Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2245 |
| ensemblid | ENSG00000102302.8 |
| hgncid | 3663 |
| symbol | FGD1 |
| name | FYVE, RhoGEF and PH domain containing 1 |
| refseq_nuc | NM_004463.3 |
| refseq_prot | NP_004454.2 |
| ensembl_nuc | ENST00000375135.4 |
| ensembl_prot | ENSP00000364277.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 54445454 |
| end | 54496234 |
| strand | - |
| ver | v1.2 |
| region | chrX:54445454-54496234 |
| region5000 | chrX:54440454-54501234 |
| regionname0 | FGD1_chrX_54445454_54496234 |
| regionname5000 | FGD1_chrX_54440454_54501234 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 961 | 247 | 68 | 44 | 98 | 11 | 24 | 74 | FGD1_chrX_54440454_54501234 | FGD1 | MHGHR others(956): Show |
chrX | 54440454 | 54501234 |
| a0002 | 0/0 | 961 | 17 | 0 | 0 | 17 | 0 | 0 | 16 | FGD1_chrX_54440454_54501234 | FGD1 | MHGHR others(956): Show |
chrX | 54440454 | 54501234 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2883 | 178 | 26 | 38 | 80 | 11 | 21 | FGD1_chrX_54440454_54501234 | FGD1 | ATGCA others(2878): Show |
chrX | 54440454 | 54501234 | ||
| a0001c0002 | 0/0 | 2883 | 61 | 36 | 6 | 17 | 0 | 2 | FGD1_chrX_54440454_54501234 | FGD1 | ATGCA others(2878): Show |
chrX | 54440454 | 54501234 | ||
| a0001c0004 | 0/0 | 2883 | 6 | 6 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | ATGCA others(2878): Show |
chrX | 54440454 | 54501234 | ||
| a0001c0005 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | ATGCA others(2878): Show |
chrX | 54440454 | 54501234 | ||
| a0001c0006 | 0/0 | 2883 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | ATGCA others(2878): Show |
chrX | 54440454 | 54501234 | ||
| a0002c0003 | 0/0 | 2883 | 17 | 0 | 0 | 17 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | ATGCA others(2878): Show |
chrX | 54440454 | 54501234 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4343 | 96 | 11 | 25 | 37 | 7 | 14 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0001c0001t0002 | 0/0 | 4343 | 51 | 0 | 9 | 37 | 1 | 4 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0001c0001t0004 | 0/0 | 4344 | 17 | 14 | 2 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4339): Show |
chrX | 54440454 | 54501234 |
| a0001c0001t0005 | 0/0 | 4344 | 6 | 0 | 1 | 4 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4339): Show |
chrX | 54440454 | 54501234 |
| a0001c0001t0006 | 0/0 | 4343 | 3 | 0 | 1 | 0 | 1 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0001c0001t0008 | 0/0 | 4343 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0001c0001t0009 | 0/0 | 4343 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0001c0001t0011 | 0/0 | 4343 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0001c0001t0012 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(5569): Show |
chrX | 54440454 | 54501234 |
| a0001c0001t0014 | 0/0 | 4343 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0001c0002t0001 | 0/0 | 4343 | 25 | 21 | 4 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0001c0002t0003 | 0/0 | 4341 | 31 | 10 | 2 | 17 | 0 | 2 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4336): Show |
chrX | 54440454 | 54501234 |
| a0001c0002t0004 | 0/0 | 4344 | 2 | 2 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4339): Show |
chrX | 54440454 | 54501234 |
| a0001c0002t0007 | 0/0 | 4341 | 2 | 2 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4336): Show |
chrX | 54440454 | 54501234 |
| a0001c0002t0010 | 0/0 | 4343 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0001c0004t0001 | 0/0 | 4343 | 6 | 6 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0001c0005t0002 | 0/0 | 4343 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0001c0006t0001 | 0/0 | 4343 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0002c0003t0002 | 0/0 | 4343 | 16 | 0 | 0 | 16 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| a0002c0003t0013 | 0/0 | 4343 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | AACTG others(4338): Show |
chrX | 54440454 | 54501234 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0006g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0009g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0011g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0012g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0001t0014g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0002t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0004t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0004t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0004t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0005t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0001c0006t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| a0002c0003t0013g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0015 | EUR | GBR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00280 | hp1 | a0001 | c0001 | t0009 | g0161 | EUR | FIN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | FIN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0221 | EAS | CHS | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0175 | EAS | CHS | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0220 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0113 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0231 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0173 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | IBS | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0089 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0094 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0195 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02027 | hp1 | a0001 | c0001 | t0012 | g0072 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0174 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02074 | hp1 | a0001 | c0001 | t0011 | g0164 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0208 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0213 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02155 | hp2 | a0002 | c0003 | t0002 | g0246 | EAS | CDX | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CDX | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | CDX | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0026 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0125 | AMR | PEL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0202 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0225 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0007 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0192 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0007 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0035 | SAS | PJL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02809 | hp2 | a0001 | c0002 | t0007 | g0250 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0200 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0228 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02896 | hp1 | a0001 | c0002 | t0010 | g0183 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0081 | AFR | ESN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ESN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | ESN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | MSL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | ESN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03195 | hp1 | a0001 | c0002 | t0004 | g0093 | AFR | ESN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | ESN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0201 | AFR | MSL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0112 | AFR | MSL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | MSL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0016 | SAS | PJL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | ESN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | ESN | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0027 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0229 | AFR | GWD | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | MSL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0224 | SAS | PJL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | STU | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0185 | SAS | BEB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03834 | hp1 | a0001 | c0006 | t0001 | g0206 | SAS | BEB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03834 | hp2 | a0001 | c0001 | t0014 | g0249 | SAS | BEB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | STU | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | YRI | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | YRI | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | YRI | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18939 | hp2 | a0002 | c0003 | t0002 | g0238 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18951 | hp2 | a0002 | c0003 | t0002 | g0245 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0204 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18960 | hp1 | a0001 | c0002 | t0003 | g0230 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18961 | hp1 | a0002 | c0003 | t0013 | g0240 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18963 | hp2 | a0001 | c0002 | t0003 | g0215 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18967 | hp1 | a0002 | c0003 | t0002 | g0234 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0209 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18971 | hp1 | a0002 | c0003 | t0002 | g0013 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18972 | hp2 | a0002 | c0003 | t0002 | g0241 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0212 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18980 | hp1 | a0002 | c0003 | t0002 | g0235 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19007 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19010 | hp1 | a0002 | c0003 | t0002 | g0236 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0203 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19011 | hp2 | a0002 | c0003 | t0002 | g0237 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0028 | AFR | LWK | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | LWK | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0111 | AFR | LWK | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19058 | hp1 | a0002 | c0003 | t0002 | g0242 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19064 | hp2 | a0002 | c0003 | t0002 | g0248 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19065 | hp1 | a0002 | c0003 | t0002 | g0243 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0219 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19074 | hp1 | a0002 | c0003 | t0002 | g0247 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19075 | hp1 | a0001 | c0005 | t0002 | g0103 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19079 | hp1 | a0002 | c0003 | t0002 | g0239 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19080 | hp1 | a0002 | c0003 | t0002 | g0013 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0218 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0216 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19091 | hp1 | a0002 | c0003 | t0002 | g0244 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0147 | AFR | YRI | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | YRI | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ASW | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA20129 | hp2 | a0001 | c0002 | t0003 | g0211 | AFR | ASW | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0170 | EUR | TSI | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | GIH | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | ACB | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | MSL | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0187 | AFR | USA | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| HG06807 | hp2 | a0001 | c0002 | t0007 | g0251 | AFR | USA | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | USA | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0106 | REF | REF | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | FGD1_chrX_54440454_54501234 | FGD1 | chrX | 54440454 | 54501234 |
