Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7102 |
| ensemblid | ENSG00000156298.13 |
| hgncid | 11854 |
| symbol | TSPAN7 |
| name | tetraspanin 7 |
| refseq_nuc | NM_004615.4 |
| refseq_prot | NP_004606.2 |
| ensembl_nuc | ENST00000378482.7 |
| ensembl_prot | ENSP00000367743.2 |
| mane_status | MANE Select |
| chr | chrX |
| start | 38561542 |
| end | 38688918 |
| strand | + |
| ver | v1.2 |
| region | chrX:38561542-38688918 |
| region5000 | chrX:38556542-38693918 |
| regionname0 | TSPAN7_chrX_38561542_38688918 |
| regionname5000 | TSPAN7_chrX_38556542_38693918 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 747 | 208 | 49 | 36 | 88 | 9 | 24 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | ATGGC others(742): Show |
chrX | 38556542 | 38693918 | ||
| a0001c0002 | 0/0 | 747 | 9 | 9 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | ATGGC others(742): Show |
chrX | 38556542 | 38693918 | ||
| a0001c0003 | 0/0 | 747 | 6 | 6 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | ATGGC others(742): Show |
chrX | 38556542 | 38693918 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1742 | 157 | 31 | 29 | 72 | 6 | 18 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | GTAGT others(1737): Show |
chrX | 38556542 | 38693918 |
| a0001c0001t0002 | 1/0 | 1742 | 47 | 14 | 7 | 16 | 3 | 6 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | GTAGT others(1737): Show |
chrX | 38556542 | 38693918 |
| a0001c0001t0003 | 0/0 | 1742 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | GTAGT others(1737): Show |
chrX | 38556542 | 38693918 |
| a0001c0001t0005 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | GTAGT others(1737): Show |
chrX | 38556542 | 38693918 |
| a0001c0002t0001 | 0/0 | 1742 | 9 | 9 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | GTAGT others(1737): Show |
chrX | 38556542 | 38693918 |
| a0001c0003t0001 | 0/0 | 1742 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | GTAGT others(1737): Show |
chrX | 38556542 | 38693918 |
| a0001c0003t0004 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | GTAGT others(1737): Show |
chrX | 38556542 | 38693918 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | GBR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | IBS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0139 | EUR | IBS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0196 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0210 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0181 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | BEB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | STU | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | YRI | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | YRI | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ASW | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ASW | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | TSI | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | GIH | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02109 | hp2 | a0001 | c0003 | t0004 | g0203 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0195 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | USA | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | USA | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | LWK | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | LWK | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0123 | REF | REF | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0122 | REF | REF | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| 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 |
|---|
| 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:38666276 | T | C | 1 | a0001c0002 | 9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
synonymous_variant | LOW | c.237T>C | p.Ala79Ala | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/8 | 242/1742 | 237/750 | 79/249 | chrX | 38666276 | |||
| chrX:38674316 | C | T | 1 | a0001c0003 | 6 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.441C>T | p.Ser147Ser | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/8 | 446/1742 | 441/750 | 147/249 | chrX | 38674316 |
| 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:38688001 | A | G | 1 | a0001c0001t0005 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 334 | chrX | 38688001 | ||||||
| chrX:38688007 | A | G | 1 | a0001c0001t0005 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*76A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 340 | chrX | 38688007 | ||||||
| chrX:38688054 | C | A | 5 | a0001c0001t0001 a0001c0001t0005 a0001c0002t0001 others(2): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*123C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 387 | chrX | 38688054 | ||||||
| chrX:38688197 | A | C | 1 | a0001c0001t0005 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*266A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 530 | chrX | 38688197 | ||||||
| chrX:38688608 | G | A | 6 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(3): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*677G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 941 | chrX | 38688608 | ||||||
| chrX:38688652 | C | T | 1 | a0001c0003t0004 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*721C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 985 | chrX | 38688652 | ||||||
| chrX:38688829 | G | A | 6 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(3): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*898G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 1162 | chrX | 38688829 |
| 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:38561712 | A | T | 2 | a0001c0002t0001g0209 a0001c0003t0001g0210 |
2 | HG02257.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.81+85A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38561712 | |||||||
| chrX:38561713 | C | T | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0002t0001g0207 others(1): Show |
4 | HG02723.hp1 HG03195.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+86C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38561713 | |||||||
| chrX:38561734 | G | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
82 | HG00621.hp1 HG00741.hp1 HG01074.hp1 others(79): Show |
intron_variant | MODIFIER | c.81+107G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38561734 | |||||||
| chrX:38561884 | CA | C | 8 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0080 others(5): Show |
8 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+267delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38561884 | ||||||
| chrX:38562069 | C | T | 5 | a0001c0001t0001g0077 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+442C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562069 | |||||||
| chrX:38562102 | T | C | 32 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(29): Show |
32 | HG01074.hp1 HG01169.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.81+475T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562102 | |||||||
| chrX:38562113 | G | A | 31 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(28): Show |
31 | HG01074.hp1 HG01169.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.81+486G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562113 | |||||||
| chrX:38562176 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.81+549T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562176 | |||||||
| chrX:38562242 | A | G | 1 | a0001c0001t0002g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.81+615A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562242 | |||||||
| chrX:38562355 | A | G | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0199 others(9): Show |
12 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.81+728A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562355 | |||||||
| chrX:38562454 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+827T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562454 | |||||||
| chrX:38562550 | G | T | 36 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
36 | HG01074.hp1 HG01169.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.81+923G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562550 | |||||||
| chrX:38562556 | G | GGGGGGAG others(8): Show |
1 | a0001c0001t0002g0193 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.81+947_81+961dupGG others(13): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38562556 | ||||||
| chrX:38562556 | GGGGGGAG others(8): Show |
G | 28 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(25): Show |
29 | HG00621.hp1 HG00741.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.81+947_81+961delGG others(13): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38562556 | ||||||
| chrX:38562558 | G | GGGGAGGA | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+934_81+940dupGA others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38562558 | ||||||
| chrX:38562682 | G | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(24): Show |
28 | HG00621.hp1 HG00741.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.81+1055G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562682 | |||||||
| chrX:38562757 | G | T | 50 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
50 | HG01074.hp1 HG01169.hp2 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.81+1130G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562757 | |||||||
| chrX:38562961 | T | A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(50): Show |
55 | HG00621.hp1 HG00741.hp1 HG01884.hp2 others(52): Show |
intron_variant | MODIFIER | c.81+1334T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562961 | |||||||
| chrX:38563296 | A | G | 47 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
47 | HG01074.hp1 HG01169.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.81+1669A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563296 | |||||||
| chrX:38563329 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.81+1702G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563329 | |||||||
| chrX:38563475 | GGA | G | 9 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0199 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+1850_81+1851del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38563475 | ||||||
| chrX:38563476 | GA | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(51): Show |
57 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.81+1850delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563476 | |||||||
| chrX:38563477 | A | G | 6 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0002t0001g0092 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+1850A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563477 | |||||||
| chrX:38563506 | A | T | 1 | a0001c0002t0001g0209 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.81+1879A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563506 | |||||||
| chrX:38563764 | A | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(90): Show |
96 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.81+2137A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563764 | |||||||
| chrX:38563808 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.81+2181G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563808 | |||||||
| chrX:38563854 | A | G | 1 | a0001c0001t0001g0028 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.81+2227A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563854 | |||||||
| chrX:38564124 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.81+2497C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564124 | |||||||
| chrX:38564282 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.81+2655C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564282 | |||||||
| chrX:38564431 | G | A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+2804G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564431 | |||||||
| chrX:38564490 | T | C | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(56): Show |
62 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.81+2863T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564490 | |||||||
| chrX:38564763 | T | C | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+3136T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564763 | |||||||
| chrX:38564799 | C | A | 1 | a0001c0001t0002g0094 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.81+3172C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564799 | |||||||
| chrX:38564978 | C | G | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+3351C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564978 | |||||||
| chrX:38564988 | C | CT | 32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(29): Show |
35 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.81+3370dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38564988 | ||||||
| chrX:38564988 | CT | C | 21 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(18): Show |
21 | HG01255.hp1 HG02055.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+3370delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38564988 | ||||||
| chrX:38565221 | C | CTTGT | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0187 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+3616_81+3619dup others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38565221 | ||||||
| chrX:38565261 | G | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+3634G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565261 | |||||||
| chrX:38565299 | A | G | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+3672A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565299 | |||||||
| chrX:38565420 | G | A | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(56): Show |
62 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.81+3793G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565420 | |||||||
| chrX:38565421 | G | T | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 others(56): Show |
62 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.81+3794G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565421 | |||||||
| chrX:38565463 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.81+3836C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565463 | |||||||
| chrX:38565825 | T | C | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0002g0097 |
3 | HG01099.hp1 HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.81+4198T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565825 | |||||||
| chrX:38565886 | G | A | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+4259G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565886 | |||||||
| chrX:38566037 | C | T | 2 | a0001c0001t0001g0197 a0001c0003t0001g0196 |
2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.81+4410C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38566037 | |||||||
| chrX:38566101 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0032 |
3 | HG02056.hp1 HG02071.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.81+4474T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38566101 | |||||||
| chrX:38566298 | C | T | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(61): Show |
67 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.81+4671C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38566298 | |||||||
| chrX:38566710 | T | A | 1 | a0001c0001t0002g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.81+5083T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38566710 | |||||||
| chrX:38566725 | A | C | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+5098A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38566725 | |||||||
| chrX:38567092 | A | AT | 26 | a0001c0001t0001g0055 a0001c0001t0001g0087 a0001c0001t0001g0089 others(23): Show |
27 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.81+5476dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38567092 | ||||||
| chrX:38567092 | A | ATT | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(53): Show |
59 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.81+5475_81+5476dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38567092 | ||||||
| chrX:38567294 | G | A | 21 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(18): Show |
21 | HG01255.hp1 HG02055.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+5667G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567294 | |||||||
| chrX:38567331 | A | T | 1 | a0001c0001t0002g0032 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.81+5704A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567331 | |||||||
| chrX:38567355 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.81+5728G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567355 | |||||||
| chrX:38567409 | AGAC | A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+5783_81+5785del others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567409 | |||||||
| chrX:38567796 | T | C | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+6169T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567796 | |||||||
| chrX:38567833 | G | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(47): Show |
53 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.81+6206G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567833 | |||||||
| chrX:38568260 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+6633C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38568260 | |||||||
| chrX:38568296 | GT | G | 24 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(21): Show |
24 | HG01255.hp1 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+6682delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38568296 | ||||||
| chrX:38568510 | G | T | 1 | a0001c0001t0002g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+6883G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38568510 | |||||||
| chrX:38568652 | T | C | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.81+7025T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38568652 | |||||||
| chrX:38568821 | T | G | 5 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | NA18953.hp1 NA18962.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+7194T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38568821 | |||||||
| chrX:38569118 | G | A | 33 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(30): Show |
33 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.81+7491G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38569118 | |||||||
| chrX:38569366 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+7739C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38569366 | |||||||
| chrX:38569435 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+7808G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38569435 | |||||||
| chrX:38569783 | G | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(92): Show |
98 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(95): Show |
intron_variant | MODIFIER | c.81+8156G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38569783 | |||||||
| chrX:38570045 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0005g0078 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.81+8418G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570045 | |||||||
| chrX:38570279 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.81+8652C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570279 | |||||||
| chrX:38570299 | G | T | 1 | a0001c0001t0002g0053 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.81+8672G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570299 | |||||||
| chrX:38570333 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.81+8706C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570333 | |||||||
| chrX:38570619 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0002g0109 |
2 | HG02602.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.81+8992T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570619 | |||||||
| chrX:38570685 | A | C | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+9058A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570685 | |||||||
| chrX:38570841 | A | T | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.81+9214A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570841 | |||||||
