Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54960 |
| ensemblid | ENSG00000046647.14 |
| hgncid | 26044 |
| symbol | GEMIN8 |
| name | gem nuclear organelle associated protein 8 |
| refseq_nuc | NM_001042479.2 |
| refseq_prot | NP_001035944.1 |
| ensembl_nuc | ENST00000680255.1 |
| ensembl_prot | ENSP00000505429.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 14006726 |
| end | 14029892 |
| strand | - |
| ver | v1.2 |
| region | chrX:14006726-14029892 |
| region5000 | chrX:14001726-14034892 |
| regionname0 | GEMIN8_chrX_14006726_14029892 |
| regionname5000 | GEMIN8_chrX_14001726_14034892 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 242 | 252 | 71 | 53 | 90 | 9 | 27 | 69 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | MAAVK others(237): Show |
chrX | 14001726 | 14034892 |
| a0002 | 0/0 | 242 | 19 | 0 | 2 | 16 | 0 | 1 | 14 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | MAAVK others(237): Show |
chrX | 14001726 | 14034892 |
| a0003 | 0/0 | 242 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | MAAVK others(237): Show |
chrX | 14001726 | 14034892 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 726 | 250 | 69 | 53 | 90 | 9 | 27 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | ATGGC others(721): Show |
chrX | 14001726 | 14034892 | ||
| a0001c0004 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | ATGGC others(721): Show |
chrX | 14001726 | 14034892 | ||
| a0001c0005 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | ATGGC others(721): Show |
chrX | 14001726 | 14034892 | ||
| a0002c0002 | 0/0 | 726 | 19 | 0 | 2 | 16 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | ATGGC others(721): Show |
chrX | 14001726 | 14034892 | ||
| a0003c0003 | 0/0 | 726 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | ATGGC others(721): Show |
chrX | 14001726 | 14034892 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3147 | 189 | 35 | 37 | 88 | 8 | 19 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0001t0002 | 0/0 | 3147 | 38 | 17 | 13 | 0 | 1 | 7 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0001t0003 | 0/0 | 3147 | 8 | 8 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0001t0004 | 0/0 | 3147 | 7 | 6 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0001t0006 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0001t0007 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0001t0008 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0001t0009 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0001t0010 | 0/0 | 3147 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0001t0011 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0001t0012 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0001t0013 | 0/0 | 3147 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0004t0004 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0001c0005t0002 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0002c0002t0002 | 0/0 | 3147 | 18 | 0 | 2 | 15 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0002c0002t0005 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| a0003c0003t0001 | 0/0 | 3147 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | AGTCG others(3142): Show |
chrX | 14001726 | 14034892 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/1 | 35 | 1 | 7 | 21 | 1 | 3 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0002 | 0/0 | 10 | 1 | 8 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 0 | 6 | 1 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0014 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0015 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0003 | 0/0 | 8 | 3 | 3 | 0 | 0 | 2 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0004g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0009g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0011g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0012g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0001t0013g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0004t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0001c0005t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0002c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0042 | EUR | FIN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00733 | hp1 | a0001 | c0001 | t0013 | g0081 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01081 | hp1 | a0001 | c0001 | t0010 | g0100 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0155 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0153 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0133 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | KHV | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03491 | hp2 | a0003 | c0003 | t0001 | g0094 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0095 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03540 | hp1 | a0001 | c0004 | t0004 | g0142 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03579 | hp1 | a0001 | c0005 | t0002 | g0130 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03831 | hp2 | a0001 | c0001 | t0012 | g0038 | SAS | BEB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | STU | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0157 | SAS | STU | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | YRI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0050 | AFR | YRI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0091 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19010 | hp2 | a0002 | c0002 | t0005 | g0154 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | LWK | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19075 | hp1 | a0001 | c0001 | t0011 | g0082 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ASW | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ASW | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | GIH | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | USA | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | USA | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | USA | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0148 | AFR | LWK | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | GEMIN8_chrX_14001726_14034892 | GEMIN8 | chrX | 14001726 | 14034892 |
