Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79836 |
| ensemblid | ENSG00000175556.17 |
| hgncid | 21152 |
| symbol | LONRF3 |
| name | LON peptidase N-terminal domain and ring finger 3 |
| refseq_nuc | NM_001031855.3 |
| refseq_prot | NP_001027026.1 |
| ensembl_nuc | ENST00000371628.8 |
| ensembl_prot | ENSP00000360690.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 118974618 |
| end | 119018355 |
| strand | + |
| ver | v1.2 |
| region | chrX:118974618-119018355 |
| region5000 | chrX:118969618-119023355 |
| regionname0 | LONRF3_chrX_118974618_119018355 |
| regionname5000 | LONRF3_chrX_118969618_119023355 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 759 | 304 | 70 | 49 | 140 | 11 | 32 | 113 | LONRF3_chrX_118969618_119023355 | LONRF3 | MESVR others(754): Show |
chrX | 118969618 | 119023355 |
| a0002 | 0/0 | 759 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | MESVR others(754): Show |
chrX | 118969618 | 119023355 |
| a0003 | 0/0 | 759 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | MESVR others(754): Show |
chrX | 118969618 | 119023355 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2277 | 144 | 7 | 26 | 96 | 5 | 9 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATGGA others(2272): Show |
chrX | 118969618 | 119023355 | ||
| a0001c0002 | 0/0 | 2277 | 106 | 44 | 12 | 31 | 5 | 14 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATGGA others(2272): Show |
chrX | 118969618 | 119023355 | ||
| a0001c0003 | 1/0 | 2277 | 25 | 2 | 9 | 7 | 1 | 5 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATGGA others(2272): Show |
chrX | 118969618 | 119023355 | ||
| a0001c0004 | 0/0 | 2277 | 20 | 10 | 1 | 5 | 0 | 4 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATGGA others(2272): Show |
chrX | 118969618 | 119023355 | ||
| a0001c0005 | 0/0 | 2277 | 7 | 6 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATGGA others(2272): Show |
chrX | 118969618 | 119023355 | ||
| a0001c0008 | 0/0 | 2277 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATGGA others(2272): Show |
chrX | 118969618 | 119023355 | ||
| a0001c0009 | 0/0 | 2277 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATGGA others(2272): Show |
chrX | 118969618 | 119023355 | ||
| a0002c0006 | 0/0 | 2277 | 4 | 4 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATGGA others(2272): Show |
chrX | 118969618 | 119023355 | ||
| a0003c0007 | 0/0 | 2277 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATGGA others(2272): Show |
chrX | 118969618 | 119023355 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3108 | 89 | 7 | 20 | 49 | 4 | 8 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0001c0001t0002 | 0/0 | 3107 | 54 | 0 | 6 | 46 | 1 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3102): Show |
chrX | 118969618 | 119023355 |
| a0001c0001t0008 | 0/0 | 3108 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0001c0002t0001 | 0/0 | 3108 | 98 | 36 | 12 | 31 | 5 | 14 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0001c0002t0003 | 0/0 | 3108 | 3 | 3 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0001c0002t0004 | 0/0 | 3108 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0001c0002t0005 | 0/0 | 3108 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0001c0002t0006 | 0/0 | 3108 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0001c0002t0007 | 0/0 | 3108 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0001c0003t0001 | 1/0 | 3108 | 16 | 2 | 9 | 0 | 1 | 3 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0001c0003t0002 | 0/0 | 3107 | 9 | 0 | 0 | 7 | 0 | 2 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3102): Show |
chrX | 118969618 | 119023355 |
| a0001c0004t0001 | 0/0 | 3108 | 20 | 10 | 1 | 5 | 0 | 4 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0001c0005t0001 | 0/0 | 3108 | 7 | 6 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0001c0008t0002 | 0/0 | 3107 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3102): Show |
chrX | 118969618 | 119023355 |
| a0001c0009t0003 | 0/0 | 3108 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0002c0006t0001 | 0/0 | 3108 | 4 | 4 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| a0003c0007t0001 | 0/0 | 3108 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | ATTAG others(3103): Show |
chrX | 118969618 | 119023355 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0001 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0002 | 0/0 | 8 | 0 | 1 | 4 | 2 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0010 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0005t0001g0004 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0005t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0008t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0009t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0002c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0002c0006t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0002c0006t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0002c0006t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0003c0007t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0150 | EUR | GBR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0099 | EUR | GBR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0137 | EUR | GBR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0125 | EUR | FIN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00639 | hp1 | a0001 | c0005 | t0001 | g0004 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0115 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00673 | hp1 | a0001 | c0003 | t0002 | g0068 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0164 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0086 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0087 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01168 | hp2 | a0003 | c0007 | t0001 | g0199 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0163 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0083 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0155 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0223 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0236 | EUR | IBS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0084 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0004 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0026 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0038 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CDX | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0247 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02451 | hp2 | a0002 | c0006 | t0001 | g0143 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02572 | hp1 | a0001 | c0005 | t0001 | g0089 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02615 | hp2 | a0002 | c0006 | t0001 | g0144 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0169 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0173 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02630 | hp1 | a0001 | c0002 | t0006 | g0165 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0107 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0168 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0128 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02809 | hp1 | a0001 | c0002 | t0005 | g0033 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02818 | hp1 | a0001 | c0002 | t0007 | g0166 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0004 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0088 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0092 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0140 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03041 | hp2 | a0002 | c0006 | t0001 | g0235 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03098 | hp1 | a0002 | c0006 | t0001 | g0020 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0162 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03239 | hp2 | a0001 | c0004 | t0001 | g0159 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0179 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0156 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0091 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0053 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0060 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03688 | hp1 | a0001 | c0003 | t0002 | g0241 | SAS | STU | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03704 | hp1 | a0001 | c0004 | t0001 | g0118 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0190 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0146 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0246 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0145 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0229 | SAS | STU | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0158 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0161 | SAS | STU | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0039 | SAS | STU | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | YRI | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18940 | hp1 | a0001 | c0001 | t0008 | g0188 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0048 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18943 | hp1 | a0001 | c0003 | t0002 | g0037 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0139 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18957 | hp2 | a0001 | c0004 | t0001 | g0058 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18968 | hp1 | a0001 | c0004 | t0001 | g0182 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18997 | hp1 | a0001 | c0003 | t0002 | g0014 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19007 | hp1 | a0001 | c0004 | t0001 | g0221 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19010 | hp1 | a0001 | c0008 | t0002 | g0082 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0148 | AFR | LWK | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19030 | hp2 | a0001 | c0009 | t0003 | g0174 | AFR | LWK | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | LWK | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19057 | hp1 | a0001 | c0004 | t0001 | g0181 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19058 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19066 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | YRI | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | ASW | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0073 | AFR | ASW | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | GIH | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0151 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0248 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0195 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0249 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0244 | REF | REF | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0010 | REF | REF | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| 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:118975145 | C | G | 1 | a0002 | 4 | HG02451.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.365C>G | p.Ala122Gly | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/11 | 528/3108 | 365/2280 | 122/759 | chrX | 118975145 | |||
| chrX:118989437 | T | A | 1 | a0003 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.1089T>A | p.Ser363Arg | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/11 | 1252/3108 | 1089/2280 | 363/759 | chrX | 118989437 |
