Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11238 |
| ensemblid | ENSG00000169239.14 |
| hgncid | 1378 |
| symbol | CA5B |
| name | carbonic anhydrase 5B |
| refseq_nuc | NM_007220.4 |
| refseq_prot | NP_009151.1 |
| ensembl_nuc | ENST00000318636.8 |
| ensembl_prot | ENSP00000314099.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 15738270 |
| end | 15788411 |
| strand | + |
| ver | v1.2 |
| region | chrX:15738270-15788411 |
| region5000 | chrX:15733270-15793411 |
| regionname0 | CA5B_chrX_15738270_15788411 |
| regionname5000 | CA5B_chrX_15733270_15793411 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 317 | 271 | 67 | 43 | 119 | 11 | 29 | 94 | CA5B_chrX_15733270_15793411 | CA5B | MVVMN others(312): Show |
chrX | 15733270 | 15793411 |
| a0002 | 0/0 | 317 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | MVVMN others(312): Show |
chrX | 15733270 | 15793411 |
| a0003 | 0/0 | 317 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | MVVMN others(312): Show |
chrX | 15733270 | 15793411 |
| a0004 | 0/0 | 317 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | MVVMN others(312): Show |
chrX | 15733270 | 15793411 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 951 | 171 | 51 | 27 | 62 | 7 | 22 | CA5B_chrX_15733270_15793411 | CA5B | ATGGT others(946): Show |
chrX | 15733270 | 15793411 | ||
| a0001c0002 | 0/0 | 951 | 99 | 16 | 16 | 56 | 4 | 7 | CA5B_chrX_15733270_15793411 | CA5B | ATGGT others(946): Show |
chrX | 15733270 | 15793411 | ||
| a0001c0004 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | ATGGT others(946): Show |
chrX | 15733270 | 15793411 | ||
| a0002c0003 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | ATGGT others(946): Show |
chrX | 15733270 | 15793411 | ||
| a0003c0005 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | ATGGT others(946): Show |
chrX | 15733270 | 15793411 | ||
| a0004c0006 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | ATGGT others(946): Show |
chrX | 15733270 | 15793411 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6837 | 100 | 21 | 12 | 50 | 3 | 13 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6832): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0003 | 0/0 | 6839 | 25 | 0 | 12 | 7 | 3 | 3 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6834): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0005 | 0/0 | 6838 | 6 | 0 | 0 | 4 | 0 | 2 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6833): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0006 | 0/0 | 6836 | 6 | 6 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6831): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0008 | 0/0 | 6839 | 6 | 6 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6834): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0009 | 0/0 | 6837 | 4 | 4 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6832): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0010 | 0/0 | 6834 | 3 | 3 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6829): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0011 | 0/0 | 6837 | 2 | 1 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6832): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0012 | 0/0 | 6834 | 2 | 1 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6829): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0013 | 0/0 | 6834 | 2 | 2 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6829): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0014 | 0/0 | 6838 | 2 | 0 | 1 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6833): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0015 | 0/0 | 6833 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6828): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0016 | 0/0 | 6833 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6828): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0017 | 0/1 | 6837 | 1 | 0 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6832): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0018 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6832): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0019 | 0/0 | 6837 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6832): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0020 | 0/0 | 6837 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6832): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0026 | 0/0 | 6834 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6829): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0027 | 0/0 | 6834 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6829): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0028 | 0/0 | 6836 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6831): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0029 | 0/0 | 6839 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6834): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0030 | 0/0 | 6839 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6834): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0031 | 0/0 | 6840 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6835): Show |
chrX | 15733270 | 15793411 |
| a0001c0001t0032 | 0/0 | 6840 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6835): Show |
chrX | 15733270 | 15793411 |
| a0001c0002t0002 | 0/0 | 6836 | 78 | 9 | 12 | 48 | 3 | 6 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6831): Show |
chrX | 15733270 | 15793411 |
| a0001c0002t0004 | 0/0 | 6837 | 11 | 2 | 3 | 6 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6832): Show |
chrX | 15733270 | 15793411 |
| a0001c0002t0007 | 0/0 | 6836 | 5 | 4 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6831): Show |
chrX | 15733270 | 15793411 |
| a0001c0002t0021 | 0/0 | 6835 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6830): Show |
chrX | 15733270 | 15793411 |
| a0001c0002t0022 | 0/0 | 6836 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6831): Show |
chrX | 15733270 | 15793411 |
| a0001c0002t0023 | 0/0 | 6836 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6831): Show |
chrX | 15733270 | 15793411 |
| a0001c0002t0024 | 0/0 | 6836 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6831): Show |
chrX | 15733270 | 15793411 |
| a0001c0002t0025 | 0/0 | 6836 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6831): Show |
chrX | 15733270 | 15793411 |
| a0001c0004t0001 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6832): Show |
chrX | 15733270 | 15793411 |
| a0002c0003t0007 | 0/0 | 6836 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6831): Show |
chrX | 15733270 | 15793411 |
| a0003c0005t0002 | 0/0 | 6836 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6831): Show |
chrX | 15733270 | 15793411 |
| a0004c0006t0001 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | GTAGC others(6832): Show |
chrX | 15733270 | 15793411 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0011g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0012g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0012g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0013g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0014g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0015g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0016g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0017g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0018g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0019g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0020g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0026g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0027g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0028g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0029g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0030g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0031g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0001t0032g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0007g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0021g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0022g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0023g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0024g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0002t0025g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0002c0003t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0003c0005t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| a0004c0006t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0246 | EUR | GBR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00280 | hp1 | a0001 | c0002 | t0025 | g0181 | EUR | FIN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0158 | EUR | FIN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00438 | hp1 | a0001 | c0002 | t0004 | g0188 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00621 | hp1 | a0001 | c0002 | t0004 | g0011 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0254 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00642 | hp1 | a0001 | c0002 | t0004 | g0177 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0247 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01071 | hp2 | a0001 | c0001 | t0012 | g0256 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0120 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0115 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0249 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01243 | hp1 | a0001 | c0002 | t0007 | g0225 | AMR | PUR | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0228 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0208 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01261 | hp1 | a0001 | c0002 | t0004 | g0242 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0187 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01496 | hp1 | a0001 | c0001 | t0014 | g0196 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0011 | EUR | IBS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0040 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0229 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01891 | hp2 | a0001 | c0001 | t0028 | g0189 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0211 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | CDX | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0099 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0026 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02293 | hp1 | a0001 | c0001 | t0011 | g0139 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02293 | hp2 | a0001 | c0002 | t0004 | g0012 | AMR | PEL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02451 | hp1 | a0001 | c0001 | t0027 | g0250 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02451 | hp2 | a0002 | c0003 | t0007 | g0239 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | KHV | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02572 | hp1 | a0001 | c0002 | t0007 | g0166 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02630 | hp1 | a0001 | c0001 | t0029 | g0062 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0097 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0194 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02717 | hp1 | a0001 | c0001 | t0016 | g0023 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02723 | hp1 | a0001 | c0001 | t0026 | g0042 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0068 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0100 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0230 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0098 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0251 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0057 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02976 | hp2 | a0001 | c0001 | t0015 | g0024 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0096 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0025 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0027 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0234 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0101 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0031 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03492 | hp1 | a0001 | c0002 | t0023 | g0173 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0028 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03516 | hp2 | a0001 | c0001 | t0032 | g0252 | AFR | ESN | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0129 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | GWD | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0255 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03669 | hp1 | a0003 | c0005 | t0002 | g0191 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0172 | SAS | STU | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03704 | hp1 | a0001 | c0001 | t0019 | g0106 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0053 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0083 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0201 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG04184 | hp1 | a0001 | c0001 | t0031 | g0030 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0066 | SAS | STU | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG04228 | hp1 | a0001 | c0001 | t0020 | g0108 | SAS | STU | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18522 | hp1 | a0001 | c0002 | t0007 | g0210 | AFR | YRI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | CHB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | CHB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0186 | AFR | YRI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18980 | hp2 | a0001 | c0002 | t0004 | g0059 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18981 | hp2 | a0001 | c0002 | t0004 | g0231 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19001 | hp1 | a0001 | c0001 | t0018 | g0095 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19005 | hp1 | a0001 | c0002 | t0004 | g0204 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19007 | hp1 | a0001 | c0002 | t0004 | g0205 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19009 | hp1 | a0004 | c0006 | t0001 | g0122 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0206 | AFR | LWK | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0056 | AFR | LWK | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19058 | hp1 | a0001 | c0002 | t0022 | g0193 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0084 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19076 | hp1 | a0001 | c0004 | t0001 | g0088 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19086 | hp1 | a0001 | c0002 | t0021 | g0199 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0244 | AFR | YRI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA20752 | hp1 | a0001 | c0001 | t0030 | g0003 | EUR | TSI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0017 | EUR | TSI | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA20905 | hp1 | a0001 | c0001 | t0014 | g0003 | SAS | GIH | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02109 | hp1 | a0001 | c0002 | t0007 | g0235 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0221 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG02486 | hp1 | a0001 | c0002 | t0007 | g0236 | AFR | ACB | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0253 | AFR | USA | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | USA | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0046 | AFR | LWK | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| NA21309 | hp2 | a0001 | c0002 | t0024 | g0222 | AFR | LWK | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0017 | g0018 | REF | REF | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0165 | REF | REF | CA5B_chrX_15733270_15793411 | CA5B | chrX | 15733270 | 15793411 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:15774323 | G | A | 1 | a0002 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.481G>A | p.Ala161Thr | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/8 | 617/6837 | 481/954 | 161/317 | chrX | 15774323 | |||
| chrX:15782588 | G | T | 1 | a0004 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.878G>T | p.Arg293Leu | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1014/6837 | 878/954 | 293/317 | chrX | 15782588 | |||
| chrX:15782623 | C | A | 1 | a0003 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.913C>A | p.Gln305Lys | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1049/6837 | 913/954 | 305/317 | chrX | 15782623 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:15775293 | G | A | 1 | a0001c0004 | 1 | NA19076.hp1 | synonymous_variant | LOW | c.603G>A | p.Pro201Pro | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/8 | 739/6837 | 603/954 | 201/317 | chrX | 15775293 | |||
| chrX:15782628 | G | A | 3 | a0001c0002 a0002c0003 a0003c0005 |
101 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
synonymous_variant | LOW | c.918G>A | p.Ala306Ala | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1054/6837 | 918/954 | 306/317 | chrX | 15782628 |
| 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:15782671 | C | A | 2 | a0001c0001t0015 a0001c0001t0016 |
2 | HG02717.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 7 | chrX | 15782671 | ||||||
| chrX:15783159 | A | G | 2 | a0001c0001t0008 a0001c0001t0032 |
7 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*495A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 495 | chrX | 15783159 | ||||||
| chrX:15783207 | A | C | 4 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0030 others(1): Show |
29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*543A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 543 | chrX | 15783207 | ||||||
| chrX:15783520 | A | G | 25 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0010 others(22): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*856A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 856 | chrX | 15783520 | ||||||
| chrX:15783623 | C | T | 2 | a0001c0001t0008 a0001c0001t0032 |
7 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*959C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 959 | chrX | 15783623 | ||||||
| chrX:15783794 | T | TA | 11 | a0001c0001t0010 a0001c0002t0002 a0001c0002t0004 others(8): Show |
104 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1143dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1144 | INFO_REALIGN_3_PRIME | chrX | 15783794 | |||||
| chrX:15783794 | TA | T | 1 | a0001c0001t0006 | 6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1143delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1143 | INFO_REALIGN_3_PRIME | chrX | 15783794 | |||||
| chrX:15783803 | A | G | 2 | a0001c0001t0015 a0001c0001t0016 |
2 | HG02717.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1139A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1139 | chrX | 15783803 | ||||||
| chrX:15783833 | G | A | 18 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0013 others(15): Show |
113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1169G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1169 | chrX | 15783833 | ||||||
| chrX:15783887 | C | CT | 11 | a0001c0001t0005 a0001c0001t0031 a0001c0001t0032 others(8): Show |
97 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1241dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1242 | INFO_REALIGN_3_PRIME | chrX | 15783887 | |||||
| chrX:15783887 | C | CTT | 2 | a0001c0001t0028 a0001c0002t0004 |
12 | HG00438.hp1 HG00621.hp1 HG00642.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1240_*1241dupTT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1242 | INFO_REALIGN_3_PRIME | chrX | 15783887 | |||||
| chrX:15784078 | G | A | 18 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0013 others(15): Show |
113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1414G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1414 | chrX | 15784078 | ||||||
| chrX:15784084 | C | T | 1 | a0001c0002t0025 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1420C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1420 | chrX | 15784084 | ||||||
| chrX:15784177 | C | T | 1 | a0001c0002t0024 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1513C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 1513 | chrX | 15784177 | ||||||
| chrX:15784677 | C | G | 7 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0014 others(4): Show |
37 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2013C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2013 | chrX | 15784677 | ||||||
| chrX:15784861 | C | T | 10 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0007 others(7): Show |
101 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*2197C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2197 | chrX | 15784861 | ||||||
| chrX:15785049 | A | G | 1 | a0001c0001t0027 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2385A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2385 | chrX | 15785049 | ||||||
| chrX:15785123 | C | T | 1 | a0001c0002t0023 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2459C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2459 | chrX | 15785123 | ||||||
| chrX:15785181 | C | G | 2 | a0001c0001t0015 a0001c0001t0016 |
2 | HG02717.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2517C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2517 | chrX | 15785181 | ||||||
| chrX:15785291 | A | G | 1 | a0001c0001t0020 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2627A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2627 | chrX | 15785291 | ||||||
| chrX:15785448 | A | G | 1 | a0001c0001t0011 | 2 | HG02293.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2784A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2784 | chrX | 15785448 | ||||||
| chrX:15785513 | G | A | 18 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0013 others(15): Show |
113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2849G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2849 | chrX | 15785513 | ||||||
| chrX:15785514 | T | C | 1 | a0001c0001t0026 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2850T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 2850 | chrX | 15785514 | ||||||
| chrX:15785864 | A | AT | 6 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0029 others(3): Show |
35 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3209dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3210 | INFO_REALIGN_3_PRIME | chrX | 15785864 | |||||
| chrX:15785867 | T | TA | 15 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0026 others(12): Show |
108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3203_*3204insA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3204 | chrX | 15785867 | ||||||
| chrX:15785902 | G | A | 3 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0016 |
5 | HG02280.hp1 HG02717.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3238G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3238 | chrX | 15785902 | ||||||
| chrX:15785983 | G | A | 1 | a0001c0001t0015 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3319G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3319 | chrX | 15785983 | ||||||
| chrX:15786091 | G | T | 1 | a0001c0001t0019 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3427G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3427 | chrX | 15786091 | ||||||
| chrX:15786263 | T | TA | 7 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0014 others(4): Show |
37 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3600dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3601 | INFO_REALIGN_3_PRIME | chrX | 15786263 | |||||
| chrX:15786385 | C | A | 1 | a0001c0001t0010 | 3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3721C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3721 | chrX | 15786385 | ||||||
| chrX:15786399 | T | C | 1 | a0001c0001t0012 | 2 | HG01071.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3735T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3735 | chrX | 15786399 | ||||||
| chrX:15786648 | ACTTC | A | 18 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0013 others(15): Show |
113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3991_*3994delTCCT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 3991 | INFO_REALIGN_3_PRIME | chrX | 15786648 | |||||
| chrX:15786860 | C | T | 3 | a0001c0002t0007 a0001c0002t0024 a0002c0003t0007 |
7 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4196C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 4196 | chrX | 15786860 | ||||||
| chrX:15786861 | G | A | 5 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0029 others(2): Show |
30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4197G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 4197 | chrX | 15786861 | ||||||
| chrX:15786863 | C | T | 1 | a0001c0001t0012 | 2 | HG01071.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4199C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 4199 | chrX | 15786863 | ||||||
| chrX:15786895 | G | A | 1 | a0001c0001t0030 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4231G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 4231 | chrX | 15786895 | ||||||
| chrX:15787668 | A | G | 5 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0029 others(2): Show |
30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5004A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5004 | chrX | 15787668 | ||||||
| chrX:15787723 | G | A | 1 | a0001c0001t0012 | 2 | HG01071.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5059G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5059 | chrX | 15787723 | ||||||
| chrX:15787735 | G | T | 25 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0010 others(22): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*5071G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5071 | chrX | 15787735 | ||||||
| chrX:15787903 | G | C | 1 | a0001c0001t0009 | 4 | HG01884.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5239G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5239 | chrX | 15787903 | ||||||
| chrX:15787979 | A | T | 1 | a0001c0001t0026 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5315A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5315 | chrX | 15787979 | ||||||
