Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11043 |
| ensemblid | ENSG00000080561.14 |
| hgncid | 7096 |
| symbol | MID2 |
| name | midline 2 |
| refseq_nuc | NM_012216.4 |
| refseq_prot | NP_036348.2 |
| ensembl_nuc | ENST00000262843.11 |
| ensembl_prot | ENSP00000262843.6 |
| mane_status | MANE Select |
| chr | chrX |
| start | 107825866 |
| end | 107931637 |
| strand | + |
| ver | v1.2 |
| region | chrX:107825866-107931637 |
| region5000 | chrX:107820866-107936637 |
| regionname0 | MID2_chrX_107825866_107931637 |
| regionname5000 | MID2_chrX_107820866_107936637 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 735 | 172 | 63 | 22 | 63 | 5 | 17 | 47 | MID2_chrX_107820866_107936637 | MID2 | MGESP others(730): Show |
chrX | 107820866 | 107936637 |
| a0002 | 0/0 | 735 | 9 | 0 | 3 | 1 | 2 | 3 | 1 | MID2_chrX_107820866_107936637 | MID2 | MGESP others(730): Show |
chrX | 107820866 | 107936637 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2205 | 143 | 53 | 21 | 49 | 4 | 14 | MID2_chrX_107820866_107936637 | MID2 | ATGGG others(2200): Show |
chrX | 107820866 | 107936637 | ||
| a0001c0002 | 0/0 | 2205 | 28 | 10 | 1 | 14 | 1 | 2 | MID2_chrX_107820866_107936637 | MID2 | ATGGG others(2200): Show |
chrX | 107820866 | 107936637 | ||
| a0001c0005 | 0/0 | 2205 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | ATGGG others(2200): Show |
chrX | 107820866 | 107936637 | ||
| a0002c0003 | 0/0 | 2205 | 8 | 0 | 2 | 1 | 2 | 3 | MID2_chrX_107820866_107936637 | MID2 | ATGGG others(2200): Show |
chrX | 107820866 | 107936637 | ||
| a0002c0004 | 0/0 | 2205 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ATGGG others(2200): Show |
chrX | 107820866 | 107936637 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7333 | 89 | 20 | 16 | 33 | 4 | 14 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0002 | 0/0 | 7333 | 13 | 4 | 1 | 8 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0003 | 0/0 | 7333 | 9 | 8 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0004 | 0/0 | 7333 | 7 | 0 | 0 | 7 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0005 | 0/0 | 7333 | 7 | 7 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0006 | 0/0 | 7333 | 3 | 2 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0007 | 0/0 | 7333 | 5 | 4 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0008 | 0/0 | 7333 | 3 | 3 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0009 | 0/0 | 7333 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0010 | 0/0 | 7333 | 2 | 2 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0011 | 0/0 | 7333 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0012 | 0/0 | 7333 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0013 | 0/0 | 7333 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0001t0014 | 0/0 | 7333 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0002t0001 | 0/0 | 7333 | 7 | 6 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0002t0002 | 0/0 | 7333 | 18 | 1 | 1 | 13 | 1 | 2 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0002t0006 | 0/0 | 7333 | 2 | 2 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0002t0009 | 0/0 | 7333 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0001c0005t0002 | 0/0 | 7333 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0002c0003t0002 | 0/0 | 7333 | 8 | 0 | 2 | 1 | 2 | 3 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| a0002c0004t0002 | 0/0 | 7333 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | ACTCC others(7328): Show |
chrX | 107820866 | 107936637 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0007g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0010g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0012g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0013g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0005t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0004t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | GBR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | FIN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00735 | hp2 | a0002 | c0003 | t0002 | g0161 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0174 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0168 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0142 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01168 | hp2 | a0002 | c0004 | t0002 | g0131 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01255 | hp1 | a0002 | c0003 | t0002 | g0162 | AMR | CLM | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01515 | hp1 | a0002 | c0003 | t0002 | g0160 | EUR | IBS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | IBS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01516 | hp2 | a0002 | c0003 | t0002 | g0138 | EUR | IBS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0169 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0147 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0137 | EAS | CDX | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0170 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0155 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02647 | hp1 | a0001 | c0002 | t0006 | g0180 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02738 | hp1 | a0001 | c0005 | t0002 | g0128 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0171 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0026 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0139 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0167 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0025 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03225 | hp1 | a0001 | c0002 | t0006 | g0179 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0129 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0130 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03704 | hp2 | a0002 | c0003 | t0002 | g0159 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03710 | hp1 | a0002 | c0003 | t0002 | g0163 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0164 | SAS | STU | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | YRI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | YRI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | YRI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18975 | hp2 | a0001 | c0001 | t0013 | g0058 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0123 | AFR | LWK | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19090 | hp1 | a0002 | c0003 | t0002 | g0165 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | YRI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0127 | EUR | TSI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | GIH | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0133 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0134 | AFR | USA | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | USA | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | USA | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA21309 | hp1 | a0001 | c0002 | t0009 | g0173 | AFR | LWK | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0110 | REF | REF | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0071 | REF | REF | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:107916061 | C | A | 1 | a0002 | 9 | HG00735.hp2 HG01168.hp2 HG01255.hp1 others(6): Show |
missense_variant | MODERATE | c.1133C>A | p.Ala378Asp | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/10 | 1694/7333 | 1133/2208 | 378/735 | chrX | 107916061 |
| 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:107840845 | A | C | 3 | a0001c0002 a0001c0005 a0002c0004 |
30 | HG01168.hp1 HG01168.hp2 HG01891.hp1 others(27): Show |
synonymous_variant | LOW | c.180A>C | p.Ser60Ser | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/10 | 741/7333 | 180/2208 | 60/735 | chrX | 107840845 | |||
| chrX:107917732 | G | A | 1 | a0001c0005 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1428G>A | p.Ala476Ala | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/10 | 1989/7333 | 1428/2208 | 476/735 | chrX | 107917732 |
| 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:107826162 | T | C | 1 | a0001c0001t0011 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-265T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/10 | 265 | chrX | 107826162 | ||||||
| chrX:107927287 | T | G | 1 | a0001c0001t0008 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*214T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 214 | chrX | 107927287 | ||||||
| chrX:107927666 | T | G | 1 | a0001c0001t0003 | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*593T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 593 | chrX | 107927666 | ||||||
| chrX:107927867 | C | T | 1 | a0001c0001t0014 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 794 | chrX | 107927867 | ||||||
| chrX:107928325 | C | G | 1 | a0001c0001t0005 | 7 | HG02922.hp1 HG02965.hp1 HG03130.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1252C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 1252 | chrX | 107928325 | ||||||
| chrX:107928414 | T | A | 3 | a0001c0001t0005 a0001c0001t0009 a0001c0002t0009 |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1341T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 1341 | chrX | 107928414 | ||||||
| chrX:107928415 | A | T | 1 | a0001c0001t0013 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1342A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 1342 | chrX | 107928415 | ||||||
| chrX:107928744 | A | C | 2 | a0001c0001t0007 a0001c0001t0011 |
6 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1671A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 1671 | chrX | 107928744 | ||||||
| chrX:107929008 | C | T | 1 | a0001c0001t0012 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1935C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 1935 | chrX | 107929008 | ||||||
| chrX:107929811 | C | A | 1 | a0001c0001t0007 | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2738C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 2738 | chrX | 107929811 | ||||||
| chrX:107930293 | T | C | 2 | a0001c0001t0006 a0001c0002t0006 |
5 | HG01243.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3220T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 3220 | chrX | 107930293 | ||||||
| chrX:107930939 | T | A | 10 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(7): Show |
49 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3866T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 3866 | chrX | 107930939 | ||||||
| chrX:107931519 | T | C | 1 | a0001c0001t0004 | 7 | NA18966.hp1 NA18973.hp2 NA18983.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4446T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 4446 | chrX | 107931519 | ||||||
| chrX:107931625 | A | G | 1 | a0001c0001t0010 | 2 | HG02486.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4552A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 4552 | chrX | 107931625 |
| 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:107826534 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4+104G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107826534 | |||||||
| chrX:107826545 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4+115G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107826545 | |||||||
| chrX:107826763 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
4 | HG02145.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4+333G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107826763 | |||||||
| chrX:107826883 | C | A | 1 | a0001c0001t0002g0006 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4+453C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107826883 | |||||||
| chrX:107826977 | A | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
58 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.4+547A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107826977 | |||||||
| chrX:107827792 | T | A | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG02630.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4+1362T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107827792 | |||||||
| chrX:107827938 | C | T | 2 | a0001c0002t0006g0179 a0001c0002t0006g0180 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4+1508C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107827938 | |||||||
| chrX:107828280 | CTCTTT | C | 13 | a0001c0001t0002g0021 a0001c0001t0005g0016 a0001c0001t0005g0017 others(10): Show |
13 | HG01243.hp1 HG02818.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.4+1866_4+1870delTC others(3): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828280 | ||||||
| chrX:107828310 | C | CT | 10 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(7): Show |
10 | HG02165.hp1 HG02622.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4+1899dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | ||||||
| chrX:107828310 | C | CTT | 24 | a0001c0001t0003g0126 a0001c0001t0007g0139 a0001c0002t0001g0144 others(21): Show |
24 | HG01109.hp1 HG01168.hp1 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.4+1898_4+1899dupTT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | ||||||
| chrX:107828310 | C | CTTT | 22 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(19): Show |
22 | HG00735.hp2 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.4+1897_4+1899dupTT others(1): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | ||||||
| chrX:107828310 | C | CTTTT | 10 | a0001c0001t0002g0178 a0001c0001t0003g0008 a0001c0001t0003g0009 others(7): Show |
10 | HG00741.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.4+1896_4+1899dupTT others(2): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | ||||||
| chrX:107828310 | CT | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
5 | HG00621.hp1 HG02165.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.4+1899delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | ||||||
| chrX:107828312 | T | TTC | 5 | a0001c0002t0002g0127 a0001c0002t0002g0129 a0001c0002t0002g0130 others(2): Show |
5 | HG01168.hp2 HG02738.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.4+1883_4+1884insCT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828312 | ||||||
| chrX:107828331 | A | G | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4+1901A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107828331 | |||||||
| chrX:107828440 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4+2010T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107828440 | |||||||
| chrX:107828480 | T | A | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG02622.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4+2050T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107828480 | |||||||
| chrX:107828902 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4+2472C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107828902 | |||||||
| chrX:107829196 | G | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
57 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.4+2766G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107829196 | |||||||
| chrX:107829243 | C | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
57 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.4+2813C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107829243 | |||||||
| chrX:107829578 | G | C | 12 | a0001c0001t0002g0021 a0001c0001t0005g0016 a0001c0001t0005g0017 others(9): Show |
12 | HG01243.hp1 HG02886.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.4+3148G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107829578 | |||||||
| chrX:107829805 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4+3375G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107829805 | |||||||
| chrX:107829818 | C | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
85 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(82): Show |
intron_variant | MODIFIER | c.4+3388C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107829818 | |||||||
| chrX:107830226 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4+3796C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107830226 | |||||||
| chrX:107830607 | G | A | 7 | a0002c0003t0002g0138 a0002c0003t0002g0159 a0002c0003t0002g0160 others(4): Show |
7 | HG00735.hp2 HG01255.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.4+4177G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107830607 | |||||||
| chrX:107830801 | T | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG02622.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4+4371T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107830801 | |||||||
| chrX:107831244 | T | C | 2 | a0001c0001t0003g0177 a0001c0001t0009g0026 |
2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4+4814T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107831244 | |||||||
| chrX:107831270 | G | A | 10 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(7): Show |
10 | HG01109.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.4+4840G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107831270 | |||||||
| chrX:107832962 | G | A | 1 | a0001c0001t0005g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4+6532G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107832962 | |||||||
| chrX:107832992 | A | G | 1 | a0001c0002t0001g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4+6562A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107832992 | |||||||
| chrX:107833201 | G | A | 3 | a0001c0001t0002g0132 a0001c0001t0008g0134 a0001c0001t0010g0133 |
3 | HG01891.hp2 HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4+6771G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833201 | |||||||
| chrX:107833411 | T | TTA | 7 | a0001c0001t0001g0040 a0001c0001t0003g0007 a0001c0001t0003g0012 others(4): Show |
7 | HG01109.hp1 HG02015.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.4+6999_4+7000dupAT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107833411 | ||||||
| chrX:107833411 | T | TTATA | 9 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
9 | HG02622.hp2 HG02723.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.4+6997_4+7000dupAT others(2): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107833411 | ||||||
| chrX:107833425 | A | T | 1 | a0002c0003t0002g0138 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4+6995A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833425 | |||||||
| chrX:107833427 | A | AT | 24 | a0001c0001t0003g0177 a0001c0001t0009g0026 a0001c0002t0001g0144 others(21): Show |
24 | HG01168.hp1 HG01168.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.4+6998dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107833427 | ||||||
| chrX:107833427 | A | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(17): Show |
20 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.4+6997A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833427 | |||||||
| chrX:107833428 | TA | T | 3 | a0001c0001t0002g0132 a0001c0001t0008g0134 a0001c0001t0010g0133 |
3 | HG01891.hp2 HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4+6999delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833428 | |||||||
| chrX:107833429 | A | AT | 6 | a0001c0001t0001g0166 a0001c0001t0007g0139 a0001c0001t0007g0167 others(3): Show |
6 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4+7007dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107833429 | ||||||
| chrX:107833429 | A | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00558.hp2 HG00673.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.4+6999A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833429 | |||||||
| chrX:107833431 | T | A | 28 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0039 others(25): Show |
28 | HG01109.hp1 HG01243.hp1 HG02622.hp1 others(25): Show |
intron_variant | MODIFIER | c.4+7001T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833431 | |||||||
| chrX:107833437 | T | A | 1 | a0001c0001t0002g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4+7007T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833437 | |||||||
| chrX:107833577 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18988.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.5-7093G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833577 | |||||||
| chrX:107834036 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5-6634T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834036 | |||||||
