Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1479 |
| ensemblid | ENSG00000176102.13 |
| hgncid | 2485 |
| symbol | CSTF3 |
| name | cleavage stimulation factor subunit 3 |
| refseq_nuc | NM_001326.3 |
| refseq_prot | NP_001317.1 |
| ensembl_nuc | ENST00000323959.9 |
| ensembl_prot | ENSP00000315791.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 33084584 |
| end | 33161480 |
| strand | - |
| ver | v1.2 |
| region | chr11:33084584-33161480 |
| region5000 | chr11:33079584-33166480 |
| regionname0 | CSTF3_chr11_33084584_33161480 |
| regionname5000 | CSTF3_chr11_33079584_33166480 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2151 | 353 | 90 | 49 | 170 | 14 | 28 | CSTF3_chr11_33079584_33166480 | CSTF3 | ATGTC others(2146): Show |
chr11 | 33079584 | 33166480 | ||
| a0001c0002 | 0/0 | 2151 | 4 | 0 | 4 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | ATGTC others(2146): Show |
chr11 | 33079584 | 33166480 | ||
| a0001c0003 | 0/0 | 2151 | 3 | 0 | 3 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | ATGTC others(2146): Show |
chr11 | 33079584 | 33166480 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2812 | 149 | 68 | 16 | 49 | 6 | 9 | CSTF3_chr11_33079584_33166480 | CSTF3 | AATTC others(2807): Show |
chr11 | 33079584 | 33166480 |
| a0001c0001t0002 | 0/0 | 2812 | 104 | 10 | 15 | 64 | 2 | 13 | CSTF3_chr11_33079584_33166480 | CSTF3 | AATTC others(2807): Show |
chr11 | 33079584 | 33166480 |
| a0001c0001t0003 | 0/1 | 2812 | 91 | 12 | 17 | 50 | 6 | 5 | CSTF3_chr11_33079584_33166480 | CSTF3 | AATTC others(2807): Show |
chr11 | 33079584 | 33166480 |
| a0001c0001t0004 | 0/0 | 2812 | 6 | 0 | 0 | 6 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | AATTC others(2807): Show |
chr11 | 33079584 | 33166480 |
| a0001c0001t0005 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | AATTC others(2807): Show |
chr11 | 33079584 | 33166480 |
| a0001c0001t0006 | 0/0 | 2812 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | AATTC others(2807): Show |
chr11 | 33079584 | 33166480 |
| a0001c0001t0007 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | AATTC others(2807): Show |
chr11 | 33079584 | 33166480 |
| a0001c0002t0002 | 0/0 | 2812 | 4 | 0 | 4 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | AATTC others(2807): Show |
chr11 | 33079584 | 33166480 |
| a0001c0003t0002 | 0/0 | 2812 | 3 | 0 | 3 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | AATTC others(2807): Show |
chr11 | 33079584 | 33166480 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0010 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0005 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0001t0007g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0002t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0003t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| a0001c0003t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0131 | EUR | GBR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | GBR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | FIN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | FIN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0116 | EUR | FIN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0014 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0014 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0191 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0019 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0067 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0165 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0019 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0122 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CDX | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | CDX | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | CDX | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | CDX | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0026 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0123 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0172 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0142 | SAS | STU | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0134 | EUR | TSI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | GIH | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | GIH | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | MSL | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | USA | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | USA | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | USA | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | USA | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | LWK | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0118 | REF | REF | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0010 | REF | REF | CSTF3_chr11_33079584_33166480 | CSTF3 | chr11 | 33079584 | 33166480 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:33090595 | A | G | 1 | a0001c0002 | 4 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
synonymous_variant | LOW | c.1578T>C | p.Asp526Asp | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/21 | 1733/2812 | 1578/2154 | 526/717 | chr11 | 33090595 | |||
| chr11:33099620 | G | A | 1 | a0001c0003 | 3 | HG01070.hp1 HG01071.hp2 HG02300.hp1 |
synonymous_variant | LOW | c.924C>T | p.Leu308Leu | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 11/21 | 1079/2812 | 924/2154 | 308/717 | chr11 | 33099620 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:33084710 | A | G | 1 | a0001c0001t0006 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 21/21 | 377 | chr11 | 33084710 | ||||||
| chr11:33085070 | C | T | 2 | a0001c0001t0003 a0001c0001t0006 |
91 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*17G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 21/21 | 17 | chr11 | 33085070 | ||||||
| chr11:33161377 | A | G | 1 | a0001c0001t0007 | 1 | HG01433.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/21 | 52 | chr11 | 33161377 | ||||||
| chr11:33161395 | A | G | 1 | a0001c0001t0004 | 6 | HG00423.hp1 HG02135.hp1 NA18945.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-70T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/21 | 70 | chr11 | 33161395 | ||||||
| chr11:33161422 | C | G | 1 | a0001c0001t0005 | 1 | NA18942.hp2 | 5_prime_UTR_variant | MODIFIER | c.-97G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/21 | 97 | chr11 | 33161422 | ||||||
| chr11:33161471 | A | G | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(3): Show |
203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-146T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/21 | chr11 | 33161471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:33085320 | CAT | C | 15 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0200 others(12): Show |
15 | HG00280.hp1 HG00733.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1952-33_1952-32del others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 20/20 | chr11 | 33085320 | |||||||
| chr11:33085362 | C | CTTTATAG | 199 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(196): Show |
224 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.1952-74_1952-73ins others(7): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 20/20 | chr11 | 33085362 | |||||||
| chr11:33085556 | T | C | 223 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(220): Show |
248 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1951+157A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 20/20 | chr11 | 33085556 | |||||||
| chr11:33085660 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1951+53G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 20/20 | chr11 | 33085660 | |||||||
| chr11:33086018 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1796-29C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086018 | |||||||
| chr11:33086146 | C | CAG | 232 | a0001c0001t0001g0023 a0001c0001t0001g0192 a0001c0001t0001g0193 others(229): Show |
258 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1796-159_1796-158d others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086146 | |||||||
| chr11:33086287 | T | G | 1 | a0001c0001t0001g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1796-298A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086287 | |||||||
| chr11:33086304 | A | G | 1 | a0001c0001t0006g0172 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1796-315T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086304 | |||||||
| chr11:33086442 | C | CT | 121 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(118): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1796-454dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086442 | |||||||
| chr11:33086442 | C | CTT | 88 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(85): Show |
94 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1796-455_1796-454d others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086442 | |||||||
| chr11:33086442 | C | CTTT | 6 | a0001c0001t0002g0020 a0001c0001t0002g0031 a0001c0001t0002g0066 others(3): Show |
7 | HG00597.hp1 HG01261.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1796-456_1796-454d others(5): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086442 | |||||||
| chr11:33086468 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1796-479C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086468 | |||||||
| chr11:33086524 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1795+464C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086524 | |||||||
| chr11:33086571 | G | A | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1795+417C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086571 | |||||||
| chr11:33086623 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1795+365T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086623 | |||||||
| chr11:33086700 | A | T | 1 | a0001c0001t0003g0186 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1795+288T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086700 | |||||||
| chr11:33086704 | C | T | 1 | a0001c0001t0003g0120 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1795+284G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086704 | |||||||
| chr11:33086720 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1795+268T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 18/20 | chr11 | 33086720 | |||||||
| chr11:33087955 | C | T | 87 | a0001c0001t0002g0006 a0001c0001t0002g0105 a0001c0001t0002g0108 others(84): Show |
105 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1642-814G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33087955 | |||||||
| chr11:33088213 | C | CTT | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1642-1073_1642-107 others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088213 | |||||||
| chr11:33088219 | A | G | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1642-1078T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088219 | |||||||
| chr11:33088289 | C | CT | 43 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(40): Show |
43 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1642-1149dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088289 | |||||||
| chr11:33088429 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1642-1288G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088429 | |||||||
| chr11:33088564 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1642-1423C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088564 | |||||||
| chr11:33088583 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1642-1442T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088583 | |||||||
| chr11:33088680 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1642-1539T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088680 | |||||||
| chr11:33088714 | G | T | 1 | a0001c0001t0003g0126 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1642-1573C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088714 | |||||||
| chr11:33088731 | C | T | 87 | a0001c0001t0002g0006 a0001c0001t0002g0105 a0001c0001t0002g0108 others(84): Show |
105 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1642-1590G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088731 | |||||||
| chr11:33088772 | A | G | 5 | a0001c0001t0002g0057 a0001c0001t0002g0062 a0001c0001t0002g0064 others(2): Show |
5 | HG02165.hp1 NA18978.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1642-1631T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088772 | |||||||
| chr11:33088881 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1641+1651C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33088881 | |||||||
| chr11:33089276 | G | A | 1 | a0001c0001t0003g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1641+1256C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089276 | |||||||
| chr11:33089344 | C | CA | 85 | a0001c0001t0002g0006 a0001c0001t0002g0049 a0001c0001t0002g0105 others(82): Show |
105 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1641+1187dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089344 | |||||||
| chr11:33089344 | CA | C | 52 | a0001c0001t0001g0023 a0001c0001t0001g0192 a0001c0001t0001g0193 others(49): Show |
53 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1641+1187delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089344 | |||||||
| chr11:33089386 | A | G | 2 | a0001c0001t0002g0112 a0001c0001t0002g0157 |
2 | NA18967.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1641+1146T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089386 | |||||||
| chr11:33089697 | T | C | 2 | a0001c0001t0002g0057 a0001c0001t0002g0064 |
2 | NA18978.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1641+835A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089697 | |||||||
| chr11:33089828 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1641+704A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089828 | |||||||
| chr11:33089894 | G | C | 1 | a0001c0001t0002g0079 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1641+638C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089894 | |||||||
| chr11:33089941 | A | G | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(83): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1641+591T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33089941 | |||||||
| chr11:33090035 | A | G | 89 | a0001c0001t0002g0006 a0001c0001t0002g0105 a0001c0001t0002g0108 others(86): Show |
109 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1641+497T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33090035 | |||||||
| chr11:33090275 | T | G | 1 | a0001c0001t0002g0105 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1641+257A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33090275 | |||||||
| chr11:33090491 | GA | G | 5 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1641+40delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 17/20 | chr11 | 33090491 | |||||||
| chr11:33090855 | A | AT | 42 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0021 others(39): Show |
51 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1446-129dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33090855 | |||||||
| chr11:33091267 | A | G | 1 | a0001c0001t0002g0013 | 2 | NA18965.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1446-540T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091267 | |||||||
| chr11:33091357 | A | C | 174 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(171): Show |
198 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1446-630T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091357 | |||||||
| chr11:33091376 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1446-649A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091376 | |||||||
| chr11:33091564 | C | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1445+707G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091564 | |||||||
| chr11:33091576 | G | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0055 |
3 | NA18965.hp2 NA18986.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1445+695C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091576 | |||||||
| chr11:33091609 | T | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1445+662A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091609 | |||||||
| chr11:33091610 | G | A | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1445+661C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091610 | |||||||
| chr11:33091758 | G | T | 4 | a0001c0001t0002g0105 a0001c0001t0002g0132 a0001c0001t0002g0133 others(1): Show |
4 | HG03688.hp2 NA18979.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1445+513C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091758 | |||||||
| chr11:33091832 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1445+439G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091832 | |||||||
| chr11:33091953 | C | T | 2 | a0001c0001t0002g0160 a0001c0001t0002g0171 |
2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1445+318G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33091953 | |||||||
| chr11:33092066 | T | G | 2 | a0001c0001t0002g0160 a0001c0001t0002g0171 |
2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1445+205A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33092066 | |||||||
| chr11:33092084 | CTG | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0308 a0001c0001t0001g0314 |
