Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4478 |
| ensemblid | ENSG00000147065.18 |
| hgncid | 7373 |
| symbol | MSN |
| name | moesin |
| refseq_nuc | NM_002444.3 |
| refseq_prot | NP_002435.1 |
| ensembl_nuc | ENST00000360270.7 |
| ensembl_prot | ENSP00000353408.5 |
| mane_status | MANE Select |
| chr | chrX |
| start | 65667654 |
| end | 65741931 |
| strand | + |
| ver | v1.2 |
| region | chrX:65667654-65741931 |
| region5000 | chrX:65662654-65746931 |
| regionname0 | MSN_chrX_65667654_65741931 |
| regionname5000 | MSN_chrX_65662654_65746931 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1731 | 170 | 52 | 26 | 67 | 7 | 16 | MSN_chrX_65662654_65746931 | MSN | ATGCC others(1726): Show |
chrX | 65662654 | 65746931 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3960 | 112 | 3 | 19 | 67 | 7 | 14 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0002 | 0/0 | 3960 | 36 | 33 | 2 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0003 | 0/0 | 3960 | 5 | 5 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0004 | 0/0 | 3960 | 4 | 3 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0005 | 0/0 | 3960 | 3 | 3 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0006 | 0/0 | 3960 | 2 | 0 | 2 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0007 | 0/0 | 3960 | 2 | 2 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0008 | 0/0 | 3960 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0009 | 0/0 | 3960 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0010 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0011 | 0/0 | 3960 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0012 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| a0001c0001t0013 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | GGCTC others(3955): Show |
chrX | 65662654 | 65746931 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0008g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0009g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0011g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0013g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01074 | hp1 | a0001 | c0001 | t0009 | g0102 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01081 | hp2 | a0001 | c0001 | t0011 | g0044 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0031 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0041 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0093 | SAS | STU | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | YRI | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | YRI | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | LWK | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0124 | AFR | LWK | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | ASW | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ASW | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | TSI | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | GIH | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0016 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | USA | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0149 | REF | REF | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0061 | REF | REF | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| 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:65667676 | G | A | 1 | a0001c0001t0008 | 1 | HG04199.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-166G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/13 | chrX | 65667676 | |||||||
| chrX:65740396 | C | T | 3 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0013 |
10 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*503C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 503 | chrX | 65740396 | ||||||
| chrX:65740569 | C | G | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(7): Show |
56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*676C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 676 | chrX | 65740569 | ||||||
| chrX:65740647 | G | A | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(7): Show |
56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*754G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 754 | chrX | 65740647 | ||||||
| chrX:65740785 | A | G | 1 | a0001c0001t0013 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*892A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 892 | chrX | 65740785 | ||||||
| chrX:65740939 | A | G | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(6): Show |
54 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1046A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1046 | chrX | 65740939 | ||||||
| chrX:65740969 | G | A | 1 | a0001c0001t0009 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1076G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1076 | chrX | 65740969 | ||||||
| chrX:65741027 | A | G | 1 | a0001c0001t0005 | 3 | HG02630.hp2 HG02896.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1134A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1134 | chrX | 65741027 | ||||||
| chrX:65741386 | A | C | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(7): Show |
56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1493A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1493 | chrX | 65741386 | ||||||
| chrX:65741557 | C | T | 2 | a0001c0001t0004 a0001c0001t0013 |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1664C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1664 | chrX | 65741557 | ||||||
| chrX:65741574 | C | G | 1 | a0001c0001t0012 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1681C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1681 | chrX | 65741574 | ||||||
| chrX:65741648 | C | G | 1 | a0001c0001t0007 | 2 | HG02258.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1755C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1755 | chrX | 65741648 | ||||||
| chrX:65741700 | C | T | 1 | a0001c0001t0011 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1807C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1807 | chrX | 65741700 | ||||||
| chrX:65741740 | G | A | 1 | a0001c0001t0007 | 2 | HG02258.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1847G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1847 | chrX | 65741740 | ||||||
| chrX:65741795 | G | A | 1 | a0001c0001t0010 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1902G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1902 | chrX | 65741795 |
| 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:65667935 | C | A | 1 | a0001c0001t0003g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.12+82C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65667935 | |||||||
| chrX:65667998 | G | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG00140.hp1 HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.12+145G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65667998 | |||||||
| chrX:65668190 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.12+337T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65668190 | |||||||
| chrX:65668595 | T | C | 41 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(38): Show |
46 | HG00738.hp1 HG01081.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.12+742T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65668595 | |||||||
| chrX:65668695 | G | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+842G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65668695 | |||||||
| chrX:65669173 | C | A | 1 | a0001c0001t0002g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.12+1320C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65669173 | |||||||
| chrX:65669667 | A | AGAGGGCT others(5): Show |
1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+1815_12+1826dup others(12): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65669667 | ||||||
| chrX:65669832 | A | C | 1 | a0001c0001t0002g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.12+1979A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65669832 | |||||||
| chrX:65669855 | T | A | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+2002T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65669855 | |||||||
| chrX:65670314 | G | A | 5 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+2461G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670314 | |||||||
| chrX:65670426 | A | G | 2 | a0001c0001t0002g0045 a0001c0001t0011g0044 |
2 | HG01081.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.12+2573A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670426 | |||||||
| chrX:65670443 | A | G | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+2590A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670443 | |||||||
| chrX:65670451 | G | T | 1 | a0001c0001t0002g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.12+2598G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670451 | |||||||
| chrX:65670896 | T | TTA | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG02071.hp1 HG02976.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+3101_12+3102dup others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | T | TTATATA | 2 | a0001c0001t0001g0052 a0001c0001t0002g0017 |
2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.12+3097_12+3102dup others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0051 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.12+3091_12+3102dup others(12): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTA | T | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG01943.hp1 HG01952.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+3101_12+3102del others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATA | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0068 a0001c0001t0001g0069 others(25): Show |
29 | HG00642.hp1 HG01099.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.12+3099_12+3102del others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATA | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0092 a0001c0001t0001g0094 others(20): Show |
25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+3097_12+3102del others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(1): Show |
T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0109 a0001c0001t0001g0110 others(18): Show |
22 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.12+3095_12+3102del others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(3): Show |
T | 20 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(17): Show |
20 | HG00140.hp1 HG01358.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.12+3093_12+3102del others(10): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(5): Show |
T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0140 a0001c0001t0001g0141 others(12): Show |
15 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.12+3091_12+3102del others(12): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(7): Show |
T | 10 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0002g0001 others(7): Show |
