Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 58517 |
| ensemblid | ENSG00000119707.14 |
| hgncid | 23244 |
| symbol | RBM25 |
| name | RNA binding motif protein 25 |
| refseq_nuc | NM_021239.3 |
| refseq_prot | NP_067062.1 |
| ensembl_nuc | ENST00000261973.12 |
| ensembl_prot | ENSP00000261973.7 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 73058534 |
| end | 73123899 |
| strand | + |
| ver | v1.2 |
| region | chr14:73058534-73123899 |
| region5000 | chr14:73053534-73128899 |
| regionname0 | RBM25_chr14_73058534_73123899 |
| regionname5000 | RBM25_chr14_73053534_73128899 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2529 | 343 | 86 | 66 | 143 | 10 | 36 | RBM25_chr14_73053534_73128899 | RBM25 | ATGTC others(2524): Show |
chr14 | 73053534 | 73128899 | ||
| a0001c0002 | 0/0 | 2529 | 43 | 3 | 9 | 29 | 0 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | ATGTC others(2524): Show |
chr14 | 73053534 | 73128899 | ||
| a0001c0003 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | ATGTC others(2524): Show |
chr14 | 73053534 | 73128899 | ||
| a0001c0004 | 0/0 | 2529 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | ATGTC others(2524): Show |
chr14 | 73053534 | 73128899 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6813 | 151 | 29 | 17 | 90 | 2 | 12 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0002 | 0/0 | 6813 | 58 | 5 | 19 | 24 | 4 | 6 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0004 | 0/0 | 6813 | 28 | 2 | 13 | 5 | 1 | 7 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0005 | 0/0 | 6814 | 18 | 11 | 5 | 1 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6809): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0006 | 0/0 | 6812 | 16 | 2 | 1 | 10 | 0 | 3 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6807): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0007 | 0/0 | 6813 | 10 | 9 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0008 | 0/0 | 6814 | 8 | 0 | 2 | 2 | 2 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6809): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0010 | 0/0 | 6813 | 6 | 6 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0011 | 0/0 | 6812 | 5 | 5 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6807): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0012 | 0/0 | 6813 | 5 | 0 | 3 | 0 | 0 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0013 | 0/0 | 6813 | 5 | 4 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0014 | 0/0 | 6813 | 3 | 0 | 0 | 3 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0015 | 0/0 | 6813 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0016 | 0/0 | 6814 | 3 | 0 | 0 | 3 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6809): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0018 | 0/0 | 6813 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0019 | 0/0 | 6814 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6809): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0020 | 0/0 | 6813 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0021 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0022 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0023 | 0/0 | 6813 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0024 | 0/0 | 6813 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0025 | 0/0 | 6812 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6807): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0026 | 0/0 | 6813 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0027 | 0/0 | 6814 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6809): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0028 | 0/0 | 6812 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6807): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0029 | 0/0 | 6813 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0030 | 0/0 | 6813 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0031 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0033 | 0/0 | 6814 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6809): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0034 | 0/0 | 6814 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6809): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0035 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0036 | 0/0 | 6814 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6809): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0037 | 0/0 | 6814 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6809): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0038 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0039 | 0/0 | 6813 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0040 | 0/1 | 6813 | 1 | 0 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0001t0041 | 0/0 | 6813 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0002t0003 | 0/0 | 6813 | 34 | 2 | 6 | 26 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0002t0009 | 0/0 | 6813 | 6 | 1 | 3 | 0 | 0 | 2 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0002t0017 | 0/0 | 6813 | 2 | 0 | 0 | 2 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0002t0032 | 0/0 | 6814 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6809): Show |
chr14 | 73053534 | 73128899 |
| a0001c0003t0001 | 0/0 | 6813 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| a0001c0004t0015 | 0/0 | 6813 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | AGACC others(6808): Show |
chr14 | 73053534 | 73128899 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0002g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0001 | 0/0 | 6 | 1 | 4 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0007g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0007g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0008g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0008g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0008g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0008g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0008g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0008g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0008g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0010g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0010g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0010g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0010g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0010g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0012g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0012g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0012g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0012g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0012g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0013g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0013g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0013