3 | HG01069.hp1 HG03239.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1445+185_1445+186d others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33092084 | |||||||
| chr11:33092107 | T | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1445+164A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33092107 | |||||||
| chr11:33092156 | G | A | 20 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0197 others(17): Show |
20 | HG00642.hp2 HG01109.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1445+115C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33092156 | |||||||
| chr11:33092211 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1445+60T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 16/20 | chr11 | 33092211 | |||||||
| chr11:33092364 | A | AT | 175 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(172): Show |
200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1376-25dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33092364 | |||||||
| chr11:33092371 | T | A | 1 | a0001c0001t0001g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1376-31A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33092371 | |||||||
| chr11:33092403 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0313 |
3 | HG00735.hp1 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1376-63A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33092403 | |||||||
| chr11:33092596 | T | C | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1376-256A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33092596 | |||||||
| chr11:33092612 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1376-272A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33092612 | |||||||
| chr11:33093011 | T | A | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1376-671A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33093011 | |||||||
| chr11:33093244 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1376-904T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33093244 | |||||||
| chr11:33093869 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0091 |
2 | HG00423.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1376-1529C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33093869 | |||||||
| chr11:33093926 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1376-1586A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33093926 | |||||||
| chr11:33094298 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1376-1958A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094298 | |||||||
| chr11:33094355 | A | G | 4 | a0001c0001t0003g0030 a0001c0001t0003g0115 a0001c0001t0003g0117 others(1): Show |
4 | HG02080.hp1 NA18939.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375+1951T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094355 | |||||||
| chr11:33094415 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1375+1891G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094415 | |||||||
| chr11:33094508 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0309 a0001c0001t0001g0310 others(3): Show |
7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1375+1798C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094508 | |||||||
| chr11:33094706 | C | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
7 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1375+1600G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094706 | |||||||
| chr11:33094841 | ATTTC | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1375+1461_1375+146 others(8): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33094841 | |||||||
| chr11:33095196 | G | A | 1 | a0001c0001t0003g0186 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1375+1110C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095196 | |||||||
| chr11:33095414 | C | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1375+892G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095414 | |||||||
| chr11:33095444 | A | G | 89 | a0001c0001t0002g0006 a0001c0001t0002g0105 a0001c0001t0002g0108 others(86): Show |
109 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1375+862T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095444 | |||||||
| chr11:33095587 | C | T | 2 | a0001c0001t0002g0089 a0001c0001t0002g0100 |
2 | NA18951.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1375+719G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095587 | |||||||
| chr11:33095597 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1375+709C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095597 | |||||||
| chr11:33095622 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1375+684G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095622 | |||||||
| chr11:33095648 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1375+658A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095648 | |||||||
| chr11:33095678 | G | C | 1 | a0001c0001t0002g0096 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1375+628C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095678 | |||||||
| chr11:33095814 | T | C | 233 | a0001c0001t0001g0023 a0001c0001t0001g0192 a0001c0001t0001g0193 others(230): Show |
259 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1375+492A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095814 | |||||||
| chr11:33095819 | C | CA | 90 | a0001c0001t0002g0006 a0001c0001t0002g0020 a0001c0001t0002g0087 others(87): Show |
111 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1375+486dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | |||||||
| chr11:33095819 | C | CAA | 82 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(79): Show |
86 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1375+485_1375+486d others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | |||||||
| chr11:33095819 | C | CAAAT | 41 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0021 others(38): Show |
49 | HG00438.hp1 HG00733.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1375+483_1375+486d others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | |||||||
| chr11:33095819 | C | CAAATAAA others(1): Show |
25 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(22): Show |
25 | HG00280.hp1 HG00642.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1375+479_1375+486d others(10): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | |||||||
| chr11:33095819 | C | CAAATAAA others(5): Show |
2 | a0001c0001t0001g0198 a0001c0001t0001g0223 |
2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1375+475_1375+486d others(14): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | |||||||
| chr11:33095819 | CAAATAAA others(5): Show |
C | 2 | a0001c0001t0001g0298 a0001c0001t0001g0302 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1375+475_1375+486d others(14): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095819 | |||||||
| chr11:33095823 | T | A | 173 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(170): Show |
198 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1375+483A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095823 | |||||||
| chr11:33095827 | T | A | 78 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0020 others(75): Show |
82 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1375+479A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095827 | |||||||
| chr11:33095831 | T | A | 23 | a0001c0001t0002g0031 a0001c0001t0002g0033 a0001c0001t0002g0035 others(20): Show |
24 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1375+475A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095831 | |||||||
| chr11:33095835 | T | A | 7 | a0001c0001t0002g0031 a0001c0001t0002g0059 a0001c0001t0002g0082 others(4): Show |
8 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375+471A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095835 | |||||||
| chr11:33095844 | A | G | 1 | a0001c0001t0003g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1375+462T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095844 | |||||||
| chr11:33095863 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1375+443T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095863 | |||||||
| chr11:33095964 | T | TTTTG | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(83): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1375+338_1375+341d others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 15/20 | chr11 | 33095964 | |||||||
| chr11:33096436 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1273-28A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 14/20 | chr11 | 33096436 | |||||||
| chr11:33096441 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1273-33T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 14/20 | chr11 | 33096441 | |||||||
| chr11:33096530 | A | G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0055 a0001c0001t0002g0079 |
4 | NA18965.hp2 NA18966.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273-122T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 14/20 | chr11 | 33096530 | |||||||
| chr11:33096591 | G | T | 230 | a0001c0001t0001g0023 a0001c0001t0001g0192 a0001c0001t0001g0193 others(227): Show |
256 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.1273-183C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 14/20 | chr11 | 33096591 | |||||||
| chr11:33096728 | A | G | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0007 others(75): Show |
95 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1272+107T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 14/20 | chr11 | 33096728 | |||||||
| chr11:33096983 | GC | G | 89 | a0001c0001t0002g0006 a0001c0001t0002g0105 a0001c0001t0002g0108 others(86): Show |
109 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
splice_region_variant&intron_variant | LOW | c.1129-6delG | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33096983 | |||||||
| chr11:33097098 | C | G | 1 | a0001c0001t0003g0125 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1129-120G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097098 | |||||||
| chr11:33097146 | A | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0309 a0001c0001t0001g0310 others(2): Show |
6 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1129-168T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097146 | |||||||
| chr11:33097152 | T | C | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1129-174A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097152 | |||||||
| chr11:33097271 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1129-293A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097271 | |||||||
| chr11:33097342 | G | T | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1129-364C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097342 | |||||||
| chr11:33097362 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1129-384C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097362 | |||||||
| chr11:33097376 | G | GT | 6 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG02717.hp2 HG03041.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129-399dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097376 | |||||||
| chr11:33097416 | C | G | 2 | a0001c0001t0002g0057 a0001c0001t0002g0064 |
2 | NA18978.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1129-438G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097416 | |||||||
| chr11:33097453 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1129-475A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097453 | |||||||
| chr11:33097558 | G | A | 1 | a0001c0001t0003g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1129-580C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097558 | |||||||
| chr11:33097580 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1129-602C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097580 | |||||||
| chr11:33097659 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1129-681C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097659 | |||||||
| chr11:33097731 | G | A | 318 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(315): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.1129-753C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097731 | |||||||
| chr11:33097794 | G | A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0032 a0001c0001t0002g0092 |
3 | NA18946.hp1 NA18971.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1129-816C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33097794 | |||||||
| chr11:33098044 | T | G | 8 | a0001c0001t0002g0105 a0001c0001t0002g0108 a0001c0001t0002g0114 others(5): Show |
9 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1128+646A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098044 | |||||||
| chr11:33098090 | T | G | 1 | a0001c0001t0002g0046 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1128+600A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098090 | |||||||
| chr11:33098241 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1128+449C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098241 | |||||||
| chr11:33098264 | T | G | 1 | a0001c0001t0001g0209 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1128+426A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098264 | |||||||
| chr11:33098468 | G | A | 1 | a0001c0001t0003g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1128+222C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098468 | |||||||
| chr11:33098492 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1128+198C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 13/20 | chr11 | 33098492 | |||||||
| chr11:33099298 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.937-148G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 11/20 | chr11 | 33099298 | |||||||
| chr11:33100036 | C | T | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.827-319G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100036 | |||||||
| chr11:33100059 | T | C | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.827-342A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100059 | |||||||
| chr11:33100123 | A | G | 178 | a0001c0001t0001g0316 a0001c0001t0002g0005 a0001c0001t0002g0006 others(175): Show |
203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.827-406T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100123 | |||||||
| chr11:33100166 | C | T | 1 | a0001c0002t0002g0008 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.827-449G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100166 | |||||||
| chr11:33100280 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.827-563C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100280 | |||||||
| chr11:33100354 | C | CA | 169 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(166): Show |
193 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.827-638dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100354 | |||||||
| chr11:33100354 | C | CAA | 7 | a0001c0001t0002g0020 a0001c0001t0002g0073 a0001c0001t0002g0081 others(4): Show |
8 | HG01346.hp2 HG01496.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-639_827-638dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100354 | |||||||
| chr11:33100354 | CA | C | 39 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(36): Show |
39 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.827-638delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100354 | |||||||
| chr11:33100860 | T | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.827-1143A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33100860 | |||||||
| chr11:33101421 | G | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.826+756C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33101421 | |||||||
| chr11:33101590 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.826+587C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33101590 | |||||||
| chr11:33101632 | A | T | 1 | a0001c0001t0002g0040 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.826+545T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33101632 | |||||||
| chr11:33101636 | C | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.826+541G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33101636 | |||||||
| chr11:33101792 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.826+385A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 10/20 | chr11 | 33101792 | |||||||
| chr11:33102348 | C | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.664-9G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102348 | |||||||
| chr11:33102396 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.664-57G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102396 | |||||||
| chr11:33102522 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.664-183G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102522 | |||||||
| chr11:33102523 | A | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.664-184T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102523 | |||||||
| chr11:33102902 | A | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.663+205T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102902 | |||||||
| chr11:33102911 | T | C | 3 | a0001c0001t0003g0135 a0001c0001t0003g0177 a0001c0001t0003g0185 |
3 | HG01346.hp2 NA18966.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.663+196A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 9/20 | chr11 | 33102911 | |||||||