| 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:14009058 | T | A | 1 | a0002 | 19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
missense_variant | MODERATE | c.584A>T | p.Glu195Val | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 815/3147 | 584/729 | 195/242 | chrX | 14009058 | |||
| chrX:14020459 | C | A | 1 | a0003 | 2 | HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.91G>T | p.Ala31Ser | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/5 | 322/3147 | 91/729 | 31/242 | chrX | 14020459 |
| 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:14009096 | G | C | 1 | a0001c0004 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.546C>G | p.Thr182Thr | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 777/3147 | 546/729 | 182/242 | chrX | 14009096 | |||
| chrX:14020415 | G | C | 1 | a0001c0005 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.135C>G | p.Ala45Ala | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/5 | 366/3147 | 135/729 | 45/242 | chrX | 14020415 |
| 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:14007033 | A | T | 1 | a0001c0001t0011 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1880T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1880 | chrX | 14007033 | ||||||
| chrX:14007140 | C | A | 1 | a0001c0001t0011 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1773G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1773 | chrX | 14007140 | ||||||
| chrX:14007543 | T | C | 1 | a0001c0001t0002 | 4 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1370A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1370 | chrX | 14007543 | ||||||
| chrX:14007567 | A | G | 1 | a0001c0001t0010 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1346T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1346 | chrX | 14007567 | ||||||
| chrX:14007677 | G | A | 1 | a0001c0001t0003 | 8 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1236C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1236 | chrX | 14007677 | ||||||
| chrX:14007688 | C | T | 1 | a0001c0001t0012 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1225 | chrX | 14007688 | ||||||
| chrX:14007818 | C | T | 1 | a0001c0001t0009 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1095 | chrX | 14007818 | ||||||
| chrX:14007821 | C | T | 1 | a0001c0001t0008 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1092G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1092 | chrX | 14007821 | ||||||
| chrX:14007836 | G | T | 1 | a0001c0001t0011 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077C>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 1077 | chrX | 14007836 | ||||||
| chrX:14008248 | A | C | 1 | a0001c0001t0007 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*665T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 665 | chrX | 14008248 | ||||||
| chrX:14008268 | C | A | 2 | a0001c0001t0004 a0001c0004t0004 |
8 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*645G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 645 | chrX | 14008268 | ||||||
| chrX:14008272 | C | T | 1 | a0001c0001t0006 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*641G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 641 | chrX | 14008272 | ||||||
| chrX:14008301 | A | T | 1 | a0001c0001t0011 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*612T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 612 | chrX | 14008301 | ||||||
| chrX:14008302 | T | A | 1 | a0001c0001t0011 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*611A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 611 | chrX | 14008302 | ||||||
| chrX:14008304 | A | G | 1 | a0001c0001t0011 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*609T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 609 | chrX | 14008304 | ||||||
| chrX:14008305 | G | A | 1 | a0001c0001t0011 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*608C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 608 | chrX | 14008305 | ||||||
| chrX:14008398 | T | C | 7 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0012 others(4): Show |
67 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*515A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 515 | chrX | 14008398 | ||||||
| chrX:14008485 | A | G | 1 | a0001c0001t0003 | 8 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*428T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 428 | chrX | 14008485 | ||||||
| chrX:14008822 | G | A | 1 | a0001c0001t0013 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 91 | chrX | 14008822 | ||||||
| chrX:14008838 | A | G | 1 | a0002c0002t0005 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*75T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 5/5 | 75 | chrX | 14008838 |
| 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:14009474 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.473-305G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009474 | |||||||
| chrX:14009563 | G | A | 1 | a0001c0001t0011g0082 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.473-394C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009563 | |||||||
| chrX:14009705 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.473-536C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009705 | |||||||
| chrX:14009942 | C | T | 2 | a0001c0001t0003g0049 a0001c0001t0009g0050 |
2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.473-773G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14009942 | |||||||
| chrX:14010028 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0083 a0001c0001t0001g0121 |
4 | HG02004.hp1 HG02300.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.473-859T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14010028 | |||||||
| chrX:14010526 | G | A | 7 | a0001c0001t0002g0031 a0001c0001t0002g0143 a0001c0001t0002g0144 others(4): Show |
12 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.473-1357C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14010526 | |||||||
| chrX:14010992 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0085 a0001c0001t0001g0102 |
6 | HG01884.hp1 HG02486.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.473-1823C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14010992 | |||||||