| chrX:15788004 | G | T | 3 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0016 |
5 | HG02280.hp1 HG02717.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5340G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5340 | chrX | 15788004 | ||||||
| chrX:15788104 | G | C | 2 | a0001c0001t0008 a0001c0001t0032 |
7 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5440G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5440 | chrX | 15788104 | ||||||
| chrX:15788123 | C | T | 1 | a0001c0001t0018 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5459C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5459 | chrX | 15788123 | ||||||
| chrX:15788159 | G | T | 2 | a0001c0001t0013 a0001c0001t0027 |
3 | HG02451.hp1 HG02965.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5495G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5495 | chrX | 15788159 | ||||||
| chrX:15788286 | A | T | 1 | a0001c0002t0022 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5622A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 8/8 | 5622 | chrX | 15788286 |
| 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:15738368 | C | T | 2 | a0001c0001t0012g0255 a0001c0001t0012g0256 |
2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-54+16C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738368 | |||||||
| chrX:15738704 | T | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(7): Show |
14 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.-54+352T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738704 | |||||||
| chrX:15738755 | C | A | 3 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 |
3 | HG01346.hp1 HG01433.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-54+403C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738755 | |||||||
| chrX:15738759 | G | A | 6 | a0001c0001t0008g0025 a0001c0001t0010g0026 a0001c0001t0010g0027 others(3): Show |
6 | HG02280.hp1 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+407G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738759 | |||||||
| chrX:15738771 | A | C | 1 | a0001c0001t0003g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-54+419A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738771 | |||||||
| chrX:15738985 | C | T | 2 | a0001c0001t0013g0253 a0001c0001t0032g0252 |
2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-54+633C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15738985 | |||||||
| chrX:15739450 | GT | G | 6 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0003g0061 others(3): Show |
6 | HG01168.hp2 HG02630.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54+1113delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15739450 | ||||||
| chrX:15739450 | GTT | G | 32 | a0001c0001t0003g0003 a0001c0001t0003g0029 a0001c0001t0003g0032 others(29): Show |
32 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-54+1112_-54+1113d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15739450 | ||||||
| chrX:15740123 | C | T | 103 | a0001c0001t0001g0182 a0001c0001t0001g0218 a0001c0001t0001g0219 others(100): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-54+1771C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15740123 | |||||||
| chrX:15740257 | G | A | 2 | a0001c0001t0015g0024 a0001c0001t0016g0023 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-54+1905G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15740257 | |||||||
| chrX:15740797 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-54+2445T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15740797 | |||||||
| chrX:15741382 | C | CA | 73 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0063 others(70): Show |
74 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.-54+3051dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15741382 | ||||||
| chrX:15741492 | T | G | 103 | a0001c0001t0001g0182 a0001c0001t0001g0218 a0001c0001t0001g0219 others(100): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-54+3140T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15741492 | |||||||
| chrX:15741510 | T | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(253): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-54+3158T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15741510 | |||||||
| chrX:15741578 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-54+3226C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15741578 | |||||||
| chrX:15741813 | G | A | 1 | a0001c0001t0018g0095 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-54+3461G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15741813 | |||||||
| chrX:15741871 | T | C | 8 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(5): Show |
8 | HG01071.hp2 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+3519T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15741871 | |||||||
| chrX:15742250 | T | A | 1 | a0001c0002t0002g0190 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-54+3898T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742250 | |||||||
| chrX:15742376 | G | GT | 98 | a0001c0001t0001g0094 a0001c0001t0001g0182 a0001c0001t0001g0218 others(95): Show |
105 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.-54+4032dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15742376 | ||||||
| chrX:15742390 | G | A | 4 | a0001c0001t0008g0025 a0001c0001t0010g0026 a0001c0001t0010g0027 others(1): Show |
4 | HG02280.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+4038G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742390 | |||||||
| chrX:15742409 | C | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-54+4057C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742409 | |||||||
| chrX:15742409 | C | G | 2 | a0001c0001t0012g0255 a0001c0001t0012g0256 |
2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-54+4057C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742409 | |||||||
| chrX:15742751 | C | G | 1 | a0001c0001t0015g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-54+4399C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742751 | |||||||
| chrX:15742801 | A | G | 2 | a0001c0001t0015g0024 a0001c0001t0016g0023 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-54+4449A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742801 | |||||||
| chrX:15742960 | C | G | 1 | a0001c0001t0003g0161 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-54+4608C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742960 | |||||||
| chrX:15742996 | C | T | 103 | a0001c0001t0001g0182 a0001c0001t0001g0218 a0001c0001t0001g0219 others(100): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-54+4644C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15742996 | |||||||
| chrX:15743564 | G | A | 1 | a0001c0002t0007g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-54+5212G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15743564 | |||||||
| chrX:15743746 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-54+5394G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15743746 | |||||||
| chrX:15743941 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-54+5589C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15743941 | |||||||
| chrX:15743955 | C | A | 92 | a0001c0001t0001g0182 a0001c0001t0001g0218 a0001c0001t0001g0219 others(89): Show |
99 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-54+5603C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15743955 | |||||||
| chrX:15744143 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-54+5791T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15744143 | |||||||
| chrX:15744409 | G | T | 1 | a0001c0002t0002g0190 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-53-5562G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15744409 | |||||||
| chrX:15744431 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-53-5540C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15744431 | |||||||
| chrX:15744551 | G | A | 1 | a0001c0001t0028g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-53-5420G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15744551 | |||||||
| chrX:15745168 | C | CA | 6 | a0001c0001t0001g0019 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG00323.hp1 HG04184.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53-4784dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745168 | ||||||
| chrX:15745183 | A | AAAAAAG | 15 | a0001c0001t0003g0029 a0001c0001t0005g0068 a0001c0001t0008g0025 others(12): Show |
16 | HG01928.hp1 HG02080.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.-53-4784_-53-4783i others(8): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745183 | ||||||
| chrX:15745183 | A | AAAAAG | 109 | a0001c0001t0001g0008 a0001c0001t0001g0159 a0001c0001t0001g0182 others(106): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-53-4763_-53-4759d others(7): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745183 | ||||||
| chrX:15745183 | A | AAAAAGAA others(3): Show |
1 | a0001c0002t0002g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-53-4768_-53-4759d others(12): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745183 | ||||||
| chrX:15745183 | AAAAAG | A | 9 | a0001c0001t0001g0094 a0001c0001t0001g0162 a0001c0001t0012g0255 others(6): Show |
9 | HG01071.hp2 HG02074.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-53-4763_-53-4759d others(7): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15745183 | ||||||
| chrX:15745715 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-53-4256G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15745715 | |||||||
| chrX:15745845 | AT | A | 30 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(27): Show |
30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.-53-4125delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15745845 | |||||||
| chrX:15745906 | A | T | 1 | a0001c0002t0002g0249 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-53-4065A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15745906 | |||||||
| chrX:15746022 | C | CT | 49 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0021 others(46): Show |
52 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-53-3924dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15746022 | ||||||
| chrX:15746022 | CT | C | 44 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(41): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-53-3924delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15746022 | ||||||
| chrX:15746022 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0008g0039 a0001c0001t0008g0040 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-53-3936_-53-3924d others(15): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15746022 | ||||||
| chrX:15746047 | T | A | 1 | a0001c0001t0003g0047 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-53-3924T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746047 | |||||||
| chrX:15746061 | GCTCTGTC others(1): Show |
G | 255 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-53-3898_-53-3891d others(10): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15746061 | ||||||
| chrX:15746069 | A | G | 1 | a0001c0002t0002g0200 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-53-3902A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746069 | |||||||
| chrX:15746079 | T | C | 134 | a0001c0001t0001g0182 a0001c0001t0001g0218 a0001c0001t0001g0219 others(131): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-53-3892T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746079 | |||||||
| chrX:15746148 | C | T | 134 | a0001c0001t0001g0182 a0001c0001t0001g0218 a0001c0001t0001g0219 others(131): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-53-3823C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746148 | |||||||
| chrX:15746324 | C | T | 30 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(27): Show |
30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.-53-3647C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746324 | |||||||
| chrX:15746354 | G | A | 10 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-53-3617G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746354 | |||||||
| chrX:15746461 | A | G | 134 | a0001c0001t0001g0182 a0001c0001t0001g0218 a0001c0001t0001g0219 others(131): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-53-3510A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746461 | |||||||
| chrX:15746593 | G | T | 2 | a0001c0001t0010g0027 a0001c0001t0010g0028 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-53-3378G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746593 | |||||||
| chrX:15746698 | G | A | 1 | a0001c0001t0008g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-53-3273G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746698 | |||||||
| chrX:15746886 | C | A | 1 | a0001c0001t0003g0161 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-53-3085C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15746886 | |||||||
| chrX:15747025 | G | A | 2 | a0001c0001t0012g0255 a0001c0001t0012g0256 |
2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-2946G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747025 | |||||||