14 | HG02280.hp1 HG02630.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.12+3089_12+3102del others(14): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(9): Show |
T | 1 | a0001c0001t0001g0148 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.12+3087_12+3102del others(16): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(11): Show |
T | 1 | a0001c0001t0001g0150 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.12+3085_12+3102del others(18): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(13): Show |
T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0038 |
3 | HG01169.hp2 HG02109.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.12+3083_12+3102del others(20): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(15): Show |
T | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0007g0039 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+3081_12+3102del others(22): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(17): Show |
T | 2 | a0001c0001t0001g0155 a0001c0001t0010g0041 |
2 | HG02630.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.12+3079_12+3102del others(24): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(19): Show |
T | 1 | a0001c0001t0002g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.12+3077_12+3102del others(26): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(21): Show |
T | 1 | a0001c0001t0002g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.12+3075_12+3102del others(28): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(25): Show |
T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.12+3071_12+3102del others(32): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670896 | TTATATAT others(33): Show |
T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0013 |
2 | HG00738.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.12+3063_12+3102del others(40): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | ||||||
| chrX:65670898 | A | T | 1 | a0001c0001t0002g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.12+3045A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670898 | |||||||
| chrX:65670944 | ATATATAT others(4): Show |
A | 3 | a0001c0001t0001g0125 a0001c0001t0002g0045 a0001c0001t0013g0124 |
3 | HG02647.hp1 NA18966.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.12+3093_12+3103del others(11): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670944 | ||||||
| chrX:65670946 | ATATATAT others(2): Show |
A | 2 | a0001c0001t0001g0060 a0001c0001t0002g0018 |
2 | HG01192.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.12+3095_12+3103del others(9): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670946 | ||||||
| chrX:65670954 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.12+3101A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670954 | |||||||
| chrX:65671009 | A | T | 1 | a0001c0001t0002g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.12+3156A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65671009 | |||||||
| chrX:65671092 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.12+3239C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65671092 | |||||||
| chrX:65671308 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.12+3455C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65671308 | |||||||
| chrX:65671691 | G | A | 1 | a0001c0001t0013g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.12+3838G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65671691 | |||||||
| chrX:65671967 | C | G | 2 | a0001c0001t0006g0031 a0001c0001t0006g0032 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.12+4114C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65671967 | |||||||
| chrX:65672221 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0138 |
2 | HG02135.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.12+4368C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65672221 | |||||||
| chrX:65672545 | A | G | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.12+4692A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65672545 | |||||||
| chrX:65672876 | C | T | 1 | a0001c0001t0002g0011 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.12+5023C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65672876 | |||||||
| chrX:65672944 | T | G | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+5091T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65672944 | |||||||
| chrX:65673459 | C | CT | 9 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0009 others(6): Show |
10 | HG00738.hp1 HG02572.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.12+5621dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65673459 | ||||||
| chrX:65673547 | C | T | 2 | a0001c0001t0002g0042 a0001c0001t0010g0041 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.12+5694C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65673547 | |||||||
| chrX:65673604 | G | A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+5751G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65673604 | |||||||
| chrX:65673864 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.12+6011A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65673864 | |||||||
| chrX:65674094 | A | C | 1 | a0001c0001t0004g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.12+6241A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674094 | |||||||
| chrX:65674266 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.12+6413C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674266 | |||||||
| chrX:65674274 | T | G | 1 | a0001c0001t0002g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.12+6421T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674274 | |||||||
| chrX:65674576 | T | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+6723T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674576 | |||||||
| chrX:65674591 | T | C | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+6738T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674591 | |||||||
| chrX:65674685 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.12+6832T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674685 | |||||||
| chrX:65675335 | T | A | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+7482T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65675335 | |||||||
| chrX:65675498 | A | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+7645A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65675498 | |||||||
| chrX:65675786 | C | T | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+7933C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65675786 | |||||||
| chrX:65675929 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+8076C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65675929 | |||||||
| chrX:65676208 | G | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+8355G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676208 | |||||||
| chrX:65676300 | G | A | 1 | a0001c0001t0007g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.12+8447G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676300 | |||||||
| chrX:65676301 | A | C | 3 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 |
3 | HG02109.hp2 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.12+8448A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676301 | |||||||
| chrX:65676637 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12+8784G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676637 | |||||||
| chrX:65676974 | G | A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+9121G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676974 | |||||||
| chrX:65676985 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+9132C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676985 | |||||||
| chrX:65677033 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.12+9180G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677033 | |||||||
| chrX:65677062 | G | A | 49 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(46): Show |
54 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.12+9209G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677062 | |||||||
| chrX:65677108 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0068 |
4 | NA18971.hp1 NA18986.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+9255G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677108 | |||||||
| chrX:65677349 | T | C | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+9496T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677349 | |||||||
| chrX:65677506 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+9653C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677506 | |||||||
| chrX:65677563 | G | C | 1 | a0001c0001t0011g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.12+9710G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677563 | |||||||
| chrX:65677626 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0002g0011 |
2 | HG01099.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.12+9773C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677626 | |||||||
| chrX:65678213 | C | CCTT | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+10361_12+10363d others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65678213 | ||||||
| chrX:65678217 | T | C | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+10364T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65678217 | |||||||
| chrX:65678220 | T | G | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+10367T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65678220 | |||||||
| chrX:65678222 | C | G | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+10369C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65678222 | |||||||
| chrX:65678295 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.12+10442G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65678295 | |||||||
| chrX:65678347 | T | C | 1 | a0001c0001t0002g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.12+10494T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65678347 | |||||||
| chrX:65679102 | T | C | 51 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(48): Show |
56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.12+11249T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65679102 | |||||||
| chrX:65679280 | G | C | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+11427G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65679280 | |||||||
| chrX:65679767 | T | A | 30 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(27): Show |
35 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.12+11914T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65679767 | |||||||
| chrX:65679869 | G | A | 1 | a0001c0001t0003g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.12+12016G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65679869 | |||||||
| chrX:65680588 | T | C | 30 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(27): Show |
35 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.12+12735T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65680588 | |||||||