| chrX:14011043 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.473-1874G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011043 | |||||||
| chrX:14011065 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.473-1896G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011065 | |||||||
| chrX:14011516 | C | CT | 22 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0054 others(19): Show |
28 | HG00558.hp1 HG00639.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.473-2348dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | |||||||
| chrX:14011516 | C | CTTTTTTT | 4 | a0001c0001t0001g0030 a0001c0001t0001g0134 a0001c0001t0003g0119 others(1): Show |
5 | HG01884.hp2 HG02055.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-2354_473-2348d others(9): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | |||||||
| chrX:14011516 | C | CTTTTTTT others(1): Show |
7 | a0001c0001t0001g0132 a0001c0001t0003g0028 a0001c0001t0003g0049 others(4): Show |
8 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.473-2355_473-2348d others(10): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | |||||||
| chrX:14011516 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.473-2357_473-2348d others(12): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | |||||||
| chrX:14011516 | CT | C | 13 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0052 others(10): Show |
14 | HG01081.hp1 HG01993.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.473-2348delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | |||||||
| chrX:14011516 | CTTTT | C | 20 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0019 others(17): Show |
35 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.473-2351_473-2348d others(6): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | |||||||
| chrX:14011516 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0055 a0001c0001t0002g0011 a0001c0001t0002g0029 others(3): Show |
10 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.473-2358_473-2348d others(13): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | |||||||
| chrX:14011516 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.473-2360_473-2348d others(15): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011516 | |||||||
| chrX:14011827 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.473-2658T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14011827 | |||||||
| chrX:14012081 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.473-2912G>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012081 | |||||||
| chrX:14012131 | A | AT | 5 | a0001c0001t0001g0025 a0001c0001t0001g0093 a0001c0001t0001g0109 others(2): Show |
6 | HG00323.hp1 HG01346.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.473-2963dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012131 | |||||||
| chrX:14012292 | AT | A | 23 | a0001c0001t0001g0053 a0001c0001t0001g0134 a0001c0001t0001g0138 others(20): Show |
33 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.473-3124delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012292 | |||||||
| chrX:14012292 | ATT | A | 21 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0019 others(18): Show |
35 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.473-3125_473-3124d others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012292 | |||||||
| chrX:14012324 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.473-3155T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012324 | |||||||
| chrX:14012403 | C | T | 15 | a0001c0001t0001g0138 a0002c0002t0002g0017 a0002c0002t0002g0032 others(12): Show |
20 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.473-3234G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012403 | |||||||
| chrX:14012855 | T | TA | 3 | a0001c0001t0002g0029 a0001c0001t0002g0129 a0001c0001t0002g0131 |
4 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-3687dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012855 | |||||||
| chrX:14012857 | T | G | 3 | a0001c0001t0002g0029 a0001c0001t0002g0129 a0001c0001t0002g0131 |
4 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-3688A>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012857 | |||||||
| chrX:14012857 | T | TG | 40 | a0001c0001t0001g0086 a0001c0001t0001g0138 a0001c0001t0002g0003 others(37): Show |
63 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.473-3689dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14012857 | |||||||
| chrX:14013320 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.473-4151A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013320 | |||||||
| chrX:14013490 | A | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0059 a0001c0001t0001g0074 others(3): Show |
12 | HG00558.hp1 HG02027.hp1 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.473-4321T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013490 | |||||||
| chrX:14013508 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.473-4339C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013508 | |||||||
| chrX:14013581 | A | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0027 others(22): Show |
36 | HG00558.hp1 HG00639.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.473-4412T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013581 | |||||||
| chrX:14013788 | GT | G | 44 | a0001c0001t0001g0053 a0001c0001t0001g0062 a0001c0001t0001g0066 others(41): Show |
68 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.473-4620delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013788 | |||||||
| chrX:14013882 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.473-4713G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013882 | |||||||
| chrX:14013891 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.473-4722A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14013891 | |||||||
| chrX:14014175 | C | T | 57 | a0001c0001t0001g0030 a0001c0001t0001g0115 a0001c0001t0001g0132 others(54): Show |
84 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.473-5006G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014175 | |||||||