| chr11:33103216 | G | T | 2 | a0001c0001t0003g0137 a0001c0001t0003g0138 |
2 | NA18954.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.586-32C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33103216 | |||||||
| chr11:33103500 | G | A | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(83): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.586-316C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33103500 | |||||||
| chr11:33103643 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.586-459C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33103643 | |||||||
| chr11:33103669 | T | C | 224 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(221): Show |
249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.586-485A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33103669 | |||||||
| chr11:33103757 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.586-573C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33103757 | |||||||
| chr11:33104424 | A | C | 1 | a0001c0001t0001g0249 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.585+1143T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104424 | |||||||
| chr11:33104441 | A | G | 1 | a0001c0001t0002g0079 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.585+1126T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104441 | |||||||
| chr11:33104458 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.585+1109G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104458 | |||||||
| chr11:33104538 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0294 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.585+1029C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104538 | |||||||
| chr11:33104543 | G | A | 4 | a0001c0001t0003g0030 a0001c0001t0003g0115 a0001c0001t0003g0117 others(1): Show |
4 | HG02080.hp1 NA18939.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+1024C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104543 | |||||||
| chr11:33104697 | T | A | 1 | a0001c0001t0002g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.585+870A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104697 | |||||||
| chr11:33104858 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.585+709C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104858 | |||||||
| chr11:33104878 | T | C | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.585+689A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104878 | |||||||
| chr11:33104937 | C | T | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.585+630G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33104937 | |||||||
| chr11:33105272 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.585+295G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33105272 | |||||||
| chr11:33105364 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.585+203T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 8/20 | chr11 | 33105364 | |||||||
| chr11:33106652 | A | G | 2 | a0001c0001t0002g0160 a0001c0001t0002g0171 |
2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.357-588T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33106652 | |||||||
| chr11:33106710 | G | T | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.357-646C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33106710 | |||||||
| chr11:33106778 | CTTTATAT others(3): Show |
C | 1 | a0001c0001t0001g0315 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.357-724_357-715del others(10): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33106778 | |||||||
| chr11:33107183 | G | T | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.356+720C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33107183 | |||||||
| chr11:33107206 | A | T | 1 | a0001c0001t0002g0063 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.356+697T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33107206 | |||||||
| chr11:33107296 | C | T | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0007 others(75): Show |
95 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.356+607G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33107296 | |||||||
| chr11:33107634 | G | GACA | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.356+266_356+268dup others(3): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 5/20 | chr11 | 33107634 | |||||||
| chr11:33108199 | C | T | 2 | a0001c0002t0002g0008 a0001c0002t0002g0122 |
4 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+187G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 4/20 | chr11 | 33108199 | |||||||
| chr11:33108451 | C | T | 77 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0007 others(74): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.226-33G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33108451 | |||||||
| chr11:33108986 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.226-568C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33108986 | |||||||
| chr11:33109251 | C | T | 1 | a0001c0001t0002g0071 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.226-833G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109251 | |||||||
| chr11:33109342 | G | C | 1 | a0001c0001t0003g0141 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.226-924C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109342 | |||||||
| chr11:33109495 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0220 |
2 | HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.226-1077C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109495 | |||||||
| chr11:33109592 | G | C | 1 | a0001c0001t0003g0126 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.226-1174C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109592 | |||||||
| chr11:33109607 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.226-1189T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109607 | |||||||
| chr11:33109666 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226-1248A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109666 | |||||||
| chr11:33109685 | C | T | 4 | a0001c0001t0002g0038 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
4 | NA18945.hp1 NA18955.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-1267G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109685 | |||||||
| chr11:33109754 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-1336T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33109754 | |||||||
| chr11:33110004 | G | A | 4 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-1586C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110004 | |||||||
| chr11:33110152 | G | C | 1 | a0001c0001t0002g0076 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.226-1734C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110152 | |||||||
| chr11:33110461 | T | C | 2 | a0001c0001t0001g0283 a0001c0001t0001g0308 |
2 | HG01167.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.226-2043A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110461 | |||||||
| chr11:33110505 | G | A | 1 | a0001c0001t0003g0131 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.226-2087C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110505 | |||||||
| chr11:33110554 | T | A | 1 | a0001c0001t0001g0309 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.226-2136A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110554 | |||||||
| chr11:33110648 | T | G | 1 | a0001c0001t0001g0270 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.226-2230A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110648 | |||||||
| chr11:33110751 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.226-2333T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110751 | |||||||
| chr11:33110881 | T | TA | 11 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0233 others(8): Show |
15 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-2464dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110881 | |||||||
| chr11:33110953 | G | A | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-2535C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33110953 | |||||||
| chr11:33111004 | G | A | 4 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-2586C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111004 | |||||||
| chr11:33111138 | G | A | 2 | a0001c0001t0003g0147 a0001c0001t0003g0148 |
2 | HG00408.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.226-2720C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111138 | |||||||
| chr11:33111285 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-2867C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111285 | |||||||
| chr11:33111292 | T | G | 1 | a0001c0001t0001g0272 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.226-2874A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111292 | |||||||
| chr11:33111318 | T | C | 90 | a0001c0001t0001g0269 a0001c0001t0002g0006 a0001c0001t0002g0105 others(87): Show |
110 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.226-2900A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111318 | |||||||
| chr11:33111366 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02258.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.226-2948C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111366 | |||||||
| chr11:33111755 | T | C | 2 | a0001c0001t0001g0290 a0001c0001t0001g0306 |
2 | HG00738.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.226-3337A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111755 | |||||||
| chr11:33111975 | C | A | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226-3557G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33111975 | |||||||
| chr11:33112011 | T | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-3593A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112011 | |||||||
| chr11:33112083 | G | A | 1 | a0001c0001t0003g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.226-3665C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112083 | |||||||
| chr11:33112255 | G | GA | 7 | a0001c0001t0001g0194 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG02027.hp2 HG02258.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-3838dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112255 | |||||||
| chr11:33112376 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.226-3958A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112376 | |||||||
| chr11:33112502 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.226-4084A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112502 | |||||||
| chr11:33112704 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.226-4286C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112704 | |||||||
| chr11:33112713 | A | C | 1 | a0001c0001t0002g0025 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.226-4295T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112713 | |||||||
| chr11:33112733 | A | G | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.226-4315T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112733 | |||||||
| chr11:33112928 | A | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-4510T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112928 | |||||||
| chr11:33112942 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226-4524A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112942 | |||||||
| chr11:33112970 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.226-4552C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33112970 | |||||||
| chr11:33113000 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0313 |
3 | HG00735.hp1 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.226-4582C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113000 | |||||||
| chr11:33113076 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-4658C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113076 | |||||||
| chr11:33113176 | A | G | 13 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0047 others(10): Show |
13 | HG02027.hp1 HG02040.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.226-4758T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113176 | |||||||
| chr11:33113206 | A | AAAAT | 38 | a0001c0001t0001g0022 a0001c0001t0001g0192 a0001c0001t0001g0193 others(35): Show |
42 | HG00642.hp2 HG00673.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.226-4792_226-4789d others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113206 | |||||||
| chr11:33113206 | A | AAAATAAA others(1): Show |
5 | a0001c0001t0001g0197 a0001c0001t0001g0271 a0001c0001t0001g0317 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-4796_226-4789d others(10): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113206 | |||||||
| chr11:33113206 | A | AAAATAAA others(5): Show |
4 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0316 others(1): Show |
4 | HG02647.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-4800_226-4789d others(14): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113206 | |||||||
| chr11:33113206 | AAAAT | A | 82 | a0001c0001t0002g0043 a0001c0001t0002g0062 a0001c0001t0002g0105 others(79): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.226-4792_226-4789d others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113206 | |||||||
| chr11:33113206 | AAAATAAA others(1): Show |
A | 85 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0002g0005 others(82): Show |
89 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.226-4796_226-4789d others(10): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113206 | |||||||
| chr11:33113247 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.226-4829C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113247 | |||||||
| chr11:33113388 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.226-4970A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113388 | |||||||
| chr11:33113399 | C | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0037 a0001c0001t0002g0046 others(4): Show |
8 | NA18964.hp1 NA18970.hp2 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.226-4981G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113399 | |||||||
| chr11:33113453 | C | T | 2 | a0001c0001t0002g0160 a0001c0001t0002g0171 |
2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.226-5035G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113453 | |||||||
| chr11:33113511 | T | C | 3 | a0001c0001t0001g0256 a0001c0001t0001g0294 a0001c0001t0001g0315 |
3 | HG02809.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.226-5093A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113511 | |||||||
| chr11:33113561 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0001t0001g0210 others(1): Show |
4 | HG02896.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-5143G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113561 | |||||||
| chr11:33113774 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.226-5356C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113774 | |||||||
| chr11:33113995 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0314 |
2 | HG01069.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.226-5577G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33113995 | |||||||
| chr11:33114367 | T | C | 2 | a0001c0001t0002g0076 a0001c0001t0002g0081 |
2 | NA18972.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.226-5949A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114367 | |||||||
| chr11:33114458 | G | GA | 80 | a0001c0001t0002g0044 a0001c0001t0002g0089 a0001c0001t0002g0092 others(77): Show |
97 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.226-6041dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114458 | |||||||
| chr11:33114463 | A | AAAAATCC others(4): Show |
1 | a0001c0001t0002g0112 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.226-6046_226-6045i others(13): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114463 | |||||||
| chr11:33114521 | T | C | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG00280.hp1 HG00733.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.226-6103A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114521 | |||||||
| chr11:33114570 | G | T | 1 | a0001c0001t0001g0270 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.226-6152C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114570 | |||||||
| chr11:33114621 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-6203G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114621 | |||||||
| chr11:33114788 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-6370T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114788 | |||||||
| chr11:33114788 | A | T | 175 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(172): Show |
199 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.226-6370T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114788 | |||||||
| chr11:33114891 | T | C | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-6473A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114891 | |||||||
| chr11:33114945 | C | A | 1 | a0001c0001t0001g0276 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.226-6527G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33114945 | |||||||
| chr11:33115012 | G | A | 4 | a0001c0001t0003g0030 a0001c0001t0003g0115 a0001c0001t0003g0117 others(1): Show |
4 | HG02080.hp1 NA18939.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-6594C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115012 | |||||||