| chrX:38571058 | T | C | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+9431T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571058 | |||||||
| chrX:38571238 | A | G | 9 | a0001c0001t0001g0009 a0001c0001t0001g0178 a0001c0001t0001g0180 others(6): Show |
10 | HG00099.hp2 HG00642.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+9611A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571238 | |||||||
| chrX:38571266 | T | C | 1 | a0001c0001t0001g0006 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.81+9639T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571266 | |||||||
| chrX:38571303 | A | G | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+9676A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571303 | |||||||
| chrX:38571345 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+9718C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571345 | |||||||
| chrX:38571498 | C | T | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.81+9871C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571498 | |||||||
| chrX:38571743 | T | TA | 11 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0194 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+10128dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38571743 | ||||||
| chrX:38571747 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.81+10120A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571747 | |||||||
| chrX:38571871 | A | C | 21 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(18): Show |
21 | HG01255.hp1 HG02055.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+10244A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571871 | |||||||
| chrX:38572010 | A | AT | 21 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(18): Show |
21 | HG01255.hp1 HG02055.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+10391dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38572010 | ||||||
| chrX:38572055 | TTGTCAAA others(10): Show |
T | 29 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(26): Show |
29 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.81+10438_81+10454d others(19): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38572055 | ||||||
| chrX:38572106 | C | A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+10479C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38572106 | |||||||
| chrX:38572624 | TCAGTTCA others(562): Show |
T | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+10998_81+11566d others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38572624 | |||||||
| chrX:38573194 | A | T | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11567A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573194 | |||||||
| chrX:38573197 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11570A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573197 | |||||||
| chrX:38573198 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11571A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573198 | |||||||
| chrX:38573200 | T | G | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11573T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573200 | |||||||
| chrX:38573203 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11576G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573203 | |||||||
| chrX:38573205 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11578C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573205 | |||||||
| chrX:38573338 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.81+11711A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573338 | |||||||
| chrX:38573571 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81+11944C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573571 | |||||||
| chrX:38573670 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.81+12043C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573670 | |||||||
| chrX:38573850 | A | AAGACCAC | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+12227_81+12233d others(9): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38573850 | ||||||
| chrX:38574005 | C | T | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG02809.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+12378C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38574005 | |||||||
| chrX:38574286 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.81+12659G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38574286 | |||||||
| chrX:38574299 | CT | C | 3 | a0001c0001t0002g0076 a0001c0001t0003g0057 a0001c0001t0003g0058 |
3 | HG02976.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.81+12677delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38574299 | ||||||
| chrX:38574739 | A | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(94): Show |
100 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(97): Show |
intron_variant | MODIFIER | c.81+13112A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38574739 | |||||||
| chrX:38574867 | C | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(53): Show |
59 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.81+13240C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38574867 | |||||||
| chrX:38575144 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.81+13517C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38575144 | |||||||
| chrX:38575559 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.81+13932T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38575559 | |||||||
| chrX:38576601 | G | A | 22 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(19): Show |
22 | HG01255.hp1 HG02055.hp1 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.81+14974G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38576601 | |||||||
| chrX:38576767 | T | C | 34 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(31): Show |
34 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.81+15140T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38576767 | |||||||
| chrX:38576769 | G | A | 14 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(11): Show |
14 | HG02257.hp1 HG02723.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+15142G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38576769 | |||||||
| chrX:38576870 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0086 |
2 | NA18944.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.81+15243G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38576870 | |||||||
| chrX:38577652 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+16025G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38577652 | |||||||
| chrX:38577719 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+16092T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38577719 | |||||||
| chrX:38577804 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.81+16177A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38577804 | |||||||
| chrX:38577810 | T | TA | 4 | a0001c0001t0001g0087 a0001c0001t0001g0185 a0001c0002t0001g0005 others(1): Show |
5 | HG01884.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+16195dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38577810 | ||||||
| chrX:38577812 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+16185A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38577812 | |||||||
| chrX:38578007 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.81+16380G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578007 | |||||||
| chrX:38578342 | T | G | 2 | a0001c0001t0001g0194 a0001c0003t0001g0195 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+16715T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578342 | |||||||
| chrX:38578391 | T | G | 1 | a0001c0003t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.81+16764T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578391 | |||||||
| chrX:38578600 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.81+16973C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578600 | |||||||
| chrX:38578745 | GA | G | 5 | a0001c0001t0001g0183 a0001c0001t0001g0197 a0001c0001t0002g0198 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+17125delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38578745 | ||||||
| chrX:38578855 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17228A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578855 | |||||||
| chrX:38578858 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17231C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578858 | |||||||
| chrX:38578864 | T | G | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17237T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578864 | |||||||
| chrX:38578865 | G | T | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17238G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578865 | |||||||
| chrX:38578866 | T | G | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17239T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578866 | |||||||
| chrX:38578867 | A | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
2 | NA19070.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.81+17240A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578867 | |||||||
| chrX:38578870 | G | T | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17243G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578870 | |||||||
| chrX:38578871 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17244G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578871 | |||||||
| chrX:38578920 | G | T | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+17293G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578920 | |||||||
| chrX:38579031 | T | G | 1 | a0001c0002t0001g0209 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.81+17404T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579031 | |||||||
| chrX:38579408 | C | T | 8 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0194 others(5): Show |
8 | HG01891.hp2 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+17781C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579408 | |||||||
| chrX:38579429 | T | A | 1 | a0001c0001t0001g0114 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.81+17802T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579429 | |||||||
| chrX:38579612 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.81+17985C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579612 | |||||||
| chrX:38579761 | T | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(98): Show |
104 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(101): Show |
intron_variant | MODIFIER | c.81+18134T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579761 | |||||||
| chrX:38579849 | A | C | 2 | a0001c0001t0002g0198 a0001c0003t0004g0203 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.81+18222A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579849 | |||||||
| chrX:38580062 | A | C | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+18435A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38580062 | |||||||
| chrX:38580206 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0119 |
3 | HG01257.hp1 HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.81+18579T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38580206 | |||||||
| chrX:38580354 | G | A | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+18727G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38580354 | |||||||
| chrX:38580516 | G | A | 10 | a0001c0001t0001g0055 a0001c0001t0001g0087 a0001c0001t0001g0089 others(7): Show |
11 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+18889G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38580516 | |||||||
| chrX:38580825 | C | T | 1 | a0001c0001t0002g0171 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.81+19198C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38580825 | |||||||
| chrX:38581250 | C | T | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+19623C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581250 | |||||||
| chrX:38581487 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.81+19860G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581487 | |||||||
| chrX:38581488 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.81+19861G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581488 | |||||||
| chrX:38581500 | C | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 |
3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+19873C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581500 | |||||||
| chrX:38581543 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.81+19916A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581543 | |||||||
| chrX:38581693 | T | G | 2 | a0001c0001t0001g0194 a0001c0003t0001g0195 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+20066T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581693 | |||||||
| chrX:38581743 | A | G | 2 | a0001c0001t0002g0029 a0001c0002t0001g0092 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.81+20116A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581743 | |||||||
| chrX:38581836 | C | T | 4 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG01109.hp1 HG01256.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+20209C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581836 | |||||||
| chrX:38581989 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 |
3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+20362C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581989 | |||||||
| chrX:38582051 | T | C | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.81+20424T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582051 | |||||||
| chrX:38582223 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.81+20596C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582223 | |||||||
| chrX:38582279 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 |
3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+20652A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582279 | |||||||
| chrX:38582294 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.81+20667T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582294 | |||||||
| chrX:38582297 | A | G | 7 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0090 others(4): Show |
8 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+20670A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582297 | |||||||
| chrX:38582753 | A | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0173 a0001c0001t0002g0109 |
3 | HG02602.hp1 HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.81+21126A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582753 | |||||||
| chrX:38582825 | T | C | 14 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(11): Show |
14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+21198T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582825 | |||||||
| chrX:38583396 | G | A | 2 | a0001c0001t0001g0194 a0001c0003t0001g0195 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+21769G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583396 | |||||||
| chrX:38583440 | A | G | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+21813A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583440 | |||||||
| chrX:38583462 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.81+21835A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583462 | |||||||
| chrX:38583531 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.81+21904T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583531 | |||||||
| chrX:38583748 | T | G | 2 | a0001c0001t0002g0198 a0001c0003t0004g0203 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.81+22121T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583748 | |||||||
| chrX:38583871 | T | A | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+22244T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583871 | |||||||
| chrX:38583935 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.81+22308C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583935 | |||||||
| chrX:38583939 | TTTTTCTT others(3): Show |
T | 2 | a0001c0001t0002g0198 a0001c0003t0004g0203 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.81+22317_81+22326d others(12): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583939 | ||||||
| chrX:38583942 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.81+22315T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583942 | |||||||
| chrX:38583949 | C | CT | 20 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(17): Show |
20 | HG01175.hp2 HG01255.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.81+22344dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583949 | ||||||
| chrX:38583949 | CT | C | 8 | a0001c0001t0001g0075 a0001c0001t0001g0128 a0001c0001t0001g0165 others(5): Show |
8 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+22344delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583949 | ||||||
| chrX:38583950 | T | C | 2 | a0001c0001t0002g0198 a0001c0003t0004g0203 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.81+22323T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583950 | |||||||
| chrX:38583980 | G | T | 7 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0090 others(4): Show |
8 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+22353G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583980 | |||||||
| chrX:38584162 | C | T | 1 | a0001c0001t0002g0053 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.81+22535C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584162 | |||||||
| chrX:38584402 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+22775G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584402 | |||||||
| chrX:38584441 | C | A | 5 | a0001c0001t0001g0110 a0001c0001t0001g0124 a0001c0001t0001g0173 others(2): Show |
5 | HG02602.hp1 HG03704.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+22814C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584441 | |||||||
| chrX:38584540 | C | T | 2 | a0001c0001t0001g0194 a0001c0003t0001g0195 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+22913C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584540 | |||||||
| chrX:38584626 | A | G | 1 | a0001c0003t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.81+22999A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584626 | |||||||
| chrX:38584670 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.81+23043T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584670 | |||||||
| chrX:38584866 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.81+23239A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584866 | |||||||
| chrX:38585342 | T | C | 6 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
6 | HG02723.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+23715T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38585342 | |||||||
| chrX:38585410 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.81+23783G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38585410 | |||||||
| chrX:38585539 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.81+23912A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38585539 | |||||||
| chrX:38585613 | T | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 |
3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+23986T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38585613 | |||||||
| chrX:38585657 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0086 |
2 | NA18944.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.81+24030A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38585657 | |||||||
| chrX:38585738 | A | ATCC | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+24113_81+24115d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38585738 | ||||||
| chrX:38586192 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.81+24565G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38586192 | |||||||
| chrX:38586310 | T | G | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+24683T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38586310 | |||||||
| chrX:38586310 | TC | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