g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0013g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0014g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0014g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0014g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0015g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0016g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0016g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0016g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0018g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0018g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0019g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0019g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0020g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0021g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0022g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0023g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0024g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0025g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0026g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0027g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0028g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0029g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0030g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0031g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0033g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0034g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0035g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0036g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0037g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0038g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0039g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0040g0364 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0001t0041g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0009g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0009g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0009g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0009g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0009g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0017g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0017g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0002t0032g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0003t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| a0001c0004t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0076 | EUR | GBR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0216 | EUR | GBR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00140 | hp1 | a0001 | c0001 | t0024 | g0224 | EUR | GBR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0326 | EUR | GBR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0018 | EUR | FIN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0095 | EUR | FIN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00408 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0153 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00544 | hp2 | a0001 | c0001 | t0006 | g0047 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00558 | hp2 | a0001 | c0001 | t0016 | g0091 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0366 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | CHS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00735 | hp1 | a0001 | c0002 | t0009 | g0131 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00738 | hp2 | a0001 | c0002 | t0009 | g0208 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0173 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0170 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0155 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01074 | hp2 | a0001 | c0001 | t0023 | g0051 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0257 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0156 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0372 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01167 | hp2 | a0001 | c0001 | t0012 | g0022 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01168 | hp2 | a0001 | c0001 | t0008 | g0016 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01169 | hp2 | a0001 | c0001 | t0012 | g0019 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01175 | hp2 | a0001 | c0001 | t0039 | g0191 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0296 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0125 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01257 | hp1 | a0001 | c0001 | t0012 | g0020 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0199 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01261 | hp2 | a0001 | c0001 | t0008 | g0012 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0367 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01358 | hp2 | a0001 | c0002 | t0009 | g0211 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0267 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01496 | hp2 | a0001 | c0001 | t0013 | g0061 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0334 | EUR | IBS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0371 | EUR | IBS | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0063 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0285 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0127 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0274 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0122 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0204 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01975 | hp1 | a0001 | c0001 | t0025 | g0041 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0368 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0130 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0157 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02055 | hp1 | a0001 | c0002 | t0009 | g0209 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0289 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02074 | hp1 | a0001 | c0001 | t0028 | g0249 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02135 | hp1 | a0001 | c0001 | t0016 | g0099 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02135 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0283 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02148 | hp1 | a0001 | c0002 | t0003 | g0121 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02148 | hp2 | a0001 | c0001 | t0041 | g0003 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CDX | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CDX | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02165 | hp1 | a0001 | c0002 | t0003 | g0169 | EAS | CDX | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | CDX | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02257 | hp2 | a0001 | c0001 | t0035 | g0123 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0183 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0298 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02523 | hp2 | a0001 | c0002 | t0003 | g0158 | EAS | KHV | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02615 | hp1 | a0001 | c0001 | t0027 | g0147 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0294 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0171 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02622 | hp2 | a0001 | c0001 | t0018 | g0278 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0292 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02683 | hp1 | a0001 | c0001 | t0033 | g0070 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0330 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02698 | hp2 | a0001 | c0001 | t0030 | g0071 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02717 | hp1 | a0001 | c0001 | t0021 | g0293 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0299 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02723 | hp2 | a0001 | c0001 | t0019 | g0281 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02735 | hp1 | a0001 | c0001 | t0008 | g0017 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02735 | hp2 | a0001 | c0001 | t0012 | g0021 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0048 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02809 | hp1 | a0001 | c0001 | t0011 | g0054 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02818 | hp1 | a0001 | c0001 | t0037 | g0148 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02818 | hp2 | a0001 | c0001 | t0038 | g0024 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0027 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0290 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02976 | hp2 | a0001 | c0001 | t0018 | g0277 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03017 | hp2 | a0001 | c0002 | t0009 | g0212 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0291 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0058 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0119 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03453 | hp1 | a0001 | c0004 | t0015 | g0025 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03453 | hp2 | a0001 | c0001 | t0019 | g0282 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0284 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0233 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03540 | hp1 | a0001 | c0001 | t0015 | g0026 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0286 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0262 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0275 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0037 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0217 | SAS | PJL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0276 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0014 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0036 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0255 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG04115 | hp1 | a0001 | c0001 | t0034 | g0259 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG04184 | hp2 | a0001 | c0001 | t0012 | g0023 | SAS | BEB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0369 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0256 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0253 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG04228 | hp1 | a0001 | c0002 | t0009 | g0161 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0370 | SAS | STU | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0295 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0062 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0167 | EAS | CHB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | CHB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0214 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0055 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18941 | hp1 | a0001 | c0001 | t0020 | g0279 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18941 | hp2 | a0001 | c0002 | t0017 | g0133 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0160 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18944 | hp1 | a0001 | c0001 | t0014 | g0351 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18944 | hp2 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18947 | hp2 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18950 | hp2 | a0001 | c0002 | t0017 | g0154 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0162 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0163 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18984 | hp1 | a0001 | c0002 | t0003 | g0152 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18985 | hp2 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0164 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18991 | hp1 | a0001 | c0001 | t0036 | g0362 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18992 | hp1 | a0001 | c0001 | t0006 | g0042 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18993 | hp1 | a0001 | c0001 | t0014 | g0178 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18994 | hp1 | a0001 | c0002 | t0032 | g0151 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18997 | hp2 | a0001 | c0001 | t0026 | g0050 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0200 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18999 | hp2 | a0001 | c0001 | t0029 | g0264 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19003 | hp2 | a0001 | c0001 | t0016 | g0073 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19009 | hp1 | a0001 | c0001 | t0014 | g0360 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0056 | AFR | LWK | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19030 | hp2 | a0001 | c0001 | t0022 | g0033 | AFR | LWK | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0134 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19063 | hp1 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19063 | hp2 | a0001 | c0001 | t0006 | g0046 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19064 | hp2 | a0001 | c0002 | t0003 | g0150 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19065 | hp1 | a0001 | c0001 | t0008 | g0015 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19067 | hp2 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0166 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19084 | hp2 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0201 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | YRI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ASW | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ASW | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0081 | EUR | TSI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0011 | EUR | TSI | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | CLM | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0052 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0297 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | ACB | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0053 | AFR | MSL | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | USA | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | USA | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0030 | AFR | USA | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| NA21309 | hp2 | a0001 | c0001 | t0031 | g0031 | AFR | LWK | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0040 | g0364 | REF | REF | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0124 | REF | REF | RBM25_chr14_73053534_73128899 | RBM25 | chr14 | 73053534 | 73128899 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:73077497 | C | T | 1 | a0001c0004 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.285C>T | p.Ser95Ser | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/19 | 472/6813 | 285/2532 | 95/843 | chr14 | 73077497 | |||
| chr14:73088047 | A | G | 1 | a0001c0003 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.429A>G | p.Ala143Ala | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/19 | 616/6813 | 429/2532 | 143/843 | chr14 | 73088047 | |||
| chr14:73114303 | A | G | 1 | a0001c0002 | 43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
synonymous_variant | LOW | c.2409A>G | p.Ser803Ser | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/19 | 2596/6813 | 2409/2532 | 803/843 | chr14 | 73114303 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:73058557 | A | T | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0013 others(2): Show |
73 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(70): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-164A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/19 | chr14 | 73058557 | |||||||
| chr14:73058578 | T | C | 1 | a0001c0001t0020 | 1 | NA18941.hp1 | 5_prime_UTR_variant | MODIFIER | c.-143T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/19 | 13064 | chr14 | 73058578 | ||||||
| chr14:73119824 | T | C | 2 | a0001c0001t0007 a0001c0001t0021 |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*19T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 19 | chr14 | 73119824 | ||||||
| chr14:73120371 | AT | A | 1 | a0001c0001t0011 | 5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*569delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 569 | INFO_REALIGN_3_PRIME | chr14 | 73120371 | |||||
| chr14:73120405 | A | G | 1 | a0001c0001t0019 | 2 | HG02723.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*600A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 600 | chr14 | 73120405 | ||||||
| chr14:73120620 | C | T | 1 | a0001c0001t0019 | 2 | HG02723.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*815C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 815 | chr14 | 73120620 | ||||||
| chr14:73120708 | T | C | 3 | a0001c0001t0011 a0001c0001t0022 a0001c0001t0023 |
7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*903T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 903 | chr14 | 73120708 | ||||||
| chr14:73120968 | C | T | 1 | a0001c0001t0010 | 6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1163C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1163 | chr14 | 73120968 | ||||||
| chr14:73121210 | T | A | 1 | a0001c0001t0022 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1405T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1405 | chr14 | 73121210 | ||||||
| chr14:73121447 | A | G | 1 | a0001c0001t0039 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1642A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1642 | chr14 | 73121447 | ||||||
| chr14:73121498 | A | G | 1 | a0001c0001t0041 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1693A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1693 | chr14 | 73121498 | ||||||
| chr14:73121520 | A | G | 1 | a0001c0001t0038 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1715A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1715 | chr14 | 73121520 | ||||||
| chr14:73121596 | G | C | 1 | a0001c0001t0024 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1791G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1791 | chr14 | 73121596 | ||||||
| chr14:73121623 | C | G | 1 | a0001c0001t0022 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1818C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1818 | chr14 | 73121623 | ||||||
| chr14:73121627 | G | C | 3 | a0001c0001t0011 a0001c0001t0022 a0001c0001t0023 |
7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1822G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1822 | chr14 | 73121627 | ||||||
| chr14:73121635 | T | C | 1 | a0001c0001t0008 | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1830T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1830 | chr14 | 73121635 | ||||||
| chr14:73121660 | G | T | 1 | a0001c0001t0037 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1855G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1855 | chr14 | 73121660 | ||||||
| chr14:73121663 | C | T | 2 | a0001c0001t0011 a0001c0001t0023 |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1858C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1858 | chr14 | 73121663 | ||||||
| chr14:73121683 | G | A | 7 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0011 others(4): Show |
33 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1878G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1878 | chr14 | 73121683 | ||||||
| chr14:73121696 | T | G | 1 | a0001c0001t0008 | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1891T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 1891 | chr14 | 73121696 | ||||||
| chr14:73121830 | T | C | 1 | a0001c0001t0027 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2025T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2025 | chr14 | 73121830 | ||||||
| chr14:73121939 | A | G | 3 | a0001c0001t0015 a0001c0001t0038 a0001c0004t0015 |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2134A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2134 | chr14 | 73121939 | ||||||
| chr14:73122202 | A | G | 2 | a0001c0001t0014 a0001c0001t0036 |
4 | NA18944.hp1 NA18991.hp1 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2397A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2397 | chr14 | 73122202 | ||||||
| chr14:73122265 | G | A | 1 | a0001c0001t0008 | 8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2460G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2460 | chr14 | 73122265 | ||||||
| chr14:73122276 | G | T | 1 | a0001c0001t0035 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2471G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2471 | chr14 | 73122276 | ||||||