| 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:118974822 | T | C | 5 | a0001c0001 a0001c0004 a0001c0005 others(2): Show |
172 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(169): Show |
synonymous_variant | LOW | c.42T>C | p.Ala14Ala | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/11 | 205/3108 | 42/2280 | 14/759 | chrX | 118974822 | |||
| chrX:118989647 | G | T | 1 | a0001c0008 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.1299G>T | p.Gly433Gly | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/11 | 1462/3108 | 1299/2280 | 433/759 | chrX | 118989647 | |||
| chrX:119009146 | C | T | 2 | a0001c0005 a0001c0009 |
8 | HG00639.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.1551C>T | p.Tyr517Tyr | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/11 | 1714/3108 | 1551/2280 | 517/759 | chrX | 119009146 | |||
| chrX:119014257 | T | C | 1 | a0001c0008 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.2025T>C | p.Tyr675Tyr | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/11 | 2188/3108 | 2025/2280 | 675/759 | chrX | 119014257 | |||
| chrX:119014266 | A | G | 3 | a0001c0002 a0001c0004 a0002c0006 |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
synonymous_variant | LOW | c.2034A>G | p.Ala678Ala | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/11 | 2197/3108 | 2034/2280 | 678/759 | chrX | 119014266 |
| 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:118974657 | G | T | 1 | a0001c0001t0008 | 1 | NA18940.hp1 | 5_prime_UTR_variant | MODIFIER | c.-124G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/11 | 124 | chrX | 118974657 | ||||||
| chrX:118974756 | C | A | 1 | a0001c0002t0005 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/11 | 25 | chrX | 118974756 | ||||||
| chrX:118974766 | C | T | 3 | a0001c0002t0003 a0001c0002t0007 a0001c0009t0003 |
5 | HG02622.hp1 HG02723.hp1 HG02818.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-15C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/11 | chrX | 118974766 | |||||||
| chrX:119017904 | G | A | 2 | a0001c0002t0006 a0001c0002t0007 |
2 | HG02630.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*214G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 214 | chrX | 119017904 | ||||||
| chrX:119018225 | G | A | 1 | a0001c0002t0004 | 2 | HG01891.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*535G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 535 | chrX | 119018225 | ||||||
| chrX:119018279 | TA | T | 3 | a0001c0001t0002 a0001c0003t0002 a0001c0008t0002 |
64 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*590delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 590 | chrX | 119018279 |
| 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:118975668 | C | G | 2 | a0001c0002t0004g0026 a0001c0004t0001g0249 |
3 | HG01891.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.817+71C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118975668 | |||||||
| chrX:118975773 | T | G | 1 | a0001c0002t0001g0027 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.817+176T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118975773 | |||||||
| chrX:118975945 | T | C | 1 | a0001c0004t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.817+348T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118975945 | |||||||
| chrX:118975988 | CCTT | C | 3 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0003g0029 |
3 | HG01106.hp1 HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.817+394_817+396del others(3): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118975988 | ||||||
| chrX:118976030 | C | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG00597.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.817+433C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976030 | |||||||
| chrX:118976103 | G | A | 1 | a0001c0002t0005g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.817+506G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976103 | |||||||
| chrX:118976190 | G | A | 19 | a0001c0001t0001g0034 a0001c0002t0001g0006 a0001c0002t0001g0012 others(16): Show |
22 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.817+593G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976190 | |||||||
| chrX:118976391 | T | C | 1 | a0001c0002t0004g0026 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.817+794T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976391 | |||||||
| chrX:118976479 | C | T | 1 | a0001c0004t0001g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.817+882C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976479 | |||||||
| chrX:118976570 | A | G | 1 | a0001c0004t0001g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.817+973A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976570 | |||||||
| chrX:118976595 | C | T | 20 | a0001c0001t0001g0034 a0001c0002t0001g0006 a0001c0002t0001g0012 others(17): Show |
23 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.817+998C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976595 | |||||||
| chrX:118976602 | G | A | 2 | a0001c0002t0001g0028 a0001c0002t0003g0029 |
2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.817+1005G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976602 | |||||||
| chrX:118976738 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.817+1141C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976738 | |||||||
| chrX:118976813 | C | T | 1 | a0001c0004t0001g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.817+1216C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976813 | |||||||
| chrX:118976814 | G | A | 1 | a0001c0002t0005g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.817+1217G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976814 | |||||||
| chrX:118976925 | C | A | 1 | a0001c0002t0001g0051 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.817+1328C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976925 | |||||||
| chrX:118977058 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.818-1287C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977058 | |||||||
| chrX:118977085 | A | G | 1 | a0001c0003t0002g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.818-1260A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977085 | |||||||
| chrX:118977088 | AAGAC | A | 4 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0052 others(1): Show |
4 | HG01106.hp1 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-1253_818-1250d others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118977088 | ||||||
| chrX:118977170 | G | GA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0064 others(91): Show |
117 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.818-1165dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118977170 | ||||||
| chrX:118977273 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0085 others(64): Show |
87 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.818-1072T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977273 | |||||||
| chrX:118977289 | A | T | 3 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0104 |
3 | NA18946.hp2 NA18991.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.818-1056A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977289 | |||||||
| chrX:118977298 | C | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 |
3 | HG01934.hp1 HG02132.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.818-1047C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977298 | |||||||
| chrX:118977378 | A | G | 25 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0028 others(22): Show |
28 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.818-967A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977378 | |||||||
| chrX:118977676 | C | T | 2 | a0001c0002t0001g0237 a0001c0003t0001g0236 |
2 | HG00639.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.818-669C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977676 | |||||||
| chrX:118977739 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.818-606C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977739 | |||||||
| chrX:118978031 | A | G | 27 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0028 others(24): Show |
31 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.818-314A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118978031 | |||||||
| chrX:118978121 | G | A | 4 | a0001c0002t0001g0017 a0001c0002t0001g0111 a0001c0002t0001g0112 others(1): Show |
5 | HG02055.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.818-224G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118978121 | |||||||
| chrX:118978219 | C | T | 1 | a0001c0003t0001g0107 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.818-126C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118978219 | |||||||
| chrX:118978511 | T | A | 5 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0052 others(2): Show |
6 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.936+48T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978511 | |||||||
| chrX:118978737 | G | C | 3 | a0001c0002t0001g0114 a0001c0002t0001g0116 a0001c0004t0001g0115 |
3 | HG00642.hp1 HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.936+274G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978737 | |||||||
| chrX:118978878 | A | G | 1 | a0001c0002t0005g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.936+415A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978878 | |||||||
| chrX:118978896 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
226 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.936+433A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978896 | |||||||
| chrX:118978897 | C | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(69): Show |
89 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.936+434C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978897 | |||||||
| chrX:118978933 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG00597.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.936+470G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978933 | |||||||
| chrX:118978945 | C | CCCTT | 8 | a0001c0002t0001g0117 a0001c0002t0001g0167 a0001c0002t0001g0170 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.936+503_936+506dup others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118978945 | ||||||
| chrX:118978998 | CT | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(175): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.936+555delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118978998 | ||||||
| chrX:118978998 | CTT | C | 25 | a0001c0001t0001g0031 a0001c0001t0002g0055 a0001c0001t0002g0056 others(22): Show |
28 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.936+554_936+555del others(2): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118978998 | ||||||
| chrX:118979003 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.936+540T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979003 | |||||||
| chrX:118979069 | C | T | 21 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0035 others(18): Show |
24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.936+606C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979069 | |||||||
| chrX:118979101 | C | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0052 |
2 | HG01106.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.936+638C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979101 | |||||||