| chrX:107834086 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0043 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.5-6584G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834086 | |||||||
| chrX:107834234 | A | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.5-6436A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834234 | |||||||
| chrX:107834554 | G | A | 1 | a0001c0001t0003g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5-6116G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834554 | |||||||
| chrX:107834740 | G | C | 1 | a0001c0002t0001g0154 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5-5930G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834740 | |||||||
| chrX:107834958 | C | T | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG02630.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.5-5712C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834958 | |||||||
| chrX:107835201 | T | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.5-5469T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107835201 | |||||||
| chrX:107835421 | C | T | 2 | a0001c0001t0008g0014 a0001c0001t0008g0015 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.5-5249C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107835421 | |||||||
| chrX:107835518 | C | T | 2 | a0001c0001t0002g0178 a0001c0001t0012g0174 |
2 | HG00741.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.5-5152C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107835518 | |||||||
| chrX:107835654 | A | ATCT | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(77): Show |
80 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.5-5014_5-5012dupCT others(1): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107835654 | ||||||
| chrX:107836400 | T | C | 10 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(7): Show |
10 | HG01109.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.5-4270T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107836400 | |||||||
| chrX:107836493 | C | T | 2 | a0001c0002t0006g0179 a0001c0002t0006g0180 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5-4177C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107836493 | |||||||
| chrX:107836516 | G | A | 1 | a0001c0002t0002g0140 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.5-4154G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107836516 | |||||||
| chrX:107836530 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.5-4140C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107836530 | |||||||
| chrX:107836542 | C | T | 7 | a0001c0001t0001g0166 a0001c0001t0007g0139 a0001c0001t0007g0167 others(4): Show |
7 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.5-4128C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107836542 | |||||||
| chrX:107836553 | CT | C | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(8): Show |
11 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.5-4103delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107836553 | ||||||
| chrX:107837299 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.5-3371G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107837299 | |||||||
| chrX:107837538 | TA | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(54): Show |
57 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.5-3120delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107837538 | ||||||
| chrX:107837539 | A | T | 3 | a0001c0001t0004g0070 a0001c0001t0004g0080 a0001c0001t0004g0095 |
3 | NA18966.hp1 NA18983.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.5-3131A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107837539 | |||||||
| chrX:107837857 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5-2813T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107837857 | |||||||
| chrX:107838520 | A | G | 2 | a0001c0001t0002g0178 a0001c0001t0012g0174 |
2 | HG00741.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.5-2150A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107838520 | |||||||
| chrX:107838787 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
85 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(82): Show |
intron_variant | MODIFIER | c.5-1883A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107838787 | |||||||
| chrX:107838874 | T | C | 7 | a0001c0001t0002g0021 a0001c0001t0005g0016 a0001c0001t0005g0017 others(4): Show |
7 | HG02922.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.5-1796T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107838874 | |||||||
| chrX:107838962 | T | C | 10 | a0001c0001t0002g0178 a0001c0001t0012g0174 a0002c0003t0002g0138 others(7): Show |
10 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.5-1708T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107838962 | |||||||
| chrX:107838984 | C | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
58 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.5-1686C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107838984 | |||||||
| chrX:107839375 | G | T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5-1295G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107839375 | |||||||
| chrX:107839379 | G | GT | 14 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0166 others(11): Show |
14 | HG01099.hp1 HG01106.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.5-1277dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107839379 | ||||||
| chrX:107839379 | G | GTT | 9 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(6): Show |
9 | HG01109.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.5-1278_5-1277dupTT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107839379 | ||||||
| chrX:107839379 | G | T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5-1291G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107839379 | |||||||
| chrX:107839434 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5-1236T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107839434 | |||||||
| chrX:107839478 | A | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): Show |
58 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.5-1192A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107839478 | |||||||
| chrX:107839734 | A | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
68 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.5-936A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107839734 | |||||||
| chrX:107840042 | A | G | 11 | a0001c0001t0002g0021 a0001c0001t0005g0016 a0001c0001t0005g0017 others(8): Show |
11 | HG01243.hp1 HG02886.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.5-628A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107840042 | |||||||
| chrX:107840243 | CAT | C | 10 | a0001c0001t0002g0178 a0001c0001t0012g0174 a0002c0003t0002g0138 others(7): Show |
10 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.5-425_5-424delTA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107840243 | ||||||
| chrX:107840332 | A | T | 8 | a0002c0003t0002g0138 a0002c0003t0002g0159 a0002c0003t0002g0160 others(5): Show |
8 | HG00735.hp2 HG01255.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.5-338A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107840332 | |||||||
| chrX:107841402 | G | A | 5 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG02622.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+17G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107841402 | |||||||
| chrX:107841423 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.720+38C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107841423 | |||||||
| chrX:107842630 | G | A | 2 | a0001c0001t0003g0177 a0001c0001t0009g0026 |
2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.720+1245G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107842630 | |||||||
| chrX:107842656 | G | T | 10 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(7): Show |
10 | HG01109.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+1271G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107842656 | |||||||
| chrX:107842911 | G | C | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.720+1526G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107842911 | |||||||
| chrX:107843333 | A | G | 7 | a0001c0001t0001g0166 a0001c0001t0007g0139 a0001c0001t0007g0167 others(4): Show |
7 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+1948A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843333 | |||||||
| chrX:107843338 | C | T | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.720+1953C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843338 | |||||||
| chrX:107843474 | G | A | 2 | a0001c0002t0006g0179 a0001c0002t0006g0180 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.720+2089G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843474 | |||||||
| chrX:107843491 | T | A | 12 | a0001c0001t0002g0021 a0001c0001t0005g0016 a0001c0001t0005g0017 others(9): Show |
12 | HG01243.hp1 HG02886.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.720+2106T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843491 | |||||||
| chrX:107843612 | T | C | 3 | a0001c0001t0002g0132 a0001c0001t0008g0134 a0001c0001t0010g0133 |
3 | HG01891.hp2 HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.720+2227T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843612 | |||||||
| chrX:107843673 | C | T | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.720+2288C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843673 | |||||||
| chrX:107843799 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.720+2414G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843799 | |||||||
| chrX:107843813 | G | A | 12 | a0001c0001t0002g0021 a0001c0001t0005g0016 a0001c0001t0005g0017 others(9): Show |
12 | HG01243.hp1 HG02886.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.720+2428G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843813 | |||||||
| chrX:107843866 | G | T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.720+2481G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843866 | |||||||
| chrX:107843873 | G | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0181 others(1): Show |
4 | HG02055.hp1 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+2488G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843873 | |||||||
| chrX:107843950 | A | G | 1 | a0001c0001t0003g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.720+2565A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843950 | |||||||
| chrX:107844230 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.720+2845G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107844230 | |||||||
| chrX:107844468 | T | G | 10 | a0001c0001t0002g0178 a0001c0001t0012g0174 a0002c0003t0002g0138 others(7): Show |
10 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+3083T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107844468 | |||||||
| chrX:107844548 | A | T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.720+3163A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107844548 | |||||||
| chrX:107844737 | C | CCTAA | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
90 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.720+3354_720+3355i others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107844737 | ||||||
| chrX:107844905 | G | T | 1 | a0001c0001t0008g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.720+3520G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107844905 | |||||||
| chrX:107845024 | G | C | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0059 others(1): Show |
4 | NA18747.hp1 NA18975.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+3639G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845024 | |||||||
| chrX:107845039 | T | A | 2 | a0001c0002t0006g0179 a0001c0002t0006g0180 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.720+3654T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845039 | |||||||
| chrX:107845039 | T | G | 49 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0038 others(46): Show |
49 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.720+3654T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845039 | |||||||
| chrX:107845451 | T | C | 5 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(2): Show |
5 | HG02717.hp1 HG02723.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+4066T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845451 | |||||||
| chrX:107845492 | A | AAC | 5 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0004g0029 others(2): Show |
5 | HG00280.hp1 HG03540.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+4140_720+4141d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845492 | ||||||
| chrX:107845492 | A | AACAC | 3 | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG01069.hp1 HG01071.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.720+4138_720+4141d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845492 | ||||||
| chrX:107845492 | AACACACA others(5): Show |
A | 1 | a0001c0001t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.720+4130_720+4141d others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845492 | ||||||
| chrX:107845519 | A | ACT | 4 | a0001c0001t0002g0178 a0001c0001t0012g0174 a0002c0003t0002g0163 others(1): Show |
4 | HG00741.hp2 HG01071.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+4135_720+4136i others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845519 | ||||||
| chrX:107845519 | A | T | 2 | a0001c0002t0002g0140 a0002c0004t0002g0131 |
2 | HG01168.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.720+4134A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845519 | |||||||
| chrX:107845521 | A | ACTCT | 2 | a0001c0002t0002g0141 a0002c0003t0002g0159 |
2 | HG03704.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.720+4137_720+4138i others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | ||||||
| chrX:107845521 | A | ACTCTCT | 3 | a0001c0001t0006g0023 a0001c0001t0006g0024 a0001c0005t0002g0128 |
3 | HG02738.hp1 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.720+4137_720+4138i others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | ||||||
| chrX:107845521 | A | ACTCTCTC others(1): Show |
6 | a0001c0001t0002g0132 a0001c0001t0003g0008 a0001c0001t0014g0171 others(3): Show |
6 | HG01168.hp1 HG01891.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+4137_720+4138i others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | ||||||
| chrX:107845521 | A | ACTCTCTC others(3): Show |
15 | a0001c0001t0002g0006 a0001c0001t0002g0051 a0001c0001t0002g0052 others(12): Show |
15 | HG00558.hp1 HG00609.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+4137_720+4138i others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | ||||||
| chrX:107845521 | A | ACTCTCTC others(5): Show |
3 | a0001c0001t0002g0048 a0001c0002t0002g0137 a0001c0002t0002g0148 |
3 | HG02165.hp1 HG03471.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.720+4137_720+4138i others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | ||||||
| chrX:107845521 | A | ACTCTCTC others(7): Show |
2 | a0001c0002t0002g0149 a0001c0002t0002g0150 |
2 | NA18973.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.720+4137_720+4138i others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | ||||||
| chrX:107845521 | A | T | 10 | a0001c0001t0002g0178 a0001c0001t0012g0174 a0001c0002t0002g0140 others(7): Show |
10 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+4136A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845521 | |||||||
| chrX:107845523 | A | ACTCTCT | 3 | a0001c0001t0001g0120 a0001c0001t0010g0123 a0001c0001t0010g0133 |
3 | HG02486.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.720+4139_720+4140i others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845523 | ||||||
| chrX:107845523 | A | ACTCTCTC others(3): Show |
1 | a0001c0001t0002g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.720+4139_720+4140i others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845523 | ||||||
| chrX:107845523 | A | ACTCTCTC others(7): Show |
1 | a0001c0002t0002g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.720+4139_720+4140i others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845523 | ||||||
| chrX:107845523 | A | T | 47 | a0001c0001t0002g0006 a0001c0001t0002g0038 a0001c0001t0002g0048 others(44): Show |
47 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.720+4138A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845523 | |||||||
| chrX:107845525 | A | ACACACAC others(3): Show |
1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.720+4141_720+4142i others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACACAC others(7): Show |
1 | a0001c0001t0005g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACACAC others(11): Show |
1 | a0001c0001t0003g0009 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.720+4141_720+4142i others(20): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACACAC others(13): Show |
1 | a0001c0001t0003g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(22): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACACAC others(25): Show |
1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(34): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACACTC others(5): Show |
4 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0027 others(1): Show |
4 | HG02922.hp1 HG02965.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+4141_720+4142i others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACACTC others(7): Show |
1 | a0001c0001t0005g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.720+4141_720+4142i others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACACTC others(9): Show |
2 | a0001c0001t0005g0020 a0001c0002t0009g0173 |
2 | HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.720+4141_720+4142i others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACACTC others(11): Show |
2 | a0001c0001t0003g0007 a0001c0001t0003g0011 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.720+4141_720+4142i others(20): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACACTC others(23): Show |
1 | a0001c0001t0003g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(32): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACTCTC others(7): Show |
1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACTCTC others(9): Show |
1 | a0001c0002t0001g0154 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.720+4141_720+4142i others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACTCTC others(11): Show |
1 | a0001c0001t0003g0012 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(20): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACTCTC others(21): Show |
1 | a0001c0001t0001g0175 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.720+4141_720+4142i others(30): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACTCTC others(23): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0176 a0001c0001t0003g0013 |
3 | HG02970.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.720+4141_720+4142i others(32): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACTCTC others(25): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.720+4141_720+4142i others(34): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACACTCTC others(27): Show |
1 | a0001c0002t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(36): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACT | 2 | a0001c0001t0001g0043 a0001c0001t0004g0109 |
2 | HG03041.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.720+4172_720+4173d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACTCT | 2 | a0001c0001t0001g0042 a0001c0001t0007g0170 |
2 | HG02258.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.720+4170_720+4173d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACTCTCTC others(1): Show |
6 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+4166_720+4173d others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACTCTCTC others(5): Show |
1 | a0001c0002t0001g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.720+4162_720+4173d others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACTCTCTC others(7): Show |
1 | a0001c0002t0001g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.720+4160_720+4173d others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | ACTCTCTC others(9): Show |