7 | HG00741.hp1 HG02027.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+24684delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38586310 | |||||||
| chrX:38586331 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.81+24704G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38586331 | |||||||
| chrX:38587168 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 |
3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+25541G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587168 | |||||||
| chrX:38587301 | T | C | 2 | a0001c0001t0001g0194 a0001c0003t0001g0195 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+25674T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587301 | |||||||
| chrX:38587348 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.81+25721T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587348 | |||||||
| chrX:38587368 | A | G | 1 | a0001c0003t0001g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81+25741A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587368 | |||||||
| chrX:38587490 | T | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 |
3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+25863T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587490 | |||||||
| chrX:38587758 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.81+26131C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587758 | |||||||
| chrX:38587806 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+26179C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587806 | |||||||
| chrX:38587968 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.81+26341A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587968 | |||||||
| chrX:38588002 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+26375G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588002 | |||||||
| chrX:38588272 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.81+26645A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588272 | |||||||
| chrX:38588335 | T | G | 1 | a0001c0001t0002g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+26708T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588335 | |||||||
| chrX:38588597 | T | G | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+26970T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588597 | |||||||
| chrX:38588613 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.81+26986G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588613 | |||||||
| chrX:38588751 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.81+27124C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588751 | |||||||
| chrX:38588891 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0178 a0001c0001t0001g0180 others(3): Show |
7 | HG00099.hp2 HG00642.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+27264C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588891 | |||||||
| chrX:38589246 | G | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0197 a0001c0003t0001g0196 |
3 | HG01884.hp2 HG04228.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.81+27619G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589246 | |||||||
| chrX:38589754 | C | T | 14 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(11): Show |
14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+28127C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589754 | |||||||
| chrX:38589769 | A | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | NA18960.hp1 NA18967.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+28142A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589769 | |||||||
| chrX:38589770 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+28143C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589770 | |||||||
| chrX:38589861 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.81+28234C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589861 | |||||||
| chrX:38589887 | T | G | 1 | a0001c0001t0001g0161 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.81+28260T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589887 | |||||||
| chrX:38590110 | T | A | 15 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(12): Show |
15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+28483T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38590110 | |||||||
| chrX:38590150 | G | A | 1 | a0001c0003t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.81+28523G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38590150 | |||||||
| chrX:38590816 | C | A | 2 | a0001c0001t0001g0194 a0001c0003t0001g0195 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+29189C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38590816 | |||||||
| chrX:38591720 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.81+30093T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38591720 | |||||||
| chrX:38592148 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02040.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.81+30521G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592148 | |||||||
| chrX:38592253 | C | T | 1 | a0001c0002t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.81+30626C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592253 | |||||||
| chrX:38592294 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.81+30667G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592294 | |||||||
| chrX:38592481 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0119 |
3 | HG01257.hp1 HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.81+30854T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592481 | |||||||
| chrX:38592644 | C | G | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.81+31017C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592644 | |||||||
| chrX:38592740 | G | T | 1 | a0001c0001t0001g0027 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+31113G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592740 | |||||||
| chrX:38592774 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.81+31147C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592774 | |||||||
| chrX:38593017 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+31390T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38593017 | |||||||
| chrX:38593509 | T | G | 14 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(11): Show |
14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+31882T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38593509 | |||||||
| chrX:38594866 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.81+33239C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38594866 | |||||||
| chrX:38595077 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0002g0029 others(1): Show |
4 | HG00741.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+33450C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595077 | |||||||
| chrX:38595215 | A | G | 14 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(11): Show |
14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+33588A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595215 | |||||||
| chrX:38595227 | T | A | 1 | a0001c0001t0001g0027 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+33600T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595227 | |||||||
| chrX:38595259 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
85 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(82): Show |
intron_variant | MODIFIER | c.81+33632G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595259 | |||||||
| chrX:38595273 | G | A | 2 | a0001c0001t0001g0194 a0001c0003t0001g0195 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+33646G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595273 | |||||||
| chrX:38595585 | C | T | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+33958C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595585 | |||||||
| chrX:38595743 | A | G | 1 | a0001c0001t0002g0120 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.81+34116A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595743 | |||||||
| chrX:38596228 | G | A | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+34601G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38596228 | |||||||
| chrX:38596281 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81+34654T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38596281 | |||||||
| chrX:38596605 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.81+34978C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38596605 | |||||||
| chrX:38596711 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+35084C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38596711 | |||||||
| chrX:38597286 | C | T | 1 | a0001c0003t0001g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81+35659C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597286 | |||||||
| chrX:38597302 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+35675T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597302 | |||||||
| chrX:38597525 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81+35898A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597525 | |||||||
| chrX:38597533 | A | C | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+35906A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597533 | |||||||
| chrX:38597708 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81+36081T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597708 | |||||||
| chrX:38597869 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36242A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597869 | |||||||
| chrX:38597871 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36244A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597871 | |||||||
| chrX:38597872 | T | A | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36245T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597872 | |||||||
| chrX:38597873 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36246A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597873 | |||||||
| chrX:38597877 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36250A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597877 | |||||||
| chrX:38597879 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36252A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597879 | |||||||
| chrX:38597884 | G | T | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36257G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597884 | |||||||
| chrX:38597935 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0075 |
2 | HG01934.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.81+36308C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597935 | |||||||
| chrX:38598276 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.81+36649C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38598276 | |||||||
| chrX:38598799 | A | T | 1 | a0001c0001t0002g0160 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.81+37172A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38598799 | |||||||
| chrX:38599065 | G | A | 2 | a0001c0001t0003g0057 a0001c0001t0003g0058 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.81+37438G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38599065 | |||||||
| chrX:38599155 | G | T | 1 | a0001c0001t0001g0004 | 2 | NA18961.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.81+37528G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38599155 | |||||||
| chrX:38600127 | T | G | 1 | a0001c0001t0002g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.81+38500T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38600127 | |||||||
| chrX:38600245 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.81+38618C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38600245 | |||||||
| chrX:38600800 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.81+39173A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38600800 | |||||||
| chrX:38600898 | T | C | 9 | a0001c0001t0001g0183 a0001c0001t0001g0197 a0001c0001t0001g0199 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+39271T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38600898 | |||||||
| chrX:38601263 | A | G | 1 | a0001c0001t0002g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+39636A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38601263 | |||||||
| chrX:38601419 | A | G | 27 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0059 others(24): Show |
27 | HG01255.hp1 HG02055.hp1 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.81+39792A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38601419 | |||||||
| chrX:38601692 | T | C | 4 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG01109.hp1 HG01256.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+40065T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38601692 | |||||||
| chrX:38601965 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.81+40338A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38601965 | |||||||
| chrX:38601989 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0027 |
3 | NA18961.hp1 NA18982.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.81+40362A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38601989 | |||||||
| chrX:38602274 | A | G | 10 | a0001c0001t0001g0009 a0001c0001t0001g0169 a0001c0001t0001g0178 others(7): Show |
11 | HG00099.hp2 HG00642.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+40647A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38602274 | |||||||
| chrX:38602615 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0027 |
3 | NA18961.hp1 NA18982.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.81+40988A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38602615 | |||||||
| chrX:38602870 | G | C | 1 | a0001c0003t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.81+41243G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38602870 | |||||||
| chrX:38602978 | A | C | 1 | a0001c0002t0001g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.81+41351A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38602978 | |||||||
| chrX:38603120 | T | C | 7 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0069 others(4): Show |
7 | HG02257.hp1 HG02896.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+41493T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38603120 | |||||||
| chrX:38603213 | A | G | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(75): Show |
81 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.81+41586A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38603213 | |||||||
| chrX:38603506 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.81+41879C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38603506 | |||||||
| chrX:38603847 | TTTTA | T | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+42240_81+42243d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38603847 | ||||||
| chrX:38604125 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+42498T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604125 | |||||||
| chrX:38604500 | G | T | 9 | a0001c0001t0001g0183 a0001c0001t0001g0197 a0001c0001t0001g0199 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+42873G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604500 | |||||||
| chrX:38604558 | C | G | 2 | a0001c0001t0001g0194 a0001c0003t0001g0195 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+42931C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604558 | |||||||
| chrX:38604760 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.81+43133C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604760 | |||||||
| chrX:38604940 | C | T | 1 | a0001c0001t0003g0079 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.81+43313C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604940 | |||||||
| chrX:38604941 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 |
3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+43314G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604941 | |||||||
| chrX:38604992 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 |
3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+43365A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604992 | |||||||
| chrX:38605040 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.81+43413G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605040 | |||||||
| chrX:38605058 | G | A | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+43431G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605058 | |||||||
| chrX:38605221 | A | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(75): Show |
81 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.81+43594A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605221 | |||||||
| chrX:38605261 | C | T | 7 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(4): Show |
7 | HG02723.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+43634C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605261 | |||||||
| chrX:38605262 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.81+43635G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605262 | |||||||
| chrX:38605465 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+43838C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605465 | |||||||
| chrX:38605592 | C | T | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+43965C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605592 | |||||||
| chrX:38605597 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+43970C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605597 | |||||||
| chrX:38605784 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0081 |
3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+44157A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605784 | |||||||
| chrX:38605881 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+44254C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605881 | |||||||
| chrX:38606077 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.81+44450A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606077 | |||||||
| chrX:38606285 | A | G | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+44658A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606285 | |||||||
| chrX:38606322 | A | G | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+44695A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606322 | |||||||
| chrX:38606368 | A | C | 1 | a0001c0001t0002g0020 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.81+44741A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606368 | |||||||
| chrX:38606371 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.81+44744G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606371 | |||||||
| chrX:38606382 | T | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(55): Show |
64 | HG00438.hp1 HG00673.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.81+44755T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606382 | |||||||
| chrX:38606470 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+44843G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606470 | |||||||
| chrX:38607049 | G | A | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+45422G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38607049 | |||||||
| chrX:38607399 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.81+45772G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38607399 | |||||||
| chrX:38607521 | C | T | 2 | a0001c0001t0002g0029 a0001c0002t0001g0092 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.81+45894C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38607521 | |||||||
| chrX:38607788 | T | C | 16 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+46161T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38607788 | |||||||
| chrX:38607862 | GA | G | 13 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(10): Show |
13 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+46251delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38607862 | ||||||
| chrX:38608085 | A | G | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+46458A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38608085 | |||||||
| chrX:38608091 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0175 |
2 | HG02132.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.81+46464G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38608091 | |||||||