| chr14:73122279 | G | GT | 10 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0016 others(7): Show |
37 | HG00323.hp1 HG00558.hp2 HG01168.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2487dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2488 | INFO_REALIGN_3_PRIME | chr14 | 73122279 | |||||
| chr14:73122279 | GT | G | 3 | a0001c0001t0006 a0001c0001t0025 a0001c0001t0028 |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2487delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2487 | INFO_REALIGN_3_PRIME | chr14 | 73122279 | |||||
| chr14:73122293 | G | C | 2 | a0001c0001t0011 a0001c0001t0023 |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2488G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2488 | chr14 | 73122293 | ||||||
| chr14:73122315 | G | A | 1 | a0001c0001t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2510G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2510 | chr14 | 73122315 | ||||||
| chr14:73122317 | C | T | 1 | a0001c0001t0021 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2512C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2512 | chr14 | 73122317 | ||||||
| chr14:73122480 | T | C | 8 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0011 others(5): Show |
38 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2675T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2675 | chr14 | 73122480 | ||||||
| chr14:73122556 | G | A | 1 | a0001c0001t0025 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2751G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2751 | chr14 | 73122556 | ||||||
| chr14:73122581 | G | A | 1 | a0001c0001t0029 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2776G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2776 | chr14 | 73122581 | ||||||
| chr14:73122589 | C | G | 1 | a0001c0001t0031 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2784C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2784 | chr14 | 73122589 | ||||||
| chr14:73122789 | C | T | 2 | a0001c0001t0004 a0001c0001t0034 |
29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2984C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 2984 | chr14 | 73122789 | ||||||
| chr14:73122910 | A | G | 3 | a0001c0001t0030 a0001c0001t0033 a0001c0002t0009 |
8 | HG00735.hp1 HG00738.hp2 HG01358.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3105A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3105 | chr14 | 73122910 | ||||||
| chr14:73122976 | C | T | 1 | a0001c0001t0010 | 6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3171C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3171 | chr14 | 73122976 | ||||||
| chr14:73122981 | C | A | 2 | a0001c0001t0011 a0001c0001t0023 |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3176C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3176 | chr14 | 73122981 | ||||||
| chr14:73123076 | A | G | 1 | a0001c0001t0018 | 2 | HG02622.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3271A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3271 | chr14 | 73123076 | ||||||
| chr14:73123188 | C | G | 19 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(16): Show |
122 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*3383C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3383 | chr14 | 73123188 | ||||||
| chr14:73123258 | A | G | 1 | a0001c0001t0012 | 5 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3453A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3453 | chr14 | 73123258 | ||||||
| chr14:73123370 | T | C | 2 | a0001c0001t0004 a0001c0001t0034 |
29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3565T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3565 | chr14 | 73123370 | ||||||
| chr14:73123604 | C | A | 1 | a0001c0002t0017 | 2 | NA18941.hp2 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3799C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 3799 | chr14 | 73123604 | ||||||
| chr14:73123838 | G | A | 2 | a0001c0001t0011 a0001c0001t0023 |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4033G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 4033 | chr14 | 73123838 | ||||||
| chr14:73123840 | T | C | 3 | a0001c0001t0006 a0001c0001t0025 a0001c0001t0026 |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4035T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 19/19 | 4035 | chr14 | 73123840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:73058764 | G | A | 13 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(10): Show |
13 | HG00323.hp1 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-16+59G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058764 | |||||||
| chr14:73058767 | G | A | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+62G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058767 | |||||||
| chr14:73058842 | G | A | 1 | a0001c0001t0002g0028 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-16+137G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058842 | |||||||
| chr14:73058843 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-16+138A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058843 | |||||||
| chr14:73058858 | G | A | 1 | a0001c0001t0008g0011 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-16+153G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058858 | |||||||
| chr14:73058966 | T | A | 1 | a0001c0001t0002g0029 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-16+261T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058966 | |||||||
| chr14:73058968 | C | T | 3 | a0001c0001t0002g0370 a0001c0001t0002g0371 a0001c0001t0002g0372 |
3 | HG01106.hp1 HG01516.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-16+263C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73058968 | |||||||
| chr14:73059002 | G | C | 1 | a0001c0001t0002g0029 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-16+297G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059002 | |||||||
| chr14:73059251 | C | T | 1 | a0001c0001t0001g0369 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-16+546C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059251 | |||||||
| chr14:73059378 | C | G | 1 | a0001c0003t0001g0368 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-16+673C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059378 | |||||||
| chr14:73059416 | C | A | 1 | a0001c0001t0013g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-16+711C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059416 | |||||||
| chr14:73059440 | C | A | 34 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(31): Show |
34 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.-16+735C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059440 | |||||||
| chr14:73059452 | A | G | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+747A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059452 | |||||||