| chrX:14014179 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.473-5010A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014179 | |||||||
| chrX:14014186 | C | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0134 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.473-5017G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014186 | |||||||
| chrX:14014361 | C | G | 1 | a0001c0001t0002g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.473-5192G>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014361 | |||||||
| chrX:14014497 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.473-5328G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014497 | |||||||
| chrX:14014824 | TTGAG | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0059 others(11): Show |
22 | HG00558.hp1 HG00639.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.472+5250_472+5253d others(6): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014824 | |||||||
| chrX:14014838 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.472+5240G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014838 | |||||||
| chrX:14014932 | C | T | 14 | a0002c0002t0002g0017 a0002c0002t0002g0032 a0002c0002t0002g0033 others(11): Show |
19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+5146G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14014932 | |||||||
| chrX:14015941 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.472+4137T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14015941 | |||||||
| chrX:14015946 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.472+4132G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14015946 | |||||||
| chrX:14015992 | A | AG | 50 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0134 others(47): Show |
76 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.472+4085dupC | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14015992 | |||||||
| chrX:14016054 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.472+4024T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016054 | |||||||
| chrX:14016218 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.472+3860C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016218 | |||||||
| chrX:14016572 | G | A | 6 | a0001c0001t0003g0028 a0001c0001t0003g0116 a0001c0001t0003g0117 others(3): Show |
7 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.472+3506C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016572 | |||||||
| chrX:14016573 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.472+3505G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016573 | |||||||
| chrX:14016693 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.472+3385T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016693 | |||||||
| chrX:14016844 | C | CA | 8 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0088 others(5): Show |
14 | HG00621.hp1 HG01175.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.472+3233dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016844 | |||||||
| chrX:14016844 | CA | C | 11 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0069 others(8): Show |
11 | HG00323.hp2 HG01099.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.472+3233delT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016844 | |||||||
| chrX:14016844 | CAAAAAAA | C | 7 | a0002c0002t0002g0017 a0002c0002t0002g0034 a0002c0002t0002g0046 others(4): Show |
10 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.472+3227_472+3233d others(9): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016844 | |||||||
| chrX:14016848 | A | ATATATAT | 2 | a0002c0002t0002g0032 a0002c0002t0002g0149 |
3 | NA18939.hp1 NA18942.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.472+3229_472+3230i others(9): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016848 | |||||||
| chrX:14016850 | A | T | 3 | a0002c0002t0002g0032 a0002c0002t0002g0149 a0002c0002t0002g0150 |
4 | NA18939.hp1 NA18942.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+3228T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016850 | |||||||
| chrX:14016852 | A | T | 4 | a0002c0002t0002g0032 a0002c0002t0002g0149 a0002c0002t0002g0150 others(1): Show |
5 | NA18939.hp1 NA18942.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+3226T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016852 | |||||||
| chrX:14016854 | A | T | 6 | a0002c0002t0002g0032 a0002c0002t0002g0033 a0002c0002t0002g0149 others(3): Show |
8 | NA18939.hp1 NA18942.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.472+3224T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016854 | |||||||
| chrX:14016856 | A | T | 13 | a0002c0002t0002g0017 a0002c0002t0002g0032 a0002c0002t0002g0033 others(10): Show |
18 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.472+3222T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016856 | |||||||
| chrX:14016858 | A | T | 14 | a0002c0002t0002g0017 a0002c0002t0002g0032 a0002c0002t0002g0033 others(11): Show |
19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+3220T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016858 | |||||||
| chrX:14016860 | A | T | 14 | a0002c0002t0002g0017 a0002c0002t0002g0032 a0002c0002t0002g0033 others(11): Show |
19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+3218T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016860 | |||||||
| chrX:14016862 | A | T | 14 | a0002c0002t0002g0017 a0002c0002t0002g0032 a0002c0002t0002g0033 others(11): Show |
19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+3216T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016862 | |||||||
| chrX:14016864 | A | T | 14 | a0002c0002t0002g0017 a0002c0002t0002g0032 a0002c0002t0002g0033 others(11): Show |
19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+3214T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016864 | |||||||
| chrX:14016865 | AAATAT | A | 6 | a0001c0001t0002g0040 a0001c0001t0002g0143 a0001c0001t0003g0116 others(3): Show |
6 | HG01975.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.472+3208_472+3212d others(7): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016865 | |||||||
| chrX:14016866 | A | AAT | 18 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(15): Show |