| chrX:38608205 | TA | T | 12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+46586delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38608205 | ||||||
| chrX:38608246 | C | T | 1 | a0001c0003t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.81+46619C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38608246 | |||||||
| chrX:38608299 | A | T | 1 | a0001c0001t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.81+46672A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38608299 | |||||||
| chrX:38608431 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.81+46804G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38608431 | |||||||
| chrX:38609042 | C | CCT | 14 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(11): Show |
14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+47415_81+47416i others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38609042 | |||||||
| chrX:38609196 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.81+47569G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38609196 | |||||||
| chrX:38609331 | A | T | 1 | a0001c0001t0002g0120 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.81+47704A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38609331 | |||||||
| chrX:38609424 | A | C | 1 | a0001c0003t0004g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.81+47797A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38609424 | |||||||
| chrX:38609839 | G | T | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+48212G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38609839 | |||||||
| chrX:38610056 | C | T | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+48429C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610056 | |||||||
| chrX:38610130 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(103): Show |
110 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(107): Show |
intron_variant | MODIFIER | c.81+48503A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610130 | |||||||
| chrX:38610219 | A | G | 14 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0183 others(11): Show |
14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+48592A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610219 | |||||||
| chrX:38610314 | C | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0085 a0001c0001t0001g0108 others(12): Show |
16 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+48687C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610314 | |||||||
| chrX:38610491 | C | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(47): Show |
53 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.81+48864C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610491 | |||||||
| chrX:38610876 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.81+49249A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610876 | |||||||
| chrX:38611014 | G | A | 2 | a0001c0001t0002g0198 a0001c0003t0004g0203 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.81+49387G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38611014 | |||||||
| chrX:38611506 | G | A | 1 | a0001c0002t0001g0209 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.81+49879G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38611506 | |||||||
| chrX:38611708 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.81+50081T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38611708 | |||||||
| chrX:38612053 | AT | A | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.81+50428delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38612053 | ||||||
| chrX:38612078 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+50451C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612078 | |||||||
| chrX:38612437 | A | G | 9 | a0001c0001t0001g0183 a0001c0001t0001g0197 a0001c0001t0001g0199 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+50810A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612437 | |||||||
| chrX:38612548 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.81+50921C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612548 | |||||||
| chrX:38612667 | G | T | 1 | a0001c0001t0002g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.81+51040G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612667 | |||||||
| chrX:38612682 | C | T | 2 | a0001c0001t0002g0080 a0001c0001t0003g0079 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+51055C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612682 | |||||||
| chrX:38612946 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.81+51319C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612946 | |||||||
| chrX:38613031 | C | G | 2 | a0001c0001t0001g0194 a0001c0003t0001g0195 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+51404C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613031 | |||||||
| chrX:38613377 | G | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG01074.hp1 HG01169.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+51750G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613377 | |||||||
| chrX:38613564 | T | C | 1 | a0001c0002t0001g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.81+51937T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613564 | |||||||
| chrX:38613741 | C | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0183 a0001c0003t0001g0066 |
3 | HG02965.hp1 HG03540.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.81+52114C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613741 | |||||||
| chrX:38613948 | A | T | 2 | a0001c0001t0002g0080 a0001c0001t0003g0079 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82-52173A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613948 | |||||||
| chrX:38613981 | T | C | 28 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0059 others(25): Show |
29 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.82-52140T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613981 | |||||||
| chrX:38614236 | T | G | 1 | a0001c0001t0002g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.82-51885T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614236 | |||||||
| chrX:38614331 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.82-51790A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614331 | |||||||
| chrX:38614457 | C | G | 1 | a0001c0001t0001g0107 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.82-51664C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614457 | |||||||
| chrX:38614583 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.82-51538A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614583 | |||||||
| chrX:38614803 | T | C | 1 | a0001c0002t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.82-51318T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614803 | |||||||
| chrX:38614830 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(80): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.82-51291A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614830 | |||||||
| chrX:38614921 | T | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.82-51200T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614921 | |||||||
| chrX:38614992 | C | CT | 8 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0087 others(5): Show |
10 | HG01257.hp2 HG01258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-51118dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38614992 | ||||||
| chrX:38614992 | CT | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(88): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.82-51118delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38614992 | ||||||
| chrX:38615034 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02145.hp1 HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.82-51087C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38615034 | |||||||
| chrX:38615554 | GT | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(76): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.82-50561delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38615554 | ||||||
| chrX:38615717 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-50404T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38615717 | |||||||
| chrX:38615756 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.82-50365C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38615756 | |||||||
| chrX:38615982 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.82-50139A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38615982 | |||||||
| chrX:38616132 | A | G | 4 | a0001c0001t0001g0108 a0001c0001t0002g0029 a0001c0001t0002g0188 others(1): Show |
4 | HG01243.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-49989A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616132 | |||||||
| chrX:38616376 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.82-49745A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616376 | |||||||
| chrX:38616389 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.82-49732T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616389 | |||||||
| chrX:38616476 | A | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(45): Show |
51 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-49645A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616476 | |||||||
| chrX:38616582 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.82-49539C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616582 | |||||||
| chrX:38616824 | A | G | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-49297A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616824 | |||||||
| chrX:38617088 | C | G | 1 | a0001c0002t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.82-49033C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38617088 | |||||||
| chrX:38617117 | A | G | 9 | a0001c0001t0002g0023 a0001c0001t0002g0065 a0001c0001t0002g0067 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-49004A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38617117 | |||||||
| chrX:38617605 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.82-48516G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38617605 | |||||||
| chrX:38617731 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.82-48390C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38617731 | |||||||
| chrX:38617940 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.82-48181G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38617940 | |||||||
| chrX:38618047 | C | T | 9 | a0001c0001t0002g0023 a0001c0001t0002g0065 a0001c0001t0002g0067 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-48074C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618047 | |||||||
| chrX:38618069 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.82-48052G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618069 | |||||||
| chrX:38618460 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.82-47661G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618460 | |||||||
| chrX:38618752 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.82-47369G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618752 | |||||||
| chrX:38618779 | T | C | 1 | a0001c0001t0002g0024 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-47342T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618779 | |||||||
| chrX:38618936 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.82-47185G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618936 | |||||||
| chrX:38618960 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0114 a0001c0001t0002g0113 |
5 | HG00438.hp1 HG01175.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-47161T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618960 | |||||||
| chrX:38618990 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.82-47131A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618990 | |||||||
| chrX:38619048 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(88): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.82-47073C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619048 | |||||||
| chrX:38619049 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.82-47072A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619049 | |||||||
| chrX:38619162 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.82-46959C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619162 | |||||||
| chrX:38619208 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02809.hp1 HG02896.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.82-46913C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619208 | |||||||
| chrX:38619246 | T | C | 9 | a0001c0001t0002g0023 a0001c0001t0002g0065 a0001c0001t0002g0067 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-46875T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619246 | |||||||
| chrX:38619285 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.82-46836G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619285 | |||||||
| chrX:38619368 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.82-46753A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619368 | |||||||
| chrX:38619753 | T | G | 2 | a0001c0001t0001g0083 a0001c0001t0002g0081 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-46368T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619753 | |||||||
| chrX:38619953 | C | T | 9 | a0001c0001t0002g0023 a0001c0001t0002g0065 a0001c0001t0002g0067 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-46168C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619953 | |||||||
| chrX:38620283 | T | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-45838T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620283 | |||||||
| chrX:38620360 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.82-45761A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620360 | |||||||
| chrX:38620615 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG00099.hp1 HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.82-45506C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620615 | |||||||
| chrX:38620640 | T | G | 1 | a0001c0002t0001g0209 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.82-45481T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620640 | |||||||
| chrX:38620827 | G | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.82-45294G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620827 | |||||||
| chrX:38620871 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-45250C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620871 | |||||||
| chrX:38621144 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.82-44977G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621144 | |||||||
| chrX:38621263 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.82-44858C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621263 | |||||||
| chrX:38621268 | T | C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(45): Show |
51 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-44853T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621268 | |||||||
| chrX:38621728 | C | CATTT | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.82-44393_82-44392i others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621728 | |||||||
| chrX:38621805 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.82-44316G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621805 | |||||||
| chrX:38621856 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.82-44265T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621856 | |||||||
| chrX:38621926 | A | C | 1 | a0001c0001t0002g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-44195A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621926 | |||||||
| chrX:38621986 | G | A | 4 | a0001c0001t0001g0089 a0001c0001t0001g0185 a0001c0001t0002g0080 others(1): Show |
4 | HG01884.hp1 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-44135G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621986 | |||||||
| chrX:38622003 | C | T | 8 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-44118C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622003 | |||||||
| chrX:38622180 | T | C | 8 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-43941T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622180 | |||||||
| chrX:38622320 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-43801G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622320 | |||||||
| chrX:38622543 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.82-43578G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622543 | |||||||
| chrX:38622550 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.82-43571C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622550 | |||||||
| chrX:38622647 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.82-43474G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622647 | |||||||
| chrX:38622672 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-43449T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622672 | |||||||
| chrX:38622679 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.82-43442C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622679 | |||||||
| chrX:38622729 | G | A | 12 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0059 others(9): Show |
12 | HG01255.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-43392G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622729 | |||||||
| chrX:38622730 | C | A | 12 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0059 others(9): Show |
12 | HG01255.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-43391C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622730 | |||||||
| chrX:38622736 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(76): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.82-43385A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622736 | |||||||
| chrX:38622751 | C | A | 1 | a0001c0001t0002g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-43370C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622751 | |||||||
| chrX:38622802 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.82-43319G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622802 | |||||||
| chrX:38622899 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.82-43222A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622899 | |||||||
| chrX:38622937 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-43184C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622937 | |||||||
| chrX:38623051 | G | A | 13 | a0001c0001t0001g0108 a0001c0001t0002g0023 a0001c0001t0002g0029 others(10): Show |
13 | HG01243.hp1 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.82-43070G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623051 | |||||||
| chrX:38623269 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0002g0081 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-42852A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623269 | |||||||
| chrX:38623302 | C | G | 2 | a0001c0001t0001g0083 a0001c0001t0002g0081 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-42819C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623302 | |||||||
| chrX:38623407 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0002g0081 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-42714C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623407 | |||||||
| chrX:38623471 | G | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.82-42650G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623471 | |||||||
| chrX:38623622 | G | GT | 47 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(44): Show |
50 | HG00609.hp1 HG00741.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-42491dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38623622 | ||||||
| chrX:38623822 | G | T | 1 | a0001c0003t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.82-42299G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623822 | |||||||
| chrX:38623833 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.82-42288T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623833 | |||||||
| chrX:38623927 | G | C | 23 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0071 others(20): Show |