| chr11:33115085 | C | T | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-6667G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115085 | |||||||
| chr11:33115115 | C | T | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.226-6697G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115115 | |||||||
| chr11:33115233 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.226-6815T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115233 | |||||||
| chr11:33115237 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0240 |
2 | NA18946.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.226-6819A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115237 | |||||||
| chr11:33115470 | T | C | 1 | a0001c0001t0003g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.226-7052A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115470 | |||||||
| chr11:33115587 | GTGACAAA others(4): Show |
G | 232 | a0001c0001t0001g0023 a0001c0001t0001g0192 a0001c0001t0001g0193 others(229): Show |
258 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.226-7180_226-7170d others(13): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115587 | |||||||
| chr11:33115599 | T | G | 232 | a0001c0001t0001g0023 a0001c0001t0001g0192 a0001c0001t0001g0193 others(229): Show |
258 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.226-7181A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115599 | |||||||
| chr11:33115600 | A | C | 232 | a0001c0001t0001g0023 a0001c0001t0001g0192 a0001c0001t0001g0193 others(229): Show |
258 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.226-7182T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115600 | |||||||
| chr11:33115691 | C | A | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.226-7273G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33115691 | |||||||
| chr11:33116133 | T | A | 1 | a0001c0001t0002g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.226-7715A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33116133 | |||||||
| chr11:33116754 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.226-8336C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33116754 | |||||||
| chr11:33116814 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.226-8396C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33116814 | |||||||
| chr11:33116874 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226-8456A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33116874 | |||||||
| chr11:33116920 | C | CT | 8 | a0001c0001t0002g0042 a0001c0001t0002g0066 a0001c0001t0002g0072 others(5): Show |
8 | HG00597.hp1 HG00733.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-8503dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33116920 | |||||||
| chr11:33117635 | A | T | 5 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-9217T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117635 | |||||||
| chr11:33117662 | A | AAT | 213 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(210): Show |
237 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.226-9246_226-9245d others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117662 | |||||||
| chr11:33117662 | A | AATAT | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-9248_226-9245d others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117662 | |||||||
| chr11:33117722 | T | C | 3 | a0001c0001t0001g0256 a0001c0001t0001g0294 a0001c0001t0001g0315 |
3 | HG02809.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.226-9304A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117722 | |||||||
| chr11:33117804 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.226-9386G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117804 | |||||||
| chr11:33117873 | G | A | 215 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(212): Show |
240 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.226-9455C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117873 | |||||||
| chr11:33117884 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.226-9466G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33117884 | |||||||
| chr11:33118081 | AT | A | 17 | a0001c0001t0001g0196 a0001c0001t0001g0200 a0001c0001t0001g0201 others(14): Show |
18 | HG01069.hp1 HG01243.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.226-9664delA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118081 | |||||||
| chr11:33118099 | T | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.226-9681A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118099 | |||||||
| chr11:33118474 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.226-10056A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118474 | |||||||
| chr11:33118476 | G | T | 212 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(209): Show |
237 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.226-10058C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118476 | |||||||
| chr11:33118587 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0269 |
3 | HG01515.hp2 HG02683.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.226-10169T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118587 | |||||||
| chr11:33118625 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.226-10207A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118625 | |||||||
| chr11:33118683 | A | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.226-10265T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118683 | |||||||
| chr11:33118747 | TA | T | 173 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(170): Show |
198 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.226-10330delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118747 | |||||||
| chr11:33118760 | C | A | 1 | a0001c0001t0001g0223 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.226-10342G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33118760 | |||||||
| chr11:33119058 | C | CT | 85 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(82): Show |
89 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.226-10641dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33119058 | |||||||
| chr11:33119120 | T | G | 1 | a0001c0001t0003g0119 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.226-10702A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33119120 | |||||||
| chr11:33119472 | A | AT | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-11055dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33119472 | |||||||
| chr11:33119474 | C | A | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-11056G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33119474 | |||||||
| chr11:33120136 | T | G | 1 | a0001c0001t0001g0292 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.226-11718A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120136 | |||||||
| chr11:33120328 | G | C | 1 | a0001c0001t0001g0274 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11910C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120328 | |||||||
| chr11:33120330 | G | T | 1 | a0001c0001t0001g0274 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11912C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120330 | |||||||
| chr11:33120332 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11914A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120332 | |||||||
| chr11:33120333 | T | A | 1 | a0001c0001t0001g0274 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11915A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120333 | |||||||
| chr11:33120334 | A | T | 1 | a0001c0001t0001g0274 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11916T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120334 | |||||||
| chr11:33120338 | T | G | 1 | a0001c0001t0001g0274 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.226-11920A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120338 | |||||||
| chr11:33120509 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.226-12091G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120509 | |||||||
| chr11:33120649 | A | T | 1 | a0001c0001t0001g0248 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.226-12231T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120649 | |||||||
| chr11:33120815 | T | C | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.226-12397A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120815 | |||||||
| chr11:33120893 | A | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.226-12475T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120893 | |||||||
| chr11:33120895 | T | C | 215 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(212): Show |
240 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.226-12477A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33120895 | |||||||
| chr11:33121028 | G | T | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226-12610C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121028 | |||||||
| chr11:33121031 | C | T | 1 | a0001c0001t0003g0144 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.226-12613G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121031 | |||||||
| chr11:33121076 | C | G | 4 | a0001c0001t0002g0050 a0001c0001t0002g0085 a0001c0001t0002g0086 others(1): Show |
4 | HG02040.hp1 HG02132.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-12658G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121076 | |||||||
| chr11:33121155 | T | G | 2 | a0001c0001t0002g0076 a0001c0001t0002g0081 |
2 | NA18972.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.226-12737A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121155 | |||||||
| chr11:33121252 | C | T | 1 | a0001c0001t0002g0061 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.226-12834G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121252 | |||||||
| chr11:33121580 | G | A | 232 | a0001c0001t0001g0023 a0001c0001t0001g0192 a0001c0001t0001g0193 others(229): Show |
258 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.226-13162C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33121580 | |||||||
| chr11:33122175 | A | T | 1 | a0001c0001t0002g0087 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.226-13757T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122175 | |||||||
| chr11:33122441 | T | C | 13 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0047 others(10): Show |
13 | HG02027.hp1 HG02040.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.226-14023A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122441 | |||||||
| chr11:33122671 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.226-14253A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122671 | |||||||
| chr11:33122785 | A | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.226-14367T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122785 | |||||||
| chr11:33122864 | C | T | 1 | a0001c0001t0003g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.226-14446G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122864 | |||||||
| chr11:33122914 | C | CA | 15 | a0001c0001t0001g0207 a0001c0001t0001g0220 a0001c0001t0001g0226 others(12): Show |
15 | HG00438.hp1 HG00544.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-14497dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122914 | |||||||
| chr11:33122914 | CA | C | 84 | a0001c0001t0001g0210 a0001c0001t0001g0272 a0001c0001t0002g0005 others(81): Show |
94 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.226-14497delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122914 | |||||||
| chr11:33122914 | CAA | C | 85 | a0001c0001t0002g0006 a0001c0001t0002g0043 a0001c0001t0002g0051 others(82): Show |
99 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.226-14498_226-1449 others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122914 | |||||||
| chr11:33122930 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.226-14512T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122930 | |||||||
| chr11:33122931 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.226-14513T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33122931 | |||||||
| chr11:33123029 | A | C | 2 | a0001c0001t0002g0070 a0001c0001t0002g0077 |
2 | HG00438.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.226-14611T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123029 | |||||||
| chr11:33123150 | T | C | 1 | a0001c0001t0004g0189 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.226-14732A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123150 | |||||||
| chr11:33123640 | C | T | 5 | a0001c0001t0002g0029 a0001c0001t0002g0032 a0001c0001t0002g0078 others(2): Show |
5 | HG00423.hp2 NA18946.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-15222G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123640 | |||||||
| chr11:33123692 | T | TA | 10 | a0001c0001t0001g0273 a0001c0001t0002g0025 a0001c0001t0002g0031 others(7): Show |
10 | HG00741.hp1 HG01109.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.226-15275dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123692 | |||||||
| chr11:33123723 | A | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.226-15305T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123723 | |||||||
| chr11:33123850 | T | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.226-15432A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33123850 | |||||||
| chr11:33124081 | C | A | 1 | a0001c0001t0001g0312 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.226-15663G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124081 | |||||||
| chr11:33124082 | A | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.226-15664T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124082 | |||||||
| chr11:33124139 | T | A | 3 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0077 |
3 | HG00438.hp2 HG02015.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.226-15721A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124139 | |||||||
| chr11:33124194 | A | C | 1 | a0001c0001t0001g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.226-15776T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124194 | |||||||
| chr11:33124231 | A | G | 2 | a0001c0001t0001g0268 a0001c0001t0007g0191 |
2 | HG01433.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.226-15813T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124231 | |||||||
| chr11:33124351 | C | G | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.226-15933G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124351 | |||||||
| chr11:33124474 | C | T | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.226-16056G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124474 | |||||||
| chr11:33124593 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.226-16175C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124593 | |||||||
| chr11:33124698 | T | G | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0007 others(75): Show |
95 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.226-16280A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124698 | |||||||
| chr11:33124868 | C | T | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.226-16450G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33124868 | |||||||
| chr11:33125080 | C | G | 4 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+16587G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125080 | |||||||
| chr11:33125387 | ACT | A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0032 a0001c0001t0002g0092 |
3 | NA18946.hp1 NA18971.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.225+16278_225+1627 others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125387 | |||||||
| chr11:33125556 | C | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+16111G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125556 | |||||||
| chr11:33125705 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.225+15962A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125705 | |||||||
| chr11:33125717 | C | T | 1 | a0001c0001t0004g0188 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.225+15950G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125717 | |||||||
| chr11:33125755 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.225+15912C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125755 | |||||||
| chr11:33125848 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.225+15819C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33125848 | |||||||
| chr11:33126018 | C | T | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(83): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.225+15649G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126018 | |||||||
| chr11:33126061 | A | G | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0315 |
3 | HG02647.hp2 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.225+15606T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126061 | |||||||
| chr11:33126182 | A | G | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+15485T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126182 | |||||||
| chr11:33126249 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0240 |
2 | NA18946.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.225+15418G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126249 | |||||||