| chrX:65680747 | T | C | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.12+12894T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65680747 | |||||||
| chrX:65681729 | A | G | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+13876A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65681729 | |||||||
| chrX:65681734 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.12+13881C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65681734 | |||||||
| chrX:65681943 | T | G | 1 | a0001c0001t0008g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.12+14090T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65681943 | |||||||
| chrX:65681957 | A | G | 8 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(5): Show |
9 | HG00738.hp1 HG02572.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+14104A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65681957 | |||||||
| chrX:65682170 | G | T | 1 | a0001c0001t0002g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.12+14317G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65682170 | |||||||
| chrX:65682237 | T | C | 51 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(48): Show |
56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.12+14384T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65682237 | |||||||
| chrX:65682823 | A | G | 1 | a0001c0001t0013g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.12+14970A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65682823 | |||||||
| chrX:65682898 | C | T | 5 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+15045C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65682898 | |||||||
| chrX:65683023 | G | A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+15170G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683023 | |||||||
| chrX:65683383 | T | TGCC | 16 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(13): Show |
17 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.12+15540_12+15542d others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683383 | ||||||
| chrX:65683393 | G | GCCA | 13 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0054 others(10): Show |
14 | HG00609.hp1 HG01069.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.12+15588_12+15590d others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | ||||||
| chrX:65683393 | G | GCCACCAC others(5): Show |
5 | a0001c0001t0001g0058 a0001c0001t0001g0071 a0001c0001t0001g0109 others(2): Show |
5 | NA18960.hp1 NA18974.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+15579_12+15590d others(14): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | ||||||
| chrX:65683393 | G | GCCACCAC others(8): Show |
3 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG02027.hp1 NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.12+15576_12+15590d others(17): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | ||||||
| chrX:65683393 | G | GCCGCCA | 3 | a0001c0001t0002g0011 a0001c0001t0002g0013 a0001c0001t0002g0025 |
3 | HG00738.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.12+15542_12+15543i others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | ||||||
| chrX:65683393 | GCCA | G | 15 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0018 others(12): Show |
19 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.12+15588_12+15590d others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | ||||||
| chrX:65683393 | GCCACCAC others(8): Show |
G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0062 a0001c0001t0001g0089 others(4): Show |
8 | HG00621.hp1 HG02083.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+15576_12+15590d others(17): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | ||||||
| chrX:65683396 | A | G | 18 | a0001c0001t0001g0052 a0001c0001t0002g0015 a0001c0001t0002g0019 others(15): Show |
18 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.12+15543A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683396 | |||||||
| chrX:65683399 | A | G | 17 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(14): Show |
21 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.12+15546A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683399 | |||||||
| chrX:65683442 | C | CCACCACC others(10): Show |
1 | a0001c0001t0001g0148 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.12+15590_12+15591i others(19): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683442 | ||||||
| chrX:65683552 | T | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0095 |
2 | HG02040.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.12+15699T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683552 | |||||||
| chrX:65683703 | A | G | 10 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(7): Show |
10 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.12+15850A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683703 | |||||||
| chrX:65683941 | TC | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
5 | HG00642.hp1 HG00735.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+16089delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683941 | |||||||
| chrX:65683942 | C | CT | 9 | a0001c0001t0001g0054 a0001c0001t0001g0080 a0001c0001t0002g0015 others(6): Show |
9 | HG00735.hp2 HG02300.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+16105dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683942 | ||||||
| chrX:65683942 | CT | C | 11 | a0001c0001t0001g0158 a0001c0001t0002g0009 a0001c0001t0002g0010 others(8): Show |
11 | HG00738.hp1 HG01081.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.12+16105delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683942 | ||||||
| chrX:65684057 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0023 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.12+16204C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684057 | |||||||
| chrX:65684065 | C | T | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+16212C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684065 | |||||||
| chrX:65684194 | G | T | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+16341G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684194 | |||||||
| chrX:65684322 | T | A | 5 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+16469T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684322 | |||||||
| chrX:65684502 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.12+16649G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684502 | |||||||
| chrX:65684507 | C | T | 4 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0010g0041 others(1): Show |
4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+16654C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684507 | |||||||
| chrX:65684532 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+16679G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684532 | |||||||
| chrX:65684777 | T | C | 1 | a0001c0001t0002g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.12+16924T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684777 | |||||||
| chrX:65684824 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.12+16971C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684824 | |||||||
| chrX:65684855 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+17002C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684855 | |||||||
| chrX:65684981 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.12+17128C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684981 | |||||||
| chrX:65685111 | T | A | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+17258T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685111 | |||||||
| chrX:65685530 | G | A | 4 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0010g0041 others(1): Show |
4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+17677G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685530 | |||||||
| chrX:65685661 | T | A | 5 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+17808T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685661 | |||||||
| chrX:65685671 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+17818C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685671 | |||||||
| chrX:65685723 | G | A | 1 | a0001c0001t0002g0010 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.12+17870G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685723 | |||||||
| chrX:65685906 | C | A | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+18053C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685906 | |||||||
| chrX:65686189 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.12+18336T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65686189 | |||||||
| chrX:65686940 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.12+19087C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65686940 | |||||||
| chrX:65687174 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+19321G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65687174 | |||||||
| chrX:65687243 | G | A | 32 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(29): Show |
37 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.12+19390G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65687243 | |||||||
| chrX:65687548 | G | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0025 others(2): Show |
6 | HG02717.hp1 HG02886.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+19695G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65687548 | |||||||
| chrX:65687936 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+20083C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65687936 | |||||||
| chrX:65688268 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.12+20415G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65688268 | |||||||
| chrX:65688297 | C | T | 1 | a0001c0001t0010g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.12+20444C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65688297 | |||||||
| chrX:65688645 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.12+20792G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65688645 | |||||||
| chrX:65689213 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.12+21360T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65689213 | |||||||
| chrX:65689220 | C | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+21367C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65689220 | |||||||
| chrX:65689927 | A | G | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+22074A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65689927 | |||||||
| chrX:65690086 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+22233T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65690086 | |||||||
| chrX:65690390 | A | G | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+22537A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65690390 | |||||||
| chrX:65690856 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0138 |
