+5121C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111629 | |||||||
| chrX:20111645 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.130+5105C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20111645 | |||||||
| chrX:20112008 | G | A | 1 | a0002c0002t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.130+4742C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20112008 | |||||||
| chrX:20112118 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.130+4632C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20112118 | |||||||
| chrX:20112327 | C | T | 1 | a0002c0002t0001g0141 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.130+4423G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20112327 | |||||||
| chrX:20113039 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.130+3711G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113039 | |||||||
| chrX:20113244 | A | G | 1 | a0001c0001t0001g0007 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.130+3506T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113244 | |||||||
| chrX:20113487 | G | A | 5 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0195 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+3263C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113487 | |||||||
| chrX:20113579 | G | A | 4 | a0002c0002t0001g0198 a0002c0002t0001g0199 a0002c0002t0001g0200 others(1): Show |
4 | HG03209.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+3171C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113579 | |||||||
| chrX:20113929 | T | C | 1 | a0002c0004t0001g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.130+2821A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113929 | |||||||
| chrX:20113983 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.130+2767A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20113983 | |||||||
| chrX:20114223 | G | C | 1 | a0002c0002t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+2527C>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114223 | |||||||
| chrX:20114454 | GCAGATTG others(36): Show |
G | 1 | a0002c0002t0001g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+2253_130+2295d others(45): Show |
MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114454 | |||||||
| chrX:20114459 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.130+2291A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114459 | |||||||
| chrX:20114685 | C | T | 10 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0134 others(7): Show |
10 | HG01070.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+2065G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114685 | |||||||
| chrX:20114756 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.130+1994A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114756 | |||||||
| chrX:20114824 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.130+1926C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114824 | |||||||
| chrX:20114985 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.130+1765C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20114985 | |||||||
| chrX:20115239 | T | TA | 9 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(6): Show |
9 | HG01496.hp2 HG02109.hp1 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.130+1510dupT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115239 | |||||||
| chrX:20115239 | TA | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0002c0002t0001g0002 others(7): Show |
11 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+1510delT | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115239 | |||||||
| chrX:20115253 | A | C | 1 | a0002c0002t0001g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.130+1497T>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115253 | |||||||
| chrX:20115259 | C | A | 3 | a0001c0001t0001g0063 a0002c0005t0001g0121 a0002c0005t0001g0122 |
3 | HG01496.hp2 HG02109.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.130+1491G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115259 | |||||||
| chrX:20115622 | T | C | 1 | a0002c0002t0002g0203 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.130+1128A>G | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115622 | |||||||
| chrX:20115666 | C | A | 3 | a0002c0002t0001g0204 a0002c0005t0001g0121 a0002c0005t0001g0122 |
3 | HG01496.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.130+1084G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20115666 | |||||||
| chrX:20116221 | G | A | 1 | a0002c0004t0001g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.130+529C>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20116221 | |||||||
| chrX:20116546 | A | G | 1 | a0001c0001t0001g0003 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.130+204T>C | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20116546 | |||||||
| chrX:20116695 | C | T | 1 | a0002c0002t0002g0123 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.130+55G>A | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20116695 | |||||||
| chrX:20116701 | C | A | 1 | a0002c0002t0001g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.130+49G>T | MAP7D2 | ENSG00000184368.16 | transcript | ENST00000379643.10 | protein_coding | 1/16 | chrX | 20116701 |