| chrX:15747071 | T | C | 1 | a0001c0002t0002g0169 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-53-2900T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747071 | |||||||
| chrX:15747073 | T | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0058 a0001c0001t0001g0060 others(39): Show |
43 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.-53-2898T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747073 | |||||||
| chrX:15747519 | G | T | 1 | a0001c0001t0003g0161 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-53-2452G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747519 | |||||||
| chrX:15747592 | A | G | 152 | a0001c0001t0001g0182 a0001c0001t0001g0218 a0001c0001t0001g0219 others(149): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-53-2379A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747592 | |||||||
| chrX:15747808 | C | A | 4 | a0001c0001t0008g0025 a0001c0001t0010g0026 a0001c0001t0010g0027 others(1): Show |
4 | HG02280.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-2163C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15747808 | |||||||
| chrX:15747899 | A | AGAGAGGA others(19): Show |
6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53-2054_-53-2029d others(28): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15747899 | ||||||
| chrX:15747899 | AGAGAGGA others(19): Show |
A | 1 | a0001c0001t0008g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-53-2054_-53-2029d others(28): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15747899 | ||||||
| chrX:15748044 | C | G | 1 | a0001c0001t0001g0128 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-53-1927C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748044 | |||||||
| chrX:15748054 | C | T | 2 | a0001c0001t0012g0255 a0001c0001t0012g0256 |
2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-1917C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748054 | |||||||
| chrX:15748197 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-53-1774G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748197 | |||||||
| chrX:15748511 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0005g0066 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-53-1460A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748511 | |||||||
| chrX:15748641 | G | A | 6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53-1330G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748641 | |||||||
| chrX:15748708 | A | AC | 80 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0069 others(77): Show |
82 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.-53-1252dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15748708 | ||||||
| chrX:15748708 | A | ACC | 24 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0077 others(21): Show |
25 | HG01106.hp1 HG01891.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.-53-1253_-53-1252d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15748708 | ||||||
| chrX:15748708 | AC | A | 16 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(13): Show |
16 | HG01071.hp2 HG01346.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.-53-1252delC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15748708 | ||||||
| chrX:15748708 | ACC | A | 26 | a0001c0001t0003g0003 a0001c0001t0003g0029 a0001c0001t0003g0032 others(23): Show |
26 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.-53-1253_-53-1252d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15748708 | ||||||
| chrX:15748720 | G | A | 6 | a0001c0001t0008g0025 a0001c0001t0010g0026 a0001c0001t0010g0027 others(3): Show |
6 | HG02280.hp1 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-53-1251G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748720 | |||||||
| chrX:15748836 | G | A | 1 | a0001c0001t0016g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-53-1135G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15748836 | |||||||
| chrX:15749152 | G | GT | 6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53-819_-53-818ins others(1): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749152 | |||||||
| chrX:15749153 | A | T | 8 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(5): Show |
8 | HG01071.hp2 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53-818A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749153 | |||||||
| chrX:15749178 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-53-793A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749178 | |||||||
| chrX:15749511 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-53-460T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749511 | |||||||
| chrX:15749514 | G | T | 2 | a0001c0002t0002g0183 a0001c0002t0002g0240 |
2 | NA18941.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-53-457G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749514 | |||||||
| chrX:15749596 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0156 |
3 | HG00438.hp2 HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-53-375G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | chrX | 15749596 | |||||||
| chrX:15749644 | AT | A | 7 | a0001c0001t0001g0109 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | HG02965.hp1 HG02976.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-53-314delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 15749644 | ||||||
| chrX:15750270 | T | C | 10 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+105T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15750270 | |||||||
| chrX:15750509 | C | A | 1 | a0001c0002t0002g0243 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.142+344C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15750509 | |||||||
| chrX:15751017 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.142+852C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751017 | |||||||
| chrX:15751539 | C | CT | 11 | a0001c0001t0005g0068 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+1387dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15751539 | ||||||
| chrX:15751667 | C | G | 4 | a0001c0001t0009g0031 a0001c0001t0009g0044 a0001c0001t0009g0046 others(1): Show |
4 | HG01884.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+1502C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751667 | |||||||
| chrX:15751667 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.142+1502C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751667 | |||||||
| chrX:15751758 | A | G | 2 | a0001c0001t0015g0024 a0001c0001t0016g0023 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.142+1593A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751758 | |||||||
| chrX:15751796 | A | G | 1 | a0001c0002t0004g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.142+1631A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751796 | |||||||
| chrX:15751829 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.142+1664G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751829 | |||||||
| chrX:15751974 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0105 |
2 | NA18961.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.142+1809C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15751974 | |||||||
| chrX:15752132 | G | A | 10 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+1967G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752132 | |||||||
| chrX:15752174 | C | T | 2 | a0001c0001t0015g0024 a0001c0001t0016g0023 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.142+2009C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752174 | |||||||
| chrX:15752184 | A | AT | 10 | a0001c0001t0008g0039 a0001c0001t0008g0040 a0001c0001t0008g0041 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+2029dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752184 | ||||||
| chrX:15752220 | G | A | 1 | a0001c0001t0026g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142+2055G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752220 | |||||||
| chrX:15752288 | G | A | 2 | a0001c0001t0003g0049 a0001c0001t0003g0061 |
2 | NA18946.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.142+2123G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752288 | |||||||
| chrX:15752320 | C | G | 1 | a0001c0001t0031g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.142+2155C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752320 | |||||||
| chrX:15752451 | C | T | 1 | a0001c0001t0028g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142+2286C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752451 | |||||||
| chrX:15752461 | T | C | 4 | a0001c0001t0003g0032 a0001c0002t0002g0167 a0001c0002t0002g0215 others(1): Show |
4 | HG01175.hp1 HG02080.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+2296T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752461 | |||||||
| chrX:15752485 | C | G | 6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+2320C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752485 | |||||||
| chrX:15752500 | C | T | 14 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+2335C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752500 | |||||||
| chrX:15752522 | A | G | 8 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(5): Show |
8 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+2357A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752522 | |||||||
| chrX:15752527 | T | C | 152 | a0001c0001t0001g0182 a0001c0001t0001g0218 a0001c0001t0001g0219 others(149): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.142+2362T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752527 | |||||||
| chrX:15752528 | A | G | 1 | a0001c0001t0003g0032 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.142+2363A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752528 | |||||||
| chrX:15752537 | A | AAC | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
111 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.142+2375_142+2376d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752537 | ||||||
| chrX:15752542 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
111 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.142+2377G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752542 | |||||||
| chrX:15752582 | A | G | 1 | a0002c0003t0007g0239 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.142+2417A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752582 | |||||||
| chrX:15752585 | C | T | 2 | a0001c0001t0012g0255 a0001c0001t0012g0256 |
2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.142+2420C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752585 | |||||||
| chrX:15752593 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0016g0023 |
2 | HG02717.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.142+2428T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752593 | |||||||
| chrX:15752617 | A | T | 1 | a0001c0002t0002g0167 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.142+2452A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752617 | |||||||
| chrX:15752618 | A | G | 1 | a0001c0002t0002g0167 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.142+2453A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752618 | |||||||
| chrX:15752622 | T | G | 2 | a0001c0001t0006g0097 a0001c0002t0002g0167 |
2 | HG02080.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.142+2457T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752622 | |||||||
| chrX:15752632 | T | G | 7 | a0001c0001t0006g0097 a0001c0001t0013g0251 a0001c0001t0013g0253 others(4): Show |
7 | HG02080.hp2 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+2467T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752632 | |||||||
| chrX:15752642 | G | A | 10 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+2477G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752642 | |||||||
| chrX:15752654 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.142+2489G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752654 | |||||||
| chrX:15752669 | G | A | 1 | a0001c0002t0002g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142+2504G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752669 | |||||||
| chrX:15752673 | C | T | 3 | a0001c0001t0013g0251 a0001c0001t0013g0253 a0001c0001t0032g0252 |
3 | HG02965.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.142+2508C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752673 | |||||||
| chrX:15752674 | G | A | 1 | a0001c0001t0026g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142+2509G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752674 | |||||||
| chrX:15752681 | C | T | 91 | a0001c0001t0001g0182 a0001c0001t0001g0245 a0001c0002t0002g0001 others(88): Show |
98 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.142+2516C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752681 | |||||||
| chrX:15752682 | G | A | 1 | a0001c0001t0026g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142+2517G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752682 | |||||||
| chrX:15752702 | G | A | 1 | a0001c0001t0026g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142+2537G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752702 | |||||||