2 | HG02135.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.12+23003G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65690856 | |||||||
| chrX:65690919 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.12+23066T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65690919 | |||||||
| chrX:65691333 | T | C | 1 | a0001c0001t0010g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.12+23480T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65691333 | |||||||
| chrX:65691405 | G | A | 4 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0010g0041 others(1): Show |
4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+23552G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65691405 | |||||||
| chrX:65691565 | T | C | 51 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(48): Show |
56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.12+23712T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65691565 | |||||||
| chrX:65691673 | T | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0059 |
2 | NA19066.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.12+23820T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65691673 | |||||||
| chrX:65691995 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0096 |
3 | NA18955.hp1 NA19085.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.12+24142G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65691995 | |||||||
| chrX:65692008 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.12+24155G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692008 | |||||||
| chrX:65692030 | C | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+24177C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692030 | |||||||
| chrX:65692202 | G | C | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+24349G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692202 | |||||||
| chrX:65692442 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(23): Show |
31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.13-24376G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692442 | |||||||
| chrX:65692613 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.13-24205T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692613 | |||||||
| chrX:65692793 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.13-24025C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692793 | |||||||
| chrX:65692794 | C | CTCACCTC others(4): Show |
1 | a0001c0001t0001g0109 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-24021_13-24020i others(13): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65692794 | ||||||
| chrX:65692823 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23995G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692823 | |||||||
| chrX:65692824 | C | G | 1 | a0001c0001t0001g0109 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23994C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692824 | |||||||
| chrX:65692825 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23993G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692825 | |||||||
| chrX:65692932 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.13-23886G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692932 | |||||||
| chrX:65693639 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.13-23179G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693639 | |||||||
| chrX:65693648 | A | G | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-23170A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693648 | |||||||
| chrX:65693792 | G | A | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-23026G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693792 | |||||||
| chrX:65693803 | C | A | 1 | a0001c0001t0001g0109 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23015C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693803 | |||||||
| chrX:65693804 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23014A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693804 | |||||||
| chrX:65693805 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23013G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693805 | |||||||
| chrX:65693880 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.13-22938C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693880 | |||||||
| chrX:65694083 | A | C | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-22735A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694083 | |||||||
| chrX:65694368 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.13-22450C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694368 | |||||||
| chrX:65694453 | C | T | 1 | a0001c0001t0004g0126 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.13-22365C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694453 | |||||||
| chrX:65694538 | G | A | 10 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0018 others(7): Show |
14 | HG01243.hp1 HG02145.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.13-22280G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694538 | |||||||
| chrX:65694588 | A | C | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.13-22230A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694588 | |||||||
| chrX:65694636 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.13-22182C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694636 | |||||||
| chrX:65694781 | A | G | 1 | a0001c0001t0011g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.13-22037A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694781 | |||||||
| chrX:65694911 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.13-21907G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694911 | |||||||
| chrX:65694914 | G | C | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.13-21904G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694914 | |||||||
| chrX:65695081 | C | CGT | 4 | a0001c0001t0001g0088 a0001c0001t0001g0107 a0001c0001t0006g0031 others(1): Show |
4 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-21709_13-21708d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695081 | ||||||
| chrX:65695081 | CGT | C | 5 | a0001c0001t0002g0010 a0001c0001t0004g0053 a0001c0001t0004g0126 others(2): Show |
5 | HG02615.hp1 HG02976.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-21709_13-21708d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695081 | ||||||
| chrX:65695081 | CGTGT | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(1): Show |
4 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-21711_13-21708d others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695081 | ||||||
| chrX:65695081 | CGTGTGT | C | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.13-21713_13-21708d others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695081 | ||||||
| chrX:65695104 | GTGT | G | 32 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(29): Show |
37 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.13-21713_13-21711d others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695104 | |||||||
| chrX:65695191 | A | G | 10 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(7): Show |
10 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.13-21627A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695191 | |||||||
| chrX:65695248 | C | G | 1 | a0001c0001t0002g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.13-21570C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695248 | |||||||
| chrX:65695266 | T | C | 2 | a0001c0001t0002g0015 a0001c0001t0012g0016 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.13-21552T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695266 | |||||||
| chrX:65695507 | C | CA | 15 | a0001c0001t0001g0059 a0001c0001t0001g0069 a0001c0001t0001g0079 others(12): Show |
15 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.13-21284dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695507 | ||||||
| chrX:65695507 | C | CAA | 8 | a0001c0001t0002g0009 a0001c0001t0003g0047 a0001c0001t0003g0048 others(5): Show |
8 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.13-21285_13-21284d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695507 | ||||||
| chrX:65695507 | CA | C | 35 | a0001c0001t0001g0054 a0001c0001t0001g0072 a0001c0001t0001g0104 others(32): Show |
40 | HG00738.hp1 HG01081.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.13-21284delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695507 | ||||||
| chrX:65695525 | A | C | 1 | a0001c0001t0002g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.13-21293A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695525 | |||||||
| chrX:65695611 | G | A | 3 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0013 |
3 | HG00738.hp1 HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.13-21207G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695611 | |||||||
| chrX:65695886 | A | AGAGTTTT others(26): Show |
38 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(35): Show |
43 | HG00738.hp1 HG01081.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.13-20930_13-20929i others(35): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695886 | ||||||
| chrX:65695933 | G | A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.13-20885G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695933 | |||||||
| chrX:65696225 | T | TCACA | 3 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0011g0044 |
3 | HG01081.hp2 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.13-20569_13-20566d others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | ||||||
| chrX:65696225 | T | TCACACA | 4 | a0001c0001t0002g0023 a0001c0001t0004g0053 a0001c0001t0004g0126 others(1): Show |
4 | HG00735.hp2 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-20571_13-20566d others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | ||||||
| chrX:65696225 | T | TCACACAC others(1): Show |
4 | a0001c0001t0002g0015 a0001c0001t0002g0046 a0001c0001t0004g0127 others(1): Show |
4 | HG02615.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-20573_13-20566d others(10): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | ||||||
| chrX:65696225 | T | TCACACAC others(3): Show |
11 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0017 others(8): Show |
12 | HG00738.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-20575_13-20566d others(12): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | ||||||
| chrX:65696225 | T | TCACACAC others(5): Show |
23 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0011 others(20): Show |
27 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.13-20577_13-20566d others(14): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | ||||||
| chrX:65696225 | T | TCACACAC others(7): Show |
1 | a0001c0001t0003g0050 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.13-20579_13-20566d others(16): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | ||||||
| chrX:65696225 | T | TCACACAC others(9): Show |
1 | a0001c0001t0002g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.13-20581_13-20566d others(18): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | ||||||