| 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:54495323 | G | A | 1 | a0002 | 17 | HG02155.hp2 NA18939.hp2 NA18951.hp2 others(14): Show |
missense_variant | MODERATE | c.110C>T | p.Ala37Val | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/18 | 912/4343 | 110/2886 | 37/961 | chrX | 54495323 |
| 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:54449194 | C | T | 1 | a0001c0005 | 1 | NA19075.hp1 | synonymous_variant | LOW | c.2223G>A | p.Glu741Glu | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 15/18 | 3025/4343 | 2223/2886 | 741/961 | chrX | 54449194 | |||
| chrX:54449671 | T | C | 2 | a0001c0002 a0001c0006 |
62 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(59): Show |
synonymous_variant | LOW | c.2136A>G | p.Pro712Pro | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 14/18 | 2938/4343 | 2136/2886 | 712/961 | chrX | 54449671 | |||
| chrX:54449716 | A | G | 2 | a0001c0002 a0001c0004 |
67 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(64): Show |
synonymous_variant | LOW | c.2091T>C | p.Thr697Thr | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 14/18 | 2893/4343 | 2091/2886 | 697/961 | chrX | 54449716 |
| 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:54445487 | T | TA | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0012 others(1): Show |
26 | HG01167.hp1 HG01255.hp1 HG01884.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*621dupT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 621 | chrX | 54445487 | ||||||
| chrX:54445499 | A | C | 1 | a0001c0001t0011 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*610T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 610 | chrX | 54445499 | ||||||
| chrX:54445505 | C | A | 1 | a0002c0003t0013 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*604G>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 604 | chrX | 54445505 | ||||||
| chrX:54445544 | CCT | C | 2 | a0001c0002t0003 a0001c0002t0007 |
33 | HG00597.hp1 HG00621.hp1 HG01081.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*563_*564delAG | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 563 | chrX | 54445544 | ||||||
| chrX:54445691 | A | G | 1 | a0001c0002t0010 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*418T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 418 | chrX | 54445691 | ||||||
| chrX:54445821 | G | GCAGCCCC others(11): Show |
1 | a0001c0001t0012 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287_*288insAGAGGG others(12): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 287 | chrX | 54445821 | ||||||
| chrX:54445825 | T | A | 1 | a0001c0001t0012 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*284A>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 284 | chrX | 54445825 | ||||||
| chrX:54445827 | A | T | 1 | a0001c0001t0012 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282T>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 282 | chrX | 54445827 | ||||||
| chrX:54445830 | G | T | 1 | a0001c0001t0012 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 279 | chrX | 54445830 | ||||||
| chrX:54445831 | A | G | 1 | a0001c0001t0012 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*278T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 278 | chrX | 54445831 | ||||||
| chrX:54445834 | A | ACACTCCT others(1205): Show |
1 | a0001c0001t0012 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274_*275insAGCTTA others(1206): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 274 | chrX | 54445834 | ||||||
| chrX:54445835 | A | C | 1 | a0001c0001t0012 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 274 | chrX | 54445835 | ||||||
| chrX:54445895 | A | G | 1 | a0001c0001t0009 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*214T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 214 | chrX | 54445895 | ||||||
| chrX:54446073 | G | A | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(3): Show |
76 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*36C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 18/18 | 36 | chrX | 54446073 | ||||||
| chrX:54495436 | C | G | 1 | a0001c0001t0006 | 3 | HG00099.hp2 HG01433.hp1 HG03492.hp1 |
5_prime_UTR_variant | MODIFIER | c.-4G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/18 | 4 | chrX | 54495436 | ||||||
| chrX:54495582 | A | G | 1 | a0001c0001t0008 | 1 | HG02647.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-150T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/18 | chrX | 54495582 | |||||||
| chrX:54495696 | G | A | 1 | a0001c0001t0014 | 1 | HG03834.hp2 | 5_prime_UTR_variant | MODIFIER | c.-264C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/18 | 264 | chrX | 54495696 | ||||||
| chrX:54495748 | T | C | 1 | a0001c0002t0007 | 2 | HG02809.hp2 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-316A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/18 | 316 | chrX | 54495748 | ||||||
| chrX:54495939 | C | G | 1 | a0001c0001t0008 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-507G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/18 | 507 | chrX | 54495939 |
| 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:54446721 | C | CT | 19 | a0001c0001t0001g0134 a0001c0001t0001g0166 a0001c0001t0001g0167 others(16): Show |
19 | HG01243.hp1 HG01255.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.2581-308dupA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 17/17 | chrX | 54446721 | |||||||
| chrX:54447582 | A | G | 3 | a0001c0002t0001g0010 a0001c0002t0001g0196 a0001c0002t0001g0223 |
4 | HG02622.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2437-128T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 16/17 | chrX | 54447582 | |||||||
| chrX:54447768 | G | T | 1 | a0001c0002t0001g0191 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2437-314C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 16/17 | chrX | 54447768 | |||||||
| chrX:54447999 | G | A | 4 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0004g0093 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2437-545C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 16/17 | chrX | 54447999 | |||||||
| chrX:54448026 | A | T | 1 | a0001c0002t0001g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2437-572T>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 16/17 | chrX | 54448026 | |||||||
| chrX:54448145 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2436+661A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 16/17 | chrX | 54448145 | |||||||
| chrX:54448186 | AT | A | 5 | a0001c0001t0001g0100 a0001c0001t0001g0126 a0001c0001t0001g0165 others(2): Show |
5 | HG01069.hp1 HG01168.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.2436+619delA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 16/17 | chrX | 54448186 | |||||||
| chrX:54448262 | C | T | 2 | a0001c0002t0003g0187 a0001c0002t0003g0192 |
2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2436+544G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 16/17 | chrX | 54448262 | |||||||
| chrX:54449056 | C | G | 15 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0171 others(12): Show |
17 | HG00735.hp1 HG01891.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.2274+87G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 15/17 | chrX | 54449056 | |||||||
| chrX:54449390 | G | A | 2 | a0001c0004t0001g0225 a0001c0004t0001g0228 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2149-122C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 14/17 | chrX | 54449390 | |||||||
| chrX:54449823 | C | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0036 others(1): Show |
4 | NA18984.hp1 NA18994.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-63G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 13/17 | chrX | 54449823 | |||||||
| chrX:54449956 | G | T | 57 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0019 others(54): Show |
61 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.2047-196C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 13/17 | chrX | 54449956 | |||||||
| chrX:54450080 | G | T | 1 | a0001c0001t0001g0169 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2046+191C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 13/17 | chrX | 54450080 | |||||||
| chrX:54450132 | A | G | 3 | a0001c0001t0002g0124 a0001c0001t0002g0179 a0001c0001t0002g0181 |
3 | HG02165.hp2 HG02523.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2046+139T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 13/17 | chrX | 54450132 | |||||||
| chrX:54450567 | T | C | 1 | a0001c0002t0001g0220 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2016-266A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54450567 | |||||||
| chrX:54450627 | A | G | 1 | a0002c0003t0002g0238 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2016-326T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54450627 | |||||||
| chrX:54450632 | A | C | 1 | a0001c0002t0003g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2016-331T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54450632 | |||||||
| chrX:54450729 | T | C | 1 | a0001c0001t0002g0097 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2016-428A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54450729 | |||||||
| chrX:54450747 | G | A | 1 | a0001c0002t0001g0210 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2016-446C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54450747 | |||||||
| chrX:54450964 | G | A | 1 | a0001c0002t0001g0191 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2016-663C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54450964 | |||||||
| chrX:54451032 | G | C | 2 | a0001c0004t0001g0225 a0001c0004t0001g0228 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2016-731C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54451032 | |||||||
| chrX:54451085 | G | GT | 64 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0019 others(61): Show |
68 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.2016-785dupA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54451085 | |||||||
| chrX:54451102 | G | A | 58 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0019 others(55): Show |
62 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.2016-801C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54451102 | |||||||
| chrX:54451107 | T | G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0008g0014 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2016-806A>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54451107 | |||||||
| chrX:54451206 | C | T | 58 | a0001c0001t0001g0159 a0001c0002t0001g0010 a0001c0002t0001g0011 others(55): Show |
62 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.2016-905G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54451206 | |||||||
| chrX:54451438 | C | T | 1 | a0001c0001t0005g0035 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2016-1137G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54451438 | |||||||
| chrX:54451501 | T | C | 1 | a0001c0005t0002g0103 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2016-1200A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54451501 | |||||||
| chrX:54451625 | A | T | 10 | a0001c0001t0004g0080 a0001c0001t0004g0083 a0001c0001t0004g0084 others(7): Show |
10 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2016-1324T>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54451625 | |||||||
| chrX:54451778 | A | G | 3 | a0001c0002t0001g0019 a0001c0002t0001g0184 a0001c0002t0001g0199 |
3 | HG02572.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2016-1477T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54451778 | |||||||
| chrX:54451888 | C | T | 72 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(69): Show |
76 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(73): Show |
intron_variant | MODIFIER | c.2016-1587G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54451888 | |||||||
| chrX:54451920 | A | G | 23 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(20): Show |