| chr11:33126303 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+15364G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126303 | |||||||
| chr11:33126398 | G | A | 10 | a0001c0001t0002g0105 a0001c0001t0002g0108 a0001c0001t0002g0114 others(7): Show |
11 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.225+15269C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126398 | |||||||
| chr11:33126407 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.225+15260C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126407 | |||||||
| chr11:33126409 | G | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.225+15258C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126409 | |||||||
| chr11:33126425 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.225+15242C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126425 | |||||||
| chr11:33126480 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.225+15187A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126480 | |||||||
| chr11:33126825 | T | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+14842A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33126825 | |||||||
| chr11:33127012 | T | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.225+14655A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127012 | |||||||
| chr11:33127025 | A | C | 2 | a0001c0001t0003g0143 a0001c0001t0003g0178 |
2 | HG01175.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.225+14642T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127025 | |||||||
| chr11:33127148 | T | G | 318 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(315): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.225+14519A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127148 | |||||||
| chr11:33127187 | A | T | 31 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(28): Show |
31 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.225+14480T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127187 | |||||||
| chr11:33127229 | T | A | 1 | a0001c0001t0002g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.225+14438A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127229 | |||||||
| chr11:33127301 | A | G | 3 | a0001c0001t0002g0029 a0001c0001t0002g0032 a0001c0001t0002g0092 |
3 | NA18946.hp1 NA18971.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.225+14366T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127301 | |||||||
| chr11:33127639 | T | C | 175 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(172): Show |
199 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.225+14028A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127639 | |||||||
| chr11:33127742 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0271 a0001c0001t0001g0296 others(2): Show |
7 | NA18955.hp2 NA18960.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+13925C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127742 | |||||||
| chr11:33127786 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0309 a0001c0001t0001g0310 others(2): Show |
6 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+13881G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33127786 | |||||||
| chr11:33128001 | T | C | 1 | a0001c0001t0003g0120 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.225+13666A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128001 | |||||||
| chr11:33128076 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.225+13591C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128076 | |||||||
| chr11:33128201 | A | C | 1 | a0001c0001t0002g0020 | 2 | HG01496.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.225+13466T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128201 | |||||||
| chr11:33128412 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.225+13255A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128412 | |||||||
| chr11:33128707 | T | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.225+12960A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128707 | |||||||
| chr11:33128849 | C | T | 4 | a0001c0001t0003g0145 a0001c0001t0003g0146 a0001c0001t0003g0152 others(1): Show |
4 | NA18957.hp2 NA18962.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+12818G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33128849 | |||||||
| chr11:33129012 | T | C | 1 | a0001c0001t0003g0120 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.225+12655A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129012 | |||||||
| chr11:33129057 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.225+12610C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129057 | |||||||
| chr11:33129138 | C | T | 175 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(172): Show |
199 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.225+12529G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129138 | |||||||
| chr11:33129192 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.225+12475T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129192 | |||||||
| chr11:33129376 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.225+12291C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129376 | |||||||
| chr11:33129394 | C | CT | 11 | a0001c0001t0001g0220 a0001c0001t0001g0267 a0001c0001t0001g0271 others(8): Show |
11 | HG01099.hp2 HG01943.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.225+12272dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129394 | |||||||
| chr11:33129394 | C | CTT | 7 | a0001c0001t0001g0194 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG02258.hp2 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+12271_225+1227 others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129394 | |||||||
| chr11:33129655 | A | G | 1 | a0001c0001t0003g0186 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.225+12012T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129655 | |||||||
| chr11:33129958 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.225+11709C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33129958 | |||||||
| chr11:33130108 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.225+11559C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33130108 | |||||||
| chr11:33130243 | C | T | 1 | a0001c0001t0004g0189 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.225+11424G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33130243 | |||||||
| chr11:33130528 | T | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.225+11139A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33130528 | |||||||
| chr11:33130657 | A | T | 1 | a0001c0001t0002g0111 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.225+11010T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33130657 | |||||||
| chr11:33131359 | C | T | 1 | a0001c0001t0003g0169 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.225+10308G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131359 | |||||||
| chr11:33131429 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+10238G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131429 | |||||||
| chr11:33131472 | T | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0309 a0001c0001t0001g0310 others(3): Show |
7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+10195A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131472 | |||||||
| chr11:33131480 | G | A | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.225+10187C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131480 | |||||||
| chr11:33131575 | G | A | 3 | a0001c0001t0001g0307 a0001c0001t0002g0020 a0001c0001t0002g0187 |
4 | HG01496.hp1 HG02486.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+10092C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131575 | |||||||
| chr11:33131584 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.225+10083G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131584 | |||||||
| chr11:33131597 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.225+10070G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131597 | |||||||
| chr11:33131613 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225+10054C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131613 | |||||||
| chr11:33131628 | C | T | 1 | a0001c0001t0003g0174 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.225+10039G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131628 | |||||||
| chr11:33131639 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.225+10028C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131639 | |||||||
| chr11:33131690 | C | CA | 98 | a0001c0001t0001g0003 a0001c0001t0001g0233 a0001c0001t0001g0234 others(95): Show |
106 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.225+9976dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131690 | |||||||
| chr11:33131713 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.225+9954C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131713 | |||||||
| chr11:33131745 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0001g0305 |
2 | HG00597.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.225+9922C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131745 | |||||||
| chr11:33131760 | G | A | 8 | a0001c0001t0002g0036 a0001c0001t0002g0042 a0001c0001t0002g0044 others(5): Show |
8 | HG00639.hp2 HG00733.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+9907C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131760 | |||||||
| chr11:33131768 | C | T | 175 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(172): Show |
199 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.225+9899G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131768 | |||||||
| chr11:33131812 | A | G | 1 | a0001c0001t0002g0057 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.225+9855T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131812 | |||||||
| chr11:33131898 | ATTGTGGT others(18): Show |
A | 4 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0001t0001g0210 others(1): Show |
4 | HG02896.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+9744_225+9768d others(27): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131898 | |||||||
| chr11:33131995 | G | A | 8 | a0001c0001t0002g0105 a0001c0001t0002g0108 a0001c0001t0002g0114 others(5): Show |
9 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+9672C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33131995 | |||||||
| chr11:33132077 | C | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.225+9590G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132077 | |||||||
| chr11:33132238 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+9429T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132238 | |||||||
| chr11:33132463 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.225+9204C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132463 | |||||||
| chr11:33132633 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.225+9034T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132633 | |||||||
| chr11:33132634 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.225+9033G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132634 | |||||||
| chr11:33132635 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.225+9032G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132635 | |||||||
| chr11:33132657 | G | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0222 a0001c0001t0001g0223 others(1): Show |
4 | HG02965.hp2 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+9010C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132657 | |||||||
| chr11:33132831 | G | A | 175 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(172): Show |
199 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.225+8836C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132831 | |||||||
| chr11:33132850 | A | T | 1 | a0001c0001t0003g0121 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.225+8817T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132850 | |||||||
| chr11:33132943 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.225+8724A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33132943 | |||||||
| chr11:33133110 | CT | C | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+8556delA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133110 | |||||||
| chr11:33133132 | G | A | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0007 others(75): Show |
95 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.225+8535C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133132 | |||||||
| chr11:33133282 | T | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+8385A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133282 | |||||||
| chr11:33133345 | C | T | 2 | a0001c0001t0002g0160 a0001c0001t0002g0171 |
2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.225+8322G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133345 | |||||||
| chr11:33133577 | C | T | 1 | a0001c0001t0003g0120 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.225+8090G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133577 | |||||||
| chr11:33133718 | A | G | 84 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(81): Show |
88 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.225+7949T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133718 | |||||||
| chr11:33133759 | G | A | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.225+7908C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133759 | |||||||
| chr11:33133833 | T | C | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+7834A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33133833 | |||||||
| chr11:33134051 | A | G | 3 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0302 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.225+7616T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134051 | |||||||
| chr11:33134268 | G | A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0032 a0001c0001t0002g0092 |
3 | NA18946.hp1 NA18971.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.225+7399C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134268 | |||||||
| chr11:33134416 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.225+7251T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134416 | |||||||
| chr11:33134586 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225+7081A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134586 | |||||||
| chr11:33134676 | AC | A | 89 | a0001c0001t0002g0006 a0001c0001t0002g0105 a0001c0001t0002g0108 others(86): Show |
109 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.225+6990delG | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134676 | |||||||
| chr11:33134706 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225+6961G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134706 | |||||||
| chr11:33134719 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0294 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.225+6948A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134719 | |||||||
| chr11:33134820 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+6847T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134820 | |||||||
| chr11:33134852 | A | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0309 a0001c0001t0001g0310 others(3): Show |
7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+6815T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33134852 | |||||||
| chr11:33135077 | C | G | 2 | a0001c0001t0002g0160 a0001c0001t0002g0171 |
2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.225+6590G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33135077 | |||||||
| chr11:33135185 | T | TA | 4 | a0001c0001t0001g0249 a0001c0001t0002g0083 a0001c0001t0002g0133 others(1): Show |
4 | HG02135.hp2 HG04115.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+6481dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33135185 | |||||||
| chr11:33135408 | C | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0314 |
2 | HG01069.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.225+6259G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33135408 | |||||||
| chr11:33135678 | T | C | 2 | a0001c0001t0001g0237 a0001c0001t0001g0289 |
2 | NA18980.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.225+5989A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33135678 | |||||||
| chr11:33135755 | CCTT | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+5909_225+5911d others(5): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33135755 | |||||||
| chr11:33136288 | C | T | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.225+5379G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136288 | |||||||
| chr11:33136590 | T | C | 4 | a0001c0001t0002g0038 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
4 | NA18945.hp1 NA18955.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+5077A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136590 | |||||||
| chr11:33136596 | T | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(83): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.225+5071A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136596 | |||||||
| chr11:33136612 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.225+5055A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136612 | |||||||
| chr11:33136687 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.225+4980A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136687 | |||||||