2 | a0001c0002t0001g0156 a0001c0002t0001g0157 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.720+4158_720+4173d others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | ||||||
| chrX:107845525 | A | T | 61 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0040 others(58): Show |
61 | HG00558.hp1 HG00609.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.720+4140A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845525 | |||||||
| chrX:107845527 | T | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(3): Show |
6 | HG00738.hp1 HG00741.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+4142T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845527 | |||||||
| chrX:107845540 | C | CTCTCTCT others(3): Show |
2 | a0001c0002t0002g0151 a0001c0002t0002g0152 |
2 | NA18960.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.720+4164_720+4165i others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845540 | ||||||
| chrX:107845876 | G | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0043 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.720+4491G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845876 | |||||||
| chrX:107845980 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.720+4595C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845980 | |||||||
| chrX:107846003 | T | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.720+4618T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846003 | |||||||
| chrX:107846071 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.720+4686G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846071 | |||||||
| chrX:107846381 | A | G | 6 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(3): Show |
6 | HG02486.hp1 HG02622.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+4996A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846381 | |||||||
| chrX:107846515 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.720+5130C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846515 | |||||||
| chrX:107846700 | G | A | 3 | a0001c0001t0002g0132 a0001c0001t0003g0013 a0001c0001t0003g0126 |
3 | HG01109.hp1 HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.720+5315G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846700 | |||||||
| chrX:107846709 | T | C | 1 | a0001c0002t0009g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.720+5324T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846709 | |||||||
| chrX:107846835 | A | G | 1 | a0001c0001t0005g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.720+5450A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846835 | |||||||
| chrX:107846965 | A | G | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 |
3 | HG00609.hp1 NA18948.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.720+5580A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846965 | |||||||
| chrX:107847004 | A | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
94 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.720+5619A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107847004 | |||||||
| chrX:107847113 | G | A | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.720+5728G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107847113 | |||||||
| chrX:107848771 | A | G | 1 | a0001c0001t0004g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.721-5838A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107848771 | |||||||
| chrX:107849033 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
178 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.721-5576A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107849033 | |||||||
| chrX:107849341 | G | C | 1 | a0001c0001t0002g0051 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.721-5268G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107849341 | |||||||
| chrX:107849348 | T | C | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.721-5261T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107849348 | |||||||
| chrX:107849429 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.721-5180A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107849429 | |||||||
| chrX:107849488 | A | C | 4 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0107 others(1): Show |
4 | HG00280.hp1 HG01516.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-5121A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107849488 | |||||||
| chrX:107850189 | GACACAC | G | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
92 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.721-4397_721-4392d others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107850189 | ||||||
| chrX:107850426 | A | G | 8 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(5): Show |
8 | HG01109.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-4183A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107850426 | |||||||
| chrX:107850590 | T | C | 1 | a0002c0003t0002g0160 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.721-4019T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107850590 | |||||||
| chrX:107851476 | A | G | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-3133A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107851476 | |||||||
| chrX:107851552 | A | G | 1 | a0001c0001t0006g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.721-3057A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107851552 | |||||||
| chrX:107851707 | A | G | 3 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0002t0002g0143 |
3 | HG02976.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.721-2902A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107851707 | |||||||
| chrX:107851767 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
94 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.721-2842G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107851767 | |||||||
| chrX:107851780 | C | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
79 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.721-2829C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107851780 | |||||||
| chrX:107851853 | CTTTTTAT others(5): Show |
C | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.721-2754_721-2743d others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851853 | ||||||
| chrX:107851855 | TTTTA | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(110): Show |
113 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.721-2711_721-2708d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | ||||||
| chrX:107851855 | TTTTATTT others(1): Show |
T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(10): Show |
13 | HG01243.hp1 HG01516.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.721-2715_721-2708d others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | ||||||
| chrX:107851855 | TTTTATTT others(5): Show |
T | 9 | a0001c0001t0002g0132 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.721-2719_721-2708d others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | ||||||
| chrX:107851855 | TTTTATTT others(9): Show |
T | 9 | a0001c0001t0001g0135 a0001c0001t0005g0016 a0001c0001t0005g0017 others(6): Show |
9 | HG02922.hp1 HG02965.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.721-2723_721-2708d others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | ||||||
| chrX:107851855 | TTTTATTT others(13): Show |
T | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.721-2727_721-2708d others(22): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | ||||||
| chrX:107851855 | TTTTATTT others(17): Show |
T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.721-2731_721-2708d others(26): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | ||||||
| chrX:107852143 | C | T | 2 | a0001c0002t0002g0151 a0001c0002t0002g0152 |
2 | NA18960.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.721-2466C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107852143 | |||||||
| chrX:107852866 | G | A | 1 | a0002c0003t0002g0159 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.721-1743G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107852866 | |||||||
| chrX:107852924 | C | T | 1 | a0001c0002t0009g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.721-1685C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107852924 | |||||||
| chrX:107853108 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.721-1501A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853108 | |||||||
| chrX:107853112 | A | G | 1 | a0001c0001t0003g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.721-1497A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853112 | |||||||
| chrX:107853141 | C | G | 18 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(15): Show |
18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.721-1468C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853141 | |||||||
| chrX:107853188 | G | A | 2 | a0001c0001t0003g0013 a0001c0001t0003g0126 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.721-1421G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853188 | |||||||
| chrX:107853424 | T | G | 1 | a0001c0002t0009g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.721-1185T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853424 | |||||||
| chrX:107853538 | G | A | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.721-1071G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853538 | |||||||
| chrX:107853590 | G | A | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.721-1019G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853590 | |||||||
| chrX:107853931 | C | G | 4 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(1): Show |
4 | HG01106.hp1 HG01884.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-678C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853931 | |||||||
| chrX:107853951 | A | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
95 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.721-658A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853951 | |||||||
| chrX:107854026 | T | C | 18 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(15): Show |
18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.721-583T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854026 | |||||||
| chrX:107854138 | T | G | 5 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0024 others(2): Show |
5 | HG01243.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-471T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854138 | |||||||
| chrX:107854206 | A | G | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.721-403A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854206 | |||||||
| chrX:107854308 | T | C | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-301T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854308 | |||||||
| chrX:107854452 | G | C | 18 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(15): Show |
18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.721-157G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854452 | |||||||
| chrX:107854541 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.721-68T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854541 | |||||||
| chrX:107854897 | C | T | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(8): Show |
11 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+193C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107854897 | |||||||
| chrX:107854911 | A | G | 18 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(15): Show |
18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.816+207A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107854911 | |||||||
| chrX:107854966 | A | G | 18 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(15): Show |
18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.816+262A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107854966 | |||||||
| chrX:107854999 | A | G | 1 | a0001c0002t0002g0142 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.816+295A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107854999 | |||||||
| chrX:107855176 | A | G | 32 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0048 others(29): Show |
32 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.816+472A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107855176 | |||||||
| chrX:107855696 | A | G | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(8): Show |
11 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+992A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107855696 | |||||||
| chrX:107855882 | C | T | 18 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(15): Show |
18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.816+1178C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107855882 | |||||||
| chrX:107856091 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.816+1387G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107856091 | |||||||
| chrX:107857183 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.816+2479T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107857183 | |||||||
| chrX:107857207 | G | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+2503G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107857207 | |||||||
| chrX:107857593 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.816+2889A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107857593 | |||||||
| chrX:107857784 | A | G | 16 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(13): Show |
16 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.816+3080A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107857784 | |||||||
| chrX:107858104 | C | A | 2 | a0001c0001t0005g0017 a0001c0001t0005g0019 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.816+3400C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107858104 | |||||||
| chrX:107858123 | A | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.816+3419A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107858123 | |||||||
| chrX:107858527 | T | C | 1 | a0001c0001t0004g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.816+3823T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107858527 | |||||||
| chrX:107858553 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.816+3849C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107858553 | |||||||
| chrX:107858733 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.816+4029T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107858733 | |||||||
| chrX:107859068 | A | G | 18 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(15): Show |
18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.816+4364A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859068 | |||||||
| chrX:107859184 | C | T | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
59 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.816+4480C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859184 | |||||||
| chrX:107859473 | G | A | 2 | a0001c0002t0006g0179 a0001c0002t0006g0180 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.816+4769G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859473 | |||||||
| chrX:107859677 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+4973C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859677 | |||||||
| chrX:107859700 | G | C | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.816+4996G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859700 | |||||||
| chrX:107859919 | A | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
95 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.816+5215A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859919 | |||||||
| chrX:107860126 | G | A | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.816+5422G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107860126 | |||||||
| chrX:107861045 | T | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(13): Show |
16 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.816+6341T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861045 | |||||||
| chrX:107861468 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+6764A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861468 | |||||||
| chrX:107861472 | T | C | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+6768T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861472 | |||||||
| chrX:107861743 | A | G | 3 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0134 |
3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.816+7039A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861743 | |||||||
| chrX:107861889 | T | C | 5 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0075 others(2): Show |
5 | HG00280.hp1 HG01516.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+7185T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861889 | |||||||
| chrX:107861987 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+7283A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861987 | |||||||
| chrX:107862235 | A | G | 1 | a0001c0005t0002g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.816+7531A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107862235 | |||||||
| chrX:107862784 | T | C | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+8080T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107862784 | |||||||
| chrX:107863141 | T | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+8437T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107863141 | |||||||
| chrX:107863325 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+8621C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107863325 | |||||||
| chrX:107863560 | C | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.816+8856C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107863560 | |||||||
| chrX:107863978 | C | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0114 |
2 | HG01433.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.816+9274C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107863978 | |||||||
| chrX:107864086 | T | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+9382T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864086 | |||||||
| chrX:107864136 | C | G | 3 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0134 |
3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.816+9432C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864136 | |||||||
| chrX:107864301 | A | G | 2 | a0001c0002t0002g0137 a0001c0002t0002g0147 |
2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.816+9597A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864301 | |||||||
| chrX:107864302 | C | A | 2 | a0001c0002t0002g0137 a0001c0002t0002g0147 |
2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.816+9598C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864302 | |||||||
| chrX:107864714 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0050 |
2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.816+10010A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864714 | |||||||
| chrX:107864726 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.816+10022A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864726 | |||||||
| chrX:107865131 | C | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+10427C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865131 | |||||||
| chrX:107865131 | C | T | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+10427C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865131 | |||||||
| chrX:107865161 | T | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+10457T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865161 | |||||||
| chrX:107865545 | C | CCT | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+10842_816+1084 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107865545 | ||||||
| chrX:107865573 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+10869G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865573 | |||||||
| chrX:107865573 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.816+10869G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865573 | |||||||
| chrX:107865605 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.816+10901A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865605 | |||||||
| chrX:107865655 | T | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+10951T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865655 | |||||||