23 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.2016-1619T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54451920 | |||||||
| chrX:54452083 | A | G | 1 | a0001c0002t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2016-1782T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54452083 | |||||||
| chrX:54452207 | A | C | 63 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0019 others(60): Show |
67 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.2016-1906T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54452207 | |||||||
| chrX:54452250 | G | C | 2 | a0001c0001t0002g0058 a0001c0001t0002g0098 |
2 | HG01070.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2016-1949C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54452250 | |||||||
| chrX:54452266 | C | CA | 31 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0039 others(28): Show |
31 | HG00642.hp1 HG01175.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.2016-1966dupT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54452266 | |||||||
| chrX:54452266 | CA | C | 51 | a0001c0001t0001g0107 a0001c0001t0001g0119 a0001c0001t0001g0122 others(48): Show |
55 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.2016-1966delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54452266 | |||||||
| chrX:54452266 | CAA | C | 7 | a0001c0002t0001g0019 a0001c0002t0001g0184 a0001c0002t0001g0190 others(4): Show |
7 | HG01099.hp1 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2016-1967_2016-196 others(6): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54452266 | |||||||
| chrX:54452575 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0155 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2016-2274C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54452575 | |||||||
| chrX:54452974 | C | A | 1 | a0001c0002t0003g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2015+2474G>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54452974 | |||||||
| chrX:54454108 | G | A | 1 | a0001c0002t0010g0183 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2015+1340C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54454108 | |||||||
| chrX:54454183 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2015+1265C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54454183 | |||||||
| chrX:54454319 | TA | T | 4 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2015+1128delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54454319 | |||||||
| chrX:54454645 | T | TA | 8 | a0001c0001t0001g0233 a0001c0001t0002g0053 a0001c0001t0002g0097 others(5): Show |
8 | HG01496.hp1 HG01517.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.2015+802dupT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54454645 | |||||||
| chrX:54454645 | T | TAA | 130 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(127): Show |
138 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.2015+801_2015+802d others(4): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54454645 | |||||||
| chrX:54454645 | TA | T | 7 | a0001c0001t0001g0116 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG00323.hp1 HG02015.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2015+802delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54454645 | |||||||
| chrX:54454939 | C | G | 4 | a0001c0002t0001g0171 a0001c0002t0001g0190 a0001c0002t0001g0191 others(1): Show |
4 | HG00735.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2015+509G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54454939 | |||||||
| chrX:54455400 | C | G | 165 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(162): Show |
173 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(170): Show |
intron_variant | MODIFIER | c.2015+48G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 12/17 | chrX | 54455400 | |||||||
| chrX:54456075 | A | G | 166 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(171): Show |
intron_variant | MODIFIER | c.1842+145T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 10/17 | chrX | 54456075 | |||||||
| chrX:54456638 | G | GT | 5 | a0001c0001t0001g0100 a0001c0001t0001g0133 a0001c0002t0001g0184 others(2): Show |
5 | HG00735.hp1 HG01168.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1637-72dupA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54456638 | |||||||
| chrX:54456638 | GT | G | 99 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(96): Show |
103 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(100): Show |
intron_variant | MODIFIER | c.1637-72delA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54456638 | |||||||
| chrX:54456725 | C | T | 2 | a0001c0002t0003g0185 a0001c0002t0003g0211 |
2 | HG03831.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1637-158G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54456725 | |||||||
| chrX:54456833 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1637-266T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54456833 | |||||||
| chrX:54456932 | C | T | 61 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(58): Show |
65 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1637-365G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54456932 | |||||||
| chrX:54457203 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1637-636C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54457203 | |||||||
| chrX:54457549 | T | A | 74 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(71): Show |
78 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(75): Show |
intron_variant | MODIFIER | c.1637-982A>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54457549 | |||||||
| chrX:54457614 | T | C | 1 | a0001c0001t0002g0047 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1637-1047A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54457614 | |||||||
| chrX:54457631 | A | G | 34 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(31): Show |
36 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1637-1064T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54457631 | |||||||
| chrX:54457644 | G | C | 1 | a0001c0001t0002g0047 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1637-1077C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54457644 | |||||||
| chrX:54457800 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1637-1233C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54457800 | |||||||
| chrX:54457813 | CA | C | 9 | a0001c0001t0001g0123 a0001c0001t0001g0182 a0001c0004t0001g0026 others(6): Show |
9 | HG01069.hp1 HG02257.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1637-1247delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54457813 | |||||||
| chrX:54458237 | C | G | 4 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0004g0093 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637-1670G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54458237 | |||||||
| chrX:54458540 | C | CA | 81 | a0001c0001t0001g0037 a0001c0001t0001g0077 a0001c0001t0001g0078 others(78): Show |
85 | HG00323.hp2 HG00642.hp1 HG01070.hp2 others(82): Show |
intron_variant | MODIFIER | c.1637-1974dupT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54458540 | |||||||
| chrX:54458540 | C | CAA | 21 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0033 others(18): Show |
21 | HG02004.hp1 HG02027.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1637-1975_1637-197 others(6): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54458540 | |||||||
| chrX:54458540 | CA | C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0128 a0001c0001t0001g0169 others(4): Show |
7 | HG02895.hp1 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1637-1974delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54458540 | |||||||
| chrX:54458815 | T | A | 4 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637-2248A>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54458815 | |||||||
| chrX:54458990 | G | T | 1 | a0001c0001t0002g0042 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1637-2423C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54458990 | |||||||
| chrX:54459061 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1637-2494A>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54459061 | |||||||
| chrX:54459217 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0158 |
2 | NA19005.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1637-2650G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54459217 | |||||||
| chrX:54459477 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1637-2910C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54459477 | |||||||
| chrX:54459578 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1637-3011T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54459578 | |||||||
| chrX:54459670 | C | G | 1 | a0001c0001t0002g0102 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1637-3103G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54459670 | |||||||
| chrX:54459732 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1637-3165G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54459732 | |||||||
| chrX:54459735 | T | G | 62 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(59): Show |
66 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1637-3168A>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54459735 | |||||||
| chrX:54459847 | T | C | 139 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(136): Show |
147 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.1637-3280A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54459847 | |||||||
| chrX:54459971 | T | TA | 74 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(71): Show |
78 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(75): Show |
intron_variant | MODIFIER | c.1637-3405dupT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54459971 | |||||||
| chrX:54460102 | TA | T | 74 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(71): Show |
78 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(75): Show |
intron_variant | MODIFIER | c.1637-3536delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460102 | |||||||
| chrX:54460109 | A | G | 1 | a0002c0003t0002g0247 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1637-3542T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460109 | |||||||
| chrX:54460146 | TA | T | 62 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(59): Show |
66 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1637-3580delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460146 | |||||||
| chrX:54460162 | G | C | 1 | a0001c0001t0002g0102 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1637-3595C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460162 | |||||||
| chrX:54460164 | C | G | 1 | a0001c0001t0002g0102 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1637-3597G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460164 | |||||||
| chrX:54460238 | C | T | 3 | a0001c0001t0002g0001 a0001c0001t0002g0020 a0001c0001t0002g0021 |
4 | NA18954.hp1 NA18969.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1637-3671G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460238 | |||||||
| chrX:54460323 | C | G | 78 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(75): Show |
82 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(79): Show |
intron_variant | MODIFIER | c.1637-3756G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460323 | |||||||
| chrX:54460417 | C | T | 1 | a0001c0002t0003g0212 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1637-3850G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460417 | |||||||
| chrX:54460441 | A | G | 1 | a0001c0002t0001g0210 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1637-3874T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460441 | |||||||
| chrX:54460525 | G | A | 2 | a0001c0002t0001g0190 a0001c0002t0001g0197 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1637-3958C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460525 | |||||||
| chrX:54460575 | T | A | 62 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(59): Show |