21 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.472+3210_472+3211d others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | |||||||
| chrX:14016866 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0014 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.472+3202_472+3211d others(12): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | |||||||
| chrX:14016866 | A | AT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0122 others(2): Show |
5 | HG00735.hp2 HG01081.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.472+3211_472+3212i others(3): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | |||||||
| chrX:14016866 | A | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(24): Show |
38 | HG00597.hp1 HG00735.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.472+3212T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | |||||||
| chrX:14016866 | AATAT | A | 13 | a0001c0001t0001g0134 a0001c0001t0002g0003 a0001c0001t0002g0019 others(10): Show |
18 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.472+3208_472+3211d others(6): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | |||||||
| chrX:14016866 | AATATAT | A | 8 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0002g0011 others(5): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.472+3206_472+3211d others(8): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016866 | |||||||
| chrX:14016867 | AT | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(2): Show |
5 | HG02083.hp1 HG02897.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.472+3210delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016867 | |||||||
| chrX:14016867 | ATAT | A | 4 | a0001c0001t0001g0030 a0001c0001t0003g0049 a0001c0001t0008g0148 others(1): Show |
5 | HG03098.hp1 HG03516.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.472+3208_472+3210d others(5): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016867 | |||||||
| chrX:14016867 | ATATAT | A | 9 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0020 others(6): Show |
16 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.472+3206_472+3210d others(7): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016867 | |||||||
| chrX:14016868 | T | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(7): Show |
15 | HG00642.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.472+3210A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016868 | |||||||
| chrX:14016872 | T | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0134 a0001c0001t0002g0041 others(4): Show |
8 | HG01884.hp2 HG01993.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.472+3206A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016872 | |||||||
| chrX:14016874 | T | A | 10 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0002g0011 others(7): Show |
15 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.472+3204A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016874 | |||||||
| chrX:14016908 | C | T | 14 | a0002c0002t0002g0017 a0002c0002t0002g0032 a0002c0002t0002g0033 others(11): Show |
19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+3170G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016908 | |||||||
| chrX:14016956 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.472+3122A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14016956 | |||||||
| chrX:14017128 | T | A | 1 | a0001c0001t0002g0042 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.472+2950A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017128 | |||||||
| chrX:14017167 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.472+2911C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017167 | |||||||
| chrX:14017375 | A | G | 43 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0002g0003 others(40): Show |
67 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.472+2703T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017375 | |||||||
| chrX:14017396 | A | G | 2 | a0001c0001t0003g0049 a0001c0001t0009g0050 |
2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.472+2682T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017396 | |||||||
| chrX:14017483 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.472+2595C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017483 | |||||||
| chrX:14017516 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.472+2562G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017516 | |||||||
| chrX:14017679 | A | C | 59 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0067 others(56): Show |
86 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.472+2399T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017679 | |||||||
| chrX:14017699 | A | G | 5 | a0001c0001t0002g0011 a0001c0001t0002g0029 a0001c0001t0002g0129 others(2): Show |
9 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.472+2379T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017699 | |||||||
| chrX:14017979 | C | A | 1 | a0001c0001t0008g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.472+2099G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017979 | |||||||
| chrX:14017987 | T | C | 23 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0019 others(20): Show |
39 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.472+2091A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14017987 | |||||||
| chrX:14018444 | G | C | 14 | a0002c0002t0002g0017 a0002c0002t0002g0032 a0002c0002t0002g0033 others(11): Show |
19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+1634C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14018444 | |||||||
| chrX:14018537 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.472+1541C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14018537 | |||||||
| chrX:14018574 | G | C | 1 | a0001c0001t0006g0091 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.472+1504C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14018574 | |||||||
| chrX:14018766 | CT | C | 21 | a0001c0001t0001g0030 a0001c0001t0001g0062 a0001c0001t0001g0071 others(18): Show |
27 | HG00597.hp1 HG01069.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.472+1311delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14018766 | |||||||