| chrX:118979177 | T | C | 1 | a0001c0002t0001g0157 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.936+714T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979177 | |||||||
| chrX:118979211 | G | A | 8 | a0001c0002t0001g0167 a0001c0002t0001g0170 a0001c0002t0003g0168 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.936+748G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979211 | |||||||
| chrX:118979245 | C | T | 1 | a0001c0002t0001g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.936+782C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979245 | |||||||
| chrX:118979282 | C | A | 21 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0035 others(18): Show |
24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.936+819C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979282 | |||||||
| chrX:118979282 | C | T | 5 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0052 others(2): Show |
6 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.936+819C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979282 | |||||||
| chrX:118979300 | C | CTTTTTTT others(3): Show |
3 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0004g0026 |
4 | HG01106.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.936+839_936+848dup others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979300 | ||||||
| chrX:118979300 | C | CTTTTTTT others(4): Show |
16 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0035 others(13): Show |
19 | HG00408.hp1 HG00544.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.936+838_936+848dup others(11): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979300 | ||||||
| chrX:118979300 | C | CTTTTTTT others(5): Show |
5 | a0001c0002t0001g0044 a0001c0002t0001g0045 a0001c0002t0001g0046 others(2): Show |
5 | HG00423.hp1 HG02071.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.936+848_936+849ins others(12): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979300 | ||||||
| chrX:118979300 | C | CTTTTTTT others(6): Show |
1 | a0001c0002t0001g0109 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.936+848_936+849ins others(13): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979300 | ||||||
| chrX:118979355 | G | A | 1 | a0001c0004t0001g0173 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.936+892G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979355 | |||||||
| chrX:118979361 | T | G | 21 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0035 others(18): Show |
24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.936+898T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979361 | |||||||
| chrX:118979454 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.936+991C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979454 | |||||||
| chrX:118979487 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0085 others(59): Show |
82 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.936+1024G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979487 | |||||||
| chrX:118979537 | GC | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0085 others(80): Show |
106 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.936+1076delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979537 | ||||||
| chrX:118979638 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0093 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.936+1175G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979638 | |||||||
| chrX:118980125 | C | T | 20 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0035 others(17): Show |
23 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.936+1662C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980125 | |||||||
| chrX:118980222 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(159): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.936+1759G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980222 | |||||||
| chrX:118980230 | A | G | 5 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0052 others(2): Show |
6 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.936+1767A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980230 | |||||||
| chrX:118980356 | T | A | 157 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(154): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.936+1893T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980356 | |||||||
| chrX:118980373 | A | T | 1 | a0001c0005t0001g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.936+1910A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980373 | |||||||
| chrX:118980570 | A | AT | 181 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(178): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.936+2116dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118980570 | ||||||
| chrX:118980632 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(189): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.936+2169A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980632 | |||||||
| chrX:118980903 | T | C | 6 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0044 others(3): Show |
7 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.937-1918T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980903 | |||||||
| chrX:118980923 | A | G | 1 | a0001c0004t0001g0173 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.937-1898A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980923 | |||||||
| chrX:118981209 | G | C | 1 | a0001c0004t0001g0182 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.937-1612G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981209 | |||||||
| chrX:118981336 | T | A | 1 | a0001c0002t0001g0028 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.937-1485T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981336 | |||||||
| chrX:118981354 | G | A | 1 | a0001c0004t0001g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.937-1467G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981354 | |||||||
| chrX:118981365 | G | T | 157 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(154): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.937-1456G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981365 | |||||||
| chrX:118981374 | A | G | 63 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0009 others(60): Show |
75 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.937-1447A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981374 | |||||||
| chrX:118981416 | T | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(180): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.937-1405T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981416 | |||||||
| chrX:118981483 | C | CA | 8 | a0001c0001t0002g0094 a0001c0001t0002g0110 a0001c0002t0001g0035 others(5): Show |
8 | HG00597.hp2 HG01169.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.937-1322dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118981483 | ||||||
| chrX:118981483 | C | CAA | 60 | a0001c0001t0001g0138 a0001c0001t0001g0210 a0001c0001t0001g0242 others(57): Show |
71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.937-1323_937-1322d others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118981483 | ||||||
| chrX:118981483 | C | CAAA | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(95): Show |
118 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.937-1324_937-1322d others(5): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118981483 | ||||||
| chrX:118982013 | G | T | 2 | a0001c0002t0001g0177 a0001c0002t0001g0178 |
2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.937-808G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118982013 | |||||||
| chrX:118982057 | C | G | 1 | a0001c0002t0005g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.937-764C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118982057 | |||||||
| chrX:118982504 | G | C | 1 | a0001c0001t0002g0110 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.937-317G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118982504 | |||||||
| chrX:118982698 | G | A | 1 | a0001c0004t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.937-123G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118982698 | |||||||
| chrX:118982773 | G | A | 26 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0028 others(23): Show |
30 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.937-48G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118982773 | |||||||
| chrX:118983090 | G | A | 2 | a0001c0004t0001g0173 a0001c0004t0001g0179 |
2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1059+147G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118983090 | |||||||
| chrX:118983100 | T | C | 52 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0018 others(49): Show |
61 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1059+157T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118983100 | |||||||
| chrX:118983627 | C | T | 83 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(80): Show |
98 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1059+684C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118983627 | |||||||
| chrX:118983843 | G | A | 3 | a0001c0002t0001g0028 a0001c0002t0001g0044 a0001c0002t0003g0029 |
3 | HG02886.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1059+900G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118983843 | |||||||
| chrX:118983928 | T | G | 10 | a0001c0002t0001g0167 a0001c0002t0003g0168 a0001c0002t0003g0169 others(7): Show |
10 | HG01884.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1059+985T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118983928 | |||||||
| chrX:118984069 | G | C | 8 | a0001c0002t0001g0167 a0001c0002t0003g0168 a0001c0002t0003g0169 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+1126G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118984069 | |||||||
| chrX:118984714 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(181): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1059+1771T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118984714 | |||||||
| chrX:118984722 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(81): Show |
102 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1059+1779C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118984722 | |||||||
| chrX:118985115 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1059+2172C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118985115 | |||||||
| chrX:118985509 | C | A | 1 | a0001c0001t0001g0183 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1059+2566C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118985509 | |||||||
| chrX:118985714 | T | C | 1 | a0001c0002t0001g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1059+2771T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118985714 | |||||||
| chrX:118985739 | A | G | 1 | a0001c0008t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1059+2796A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118985739 | |||||||
| chrX:118986050 | AAACACAC others(4): Show |
A | 1 | a0001c0001t0001g0208 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1059+3109_1059+311 others(15): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986050 | ||||||
| chrX:118986051 | A | AAC | 4 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 others(1): Show |
4 | HG00621.hp1 HG02258.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+3158_1059+315 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | ||||||