| chrX:65696225 | T | TCACACAC others(11): Show |
2 | a0001c0001t0002g0010 a0001c0001t0002g0024 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.13-20583_13-20566d others(20): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | ||||||
| chrX:65696480 | G | C | 1 | a0001c0001t0001g0005 | 2 | HG00609.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.13-20338G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65696480 | |||||||
| chrX:65696546 | C | A | 1 | a0001c0001t0013g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.13-20272C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65696546 | |||||||
| chrX:65697013 | G | C | 27 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(24): Show |
32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.13-19805G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65697013 | |||||||
| chrX:65698232 | G | A | 9 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0109 others(6): Show |
9 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.13-18586G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65698232 | |||||||
| chrX:65699052 | A | T | 26 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(23): Show |
31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.13-17766A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699052 | |||||||
| chrX:65699059 | G | T | 1 | a0001c0001t0002g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.13-17759G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699059 | |||||||
| chrX:65699315 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0004g0126 |
2 | NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.13-17503G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699315 | |||||||
| chrX:65699641 | C | T | 6 | a0001c0001t0001g0098 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | NA18970.hp1 NA18989.hp1 NA19067.hp1 others(3): Show |
intron_variant | MODIFIER | c.13-17177C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699641 | |||||||
| chrX:65699748 | C | CA | 5 | a0001c0001t0001g0051 a0001c0001t0001g0059 a0001c0001t0001g0080 others(2): Show |
5 | HG02135.hp1 HG02300.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-17048dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65699748 | ||||||
| chrX:65699748 | CA | C | 32 | a0001c0001t0001g0067 a0001c0001t0001g0138 a0001c0001t0001g0153 others(29): Show |
37 | HG01081.hp2 HG01167.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.13-17048delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65699748 | ||||||
| chrX:65699748 | CAA | C | 10 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(7): Show |
10 | HG00738.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.13-17049_13-17048d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65699748 | ||||||
| chrX:65699748 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-17060_13-17048d others(15): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65699748 | ||||||
| chrX:65699759 | A | G | 1 | a0001c0001t0002g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13-17059A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699759 | |||||||
| chrX:65699791 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-17027C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699791 | |||||||
| chrX:65699921 | T | C | 6 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(3): Show |
6 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.13-16897T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699921 | |||||||
| chrX:65700350 | G | A | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-16468G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65700350 | |||||||
| chrX:65700379 | T | C | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-16439T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65700379 | |||||||
| chrX:65700800 | C | T | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-16018C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65700800 | |||||||
| chrX:65700841 | A | G | 39 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(36): Show |
44 | HG00738.hp1 HG01081.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.13-15977A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65700841 | |||||||
| chrX:65700968 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.13-15850A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65700968 | |||||||
| chrX:65701770 | A | G | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-15048A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65701770 | |||||||
| chrX:65701995 | G | A | 4 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0010g0041 others(1): Show |
4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-14823G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65701995 | |||||||
| chrX:65702007 | C | CT | 16 | a0001c0001t0001g0062 a0001c0001t0001g0086 a0001c0001t0001g0103 others(13): Show |
16 | HG00673.hp1 HG00735.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.13-14795dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65702007 | ||||||
| chrX:65702022 | T | C | 2 | a0001c0001t0006g0031 a0001c0001t0006g0032 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.13-14796T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702022 | |||||||
| chrX:65702164 | C | T | 5 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-14654C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702164 | |||||||
| chrX:65702259 | C | T | 1 | a0001c0001t0007g0040 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.13-14559C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702259 | |||||||
| chrX:65702260 | G | A | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-14558G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702260 | |||||||
| chrX:65702499 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-14319C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702499 | |||||||
| chrX:65702659 | CTG | C | 26 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(23): Show |
31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.13-14157_13-14156d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65702659 | ||||||
| chrX:65702967 | A | G | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-13851A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702967 | |||||||
| chrX:65703023 | T | A | 5 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-13795T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703023 | |||||||
| chrX:65703327 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.13-13491A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703327 | |||||||
| chrX:65703803 | C | T | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-13015C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703803 | |||||||
| chrX:65703814 | T | C | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-13004T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703814 | |||||||
| chrX:65703815 | G | T | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-13003G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703815 | |||||||
| chrX:65703817 | T | TC | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-13001_13-13000i others(3): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703817 | |||||||
| chrX:65703904 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13-12914G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703904 | |||||||
| chrX:65704374 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.13-12444T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65704374 | |||||||
| chrX:65704433 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.13-12385G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65704433 | |||||||
| chrX:65704667 | G | GT | 27 | a0001c0001t0001g0106 a0001c0001t0002g0001 a0001c0001t0002g0002 others(24): Show |
32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.13-12141dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65704667 | ||||||
| chrX:65704771 | G | GT | 6 | a0001c0001t0001g0008 a0001c0001t0002g0046 a0001c0001t0004g0053 others(3): Show |
6 | HG01256.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.13-12031dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65704771 | ||||||
| chrX:65704855 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.13-11963C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65704855 | |||||||
| chrX:65704923 | C | A | 1 | a0001c0001t0002g0010 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13-11895C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65704923 | |||||||
| chrX:65705063 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0123 |
2 | NA18995.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.13-11755G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705063 | |||||||
| chrX:65705203 | C | G | 39 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(36): Show |
44 | HG00738.hp1 HG01081.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.13-11615C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705203 | |||||||
| chrX:65705563 | A | G | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-11255A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705563 | |||||||
| chrX:65705641 | T | G | 1 | a0001c0001t0001g0150 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.13-11177T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705641 | |||||||
| chrX:65705665 | C | T | 1 | a0001c0001t0009g0102 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.13-11153C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705665 | |||||||
| chrX:65705905 | T | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-10913T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705905 | |||||||
| chrX:65706466 | C | T | 49 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(46): Show |
54 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.13-10352C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65706466 | |||||||
| chrX:65706836 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0024 a0001c0001t0002g0027 |
3 | HG02145.hp1 HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.13-9982G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65706836 | |||||||
| chrX:65707333 | G | A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.13-9485G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65707333 | |||||||
| chrX:65707410 | A | G | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-9408A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65707410 | |||||||
| chrX:65707545 | G | C | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-9273G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65707545 | |||||||
| chrX:65708037 | A | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0120 |
2 | HG00673.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.13-8781A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708037 | |||||||
| chrX:65708075 | T | C | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-8743T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708075 | |||||||