66 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1637-4008A>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460575 | |||||||
| chrX:54460613 | T | C | 62 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(59): Show |
66 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1637-4046A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460613 | |||||||
| chrX:54460695 | C | T | 62 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(59): Show |
66 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1637-4128G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460695 | |||||||
| chrX:54460744 | A | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0154 |
2 | HG01109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1637-4177T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54460744 | |||||||
| chrX:54461457 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1636+3994G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54461457 | |||||||
| chrX:54461458 | G | A | 45 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(42): Show |
48 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(45): Show |
intron_variant | MODIFIER | c.1636+3993C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54461458 | |||||||
| chrX:54461600 | C | CA | 78 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0001g0077 others(75): Show |
83 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1636+3850dupT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54461600 | |||||||
| chrX:54461600 | C | CAA | 21 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 others(18): Show |
21 | HG01258.hp1 HG02080.hp1 HG02148.hp1 others(18): Show |
intron_variant | MODIFIER | c.1636+3849_1636+385 others(6): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54461600 | |||||||
| chrX:54461600 | CA | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0101 a0001c0001t0001g0120 others(2): Show |
5 | HG02895.hp1 HG03490.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1636+3850delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54461600 | |||||||
| chrX:54461600 | CAAAAAAA | C | 28 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(25): Show |
28 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1636+3844_1636+385 others(11): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54461600 | |||||||
| chrX:54461648 | G | A | 58 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(55): Show |
62 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1636+3803C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54461648 | |||||||
| chrX:54461755 | A | G | 166 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(171): Show |
intron_variant | MODIFIER | c.1636+3696T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54461755 | |||||||
| chrX:54461961 | C | T | 1 | a0001c0001t0005g0125 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1636+3490G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54461961 | |||||||
| chrX:54462173 | G | A | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0099 |
3 | HG01257.hp2 HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1636+3278C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54462173 | |||||||
| chrX:54462181 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0014g0249 |
2 | HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1636+3270G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54462181 | |||||||
| chrX:54462389 | C | CT | 35 | a0001c0001t0001g0109 a0001c0001t0001g0117 a0001c0001t0001g0141 others(32): Show |
35 | HG00621.hp1 HG01884.hp2 HG02015.hp1 others(32): Show |
intron_variant | MODIFIER | c.1636+3061dupA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54462389 | |||||||
| chrX:54462389 | CT | C | 7 | a0001c0001t0001g0108 a0001c0001t0001g0119 a0001c0001t0001g0198 others(4): Show |
7 | HG01257.hp1 HG01517.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1636+3061delA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54462389 | |||||||
| chrX:54462417 | G | A | 2 | a0001c0001t0002g0045 a0001c0001t0002g0064 |
2 | NA18982.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1636+3034C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54462417 | |||||||
| chrX:54462428 | C | T | 2 | a0001c0002t0001g0019 a0001c0002t0010g0183 |
2 | HG02896.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1636+3023G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54462428 | |||||||
| chrX:54462765 | C | CT | 99 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(96): Show |
103 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1636+2685dupA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54462765 | |||||||
| chrX:54462765 | CT | C | 8 | a0001c0001t0001g0105 a0001c0001t0001g0126 a0001c0001t0001g0128 others(5): Show |
8 | HG01515.hp1 HG02523.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.1636+2685delA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54462765 | |||||||
| chrX:54462979 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1636+2472C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54462979 | |||||||
| chrX:54463489 | C | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0091 |
2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1636+1962G>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54463489 | |||||||
| chrX:54464046 | C | G | 26 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(23): Show |
26 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1636+1405G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54464046 | |||||||
| chrX:54464111 | A | G | 79 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(76): Show |
83 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(80): Show |
intron_variant | MODIFIER | c.1636+1340T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54464111 | |||||||
| chrX:54464127 | C | CT | 42 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0078 others(39): Show |
42 | HG00642.hp1 HG01069.hp1 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.1636+1323dupA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54464127 | |||||||
| chrX:54464127 | C | CTT | 72 | a0001c0001t0001g0039 a0001c0001t0002g0001 a0001c0001t0002g0002 others(69): Show |
76 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(73): Show |
intron_variant | MODIFIER | c.1636+1322_1636+132 others(6): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54464127 | |||||||
| chrX:54464127 | C | CTTT | 6 | a0001c0001t0002g0062 a0001c0001t0002g0181 a0001c0001t0005g0034 others(3): Show |
6 | HG02622.hp1 NA18906.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.1636+1321_1636+132 others(7): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54464127 | |||||||
| chrX:54464127 | CT | C | 12 | a0001c0001t0001g0018 a0001c0001t0001g0120 a0001c0001t0001g0136 others(9): Show |
12 | HG00738.hp1 HG02809.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.1636+1323delA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54464127 | |||||||
| chrX:54464253 | C | G | 1 | a0001c0001t0014g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1636+1198G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54464253 | |||||||
| chrX:54464443 | G | A | 2 | a0001c0002t0001g0210 a0001c0002t0001g0220 |
2 | HG00738.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1636+1008C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54464443 | |||||||
| chrX:54464519 | T | C | 62 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(59): Show |
66 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1636+932A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54464519 | |||||||
| chrX:54464794 | G | A | 79 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(76): Show |
83 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(80): Show |
intron_variant | MODIFIER | c.1636+657C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54464794 | |||||||
| chrX:54464967 | A | G | 1 | a0001c0001t0009g0161 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1636+484T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54464967 | |||||||
| chrX:54465200 | G | C | 23 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(20): Show |
23 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1636+251C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54465200 | |||||||
| chrX:54465430 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0101 others(10): Show |
14 | HG01069.hp1 HG01261.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1636+21C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 8/17 | chrX | 54465430 | |||||||
| chrX:54465917 | A | G | 166 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(163): Show |
174 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(171): Show |
intron_variant | MODIFIER | c.1341-65T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54465917 | |||||||
| chrX:54466048 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1341-196G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466048 | |||||||
| chrX:54466276 | G | C | 4 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1341-424C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466276 | |||||||
| chrX:54466341 | TA | T | 78 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(75): Show |
82 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(79): Show |
intron_variant | MODIFIER | c.1341-490delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466341 | |||||||
| chrX:54466453 | A | G | 62 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(59): Show |
66 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1341-601T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466453 | |||||||
| chrX:54466578 | T | C | 1 | a0001c0004t0001g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1341-726A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466578 | |||||||
| chrX:54466755 | G | GT | 77 | a0001c0001t0001g0078 a0001c0001t0001g0131 a0001c0001t0001g0134 others(74): Show |
81 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.1341-904dupA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466755 | |||||||
| chrX:54466758 | T | TG | 61 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(58): Show |
65 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1341-907_1341-906i others(3): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466758 | |||||||
| chrX:54466759 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1341-907A>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466759 | |||||||
| chrX:54466810 | T | C | 34 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(31): Show |
36 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1341-958A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466810 | |||||||
| chrX:54466811 | A | G | 34 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(31): Show |
36 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1341-959T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466811 | |||||||
| chrX:54466812 | C | G | 34 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(31): Show |
36 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1341-960G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466812 | |||||||
| chrX:54466898 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1340+886G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54466898 | |||||||
| chrX:54467104 | C | T | 1 | a0001c0002t0001g0220 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1340+680G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54467104 | |||||||
| chrX:54467263 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1340+521A>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54467263 | |||||||
| chrX:54467358 | CT | C | 77 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0002g0001 others(74): Show |
81 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(78): Show |
intron_variant | MODIFIER | c.1340+425delA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54467358 | |||||||