| chrX:15752703 | C | T | 1 | a0001c0001t0026g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142+2538C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752703 | |||||||
| chrX:15752704 | G | A | 1 | a0001c0001t0010g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.142+2539G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752704 | |||||||
| chrX:15752716 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.142+2551C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752716 | |||||||
| chrX:15752719 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0003g0161 |
2 | HG01934.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.142+2554T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752719 | |||||||
| chrX:15752720 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.142+2555G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752720 | |||||||
| chrX:15752724 | CA | C | 101 | a0001c0001t0001g0111 a0001c0001t0001g0182 a0001c0001t0001g0245 others(98): Show |
108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.142+2573delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752724 | ||||||
| chrX:15752851 | A | G | 30 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(27): Show |
30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.142+2686A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752851 | |||||||
| chrX:15752914 | C | G | 6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+2749C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752914 | |||||||
| chrX:15752987 | G | GC | 13 | a0001c0001t0001g0080 a0001c0001t0001g0087 a0001c0001t0001g0091 others(10): Show |
13 | HG01071.hp2 HG01496.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+2829dupC | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15752987 | ||||||
| chrX:15752993 | C | G | 6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+2828C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752993 | |||||||
| chrX:15752994 | C | T | 1 | a0001c0001t0005g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.142+2829C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15752994 | |||||||
| chrX:15753040 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.142+2875C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753040 | |||||||
| chrX:15753501 | T | C | 1 | a0001c0002t0023g0173 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.142+3336T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753501 | |||||||
| chrX:15753632 | G | C | 2 | a0001c0001t0011g0129 a0001c0001t0011g0139 |
2 | HG02293.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.142+3467G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753632 | |||||||
| chrX:15753665 | T | G | 4 | a0001c0002t0002g0220 a0001c0002t0002g0244 a0001c0002t0004g0186 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+3500T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753665 | |||||||
| chrX:15753707 | G | A | 1 | a0001c0002t0024g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.142+3542G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753707 | |||||||
| chrX:15753773 | G | C | 1 | a0001c0001t0009g0057 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+3608G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753773 | |||||||
| chrX:15753894 | GA | G | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+3730delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753894 | |||||||
| chrX:15753917 | T | C | 1 | a0001c0001t0028g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142+3752T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15753917 | |||||||
| chrX:15754349 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.142+4184G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15754349 | |||||||
| chrX:15754462 | G | C | 1 | a0001c0001t0003g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.142+4297G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15754462 | |||||||
| chrX:15754776 | G | A | 1 | a0001c0001t0008g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.142+4611G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15754776 | |||||||
| chrX:15755357 | A | G | 30 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(27): Show |
30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.142+5192A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15755357 | |||||||
| chrX:15755362 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0005g0066 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.142+5197A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15755362 | |||||||
| chrX:15755372 | A | G | 1 | a0001c0002t0002g0200 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.142+5207A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15755372 | |||||||
| chrX:15755385 | T | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0086 others(2): Show |
6 | HG02145.hp1 HG02976.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+5220T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15755385 | |||||||
| chrX:15755820 | G | A | 34 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(31): Show |
34 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.142+5655G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15755820 | |||||||
| chrX:15756210 | A | G | 1 | a0001c0002t0002g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.142+6045A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15756210 | |||||||
| chrX:15756754 | T | A | 2 | a0001c0002t0004g0204 a0001c0002t0004g0205 |
2 | NA19005.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.142+6589T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15756754 | |||||||
| chrX:15756776 | C | T | 1 | a0001c0002t0002g0238 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.142+6611C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15756776 | |||||||
| chrX:15756783 | A | G | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+6618A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15756783 | |||||||
| chrX:15756792 | T | C | 4 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(1): Show |
4 | HG01884.hp1 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+6627T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15756792 | |||||||
| chrX:15757054 | C | CA | 33 | a0001c0001t0001g0130 a0001c0001t0003g0003 a0001c0001t0003g0015 others(30): Show |
33 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.142+6906dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757054 | ||||||
| chrX:15757054 | C | CAA | 6 | a0001c0001t0003g0029 a0001c0001t0003g0047 a0001c0001t0003g0049 others(3): Show |
6 | HG00741.hp1 NA18942.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+6905_142+6906d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757054 | ||||||
| chrX:15757147 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.142+6982G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15757147 | |||||||
| chrX:15757407 | G | A | 29 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(26): Show |
29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.143-7171G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15757407 | |||||||
| chrX:15757707 | C | CA | 31 | a0001c0001t0001g0021 a0001c0001t0001g0063 a0001c0001t0001g0081 others(28): Show |
31 | HG00438.hp1 HG00741.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-6855dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757707 | ||||||
| chrX:15757707 | CA | C | 21 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0087 others(18): Show |
21 | HG01496.hp2 HG02165.hp2 HG03710.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-6855delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15757707 | ||||||
| chrX:15757761 | G | A | 96 | a0001c0001t0005g0065 a0001c0001t0005g0084 a0001c0002t0002g0001 others(93): Show |
103 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.143-6817G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15757761 | |||||||
| chrX:15758243 | G | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-6335G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758243 | |||||||
| chrX:15758278 | T | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-6300T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758278 | |||||||
| chrX:15758461 | G | A | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.143-6117G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758461 | |||||||
| chrX:15758518 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.143-6060A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758518 | |||||||
| chrX:15758599 | C | T | 1 | a0001c0001t0016g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.143-5979C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758599 | |||||||
| chrX:15758968 | C | T | 1 | a0001c0002t0002g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.143-5610C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15758968 | |||||||
| chrX:15759114 | C | T | 104 | a0001c0001t0005g0065 a0001c0001t0005g0084 a0001c0001t0012g0255 others(101): Show |
111 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.143-5464C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759114 | |||||||
| chrX:15759418 | G | A | 1 | a0001c0002t0002g0241 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.143-5160G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759418 | |||||||
| chrX:15759645 | A | T | 95 | a0001c0001t0005g0065 a0001c0001t0005g0084 a0001c0002t0002g0001 others(92): Show |
102 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.143-4933A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759645 | |||||||
| chrX:15759651 | A | G | 2 | a0001c0001t0003g0032 a0001c0001t0003g0054 |
2 | HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.143-4927A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759651 | |||||||
| chrX:15759734 | C | CTTT | 5 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(2): Show |
5 | HG01884.hp1 HG02647.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4814_143-4812d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | ||||||
| chrX:15759734 | C | CTTTT | 6 | a0001c0001t0006g0099 a0001c0001t0006g0100 a0001c0001t0006g0101 others(3): Show |
6 | HG01884.hp2 HG02258.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-4815_143-4812d others(6): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | ||||||
| chrX:15759734 | C | CTTTTT | 5 | a0001c0001t0008g0039 a0001c0001t0009g0031 a0001c0001t0009g0046 others(2): Show |
5 | HG02970.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-4816_143-4812d others(7): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | ||||||
| chrX:15759734 | CT | C | 10 | a0001c0001t0001g0145 a0001c0001t0003g0033 a0001c0001t0003g0037 others(7): Show |
10 | HG00741.hp1 HG01192.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.143-4812delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | ||||||
| chrX:15759734 | CTT | C | 29 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0105 others(26): Show |
29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.143-4813_143-4812d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | ||||||
| chrX:15759734 | CTTT | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0058 others(62): Show |
68 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.143-4814_143-4812d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | ||||||
| chrX:15759734 | CTTTT | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.143-4815_143-4812d others(6): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | ||||||
| chrX:15759734 | CTTTTT | C | 7 | a0001c0001t0005g0084 a0001c0001t0013g0251 a0001c0001t0013g0253 others(4): Show |
7 | HG01257.hp1 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-4816_143-4812d others(7): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15759734 | ||||||
| chrX:15759928 | A | G | 1 | a0001c0001t0009g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.143-4650A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759928 | |||||||
| chrX:15759966 | C | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0128 |
2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.143-4612C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759966 | |||||||
| chrX:15759973 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0128 |
2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.143-4605T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759973 | |||||||
| chrX:15759974 | G | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0128 |
2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.143-4604G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15759974 | |||||||
| chrX:15760032 | G | A | 1 | a0001c0001t0010g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.143-4546G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760032 | |||||||
| chrX:15760111 | T | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-4467T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760111 | |||||||
| chrX:15760563 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.143-4015G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760563 | |||||||