| chrX:118986051 | A | AACAC | 3 | a0001c0001t0002g0081 a0001c0001t0002g0180 a0001c0004t0001g0088 |
3 | HG02922.hp1 NA18959.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1059+3156_1059+315 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | ||||||
| chrX:118986051 | AAC | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0097 others(42): Show |
66 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1059+3158_1059+315 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | ||||||
| chrX:118986051 | AACAC | A | 21 | a0001c0001t0002g0007 a0001c0001t0002g0055 a0001c0001t0002g0059 others(18): Show |
24 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1059+3156_1059+315 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | ||||||
| chrX:118986051 | AACACAC | A | 15 | a0001c0001t0001g0085 a0001c0001t0001g0138 a0001c0001t0001g0230 others(12): Show |
15 | HG00140.hp1 HG01106.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.1059+3154_1059+315 others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | ||||||
| chrX:118986051 | AACACACA others(1): Show |
A | 53 | a0001c0001t0001g0024 a0001c0001t0001g0183 a0001c0001t0001g0200 others(50): Show |
62 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.1059+3152_1059+315 others(12): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | ||||||
| chrX:118986051 | AACACACA others(3): Show |
A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(64): Show |
84 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1059+3150_1059+315 others(14): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | ||||||
| chrX:118986051 | AACACACA others(5): Show |
A | 4 | a0001c0001t0001g0240 a0001c0001t0008g0188 a0001c0002t0001g0021 others(1): Show |
5 | HG00741.hp2 HG01109.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+3148_1059+315 others(16): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | ||||||
| chrX:118986051 | AACACACA others(7): Show |
A | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0238 others(10): Show |
15 | HG01243.hp1 HG01934.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1059+3146_1059+315 others(18): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | ||||||
| chrX:118986051 | AACACACA others(9): Show |
A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | HG01257.hp2 HG01258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1059+3144_1059+315 others(20): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | ||||||
| chrX:118986051 | AACACACA others(11): Show |
A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0005g0033 |
3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1059+3142_1059+315 others(22): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | ||||||
| chrX:118986091 | CACACACA others(4): Show |
C | 1 | a0001c0001t0001g0209 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1059+3150_1059+316 others(15): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986091 | ||||||
| chrX:118986529 | A | G | 24 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0206 others(21): Show |
27 | HG00323.hp2 HG00609.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1060-2879A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986529 | |||||||
| chrX:118986622 | G | A | 1 | a0001c0002t0001g0125 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1060-2786G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986622 | |||||||
| chrX:118986681 | C | T | 94 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(91): Show |
109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1060-2727C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986681 | |||||||
| chrX:118986686 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1060-2722C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986686 | |||||||
| chrX:118986972 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1060-2436A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986972 | |||||||
| chrX:118986981 | C | T | 1 | a0001c0004t0001g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1060-2427C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986981 | |||||||
| chrX:118987153 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1060-2255C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987153 | |||||||
| chrX:118987283 | G | A | 4 | a0001c0002t0001g0117 a0001c0002t0001g0126 a0001c0002t0001g0127 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-2125G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987283 | |||||||
| chrX:118987295 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1060-2113T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987295 | |||||||
| chrX:118987419 | A | T | 84 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(81): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1060-1989A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987419 | |||||||
| chrX:118987424 | C | T | 94 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(91): Show |
109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1060-1984C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987424 | |||||||
| chrX:118987445 | G | GT | 15 | a0001c0001t0001g0234 a0001c0001t0002g0075 a0001c0002t0001g0020 others(12): Show |
15 | HG00741.hp1 HG01123.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1060-1935dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | ||||||
| chrX:118987445 | G | GTT | 63 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(60): Show |
78 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1060-1936_1060-193 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | ||||||
| chrX:118987445 | G | GTTT | 14 | a0001c0001t0001g0211 a0001c0002t0001g0035 a0001c0002t0001g0045 others(11): Show |
14 | HG00323.hp1 HG00423.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1060-1937_1060-193 others(7): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | ||||||
| chrX:118987445 | G | GTTTT | 43 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0024 others(40): Show |
53 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1060-1938_1060-193 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | ||||||
| chrX:118987445 | G | GTTTTT | 26 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0031 others(23): Show |
31 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1060-1939_1060-193 others(9): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | ||||||
| chrX:118987445 | G | GTTTTTT | 8 | a0001c0001t0001g0100 a0001c0001t0001g0184 a0001c0001t0001g0185 others(5): Show |
8 | HG00609.hp1 HG00733.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1060-1940_1060-193 others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | ||||||
| chrX:118987445 | G | GTTTTTTT | 8 | a0001c0001t0008g0188 a0001c0002t0001g0017 a0001c0002t0001g0111 others(5): Show |
9 | HG02257.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-1941_1060-193 others(11): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | ||||||
| chrX:118987445 | GT | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0085 others(38): Show |
55 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1060-1935delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | ||||||
| chrX:118987455 | T | G | 1 | a0001c0002t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1060-1953T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987455 | |||||||
| chrX:118987599 | C | T | 4 | a0001c0002t0001g0028 a0001c0002t0001g0140 a0001c0002t0001g0142 others(1): Show |
4 | HG02886.hp1 HG03017.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-1809C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987599 | |||||||
| chrX:118987829 | T | C | 1 | a0003c0007t0001g0199 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1060-1579T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987829 | |||||||
| chrX:118988028 | A | G | 6 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0044 others(3): Show |
7 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-1380A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988028 | |||||||
| chrX:118988032 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0093 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1060-1376C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988032 | |||||||
| chrX:118988056 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1060-1352C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988056 | |||||||
| chrX:118988164 | G | A | 10 | a0001c0002t0001g0167 a0001c0002t0003g0168 a0001c0002t0003g0169 others(7): Show |
10 | HG01884.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1060-1244G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988164 | |||||||
| chrX:118988331 | C | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(189): Show |
226 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1060-1077C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988331 | |||||||
| chrX:118988557 | T | C | 100 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(97): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1060-851T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988557 | |||||||
| chrX:118988729 | T | G | 1 | a0001c0002t0001g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1060-679T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988729 | |||||||
| chrX:118988766 | A | T | 1 | a0001c0002t0001g0045 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1060-642A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988766 | |||||||
| chrX:118988799 | CT | C | 52 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0184 others(49): Show |
57 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1060-594delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118988799 | ||||||
| chrX:118988941 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0228 |
2 | HG00609.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1060-467A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988941 | |||||||
| chrX:118989014 | A | C | 1 | a0001c0003t0002g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1060-394A>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118989014 | |||||||
| chrX:118989127 | A | G | 84 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(81): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1060-281A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118989127 | |||||||
| chrX:118989201 | G | T | 1 | a0001c0004t0001g0139 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1060-207G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118989201 | |||||||
| chrX:118989711 | A | G | 1 | a0001c0004t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1324+39A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | chrX | 118989711 | |||||||
| chrX:118989802 | G | T | 84 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(81): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1324+130G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | chrX | 118989802 | |||||||
| chrX:118989927 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1324+255G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | chrX | 118989927 | |||||||
| chrX:118989976 | G | A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0005g0033 |
3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1324+304G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | chrX | 118989976 | |||||||