| chr14:73059496 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-16+791G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059496 | |||||||
| chr14:73059599 | C | T | 2 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | HG00639.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-16+894C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059599 | |||||||
| chr14:73059771 | A | G | 1 | a0001c0001t0001g0365 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-16+1066A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059771 | |||||||
| chr14:73059824 | T | C | 9 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0064 others(6): Show |
9 | HG01496.hp2 HG01884.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+1119T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059824 | |||||||
| chr14:73059881 | T | C | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+1176T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059881 | |||||||
| chr14:73059905 | G | A | 58 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0029 others(55): Show |
58 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-16+1200G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73059905 | |||||||
| chr14:73060084 | G | C | 20 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(17): Show |
20 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+1379G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060084 | |||||||
| chr14:73060133 | GGTTCAAG others(5084): Show |
G | 2 | a0001c0001t0008g0017 a0001c0001t0008g0018 |
2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-16+1436_-15-6396d others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73060133 | ||||||
| chr14:73060205 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0215 |
2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-16+1500A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060205 | |||||||
| chr14:73060259 | G | A | 1 | a0001c0001t0001g0365 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-16+1554G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060259 | |||||||
| chr14:73060424 | G | T | 1 | a0001c0002t0003g0201 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-16+1719G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060424 | |||||||
| chr14:73060545 | A | G | 53 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0057 others(50): Show |
55 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-16+1840A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060545 | |||||||
| chr14:73060595 | A | G | 1 | a0001c0001t0020g0279 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-16+1890A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060595 | |||||||
| chr14:73060967 | A | G | 1 | a0001c0001t0007g0295 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-16+2262A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73060967 | |||||||
| chr14:73060985 | C | CTT | 25 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(22): Show |
31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-16+2281_-16+2282i others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73060985 | ||||||
| chr14:73061071 | T | C | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+2366T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061071 | |||||||
| chr14:73061092 | C | T | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+2387C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061092 | |||||||
| chr14:73061162 | A | T | 1 | a0001c0001t0006g0045 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-16+2457A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061162 | |||||||
| chr14:73061245 | A | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0204 a0001c0001t0004g0267 others(2): Show |
6 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+2540A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061245 | |||||||
| chr14:73061421 | A | G | 3 | a0001c0001t0002g0072 a0001c0001t0002g0076 a0001c0001t0002g0112 |
3 | HG00099.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-16+2716A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061421 | |||||||
| chr14:73061481 | C | T | 119 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(116): Show |
128 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.-16+2776C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061481 | |||||||
| chr14:73061528 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-16+2823G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061528 | |||||||
| chr14:73061715 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-16+3010C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061715 | |||||||
| chr14:73061772 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-16+3067T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061772 | |||||||
| chr14:73061930 | C | T | 4 | a0001c0001t0001g0185 a0001c0001t0001g0241 a0001c0001t0001g0243 others(1): Show |
4 | HG02155.hp2 NA18954.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+3225C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061930 | |||||||
| chr14:73061937 | G | A | 94 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0126 others(91): Show |
95 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.-16+3232G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061937 | |||||||
| chr14:73061956 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-16+3251G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73061956 | |||||||
| chr14:73062064 | G | A | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+3359G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062064 | |||||||
| chr14:73062077 | G | C | 1 | a0001c0001t0006g0045 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-16+3372G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062077 | |||||||
| chr14:73062386 | A | G | 58 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0029 others(55): Show |
58 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-16+3681A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062386 | |||||||
| chr14:73062442 | G | A | 3 | a0001c0001t0012g0019 a0001c0001t0012g0020 a0001c0001t0012g0022 |
3 | HG01167.hp2 HG01169.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.-16+3737G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062442 | |||||||
| chr14:73062557 | G | A | 1 | a0001c0001t0031g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-16+3852G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062557 | |||||||
| chr14:73062628 | A | G | 1 | a0001c0001t0005g0143 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-16+3923A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062628 | |||||||
| chr14:73062654 | G | C | 22 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(19): Show |
28 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-16+3949G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062654 | |||||||