| chrX:14019253 | A | G | 42 | a0001c0001t0001g0138 a0001c0001t0002g0003 a0001c0001t0002g0011 others(39): Show |
66 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.472+825T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019253 | |||||||
| chrX:14019315 | G | A | 3 | a0002c0002t0002g0017 a0002c0002t0002g0046 a0002c0002t0002g0156 |
5 | HG00597.hp1 HG02523.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+763C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019315 | |||||||
| chrX:14019419 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.472+659G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019419 | |||||||
| chrX:14019545 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0093 |
3 | HG00323.hp1 HG01346.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.472+533C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019545 | |||||||
| chrX:14019592 | G | A | 15 | a0001c0001t0001g0138 a0002c0002t0002g0017 a0002c0002t0002g0032 others(12): Show |
20 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.472+486C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019592 | |||||||
| chrX:14019723 | TATATAAA others(9): Show |
T | 1 | a0001c0001t0001g0072 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.472+339_472+354del others(16): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019723 | |||||||
| chrX:14019772 | A | G | 42 | a0001c0001t0001g0138 a0001c0001t0002g0003 a0001c0001t0002g0011 others(39): Show |
66 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.472+306T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019772 | |||||||
| chrX:14019786 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.472+292C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019786 | |||||||
| chrX:14019993 | T | C | 14 | a0002c0002t0002g0017 a0002c0002t0002g0032 a0002c0002t0002g0033 others(11): Show |
19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.472+85A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 4/4 | chrX | 14019993 | |||||||
| chrX:14020653 | C | CT | 44 | a0001c0001t0001g0138 a0001c0001t0002g0003 a0001c0001t0002g0011 others(41): Show |
69 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.16-120_16-119insA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14020653 | |||||||
| chrX:14020819 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0134 others(2): Show |
6 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-285C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14020819 | |||||||
| chrX:14021100 | T | C | 7 | a0001c0001t0003g0028 a0001c0001t0003g0049 a0001c0001t0003g0116 others(4): Show |
8 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+364A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021100 | |||||||
| chrX:14021147 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG00323.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.15+317T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021147 | |||||||
| chrX:14021196 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0096 |
5 | HG02132.hp1 HG02523.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+268C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021196 | |||||||
| chrX:14021225 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.15+239A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021225 | |||||||
| chrX:14021230 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0071 |
3 | HG00438.hp1 HG02135.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.15+234G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021230 | |||||||
| chrX:14021312 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.15+152C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 3/4 | chrX | 14021312 | |||||||
| chrX:14021646 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-33-135G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021646 | |||||||
| chrX:14021759 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-33-248A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021759 | |||||||
| chrX:14021814 | G | GTA | 24 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(21): Show |
48 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-33-305_-33-304dup others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | |||||||
| chrX:14021814 | G | GTATA | 8 | a0001c0001t0001g0016 a0001c0001t0001g0051 a0001c0001t0001g0107 others(5): Show |
10 | HG01070.hp2 HG02109.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-33-307_-33-304dup others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | |||||||
| chrX:14021814 | G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0146 a0001c0001t0003g0049 |
2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-33-313_-33-304dup others(10): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | |||||||
| chrX:14021814 | G | GTATATAT others(5): Show |
5 | a0001c0001t0001g0022 a0001c0001t0001g0066 a0001c0001t0001g0112 others(2): Show |
6 | HG01074.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-315_-33-304dup others(12): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | |||||||
| chrX:14021814 | G | GTATATAT others(7): Show |
4 | a0001c0001t0001g0048 a0001c0001t0001g0147 a0001c0001t0003g0118 others(1): Show |
4 | HG02293.hp1 HG02922.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33-317_-33-304dup others(14): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | |||||||
| chrX:14021814 | G | GTATATAT others(9): Show |
2 | a0001c0001t0003g0028 a0001c0001t0003g0120 |
3 | HG02622.hp1 HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-33-319_-33-304dup others(16): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | |||||||
| chrX:14021814 | G | GTGTATAT others(11): Show |
1 | a0001c0001t0001g0067 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-33-304_-33-303ins others(18): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | |||||||
| chrX:14021814 | GTA | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0063 others(2): Show |
8 | HG00558.hp2 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33-305_-33-304del others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | |||||||