| chrX:54467440 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1340+344G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54467440 | |||||||
| chrX:54467531 | T | A | 1 | a0001c0002t0003g0231 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1340+253A>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54467531 | |||||||
| chrX:54467775 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1340+9C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 6/17 | chrX | 54467775 | |||||||
| chrX:54468084 | T | C | 1 | a0001c0002t0001g0011 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1192-152A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 5/17 | chrX | 54468084 | |||||||
| chrX:54468152 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1192-220C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 5/17 | chrX | 54468152 | |||||||
| chrX:54468667 | G | A | 2 | a0001c0002t0001g0019 a0001c0002t0010g0183 |
2 | HG02896.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1191+120C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 5/17 | chrX | 54468667 | |||||||
| chrX:54468936 | C | A | 1 | a0001c0002t0001g0199 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1102-60G>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 4/17 | chrX | 54468936 | |||||||
| chrX:54469277 | A | T | 1 | a0001c0002t0001g0186 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1102-401T>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 4/17 | chrX | 54469277 | |||||||
| chrX:54469565 | T | C | 1 | a0001c0002t0003g0211 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1101+451A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 4/17 | chrX | 54469565 | |||||||
| chrX:54469750 | G | C | 4 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+266C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 4/17 | chrX | 54469750 | |||||||
| chrX:54469830 | G | A | 1 | a0001c0002t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1101+186C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 4/17 | chrX | 54469830 | |||||||
| chrX:54469983 | TGGACCTG others(16): Show |
T | 1 | a0001c0001t0002g0102 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1101+10_1101+32del others(23): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 4/17 | chrX | 54469983 | |||||||
| chrX:54469996 | C | G | 4 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0004g0093 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+20G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 4/17 | chrX | 54469996 | |||||||
| chrX:54470512 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.660-55G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 3/17 | chrX | 54470512 | |||||||
| chrX:54470556 | A | G | 79 | a0001c0001t0001g0076 a0001c0001t0002g0001 a0001c0001t0002g0002 others(76): Show |
83 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(80): Show |
intron_variant | MODIFIER | c.659+27T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 3/17 | chrX | 54470556 | |||||||
| chrX:54470770 | C | T | 6 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0133 others(3): Show |
6 | NA18955.hp1 NA18959.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-10G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 2/17 | chrX | 54470770 | |||||||
| chrX:54470782 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.482-22T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 2/17 | chrX | 54470782 | |||||||
| chrX:54470873 | G | A | 74 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(71): Show |
78 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(75): Show |
intron_variant | MODIFIER | c.482-113C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 2/17 | chrX | 54470873 | |||||||
| chrX:54470914 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.482-154G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 2/17 | chrX | 54470914 | |||||||
| chrX:54470988 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.482-228T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 2/17 | chrX | 54470988 | |||||||
| chrX:54471007 | C | CA | 28 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(25): Show |
28 | HG00140.hp1 HG00642.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.482-248dupT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 2/17 | chrX | 54471007 | |||||||
| chrX:54471007 | CA | C | 69 | a0001c0001t0001g0018 a0001c0001t0001g0130 a0001c0001t0001g0143 others(66): Show |
73 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.482-248delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 2/17 | chrX | 54471007 | |||||||
| chrX:54471069 | C | G | 18 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0171 others(15): Show |
20 | HG00735.hp1 HG01891.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.481+245G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 2/17 | chrX | 54471069 | |||||||
| chrX:54471123 | A | C | 1 | a0001c0002t0001g0210 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.481+191T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 2/17 | chrX | 54471123 | |||||||
| chrX:54471194 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0148 |
2 | NA18972.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.481+120G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 2/17 | chrX | 54471194 | |||||||
| chrX:54471812 | C | T | 140 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(137): Show |
148 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.308-325G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54471812 | |||||||
| chrX:54472273 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.308-786C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54472273 | |||||||
| chrX:54472280 | GA | G | 28 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(25): Show |
28 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.308-794delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54472280 | |||||||
| chrX:54473343 | C | A | 55 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(52): Show |
59 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.308-1856G>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54473343 | |||||||
| chrX:54473798 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.308-2311T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54473798 | |||||||
| chrX:54473940 | T | C | 140 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(137): Show |
148 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.308-2453A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54473940 | |||||||
| chrX:54473982 | A | AAT | 8 | a0001c0001t0002g0030 a0001c0001t0002g0045 a0001c0001t0002g0056 others(5): Show |
8 | HG02622.hp1 NA18747.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.308-2496_308-2495i others(4): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54473982 | |||||||
| chrX:54473984 | A | AAT | 6 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0001g0220 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-2498_308-2497i others(4): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54473984 | |||||||
| chrX:54473984 | A | T | 78 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(75): Show |
82 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(79): Show |
intron_variant | MODIFIER | c.308-2497T>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54473984 | |||||||
| chrX:54473986 | A | T | 141 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0001g0205 others(138): Show |
149 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.308-2499T>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54473986 | |||||||
| chrX:54473988 | A | T | 217 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.308-2501T>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54473988 | |||||||
| chrX:54474120 | G | A | 140 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(137): Show |
148 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.308-2633C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54474120 | |||||||
| chrX:54474511 | C | T | 4 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-3024G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54474511 | |||||||
| chrX:54474652 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.308-3165G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54474652 | |||||||
| chrX:54474658 | C | G | 1 | a0001c0002t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.308-3171G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54474658 | |||||||
| chrX:54474728 | T | C | 65 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(62): Show |
69 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.308-3241A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54474728 | |||||||
| chrX:54475505 | GTTTAGGA others(31): Show |
G | 63 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(60): Show |
67 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.308-4056_308-4019d others(40): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54475505 | |||||||
| chrX:54475639 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.308-4152G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54475639 | |||||||
| chrX:54475894 | C | T | 1 | a0001c0001t0006g0016 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.308-4407G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54475894 | |||||||
| chrX:54476053 | G | A | 1 | a0001c0002t0001g0210 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.308-4566C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54476053 | |||||||
| chrX:54476067 | A | AAAAC | 3 | a0001c0002t0001g0096 a0001c0002t0004g0093 a0001c0002t0004g0094 |
3 | HG01884.hp2 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.308-4584_308-4581d others(6): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54476067 | |||||||
| chrX:54476222 | A | G | 65 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(62): Show |
69 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.308-4735T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54476222 | |||||||
| chrX:54476357 | CT | C | 6 | a0001c0001t0001g0127 a0001c0001t0001g0140 a0001c0001t0001g0143 others(3): Show |
6 | HG01167.hp1 HG02897.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-4871delA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54476357 | |||||||
| chrX:54476357 | CTT | C | 65 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(62): Show |
69 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.308-4872_308-4871d others(4): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54476357 | |||||||
| chrX:54476755 | C | T | 65 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(62): Show |
69 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.308-5268G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54476755 | |||||||
| chrX:54476880 | C | T | 1 | a0001c0002t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.308-5393G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54476880 | |||||||
| chrX:54476935 | G | C | 61 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(58): Show |
65 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.308-5448C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54476935 | |||||||
| chrX:54477091 | G | A | 65 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(62): Show |
69 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.308-5604C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477091 | |||||||
| chrX:54477215 | G | C | 1 | a0001c0002t0001g0220 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.308-5728C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477215 | |||||||
| chrX:54477258 | C | A | 1 | a0001c0002t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.308-5771G>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477258 | |||||||
| chrX:54477293 | C | T | 65 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(62): Show |
69 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.308-5806G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477293 | |||||||