| chrX:65708138 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13-8680G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708138 | |||||||
| chrX:65708583 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.13-8235G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708583 | |||||||
| chrX:65708705 | C | T | 1 | a0001c0001t0002g0011 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13-8113C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708705 | |||||||
| chrX:65708775 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.13-8043C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708775 | |||||||
| chrX:65708808 | G | C | 4 | a0001c0001t0002g0001 a0001c0001t0002g0029 a0001c0001t0005g0001 others(1): Show |
8 | HG01243.hp1 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.13-8010G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708808 | |||||||
| chrX:65709040 | C | T | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-7778C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65709040 | |||||||
| chrX:65709096 | G | C | 1 | a0001c0001t0002g0010 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13-7722G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65709096 | |||||||
| chrX:65709495 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.13-7323C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65709495 | |||||||
| chrX:65709843 | C | G | 1 | a0001c0001t0003g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.13-6975C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65709843 | |||||||
| chrX:65710310 | C | T | 2 | a0001c0001t0006g0031 a0001c0001t0006g0032 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.13-6508C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65710310 | |||||||
| chrX:65710420 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.13-6398T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65710420 | |||||||
| chrX:65710537 | G | T | 1 | a0001c0001t0002g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13-6281G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65710537 | |||||||
| chrX:65710883 | GTAT | G | 33 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(30): Show |
38 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(35): Show |
intron_variant | MODIFIER | c.13-5924_13-5922del others(3): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65710883 | ||||||
| chrX:65710980 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.13-5838G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65710980 | |||||||
| chrX:65711249 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.13-5569T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65711249 | |||||||
| chrX:65711697 | G | T | 1 | a0001c0001t0004g0139 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.13-5121G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65711697 | |||||||
| chrX:65711701 | C | G | 1 | a0001c0001t0002g0010 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13-5117C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65711701 | |||||||
| chrX:65711996 | A | G | 5 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-4822A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65711996 | |||||||
| chrX:65712172 | A | T | 1 | a0001c0001t0002g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.13-4646A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65712172 | |||||||
| chrX:65712416 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0120 |
2 | HG00673.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.13-4402A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65712416 | |||||||
| chrX:65712602 | C | G | 1 | a0001c0001t0002g0026 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.13-4216C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65712602 | |||||||
| chrX:65712914 | G | A | 5 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-3904G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65712914 | |||||||
| chrX:65713028 | G | A | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-3790G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65713028 | |||||||
| chrX:65713157 | C | A | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-3661C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65713157 | |||||||
| chrX:65713918 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0116 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.13-2900T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65713918 | |||||||
| chrX:65713977 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.13-2841G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65713977 | |||||||
| chrX:65713989 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.13-2829A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65713989 | |||||||
| chrX:65714208 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.13-2610A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714208 | |||||||
| chrX:65714279 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-2539C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714279 | |||||||
| chrX:65714391 | A | T | 10 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(7): Show |
10 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.13-2427A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714391 | |||||||
| chrX:65714458 | T | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0091 a0001c0001t0001g0119 |
3 | NA18943.hp1 NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.13-2360T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714458 | |||||||
| chrX:65714720 | T | A | 1 | a0001c0001t0002g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.13-2098T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714720 | |||||||
| chrX:65714859 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.13-1959C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714859 | |||||||
| chrX:65714908 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.13-1910C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714908 | |||||||
| chrX:65714926 | G | T | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-1892G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714926 | |||||||
| chrX:65714949 | A | G | 1 | a0001c0001t0002g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.13-1869A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714949 | |||||||
| chrX:65714979 | A | ATAGAGTT others(967): Show |
1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-1825_13-1824ins others(974): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65714979 | ||||||
| chrX:65715281 | T | TAGGATTG others(6): Show |
1 | a0001c0001t0002g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.13-1536_13-1524dup others(13): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65715281 | ||||||
| chrX:65715717 | G | A | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-1101G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65715717 | |||||||
| chrX:65716178 | C | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0141 |
2 | NA18962.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.13-640C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65716178 | |||||||
| chrX:65716287 | T | G | 5 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-531T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65716287 | |||||||
| chrX:65716437 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.13-381G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65716437 | |||||||
| chrX:65716572 | G | A | 1 | a0001c0001t0002g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.13-246G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65716572 | |||||||
| chrX:65716604 | T | C | 2 | a0001c0001t0002g0018 a0001c0001t0002g0027 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.13-214T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65716604 | |||||||
| chrX:65717108 | A | C | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+207A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717108 | |||||||
| chrX:65717108 | A | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.96+207A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717108 | |||||||
| chrX:65717289 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0142 |
2 | HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.96+388G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717289 | |||||||
| chrX:65717431 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.96+530C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717431 | |||||||
| chrX:65717435 | A | G | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+534A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717435 | |||||||
| chrX:65717746 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.96+845G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717746 | |||||||
| chrX:65717909 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(23): Show |
31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.96+1008G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717909 | |||||||
| chrX:65718148 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.96+1247A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718148 | |||||||
| chrX:65718175 | T | C | 27 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(24): Show |
32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.96+1274T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718175 | |||||||
| chrX:65718277 | G | C | 51 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(48): Show |
56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.96+1376G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718277 | |||||||
| chrX:65718470 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.96+1569A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718470 | |||||||
| chrX:65718583 | T | G | 1 | a0001c0001t0002g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.96+1682T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718583 | |||||||
| chrX:65718728 | G | A | 1 | a0001c0001t0002g0021 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.96+1827G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718728 | |||||||
| chrX:65718818 | T | TAAAAAAA others(1): Show |
22 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(19): Show |
27 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.96+1927_96+1934dup others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65718818 | ||||||
| chrX:65718818 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+1925_96+1934dup others(10): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65718818 | ||||||
| chrX:65718818 | TA | T | 7 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0136 others(4): Show |
7 | HG02015.hp1 HG02074.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+1934delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65718818 | ||||||
| chrX:65719414 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.96+2513G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65719414 | |||||||