| chrX:118990277 | C | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(181): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1325-193C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | chrX | 118990277 | |||||||
| chrX:118990731 | G | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(77): Show |
98 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1415+171G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118990731 | |||||||
| chrX:118990967 | C | G | 10 | a0001c0002t0001g0167 a0001c0002t0003g0168 a0001c0002t0003g0169 others(7): Show |
10 | HG01884.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1415+407C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118990967 | |||||||
| chrX:118991255 | C | A | 107 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(104): Show |
123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1415+695C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118991255 | |||||||
| chrX:118991393 | A | AT | 113 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(110): Show |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1415+833_1415+834i others(3): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118991393 | |||||||
| chrX:118991864 | A | AT | 110 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(107): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1415+1313dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118991864 | ||||||
| chrX:118992335 | C | T | 24 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0020 others(21): Show |
27 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1415+1775C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992335 | |||||||
| chrX:118992672 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1415+2112G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992672 | |||||||
| chrX:118992766 | A | C | 1 | a0001c0003t0001g0158 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1415+2206A>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992766 | |||||||
| chrX:118992775 | A | T | 110 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(107): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1415+2215A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992775 | |||||||
| chrX:118992778 | A | G | 110 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(107): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1415+2218A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992778 | |||||||
| chrX:118992810 | T | C | 100 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(97): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1415+2250T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992810 | |||||||
| chrX:118993121 | C | CCA | 109 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(106): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1415+2562_1415+256 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118993121 | ||||||
| chrX:118993126 | C | T | 1 | a0001c0002t0001g0042 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1415+2566C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993126 | |||||||
| chrX:118993127 | C | A | 1 | a0001c0002t0006g0165 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1415+2567C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993127 | |||||||
| chrX:118993128 | C | G | 1 | a0001c0004t0001g0088 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1415+2568C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993128 | |||||||
| chrX:118993129 | C | A | 109 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(106): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1415+2569C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993129 | |||||||
| chrX:118993193 | T | A | 110 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(107): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1415+2633T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993193 | |||||||
| chrX:118993435 | T | G | 10 | a0001c0002t0001g0017 a0001c0002t0001g0111 a0001c0002t0001g0112 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1415+2875T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993435 | |||||||
| chrX:118993562 | A | G | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0005g0033 |
3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1415+3002A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993562 | |||||||
| chrX:118994056 | A | T | 113 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(110): Show |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1415+3496A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994056 | |||||||
| chrX:118994173 | C | T | 1 | a0001c0003t0001g0236 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1415+3613C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994173 | |||||||
| chrX:118994177 | A | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0077 |
3 | NA18972.hp1 NA19002.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1415+3617A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994177 | |||||||
| chrX:118994228 | T | G | 9 | a0001c0002t0001g0009 a0001c0002t0001g0021 a0001c0002t0001g0027 others(6): Show |
12 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1415+3668T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994228 | |||||||
| chrX:118994408 | A | AT | 110 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(107): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1415+3861dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118994408 | ||||||
| chrX:118994456 | C | T | 1 | a0001c0003t0001g0164 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1415+3896C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994456 | |||||||
| chrX:118994468 | A | G | 2 | a0001c0002t0001g0030 a0001c0002t0001g0052 |
2 | HG01106.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1415+3908A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994468 | |||||||
| chrX:118994506 | G | A | 1 | a0001c0002t0005g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1415+3946G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994506 | |||||||
| chrX:118994526 | C | T | 1 | a0001c0002t0001g0133 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1415+3966C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994526 | |||||||
| chrX:118994601 | C | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0005g0033 |
3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1415+4041C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994601 | |||||||
| chrX:118994901 | G | A | 1 | a0001c0003t0002g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1415+4341G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994901 | |||||||
| chrX:118995051 | T | G | 13 | a0001c0002t0001g0017 a0001c0002t0001g0105 a0001c0002t0001g0106 others(10): Show |
14 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1415+4491T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995051 | |||||||
| chrX:118995316 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1415+4756A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995316 | |||||||
| chrX:118995397 | T | C | 1 | a0001c0002t0001g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1415+4837T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995397 | |||||||
| chrX:118995462 | C | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0196 others(2): Show |
5 | HG00280.hp1 HG00733.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1415+4902C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995462 | |||||||
| chrX:118995611 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1415+5051G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995611 | |||||||
| chrX:118995805 | A | C | 6 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0044 others(3): Show |
7 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1415+5245A>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995805 | |||||||
| chrX:118996029 | G | T | 1 | a0001c0002t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1415+5469G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996029 | |||||||
| chrX:118996100 | A | G | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0005g0033 |
3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1415+5540A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996100 | |||||||
| chrX:118996105 | G | A | 10 | a0001c0002t0001g0167 a0001c0002t0003g0168 a0001c0002t0003g0169 others(7): Show |
10 | HG01884.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1415+5545G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996105 | |||||||
| chrX:118996166 | T | C | 1 | a0001c0002t0001g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1415+5606T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996166 | |||||||
| chrX:118996217 | G | A | 94 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(91): Show |
109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1415+5657G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996217 | |||||||
| chrX:118996478 | A | G | 3 | a0001c0002t0001g0140 a0001c0002t0001g0142 a0001c0002t0001g0146 |
3 | HG03017.hp1 HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1415+5918A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996478 | |||||||
| chrX:118996660 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(243): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1415+6100T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996660 | |||||||
| chrX:118996704 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1415+6144C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996704 | |||||||
| chrX:118996767 | A | G | 5 | a0001c0002t0001g0019 a0001c0002t0001g0132 a0001c0002t0001g0153 others(2): Show |
6 | HG02083.hp1 NA18941.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1415+6207A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996767 | |||||||
| chrX:118996921 | C | CA | 6 | a0001c0001t0001g0032 a0001c0001t0001g0100 a0001c0001t0001g0213 others(3): Show |
6 | HG00597.hp1 HG01256.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1415+6378dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118996921 | ||||||
| chrX:118996921 | CA | C | 73 | a0001c0001t0001g0138 a0001c0001t0001g0225 a0001c0001t0002g0072 others(70): Show |
85 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1415+6378delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118996921 | ||||||
| chrX:118997048 | A | G | 21 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0035 others(18): Show |
24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1415+6488A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118997048 | |||||||
| chrX:118997468 | C | A | 1 | a0001c0001t0008g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1415+6908C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118997468 | |||||||
| chrX:118997722 | T | G | 1 | a0001c0004t0001g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1415+7162T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118997722 | |||||||
| chrX:118997785 | A | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 |
3 | HG01934.hp1 HG02132.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1415+7225A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118997785 | |||||||
| chrX:118997865 | A | G | 96 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(93): Show |
111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1415+7305A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118997865 | |||||||