| chrX:54477321 | A | T | 1 | a0001c0002t0004g0094 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.308-5834T>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477321 | |||||||
| chrX:54477338 | C | T | 1 | a0001c0001t0004g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.308-5851G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477338 | |||||||
| chrX:54477355 | G | A | 2 | a0001c0002t0001g0184 a0001c0002t0001g0199 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.308-5868C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477355 | |||||||
| chrX:54477370 | C | A | 1 | a0001c0002t0003g0200 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.308-5883G>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477370 | |||||||
| chrX:54477411 | T | C | 65 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(62): Show |
69 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.308-5924A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477411 | |||||||
| chrX:54477433 | A | AT | 56 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(53): Show |
60 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.308-5947dupA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477433 | |||||||
| chrX:54477554 | C | T | 3 | a0001c0001t0002g0044 a0001c0001t0002g0049 a0001c0001t0002g0051 |
3 | HG02602.hp1 HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.308-6067G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477554 | |||||||
| chrX:54477564 | A | G | 1 | a0001c0002t0010g0183 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.308-6077T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477564 | |||||||
| chrX:54477656 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0075 others(5): Show |
10 | HG00597.hp2 HG00609.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.308-6169G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477656 | |||||||
| chrX:54477918 | G | C | 1 | a0001c0001t0014g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.308-6431C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54477918 | |||||||
| chrX:54478025 | G | A | 65 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(62): Show |
69 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.308-6538C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54478025 | |||||||
| chrX:54478122 | C | A | 65 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(62): Show |
69 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.308-6635G>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54478122 | |||||||
| chrX:54478132 | T | TATTGTAT others(18): Show |
3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0008g0014 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.308-6670_308-6646d others(27): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54478132 | |||||||
| chrX:54478332 | T | A | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0008g0014 others(5): Show |
8 | HG01884.hp2 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.308-6845A>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54478332 | |||||||
| chrX:54478418 | T | A | 60 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(57): Show |
64 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.308-6931A>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54478418 | |||||||
| chrX:54478531 | T | C | 2 | a0001c0004t0001g0225 a0001c0004t0001g0228 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.308-7044A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54478531 | |||||||
| chrX:54478943 | C | T | 2 | a0001c0002t0003g0209 a0001c0002t0003g0216 |
2 | NA18969.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.308-7456G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54478943 | |||||||
| chrX:54479633 | C | T | 23 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(20): Show |
23 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.308-8146G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54479633 | |||||||
| chrX:54479700 | G | A | 1 | a0001c0002t0003g0215 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.308-8213C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54479700 | |||||||
| chrX:54479780 | C | CA | 20 | a0001c0001t0001g0039 a0001c0001t0001g0075 a0001c0001t0001g0105 others(17): Show |
20 | HG01358.hp1 HG01884.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.308-8294dupT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54479780 | |||||||
| chrX:54479780 | CA | C | 48 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(45): Show |
50 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.308-8294delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54479780 | |||||||
| chrX:54479889 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.308-8402G>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54479889 | |||||||
| chrX:54479982 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.308-8495G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54479982 | |||||||
| chrX:54480024 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.308-8537G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54480024 | |||||||
| chrX:54480148 | T | C | 61 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0226 others(58): Show |
64 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.308-8661A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54480148 | |||||||
| chrX:54480345 | T | C | 1 | a0001c0002t0001g0096 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.308-8858A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54480345 | |||||||
| chrX:54480552 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.308-9065C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54480552 | |||||||
| chrX:54480691 | G | A | 9 | a0001c0001t0001g0123 a0001c0001t0001g0142 a0001c0001t0001g0143 others(6): Show |
9 | HG02056.hp1 HG02135.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.308-9204C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54480691 | |||||||
| chrX:54480854 | G | A | 2 | a0001c0002t0003g0209 a0001c0002t0003g0216 |
2 | NA18969.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.308-9367C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54480854 | |||||||
| chrX:54480899 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.308-9412C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54480899 | |||||||
| chrX:54480939 | A | G | 1 | a0001c0002t0010g0183 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.308-9452T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54480939 | |||||||
| chrX:54480945 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0009g0161 |
2 | HG00280.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.308-9458G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54480945 | |||||||
| chrX:54481022 | A | G | 2 | a0001c0002t0003g0200 a0001c0002t0003g0201 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.308-9535T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54481022 | |||||||
| chrX:54481114 | A | G | 1 | a0001c0002t0003g0175 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.308-9627T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54481114 | |||||||
| chrX:54481132 | C | G | 1 | a0001c0002t0010g0183 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.308-9645G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54481132 | |||||||
| chrX:54481277 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.308-9790G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54481277 | |||||||
| chrX:54481425 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.308-9938G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54481425 | |||||||
| chrX:54481576 | G | C | 17 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0171 others(14): Show |
19 | HG00735.hp1 HG01891.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.308-10089C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54481576 | |||||||
| chrX:54481707 | G | A | 1 | a0001c0004t0001g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.308-10220C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54481707 | |||||||
| chrX:54481779 | T | C | 51 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(48): Show |
54 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.308-10292A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54481779 | |||||||
| chrX:54482226 | G | A | 60 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0226 others(57): Show |
63 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.308-10739C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482226 | |||||||
| chrX:54482230 | A | G | 60 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0226 others(57): Show |
63 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.308-10743T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482230 | |||||||
| chrX:54482236 | G | GCA | 9 | a0001c0001t0001g0105 a0001c0001t0001g0146 a0001c0001t0001g0169 others(6): Show |
10 | HG01934.hp1 HG02074.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.308-10751_308-1075 others(6): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCACA | 6 | a0001c0001t0001g0148 a0001c0002t0001g0186 a0001c0002t0003g0192 others(3): Show |
6 | HG02280.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.308-10753_308-1075 others(8): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCACACA | 10 | a0001c0002t0001g0010 a0001c0002t0001g0188 a0001c0002t0001g0189 others(7): Show |
11 | HG01891.hp2 HG02622.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.308-10755_308-1075 others(10): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCACACAC others(1): Show |
30 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(27): Show |
31 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.308-10757_308-1075 others(12): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCACACAC others(3): Show |
47 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(44): Show |
52 | HG01070.hp2 HG01074.hp1 HG02027.hp1 others(49): Show |
intron_variant | MODIFIER | c.308-10759_308-1075 others(14): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCACACAC others(5): Show |
12 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0061 others(9): Show |
12 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.308-10761_308-1075 others(16): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCACACAC others(7): Show |
5 | a0001c0001t0002g0067 a0001c0004t0001g0225 a0002c0003t0002g0234 others(2): Show |
5 | HG02148.hp1 HG02622.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.308-10763_308-1075 others(18): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCACACAC others(9): Show |
8 | a0001c0001t0004g0083 a0001c0001t0004g0087 a0001c0001t0004g0088 others(5): Show |
8 | HG00738.hp1 HG01884.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.308-10765_308-1075 others(20): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCACACAC others(11): Show |
6 | a0001c0001t0001g0038 a0001c0001t0004g0023 a0001c0001t0004g0024 others(3): Show |
6 | HG01175.hp1 HG02970.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-10767_308-1075 others(22): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCACACAC others(13): Show |
5 | a0001c0001t0001g0039 a0001c0001t0001g0091 a0001c0001t0004g0084 others(2): Show |
5 | HG00642.hp1 HG01167.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.308-10769_308-1075 others(24): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCACACAC others(21): Show |
1 | a0001c0001t0004g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.308-10777_308-1075 others(32): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCAGCGCG others(12): Show |
1 | a0001c0001t0001g0226 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.308-10750_308-1074 others(23): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCGCACA | 3 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 |
3 | HG02257.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.308-10750_308-1074 others(10): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCGCACAC others(3): Show |
4 | a0001c0001t0002g0049 a0001c0001t0002g0051 a0001c0002t0003g0185 others(1): Show |