| chrX:107865758 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.816+11054C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865758 | |||||||
| chrX:107865764 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
95 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.816+11060C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865764 | |||||||
| chrX:107865839 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+11135A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865839 | |||||||
| chrX:107865993 | G | C | 1 | a0001c0002t0009g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.816+11289G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865993 | |||||||
| chrX:107865995 | G | T | 5 | a0002c0003t0002g0138 a0002c0003t0002g0159 a0002c0003t0002g0160 others(2): Show |
5 | HG01515.hp1 HG01516.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+11291G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865995 | |||||||
| chrX:107866070 | C | T | 4 | a0001c0001t0002g0060 a0001c0002t0002g0136 a0001c0002t0002g0141 others(1): Show |
4 | NA18944.hp1 NA18945.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+11366C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107866070 | |||||||
| chrX:107866225 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.816+11521A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107866225 | |||||||
| chrX:107866421 | AAACAC | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0125 a0001c0001t0008g0015 |
3 | HG02630.hp1 HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.816+11719_816+1172 others(9): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866421 | ||||||
| chrX:107866422 | A | AAC | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0003g0011 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+11772_816+1177 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | ||||||
| chrX:107866422 | AAC | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0114 a0001c0001t0001g0176 |
3 | HG01433.hp1 HG03704.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.816+11772_816+1177 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | ||||||
| chrX:107866422 | AACAC | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0072 others(13): Show |
16 | HG00642.hp1 HG01099.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.816+11770_816+1177 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | ||||||
| chrX:107866422 | AACACAC | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(54): Show |
57 | HG00140.hp1 HG00558.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.816+11768_816+1177 others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | ||||||
| chrX:107866422 | AACACACA others(1): Show |
A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0045 others(17): Show |
20 | HG00280.hp1 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.816+11766_816+1177 others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | ||||||
| chrX:107866422 | AACACACA others(3): Show |
A | 20 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0102 others(17): Show |
20 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.816+11764_816+1177 others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | ||||||
| chrX:107866422 | AACACACA others(5): Show |
A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0048 others(26): Show |
29 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.816+11762_816+1177 others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | ||||||
| chrX:107866422 | AACACACA others(7): Show |
A | 2 | a0001c0001t0003g0177 a0001c0001t0014g0171 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.816+11760_816+1177 others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | ||||||
| chrX:107866422 | AACACACA others(9): Show |
A | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.816+11758_816+1177 others(20): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | ||||||
| chrX:107866422 | AACACACA others(13): Show |
A | 4 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0002t0006g0179 others(1): Show |
4 | HG01243.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+11754_816+1177 others(24): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | ||||||
| chrX:107866422 | AACACACA others(15): Show |
A | 12 | a0001c0001t0002g0038 a0001c0001t0002g0178 a0001c0001t0006g0024 others(9): Show |
12 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+11752_816+1177 others(26): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | ||||||
| chrX:107866464 | CACACACA others(6): Show |
C | 1 | a0002c0004t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.816+11765_816+1177 others(17): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866464 | ||||||
| chrX:107866817 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+12113A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107866817 | |||||||
| chrX:107867317 | AT | A | 36 | a0001c0001t0001g0078 a0001c0001t0001g0120 a0001c0001t0001g0121 others(33): Show |
36 | HG00642.hp1 HG01106.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.816+12630delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107867317 | ||||||
| chrX:107867335 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+12631G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107867335 | |||||||
| chrX:107867493 | C | A | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.816+12789C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107867493 | |||||||
| chrX:107867514 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.816+12810A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107867514 | |||||||
| chrX:107867764 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+13060A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107867764 | |||||||
| chrX:107867978 | A | T | 49 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0038 others(46): Show |
49 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.816+13274A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107867978 | |||||||
| chrX:107868003 | A | G | 35 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(32): Show |
35 | HG01106.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.816+13299A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107868003 | |||||||
| chrX:107868178 | T | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
95 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.816+13474T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107868178 | |||||||
| chrX:107868219 | T | C | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+13515T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107868219 | |||||||
| chrX:107868389 | A | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 |
3 | HG02622.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.816+13685A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107868389 | |||||||
| chrX:107869091 | G | A | 2 | a0001c0001t0007g0139 a0001c0001t0007g0167 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.816+14387G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869091 | |||||||
| chrX:107869485 | T | G | 1 | a0001c0001t0008g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.816+14781T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869485 | |||||||
| chrX:107869590 | G | T | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+14886G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869590 | |||||||
| chrX:107869712 | T | C | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+15008T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869712 | |||||||
| chrX:107869833 | TA | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+15139delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107869833 | ||||||
| chrX:107869838 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+15134A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869838 | |||||||
| chrX:107869882 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.816+15178T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869882 | |||||||
| chrX:107870060 | T | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+15356T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107870060 | |||||||
| chrX:107870222 | T | G | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+15518T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107870222 | |||||||
| chrX:107870519 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+15815G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107870519 | |||||||
| chrX:107870621 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0066 |
2 | HG02698.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.816+15917G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107870621 | |||||||
| chrX:107870753 | C | CT | 51 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0049 others(48): Show |
51 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.816+16067dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107870753 | ||||||
| chrX:107870753 | C | CTT | 8 | a0001c0001t0001g0124 a0001c0001t0002g0105 a0001c0002t0001g0154 others(5): Show |
8 | HG02572.hp1 HG02738.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+16066_816+1606 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107870753 | ||||||
| chrX:107870753 | C | CTTT | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0175 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+16065_816+1606 others(7): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107870753 | ||||||
| chrX:107870753 | C | CTTTT | 8 | a0001c0001t0001g0005 a0001c0001t0005g0016 a0001c0001t0005g0017 others(5): Show |
8 | HG02145.hp1 HG02922.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+16064_816+1606 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107870753 | ||||||
| chrX:107871023 | T | C | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+16319T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871023 | |||||||
| chrX:107871258 | C | T | 1 | a0001c0005t0002g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.816+16554C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871258 | |||||||
| chrX:107871282 | G | A | 2 | a0001c0001t0010g0123 a0001c0001t0010g0133 |
2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.816+16578G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871282 | |||||||
| chrX:107871317 | C | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.816+16613C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871317 | |||||||
| chrX:107871386 | G | A | 32 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0048 others(29): Show |
32 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.816+16682G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871386 | |||||||
| chrX:107871400 | G | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+16696G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871400 | |||||||
| chrX:107871499 | A | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.816+16795A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871499 | |||||||
| chrX:107871527 | T | C | 10 | a0001c0001t0001g0166 a0001c0001t0003g0007 a0001c0001t0003g0008 others(7): Show |
10 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.816+16823T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871527 | |||||||
| chrX:107871726 | A | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.816+17022A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871726 | |||||||
| chrX:107871760 | C | T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.816+17056C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871760 | |||||||
| chrX:107871783 | T | G | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.816+17079T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871783 | |||||||
| chrX:107871786 | T | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+17082T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871786 | |||||||
| chrX:107871811 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+17107A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871811 | |||||||
| chrX:107871868 | C | A | 1 | a0001c0002t0002g0151 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.816+17164C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871868 | |||||||
| chrX:107872020 | C | T | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+17316C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107872020 | |||||||
| chrX:107872214 | CCTGA | C | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 others(2): Show |
5 | HG02486.hp1 HG02622.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+17514_816+1751 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107872214 | ||||||
| chrX:107872254 | A | G | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+17550A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107872254 | |||||||
| chrX:107872320 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+17616A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107872320 | |||||||
| chrX:107872801 | A | G | 1 | a0001c0002t0002g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.816+18097A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107872801 | |||||||
| chrX:107873505 | T | C | 1 | a0001c0001t0007g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.816+18801T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107873505 | |||||||
| chrX:107874245 | A | C | 1 | a0001c0001t0002g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.816+19541A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107874245 | |||||||
| chrX:107874492 | T | A | 11 | a0001c0001t0002g0178 a0001c0001t0012g0174 a0002c0003t0002g0138 others(8): Show |
11 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+19788T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107874492 | |||||||
| chrX:107875258 | C | G | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+20554C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875258 | |||||||
| chrX:107875391 | C | G | 32 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0048 others(29): Show |
32 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.816+20687C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875391 | |||||||
| chrX:107875657 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 |
3 | HG02622.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.816+20953G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875657 | |||||||
| chrX:107875829 | T | C | 15 | a0001c0001t0001g0166 a0001c0001t0005g0016 a0001c0001t0005g0017 others(12): Show |
15 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.816+21125T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875829 | |||||||
| chrX:107875864 | C | T | 1 | a0001c0001t0010g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.816+21160C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875864 | |||||||
| chrX:107875893 | T | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+21189T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875893 | |||||||
| chrX:107876142 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.816+21438C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107876142 | |||||||
| chrX:107876277 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.816+21573A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107876277 | |||||||
| chrX:107876409 | A | C | 1 | a0001c0001t0002g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.816+21705A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107876409 | |||||||
| chrX:107876685 | TCAGCTG | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0114 |
2 | HG01433.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.816+21985_816+2199 others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107876685 | ||||||
| chrX:107876719 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.816+22015G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107876719 | |||||||
| chrX:107876888 | A | G | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+22184A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107876888 | |||||||
| chrX:107877178 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+22474G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107877178 | |||||||
| chrX:107877694 | T | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+22990T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107877694 | |||||||
| chrX:107878012 | GA | G | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+23320delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107878012 | ||||||
| chrX:107878062 | A | T | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+23358A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107878062 | |||||||
| chrX:107878358 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+23654A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107878358 | |||||||
| chrX:107878640 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.816+23936C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107878640 | |||||||
| chrX:107878939 | T | C | 1 | a0001c0001t0008g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.816+24235T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107878939 | |||||||
| chrX:107879107 | G | A | 1 | a0001c0001t0004g0109 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.816+24403G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107879107 | |||||||
| chrX:107879187 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.816+24483T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107879187 | |||||||
| chrX:107879243 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.816+24539G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107879243 | |||||||
| chrX:107879528 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-24430C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107879528 | |||||||
| chrX:107880246 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-23712C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107880246 | |||||||
| chrX:107880329 | CA | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | NA18986.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.817-23627delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107880329 | ||||||
| chrX:107880360 | G | A | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-23598G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107880360 | |||||||
| chrX:107880558 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.817-23400A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107880558 | |||||||
| chrX:107880682 | G | A | 7 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(4): Show |
7 | HG02922.hp1 HG02965.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-23276G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107880682 | |||||||
| chrX:107880921 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-23037A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107880921 | |||||||
| chrX:107881146 | T | C | 9 | a0002c0003t0002g0138 a0002c0003t0002g0159 a0002c0003t0002g0160 others(6): Show |
9 | HG00735.hp2 HG01168.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-22812T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881146 | |||||||
| chrX:107881468 | T | C | 1 | a0001c0002t0002g0151 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.817-22490T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881468 | |||||||
| chrX:107881477 | C | T | 3 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0134 |
3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.817-22481C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881477 | |||||||
| chrX:107881506 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.817-22452G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881506 | |||||||
| chrX:107881684 | G | A | 2 | a0001c0001t0008g0014 a0001c0001t0008g0015 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.817-22274G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881684 | |||||||
| chrX:107881701 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.817-22257A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881701 | |||||||
| chrX:107881739 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-22219A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881739 | |||||||
| chrX:107881757 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.817-22201C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881757 | |||||||