| chr11:33136908 | T | C | 5 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+4759A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136908 | |||||||
| chr11:33136915 | C | CT | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+4751dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33136915 | |||||||
| chr11:33137020 | T | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(83): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.225+4647A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33137020 | |||||||
| chr11:33137115 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.225+4552C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33137115 | |||||||
| chr11:33137258 | C | A | 1 | a0001c0001t0003g0181 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.225+4409G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33137258 | |||||||
| chr11:33137989 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.225+3678A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33137989 | |||||||
| chr11:33138128 | G | C | 1 | a0001c0001t0002g0054 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.225+3539C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138128 | |||||||
| chr11:33138172 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+3495G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138172 | |||||||
| chr11:33138222 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.225+3445T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138222 | |||||||
| chr11:33138459 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.225+3208A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138459 | |||||||
| chr11:33138671 | T | G | 1 | a0001c0001t0003g0186 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.225+2996A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138671 | |||||||
| chr11:33138830 | T | A | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.225+2837A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138830 | |||||||
| chr11:33138982 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.225+2685A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33138982 | |||||||
| chr11:33139081 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.225+2586G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139081 | |||||||
| chr11:33139138 | A | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0294 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.225+2529T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139138 | |||||||
| chr11:33139442 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.225+2225G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139442 | |||||||
| chr11:33139503 | T | A | 1 | a0001c0001t0002g0110 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.225+2164A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139503 | |||||||
| chr11:33139514 | G | T | 1 | a0001c0001t0002g0077 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.225+2153C>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139514 | |||||||
| chr11:33139744 | G | A | 85 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(82): Show |
89 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.225+1923C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139744 | |||||||
| chr11:33139835 | A | C | 1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.225+1832T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139835 | |||||||
| chr11:33139915 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.225+1752A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139915 | |||||||
| chr11:33139955 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.225+1712C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33139955 | |||||||
| chr11:33140463 | A | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.225+1204T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33140463 | |||||||
| chr11:33140494 | C | T | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.225+1173G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33140494 | |||||||
| chr11:33140850 | A | AC | 6 | a0001c0001t0001g0023 a0001c0001t0001g0309 a0001c0001t0001g0310 others(3): Show |
7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+816dupG | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33140850 | |||||||
| chr11:33140907 | T | C | 5 | a0001c0001t0002g0039 a0001c0001t0002g0050 a0001c0001t0002g0085 others(2): Show |
5 | HG02027.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+760A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33140907 | |||||||
| chr11:33141091 | TGATTAAA others(3): Show |
T | 1 | a0001c0001t0001g0304 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.225+566_225+575del others(10): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 3/20 | chr11 | 33141091 | |||||||
| chr11:33142219 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.28-233T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142219 | |||||||
| chr11:33142336 | GAT | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-352_28-351delAT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142336 | |||||||
| chr11:33142384 | C | A | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.28-398G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142384 | |||||||
| chr11:33142476 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.28-490A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142476 | |||||||
| chr11:33142510 | T | A | 2 | a0001c0001t0002g0076 a0001c0001t0002g0081 |
2 | NA18972.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.28-524A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142510 | |||||||
| chr11:33142571 | A | G | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(83): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.28-585T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142571 | |||||||
| chr11:33142573 | A | G | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.28-587T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142573 | |||||||
| chr11:33142603 | A | G | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(83): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.28-617T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142603 | |||||||
| chr11:33142616 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.28-630C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142616 | |||||||
| chr11:33142729 | CAT | C | 2 | a0001c0001t0001g0242 a0001c0001t0002g0006 |
4 | HG02559.hp1 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-745_28-744delAT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142729 | |||||||
| chr11:33142909 | C | G | 4 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-923G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142909 | |||||||
| chr11:33142981 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-995A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33142981 | |||||||
| chr11:33143037 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-1051C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143037 | |||||||
| chr11:33143072 | T | C | 1 | a0001c0001t0003g0167 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.28-1086A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143072 | |||||||
| chr11:33143353 | T | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0218 |
3 | HG02723.hp2 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.28-1367A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143353 | |||||||
| chr11:33143558 | A | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-1572T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143558 | |||||||
| chr11:33143569 | T | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-1583A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143569 | |||||||
| chr11:33143723 | T | C | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0217 others(1): Show |
4 | HG02630.hp2 HG02723.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1737A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143723 | |||||||
| chr11:33143863 | G | A | 1 | a0001c0001t0004g0189 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.28-1877C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143863 | |||||||
| chr11:33143938 | C | T | 31 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(28): Show |
31 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.28-1952G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33143938 | |||||||
| chr11:33144120 | C | T | 5 | a0001c0001t0003g0153 a0001c0001t0003g0154 a0001c0001t0003g0155 others(2): Show |
5 | HG02145.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-2134G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144120 | |||||||
| chr11:33144129 | C | T | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.28-2143G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144129 | |||||||
| chr11:33144132 | T | C | 1 | a0001c0001t0003g0149 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.28-2146A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144132 | |||||||
| chr11:33144137 | TTTAGTGG others(2): Show |
T | 88 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(85): Show |
93 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.28-2160_28-2152del others(9): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144137 | |||||||
| chr11:33144138 | TTAGTGGA others(1): Show |
T | 89 | a0001c0001t0002g0006 a0001c0001t0002g0105 a0001c0001t0002g0108 others(86): Show |
109 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.28-2160_28-2153del others(8): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144138 | |||||||
| chr11:33144269 | G | A | 7 | a0001c0001t0003g0019 a0001c0001t0003g0143 a0001c0001t0003g0144 others(4): Show |
8 | HG00741.hp2 HG01099.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-2283C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144269 | |||||||
| chr11:33144402 | G | A | 2 | a0001c0001t0002g0112 a0001c0001t0002g0157 |
2 | NA18967.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.28-2416C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144402 | |||||||
| chr11:33144425 | T | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-2439A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144425 | |||||||
| chr11:33144516 | T | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-2530A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144516 | |||||||
| chr11:33144630 | A | C | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.28-2644T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144630 | |||||||
| chr11:33144632 | G | C | 1 | a0001c0001t0002g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.28-2646C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144632 | |||||||
| chr11:33144684 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.28-2698T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144684 | |||||||
| chr11:33144685 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0022 others(21): Show |
30 | HG00438.hp1 HG00673.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.28-2699C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144685 | |||||||
| chr11:33144694 | T | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-2708A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144694 | |||||||
| chr11:33144749 | G | C | 8 | a0001c0001t0002g0105 a0001c0001t0002g0108 a0001c0001t0002g0114 others(5): Show |
9 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-2763C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144749 | |||||||
| chr11:33144919 | G | C | 1 | a0001c0001t0001g0286 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.28-2933C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144919 | |||||||
| chr11:33144924 | T | C | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.28-2938A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144924 | |||||||
| chr11:33144977 | TA | T | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.28-2992delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33144977 | |||||||
| chr11:33145279 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.28-3293A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145279 | |||||||
| chr11:33145421 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.28-3435C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145421 | |||||||
| chr11:33145502 | A | G | 5 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-3516T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145502 | |||||||
| chr11:33145565 | C | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0032 |
2 | NA18946.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.28-3579G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145565 | |||||||
| chr11:33145691 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0021 others(37): Show |
49 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.28-3705C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145691 | |||||||
| chr11:33145827 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-3841T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145827 | |||||||
| chr11:33145957 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.28-3971G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33145957 | |||||||
| chr11:33146066 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0265 |
2 | NA18954.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.28-4080G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146066 | |||||||
| chr11:33146088 | A | C | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.28-4102T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146088 | |||||||
| chr11:33146238 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-4252C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146238 | |||||||
| chr11:33146252 | G | GA | 10 | a0001c0001t0002g0105 a0001c0001t0002g0108 a0001c0001t0002g0114 others(7): Show |
11 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-4267dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146252 | |||||||
| chr11:33146528 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.28-4542C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146528 | |||||||
| chr11:33146623 | T | TA | 92 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0021 others(89): Show |
102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.28-4638dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146623 | |||||||
| chr11:33146623 | T | TAA | 175 | a0001c0001t0001g0296 a0001c0001t0002g0005 a0001c0001t0002g0006 others(172): Show |
200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.28-4639_28-4638dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146623 | |||||||
| chr11:33146753 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0314 |
2 | HG01069.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.28-4767G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146753 | |||||||
| chr11:33146855 | GA | G | 84 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(81): Show |
88 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.28-4870delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33146855 | |||||||
| chr11:33147060 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.28-5074C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147060 | |||||||
| chr11:33147207 | A | T | 1 | a0001c0001t0003g0119 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.28-5221T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147207 | |||||||
| chr11:33147224 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.28-5238C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147224 | |||||||
| chr11:33147254 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-5268C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147254 | |||||||
| chr11:33147317 | C | G | 1 | a0001c0002t0002g0008 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.28-5331G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147317 | |||||||
| chr11:33147348 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0309 a0001c0001t0001g0310 others(3): Show |
7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-5362C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147348 | |||||||
| chr11:33147412 | T | C | 13 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0047 others(10): Show |
13 | HG02027.hp1 HG02040.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.28-5426A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147412 | |||||||
| chr11:33147486 | T | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28-5500A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147486 | |||||||
| chr11:33147520 | A | G | 215 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(212): Show |
240 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.28-5534T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147520 | |||||||
| chr11:33147555 | C | G | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-5569G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147555 | |||||||
| chr11:33147618 | T | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(83): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.28-5632A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147618 | |||||||
| chr11:33147785 | A | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-5799T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147785 | |||||||