| chrX:14021814 | GTATA | G | 6 | a0001c0001t0001g0068 a0001c0001t0001g0132 a0001c0001t0001g0134 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-307_-33-304del others(4): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | |||||||
| chrX:14021814 | GTATATAT others(9): Show |
G | 29 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0018 others(26): Show |
49 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.-33-319_-33-304del others(16): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021814 | |||||||
| chrX:14021816 | A | G | 14 | a0001c0001t0001g0138 a0002c0002t0002g0017 a0002c0002t0002g0032 others(11): Show |
19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.-33-305T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021816 | |||||||
| chrX:14021819 | T | TATATATA others(38): Show |
1 | a0001c0001t0001g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-33-309_-33-308ins others(45): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021819 | |||||||
| chrX:14021832 | A | G | 29 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0018 others(26): Show |
49 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.-33-321T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021832 | |||||||
| chrX:14021913 | TATGTATA | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0068 a0001c0001t0001g0132 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33-409_-33-403del others(7): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021913 | |||||||
| chrX:14021965 | CAT | C | 8 | a0001c0001t0001g0060 a0001c0001t0003g0028 a0001c0001t0003g0049 others(5): Show |
9 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-456_-33-455del others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14021965 | |||||||
| chrX:14022004 | TATGTATG others(7): Show |
T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-33-507_-33-494del others(14): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022004 | |||||||
| chrX:14022048 | G | GTA | 10 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(7): Show |
21 | HG00140.hp1 HG01168.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.-33-539_-33-538dup others(2): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022048 | |||||||
| chrX:14022338 | T | C | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-33-827A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022338 | |||||||
| chrX:14022362 | C | T | 1 | a0001c0001t0004g0141 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-33-851G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022362 | |||||||
| chrX:14022599 | C | CT | 4 | a0001c0001t0002g0019 a0001c0001t0002g0035 a0001c0001t0002g0036 others(1): Show |
5 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33-1089dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022599 | |||||||
| chrX:14022599 | CT | C | 15 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0137 others(12): Show |
20 | HG02015.hp1 HG02145.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-33-1089delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14022599 | |||||||
| chrX:14023041 | A | G | 1 | a0001c0001t0002g0018 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-33-1530T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023041 | |||||||
| chrX:14023156 | T | G | 1 | a0001c0001t0002g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-33-1645A>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023156 | |||||||
| chrX:14023224 | G | A | 15 | a0001c0001t0001g0138 a0002c0002t0002g0017 a0002c0002t0002g0032 others(12): Show |
20 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.-33-1713C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023224 | |||||||
| chrX:14023382 | C | CT | 21 | a0001c0001t0001g0030 a0001c0001t0001g0065 a0001c0001t0001g0132 others(18): Show |
27 | HG00597.hp1 HG01884.hp2 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.-33-1872dupA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023382 | |||||||
| chrX:14023382 | C | T | 1 | a0001c0001t0008g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-33-1871G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023382 | |||||||
| chrX:14023382 | CT | C | 4 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0002g0031 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-1872delA | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023382 | |||||||
| chrX:14023402 | C | T | 5 | a0001c0001t0002g0011 a0001c0001t0002g0029 a0001c0001t0002g0129 others(2): Show |
9 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-1891G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023402 | |||||||
| chrX:14023527 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-33-2016C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023527 | |||||||
| chrX:14023648 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-33-2137T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023648 | |||||||
| chrX:14023672 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0134 others(2): Show |
6 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-2161G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023672 | |||||||
| chrX:14023747 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-33-2236C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14023747 | |||||||
| chrX:14024261 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-34+1879C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024261 | |||||||
| chrX:14024283 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0158 |
2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-34+1857C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024283 | |||||||
| chrX:14024367 | C | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0063 a0001c0001t0001g0064 others(4): Show |
8 | HG00639.hp2 HG01884.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+1773G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024367 | |||||||
| chrX:14024396 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0134 others(2): Show |
6 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+1744C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024396 | |||||||
| chrX:14024522 | A | C | 23 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0019 others(20): Show |
39 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-34+1618T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024522 | |||||||