24 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.82-42194G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623927 | |||||||
| chrX:38624069 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.82-42052G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624069 | |||||||
| chrX:38624239 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.82-41882G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624239 | |||||||
| chrX:38624298 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.82-41823A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624298 | |||||||
| chrX:38624663 | C | G | 1 | a0001c0001t0001g0176 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.82-41458C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624663 | |||||||
| chrX:38624679 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.82-41442T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624679 | |||||||
| chrX:38624680 | T | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.82-41441T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624680 | |||||||
| chrX:38624742 | C | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.82-41379C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624742 | |||||||
| chrX:38625062 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0082 |
2 | HG01255.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82-41059C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38625062 | |||||||
| chrX:38625351 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02615.hp1 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.82-40770G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38625351 | |||||||
| chrX:38625410 | GGTTCTAG others(18): Show |
G | 1 | a0001c0001t0001g0114 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.82-40708_82-40684d others(27): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38625410 | ||||||
| chrX:38625679 | T | A | 1 | a0001c0001t0001g0134 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.82-40442T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38625679 | |||||||
| chrX:38625725 | T | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.82-40396T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38625725 | |||||||
| chrX:38626585 | G | T | 8 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-39536G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38626585 | |||||||
| chrX:38626628 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.82-39493A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38626628 | |||||||
| chrX:38626713 | G | A | 12 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0072 others(9): Show |
12 | HG01255.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-39408G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38626713 | |||||||
| chrX:38626738 | C | A | 2 | a0001c0001t0001g0018 a0001c0003t0001g0066 |
2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-39383C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38626738 | |||||||
| chrX:38626836 | G | A | 1 | a0001c0001t0002g0024 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-39285G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38626836 | |||||||
| chrX:38627173 | G | A | 33 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(30): Show |
33 | HG00621.hp1 HG01106.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.82-38948G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627173 | |||||||
| chrX:38627359 | G | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0020 |
2 | NA18948.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.82-38762G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627359 | |||||||
| chrX:38627366 | C | T | 9 | a0001c0001t0001g0075 a0001c0001t0002g0023 a0001c0001t0002g0065 others(6): Show |
9 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-38755C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627366 | |||||||
| chrX:38627572 | C | T | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.82-38549C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627572 | |||||||
| chrX:38627772 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-38349G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627772 | |||||||
| chrX:38627853 | C | T | 11 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0197 others(8): Show |
11 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.82-38268C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627853 | |||||||
| chrX:38628126 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.82-37995G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628126 | |||||||
| chrX:38628336 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.82-37785G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628336 | |||||||
| chrX:38628358 | G | A | 1 | a0001c0003t0001g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.82-37763G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628358 | |||||||
| chrX:38628465 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-37656C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628465 | |||||||
| chrX:38628466 | G | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0188 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.82-37655G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628466 | |||||||
| chrX:38628543 | C | T | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-37578C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628543 | |||||||
| chrX:38628600 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0073 |
2 | HG02895.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.82-37521C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628600 | |||||||
| chrX:38628757 | CACATTT | C | 2 | a0001c0001t0001g0083 a0001c0001t0002g0081 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-37361_82-37356d others(8): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38628757 | ||||||
| chrX:38629076 | A | G | 1 | a0001c0001t0002g0024 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-37045A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38629076 | |||||||
| chrX:38629265 | C | T | 2 | a0001c0001t0001g0018 a0001c0003t0001g0066 |
2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-36856C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38629265 | |||||||
| chrX:38629357 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.82-36764A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38629357 | |||||||
| chrX:38629376 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0002g0081 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-36745A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38629376 | |||||||
| chrX:38629481 | C | G | 1 | a0001c0001t0002g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-36640C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38629481 | |||||||
| chrX:38630005 | T | C | 1 | a0001c0001t0002g0024 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-36116T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630005 | |||||||
| chrX:38630059 | A | G | 2 | a0001c0001t0001g0018 a0001c0003t0001g0066 |
2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-36062A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630059 | |||||||
| chrX:38630290 | T | C | 8 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-35831T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630290 | |||||||
| chrX:38630428 | T | C | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-35693T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630428 | |||||||
| chrX:38630479 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.82-35642G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630479 | |||||||
| chrX:38630590 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.82-35531A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630590 | |||||||
| chrX:38630849 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.82-35272A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630849 | |||||||
| chrX:38630975 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.82-35146A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630975 | |||||||
| chrX:38631288 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-34833C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38631288 | |||||||
| chrX:38631309 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.82-34812C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38631309 | |||||||
| chrX:38631442 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-34679G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38631442 | |||||||
| chrX:38631591 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.82-34530A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38631591 | |||||||
| chrX:38631592 | C | T | 8 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-34529C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38631592 | |||||||
| chrX:38632294 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.82-33827A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38632294 | |||||||
| chrX:38632450 | G | A | 1 | a0001c0001t0002g0024 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-33671G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38632450 | |||||||
| chrX:38632616 | T | C | 1 | a0001c0001t0002g0138 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.82-33505T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38632616 | |||||||
| chrX:38632839 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.82-33282A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38632839 | |||||||
| chrX:38634238 | C | T | 38 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(35): Show |
38 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-31883C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38634238 | |||||||
| chrX:38634861 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.82-31260G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38634861 | |||||||
| chrX:38635002 | GC | G | 5 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0185 others(2): Show |
5 | HG01884.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-31115delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38635002 | ||||||
| chrX:38635247 | G | A | 6 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-30874G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38635247 | |||||||
| chrX:38635483 | G | C | 8 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-30638G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38635483 | |||||||
| chrX:38635813 | G | A | 68 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0030 others(65): Show |
69 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(66): Show |
intron_variant | MODIFIER | c.82-30308G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38635813 | |||||||
| chrX:38635940 | C | A | 1 | a0001c0001t0001g0041 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.82-30181C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38635940 | |||||||
| chrX:38636066 | T | C | 5 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0185 others(2): Show |
5 | HG01884.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-30055T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636066 | |||||||
| chrX:38636075 | G | GTTAT | 40 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0030 others(37): Show |
41 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.82-30015_82-30012d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636075 | ||||||
| chrX:38636075 | G | GTTATTTA others(1): Show |
15 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0056 others(12): Show |
15 | HG00621.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.82-30019_82-30012d others(10): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636075 | ||||||
| chrX:38636075 | G | GTTATTTA others(5): Show |
3 | a0001c0001t0001g0075 a0001c0001t0002g0024 a0001c0001t0002g0081 |
3 | HG03209.hp1 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.82-30023_82-30012d others(14): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636075 | ||||||
| chrX:38636075 | G | GTTATTTA others(9): Show |
1 | a0001c0001t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.82-30027_82-30012d others(18): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636075 | ||||||
| chrX:38636075 | GTTAT | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.82-30015_82-30012d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636075 | ||||||
| chrX:38636329 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.82-29792C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636329 | |||||||
| chrX:38636472 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.82-29649A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636472 | |||||||
| chrX:38636697 | A | G | 2 | a0001c0001t0001g0018 a0001c0003t0001g0066 |
2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-29424A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636697 | |||||||
| chrX:38636734 | C | T | 8 | a0001c0001t0002g0023 a0001c0001t0002g0065 a0001c0001t0002g0067 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-29387C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636734 | |||||||
| chrX:38636737 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.82-29384G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636737 | |||||||
| chrX:38636758 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.82-29363C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636758 | |||||||
| chrX:38636851 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.82-29270T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636851 | |||||||
| chrX:38636941 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-29180C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636941 | |||||||
| chrX:38637046 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.82-29075C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637046 | |||||||
| chrX:38637048 | A | G | 8 | a0001c0001t0002g0023 a0001c0001t0002g0065 a0001c0001t0002g0067 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-29073A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637048 | |||||||
| chrX:38637065 | C | G | 1 | a0001c0001t0001g0176 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.82-29056C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637065 | |||||||
| chrX:38637074 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.82-29047A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637074 | |||||||
| chrX:38637367 | G | A | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-28754G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637367 | |||||||
| chrX:38637421 | T | G | 33 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(30): Show |
33 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.82-28700T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637421 | |||||||
| chrX:38637609 | C | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.82-28512C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637609 | |||||||
| chrX:38638006 | A | G | 1 | a0001c0001t0002g0024 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-28115A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638006 | |||||||
| chrX:38638035 | GAA | G | 5 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0185 others(2): Show |
5 | HG01884.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-28084_82-28083d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38638035 | ||||||
| chrX:38638297 | C | T | 2 | a0001c0001t0001g0018 a0001c0003t0001g0066 |
2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-27824C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638297 | |||||||
| chrX:38638655 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82-27466A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638655 | |||||||
| chrX:38638657 | C | A | 10 | a0001c0001t0001g0056 a0001c0001t0001g0197 a0001c0001t0002g0023 others(7): Show |
10 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-27464C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638657 | |||||||
| chrX:38638819 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.82-27302G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638819 | |||||||
| chrX:38638873 | CT | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.82-27244delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38638873 | ||||||
| chrX:38638889 | A | G | 1 | a0001c0001t0001g0015 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.82-27232A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638889 | |||||||
| chrX:38639216 | T | A | 1 | a0001c0001t0001g0131 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.82-26905T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38639216 | |||||||
| chrX:38639252 | G | A | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-26869G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38639252 | |||||||
| chrX:38639610 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.82-26511C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38639610 | |||||||
| chrX:38639680 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.82-26441C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38639680 | |||||||
| chrX:38639692 | G | T | 10 | a0001c0001t0001g0018 a0001c0001t0002g0023 a0001c0001t0002g0065 others(7): Show |
10 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-26429G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38639692 | |||||||
| chrX:38640173 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.82-25948G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640173 | |||||||
| chrX:38640315 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0002g0024 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.82-25806C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640315 | |||||||
| chrX:38640809 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0194 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.82-25312C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640809 | |||||||
| chrX:38640834 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.82-25287A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640834 | |||||||
| chrX:38640835 | A | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.82-25286A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640835 | |||||||
| chrX:38640902 | G | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0073 others(1): Show |
4 | HG02055.hp1 HG02895.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-25219G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640902 | |||||||
| chrX:38641121 | C | T | 10 | a0001c0001t0001g0056 a0001c0001t0001g0197 a0001c0001t0002g0023 others(7): Show |
10 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-25000C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641121 | |||||||
| chrX:38641255 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.82-24866C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641255 | |||||||
| chrX:38641405 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.82-24716G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641405 | |||||||
| chrX:38641425 | C | T | 5 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0185 others(2): Show |
5 | HG01884.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-24696C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641425 | |||||||
| chrX:38641439 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-24682A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641439 | |||||||
| chrX:38641483 | G | A | 1 | a0001c0001t0003g0079 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.82-24638G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641483 | |||||||
| chrX:38642235 | G | T | 68 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0030 others(65): Show |
69 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(66): Show |
intron_variant | MODIFIER | c.82-23886G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38642235 | |||||||
| chrX:38642394 | G | A | 2 | a0001c0003t0001g0181 a0001c0003t0001g0210 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.82-23727G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38642394 | |||||||
| chrX:38642455 | A | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0084 others(7): Show |