| chr14:73062690 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-16+3985A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062690 | |||||||
| chr14:73062859 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-16+4154C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062859 | |||||||
| chr14:73062867 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-16+4162C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73062867 | |||||||
| chr14:73063085 | A | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+4380A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063085 | |||||||
| chr14:73063087 | G | T | 2 | a0001c0001t0007g0296 a0001c0001t0007g0297 |
2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-16+4382G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063087 | |||||||
| chr14:73063222 | TC | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0223 a0001c0001t0001g0226 others(6): Show |
10 | NA18946.hp1 NA18953.hp1 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16+4518delC | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063222 | |||||||
| chr14:73063235 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 |
4 | HG02647.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+4530C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063235 | |||||||
| chr14:73063275 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-16+4570G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063275 | |||||||
| chr14:73063321 | T | C | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-16+4616T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063321 | |||||||
| chr14:73063450 | G | A | 37 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(34): Show |
37 | HG00408.hp2 HG00544.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.-16+4745G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063450 | |||||||
| chr14:73063487 | T | C | 4 | a0001c0001t0002g0069 a0001c0001t0002g0088 a0001c0001t0030g0071 others(1): Show |
4 | HG02683.hp1 HG02698.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+4782T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063487 | |||||||
| chr14:73063672 | C | T | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+4967C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063672 | |||||||
| chr14:73063871 | T | C | 20 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(17): Show |
20 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+5166T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063871 | |||||||
| chr14:73063873 | G | T | 1 | a0001c0001t0002g0074 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-16+5168G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063873 | |||||||
| chr14:73063895 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-16+5190C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063895 | |||||||
| chr14:73063970 | T | C | 144 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0137 others(141): Show |
154 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-16+5265T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73063970 | |||||||
| chr14:73064548 | C | T | 2 | a0001c0001t0008g0012 a0001c0001t0008g0016 |
2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-16+5843C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064548 | |||||||
| chr14:73064676 | A | T | 1 | a0001c0001t0002g0098 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-16+5971A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064676 | |||||||
| chr14:73064700 | G | A | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+5995G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064700 | |||||||
| chr14:73064752 | T | C | 3 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 |
3 | HG02055.hp2 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-16+6047T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064752 | |||||||
| chr14:73064916 | A | G | 4 | a0001c0001t0005g0122 a0001c0001t0005g0125 a0001c0001t0005g0127 others(1): Show |
4 | HG01256.hp2 HG01928.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+6211A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064916 | |||||||
| chr14:73064954 | CT | C | 8 | a0001c0001t0001g0305 a0001c0001t0001g0357 a0001c0001t0011g0052 others(5): Show |
8 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+6264delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73064954 | ||||||
| chr14:73064980 | T | G | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.-16+6275T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73064980 | |||||||
| chr14:73065025 | A | G | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-16+6320A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065025 | |||||||
| chr14:73065045 | G | T | 19 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(16): Show |
19 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-16+6340G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065045 | |||||||
| chr14:73065091 | C | G | 94 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0126 others(91): Show |
95 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.-16+6386C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065091 | |||||||
| chr14:73065118 | TTTTGTTT others(1): Show |
T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 |
4 | HG02647.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+6429_-16+6436d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73065118 | ||||||
| chr14:73065270 | A | G | 63 | a0001c0001t0001g0010 a0001c0001t0001g0303 a0001c0001t0001g0304 others(60): Show |
64 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-15-6357A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065270 | |||||||
| chr14:73065316 | C | T | 1 | a0001c0001t0001g0363 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-15-6311C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065316 | |||||||
| chr14:73065429 | A | AT | 10 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0005g0300 others(7): Show |
10 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-6184dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73065429 | ||||||
| chr14:73065569 | C | T | 11 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15-6058C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065569 | |||||||
| chr14:73065603 | A | G | 1 | a0001c0001t0001g0361 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-15-6024A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065603 | |||||||
| chr14:73065752 | A | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-5875A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065752 | |||||||
| chr14:73065856 | A | AGAGTTTT others(326): Show |
2 | a0001c0001t0001g0009 a0001c0001t0001g0287 |
3 | HG02976.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-15-5757_-15-5756i others(335): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73065856 | ||||||