4 | HG02602.hp1 HG02735.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-10750_308-1074 others(14): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCGCACAC others(9): Show |
1 | a0001c0001t0001g0198 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.308-10750_308-1074 others(20): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCGCGCAC others(9): Show |
1 | a0001c0001t0001g0227 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.308-10750_308-1074 others(20): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCGCGCGC others(9): Show |
1 | a0001c0001t0008g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.308-10750_308-1074 others(20): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCGCGCGC others(15): Show |
2 | a0001c0001t0001g0037 a0001c0001t0001g0082 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.308-10750_308-1074 others(26): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482236 | G | GCGCGCGC others(17): Show |
1 | a0001c0001t0001g0090 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.308-10750_308-1074 others(28): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482236 | |||||||
| chrX:54482238 | A | G | 4 | a0001c0002t0001g0019 a0001c0002t0001g0096 a0001c0002t0004g0093 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.308-10751T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482238 | |||||||
| chrX:54482240 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.308-10753T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482240 | |||||||
| chrX:54482242 | A | G | 1 | a0001c0002t0001g0095 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.308-10755T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482242 | |||||||
| chrX:54482279 | G | A | 1 | a0001c0002t0003g0219 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.308-10792C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482279 | |||||||
| chrX:54482491 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0014g0249 |
2 | HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.308-11004C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482491 | |||||||
| chrX:54482541 | C | T | 2 | a0001c0004t0001g0225 a0001c0004t0001g0228 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.308-11054G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482541 | |||||||
| chrX:54482851 | C | T | 51 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(48): Show |
54 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.308-11364G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482851 | |||||||
| chrX:54482929 | G | T | 53 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(50): Show |
56 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.308-11442C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54482929 | |||||||
| chrX:54483061 | C | T | 2 | a0001c0002t0003g0187 a0001c0002t0003g0192 |
2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.308-11574G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54483061 | |||||||
| chrX:54483302 | A | G | 51 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(48): Show |
54 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.308-11815T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54483302 | |||||||
| chrX:54483390 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.307+11736C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54483390 | |||||||
| chrX:54483401 | C | T | 2 | a0001c0002t0003g0200 a0001c0002t0003g0201 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.307+11725G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54483401 | |||||||
| chrX:54483425 | C | T | 1 | a0001c0002t0001g0229 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.307+11701G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54483425 | |||||||
| chrX:54483514 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.307+11612G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54483514 | |||||||
| chrX:54483538 | G | A | 1 | a0001c0001t0004g0092 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.307+11588C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54483538 | |||||||
| chrX:54484022 | C | T | 51 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(48): Show |
54 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.307+11104G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54484022 | |||||||
| chrX:54484148 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.307+10978G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54484148 | |||||||
| chrX:54484266 | G | A | 1 | a0001c0001t0002g0097 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.307+10860C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54484266 | |||||||
| chrX:54484269 | C | G | 1 | a0001c0002t0001g0186 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.307+10857G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54484269 | |||||||
| chrX:54484278 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.307+10848G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54484278 | |||||||
| chrX:54484466 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0014g0249 |
2 | HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.307+10660G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54484466 | |||||||
| chrX:54484480 | C | T | 67 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(64): Show |
71 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.307+10646G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54484480 | |||||||
| chrX:54484497 | A | G | 27 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(24): Show |
27 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.307+10629T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54484497 | |||||||
| chrX:54484645 | A | AC | 155 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(152): Show |
162 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(159): Show |
intron_variant | MODIFIER | c.307+10480_307+1048 others(5): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54484645 | |||||||
| chrX:54484812 | G | C | 1 | a0001c0002t0003g0209 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.307+10314C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54484812 | |||||||
| chrX:54485073 | C | G | 2 | a0001c0002t0003g0200 a0001c0002t0003g0201 |
2 | HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.307+10053G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54485073 | |||||||
| chrX:54485176 | A | C | 1 | a0001c0002t0001g0019 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.307+9950T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54485176 | |||||||
| chrX:54485583 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.307+9543G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54485583 | |||||||
| chrX:54485597 | T | C | 51 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(48): Show |
54 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.307+9529A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54485597 | |||||||
| chrX:54485690 | T | C | 2 | a0002c0003t0002g0235 a0002c0003t0002g0236 |
2 | NA18980.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.307+9436A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54485690 | |||||||
| chrX:54485780 | CT | C | 154 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(151): Show |
161 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(158): Show |
intron_variant | MODIFIER | c.307+9345delA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54485780 | |||||||
| chrX:54485919 | C | T | 2 | a0001c0002t0001g0184 a0001c0002t0001g0199 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.307+9207G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54485919 | |||||||
| chrX:54486003 | G | C | 1 | a0002c0003t0002g0247 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.307+9123C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486003 | |||||||
| chrX:54486117 | C | T | 1 | a0001c0002t0001g0019 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.307+9009G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486117 | |||||||
| chrX:54486253 | A | AC | 25 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(22): Show |
25 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.307+8872_307+8873i others(3): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486253 | |||||||
| chrX:54486272 | C | T | 76 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(73): Show |
79 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.307+8854G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486272 | |||||||
| chrX:54486281 | G | A | 2 | a0001c0004t0001g0225 a0001c0004t0001g0228 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.307+8845C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486281 | |||||||
| chrX:54486342 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.307+8784C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486342 | |||||||
| chrX:54486667 | C | T | 1 | a0001c0002t0003g0211 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.307+8459G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486667 | |||||||
| chrX:54486678 | G | A | 51 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(48): Show |
54 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.307+8448C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486678 | |||||||
| chrX:54486773 | G | T | 49 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(46): Show |
52 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.307+8353C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486773 | |||||||
| chrX:54486781 | G | A | 5 | a0001c0001t0008g0014 a0001c0002t0001g0095 a0001c0002t0001g0096 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+8345C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486781 | |||||||
| chrX:54486909 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.307+8217G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486909 | |||||||
| chrX:54486920 | G | A | 1 | a0002c0003t0002g0237 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.307+8206C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54486920 | |||||||
| chrX:54487030 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.307+8096G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54487030 | |||||||
| chrX:54487077 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.307+8049G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54487077 | |||||||
| chrX:54487285 | T | C | 1 | a0001c0001t0004g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.307+7841A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54487285 | |||||||
| chrX:54487394 | G | T | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0004t0001g0225 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+7732C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54487394 | |||||||
| chrX:54487677 | T | C | 1 | a0001c0001t0008g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.307+7449A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54487677 | |||||||
| chrX:54487799 | A | C | 1 | a0001c0001t0008g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.307+7327T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54487799 | |||||||
| chrX:54487935 | G | C | 1 | a0001c0002t0010g0183 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.307+7191C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54487935 | |||||||
| chrX:54487964 | A | C | 125 | a0001c0001t0001g0165 a0001c0001t0001g0205 a0001c0001t0001g0214 others(122): Show |
132 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.307+7162T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54487964 | |||||||
| chrX:54488005 | C | T | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0004t0001g0225 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+7121G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488005 | |||||||
| chrX:54488029 | G | A | 28 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(25): Show |
29 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.307+7097C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488029 | |||||||