10 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-23666A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38642455 | |||||||
| chrX:38642875 | G | A | 31 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(28): Show |
31 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.82-23246G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38642875 | |||||||
| chrX:38642968 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0185 |
2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.82-23153A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38642968 | |||||||
| chrX:38643057 | TTAAATGT others(12): Show |
T | 1 | a0001c0001t0001g0172 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82-23062_82-23044d others(21): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643057 | ||||||
| chrX:38643144 | C | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0185 a0001c0001t0002g0080 others(1): Show |
4 | HG01884.hp1 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-22977C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643144 | |||||||
| chrX:38643145 | G | A | 10 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0084 others(7): Show |
10 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-22976G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643145 | |||||||
| chrX:38643239 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.82-22882G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643239 | |||||||
| chrX:38643336 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0082 a0001c0001t0001g0090 |
3 | HG01255.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82-22785G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643336 | |||||||
| chrX:38643672 | C | CA | 10 | a0001c0001t0001g0077 a0001c0001t0001g0087 a0001c0001t0001g0194 others(7): Show |
11 | HG01884.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.82-22426dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | ||||||
| chrX:38643672 | C | CAA | 31 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(28): Show |
31 | HG01175.hp2 HG01934.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.82-22427_82-22426d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | ||||||
| chrX:38643672 | C | CAAA | 5 | a0001c0001t0001g0103 a0001c0001t0001g0134 a0001c0001t0002g0020 others(2): Show |
5 | HG01106.hp1 NA18948.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-22428_82-22426d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | ||||||
| chrX:38643672 | CA | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(90): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.82-22426delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | ||||||
| chrX:38643672 | CAA | C | 6 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-22427_82-22426d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | ||||||
| chrX:38643824 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.82-22297G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643824 | |||||||
| chrX:38643850 | A | G | 10 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0084 others(7): Show |
10 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-22271A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643850 | |||||||
| chrX:38643869 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.82-22252C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643869 | |||||||
| chrX:38643918 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-22203A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643918 | |||||||
| chrX:38644005 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-22116C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644005 | |||||||
| chrX:38644053 | G | T | 1 | a0001c0001t0001g0041 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.82-22068G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644053 | |||||||
| chrX:38644098 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.82-22023T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644098 | |||||||
| chrX:38644169 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.82-21952G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644169 | |||||||
| chrX:38644391 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.82-21730C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644391 | |||||||
| chrX:38644584 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.82-21537G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644584 | |||||||
| chrX:38644604 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0130 |
2 | NA18952.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.82-21517G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644604 | |||||||
| chrX:38644909 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.82-21212A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644909 | |||||||
| chrX:38644936 | G | A | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-21185G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644936 | |||||||
| chrX:38645360 | G | A | 12 | a0001c0001t0001g0018 a0001c0001t0001g0083 a0001c0001t0002g0023 others(9): Show |
12 | HG01891.hp2 HG02257.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.82-20761G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38645360 | |||||||
| chrX:38645553 | G | GA | 17 | a0001c0001t0001g0056 a0001c0001t0001g0077 a0001c0001t0001g0084 others(14): Show |
18 | HG01884.hp2 HG02109.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.82-20556dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38645553 | ||||||
| chrX:38645685 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.82-20436C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38645685 | |||||||
| chrX:38645918 | T | TA | 43 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(40): Show |
44 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.82-20202dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38645918 | ||||||
| chrX:38646132 | T | C | 1 | a0001c0002t0001g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82-19989T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646132 | |||||||
| chrX:38646146 | T | TAAA | 9 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0084 others(6): Show |
9 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-19967_82-19965d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38646146 | ||||||
| chrX:38646239 | T | C | 33 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(30): Show |
33 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.82-19882T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646239 | |||||||
| chrX:38646453 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0082 a0001c0001t0001g0090 |
3 | HG01255.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82-19668G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646453 | |||||||
| chrX:38646652 | T | C | 1 | a0001c0001t0002g0024 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-19469T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646652 | |||||||
| chrX:38646749 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.82-19372T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646749 | |||||||
| chrX:38646777 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.82-19344G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646777 | |||||||
| chrX:38646873 | C | T | 9 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0084 others(6): Show |
9 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-19248C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646873 | |||||||
| chrX:38647272 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-18849T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38647272 | |||||||
| chrX:38647311 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.82-18810T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38647311 | |||||||
| chrX:38647406 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-18715C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38647406 | |||||||
| chrX:38647747 | TG | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.82-18372delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38647747 | ||||||
| chrX:38647827 | G | A | 6 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-18294G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38647827 | |||||||
| chrX:38648191 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0005g0078 a0001c0002t0001g0074 |
3 | HG02615.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.82-17930T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648191 | |||||||
| chrX:38648193 | A | G | 3 | a0001c0001t0001g0089 a0001c0001t0005g0078 a0001c0002t0001g0074 |
3 | HG02615.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.82-17928A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648193 | |||||||
| chrX:38648279 | T | C | 6 | a0001c0001t0001g0056 a0001c0001t0001g0087 a0001c0001t0001g0197 others(3): Show |
7 | HG02559.hp2 HG02818.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-17842T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648279 | |||||||
| chrX:38648475 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.82-17646G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648475 | |||||||
| chrX:38648503 | G | C | 1 | a0001c0001t0001g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.82-17618G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648503 | |||||||
| chrX:38648544 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.82-17577G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648544 | |||||||
| chrX:38648591 | G | C | 7 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0084 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-17530G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648591 | |||||||
| chrX:38648678 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0002g0023 a0001c0001t0002g0065 others(7): Show |
10 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-17443C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648678 | |||||||
| chrX:38648732 | G | A | 5 | a0001c0001t0002g0102 a0001c0001t0002g0139 a0001c0001t0002g0149 others(2): Show |
5 | HG00099.hp2 HG00642.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-17389G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648732 | |||||||
| chrX:38648917 | C | CA | 10 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0033 others(7): Show |
11 | HG00280.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.82-17187dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38648917 | ||||||
| chrX:38648977 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0005g0078 a0001c0002t0001g0074 |
3 | HG02615.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.82-17144G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648977 | |||||||
| chrX:38648981 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.82-17140G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648981 | |||||||
| chrX:38648983 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0190 a0001c0001t0001g0191 |
5 | HG00609.hp1 NA18965.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-17138C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648983 | |||||||
| chrX:38649067 | C | A | 1 | a0001c0001t0001g0039 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.82-17054C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649067 | |||||||
| chrX:38649207 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.82-16914G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649207 | |||||||
| chrX:38649285 | G | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.82-16836G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649285 | |||||||
| chrX:38649327 | T | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0089 others(6): Show |
9 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-16794T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649327 | |||||||
| chrX:38649449 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.82-16672T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649449 | |||||||
| chrX:38649633 | G | A | 1 | a0001c0002t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.82-16488G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649633 | |||||||
| chrX:38649926 | T | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0077 a0001c0001t0001g0084 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-16195T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649926 | |||||||
| chrX:38650160 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.82-15961G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38650160 | |||||||
| chrX:38650185 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.82-15936C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38650185 | |||||||
| chrX:38650472 | CTGTGAG | C | 30 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(27): Show |
30 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.82-15646_82-15641d others(8): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38650472 | ||||||
| chrX:38650488 | G | C | 3 | a0001c0001t0001g0060 a0001c0003t0001g0196 a0001c0003t0004g0203 |
3 | HG01884.hp2 HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.82-15633G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38650488 | |||||||
| chrX:38650570 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-15551C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38650570 | |||||||
| chrX:38650890 | G | T | 65 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0030 others(62): Show |
66 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(63): Show |
intron_variant | MODIFIER | c.82-15231G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38650890 | |||||||
| chrX:38651050 | C | CAT | 5 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0205 others(2): Show |
5 | HG01261.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-15049_82-15048d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | ||||||
| chrX:38651050 | C | CATATATA others(7): Show |
2 | a0001c0001t0001g0185 a0001c0001t0002g0067 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.82-15061_82-15048d others(16): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | ||||||
| chrX:38651050 | C | CATATATA others(9): Show |
4 | a0001c0001t0002g0023 a0001c0001t0002g0069 a0001c0001t0002g0076 others(1): Show |
4 | HG02630.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-15063_82-15048d others(18): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | ||||||
| chrX:38651050 | C | CATATATA others(11): Show |
1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-15065_82-15048d others(20): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | ||||||
| chrX:38651050 | C | CATATATA others(15): Show |
2 | a0001c0001t0002g0065 a0001c0001t0003g0057 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.82-15069_82-15048d others(24): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | ||||||
| chrX:38651050 | C | CATATATA others(19): Show |
1 | a0001c0001t0003g0058 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.82-15048_82-15047i others(28): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | ||||||
| chrX:38651050 | CAT | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.82-15049_82-15048d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | ||||||
| chrX:38651050 | CATAT | C | 46 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(43): Show |
47 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.82-15051_82-15048d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | ||||||
| chrX:38651058 | T | G | 10 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0087 others(7): Show |
11 | HG01884.hp2 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.82-15063T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651058 | |||||||
| chrX:38651204 | G | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0036 others(15): Show |
19 | HG00280.hp1 HG00438.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-14917G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651204 | |||||||
| chrX:38651582 | G | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.82-14539G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651582 | |||||||
| chrX:38651600 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.82-14521G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651600 | |||||||
| chrX:38651686 | G | A | 9 | a0001c0001t0001g0185 a0001c0001t0002g0023 a0001c0001t0002g0065 others(6): Show |
9 | HG01884.hp1 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-14435G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651686 | |||||||
| chrX:38651829 | A | G | 5 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0194 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-14292A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651829 | |||||||
| chrX:38652131 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.82-13990C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38652131 | |||||||
| chrX:38652241 | T | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0089 a0001c0001t0001g0091 others(4): Show |
7 | HG01891.hp2 HG02615.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-13880T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38652241 | |||||||
| chrX:38652777 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.82-13344C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38652777 | |||||||
| chrX:38652874 | C | T | 1 | a0001c0003t0004g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82-13247C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38652874 | |||||||
| chrX:38652880 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.82-13241A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38652880 | |||||||
| chrX:38653012 | C | T | 40 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(37): Show |
41 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.82-13109C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653012 | |||||||
| chrX:38653053 | C | T | 2 | a0001c0001t0002g0080 a0001c0003t0001g0195 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.82-13068C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653053 | |||||||
| chrX:38653118 | G | A | 1 | a0001c0001t0002g0127 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.82-13003G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653118 | |||||||
| chrX:38653192 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-12929C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653192 | |||||||
| chrX:38653193 | G | A | 27 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(24): Show |
27 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.82-12928G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653193 | |||||||
| chrX:38653328 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.82-12793G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653328 | |||||||
| chrX:38653359 | A | G | 40 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(37): Show |
41 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.82-12762A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653359 | |||||||
| chrX:38654194 | G | A | 29 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0038 others(26): Show |
29 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.82-11927G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38654194 | |||||||
| chrX:38654257 | G | C | 2 | a0001c0001t0002g0080 a0001c0003t0001g0195 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.82-11864G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38654257 | |||||||
| chrX:38654720 | CATGAATA others(2): Show |
C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.82-11390_82-11382d others(11): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38654720 | ||||||
| chrX:38654975 | T | G | 1 | a0001c0002t0001g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82-11146T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38654975 | |||||||
| chrX:38655206 | G | A | 1 | a0001c0001t0002g0160 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10915G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655206 | |||||||
| chrX:38655490 | G | GT | 8 | a0001c0001t0002g0102 a0001c0001t0002g0120 a0001c0001t0002g0138 others(5): Show |
8 | HG00099.hp2 HG00642.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-10621dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38655490 | ||||||