| chrX:107881831 | T | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-22127T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881831 | |||||||
| chrX:107881863 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.817-22095A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881863 | |||||||
| chrX:107882047 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0043 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.817-21911C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882047 | |||||||
| chrX:107882372 | A | G | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.817-21586A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882372 | |||||||
| chrX:107882456 | T | C | 2 | a0001c0001t0002g0132 a0001c0001t0014g0171 |
2 | HG01891.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.817-21502T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882456 | |||||||
| chrX:107882505 | G | GA | 15 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(12): Show |
15 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.817-21445dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107882505 | ||||||
| chrX:107882555 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-21403C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882555 | |||||||
| chrX:107882774 | C | G | 49 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0038 others(46): Show |
49 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.817-21184C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882774 | |||||||
| chrX:107882892 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.817-21066G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882892 | |||||||
| chrX:107882958 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.817-21000C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882958 | |||||||
| chrX:107883013 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-20945A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883013 | |||||||
| chrX:107883075 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-20883A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883075 | |||||||
| chrX:107883088 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-20870A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883088 | |||||||
| chrX:107883233 | G | A | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-20725G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883233 | |||||||
| chrX:107883385 | A | C | 6 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(3): Show |
6 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-20573A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883385 | |||||||
| chrX:107883397 | T | A | 1 | a0001c0001t0014g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.817-20561T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883397 | |||||||
| chrX:107884115 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.817-19843T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884115 | |||||||
| chrX:107884398 | T | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-19560T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884398 | |||||||
| chrX:107884614 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-19344C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884614 | |||||||
| chrX:107884683 | C | CA | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-19270dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107884683 | ||||||
| chrX:107884728 | A | T | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.817-19230A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884728 | |||||||
| chrX:107884747 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.817-19211C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884747 | |||||||
| chrX:107884878 | T | C | 1 | a0001c0001t0004g0029 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.817-19080T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884878 | |||||||
| chrX:107885093 | G | GGAGA | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.817-18864_817-1886 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107885093 | ||||||
| chrX:107885102 | C | CTTAT | 3 | a0001c0002t0002g0149 a0001c0002t0006g0179 a0001c0002t0006g0180 |
3 | HG02647.hp1 HG03225.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.817-18829_817-1882 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107885102 | ||||||
| chrX:107885102 | C | CTTATTTA others(1): Show |
4 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(1): Show |
4 | HG01106.hp1 HG01884.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-18833_817-1882 others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107885102 | ||||||
| chrX:107885102 | C | CTTATTTA others(5): Show |
2 | a0001c0001t0001g0050 a0001c0001t0007g0170 |
2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.817-18837_817-1882 others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107885102 | ||||||
| chrX:107885386 | T | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-18572T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885386 | |||||||
| chrX:107885391 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-18567G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885391 | |||||||
| chrX:107885402 | G | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-18556G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885402 | |||||||
| chrX:107885518 | T | A | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.817-18440T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885518 | |||||||
| chrX:107885645 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.817-18313G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885645 | |||||||
| chrX:107885655 | A | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-18303A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885655 | |||||||
| chrX:107885719 | A | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-18239A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885719 | |||||||
| chrX:107885720 | G | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-18238G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885720 | |||||||
| chrX:107885776 | G | A | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.817-18182G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885776 | |||||||
| chrX:107885893 | T | C | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.817-18065T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885893 | |||||||
| chrX:107885969 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-17989A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885969 | |||||||
| chrX:107886025 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-17933C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886025 | |||||||
| chrX:107886119 | T | G | 33 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0038 others(30): Show |
33 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.817-17839T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886119 | |||||||
| chrX:107886337 | C | A | 1 | a0001c0002t0002g0129 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.817-17621C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886337 | |||||||
| chrX:107886394 | G | T | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-17564G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886394 | |||||||
| chrX:107886559 | T | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.817-17399T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886559 | |||||||
| chrX:107886790 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.817-17168T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886790 | |||||||
| chrX:107886808 | T | G | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.817-17150T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886808 | |||||||
| chrX:107886945 | A | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0075 others(2): Show |
5 | HG00280.hp1 HG01516.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-17013A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886945 | |||||||
| chrX:107886955 | A | T | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.817-17003A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886955 | |||||||
| chrX:107887177 | A | C | 10 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 others(7): Show |
10 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-16781A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887177 | |||||||
| chrX:107887202 | A | C | 1 | a0001c0001t0003g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.817-16756A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887202 | |||||||
| chrX:107887254 | G | A | 1 | a0001c0001t0003g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.817-16704G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887254 | |||||||
| chrX:107887300 | C | G | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.817-16658C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887300 | |||||||
| chrX:107887306 | C | A | 1 | a0001c0001t0004g0109 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.817-16652C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887306 | |||||||
| chrX:107887335 | G | A | 2 | a0001c0001t0003g0013 a0001c0001t0003g0126 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.817-16623G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887335 | |||||||
| chrX:107887385 | C | G | 10 | a0001c0001t0001g0166 a0001c0001t0005g0016 a0001c0001t0005g0017 others(7): Show |
10 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-16573C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887385 | |||||||
| chrX:107887496 | G | C | 9 | a0002c0003t0002g0138 a0002c0003t0002g0159 a0002c0003t0002g0160 others(6): Show |
9 | HG00735.hp2 HG01168.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-16462G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887496 | |||||||
| chrX:107887671 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0114 |
2 | HG01433.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.817-16287A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887671 | |||||||
| chrX:107887856 | A | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
59 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.817-16102A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887856 | |||||||
| chrX:107888528 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-15430A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107888528 | |||||||
| chrX:107888686 | C | T | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
59 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.817-15272C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107888686 | |||||||
| chrX:107888942 | A | C | 34 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 others(31): Show |
34 | HG01106.hp1 HG01109.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.817-15016A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107888942 | |||||||
| chrX:107889044 | A | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-14914A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889044 | |||||||
| chrX:107889075 | A | G | 5 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(2): Show |
5 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-14883A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889075 | |||||||
| chrX:107889221 | G | T | 3 | a0001c0001t0002g0105 a0001c0002t0002g0137 a0001c0002t0002g0147 |
3 | HG02056.hp1 HG02165.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.817-14737G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889221 | |||||||
| chrX:107889409 | G | A | 2 | a0001c0001t0002g0132 a0001c0001t0014g0171 |
2 | HG01891.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.817-14549G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889409 | |||||||
| chrX:107889410 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.817-14548G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889410 | |||||||
| chrX:107889481 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.817-14477G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889481 | |||||||
| chrX:107889489 | C | T | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-14469C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889489 | |||||||
| chrX:107889606 | C | A | 11 | a0001c0001t0002g0178 a0001c0001t0012g0174 a0002c0003t0002g0138 others(8): Show |
11 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.817-14352C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889606 | |||||||
| chrX:107889738 | G | A | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-14220G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889738 | |||||||
| chrX:107889748 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-14210G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889748 | |||||||
| chrX:107889809 | G | A | 1 | a0001c0001t0003g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.817-14149G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889809 | |||||||
| chrX:107889948 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.817-14010T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889948 | |||||||
| chrX:107890873 | T | C | 1 | a0001c0001t0008g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.817-13085T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107890873 | |||||||
| chrX:107891072 | C | T | 2 | a0001c0002t0002g0137 a0001c0002t0002g0147 |
2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.817-12886C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891072 | |||||||
| chrX:107891081 | A | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.817-12877A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891081 | |||||||
| chrX:107891121 | C | T | 6 | a0001c0001t0002g0006 a0001c0001t0002g0051 a0001c0001t0002g0052 others(3): Show |
6 | HG00558.hp1 HG00609.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-12837C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891121 | |||||||
| chrX:107891201 | G | A | 1 | a0001c0001t0004g0080 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.817-12757G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891201 | |||||||
| chrX:107891279 | C | CT | 6 | a0001c0001t0001g0100 a0001c0001t0002g0105 a0001c0002t0001g0154 others(3): Show |
6 | HG02572.hp1 HG02886.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-12660dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107891279 | ||||||
| chrX:107891279 | CT | C | 16 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0061 others(13): Show |
16 | HG01069.hp1 HG01891.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.817-12660delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107891279 | ||||||
| chrX:107891342 | G | A | 3 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0134 |
3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.817-12616G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891342 | |||||||
| chrX:107891405 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-12553C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891405 | |||||||
| chrX:107891429 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-12529C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891429 | |||||||
| chrX:107891505 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-12453C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891505 | |||||||
| chrX:107891525 | C | T | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.817-12433C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891525 | |||||||
| chrX:107891722 | T | C | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.817-12236T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891722 | |||||||
| chrX:107891823 | C | G | 1 | a0001c0002t0009g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.817-12135C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891823 | |||||||
| chrX:107892201 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.817-11757C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892201 | |||||||
| chrX:107892349 | A | G | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.817-11609A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892349 | |||||||
| chrX:107892382 | T | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-11576T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892382 | |||||||
| chrX:107892534 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.817-11424C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892534 | |||||||
| chrX:107892762 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-11196A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892762 | |||||||
| chrX:107892785 | C | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-11173C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892785 | |||||||
| chrX:107893049 | A | T | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-10909A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107893049 | |||||||
| chrX:107893163 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
94 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.817-10795A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107893163 | |||||||
| chrX:107893275 | A | G | 1 | a0001c0002t0002g0142 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.817-10683A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107893275 | |||||||
| chrX:107893659 | A | G | 1 | a0001c0001t0003g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.817-10299A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107893659 | |||||||
| chrX:107893858 | T | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
60 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.817-10100T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107893858 | |||||||
| chrX:107894012 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.817-9946C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894012 | |||||||
| chrX:107894016 | ACCT | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-9938_817-9936d others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894016 | ||||||
| chrX:107894196 | C | CT | 5 | a0001c0001t0001g0100 a0001c0001t0002g0060 a0001c0002t0002g0136 others(2): Show |
5 | NA18944.hp1 NA18945.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-9751dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894196 | ||||||
| chrX:107894219 | A | G | 1 | a0001c0001t0005g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.817-9739A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894219 | |||||||
| chrX:107894765 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.817-9193C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894765 | |||||||
| chrX:107894828 | A | AGT | 6 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0134 others(3): Show |
6 | HG01071.hp1 HG01255.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-9094_817-9093d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894828 | ||||||
| chrX:107894828 | AGT | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(13): Show |
16 | HG00735.hp2 HG01516.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.817-9094_817-9093d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894828 | ||||||
| chrX:107894860 | T | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-9098T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894860 | |||||||
| chrX:107894861 | G | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-9097G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894861 | |||||||
| chrX:107894862 | T | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-9096T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894862 | |||||||
| chrX:107894863 | G | GAA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(6): Show |
9 | HG00738.hp1 HG00741.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-9095_817-9094i others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894863 | |||||||
| chrX:107894864 | T | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(15): Show |
18 | HG00738.hp1 HG00741.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.817-9094T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894864 | |||||||
| chrX:107894864 | T | TGTGAAA | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0068 others(2): Show |