| chr11:33147865 | T | G | 1 | a0001c0001t0002g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.28-5879A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33147865 | |||||||
| chr11:33148097 | C | T | 3 | a0001c0001t0001g0196 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG01243.hp1 HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.28-6111G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148097 | |||||||
| chr11:33148141 | C | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-6155G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148141 | |||||||
| chr11:33148186 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.28-6200T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148186 | |||||||
| chr11:33148192 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0309 a0001c0001t0001g0310 others(3): Show |
7 | HG00735.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-6206G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148192 | |||||||
| chr11:33148434 | C | T | 1 | a0001c0001t0003g0174 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.28-6448G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148434 | |||||||
| chr11:33148466 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.28-6480C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148466 | |||||||
| chr11:33148534 | T | TAAAAATA others(180): Show |
1 | a0001c0001t0001g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(187): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(181): Show |
1 | a0001c0001t0001g0230 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(188): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(185): Show |
1 | a0001c0001t0001g0241 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(192): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(186): Show |
1 | a0001c0001t0001g0242 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(193): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(187): Show |
1 | a0001c0001t0001g0240 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(194): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(188): Show |
1 | a0001c0001t0001g0238 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(195): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(195): Show |
2 | a0001c0001t0001g0237 a0001c0001t0001g0306 |
2 | HG00738.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.28-6549_28-6548ins others(202): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(196): Show |
1 | a0001c0001t0001g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(203): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(197): Show |
4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0289 others(1): Show |
4 | HG01358.hp1 NA18939.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-6549_28-6548ins others(204): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(199): Show |
2 | a0001c0001t0001g0246 a0001c0001t0001g0249 |
2 | HG04115.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.28-6549_28-6548ins others(206): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(200): Show |
2 | a0001c0001t0001g0231 a0001c0001t0001g0239 |
2 | HG00323.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.28-6549_28-6548ins others(207): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(205): Show |
1 | a0001c0001t0001g0248 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(212): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(209): Show |
1 | a0001c0001t0001g0291 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(216): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148534 | T | TAAAAATA others(204): Show |
1 | a0001c0001t0001g0247 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.28-6549_28-6548ins others(211): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148534 | |||||||
| chr11:33148572 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-6586A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148572 | |||||||
| chr11:33148596 | T | C | 3 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 |
3 | HG02080.hp2 HG02129.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.28-6610A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148596 | |||||||
| chr11:33148694 | C | CA | 80 | a0001c0001t0001g0311 a0001c0001t0002g0005 a0001c0001t0002g0025 others(77): Show |
83 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.28-6709dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148694 | |||||||
| chr11:33148694 | C | CAA | 16 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0034 others(13): Show |
18 | HG00438.hp2 HG01981.hp2 HG04204.hp2 others(15): Show |
intron_variant | MODIFIER | c.28-6710_28-6709dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148694 | |||||||
| chr11:33148825 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0240 |
2 | NA18946.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.28-6839G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148825 | |||||||
| chr11:33148837 | A | G | 7 | a0001c0001t0001g0194 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG02258.hp2 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-6851T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148837 | |||||||
| chr11:33148844 | T | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0013 others(83): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.28-6858A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148844 | |||||||
| chr11:33148856 | C | CTG | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.28-6872_28-6871dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148856 | |||||||
| chr11:33148860 | G | GT | 139 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(136): Show |
157 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.28-6875dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148860 | |||||||
| chr11:33148860 | G | GTT | 40 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0034 others(37): Show |
45 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.28-6876_28-6875dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148860 | |||||||
| chr11:33148860 | GT | G | 35 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(32): Show |
35 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-6875delA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148860 | |||||||
| chr11:33148866 | T | G | 4 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-6880A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148866 | |||||||
| chr11:33148915 | A | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-6929T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148915 | |||||||
| chr11:33148971 | C | T | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-6985G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33148971 | |||||||
| chr11:33149307 | A | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-7321T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33149307 | |||||||
| chr11:33149714 | T | A | 2 | a0001c0001t0002g0160 a0001c0001t0002g0171 |
2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.28-7728A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33149714 | |||||||
| chr11:33149982 | G | A | 1 | a0001c0001t0003g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.28-7996C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33149982 | |||||||
| chr11:33150033 | C | A | 1 | a0001c0001t0003g0152 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.28-8047G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150033 | |||||||
| chr11:33150034 | A | AAAC | 83 | a0001c0001t0002g0105 a0001c0001t0002g0114 a0001c0001t0002g0132 others(80): Show |
100 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.28-8051_28-8049dup others(3): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150034 | |||||||
| chr11:33150034 | A | AAACAAC | 87 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(84): Show |
92 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.28-8054_28-8049dup others(6): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150034 | |||||||
| chr11:33150034 | A | AAACAACA others(2): Show |
3 | a0001c0001t0002g0013 a0001c0001t0002g0055 a0001c0001t0002g0079 |
4 | NA18965.hp2 NA18966.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-8057_28-8049dup others(9): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150034 | |||||||
| chr11:33150034 | A | C | 1 | a0001c0001t0003g0152 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.28-8048T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150034 | |||||||
| chr11:33150122 | G | A | 5 | a0001c0001t0003g0153 a0001c0001t0003g0154 a0001c0001t0003g0155 others(2): Show |
5 | HG02145.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-8136C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150122 | |||||||
| chr11:33150153 | T | A | 1 | a0001c0001t0001g0220 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.28-8167A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150153 | |||||||
| chr11:33150196 | C | G | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.28-8210G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150196 | |||||||
| chr11:33150219 | T | TA | 44 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(41): Show |
44 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.28-8234dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150219 | |||||||
| chr11:33150219 | TA | T | 167 | a0001c0001t0001g0236 a0001c0001t0001g0253 a0001c0001t0001g0282 others(164): Show |
190 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.28-8234delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150219 | |||||||
| chr11:33150219 | TAA | T | 8 | a0001c0001t0002g0046 a0001c0001t0002g0089 a0001c0001t0002g0112 others(5): Show |
8 | HG01256.hp2 HG02015.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-8235_28-8234del others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150219 | |||||||
| chr11:33150250 | G | GAA | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.28-8266_28-8265dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150250 | |||||||
| chr11:33150420 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.28-8434G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150420 | |||||||
| chr11:33150673 | T | C | 5 | a0001c0001t0002g0079 a0001c0001t0003g0145 a0001c0001t0003g0146 others(2): Show |
5 | NA18957.hp2 NA18962.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-8687A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150673 | |||||||
| chr11:33150855 | C | CA | 12 | a0001c0001t0001g0276 a0001c0001t0001g0287 a0001c0001t0001g0303 others(9): Show |
13 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.28-8870dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33150855 | |||||||
| chr11:33151217 | A | T | 1 | a0001c0001t0006g0172 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.28-9231T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151217 | |||||||
| chr11:33151257 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.28-9271G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151257 | |||||||
| chr11:33151585 | T | C | 1 | a0001c0001t0002g0082 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.28-9599A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151585 | |||||||
| chr11:33151601 | C | T | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0007 others(75): Show |
95 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.28-9615G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151601 | |||||||
| chr11:33151611 | T | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0199 a0001c0001t0001g0208 others(1): Show |
4 | HG02258.hp2 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-9625A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151611 | |||||||
| chr11:33151707 | T | C | 89 | a0001c0001t0002g0006 a0001c0001t0002g0105 a0001c0001t0002g0108 others(86): Show |
109 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.27+9592A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151707 | |||||||
| chr11:33151735 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.27+9564C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151735 | |||||||
| chr11:33151807 | T | C | 1 | a0001c0001t0001g0312 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.27+9492A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33151807 | |||||||
| chr11:33152069 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27+9230G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152069 | |||||||
| chr11:33152182 | G | A | 1 | a0001c0001t0003g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.27+9117C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152182 | |||||||
| chr11:33152185 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27+9114C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152185 | |||||||
| chr11:33152269 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.27+9030C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152269 | |||||||
| chr11:33152294 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.27+9005C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152294 | |||||||
| chr11:33152317 | T | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+8982A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152317 | |||||||
| chr11:33152327 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.27+8972G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152327 | |||||||
| chr11:33152362 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.27+8937G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152362 | |||||||
| chr11:33152433 | T | G | 1 | a0001c0001t0001g0247 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.27+8866A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152433 | |||||||
| chr11:33152471 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27+8828A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152471 | |||||||
| chr11:33152498 | C | T | 215 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(212): Show |
240 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.27+8801G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152498 | |||||||
| chr11:33152544 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27+8755C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152544 | |||||||
| chr11:33152731 | T | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.27+8568A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152731 | |||||||
| chr11:33152749 | A | C | 1 | a0001c0001t0002g0006 | 3 | HG02559.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.27+8550T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152749 | |||||||
| chr11:33152857 | G | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.27+8442C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152857 | |||||||
| chr11:33152995 | G | A | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.27+8304C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152995 | |||||||
| chr11:33152999 | T | G | 1 | a0001c0001t0002g0088 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.27+8300A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33152999 | |||||||
| chr11:33153018 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.27+8281C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153018 | |||||||
| chr11:33153182 | A | G | 78 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0007 others(75): Show |
95 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.27+8117T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153182 | |||||||
| chr11:33153298 | A | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.27+8001T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153298 | |||||||
| chr11:33153384 | C | A | 3 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 |
3 | HG02717.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.27+7915G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153384 | |||||||
| chr11:33153449 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.27+7850C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153449 | |||||||
| chr11:33153512 | A | C | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.27+7787T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153512 | |||||||
| chr11:33153629 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.27+7670A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153629 | |||||||
| chr11:33153643 | A | C | 1 | a0001c0001t0002g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.27+7656T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153643 | |||||||
| chr11:33153675 | C | A | 1 | a0001c0001t0001g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+7624G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153675 | |||||||
| chr11:33153712 | C | CA | 106 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0237 others(103): Show |
126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.27+7586dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153712 | |||||||
| chr11:33153712 | C | CAA | 86 | a0001c0001t0001g0232 a0001c0001t0001g0248 a0001c0001t0001g0249 others(83): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.27+7585_27+7586dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153712 | |||||||
| chr11:33153795 | C | T | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.27+7504G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153795 | |||||||