| chrX:54488269 | C | CA | 66 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0068 others(63): Show |
72 | HG00140.hp1 HG00673.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.307+6856dupT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488269 | |||||||
| chrX:54488269 | C | CAA | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0040 others(26): Show |
32 | HG00609.hp1 HG01109.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.307+6855_307+6856d others(4): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488269 | |||||||
| chrX:54488269 | C | CAAA | 11 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0107 others(8): Show |
11 | HG00280.hp1 HG00597.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.307+6854_307+6856d others(5): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488269 | |||||||
| chrX:54488269 | CA | C | 19 | a0001c0001t0002g0046 a0001c0001t0002g0048 a0001c0001t0002g0049 others(16): Show |
19 | HG00597.hp1 HG00738.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.307+6856delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488269 | |||||||
| chrX:54488269 | CAA | C | 28 | a0001c0001t0001g0214 a0001c0001t0001g0233 a0001c0001t0002g0047 others(25): Show |
31 | HG00621.hp1 HG01361.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.307+6855_307+6856d others(4): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488269 | |||||||
| chrX:54488269 | CAAA | C | 38 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(35): Show |
38 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.307+6854_307+6856d others(5): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488269 | |||||||
| chrX:54488269 | CAAAA | C | 12 | a0001c0001t0001g0082 a0001c0001t0004g0022 a0001c0001t0004g0023 others(9): Show |
12 | HG01243.hp1 HG01255.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.307+6853_307+6856d others(6): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488269 | |||||||
| chrX:54488269 | CAAAAAAA others(9): Show |
C | 2 | a0001c0002t0003g0111 a0001c0002t0003g0112 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.307+6841_307+6856d others(18): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488269 | |||||||
| chrX:54488269 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0176 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.307+6839_307+6856d others(20): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488269 | |||||||
| chrX:54488401 | C | T | 1 | a0001c0002t0004g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.307+6725G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488401 | |||||||
| chrX:54488415 | C | G | 52 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(49): Show |
55 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.307+6711G>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488415 | |||||||
| chrX:54488454 | G | A | 51 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0232 others(48): Show |
54 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.307+6672C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488454 | |||||||
| chrX:54488509 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA18955.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.307+6617G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488509 | |||||||
| chrX:54488527 | G | C | 27 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(24): Show |
27 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.307+6599C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488527 | |||||||
| chrX:54488700 | A | G | 1 | a0001c0004t0001g0026 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.307+6426T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488700 | |||||||
| chrX:54488744 | C | T | 1 | a0001c0004t0001g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.307+6382G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54488744 | |||||||
| chrX:54489106 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.307+6020T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54489106 | |||||||
| chrX:54489347 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.307+5779G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54489347 | |||||||
| chrX:54489593 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.307+5533G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54489593 | |||||||
| chrX:54489628 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.307+5498T>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54489628 | |||||||
| chrX:54489857 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01069.hp1 HG01261.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+5269C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54489857 | |||||||
| chrX:54489945 | A | C | 4 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.307+5181T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54489945 | |||||||
| chrX:54490119 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.307+5007C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54490119 | |||||||
| chrX:54490406 | C | A | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0004t0001g0225 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+4720G>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54490406 | |||||||
| chrX:54490663 | C | T | 27 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(24): Show |
27 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.307+4463G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54490663 | |||||||
| chrX:54490664 | G | T | 1 | a0002c0003t0002g0239 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.307+4462C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54490664 | |||||||
| chrX:54490903 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.307+4223G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54490903 | |||||||
| chrX:54491021 | C | T | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0004t0001g0225 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+4105G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54491021 | |||||||
| chrX:54491073 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.307+4053G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54491073 | |||||||
| chrX:54491183 | T | C | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0004t0001g0225 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+3943A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54491183 | |||||||
| chrX:54491334 | A | T | 3 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG02165.hp1 NA18612.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.307+3792T>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54491334 | |||||||
| chrX:54492051 | G | A | 1 | a0001c0002t0003g0231 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.307+3075C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54492051 | |||||||
| chrX:54492466 | C | T | 16 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0171 others(13): Show |
18 | HG00735.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.307+2660G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54492466 | |||||||
| chrX:54492601 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0004g0170 |
2 | NA18980.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.307+2525A>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54492601 | |||||||
| chrX:54492614 | C | T | 1 | a0001c0002t0003g0185 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.307+2512G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54492614 | |||||||
| chrX:54492615 | A | C | 1 | a0001c0002t0003g0185 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.307+2511T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54492615 | |||||||
| chrX:54492914 | CA | C | 137 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(134): Show |
144 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.307+2211delT | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54492914 | |||||||
| chrX:54492966 | T | G | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0004t0001g0225 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+2160A>C | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54492966 | |||||||
| chrX:54493067 | G | T | 1 | a0001c0002t0001g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.307+2059C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54493067 | |||||||
| chrX:54493152 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.307+1974G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54493152 | |||||||
| chrX:54493202 | G | C | 1 | a0001c0002t0003g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.307+1924C>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54493202 | |||||||
| chrX:54493302 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.307+1824C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54493302 | |||||||
| chrX:54493653 | G | T | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0004t0001g0225 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+1473C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54493653 | |||||||
| chrX:54493824 | A | C | 88 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(85): Show |
91 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.307+1302T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54493824 | |||||||
| chrX:54494109 | G | A | 1 | a0001c0002t0010g0183 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.307+1017C>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54494109 | |||||||
| chrX:54494391 | C | T | 1 | a0001c0001t0004g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.307+735G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54494391 | |||||||
| chrX:54494402 | C | CT | 59 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(56): Show |
63 | HG00323.hp2 HG00673.hp1 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.307+723dupA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54494402 | |||||||
| chrX:54494402 | C | CTT | 16 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(13): Show |
16 | HG02257.hp1 HG02738.hp1 HG03540.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+722_307+723dup others(2): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54494402 | |||||||
| chrX:54494402 | CT | C | 13 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(10): Show |
13 | HG00621.hp1 HG01069.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.307+723delA | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54494402 | |||||||
| chrX:54494402 | CTT | C | 47 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0001g0214 others(44): Show |
50 | HG00099.hp1 HG00597.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.307+722_307+723del others(2): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54494402 | |||||||
| chrX:54494402 | CTTT | C | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0008g0014 others(5): Show |
8 | HG01099.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.307+721_307+723del others(3): Show |
FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54494402 | |||||||
| chrX:54494427 | TC | T | 4 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0024 others(1): Show |
4 | HG02970.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.307+698delG | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54494427 | |||||||
| chrX:54494692 | A | C | 3 | a0001c0001t0002g0001 a0001c0001t0002g0020 a0001c0001t0002g0021 |
4 | NA18954.hp1 NA18969.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.307+434T>G | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54494692 | |||||||
| chrX:54494716 | C | T | 1 | a0001c0002t0001g0019 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.307+410G>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54494716 | |||||||
| chrX:54494754 | G | T | 1 | a0001c0001t0001g0018 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.307+372C>A | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54494754 | |||||||
| chrX:54495026 | C | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.307+100G>T | FGD1 | ENSG00000102302.8 | transcript | ENST00000375135.4 | protein_coding | 1/17 | chrX | 54495026 |