| chrX:15760595 | A | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-3983A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760595 | |||||||
| chrX:15760635 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.143-3943A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760635 | |||||||
| chrX:15760668 | C | G | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.143-3910C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760668 | |||||||
| chrX:15760672 | T | C | 6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-3906T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15760672 | |||||||
| chrX:15761031 | T | C | 2 | a0001c0002t0002g0183 a0001c0002t0002g0240 |
2 | NA18941.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.143-3547T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761031 | |||||||
| chrX:15761058 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(5): Show |
12 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-3520C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761058 | |||||||
| chrX:15761088 | C | T | 9 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-3490C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761088 | |||||||
| chrX:15761179 | C | CT | 29 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(26): Show |
29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.143-3393dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 15761179 | ||||||
| chrX:15761402 | G | A | 3 | a0001c0001t0013g0251 a0001c0001t0013g0253 a0001c0001t0027g0250 |
3 | HG02451.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.143-3176G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761402 | |||||||
| chrX:15761564 | A | G | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.143-3014A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761564 | |||||||
| chrX:15761841 | A | G | 7 | a0001c0001t0001g0080 a0001c0001t0001g0111 a0001c0001t0001g0127 others(4): Show |
7 | HG01496.hp2 HG02148.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-2737A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761841 | |||||||
| chrX:15761985 | C | T | 9 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-2593C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15761985 | |||||||
| chrX:15762129 | G | A | 29 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(26): Show |
29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.143-2449G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762129 | |||||||
| chrX:15762146 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.143-2432T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762146 | |||||||
| chrX:15762294 | C | A | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.143-2284C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762294 | |||||||
| chrX:15762370 | T | C | 1 | a0001c0002t0002g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.143-2208T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762370 | |||||||
| chrX:15762425 | A | G | 103 | a0001c0001t0005g0065 a0001c0001t0005g0084 a0001c0001t0012g0255 others(100): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.143-2153A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762425 | |||||||
| chrX:15762442 | C | G | 1 | a0001c0001t0003g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.143-2136C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762442 | |||||||
| chrX:15762503 | G | A | 1 | a0001c0002t0023g0173 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.143-2075G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762503 | |||||||
| chrX:15762524 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0005g0124 a0001c0002t0021g0199 |
3 | NA19056.hp1 NA19086.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.143-2054C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762524 | |||||||
| chrX:15762534 | C | T | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-2044C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762534 | |||||||
| chrX:15762576 | G | A | 2 | a0001c0001t0015g0024 a0001c0001t0016g0023 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.143-2002G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762576 | |||||||
| chrX:15762641 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.143-1937G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762641 | |||||||
| chrX:15762728 | T | C | 6 | a0001c0001t0003g0029 a0001c0001t0003g0047 a0001c0001t0003g0049 others(3): Show |
6 | NA18942.hp1 NA18946.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-1850T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15762728 | |||||||
| chrX:15763103 | A | G | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-1475A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763103 | |||||||
| chrX:15763282 | G | A | 2 | a0001c0001t0015g0024 a0001c0001t0016g0023 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.143-1296G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763282 | |||||||
| chrX:15763542 | C | T | 1 | a0001c0002t0024g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.143-1036C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763542 | |||||||
| chrX:15763592 | C | G | 155 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(152): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.143-986C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763592 | |||||||
| chrX:15763876 | G | A | 1 | a0001c0002t0007g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.143-702G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763876 | |||||||
| chrX:15763908 | C | G | 1 | a0001c0001t0008g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.143-670C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15763908 | |||||||
| chrX:15764201 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.143-377T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15764201 | |||||||
| chrX:15764274 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.143-304G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15764274 | |||||||
| chrX:15764320 | A | G | 104 | a0001c0001t0001g0137 a0001c0001t0005g0065 a0001c0001t0005g0084 others(101): Show |
111 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.143-258A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15764320 | |||||||
| chrX:15764327 | C | T | 39 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(36): Show |
39 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.143-251C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15764327 | |||||||
| chrX:15764440 | G | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-138G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 2/7 | chrX | 15764440 | |||||||
| chrX:15765611 | T | A | 1 | a0001c0002t0002g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.340+836T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15765611 | |||||||
| chrX:15765644 | C | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0073 a0001c0001t0001g0102 others(3): Show |
6 | HG02523.hp1 NA18942.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+869C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15765644 | |||||||
| chrX:15766155 | CA | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.340+1403delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15766155 | ||||||
| chrX:15766155 | CAA | C | 92 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0003g0037 others(89): Show |
99 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.340+1402_340+1403d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15766155 | ||||||
| chrX:15766155 | CAAA | C | 11 | a0001c0002t0002g0012 a0001c0002t0002g0168 a0001c0002t0002g0170 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.340+1401_340+1403d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15766155 | ||||||
| chrX:15766375 | A | G | 8 | a0001c0001t0001g0137 a0001c0001t0012g0255 a0001c0001t0012g0256 others(5): Show |
8 | HG01071.hp2 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.340+1600A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15766375 | |||||||
| chrX:15767289 | T | C | 4 | a0001c0001t0003g0033 a0001c0001t0003g0036 a0001c0001t0003g0038 others(1): Show |
4 | HG00323.hp2 HG01192.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+2514T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767289 | |||||||
| chrX:15767404 | A | AT | 8 | a0001c0001t0001g0125 a0001c0001t0006g0096 a0001c0001t0006g0097 others(5): Show |
8 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.340+2644dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15767404 | ||||||
| chrX:15767535 | G | A | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.340+2760G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767535 | |||||||
| chrX:15767770 | A | G | 1 | a0002c0003t0007g0239 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.340+2995A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767770 | |||||||
| chrX:15767810 | G | A | 29 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(26): Show |
29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.340+3035G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767810 | |||||||
| chrX:15767849 | C | T | 6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+3074C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767849 | |||||||
| chrX:15767897 | C | CT | 124 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0093 others(121): Show |
131 | HG00140.hp1 HG00280.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.340+3141dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15767897 | ||||||
| chrX:15767897 | C | CTT | 9 | a0001c0002t0002g0174 a0001c0002t0002g0175 a0001c0002t0002g0178 others(6): Show |
9 | HG00438.hp1 HG01109.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.340+3140_340+3141d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15767897 | ||||||
| chrX:15767938 | G | A | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.340+3163G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767938 | |||||||
| chrX:15767974 | C | T | 1 | a0001c0002t0007g0210 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.340+3199C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767974 | |||||||
| chrX:15767986 | C | T | 2 | a0001c0001t0015g0024 a0001c0001t0016g0023 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.340+3211C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15767986 | |||||||
| chrX:15768010 | C | T | 1 | a0001c0001t0026g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.340+3235C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15768010 | |||||||
| chrX:15768176 | T | C | 116 | a0001c0001t0005g0065 a0001c0001t0005g0084 a0001c0001t0006g0096 others(113): Show |
123 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.340+3401T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15768176 | |||||||
| chrX:15768410 | A | G | 1 | a0001c0001t0009g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.340+3635A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15768410 | |||||||
| chrX:15768606 | T | C | 1 | a0001c0001t0011g0139 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.340+3831T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15768606 | |||||||
| chrX:15768752 | A | G | 2 | a0001c0001t0009g0044 a0001c0001t0009g0046 |
2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.341-3744A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15768752 | |||||||
| chrX:15769229 | A | G | 96 | a0001c0001t0005g0065 a0001c0001t0005g0084 a0001c0002t0002g0001 others(93): Show |
103 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.341-3267A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15769229 | |||||||
| chrX:15769624 | T | A | 1 | a0001c0002t0002g0202 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.341-2872T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15769624 | |||||||
| chrX:15769701 | C | G | 6 | a0001c0002t0007g0166 a0001c0002t0007g0210 a0001c0002t0007g0235 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-2795C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15769701 | |||||||
| chrX:15769706 | T | G | 2 | a0001c0001t0001g0071 a0004c0006t0001g0122 |
2 | HG00597.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.341-2790T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15769706 | |||||||
| chrX:15769828 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.341-2668G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15769828 | |||||||
| chrX:15770188 | C | T | 2 | a0001c0001t0015g0024 a0001c0001t0016g0023 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.341-2308C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770188 | |||||||
| chrX:15770205 | T | C | 146 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(143): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.341-2291T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770205 | |||||||
| chrX:15770417 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.341-2079A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770417 | |||||||
| chrX:15770444 | T | G | 1 | a0001c0001t0001g0105 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.341-2052T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770444 | |||||||