| chrX:65719535 | T | A | 5 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+2634T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65719535 | |||||||
| chrX:65719924 | T | C | 4 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0010g0041 others(1): Show |
4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+3023T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65719924 | |||||||
| chrX:65720427 | G | A | 4 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0010g0041 others(1): Show |
4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+3526G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65720427 | |||||||
| chrX:65720456 | G | A | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+3555G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65720456 | |||||||
| chrX:65720588 | G | A | 1 | a0001c0001t0003g0049 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.96+3687G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65720588 | |||||||
| chrX:65721034 | A | G | 1 | a0001c0001t0001g0003 | 2 | NA18994.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.96+4133A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65721034 | |||||||
| chrX:65721188 | A | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(48): Show |
56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.96+4287A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65721188 | |||||||
| chrX:65721233 | A | G | 1 | a0001c0001t0002g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.96+4332A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65721233 | |||||||
| chrX:65721312 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.96+4411C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65721312 | |||||||
| chrX:65721519 | C | CT | 27 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(24): Show |
32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.96+4620dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65721519 | ||||||
| chrX:65721772 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.96+4871C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65721772 | |||||||
| chrX:65722401 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0072 |
2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.97-5413G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722401 | |||||||
| chrX:65722404 | C | CGT | 9 | a0001c0001t0001g0058 a0001c0001t0001g0082 a0001c0001t0001g0108 others(6): Show |
9 | HG00738.hp1 HG02135.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-5373_97-5372dup others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | ||||||
| chrX:65722404 | C | CGTGT | 14 | a0001c0001t0002g0010 a0001c0001t0002g0027 a0001c0001t0002g0028 others(11): Show |
14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.97-5375_97-5372dup others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | ||||||
| chrX:65722404 | C | CGTGTGT | 7 | a0001c0001t0002g0012 a0001c0001t0002g0023 a0001c0001t0002g0030 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-5377_97-5372dup others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | ||||||
| chrX:65722404 | C | CGTGTGTG others(1): Show |
15 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(12): Show |
20 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-5379_97-5372dup others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | ||||||
| chrX:65722404 | C | CGTGTGTG others(3): Show |
5 | a0001c0001t0002g0019 a0001c0001t0002g0037 a0001c0001t0002g0038 others(2): Show |
5 | HG00735.hp2 HG02109.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-5381_97-5372dup others(10): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | ||||||
| chrX:65722404 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0002g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97-5383_97-5372dup others(12): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | ||||||
| chrX:65722404 | CGT | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0094 a0001c0001t0001g0110 others(11): Show |
14 | HG00140.hp1 HG00323.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.97-5373_97-5372del others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | ||||||
| chrX:65722404 | CGTGTGT | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0002g0015 |
3 | HG02809.hp1 NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.97-5377_97-5372del others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | ||||||
| chrX:65722463 | C | T | 2 | a0001c0001t0006g0031 a0001c0001t0006g0032 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.97-5351C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722463 | |||||||
| chrX:65722509 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0136 |
3 | HG02015.hp1 HG02074.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.97-5305G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722509 | |||||||
| chrX:65722666 | C | T | 26 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(23): Show |
31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.97-5148C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722666 | |||||||
| chrX:65722695 | C | T | 27 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(24): Show |
32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.97-5119C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722695 | |||||||
| chrX:65722857 | T | C | 27 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(24): Show |
32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.97-4957T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722857 | |||||||
| chrX:65723082 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.97-4732C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723082 | |||||||
| chrX:65723164 | T | C | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-4650T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723164 | |||||||
| chrX:65723208 | T | C | 25 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(22): Show |
30 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.97-4606T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723208 | |||||||
| chrX:65723272 | A | G | 3 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0117 |
3 | HG02602.hp1 HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.97-4542A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723272 | |||||||
| chrX:65723384 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0013 |
2 | HG00738.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.97-4430C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723384 | |||||||
| chrX:65723718 | A | G | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97-4096A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723718 | |||||||
| chrX:65723817 | C | G | 27 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(24): Show |
32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.97-3997C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723817 | |||||||
| chrX:65723900 | G | A | 1 | a0001c0001t0010g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97-3914G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723900 | |||||||
| chrX:65724122 | C | T | 4 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0010g0041 others(1): Show |
4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-3692C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724122 | |||||||
| chrX:65724206 | G | A | 1 | a0001c0001t0002g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.97-3608G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724206 | |||||||
| chrX:65724307 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97-3507G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724307 | |||||||
| chrX:65724391 | G | A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.97-3423G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724391 | |||||||
| chrX:65724677 | T | TTTTG | 44 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(41): Show |
49 | HG00735.hp2 HG00738.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.97-3113_97-3110dup others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65724677 | ||||||
| chrX:65724677 | TTTTG | T | 3 | a0001c0001t0001g0052 a0001c0001t0002g0045 a0001c0001t0011g0044 |
3 | HG01081.hp2 HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.97-3113_97-3110del others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65724677 | ||||||
| chrX:65724721 | C | T | 1 | a0001c0001t0008g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.97-3093C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724721 | |||||||
| chrX:65724777 | C | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.97-3037C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724777 | |||||||
| chrX:65724780 | A | G | 27 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(24): Show |
32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.97-3034A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724780 | |||||||
| chrX:65724847 | C | T | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-2967C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724847 | |||||||
| chrX:65724978 | C | T | 1 | a0001c0001t0011g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.97-2836C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724978 | |||||||
| chrX:65725244 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.97-2570C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65725244 | |||||||
| chrX:65725647 | A | C | 1 | a0001c0001t0010g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97-2167A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65725647 | |||||||
| chrX:65725784 | C | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0142 |
2 | HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.97-2030C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65725784 | |||||||
| chrX:65726122 | A | G | 3 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0117 |
3 | HG02602.hp1 HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.97-1692A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65726122 | |||||||
| chrX:65726469 | T | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0064 others(15): Show |
19 | HG01069.hp1 HG01256.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.97-1345T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65726469 | |||||||
| chrX:65726569 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.97-1245T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65726569 | |||||||
| chrX:65727365 | G | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-449G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65727365 | |||||||
| chrX:65727709 | C | A | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-105C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65727709 | |||||||
| chrX:65727758 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.97-56C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65727758 | |||||||
| chrX:65727978 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.192+69T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65727978 | |||||||