| chrX:38655671 | C | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0071 others(4): Show |
7 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-10450C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655671 | |||||||
| chrX:38655695 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.82-10426G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655695 | |||||||
| chrX:38655915 | G | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.82-10206G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655915 | |||||||
| chrX:38655942 | G | T | 1 | a0001c0001t0002g0160 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10179G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655942 | |||||||
| chrX:38656162 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.82-9959G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38656162 | |||||||
| chrX:38656279 | A | G | 4 | a0001c0002t0001g0074 a0001c0002t0001g0207 a0001c0002t0001g0208 others(1): Show |
4 | HG02257.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-9842A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38656279 | |||||||
| chrX:38656781 | T | G | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-9340T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38656781 | |||||||
| chrX:38657202 | G | C | 36 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(33): Show |
38 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-8919G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38657202 | |||||||
| chrX:38657697 | T | A | 18 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0087 others(15): Show |
19 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-8424T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38657697 | |||||||
| chrX:38657705 | G | A | 2 | a0001c0003t0001g0181 a0001c0003t0001g0210 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.82-8416G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38657705 | |||||||
| chrX:38658040 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.82-8081C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38658040 | |||||||
| chrX:38658115 | T | TAA | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.82-8004_82-8003dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38658115 | ||||||
| chrX:38658347 | A | AT | 8 | a0001c0001t0001g0049 a0001c0001t0002g0023 a0001c0001t0002g0065 others(5): Show |
8 | HG01884.hp2 HG02257.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-7759dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38658347 | ||||||
| chrX:38658347 | AT | A | 18 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0087 others(15): Show |
19 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-7759delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38658347 | ||||||
| chrX:38658426 | C | T | 3 | a0001c0001t0001g0083 a0001c0001t0002g0081 a0001c0003t0001g0195 |
3 | HG01891.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.82-7695C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38658426 | |||||||
| chrX:38659001 | T | TAC | 4 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0002g0198 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-7083_82-7082dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | ||||||
| chrX:38659001 | TAC | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0060 others(19): Show |
25 | HG00609.hp1 HG01099.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-7083_82-7082del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | ||||||
| chrX:38659001 | TACAC | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(119): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.82-7085_82-7082del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | ||||||
| chrX:38659001 | TACACAC | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0077 a0001c0001t0001g0083 others(8): Show |
11 | HG01891.hp2 HG01975.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.82-7087_82-7082del others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | ||||||
| chrX:38659001 | TACACACA others(3): Show |
T | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-7091_82-7082del others(10): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | ||||||
| chrX:38659001 | TACACACA others(7): Show |
T | 36 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(33): Show |
38 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-7095_82-7082del others(14): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | ||||||
| chrX:38659038 | A | C | 1 | a0001c0003t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.82-7083A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659038 | |||||||
| chrX:38659069 | C | CAA | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.82-7052_82-7051ins others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659069 | |||||||
| chrX:38659280 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.82-6841C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659280 | |||||||
| chrX:38659657 | A | T | 36 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(33): Show |
38 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-6464A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659657 | |||||||
| chrX:38659664 | A | AT | 52 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(49): Show |
55 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.82-6442dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659664 | ||||||
| chrX:38659664 | A | ATT | 6 | a0001c0001t0001g0116 a0001c0001t0001g0126 a0001c0001t0001g0140 others(3): Show |
6 | HG01109.hp1 HG04228.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-6443_82-6442dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659664 | ||||||
| chrX:38659664 | A | ATTT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
91 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.82-6444_82-6442dup others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659664 | ||||||
| chrX:38659724 | T | G | 2 | a0001c0001t0002g0081 a0001c0003t0001g0195 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.82-6397T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659724 | |||||||
| chrX:38659773 | A | T | 12 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0071 others(9): Show |
13 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.82-6348A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659773 | |||||||
| chrX:38659823 | CT | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0060 others(10): Show |
13 | HG01891.hp2 HG02145.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.82-6277delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659823 | ||||||
| chrX:38659823 | CTT | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(39): Show |
45 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.82-6278_82-6277del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659823 | ||||||
| chrX:38659823 | CTTT | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(95): Show |
103 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.82-6279_82-6277del others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659823 | ||||||
| chrX:38659823 | CTTTT | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0059 others(10): Show |
14 | HG02559.hp2 HG02572.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.82-6280_82-6277del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659823 | ||||||
| chrX:38659861 | C | G | 1 | a0001c0001t0001g0131 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.82-6260C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659861 | |||||||
| chrX:38659880 | A | G | 2 | a0001c0003t0001g0066 a0001c0003t0001g0196 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.82-6241A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659880 | |||||||
| chrX:38659987 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.82-6134C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659987 | |||||||
| chrX:38660025 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.82-6096C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660025 | |||||||
| chrX:38660422 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.82-5699C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660422 | |||||||
| chrX:38660432 | C | G | 3 | a0001c0003t0001g0066 a0001c0003t0001g0196 a0001c0003t0004g0203 |
3 | HG01884.hp2 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.82-5689C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660432 | |||||||
| chrX:38660562 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0001t0001g0104 others(1): Show |
4 | NA18962.hp1 NA18963.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-5559G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660562 | |||||||
| chrX:38660562 | G | T | 6 | a0001c0001t0002g0023 a0001c0001t0002g0065 a0001c0001t0002g0067 others(3): Show |
6 | HG02257.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-5559G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660562 | |||||||
| chrX:38660584 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.82-5537A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660584 | |||||||
| chrX:38660766 | A | G | 36 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(33): Show |
38 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-5355A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660766 | |||||||
| chrX:38660849 | T | C | 5 | a0001c0001t0002g0023 a0001c0001t0002g0065 a0001c0001t0002g0067 others(2): Show |
5 | HG02257.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-5272T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660849 | |||||||
| chrX:38661376 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.82-4745A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38661376 | |||||||
| chrX:38661676 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.82-4445G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38661676 | |||||||
| chrX:38661770 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.82-4351C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38661770 | |||||||
| chrX:38661834 | T | TA | 52 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(49): Show |
54 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.82-4277dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38661834 | ||||||
| chrX:38661954 | T | A | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-4167T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38661954 | |||||||
| chrX:38661958 | T | C | 13 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0071 others(10): Show |
14 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.82-4163T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38661958 | |||||||
| chrX:38662000 | G | T | 4 | a0001c0002t0001g0074 a0001c0002t0001g0207 a0001c0002t0001g0208 others(1): Show |
4 | HG02257.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-4121G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662000 | |||||||
| chrX:38662060 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.82-4061G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662060 | |||||||
| chrX:38662335 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.82-3786G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662335 | |||||||
| chrX:38662445 | G | C | 3 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0079 |
3 | HG02630.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.82-3676G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662445 | |||||||
| chrX:38662483 | G | T | 1 | a0001c0001t0002g0069 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.82-3638G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662483 | |||||||
| chrX:38662542 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.82-3579G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662542 | |||||||
| chrX:38662602 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-3519G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662602 | |||||||
| chrX:38662609 | AG | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.82-3510delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38662609 | ||||||
| chrX:38662806 | G | T | 4 | a0001c0002t0001g0074 a0001c0002t0001g0207 a0001c0002t0001g0208 others(1): Show |
4 | HG02257.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-3315G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662806 | |||||||
| chrX:38662953 | T | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(40): Show |
45 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.82-3168T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662953 | |||||||
| chrX:38662982 | C | T | 7 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0083 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-3139C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662982 | |||||||
| chrX:38663081 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.82-3040C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663081 | |||||||
| chrX:38663152 | TAC | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.82-2941_82-2940del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38663152 | ||||||
| chrX:38663152 | TACAC | T | 43 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(40): Show |
45 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.82-2943_82-2940del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38663152 | ||||||
| chrX:38663178 | C | G | 16 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-2943C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663178 | |||||||
| chrX:38663180 | CAG | C | 16 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-2939_82-2938del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38663180 | ||||||
| chrX:38663184 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-2937C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663184 | |||||||
| chrX:38663203 | T | C | 1 | a0001c0001t0002g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-2918T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663203 | |||||||
| chrX:38663254 | C | G | 16 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-2867C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663254 | |||||||
| chrX:38663369 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82-2752G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663369 | |||||||
| chrX:38663410 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.82-2711G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663410 | |||||||
| chrX:38663443 | G | A | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-2678G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663443 | |||||||
| chrX:38663626 | G | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0190 a0001c0001t0001g0191 |
5 | HG00609.hp1 NA18965.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-2495G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663626 | |||||||
| chrX:38663668 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.82-2453T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663668 | |||||||
| chrX:38663858 | G | C | 6 | a0001c0003t0001g0066 a0001c0003t0001g0181 a0001c0003t0001g0195 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-2263G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663858 | |||||||
| chrX:38664018 | C | T | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-2103C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664018 | |||||||
| chrX:38664085 | G | T | 6 | a0001c0003t0001g0066 a0001c0003t0001g0181 a0001c0003t0001g0195 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-2036G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664085 | |||||||
| chrX:38664443 | G | T | 1 | a0001c0003t0004g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82-1678G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664443 | |||||||
| chrX:38664621 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.82-1500T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664621 | |||||||
| chrX:38664832 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.82-1289G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664832 | |||||||
| chrX:38664876 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
96 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.82-1245C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664876 | |||||||
| chrX:38664932 | G | A | 16 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-1189G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664932 | |||||||
| chrX:38664999 | G | A | 4 | a0001c0002t0001g0074 a0001c0002t0001g0207 a0001c0002t0001g0208 others(1): Show |
4 | HG02257.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-1122G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664999 | |||||||
| chrX:38665162 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-959C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38665162 | |||||||
| chrX:38665398 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.82-723G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38665398 | |||||||
| chrX:38665597 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.82-524A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38665597 | |||||||
| chrX:38665719 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-402T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38665719 | |||||||
| chrX:38665989 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.82-132G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38665989 | |||||||
| chrX:38666371 | A | G | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.270+62A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38666371 | |||||||
| chrX:38666371 | A | T | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.270+62A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38666371 | |||||||
| chrX:38666597 | CT | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.270+302delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 38666597 | ||||||
| chrX:38666597 | CTT | C | 9 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0002g0081 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+301_270+302del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 38666597 | ||||||
| chrX:38666791 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.270+482G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38666791 | |||||||
| chrX:38666797 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.270+488T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38666797 | |||||||
| chrX:38666807 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
96 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.270+498G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38666807 | |||||||
| chrX:38667161 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.270+852T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667161 | |||||||
| chrX:38667283 | C | G | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.270+974C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667283 | |||||||
| chrX:38667366 | G | A | 8 | a0001c0002t0001g0005 a0001c0002t0001g0068 a0001c0002t0001g0074 others(5): Show |
9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+1057G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667366 | |||||||
| chrX:38667505 | A | G | 3 | a0001c0001t0003g0057 a0001c0001t0003g0058 a0001c0001t0003g0079 |
3 | HG02630.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.270+1196A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667505 | |||||||
| chrX:38667506 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.270+1197C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667506 | |||||||
| chrX:38667595 | A | G | 36 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(33): Show |
38 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.270+1286A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667595 | |||||||
| chrX:38668119 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.270+1810T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38668119 | |||||||
| chrX:38668168 | T | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0071 others(5): Show |
8 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.270+1859T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38668168 | |||||||