| chrX:118998097 | T | C | 3 | a0001c0003t0001g0083 a0001c0003t0001g0086 a0001c0003t0001g0087 |
3 | HG01099.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1415+7537T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998097 | |||||||
| chrX:118998185 | C | CA | 116 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(113): Show |
133 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1415+7626dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118998185 | ||||||
| chrX:118998259 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1415+7699A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998259 | |||||||
| chrX:118998320 | G | C | 3 | a0001c0003t0002g0037 a0001c0003t0002g0038 a0001c0003t0002g0048 |
3 | HG02027.hp1 NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1415+7760G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998320 | |||||||
| chrX:118998500 | G | A | 2 | a0001c0004t0001g0091 a0001c0004t0001g0092 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1416-7621G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998500 | |||||||
| chrX:118998515 | G | A | 2 | a0001c0002t0001g0167 a0001c0002t0003g0169 |
2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1416-7606G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998515 | |||||||
| chrX:118998724 | C | A | 1 | a0001c0004t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1416-7397C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998724 | |||||||
| chrX:118998742 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1416-7379C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998742 | |||||||
| chrX:118998744 | C | T | 1 | a0001c0002t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1416-7377C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998744 | |||||||
| chrX:118998823 | C | A | 1 | a0001c0002t0005g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1416-7298C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998823 | |||||||
| chrX:118998940 | G | A | 10 | a0001c0002t0001g0017 a0001c0002t0001g0111 a0001c0002t0001g0112 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416-7181G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998940 | |||||||
| chrX:118999058 | G | A | 1 | a0001c0002t0003g0029 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1416-7063G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999058 | |||||||
| chrX:118999113 | C | T | 1 | a0001c0002t0006g0165 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1416-7008C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999113 | |||||||
| chrX:118999145 | C | T | 1 | a0001c0001t0008g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1416-6976C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999145 | |||||||
| chrX:118999148 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1416-6973T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999148 | |||||||
| chrX:118999228 | A | G | 9 | a0001c0002t0001g0009 a0001c0002t0001g0021 a0001c0002t0001g0027 others(6): Show |
12 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1416-6893A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999228 | |||||||
| chrX:118999334 | C | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0093 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1416-6787C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999334 | |||||||
| chrX:118999466 | GTAGACT | G | 10 | a0001c0002t0001g0017 a0001c0002t0001g0111 a0001c0002t0001g0112 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416-6653_1416-664 others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118999466 | ||||||
| chrX:118999661 | A | C | 1 | a0001c0008t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1416-6460A>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999661 | |||||||
| chrX:118999761 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1416-6360G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999761 | |||||||
| chrX:118999825 | C | T | 1 | a0001c0008t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1416-6296C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999825 | |||||||
| chrX:119000169 | T | A | 1 | a0001c0001t0001g0025 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1416-5952T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000169 | |||||||
| chrX:119000300 | T | A | 1 | a0001c0001t0001g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1416-5821T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000300 | |||||||
| chrX:119000324 | A | G | 2 | a0001c0002t0001g0140 a0001c0002t0001g0146 |
2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1416-5797A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000324 | |||||||
| chrX:119000478 | C | G | 10 | a0001c0002t0001g0167 a0001c0002t0003g0168 a0001c0002t0003g0169 others(7): Show |
10 | HG01884.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1416-5643C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000478 | |||||||
| chrX:119000566 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1416-5555C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000566 | |||||||
| chrX:119000775 | TTCTC | T | 3 | a0001c0003t0001g0010 a0001c0003t0001g0164 a0001c0003t0002g0241 |
3 | HG00741.hp1 HG01168.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1416-5285_1416-528 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTC | T | 8 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0057 others(5): Show |
8 | HG01074.hp1 HG01169.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1416-5287_1416-528 others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(1): Show |
T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0064 a0001c0001t0001g0085 others(11): Show |
14 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.1416-5289_1416-528 others(12): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(3): Show |
T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0098 a0001c0001t0002g0001 others(14): Show |
20 | HG00099.hp2 HG00621.hp1 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.1416-5291_1416-528 others(14): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(5): Show |
T | 8 | a0001c0001t0002g0016 a0001c0001t0002g0059 a0001c0001t0002g0065 others(5): Show |
8 | HG00673.hp1 HG01928.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1416-5293_1416-528 others(16): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(7): Show |
T | 14 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0007 others(11): Show |
18 | HG01261.hp1 HG01978.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.1416-5295_1416-528 others(18): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(9): Show |
T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0234 a0001c0001t0002g0008 others(17): Show |
23 | HG00438.hp2 HG00639.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1416-5297_1416-528 others(20): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(11): Show |
T | 23 | a0001c0001t0002g0074 a0001c0002t0001g0002 a0001c0002t0001g0006 others(20): Show |
26 | HG00140.hp1 HG01192.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.1416-5299_1416-528 others(22): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(13): Show |
T | 35 | a0001c0001t0001g0101 a0001c0002t0001g0002 a0001c0002t0001g0018 others(32): Show |
36 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1416-5301_1416-528 others(24): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(15): Show |
T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0194 others(18): Show |
24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1416-5303_1416-528 others(26): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(17): Show |
T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0138 others(13): Show |
19 | HG02083.hp1 HG02280.hp1 HG02738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1416-5305_1416-528 others(28): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(19): Show |
T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(50): Show |
59 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1416-5307_1416-528 others(30): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(21): Show |
T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0189 others(15): Show |
20 | HG00323.hp2 HG00438.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1416-5309_1416-528 others(32): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(23): Show |
T | 9 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0184 others(6): Show |
9 | HG00280.hp1 HG00733.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1416-5311_1416-528 others(34): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(25): Show |
T | 14 | a0001c0002t0001g0017 a0001c0002t0001g0105 a0001c0002t0001g0106 others(11): Show |
15 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1416-5313_1416-528 others(36): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000775 | TTCTCTCT others(29): Show |
T | 1 | a0001c0001t0001g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1416-5317_1416-528 others(40): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | ||||||
| chrX:119000849 | C | T | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0005g0033 |
3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1416-5272C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000849 | |||||||
| chrX:119000971 | G | T | 21 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0035 others(18): Show |
24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1416-5150G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000971 | |||||||
| chrX:119001189 | C | G | 24 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0100 others(21): Show |
27 | HG00323.hp2 HG00609.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1416-4932C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119001189 | |||||||
| chrX:119001746 | G | A | 1 | a0001c0003t0001g0236 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1416-4375G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119001746 | |||||||
| chrX:119001788 | T | A | 2 | a0001c0002t0001g0028 a0001c0002t0003g0029 |
2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1416-4333T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119001788 | |||||||
| chrX:119001960 | T | C | 65 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0009 others(62): Show |
77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1416-4161T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119001960 | |||||||
| chrX:119002005 | C | T | 1 | a0001c0002t0001g0237 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1416-4116C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002005 | |||||||
| chrX:119002262 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1416-3859C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002262 | |||||||
| chrX:119002285 | C | G | 10 | a0001c0002t0001g0017 a0001c0002t0001g0111 a0001c0002t0001g0112 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416-3836C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002285 | |||||||
| chrX:119002311 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0001g0101 a0001c0003t0001g0083 others(2): Show |
5 | HG01099.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1416-3810C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002311 | |||||||
| chrX:119002451 | A | G | 117 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0006 others(114): Show |
134 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1416-3670A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002451 | |||||||