5 | HG00280.hp1 HG01516.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-9093_817-9092i others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894864 | ||||||
| chrX:107894864 | T | TGTGTGAA others(1): Show |
56 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0031 others(53): Show |
56 | HG00140.hp1 HG00642.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.817-9093_817-9092i others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894864 | ||||||
| chrX:107894864 | T | TGTGTGTG others(3): Show |
24 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0061 others(21): Show |
24 | HG01069.hp1 HG01071.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.817-9093_817-9092i others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894864 | ||||||
| chrX:107894864 | T | TGTGTGTG others(5): Show |
6 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0043 others(3): Show |
6 | HG00621.hp1 HG01109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-9093_817-9092i others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894864 | ||||||
| chrX:107894864 | T | TGTGTGTG others(9): Show |
2 | a0001c0001t0003g0013 a0001c0001t0003g0177 |
2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.817-9093_817-9092i others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894864 | ||||||
| chrX:107894867 | A | AAGAG | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0072 others(5): Show |
8 | HG01258.hp1 HG02486.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.817-9075_817-9072d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894867 | ||||||
| chrX:107894867 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0030 others(108): Show |
111 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.817-9091A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894867 | |||||||
| chrX:107894912 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-9046A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894912 | |||||||
| chrX:107895030 | A | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.817-8928A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895030 | |||||||
| chrX:107895215 | T | TG | 19 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 others(16): Show |
19 | HG01516.hp2 HG02258.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.817-8733dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107895215 | ||||||
| chrX:107895221 | G | GC | 2 | a0001c0001t0003g0013 a0001c0001t0003g0126 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.817-8737_817-8736i others(3): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895221 | |||||||
| chrX:107895224 | G | T | 1 | a0001c0001t0003g0008 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.817-8734G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895224 | |||||||
| chrX:107895304 | C | A | 32 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0048 others(29): Show |
32 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.817-8654C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895304 | |||||||
| chrX:107895480 | C | T | 10 | a0001c0001t0001g0166 a0001c0001t0005g0016 a0001c0001t0005g0017 others(7): Show |
10 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-8478C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895480 | |||||||
| chrX:107895543 | G | A | 1 | a0001c0001t0008g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.817-8415G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895543 | |||||||
| chrX:107895787 | A | G | 2 | a0001c0001t0004g0080 a0001c0001t0004g0095 |
2 | NA18966.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.817-8171A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895787 | |||||||
| chrX:107896097 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.817-7861G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896097 | |||||||
| chrX:107896238 | C | T | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-7720C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896238 | |||||||
| chrX:107896408 | G | A | 4 | a0001c0001t0002g0060 a0001c0002t0002g0136 a0001c0002t0002g0141 others(1): Show |
4 | NA18944.hp1 NA18945.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-7550G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896408 | |||||||
| chrX:107896584 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-7374A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896584 | |||||||
| chrX:107896800 | CCT | C | 2 | a0001c0001t0002g0132 a0001c0001t0014g0171 |
2 | HG01891.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.817-7146_817-7145d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107896800 | ||||||
| chrX:107896812 | T | A | 1 | a0001c0002t0002g0140 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.817-7146T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896812 | |||||||
| chrX:107896812 | T | TCA | 6 | a0001c0001t0001g0166 a0001c0002t0001g0154 a0001c0002t0001g0155 others(3): Show |
6 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-7128_817-7127d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107896812 | ||||||
| chrX:107896814 | A | T | 2 | a0001c0001t0001g0103 a0001c0001t0005g0020 |
2 | HG03130.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.817-7144A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896814 | |||||||
| chrX:107896832 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.817-7126G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896832 | |||||||
| chrX:107896904 | T | C | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.817-7054T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896904 | |||||||
| chrX:107897319 | A | T | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-6639A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107897319 | |||||||
| chrX:107897627 | G | C | 1 | a0001c0001t0003g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.817-6331G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107897627 | |||||||
| chrX:107898001 | C | CT | 3 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0024 |
3 | HG01243.hp1 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.817-5951dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107898001 | ||||||
| chrX:107898022 | C | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-5936C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107898022 | |||||||
| chrX:107898327 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.817-5631G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107898327 | |||||||
| chrX:107898396 | C | T | 2 | a0002c0003t0002g0161 a0002c0003t0002g0162 |
2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.817-5562C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107898396 | |||||||
| chrX:107898528 | AT | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG01074.hp1 HG01433.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-5428delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107898528 | ||||||
| chrX:107898916 | T | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-5042T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107898916 | |||||||
| chrX:107898967 | T | C | 49 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0038 others(46): Show |
49 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.817-4991T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107898967 | |||||||
| chrX:107899097 | T | C | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.817-4861T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899097 | |||||||
| chrX:107899162 | T | G | 3 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0134 |
3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.817-4796T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899162 | |||||||
| chrX:107899176 | T | TC | 4 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(1): Show |
4 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-4777dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899176 | ||||||
| chrX:107899182 | T | C | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-4776T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899182 | |||||||
| chrX:107899182 | T | TC | 21 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(18): Show |
21 | HG00642.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.817-4766dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899182 | ||||||
| chrX:107899193 | A | C | 1 | a0001c0002t0002g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.817-4765A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899193 | |||||||
| chrX:107899457 | G | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-4501G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899457 | |||||||
| chrX:107899741 | A | AT | 11 | a0001c0001t0001g0100 a0001c0001t0002g0178 a0001c0001t0012g0174 others(8): Show |
11 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.817-4209dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899741 | ||||||
| chrX:107899796 | G | A | 1 | a0001c0002t0001g0144 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.817-4162G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899796 | |||||||
| chrX:107899948 | G | A | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.817-4010G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899948 | |||||||
| chrX:107900187 | A | C | 2 | a0001c0001t0002g0132 a0001c0001t0014g0171 |
2 | HG01891.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.817-3771A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107900187 | |||||||
| chrX:107901105 | C | T | 1 | a0001c0001t0004g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.817-2853C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107901105 | |||||||
| chrX:107901328 | AAGTAGCA others(8): Show |
A | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817-2629_817-2615d others(17): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107901328 | |||||||
| chrX:107901378 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.817-2580G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107901378 | |||||||
| chrX:107901423 | G | A | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-2535G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107901423 | |||||||
| chrX:107901487 | A | C | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-2471A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107901487 | |||||||
| chrX:107902071 | C | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-1887C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107902071 | |||||||
| chrX:107902300 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-1658T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107902300 | |||||||
| chrX:107902322 | C | T | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-1636C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107902322 | |||||||
| chrX:107902602 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-1356C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107902602 | |||||||
| chrX:107903048 | A | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-910A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107903048 | |||||||
| chrX:107903325 | G | GT | 35 | a0001c0001t0001g0037 a0001c0001t0001g0104 a0001c0001t0002g0006 others(32): Show |
35 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.817-620dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107903325 | ||||||
| chrX:107903325 | GT | G | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-620delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107903325 | ||||||
| chrX:107903379 | G | C | 10 | a0001c0001t0002g0178 a0001c0001t0012g0174 a0002c0003t0002g0138 others(7): Show |
10 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-579G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107903379 | |||||||
| chrX:107903492 | A | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-466A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107903492 | |||||||
| chrX:107903505 | AAAATTAG others(8): Show |
A | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.817-450_817-436del others(15): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107903505 | ||||||
| chrX:107904072 | C | T | 2 | a0001c0001t0008g0014 a0001c0001t0008g0015 |
2 | HG02630.hp1 HG02818.hp2 |
splice_region_variant&intron_variant | LOW | c.924+7C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | chrX | 107904072 | |||||||
| chrX:107904132 | A | G | 3 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0011 |
3 | HG02723.hp1 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.924+67A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | chrX | 107904132 | |||||||
| chrX:107904229 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.924+164C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | chrX | 107904229 | |||||||
| chrX:107904318 | A | C | 1 | a0001c0001t0001g0072 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.924+253A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | chrX | 107904318 | |||||||
| chrX:107904601 | AAACCAGA others(4): Show |
A | 1 | a0001c0001t0004g0109 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.924+537_924+547del others(11): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | chrX | 107904601 | |||||||
| chrX:107905813 | C | CAGCTCTT others(12): Show |
1 | a0001c0001t0005g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1073+188_1073+206d others(21): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107905813 | ||||||
| chrX:107906201 | T | C | 1 | a0001c0001t0003g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1073+575T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906201 | |||||||
| chrX:107906557 | C | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.1073+931C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906557 | |||||||
| chrX:107906648 | C | G | 1 | a0001c0001t0013g0058 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1073+1022C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906648 | |||||||
| chrX:107906649 | G | C | 1 | a0001c0001t0013g0058 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1073+1023G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906649 | |||||||
| chrX:107906650 | A | ATCTTGGC others(13): Show |
1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1073+1026_1073+104 others(24): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906650 | ||||||
| chrX:107906841 | C | CTCCCAAA others(18): Show |
1 | a0001c0001t0001g0098 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1073+1217_1073+124 others(29): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906841 | ||||||
| chrX:107906866 | G | A | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+1240G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906866 | |||||||
| chrX:107906984 | TGTCTTCG others(8): Show |
T | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1073+1359_1073+137 others(19): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906984 | |||||||
| chrX:107906990 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1073+1364C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906990 | |||||||
| chrX:107907037 | T | C | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 others(2): Show |
5 | HG02486.hp1 HG02622.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+1411T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907037 | |||||||
| chrX:107907257 | C | T | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+1631C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907257 | |||||||
| chrX:107907543 | A | G | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1073+1917A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907543 | |||||||
| chrX:107907588 | T | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+1962T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907588 | |||||||
| chrX:107907595 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+1969A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907595 | |||||||
| chrX:107907627 | C | CA | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0112 others(2): Show |
5 | HG00735.hp1 HG01884.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073+2008dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907627 | ||||||
| chrX:107907887 | A | T | 10 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 others(7): Show |
10 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1073+2261A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907887 | |||||||
| chrX:107908057 | GGCACAGG others(3): Show |
G | 1 | a0001c0001t0001g0104 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1073+2433_1073+244 others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908057 | ||||||
| chrX:107908256 | G | GCCACTAC others(4): Show |
1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1073+2631_1073+264 others(15): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908256 | ||||||
| chrX:107908553 | T | C | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+2927T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908553 | |||||||
| chrX:107908553 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+2927T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908553 | |||||||
| chrX:107908564 | TA | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0115 a0002c0003t0002g0164 |
3 | HG04204.hp1 NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1073+2944delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908564 | ||||||
| chrX:107908566 | A | AAAAATGT others(12): Show |
1 | a0001c0001t0001g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1073+2943_1073+296 others(23): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908566 | ||||||
| chrX:107908682 | A | G | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+3056A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908682 | |||||||
| chrX:107908696 | T | TA | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
79 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1073+3088dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908696 | ||||||
| chrX:107908696 | T | TAA | 20 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0002g0038 others(17): Show |
20 | HG01243.hp1 HG02486.hp1 HG02622.hp2 others(17): Show |
intron_variant | MODIFIER | c.1073+3087_1073+308 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908696 | ||||||
| chrX:107908696 | TA | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | HG02015.hp1 NA18962.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+3088delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908696 | ||||||
| chrX:107908715 | G | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+3089G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908715 | |||||||
| chrX:107909087 | G | A | 3 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0024 |
3 | HG01243.hp1 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1073+3461G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909087 | |||||||
| chrX:107909106 | TATTCCTA others(28): Show |
T | 1 | a0001c0001t0001g0118 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1073+3482_1073+351 others(39): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909106 | ||||||
| chrX:107909179 | G | GTCTTGGT others(5): Show |
1 | a0001c0001t0004g0109 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1073+3554_1073+356 others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909179 | ||||||
| chrX:107909254 | C | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+3628C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909254 | |||||||
| chrX:107909280 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+3654A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909280 | |||||||
| chrX:107909321 | G | GA | 2 | a0001c0001t0001g0100 a0002c0003t0002g0164 |
2 | HG04204.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1073+3697dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909321 | ||||||
| chrX:107909326 | C | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
95 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.1073+3700C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909326 | |||||||
| chrX:107909355 | AG | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0112 a0001c0001t0001g0115 |
3 | HG01884.hp1 NA19062.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1073+3732delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909355 | ||||||