| chrX:15770731 | CTCTT | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0159 |
3 | HG01069.hp1 HG01071.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.341-1754_341-1751d others(6): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15770731 | ||||||
| chrX:15770733 | CTT | C | 80 | a0001c0001t0005g0065 a0001c0001t0005g0084 a0001c0002t0002g0001 others(77): Show |
87 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.341-1761_341-1760d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15770733 | ||||||
| chrX:15770829 | G | A | 2 | a0001c0001t0012g0255 a0001c0001t0012g0256 |
2 | HG01071.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.341-1667G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770829 | |||||||
| chrX:15770932 | T | A | 4 | a0001c0001t0009g0031 a0001c0001t0009g0044 a0001c0001t0009g0046 others(1): Show |
4 | HG01884.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-1564T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15770932 | |||||||
| chrX:15771084 | G | T | 1 | a0001c0001t0026g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.341-1412G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771084 | |||||||
| chrX:15771201 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.341-1295C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771201 | |||||||
| chrX:15771204 | C | CA | 10 | a0001c0001t0001g0069 a0001c0001t0001g0121 a0001c0001t0001g0125 others(7): Show |
10 | HG02083.hp1 HG02280.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.341-1272dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771204 | ||||||
| chrX:15771204 | C | CAA | 92 | a0001c0001t0001g0114 a0001c0001t0005g0065 a0001c0001t0005g0084 others(89): Show |
98 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.341-1273_341-1272d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771204 | ||||||
| chrX:15771204 | C | CAAA | 12 | a0001c0001t0027g0250 a0001c0002t0002g0010 a0001c0002t0002g0012 others(9): Show |
13 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.341-1274_341-1272d others(5): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771204 | ||||||
| chrX:15771370 | CA | C | 148 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(145): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.341-1113delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771370 | ||||||
| chrX:15771423 | T | TTG | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.341-1055_341-1054d others(4): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771423 | ||||||
| chrX:15771435 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-1061G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771435 | |||||||
| chrX:15771593 | A | AT | 39 | a0001c0001t0001g0072 a0001c0001t0003g0003 a0001c0001t0003g0015 others(36): Show |
39 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.341-886dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771593 | ||||||
| chrX:15771593 | AT | A | 6 | a0001c0001t0001g0060 a0001c0001t0015g0024 a0001c0001t0016g0023 others(3): Show |
6 | HG01168.hp2 HG02523.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-886delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771593 | ||||||
| chrX:15771610 | T | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.341-886T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771610 | |||||||
| chrX:15771769 | C | T | 155 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(152): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.341-727C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771769 | |||||||
| chrX:15771864 | A | AT | 43 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0077 others(40): Show |
44 | HG01069.hp1 HG01106.hp1 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.341-621dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 15771864 | ||||||
| chrX:15771864 | A | G | 2 | a0001c0001t0010g0027 a0001c0001t0010g0028 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.341-632A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15771864 | |||||||
| chrX:15772124 | A | G | 3 | a0001c0001t0013g0251 a0001c0001t0013g0253 a0001c0001t0027g0250 |
3 | HG02451.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.341-372A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15772124 | |||||||
| chrX:15772210 | A | G | 30 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(27): Show |
30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.341-286A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15772210 | |||||||
| chrX:15772263 | G | T | 1 | a0001c0001t0013g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.341-233G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 3/7 | chrX | 15772263 | |||||||
| chrX:15772711 | A | G | 1 | a0001c0001t0010g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.459+97A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15772711 | |||||||
| chrX:15772890 | A | G | 2 | a0001c0001t0008g0043 a0001c0001t0008g0045 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.459+276A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15772890 | |||||||
| chrX:15772926 | G | T | 2 | a0001c0001t0015g0024 a0001c0001t0016g0023 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.459+312G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15772926 | |||||||
| chrX:15772957 | A | G | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.459+343A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15772957 | |||||||
| chrX:15773099 | A | G | 1 | a0001c0002t0002g0230 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.459+485A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773099 | |||||||
| chrX:15773110 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.459+496A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773110 | |||||||
| chrX:15773274 | T | G | 4 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(1): Show |
4 | HG01884.hp1 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+660T>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773274 | |||||||
| chrX:15773345 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0005g0068 |
2 | HG02683.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.459+731G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773345 | |||||||
| chrX:15773385 | A | G | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.459+771A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773385 | |||||||
| chrX:15773402 | AT | A | 22 | a0001c0001t0001g0093 a0001c0001t0001g0131 a0001c0001t0001g0152 others(19): Show |
22 | HG00597.hp1 HG01109.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+813delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 15773402 | ||||||
| chrX:15773402 | ATT | A | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.459+812_459+813del others(2): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 15773402 | ||||||
| chrX:15773534 | C | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0128 |
2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.460-768C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773534 | |||||||
| chrX:15773552 | A | G | 1 | a0001c0002t0002g0176 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.460-750A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773552 | |||||||
| chrX:15773661 | G | A | 1 | a0001c0001t0003g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.460-641G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773661 | |||||||
| chrX:15773667 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0123 |
2 | HG01168.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.460-635C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773667 | |||||||
| chrX:15773688 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.460-614C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773688 | |||||||
| chrX:15773771 | C | T | 1 | a0001c0001t0027g0250 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.460-531C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773771 | |||||||
| chrX:15773870 | A | T | 1 | a0001c0002t0002g0209 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.460-432A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773870 | |||||||
| chrX:15773943 | A | G | 1 | a0001c0001t0028g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.460-359A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773943 | |||||||
| chrX:15773975 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0156 |
3 | HG00438.hp2 HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.460-327G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15773975 | |||||||
| chrX:15774012 | G | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0039 a0001c0001t0008g0040 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-290G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15774012 | |||||||
| chrX:15774253 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.460-49G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 4/7 | chrX | 15774253 | |||||||
| chrX:15774404 | T | A | 155 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(152): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
splice_region_variant&intron_variant | LOW | c.555+7T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774404 | |||||||
| chrX:15774571 | C | G | 1 | a0001c0002t0002g0233 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.555+174C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774571 | |||||||
| chrX:15774577 | T | C | 1 | a0001c0001t0027g0250 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.555+180T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774577 | |||||||
| chrX:15774650 | A | G | 1 | a0001c0001t0003g0035 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.555+253A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774650 | |||||||
| chrX:15774806 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0155 |
2 | NA18946.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.555+409C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774806 | |||||||
| chrX:15774839 | C | T | 1 | a0001c0002t0002g0248 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.556-407C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774839 | |||||||
| chrX:15774855 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.556-391T>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 5/7 | chrX | 15774855 | |||||||
| chrX:15775365 | C | T | 1 | a0001c0002t0002g0195 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.618+57C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775365 | |||||||
| chrX:15775440 | C | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(5): Show |
12 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.618+132C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775440 | |||||||
| chrX:15775465 | GTCA | G | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.618+162_618+164del others(3): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 15775465 | ||||||
| chrX:15775480 | G | C | 1 | a0001c0001t0009g0057 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.618+172G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775480 | |||||||
| chrX:15775626 | G | T | 103 | a0001c0001t0005g0065 a0001c0001t0005g0084 a0001c0001t0012g0255 others(100): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.618+318G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775626 | |||||||
| chrX:15775651 | C | A | 116 | a0001c0001t0005g0065 a0001c0001t0005g0084 a0001c0001t0008g0025 others(113): Show |
123 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.618+343C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775651 | |||||||
| chrX:15775807 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0086 others(5): Show |
9 | HG02145.hp1 HG02293.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.618+499C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775807 | |||||||
| chrX:15775812 | A | C | 1 | a0001c0001t0001g0218 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.618+504A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775812 | |||||||
| chrX:15775847 | C | A | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.618+539C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775847 | |||||||
| chrX:15775885 | C | T | 1 | a0001c0002t0002g0212 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.618+577C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15775885 | |||||||
| chrX:15776066 | C | T | 1 | a0001c0001t0015g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.619-648C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776066 | |||||||
| chrX:15776067 | A | G | 1 | a0001c0001t0015g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.619-647A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776067 | |||||||
| chrX:15776155 | A | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
112 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.619-559A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776155 | |||||||
| chrX:15776193 | G | T | 6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-521G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776193 | |||||||