| chrX:119002734 | G | A | 1 | a0001c0003t0002g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1416-3387G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002734 | |||||||
| chrX:119002806 | T | A | 3 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0005g0033 |
3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1416-3315T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002806 | |||||||
| chrX:119003362 | C | T | 6 | a0001c0001t0002g0013 a0001c0001t0002g0062 a0001c0001t0002g0069 others(3): Show |
7 | HG00621.hp1 NA18952.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1416-2759C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119003362 | |||||||
| chrX:119003500 | C | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(67): Show |
87 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1416-2621C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119003500 | |||||||
| chrX:119003750 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1416-2371T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119003750 | |||||||
| chrX:119003856 | C | T | 65 | a0001c0001t0001g0138 a0001c0002t0001g0002 a0001c0002t0001g0009 others(62): Show |
77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1416-2265C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119003856 | |||||||
| chrX:119003980 | CGTGT | C | 10 | a0001c0002t0001g0017 a0001c0002t0001g0111 a0001c0002t0001g0112 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416-2134_1416-213 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119003980 | ||||||
| chrX:119003985 | G | C | 1 | a0001c0001t0002g0055 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1416-2136G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119003985 | |||||||
| chrX:119004100 | GT | G | 10 | a0001c0002t0001g0017 a0001c0002t0001g0111 a0001c0002t0001g0112 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416-2014delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119004100 | ||||||
| chrX:119004233 | A | G | 2 | a0001c0004t0001g0173 a0001c0004t0001g0179 |
2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1416-1888A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119004233 | |||||||
| chrX:119004464 | A | G | 2 | a0001c0002t0001g0030 a0001c0002t0001g0052 |
2 | HG01106.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1416-1657A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119004464 | |||||||
| chrX:119004568 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1416-1553C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119004568 | |||||||
| chrX:119004576 | G | A | 1 | a0001c0008t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1416-1545G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119004576 | |||||||
| chrX:119004851 | G | A | 4 | a0001c0002t0001g0117 a0001c0002t0001g0126 a0001c0002t0001g0127 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1416-1270G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119004851 | |||||||
| chrX:119005060 | T | G | 12 | a0001c0002t0001g0167 a0001c0002t0003g0168 a0001c0002t0003g0169 others(9): Show |
12 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1416-1061T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119005060 | |||||||
| chrX:119005340 | A | G | 1 | a0001c0002t0001g0030 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1416-781A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119005340 | |||||||
| chrX:119005428 | A | ATG | 11 | a0001c0002t0001g0017 a0001c0002t0001g0052 a0001c0002t0001g0111 others(8): Show |
12 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1416-691_1416-690d others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119005428 | ||||||
| chrX:119005778 | G | A | 1 | a0001c0002t0005g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1416-343G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119005778 | |||||||
| chrX:119006017 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1416-104C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119006017 | |||||||
| chrX:119006398 | C | CT | 28 | a0001c0001t0001g0098 a0001c0001t0001g0187 a0001c0001t0001g0202 others(25): Show |
29 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1530+184dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006398 | ||||||
| chrX:119006398 | C | CTT | 11 | a0001c0002t0001g0017 a0001c0002t0001g0052 a0001c0002t0001g0111 others(8): Show |
12 | HG00673.hp1 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1530+183_1530+184d others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006398 | ||||||
| chrX:119006398 | C | CTTT | 6 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0044 others(3): Show |
7 | HG01106.hp1 HG01891.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+182_1530+184d others(5): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006398 | ||||||
| chrX:119006398 | C | T | 1 | a0001c0002t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1530+163C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006398 | |||||||
| chrX:119006398 | CT | C | 16 | a0001c0001t0001g0138 a0001c0001t0001g0193 a0001c0001t0001g0200 others(13): Show |
16 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1530+184delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006398 | ||||||
| chrX:119006562 | G | A | 11 | a0001c0002t0001g0017 a0001c0002t0001g0052 a0001c0002t0001g0111 others(8): Show |
12 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1530+327G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006562 | |||||||
| chrX:119006568 | T | TTTTTG | 65 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(62): Show |
82 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1530+366_1530+370d others(7): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006568 | ||||||
| chrX:119006568 | T | TTTTTGTT others(3): Show |
8 | a0001c0001t0001g0085 a0001c0001t0001g0194 a0001c0001t0001g0216 others(5): Show |
8 | HG00609.hp1 HG00733.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1530+361_1530+370d others(12): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006568 | ||||||
| chrX:119006568 | TTTTTG | T | 117 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0009 others(114): Show |
134 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1530+366_1530+370d others(7): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006568 | ||||||
| chrX:119006688 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1530+453T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006688 | |||||||
| chrX:119006743 | C | T | 1 | a0001c0004t0001g0229 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1530+508C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006743 | |||||||
| chrX:119006831 | A | G | 1 | a0001c0002t0001g0028 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1530+596A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006831 | |||||||
| chrX:119006834 | C | T | 1 | a0001c0002t0001g0028 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1530+599C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006834 | |||||||
| chrX:119006883 | C | T | 65 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0018 others(62): Show |
77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1530+648C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006883 | |||||||
| chrX:119007511 | T | C | 2 | a0001c0002t0006g0165 a0001c0002t0007g0166 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1530+1276T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119007511 | |||||||
| chrX:119007572 | C | T | 1 | a0001c0004t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1530+1337C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119007572 | |||||||
| chrX:119007732 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1531-1394T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119007732 | |||||||
| chrX:119008130 | T | G | 2 | a0001c0004t0001g0088 a0001c0004t0001g0248 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1531-996T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119008130 | |||||||
| chrX:119008384 | T | G | 1 | a0001c0001t0002g0074 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1531-742T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119008384 | |||||||
| chrX:119008661 | C | A | 1 | a0001c0009t0003g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1531-465C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119008661 | |||||||
| chrX:119008965 | A | G | 5 | a0001c0002t0001g0019 a0001c0002t0001g0132 a0001c0002t0001g0153 others(2): Show |
6 | HG02083.hp1 NA18941.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1531-161A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119008965 | |||||||
| chrX:119009080 | A | G | 113 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0009 others(110): Show |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1531-46A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119009080 | |||||||
| chrX:119009288 | G | A | 2 | a0001c0001t0002g0057 a0001c0001t0002g0078 |
2 | NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1652+41G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009288 | |||||||
| chrX:119009568 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1652+321G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009568 | |||||||
| chrX:119009695 | A | G | 1 | a0001c0009t0003g0174 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1652+448A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009695 | |||||||
| chrX:119009756 | C | T | 1 | a0001c0002t0005g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1652+509C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009756 | |||||||
| chrX:119009855 | C | T | 55 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0019 others(52): Show |
64 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1652+608C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009855 | |||||||
| chrX:119009856 | G | A | 1 | a0001c0004t0001g0249 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1652+609G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009856 | |||||||
| chrX:119009863 | G | A | 19 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0035 others(16): Show |
22 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1652+616G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009863 | |||||||
| chrX:119009894 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1652+647C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009894 | |||||||
| chrX:119010098 | A | T | 1 | a0001c0002t0001g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1652+851A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010098 | |||||||
| chrX:119010168 | G | A | 4 | a0001c0002t0001g0028 a0001c0002t0001g0044 a0001c0002t0003g0029 others(1): Show |
5 | HG01891.hp1 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1652+921G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010168 | |||||||
| chrX:119010197 | A | G | 19 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0035 others(16): Show |
22 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1652+950A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010197 | |||||||
| chrX:119010208 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(67): Show |
87 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1652+961C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010208 | |||||||