| chrX:107909371 | T | C | 2 | a0001c0001t0009g0026 a0001c0002t0009g0173 |
2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1073+3745T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909371 | |||||||
| chrX:107909383 | TG | T | 2 | a0001c0001t0001g0100 a0001c0001t0003g0007 |
2 | HG03098.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1073+3759delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909383 | ||||||
| chrX:107909500 | C | CT | 2 | a0001c0001t0001g0005 a0002c0003t0002g0164 |
2 | HG02145.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1073+3875dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909500 | ||||||
| chrX:107909534 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1073+3908G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909534 | |||||||
| chrX:107909589 | GC | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0112 |
2 | HG01884.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1073+3965delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909589 | ||||||
| chrX:107909738 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1073+4112T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909738 | |||||||
| chrX:107909997 | AT | A | 3 | a0001c0001t0001g0112 a0002c0003t0002g0160 a0002c0003t0002g0164 |
3 | HG01515.hp1 HG01884.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1073+4377delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909997 | ||||||
| chrX:107910104 | A | T | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+4478A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910104 | |||||||
| chrX:107910134 | CT | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0074 |
2 | HG02145.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1073+4511delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910134 | ||||||
| chrX:107910148 | TC | T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0115 a0001c0002t0001g0156 |
3 | HG02970.hp1 NA19082.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1073+4526delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910148 | ||||||
| chrX:107910168 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1073+4542C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910168 | |||||||
| chrX:107910238 | G | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+4612G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910238 | |||||||
| chrX:107910362 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1073+4736T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910362 | |||||||
| chrX:107910384 | CT | C | 2 | a0001c0001t0001g0117 a0001c0002t0002g0141 |
2 | HG04115.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1073+4761delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910384 | ||||||
| chrX:107910557 | GT | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0106 a0001c0002t0002g0136 |
3 | HG00558.hp2 NA18944.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1073+4937delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910557 | ||||||
| chrX:107910580 | G | GT | 3 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0001g0100 |
3 | HG00735.hp1 NA18994.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1073+4960dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910580 | ||||||
| chrX:107910594 | C | CT | 3 | a0001c0001t0001g0117 a0002c0003t0002g0138 a0002c0003t0002g0164 |
3 | HG01516.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1073+4969dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910594 | ||||||
| chrX:107910673 | CT | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0074 others(1): Show |
4 | HG02735.hp1 HG04204.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+5051delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910673 | ||||||
| chrX:107910680 | TA | T | 2 | a0001c0001t0001g0074 a0002c0003t0002g0164 |
2 | HG04204.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1073+5056delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910680 | ||||||
| chrX:107910694 | A | AT | 2 | a0001c0001t0001g0106 a0002c0003t0002g0138 |
2 | HG00558.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1073+5069dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910694 | ||||||
| chrX:107910728 | G | GT | 4 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0074 others(1): Show |
4 | HG03540.hp1 NA19062.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+5107dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910728 | ||||||
| chrX:107910739 | A | T | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1073+5113A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910739 | |||||||
| chrX:107910767 | A | ATTCTTTC others(271): Show |
1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1073+5143_1073+514 others(282): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910767 | ||||||
| chrX:107910767 | A | ATTTTCCT others(259): Show |
1 | a0001c0001t0001g0085 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(270): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910767 | ||||||
| chrX:107910768 | T | TTTTCCTT others(146): Show |
1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+5154_1073+515 others(157): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(297): Show |
1 | a0001c0001t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+5154_1073+515 others(308): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(277): Show |
1 | a0001c0001t0001g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+5154_1073+515 others(288): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(252): Show |
1 | a0001c0001t0001g0039 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1073+5159_1073+516 others(263): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(221): Show |
1 | a0001c0001t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1073+5159_1073+516 others(232): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(324): Show |
1 | a0001c0001t0004g0109 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1073+5162_1073+516 others(335): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(292): Show |
1 | a0001c0001t0001g0117 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1073+5164_1073+516 others(303): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(333): Show |
1 | a0001c0001t0001g0086 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1073+5182_1073+518 others(344): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(250): Show |
1 | a0001c0001t0001g0082 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(261): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(168): Show |
1 | a0001c0001t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(179): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(228): Show |
1 | a0001c0001t0004g0029 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(239): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(285): Show |
1 | a0001c0001t0001g0046 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(296): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(153): Show |
1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(164): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(158): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0108 |
2 | HG01516.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(169): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(173): Show |
1 | a0001c0001t0001g0107 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(184): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(178): Show |
2 | a0001c0001t0001g0061 a0001c0001t0001g0111 |
2 | HG00673.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(189): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(183): Show |
2 | a0001c0001t0001g0062 a0001c0001t0001g0072 |
2 | HG01071.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(194): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(188): Show |
1 | a0001c0001t0001g0049 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(199): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(203): Show |
4 | a0001c0001t0001g0059 a0001c0001t0001g0075 a0001c0001t0001g0084 others(1): Show |
4 | HG03688.hp1 NA18953.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(214): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(208): Show |
2 | a0001c0001t0001g0063 a0001c0001t0001g0093 |
2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(219): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(213): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0064 a0001c0001t0001g0125 |
3 | HG02622.hp1 HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(224): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(218): Show |
3 | a0001c0001t0001g0067 a0001c0001t0001g0092 a0001c0001t0001g0096 |
3 | HG03704.hp1 NA18955.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(229): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(223): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0104 |
2 | HG00280.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(234): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(233): Show |
3 | a0001c0001t0001g0056 a0001c0001t0001g0120 a0001c0001t0001g0181 |
3 | HG02630.hp2 HG02976.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(244): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(238): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0065 |
2 | HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(249): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(243): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0088 others(2): Show |
5 | HG00738.hp1 HG02132.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(254): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(248): Show |
5 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0078 others(2): Show |
5 | HG00642.hp1 HG02922.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(259): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(253): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0101 |
2 | HG00140.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(264): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(258): Show |
3 | a0001c0001t0001g0083 a0001c0001t0001g0097 a0001c0001t0001g0118 |
3 | HG00735.hp1 NA18961.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(269): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(263): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0116 |
2 | HG01099.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(274): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(268): Show |
4 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0001g0057 others(1): Show |
4 | HG01433.hp1 HG02040.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(279): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(283): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0094 |
2 | HG02602.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(294): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(288): Show |
1 | a0001c0001t0004g0080 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(299): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(293): Show |
1 | a0001c0001t0001g0002 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(304): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(298): Show |
1 | a0001c0001t0001g0040 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(309): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(303): Show |
1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(314): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(308): Show |
1 | a0001c0001t0004g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(319): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(333): Show |
1 | a0001c0001t0001g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(344): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(343): Show |
1 | a0001c0001t0004g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(354): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(200): Show |
1 | a0001c0001t0001g0030 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(211): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(229): Show |
1 | a0001c0001t0001g0100 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(240): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(165): Show |
1 | a0001c0001t0002g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1074-5181_1074-518 others(176): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(129): Show |
1 | a0001c0002t0001g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074-5185_1074-518 others(140): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(229): Show |
1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1073+5185_1073+518 others(240): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(172): Show |
1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1073+5181_1073+518 others(183): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(323): Show |
1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1073+5181_1073+518 others(334): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910768 | T | TTTTCCTT others(217): Show |
1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+5165_1073+516 others(228): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | ||||||
| chrX:107910771 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1073+5145T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910771 | |||||||
| chrX:107910788 | C | CTTTCCTT others(200): Show |
1 | a0001c0001t0001g0090 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1074-5175_1074-517 others(211): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910788 | ||||||
| chrX:107910795 | T | TTCCCTTT others(294): Show |
1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1073+5172_1073+517 others(305): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910795 | ||||||
| chrX:107910797 | C | CCTTTCCT others(352): Show |
1 | a0001c0001t0001g0087 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(363): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910797 | ||||||
| chrX:107910797 | C | CCTTTCCT others(176): Show |
1 | a0001c0001t0006g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1074-5185_1074-518 others(187): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910797 | ||||||
| chrX:107910803 | C | CTTTCCTT others(350): Show |
1 | a0001c0001t0001g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(361): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910803 | ||||||
| chrX:107910807 | C | CCTTTCCC others(281): Show |
1 | a0001c0001t0001g0032 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+5187_1073+518 others(292): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910807 | ||||||
| chrX:107910809 | T | TTTCCTTT others(228): Show |
1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(239): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910809 | ||||||
| chrX:107910834 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1074-5168T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910834 | |||||||
| chrX:107910834 | T | TTCCTTTC others(274): Show |
1 | a0001c0001t0001g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-5167_1074-516 others(285): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910834 | ||||||
| chrX:107910835 | T | C | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-5167T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910835 | |||||||
| chrX:107910836 | T | TCCTTTCC others(267): Show |
1 | a0001c0001t0001g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(278): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910836 | ||||||
| chrX:107910836 | T | TCTTTCCT others(294): Show |
1 | a0001c0001t0004g0081 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1074-5165_1074-516 others(305): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910836 | ||||||
| chrX:107910837 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-5165C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910837 | |||||||
| chrX:107910838 | C | CCTTCCCT others(209): Show |
1 | a0001c0001t0002g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1074-5162_1074-516 others(220): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910838 | ||||||
| chrX:107910838 | C | CT | 5 | a0001c0001t0001g0005 a0001c0001t0002g0038 a0001c0001t0002g0132 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCCT others(264): Show |
1 | a0001c0001t0002g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(275): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCCT others(244): Show |
1 | a0001c0001t0002g0053 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(255): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCCT others(214): Show |
1 | a0001c0001t0002g0006 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(225): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(239): Show |
1 | a0001c0002t0002g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(250): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(306): Show |
1 | a0001c0001t0002g0052 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(317): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(244): Show |
1 | a0001c0001t0002g0051 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(255): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(224): Show |
1 | a0001c0001t0002g0054 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(235): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(199): Show |
1 | a0001c0002t0002g0148 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(210): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(239): Show |
1 | a0001c0001t0002g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(250): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(194): Show |
1 | a0001c0002t0002g0150 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(205): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(169): Show |
1 | a0001c0002t0002g0129 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(180): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(173): Show |
1 | a0001c0002t0002g0142 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(184): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(193): Show |
1 | a0001c0002t0002g0149 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(204): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(218): Show |
1 | a0002c0003t0002g0138 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(229): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(194): Show |
1 | a0001c0002t0002g0137 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(205): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(228): Show |
1 | a0001c0002t0002g0140 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(239): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(194): Show |
1 | a0001c0002t0002g0145 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(205): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(199): Show |
1 | a0001c0002t0002g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(210): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(204): Show |
1 | a0001c0002t0002g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(215): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(174): Show |
2 | a0001c0001t0013g0058 a0001c0002t0001g0144 |
2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(185): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(269): Show |
1 | a0001c0002t0002g0147 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(280): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(229): Show |
1 | a0001c0001t0002g0105 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(240): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(225): Show |
1 | a0001c0005t0002g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(236): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(189): Show |
1 | a0001c0002t0002g0151 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(200): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(204): Show |
1 | a0001c0002t0002g0146 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(215): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(240): Show |
1 | a0001c0002t0002g0136 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(251): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(219): Show |