| chrX:38668173 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.270+1864C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38668173 | |||||||
| chrX:38668513 | G | C | 3 | a0001c0003t0001g0066 a0001c0003t0001g0196 a0001c0003t0004g0203 |
3 | HG01884.hp2 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.270+2204G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38668513 | |||||||
| chrX:38668935 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.271-2441T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38668935 | |||||||
| chrX:38668936 | A | AT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
95 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.271-2429dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 38668936 | ||||||
| chrX:38668936 | AT | A | 26 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(23): Show |
27 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.271-2429delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 38668936 | ||||||
| chrX:38669637 | G | A | 6 | a0001c0003t0001g0066 a0001c0003t0001g0181 a0001c0003t0001g0195 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-1739G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38669637 | |||||||
| chrX:38670219 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.271-1157A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670219 | |||||||
| chrX:38670254 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0071 others(4): Show |
7 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-1122A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670254 | |||||||
| chrX:38670286 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.271-1090G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670286 | |||||||
| chrX:38670374 | C | G | 48 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(45): Show |
50 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.271-1002C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670374 | |||||||
| chrX:38670495 | A | G | 6 | a0001c0003t0001g0066 a0001c0003t0001g0181 a0001c0003t0001g0195 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-881A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670495 | |||||||
| chrX:38670883 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.271-493G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670883 | |||||||
| chrX:38671133 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02572.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-243G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38671133 | |||||||
| chrX:38671791 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0071 others(6): Show |
9 | HG02055.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.345+341C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38671791 | |||||||
| chrX:38671823 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345+373C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38671823 | |||||||
| chrX:38671853 | G | A | 1 | a0001c0003t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.345+403G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38671853 | |||||||
| chrX:38671889 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345+439A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38671889 | |||||||
| chrX:38671904 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345+454T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38671904 | |||||||
| chrX:38672224 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0112 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+774A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38672224 | |||||||
| chrX:38672309 | T | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02615.hp1 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.345+859T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38672309 | |||||||
| chrX:38672360 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.345+910C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38672360 | |||||||
| chrX:38672619 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.345+1169C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38672619 | |||||||
| chrX:38673364 | C | CT | 19 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0114 others(16): Show |
20 | HG01169.hp1 HG01884.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.346-836dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 38673364 | ||||||
| chrX:38673364 | CT | C | 18 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0073 others(15): Show |
18 | HG00099.hp2 HG01069.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.346-836delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 38673364 | ||||||
| chrX:38673982 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.346-239A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38673982 | |||||||
| chrX:38674036 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0115 a0001c0001t0001g0119 others(2): Show |
6 | HG01257.hp1 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.346-185G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38674036 | |||||||
| chrX:38674782 | G | C | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.441+466G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | chrX | 38674782 | |||||||
| chrX:38675046 | G | A | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-659G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | chrX | 38675046 | |||||||
| chrX:38675149 | C | G | 4 | a0001c0001t0002g0155 a0001c0001t0002g0167 a0001c0001t0002g0177 others(1): Show |
4 | HG01071.hp1 HG01106.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-556C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | chrX | 38675149 | |||||||
| chrX:38675410 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.442-295G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | chrX | 38675410 | |||||||
| chrX:38675679 | T | A | 1 | a0001c0002t0001g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-26T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | chrX | 38675679 | |||||||
| chrX:38675920 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.597+60A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38675920 | |||||||
| chrX:38676156 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.597+296G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38676156 | |||||||
| chrX:38676323 | T | C | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.597+463T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38676323 | |||||||
| chrX:38676876 | C | T | 1 | a0001c0003t0004g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.597+1016C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38676876 | |||||||
| chrX:38677039 | A | G | 13 | a0001c0001t0002g0081 a0001c0002t0001g0005 a0001c0002t0001g0068 others(10): Show |
14 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+1179A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38677039 | |||||||
| chrX:38677067 | C | CT | 5 | a0001c0001t0002g0081 a0001c0003t0001g0181 a0001c0003t0001g0195 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+1215dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38677067 | ||||||
| chrX:38677343 | T | G | 1 | a0001c0001t0002g0019 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.597+1483T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38677343 | |||||||
| chrX:38677917 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG00099.hp1 HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.597+2057T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38677917 | |||||||
| chrX:38678235 | C | G | 2 | a0001c0001t0003g0057 a0001c0001t0003g0058 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.597+2375C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38678235 | |||||||
| chrX:38678413 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.597+2553G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38678413 | |||||||
| chrX:38678636 | C | A | 8 | a0001c0002t0001g0005 a0001c0002t0001g0068 a0001c0002t0001g0074 others(5): Show |
9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-2568C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38678636 | |||||||
| chrX:38679017 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.598-2187G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679017 | |||||||
| chrX:38679259 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.598-1945C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679259 | |||||||
| chrX:38679271 | C | G | 24 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(21): Show |
25 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.598-1933C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679271 | |||||||
| chrX:38679312 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.598-1892C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679312 | |||||||
| chrX:38679348 | C | A | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.598-1856C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679348 | |||||||
| chrX:38679363 | A | T | 8 | a0001c0002t0001g0005 a0001c0002t0001g0068 a0001c0002t0001g0074 others(5): Show |
9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-1841A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679363 | |||||||
| chrX:38679720 | C | CA | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
123 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.598-1474dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38679720 | ||||||
| chrX:38680128 | C | T | 5 | a0001c0001t0002g0151 a0001c0001t0002g0155 a0001c0001t0002g0167 others(2): Show |
5 | HG01071.hp1 HG01106.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-1076C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680128 | |||||||
| chrX:38680207 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0115 a0001c0001t0001g0119 others(2): Show |
6 | HG01257.hp1 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-997A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680207 | |||||||
| chrX:38680311 | T | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.598-893T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680311 | |||||||
| chrX:38680346 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.598-858G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680346 | |||||||
| chrX:38680462 | C | T | 5 | a0001c0001t0001g0075 a0001c0003t0001g0181 a0001c0003t0001g0195 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-742C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680462 | |||||||
| chrX:38680535 | C | G | 1 | a0001c0001t0002g0024 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.598-669C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680535 | |||||||
| chrX:38680538 | A | ATTCT | 3 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0206 |
3 | HG02615.hp1 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.598-665_598-662dup others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680538 | ||||||
| chrX:38680539 | T | TTC | 21 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0036 others(18): Show |
22 | HG00609.hp1 HG00642.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.598-621_598-620dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | T | TTCTC | 7 | a0001c0001t0001g0056 a0001c0001t0001g0082 a0001c0001t0001g0085 others(4): Show |
7 | HG00438.hp2 HG02145.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.598-623_598-620dup others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | T | TTCTCTC | 8 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0086 others(5): Show |
8 | HG00280.hp1 HG01099.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-625_598-620dup others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | T | TTCTCTCT others(1): Show |
2 | a0001c0001t0001g0098 a0001c0001t0002g0135 |
2 | HG03704.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.598-627_598-620dup others(8): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | T | TTCTCTCT others(3): Show |
4 | a0001c0001t0001g0042 a0001c0001t0001g0059 a0001c0001t0001g0071 others(1): Show |
4 | HG00621.hp1 HG02055.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-629_598-620dup others(10): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | T | TTCTCTCT others(9): Show |
1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.598-635_598-620dup others(16): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | TTC | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0050 others(23): Show |
27 | HG00099.hp1 HG00438.hp1 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.598-621_598-620del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | TTCTC | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
84 | HG00140.hp1 HG00673.hp1 HG01069.hp1 others(81): Show |
intron_variant | MODIFIER | c.598-623_598-620del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | TTCTCTCT others(1): Show |
T | 4 | a0001c0001t0001g0137 a0001c0001t0001g0145 a0001c0003t0001g0181 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-627_598-620del others(8): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | TTCTCTCT others(3): Show |
T | 2 | a0001c0001t0001g0147 a0001c0003t0001g0195 |
2 | HG03471.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.598-629_598-620del others(10): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | TTCTCTCT others(5): Show |
T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0132 |
2 | HG00741.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.598-631_598-620del others(12): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | TTCTCTCT others(9): Show |
T | 1 | a0001c0001t0001g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.598-635_598-620del others(16): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680539 | TTCTCTCT others(15): Show |
T | 8 | a0001c0002t0001g0005 a0001c0002t0001g0068 a0001c0002t0001g0074 others(5): Show |
9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-641_598-620del others(22): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | ||||||
| chrX:38680707 | T | C | 2 | a0001c0003t0001g0181 a0001c0003t0001g0210 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.598-497T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680707 | |||||||
| chrX:38680796 | G | A | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.598-408G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680796 | |||||||
| chrX:38680862 | T | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0073 |
2 | HG02895.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.598-342T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680862 | |||||||
| chrX:38680924 | A | C | 2 | a0001c0003t0001g0181 a0001c0003t0001g0210 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.598-280A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680924 | |||||||
| chrX:38681009 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.598-195T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38681009 | |||||||
| chrX:38681124 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.598-80T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38681124 | |||||||
| chrX:38681582 | G | A | 40 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
42 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.681+295G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38681582 | |||||||
| chrX:38681689 | A | G | 27 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(24): Show |
28 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.681+402A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38681689 | |||||||
| chrX:38681800 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0116 a0001c0001t0001g0117 others(5): Show |
8 | HG01109.hp1 HG01256.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.681+513G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38681800 | |||||||
| chrX:38681843 | T | C | 15 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0073 others(12): Show |
16 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.681+556T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38681843 | |||||||
| chrX:38681981 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.681+694T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38681981 | |||||||
| chrX:38682185 | TA | T | 27 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 others(24): Show |
28 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.681+899delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38682185 | |||||||
| chrX:38682671 | A | G | 4 | a0001c0002t0001g0005 a0001c0002t0001g0068 a0001c0002t0001g0088 others(1): Show |
5 | HG02559.hp2 HG02818.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+1384A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38682671 | |||||||
| chrX:38683055 | C | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.681+1768C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38683055 | |||||||
| chrX:38683428 | G | A | 1 | a0001c0003t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.681+2141G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38683428 | |||||||
| chrX:38683941 | T | G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0073 |
3 | HG02055.hp1 HG02895.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.681+2654T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38683941 | |||||||
| chrX:38684257 | C | G | 8 | a0001c0002t0001g0005 a0001c0002t0001g0068 a0001c0002t0001g0074 others(5): Show |
9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.681+2970C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38684257 | |||||||
| chrX:38684349 | CCT | C | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.681+3064_681+3065d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 38684349 | ||||||
| chrX:38685120 | T | C | 8 | a0001c0002t0001g0005 a0001c0002t0001g0068 a0001c0002t0001g0074 others(5): Show |
9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-2479T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685120 | |||||||
| chrX:38685171 | G | A | 8 | a0001c0002t0001g0005 a0001c0002t0001g0068 a0001c0002t0001g0074 others(5): Show |
9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-2428G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685171 | |||||||
| chrX:38685457 | T | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0073 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.682-2142T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685457 | |||||||
| chrX:38685620 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.682-1979G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685620 | |||||||
| chrX:38685674 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.682-1925G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685674 | |||||||
| chrX:38685680 | C | T | 4 | a0001c0002t0001g0005 a0001c0002t0001g0068 a0001c0002t0001g0088 others(1): Show |
5 | HG02559.hp2 HG02818.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-1919C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685680 | |||||||
| chrX:38685748 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.682-1851T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685748 | |||||||
| chrX:38685768 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.682-1831T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685768 | |||||||
| chrX:38686651 | G | A | 1 | a0001c0001t0002g0024 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.682-948G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38686651 | |||||||
| chrX:38686975 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.682-624C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38686975 | |||||||
| chrX:38687026 | A | G | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.682-573A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38687026 | |||||||
| chrX:38687140 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.682-459A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38687140 | |||||||
| chrX:38687572 | C | T | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0077 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.682-27C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38687572 | |||||||
| chrX:38687755 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.*7+81C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 7/7 | chrX | 38687755 |