| chr11:33153805 | G | A | 175 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(172): Show |
199 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.27+7494C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153805 | |||||||
| chr11:33153871 | C | T | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.27+7428G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153871 | |||||||
| chr11:33153939 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.27+7360G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33153939 | |||||||
| chr11:33154107 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.27+7192G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154107 | |||||||
| chr11:33154212 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.27+7087C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154212 | |||||||
| chr11:33154240 | T | C | 1 | a0001c0002t0002g0008 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.27+7059A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154240 | |||||||
| chr11:33154352 | A | C | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.27+6947T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154352 | |||||||
| chr11:33154486 | ACTTT | A | 153 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(150): Show |
177 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.27+6809_27+6812del others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154486 | |||||||
| chr11:33154487 | CTTTCT | C | 7 | a0001c0001t0002g0038 a0001c0001t0003g0030 a0001c0001t0003g0115 others(4): Show |
7 | HG00323.hp2 HG01256.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+6807_27+6811del others(5): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154487 | |||||||
| chr11:33154488 | TTTC | T | 15 | a0001c0001t0002g0028 a0001c0001t0002g0039 a0001c0001t0002g0040 others(12): Show |
15 | HG00408.hp1 HG00423.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.27+6808_27+6810del others(3): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154488 | |||||||
| chr11:33154491 | C | CT | 7 | a0001c0001t0001g0237 a0001c0001t0001g0251 a0001c0001t0001g0252 others(4): Show |
7 | HG00099.hp2 HG02148.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+6807dupA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154491 | |||||||
| chr11:33154491 | CT | C | 51 | a0001c0001t0001g0023 a0001c0001t0001g0192 a0001c0001t0001g0193 others(48): Show |
52 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.27+6807delA | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154491 | |||||||
| chr11:33154496 | T | C | 35 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(32): Show |
35 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.27+6803A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154496 | |||||||
| chr11:33154497 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0228 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.27+6802A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154497 | |||||||
| chr11:33154582 | C | T | 1 | a0001c0001t0003g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.27+6717G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154582 | |||||||
| chr11:33154583 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.27+6716C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154583 | |||||||
| chr11:33154608 | T | C | 175 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(172): Show |
199 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.27+6691A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154608 | |||||||
| chr11:33154699 | A | G | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.27+6600T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154699 | |||||||
| chr11:33154943 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.27+6356G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154943 | |||||||
| chr11:33154976 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.27+6323G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33154976 | |||||||
| chr11:33155018 | T | C | 178 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(175): Show |
203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.27+6281A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155018 | |||||||
| chr11:33155115 | G | A | 37 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0019 others(34): Show |
42 | HG00408.hp1 HG00741.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.27+6184C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155115 | |||||||
| chr11:33155128 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+6171C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155128 | |||||||
| chr11:33155217 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+6082C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155217 | |||||||
| chr11:33155249 | C | A | 178 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(175): Show |
203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.27+6050G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155249 | |||||||
| chr11:33155268 | G | C | 1 | a0001c0001t0002g0085 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.27+6031C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155268 | |||||||
| chr11:33155280 | C | T | 8 | a0001c0001t0001g0256 a0001c0001t0001g0294 a0001c0001t0001g0315 others(5): Show |
8 | HG02717.hp2 HG02809.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+6019G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155280 | |||||||
| chr11:33155283 | G | C | 1 | a0001c0001t0001g0288 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.27+6016C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155283 | |||||||
| chr11:33155343 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.27+5956C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155343 | |||||||
| chr11:33155386 | T | TA | 213 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(210): Show |
238 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.27+5912dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155386 | |||||||
| chr11:33155386 | TA | T | 7 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(4): Show |
7 | HG02723.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+5912delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155386 | |||||||
| chr11:33155542 | T | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+5757A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155542 | |||||||
| chr11:33155543 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+5756G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155543 | |||||||
| chr11:33155846 | G | A | 175 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(172): Show |
199 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.27+5453C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155846 | |||||||
| chr11:33155864 | TA | T | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.27+5434delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155864 | |||||||
| chr11:33155971 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.27+5328G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33155971 | |||||||
| chr11:33156289 | CAT | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+5008_27+5009del others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156289 | |||||||
| chr11:33156320 | C | G | 1 | a0001c0001t0002g0105 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27+4979G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156320 | |||||||
| chr11:33156410 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.27+4889C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156410 | |||||||
| chr11:33156491 | CATT | C | 9 | a0001c0001t0003g0002 a0001c0001t0003g0109 a0001c0001t0003g0147 others(6): Show |
12 | HG00408.hp1 HG02015.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.27+4805_27+4807del others(3): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156491 | |||||||
| chr11:33156792 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.27+4507G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156792 | |||||||
| chr11:33156955 | A | G | 1 | a0001c0001t0003g0159 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.27+4344T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33156955 | |||||||
| chr11:33157163 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.27+4136C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157163 | |||||||
| chr11:33157224 | G | C | 1 | a0001c0001t0002g0158 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.27+4075C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157224 | |||||||
| chr11:33157245 | C | A | 1 | a0001c0001t0001g0210 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.27+4054G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157245 | |||||||
| chr11:33157304 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.27+3995C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157304 | |||||||
| chr11:33157322 | T | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.27+3977A>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157322 | |||||||
| chr11:33157323 | C | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.27+3976G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157323 | |||||||
| chr11:33157324 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.27+3975G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157324 | |||||||
| chr11:33157325 | A | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.27+3974T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157325 | |||||||
| chr11:33157776 | A | T | 1 | a0001c0001t0002g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27+3523T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157776 | |||||||
| chr11:33157890 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.27+3409A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157890 | |||||||
| chr11:33157913 | A | G | 1 | a0001c0001t0002g0034 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.27+3386T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33157913 | |||||||
| chr11:33158223 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.27+3076T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158223 | |||||||
| chr11:33158285 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.27+3014G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158285 | |||||||
| chr11:33158475 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.27+2824T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158475 | |||||||
| chr11:33158596 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.27+2703C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158596 | |||||||
| chr11:33158602 | C | A | 1 | a0001c0001t0003g0152 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.27+2697G>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158602 | |||||||
| chr11:33158842 | C | CAA | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+2455_27+2456dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158842 | |||||||
| chr11:33158927 | TGAGACTA others(5): Show |
T | 1 | a0001c0001t0002g0158 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.27+2360_27+2371del others(12): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158927 | |||||||
| chr11:33158960 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.27+2339T>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158960 | |||||||
| chr11:33158987 | T | TA | 11 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(8): Show |
11 | HG00280.hp2 HG00597.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+2311dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158987 | |||||||
| chr11:33158999 | C | G | 1 | a0001c0001t0007g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.27+2300G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33158999 | |||||||
| chr11:33159104 | ATT | A | 5 | a0001c0001t0003g0153 a0001c0001t0003g0154 a0001c0001t0003g0155 others(2): Show |
5 | HG02145.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+2193_27+2194del others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159104 | |||||||
| chr11:33159180 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.27+2119C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159180 | |||||||
| chr11:33159312 | T | C | 89 | a0001c0001t0002g0006 a0001c0001t0002g0105 a0001c0001t0002g0108 others(86): Show |
109 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.27+1987A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159312 | |||||||
| chr11:33159353 | T | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+1946A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159353 | |||||||
| chr11:33159530 | A | G | 20 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(17): Show |
20 | HG00323.hp1 HG00544.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.27+1769T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159530 | |||||||
| chr11:33159595 | C | CA | 46 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(43): Show |
49 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.27+1703dupT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | |||||||
| chr11:33159595 | C | CAA | 60 | a0001c0001t0001g0194 a0001c0001t0001g0306 a0001c0001t0001g0307 others(57): Show |
77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.27+1702_27+1703dup others(2): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | |||||||
| chr11:33159595 | C | CAAA | 50 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(47): Show |
50 | HG00735.hp2 HG00741.hp2 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.27+1701_27+1703dup others(3): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | |||||||
| chr11:33159595 | C | CAAAA | 17 | a0001c0001t0001g0023 a0001c0001t0001g0211 a0001c0001t0001g0212 others(14): Show |
18 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.27+1700_27+1703dup others(4): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | |||||||
| chr11:33159595 | C | CAAAAA | 8 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG00642.hp2 HG03139.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+1699_27+1703dup others(5): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | |||||||
| chr11:33159595 | CA | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
17 | HG00323.hp1 HG01261.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.27+1703delT | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159595 | |||||||
| chr11:33159664 | G | A | 1 | a0001c0001t0003g0186 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.27+1635C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159664 | |||||||
| chr11:33159712 | A | T | 1 | a0001c0001t0003g0030 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.27+1587T>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159712 | |||||||
| chr11:33159731 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.27+1568A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159731 | |||||||
| chr11:33159799 | T | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+1500A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159799 | |||||||
| chr11:33159915 | G | C | 1 | a0001c0001t0001g0315 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.27+1384C>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33159915 | |||||||
| chr11:33160321 | C | T | 1 | a0001c0001t0002g0029 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.27+978G>A | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160321 | |||||||
| chr11:33160572 | TCTGAATA others(16): Show |
T | 1 | a0001c0001t0002g0028 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.27+704_27+726delTT others(21): Show |
CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160572 | |||||||
| chr11:33160710 | T | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG01891.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.27+589A>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160710 | |||||||
| chr11:33160732 | A | G | 38 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(35): Show |
38 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.27+567T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160732 | |||||||
| chr11:33160762 | G | A | 177 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(174): Show |
202 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.27+537C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160762 | |||||||
| chr11:33160825 | T | C | 5 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+474A>G | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160825 | |||||||
| chr11:33160846 | A | G | 176 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0012 others(173): Show |
200 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.27+453T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33160846 | |||||||
| chr11:33161006 | A | G | 1 | a0001c0003t0002g0026 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.27+293T>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33161006 | |||||||
| chr11:33161088 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0187 |
3 | HG01496.hp1 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.27+211C>T | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33161088 | |||||||
| chr11:33161153 | C | G | 1 | a0001c0001t0002g0025 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.27+146G>C | CSTF3 | ENSG00000176102.13 | transcript | ENST00000323959.9 | protein_coding | 1/20 | chr11 | 33161153 |