| chrX:65728127 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0109 others(1): Show |
4 | NA18960.hp1 NA19000.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+218G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65728127 | |||||||
| chrX:65728336 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.192+427C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65728336 | |||||||
| chrX:65728630 | GA | G | 6 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(3): Show |
6 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.192+732delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chrX | 65728630 | ||||||
| chrX:65728662 | T | G | 7 | a0001c0001t0002g0015 a0001c0001t0002g0042 a0001c0001t0002g0045 others(4): Show |
7 | HG01081.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+753T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65728662 | |||||||
| chrX:65728828 | C | T | 26 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(23): Show |
31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-610C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65728828 | |||||||
| chrX:65729141 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.193-297A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65729141 | |||||||
| chrX:65729995 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.467+283T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65729995 | |||||||
| chrX:65730029 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.467+317T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730029 | |||||||
| chrX:65730039 | T | C | 1 | a0001c0001t0002g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.467+327T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730039 | |||||||
| chrX:65730117 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0095 |
2 | HG02040.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.467+405G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730117 | |||||||
| chrX:65730128 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.467+416T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730128 | |||||||
| chrX:65730262 | G | A | 1 | a0001c0001t0002g0011 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.467+550G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730262 | |||||||
| chrX:65730384 | C | T | 1 | a0001c0001t0002g0010 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.467+672C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730384 | |||||||
| chrX:65731212 | T | C | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.551+22T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 5/12 | chrX | 65731212 | |||||||
| chrX:65732980 | G | T | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.699-204G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 6/12 | chrX | 65732980 | |||||||
| chrX:65733076 | G | A | 4 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0117 others(1): Show |
4 | HG02602.hp1 HG02735.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.699-108G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 6/12 | chrX | 65733076 | |||||||
| chrX:65733430 | T | C | 7 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0019 others(4): Show |
8 | HG02717.hp1 HG02886.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.795+150T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65733430 | |||||||
| chrX:65733676 | C | CCT | 5 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0109 others(2): Show |
5 | HG02809.hp1 NA18960.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.795+413_795+414dup others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65733676 | ||||||
| chrX:65733676 | CCTCT | C | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.795+411_795+414del others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65733676 | ||||||
| chrX:65733813 | C | G | 1 | a0001c0001t0004g0053 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.795+533C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65733813 | |||||||
| chrX:65733863 | G | A | 49 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(46): Show |
54 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.795+583G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65733863 | |||||||
| chrX:65733892 | G | A | 4 | a0001c0001t0004g0053 a0001c0001t0004g0127 a0001c0001t0004g0139 others(1): Show |
4 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+612G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65733892 | |||||||
| chrX:65733917 | G | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0019 others(4): Show |
8 | HG02717.hp1 HG02886.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.795+637G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65733917 | |||||||
| chrX:65733962 | C | CT | 37 | a0001c0001t0001g0153 a0001c0001t0002g0001 a0001c0001t0002g0002 others(34): Show |
42 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.795+692dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65733962 | ||||||
| chrX:65734011 | A | G | 1 | a0001c0001t0004g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.795+731A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65734011 | |||||||
| chrX:65734522 | G | A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.796-745G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65734522 | |||||||
| chrX:65734996 | G | T | 1 | a0001c0001t0002g0012 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.796-271G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65734996 | |||||||
| chrX:65735044 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.796-223A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65735044 | |||||||
| chrX:65735560 | C | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.959+130C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65735560 | |||||||
| chrX:65735698 | A | G | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.959+268A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65735698 | |||||||
| chrX:65735842 | A | G | 1 | a0001c0001t0012g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.959+412A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65735842 | |||||||
| chrX:65735906 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.959+476C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65735906 | |||||||
| chrX:65736096 | G | A | 5 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.959+666G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736096 | |||||||
| chrX:65736134 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.960-661A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736134 | |||||||
| chrX:65736139 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.960-656C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736139 | |||||||
| chrX:65736307 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.960-488C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736307 | |||||||
| chrX:65736437 | C | CT | 6 | a0001c0001t0001g0114 a0001c0001t0001g0147 a0001c0001t0002g0042 others(3): Show |
6 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.960-342dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 65736437 | ||||||
| chrX:65736437 | CT | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0064 a0001c0001t0002g0001 others(30): Show |
38 | HG01243.hp1 HG01256.hp1 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.960-342delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 65736437 | ||||||
| chrX:65736451 | T | C | 5 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(2): Show |
5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.960-344T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736451 | |||||||
| chrX:65736598 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.960-197C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736598 | |||||||
| chrX:65736640 | G | C | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.960-155G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736640 | |||||||
| chrX:65736749 | G | A | 39 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(36): Show |
44 | HG00738.hp1 HG01081.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.960-46G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736749 | |||||||
| chrX:65737711 | A | T | 1 | a0001c0001t0001g0133 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1251+373A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65737711 | |||||||
| chrX:65737807 | AACCC | A | 51 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0009 others(48): Show |
56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.1251+475_1251+478d others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 65737807 | ||||||
| chrX:65737926 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1251+588T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65737926 | |||||||
| chrX:65738072 | C | T | 1 | a0001c0001t0002g0011 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1252-453C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65738072 | |||||||
| chrX:65738228 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0150 |
2 | NA18953.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1252-297C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65738228 | |||||||
| chrX:65738396 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1252-129G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65738396 | |||||||
| chrX:65738521 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG02572.hp1 | splice_region_variant&intron_variant | LOW | c.1252-4G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65738521 | |||||||
| chrX:65738631 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1344+14C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 11/12 | chrX | 65738631 | |||||||
| chrX:65738731 | C | T | 5 | a0001c0001t0004g0053 a0001c0001t0004g0126 a0001c0001t0004g0127 others(2): Show |
5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1344+114C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 11/12 | chrX | 65738731 | |||||||
| chrX:65738894 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0136 |
2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1345-76C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 11/12 | chrX | 65738894 | |||||||
| chrX:65739543 | AT | A | 10 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0048 others(7): Show |
10 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1570-177delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 65739543 | ||||||
| chrX:65739703 | C | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0035 |
2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1570-26C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 12/12 | chrX | 65739703 | |||||||
| chrX:65739715 | A | G | 37 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(34): Show |
42 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.1570-14A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 12/12 | chrX | 65739715 |