| chrX:119010484 | G | GT | 7 | a0001c0001t0001g0192 a0001c0001t0002g0061 a0001c0002t0001g0130 others(4): Show |
7 | HG02630.hp2 HG02738.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1652+1247dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 119010484 | ||||||
| chrX:119010777 | T | C | 8 | a0001c0002t0001g0167 a0001c0002t0003g0168 a0001c0002t0003g0169 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1653-1038T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010777 | |||||||
| chrX:119010890 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1653-925G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010890 | |||||||
| chrX:119011108 | C | T | 11 | a0001c0002t0001g0017 a0001c0002t0001g0052 a0001c0002t0001g0111 others(8): Show |
12 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1653-707C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119011108 | |||||||
| chrX:119011112 | T | TA | 6 | a0001c0002t0001g0009 a0001c0002t0001g0021 a0001c0002t0001g0040 others(3): Show |
9 | HG00673.hp1 HG01109.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1653-686dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 119011112 | ||||||
| chrX:119011112 | TA | T | 12 | a0001c0001t0001g0198 a0001c0001t0002g0067 a0001c0001t0002g0095 others(9): Show |
12 | HG01257.hp1 HG02559.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.1653-686delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 119011112 | ||||||
| chrX:119011280 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1653-535T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119011280 | |||||||
| chrX:119011369 | G | C | 1 | a0001c0003t0002g0048 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1653-446G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119011369 | |||||||
| chrX:119011457 | G | T | 11 | a0001c0002t0001g0017 a0001c0002t0001g0052 a0001c0002t0001g0111 others(8): Show |
12 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1653-358G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119011457 | |||||||
| chrX:119011514 | A | G | 1 | a0001c0003t0001g0158 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1653-301A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119011514 | |||||||
| chrX:119012013 | T | C | 3 | a0001c0002t0001g0140 a0001c0002t0001g0142 a0001c0002t0001g0146 |
3 | HG03017.hp1 HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1811+40T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012013 | |||||||
| chrX:119012050 | G | A | 2 | a0001c0004t0001g0173 a0001c0004t0001g0179 |
2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1811+77G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012050 | |||||||
| chrX:119012375 | G | A | 4 | a0001c0005t0001g0004 a0001c0005t0001g0073 a0001c0005t0001g0089 others(1): Show |
8 | HG00639.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1811+402G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012375 | |||||||
| chrX:119012618 | A | G | 1 | a0001c0002t0001g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1812-421A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012618 | |||||||
| chrX:119012847 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(67): Show |
87 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1812-192C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012847 | |||||||
| chrX:119012925 | A | G | 1 | a0002c0006t0001g0235 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1812-114A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012925 | |||||||
| chrX:119013270 | G | T | 101 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0009 others(98): Show |
117 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1974+69G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013270 | |||||||
| chrX:119013502 | G | A | 113 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0009 others(110): Show |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1974+301G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013502 | |||||||
| chrX:119013655 | C | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(186): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1974+454C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013655 | |||||||
| chrX:119013838 | G | A | 1 | a0001c0002t0001g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1975-369G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013838 | |||||||
| chrX:119013891 | G | A | 1 | a0001c0004t0001g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1975-316G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013891 | |||||||
| chrX:119013893 | C | G | 1 | a0001c0001t0002g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1975-314C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013893 | |||||||
| chrX:119013961 | C | T | 8 | a0001c0002t0001g0009 a0001c0002t0001g0021 a0001c0002t0001g0027 others(5): Show |
11 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1975-246C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013961 | |||||||
| chrX:119014104 | T | C | 1 | a0001c0004t0001g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1975-103T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119014104 | |||||||
| chrX:119014473 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2124+117G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119014473 | |||||||
| chrX:119014659 | C | T | 11 | a0001c0002t0001g0017 a0001c0002t0001g0052 a0001c0002t0001g0111 others(8): Show |
12 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2124+303C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119014659 | |||||||
| chrX:119015168 | G | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(187): Show |
224 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.2124+812G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015168 | |||||||
| chrX:119015235 | T | C | 96 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0009 others(93): Show |
111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2124+879T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015235 | |||||||
| chrX:119015306 | G | A | 102 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0009 others(99): Show |
118 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2124+950G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015306 | |||||||
| chrX:119015403 | G | A | 96 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0009 others(93): Show |
111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2124+1047G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015403 | |||||||
| chrX:119015437 | G | A | 1 | a0001c0003t0001g0162 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2124+1081G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015437 | |||||||
| chrX:119015476 | C | A | 5 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0044 others(2): Show |
6 | HG01106.hp1 HG01891.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2124+1120C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015476 | |||||||
| chrX:119015552 | G | A | 1 | a0001c0001t0002g0099 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2124+1196G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015552 | |||||||
| chrX:119015662 | A | G | 1 | a0001c0002t0005g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2124+1306A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015662 | |||||||
| chrX:119016026 | G | A | 1 | a0001c0002t0001g0160 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-1509G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016026 | |||||||
| chrX:119016027 | A | G | 1 | a0001c0002t0001g0160 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-1508A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016027 | |||||||
| chrX:119016053 | T | C | 113 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0009 others(110): Show |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.2125-1482T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016053 | |||||||
| chrX:119016095 | C | T | 17 | a0001c0002t0001g0006 a0001c0002t0001g0012 a0001c0002t0001g0035 others(14): Show |
20 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.2125-1440C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016095 | |||||||
| chrX:119016258 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2125-1277A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016258 | |||||||
| chrX:119016274 | G | C | 2 | a0001c0001t0002g0059 a0001c0001t0002g0093 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.2125-1261G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016274 | |||||||
| chrX:119016330 | A | ATTTC | 56 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0023 others(53): Show |
68 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.2125-1185_2125-118 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016330 | ||||||
| chrX:119016330 | A | ATTTCTTT others(1): Show |
13 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(10): Show |
18 | HG00544.hp1 HG00597.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.2125-1189_2125-118 others(12): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016330 | ||||||
| chrX:119016350 | C | CT | 94 | a0001c0001t0001g0101 a0001c0001t0002g0067 a0001c0002t0001g0002 others(91): Show |
110 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2125-1169dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016350 | ||||||
| chrX:119016350 | C | CTT | 16 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0044 others(13): Show |
17 | HG00140.hp1 HG01106.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2125-1170_2125-116 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016350 | ||||||
| chrX:119016501 | C | A | 1 | a0001c0002t0005g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2125-1034C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016501 | |||||||
| chrX:119016502 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2125-1033C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016502 | |||||||
| chrX:119016503 | G | T | 6 | a0001c0002t0001g0012 a0001c0002t0001g0035 a0001c0002t0001g0040 others(3): Show |
7 | NA18956.hp1 NA18960.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125-1032G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016503 | |||||||
| chrX:119016504 | C | A | 84 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0009 others(81): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.2125-1031C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016504 | |||||||
| chrX:119016671 | A | C | 1 | a0001c0002t0001g0160 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-864A>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016671 | |||||||
| chrX:119016695 | C | A | 5 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0044 others(2): Show |
6 | HG01106.hp1 HG01891.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2125-840C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016695 | |||||||
| chrX:119016704 | A | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(187): Show |
224 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.2125-831A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016704 | |||||||
| chrX:119017181 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2125-354C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119017181 | |||||||
| chrX:119017187 | G | A | 1 | a0001c0002t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2125-348G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119017187 |