| chrX:14024574 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-34+1566G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14024574 | |||||||
| chrX:14025023 | T | C | 49 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0134 others(46): Show |
75 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-34+1117A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025023 | |||||||
| chrX:14025055 | T | A | 1 | a0001c0001t0001g0059 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-34+1085A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025055 | |||||||
| chrX:14025348 | A | C | 1 | a0001c0001t0001g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-34+792T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025348 | |||||||
| chrX:14025412 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-34+728G>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025412 | |||||||
| chrX:14025419 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18974.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-34+721A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025419 | |||||||
| chrX:14025439 | C | A | 44 | a0001c0001t0001g0138 a0001c0001t0002g0003 a0001c0001t0002g0011 others(41): Show |
69 | HG00280.hp1 HG00597.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.-34+701G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025439 | |||||||
| chrX:14025475 | A | T | 23 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0019 others(20): Show |
39 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-34+665T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14025475 | |||||||
| chrX:14026099 | TTGGTCTT others(3): Show |
T | 1 | a0001c0001t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-34+31_-34+40delTT others(8): Show |
GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14026099 | |||||||
| chrX:14026123 | G | A | 23 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0019 others(20): Show |
39 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-34+17C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 2/4 | chrX | 14026123 | |||||||
| chrX:14026339 | G | A | 29 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0018 others(26): Show |
49 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.-115-118C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14026339 | |||||||
| chrX:14026396 | A | T | 1 | a0001c0001t0001g0059 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-115-175T>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14026396 | |||||||
| chrX:14026424 | C | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0132 a0001c0001t0001g0134 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-115-203G>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14026424 | |||||||
| chrX:14026712 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(8): Show |
22 | HG00140.hp1 HG01168.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.-115-491T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14026712 | |||||||
| chrX:14027263 | T | C | 1 | a0002c0002t0002g0157 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-115-1042A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14027263 | |||||||
| chrX:14027360 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-115-1139T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14027360 | |||||||
| chrX:14027488 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-115-1267A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14027488 | |||||||
| chrX:14027809 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
13 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.-115-1588C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14027809 | |||||||
| chrX:14028006 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-116+1771T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028006 | |||||||
| chrX:14028475 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-116+1302C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028475 | |||||||
| chrX:14028619 | T | TA | 24 | a0001c0001t0001g0140 a0001c0001t0002g0003 a0001c0001t0002g0018 others(21): Show |
40 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.-116+1157dupT | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028619 | |||||||
| chrX:14028628 | A | C | 2 | a0001c0001t0003g0049 a0001c0001t0009g0050 |
2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-116+1149T>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028628 | |||||||
| chrX:14028643 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02572.hp1 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-116+1134A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028643 | |||||||
| chrX:14028783 | T | C | 1 | a0001c0001t0008g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-116+994A>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028783 | |||||||
| chrX:14028936 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0048 |
4 | HG02293.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-116+841T>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14028936 | |||||||
| chrX:14029112 | G | C | 14 | a0002c0002t0002g0017 a0002c0002t0002g0032 a0002c0002t0002g0033 others(11): Show |
19 | HG00597.hp1 HG01975.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.-116+665C>G | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14029112 | |||||||
| chrX:14029152 | C | G | 1 | a0002c0002t0002g0046 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-116+625G>C | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14029152 | |||||||
| chrX:14029242 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-116+535C>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14029242 | |||||||
| chrX:14029334 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-116+443A>T | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14029334 | |||||||
| chrX:14029715 | G | T | 16 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0019 others(13): Show |
27 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-116+62C>A | GEMIN8 | ENSG00000046647.14 | transcript | ENST00000680255.1 | protein_coding | 1/4 | chrX | 14029715 |