1 | a0001c0002t0002g0152 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(230): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(79): Show |
1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(90): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(119): Show |
3 | a0001c0001t0005g0028 a0001c0001t0007g0168 a0001c0001t0009g0026 |
3 | HG01106.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(130): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(124): Show |
1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(135): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(134): Show |
2 | a0001c0001t0005g0020 a0001c0001t0014g0171 |
2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(145): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(139): Show |
3 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0169 |
3 | HG01884.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(150): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(144): Show |
1 | a0001c0001t0003g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(155): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(149): Show |
5 | a0001c0001t0003g0177 a0001c0001t0007g0170 a0001c0001t0008g0014 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(160): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(169): Show |
1 | a0001c0001t0002g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(180): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(154): Show |
4 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0005g0018 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(165): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(159): Show |
1 | a0002c0003t0002g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(170): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(159): Show |
3 | a0001c0001t0003g0007 a0001c0001t0005g0016 a0001c0001t0006g0023 |
3 | HG02886.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(170): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(248): Show |
1 | a0001c0001t0001g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(259): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(164): Show |
2 | a0001c0001t0001g0175 a0001c0001t0003g0009 |
2 | HG02451.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(175): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(169): Show |
1 | a0002c0003t0002g0165 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(180): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(169): Show |
4 | a0001c0001t0001g0122 a0001c0001t0005g0027 a0001c0001t0006g0022 others(1): Show |
4 | HG01243.hp1 HG02486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(180): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(174): Show |
3 | a0001c0001t0001g0124 a0001c0001t0003g0008 a0001c0002t0001g0172 |
3 | HG01891.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(185): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(179): Show |
1 | a0001c0002t0001g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(190): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(184): Show |
1 | a0002c0003t0002g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(195): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(183): Show |
1 | a0001c0001t0001g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(194): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(184): Show |
3 | a0001c0001t0001g0176 a0001c0001t0003g0012 a0001c0002t0001g0157 |
3 | HG02717.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(195): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(189): Show |
2 | a0001c0001t0001g0004 a0001c0001t0008g0134 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(200): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(199): Show |
1 | a0002c0003t0002g0159 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(210): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(199): Show |
3 | a0001c0002t0006g0179 a0001c0002t0006g0180 a0001c0002t0009g0173 |
3 | HG02647.hp1 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(210): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(204): Show |
1 | a0001c0001t0001g0003 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(215): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(209): Show |
1 | a0001c0001t0003g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(220): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(219): Show |
2 | a0002c0003t0002g0163 a0002c0004t0002g0131 |
2 | HG01168.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(230): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(229): Show |
1 | a0001c0001t0012g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(240): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(224): Show |
1 | a0001c0001t0005g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(235): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(234): Show |
1 | a0001c0001t0002g0060 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(245): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(239): Show |
1 | a0001c0001t0005g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(250): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(259): Show |
1 | a0001c0002t0002g0153 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(270): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(236): Show |
1 | a0002c0003t0002g0160 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(247): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(194): Show |
1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(205): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | CTTTCCTT others(187): Show |
1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(198): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910838 | C | T | 1 | a0001c0002t0001g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074-5164C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | |||||||
| chrX:107910845 | CT | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0119 |
2 | HG01952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1074-5154delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910845 | ||||||
| chrX:107910855 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1074-5147C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910855 | |||||||
| chrX:107910971 | A | T | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1074-5031A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910971 | |||||||
| chrX:107910997 | G | C | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-5005G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910997 | |||||||
| chrX:107911113 | CA | C | 2 | a0001c0001t0001g0106 a0001c0001t0002g0038 |
2 | HG00558.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1074-4886delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911113 | ||||||
| chrX:107911117 | G | A | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1074-4885G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911117 | |||||||
| chrX:107911130 | AG | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0115 |
2 | NA19091.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1074-4870delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911130 | ||||||
| chrX:107911267 | C | T | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-4735C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911267 | |||||||
| chrX:107911269 | T | C | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-4733T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911269 | |||||||
| chrX:107911270 | C | T | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-4732C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911270 | |||||||
| chrX:107911304 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1074-4698T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911304 | |||||||
| chrX:107911396 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1074-4606T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911396 | |||||||
| chrX:107911488 | C | CT | 3 | a0001c0001t0001g0074 a0001c0001t0001g0100 a0001c0001t0004g0081 |
3 | NA18994.hp1 NA19060.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1074-4508dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911488 | ||||||
| chrX:107911555 | AT | A | 3 | a0001c0001t0001g0087 a0001c0001t0002g0038 a0001c0002t0002g0136 |
3 | HG01261.hp1 NA18522.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1074-4442delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911555 | ||||||
| chrX:107911574 | TA | T | 2 | a0001c0001t0001g0032 a0001c0002t0002g0141 |
2 | NA19079.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1074-4425delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911574 | ||||||
| chrX:107911697 | TG | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0181 |
2 | HG02630.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1074-4303delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911697 | ||||||
| chrX:107911782 | TG | T | 2 | a0001c0001t0001g0073 a0002c0003t0002g0164 |
2 | HG04204.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1074-4218delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911782 | ||||||
| chrX:107911928 | A | G | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-4074A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911928 | |||||||
| chrX:107912379 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1074-3623A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107912379 | |||||||
| chrX:107912871 | A | G | 2 | a0001c0002t0006g0179 a0001c0002t0006g0180 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1074-3131A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107912871 | |||||||
| chrX:107913015 | C | T | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1074-2987C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913015 | |||||||
| chrX:107913034 | T | A | 1 | a0001c0001t0001g0032 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2968T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913034 | |||||||
| chrX:107913064 | A | G | 1 | a0001c0001t0004g0029 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1074-2938A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913064 | |||||||
| chrX:107913368 | C | A | 1 | a0001c0001t0001g0032 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2634C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913368 | |||||||
| chrX:107913549 | G | T | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-2453G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913549 | |||||||
| chrX:107913590 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 |
3 | HG02622.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1074-2412C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913590 | |||||||
| chrX:107913850 | C | T | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-2152C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913850 | |||||||
| chrX:107913926 | C | T | 7 | a0001c0001t0001g0078 a0001c0001t0001g0086 a0001c0001t0001g0096 others(4): Show |
7 | HG00642.hp1 HG02027.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074-2076C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913926 | |||||||
| chrX:107914019 | G | A | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-1983G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914019 | |||||||
| chrX:107914150 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074-1852T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914150 | |||||||
| chrX:107914182 | G | A | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-1820G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914182 | |||||||
| chrX:107914205 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1074-1797T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914205 | |||||||
| chrX:107914286 | T | C | 1 | a0001c0001t0012g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1074-1716T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914286 | |||||||
| chrX:107914551 | T | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-1451T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914551 | |||||||
| chrX:107914603 | C | T | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-1399C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914603 | |||||||
| chrX:107914824 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1074-1178A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914824 | |||||||
| chrX:107915113 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1074-889A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107915113 | |||||||
| chrX:107915428 | GC | G | 10 | a0001c0001t0001g0166 a0001c0001t0005g0016 a0001c0001t0005g0017 others(7): Show |
10 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074-572delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107915428 | ||||||
| chrX:107915557 | C | CA | 8 | a0001c0001t0001g0032 a0001c0001t0001g0067 a0001c0001t0001g0104 others(5): Show |
8 | HG01192.hp1 HG02738.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1074-432dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107915557 | ||||||
| chrX:107915673 | C | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-329C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107915673 | |||||||
| chrX:107915710 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1074-292G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107915710 | |||||||
| chrX:107915776 | T | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 |
3 | HG02622.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1074-226T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107915776 | |||||||
| chrX:107916196 | T | C | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1201+67T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107916196 | |||||||
| chrX:107916457 | A | G | 1 | a0001c0001t0010g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1201+328A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107916457 | |||||||
| chrX:107916869 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202-637A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107916869 | |||||||
| chrX:107917139 | C | CTA | 6 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 others(3): Show |
6 | HG02258.hp1 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202-354_1202-353d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107917139 | ||||||
| chrX:107917139 | C | CTATA | 4 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(1): Show |
4 | HG01106.hp1 HG01884.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202-356_1202-353d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107917139 | ||||||
| chrX:107917352 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1202-154T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107917352 | |||||||
| chrX:107917423 | G | C | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1202-83G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107917423 | |||||||
| chrX:107917428 | C | T | 1 | a0001c0002t0002g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1202-78C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107917428 | |||||||
| chrX:107917429 | G | A | 1 | a0002c0003t0002g0160 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1202-77G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107917429 | |||||||
| chrX:107918113 | C | T | 9 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1435+374C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107918113 | |||||||
| chrX:107918269 | A | G | 26 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0048 others(23): Show |
26 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1435+530A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107918269 | |||||||
| chrX:107918293 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1435+554T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107918293 | |||||||
| chrX:107918370 | A | G | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435+631A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107918370 | |||||||
| chrX:107919254 | G | T | 1 | a0001c0002t0002g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1435+1515G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107919254 | |||||||
| chrX:107919862 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1435+2123T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107919862 | |||||||
| chrX:107920537 | A | G | 1 | a0001c0002t0002g0137 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1435+2798A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107920537 | |||||||
| chrX:107920708 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1435+2969A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107920708 | |||||||
| chrX:107920991 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1435+3252G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107920991 | |||||||
| chrX:107921624 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1436-2719C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107921624 | |||||||
| chrX:107921859 | C | G | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1436-2484C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107921859 | |||||||
| chrX:107922074 | A | G | 2 | a0001c0001t0008g0014 a0001c0001t0008g0015 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1436-2269A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107922074 | |||||||
| chrX:107922259 | A | G | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1436-2084A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107922259 | |||||||
| chrX:107922995 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1436-1348G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107922995 | |||||||
| chrX:107923052 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1436-1291A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923052 | |||||||
| chrX:107923054 | A | G | 5 | a0001c0001t0007g0139 a0001c0001t0007g0167 a0001c0001t0007g0168 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1436-1289A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923054 | |||||||
| chrX:107923071 | C | T | 1 | a0001c0002t0002g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1436-1272C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923071 | |||||||
| chrX:107923136 | A | G | 1 | a0001c0002t0002g0142 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1436-1207A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923136 | |||||||
| chrX:107923611 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1436-732A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923611 | |||||||
| chrX:107923760 | T | G | 3 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0134 |
3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1436-583T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923760 | |||||||
| chrX:107924583 | A | G | 9 | a0001c0001t0005g0016 a0001c0001t0005g0017 a0001c0001t0005g0018 others(6): Show |
9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597+79A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107924583 | |||||||
| chrX:107924611 | G | C | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1597+107G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107924611 | |||||||
| chrX:107924695 | T | C | 2 | a0001c0002t0002g0151 a0001c0002t0002g0152 |
2 | NA18960.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1597+191T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107924695 | |||||||
| chrX:107924729 | G | A | 11 | a0001c0001t0002g0178 a0001c0001t0012g0174 a0002c0003t0002g0138 others(8): Show |
11 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1597+225G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107924729 | |||||||
| chrX:107925069 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1597+565C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107925069 | |||||||
| chrX:107925229 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1597+725C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107925229 | |||||||
| chrX:107925870 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1598-224A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107925870 | |||||||
| chrX:107926636 | A | C | 5 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0156 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1806-35A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 9/9 | chrX | 107926636 |