| chrX:15776263 | C | T | 2 | a0001c0002t0002g0187 a0001c0002t0025g0181 |
2 | HG00280.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.619-451C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776263 | |||||||
| chrX:15776290 | G | T | 1 | a0001c0001t0005g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.619-424G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776290 | |||||||
| chrX:15776326 | G | A | 3 | a0001c0001t0013g0251 a0001c0001t0013g0253 a0001c0001t0027g0250 |
3 | HG02451.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.619-388G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776326 | |||||||
| chrX:15776338 | C | CA | 105 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0081 others(102): Show |
112 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.619-357dupA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 15776338 | ||||||
| chrX:15776338 | C | CAA | 7 | a0001c0002t0002g0172 a0001c0002t0002g0179 a0001c0002t0002g0195 others(4): Show |
7 | HG01243.hp1 HG03688.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.619-358_619-357dup others(2): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 15776338 | ||||||
| chrX:15776404 | G | A | 30 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(27): Show |
30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.619-310G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776404 | |||||||
| chrX:15776545 | T | C | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.619-169T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776545 | |||||||
| chrX:15776614 | C | T | 7 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0001c0001t0001g0071 others(4): Show |
7 | HG00597.hp2 HG01168.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.619-100C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776614 | |||||||
| chrX:15776641 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.619-73G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776641 | |||||||
| chrX:15776653 | T | C | 6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-61T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 6/7 | chrX | 15776653 | |||||||
| chrX:15776882 | C | A | 1 | a0001c0001t0003g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.774+13C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15776882 | |||||||
| chrX:15776975 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.774+106A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15776975 | |||||||
| chrX:15777358 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.774+489T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777358 | |||||||
| chrX:15777431 | A | T | 1 | a0001c0002t0002g0238 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.774+562A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777431 | |||||||
| chrX:15777541 | C | G | 47 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(44): Show |
47 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.774+672C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777541 | |||||||
| chrX:15777680 | A | G | 1 | a0001c0001t0013g0253 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.774+811A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777680 | |||||||
| chrX:15777817 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0128 |
2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.774+948T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777817 | |||||||
| chrX:15777976 | C | T | 1 | a0001c0001t0026g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.774+1107C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15777976 | |||||||
| chrX:15778078 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.774+1209A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15778078 | |||||||
| chrX:15778367 | T | C | 6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+1498T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15778367 | |||||||
| chrX:15778396 | C | A | 2 | a0001c0002t0002g0208 a0001c0002t0002g0228 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.774+1527C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15778396 | |||||||
| chrX:15778632 | G | A | 3 | a0001c0002t0002g0197 a0001c0002t0002g0207 a0001c0002t0004g0231 |
3 | HG02523.hp2 NA18969.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.774+1763G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15778632 | |||||||
| chrX:15778828 | A | G | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.774+1959A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15778828 | |||||||
| chrX:15779304 | C | A | 1 | a0001c0002t0002g0226 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.774+2435C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15779304 | |||||||
| chrX:15779346 | A | T | 1 | a0001c0002t0007g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.774+2477A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15779346 | |||||||
| chrX:15779631 | G | T | 29 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(26): Show |
29 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.774+2762G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15779631 | |||||||
| chrX:15779638 | A | C | 1 | a0001c0001t0018g0095 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.774+2769A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15779638 | |||||||
| chrX:15779927 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.775-2558C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15779927 | |||||||
| chrX:15780081 | C | T | 78 | a0001c0002t0002g0001 a0001c0002t0002g0009 a0001c0002t0002g0010 others(75): Show |
85 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.775-2404C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780081 | |||||||
| chrX:15780104 | A | G | 30 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(27): Show |
30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.775-2381A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780104 | |||||||
| chrX:15780134 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0086 others(3): Show |
7 | HG02145.hp1 HG02976.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-2351A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780134 | |||||||
| chrX:15780196 | A | T | 2 | a0001c0001t0010g0027 a0001c0001t0010g0028 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.775-2289A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780196 | |||||||
| chrX:15780276 | C | CG | 30 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(27): Show |
30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.775-2209_775-2208i others(3): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780276 | |||||||
| chrX:15780277 | A | T | 30 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(27): Show |
30 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.775-2208A>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780277 | |||||||
| chrX:15780277 | AT | A | 106 | a0001c0001t0001g0080 a0001c0001t0001g0119 a0001c0001t0010g0026 others(103): Show |
113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.775-2193delT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15780277 | ||||||
| chrX:15780318 | G | C | 3 | a0001c0001t0010g0026 a0001c0001t0010g0027 a0001c0001t0010g0028 |
3 | HG02280.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.775-2167G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780318 | |||||||
| chrX:15780340 | T | C | 1 | a0001c0002t0002g0237 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.775-2145T>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780340 | |||||||
| chrX:15780367 | C | G | 41 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(38): Show |
41 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.775-2118C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780367 | |||||||
| chrX:15780403 | G | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG02630.hp2 HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.775-2082G>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780403 | |||||||
| chrX:15780460 | A | G | 41 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(38): Show |
41 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.775-2025A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780460 | |||||||
| chrX:15780523 | C | T | 6 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-1962C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780523 | |||||||
| chrX:15780626 | A | G | 2 | a0001c0002t0002g0208 a0001c0002t0002g0228 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.775-1859A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780626 | |||||||
| chrX:15780681 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.775-1804C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780681 | |||||||
| chrX:15780776 | G | A | 3 | a0001c0002t0002g0220 a0001c0002t0002g0244 a0001c0002t0004g0221 |
3 | HG02109.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.775-1709G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780776 | |||||||
| chrX:15780976 | G | C | 41 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(38): Show |
41 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.775-1509G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15780976 | |||||||
| chrX:15780981 | C | CT | 13 | a0001c0001t0006g0096 a0001c0001t0006g0097 a0001c0001t0006g0098 others(10): Show |
13 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.775-1490dupT | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15780981 | ||||||
| chrX:15781028 | G | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0140 |
2 | NA18952.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.775-1457G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781028 | |||||||
| chrX:15781085 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.775-1400A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781085 | |||||||
| chrX:15781104 | A | C | 1 | a0001c0002t0007g0236 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.775-1381A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781104 | |||||||
| chrX:15781123 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.775-1362A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781123 | |||||||
| chrX:15781780 | C | T | 1 | a0001c0002t0002g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.775-705C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781780 | |||||||
| chrX:15781865 | G | C | 2 | a0001c0001t0015g0024 a0001c0001t0016g0023 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.775-620G>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781865 | |||||||
| chrX:15781890 | G | A | 1 | a0001c0001t0008g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.775-595G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781890 | |||||||
| chrX:15781918 | TA | T | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.775-559delA | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15781918 | ||||||
| chrX:15781925 | AAC | A | 101 | a0001c0001t0012g0255 a0001c0001t0012g0256 a0001c0001t0013g0251 others(98): Show |
108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.775-558_775-557del others(2): Show |
CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 15781925 | ||||||
| chrX:15781926 | A | C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0090 a0001c0001t0001g0147 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-559A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781926 | |||||||
| chrX:15781927 | C | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0090 a0001c0001t0001g0147 others(2): Show |
5 | HG01106.hp1 HG01884.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-558C>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781927 | |||||||
| chrX:15781928 | A | C | 101 | a0001c0001t0012g0255 a0001c0001t0012g0256 a0001c0001t0013g0251 others(98): Show |
108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.775-557A>C | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15781928 | |||||||
| chrX:15782074 | G | A | 1 | a0001c0001t0008g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.775-411G>A | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15782074 | |||||||
| chrX:15782278 | C | T | 1 | a0001c0002t0002g0192 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.775-207C>T | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15782278 | |||||||
| chrX:15782282 | A | G | 41 | a0001c0001t0003g0003 a0001c0001t0003g0015 a0001c0001t0003g0016 others(38): Show |
41 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.775-203A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15782282 | |||||||
| chrX:15782475 | C | G | 1 | a0001c0001t0028g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.775-10C>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15782475 | |||||||
| chrX:15782477 | A | G | 94 | a0001c0002t0002g0001 a0001c0002t0002g0009 a0001c0002t0002g0010 others(91): Show |
101 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
splice_region_variant&intron_variant | LOW | c.775-8A>G | CA5B | ENSG00000169239.14 | transcript | ENST00000318636.8 | protein_coding | 7/7 | chrX | 15782477 |