| chr14:73065856 | A | AGAGTTTT others(327): Show |
1 | a0001c0001t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-15-5757_-15-5756i others(336): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73065856 | ||||||
| chr14:73065947 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-15-5680T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065947 | |||||||
| chr14:73065962 | T | C | 1 | a0001c0002t0003g0117 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-15-5665T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065962 | |||||||
| chr14:73065968 | A | G | 72 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0029 others(69): Show |
73 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-15-5659A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73065968 | |||||||
| chr14:73066180 | C | T | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-5447C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066180 | |||||||
| chr14:73066195 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0118 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-15-5432G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066195 | |||||||
| chr14:73066244 | T | C | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-15-5383T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066244 | |||||||
| chr14:73066260 | T | C | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-15-5367T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066260 | |||||||
| chr14:73066413 | A | G | 20 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(17): Show |
20 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-5214A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066413 | |||||||
| chr14:73066504 | G | A | 1 | a0001c0002t0003g0119 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-15-5123G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066504 | |||||||
| chr14:73066508 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-15-5119G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066508 | |||||||
| chr14:73066576 | G | A | 1 | a0001c0002t0003g0121 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-15-5051G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066576 | |||||||
| chr14:73066637 | A | G | 2 | a0001c0001t0019g0281 a0001c0001t0019g0282 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-15-4990A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066637 | |||||||
| chr14:73066646 | CA | C | 217 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(214): Show |
223 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.-15-4962delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73066646 | ||||||
| chr14:73066646 | CAA | C | 94 | a0001c0001t0001g0006 a0001c0001t0001g0215 a0001c0001t0001g0220 others(91): Show |
101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.-15-4963_-15-4962d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73066646 | ||||||
| chr14:73066646 | CAAA | C | 22 | a0001c0001t0004g0280 a0001c0001t0006g0034 a0001c0001t0006g0035 others(19): Show |
22 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-15-4964_-15-4962d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73066646 | ||||||
| chr14:73066646 | CAAAA | C | 7 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(4): Show |
7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15-4965_-15-4962d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73066646 | ||||||
| chr14:73066757 | G | A | 4 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG00609.hp1 NA18980.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-4870G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066757 | |||||||
| chr14:73066951 | A | G | 1 | a0001c0002t0009g0212 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-15-4676A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066951 | |||||||
| chr14:73066994 | T | C | 20 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(17): Show |
20 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-4633T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73066994 | |||||||
| chr14:73067066 | A | AG | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-4561_-15-4560i others(3): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067066 | |||||||
| chr14:73067067 | A | AT | 25 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0269 others(22): Show |
25 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-15-4540dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067067 | ||||||
| chr14:73067067 | A | ATT | 54 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0029 others(51): Show |
54 | HG00323.hp2 HG00558.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-15-4541_-15-4540d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067067 | ||||||
| chr14:73067067 | A | ATTT | 6 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0111 others(3): Show |
6 | HG01069.hp1 HG01167.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-4542_-15-4540d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067067 | ||||||
| chr14:73067067 | A | T | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-4560A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067067 | |||||||
| chr14:73067068 | T | G | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-15-4559T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067068 | |||||||
| chr14:73067072 | T | A | 1 | a0001c0001t0001g0306 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-15-4555T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067072 | |||||||
| chr14:73067090 | T | C | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-4537T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067090 | |||||||
| chr14:73067150 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0369 |
3 | HG03017.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-15-4477A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067150 | |||||||
| chr14:73067172 | C | T | 8 | a0001c0001t0002g0370 a0001c0001t0002g0371 a0001c0001t0002g0372 others(5): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15-4455C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067172 | |||||||
| chr14:73067604 | A | AT | 36 | a0001c0001t0001g0203 a0001c0001t0001g0266 a0001c0001t0001g0358 others(33): Show |
37 | HG00323.hp1 HG00408.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15-4006dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067604 | ||||||
| chr14:73067604 | AT | A | 6 | a0001c0001t0001g0307 a0001c0001t0002g0078 a0001c0001t0002g0079 others(3): Show |
6 | HG02165.hp2 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-4006delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067604 | ||||||
| chr14:73067621 | T | G | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-15-4006T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067621 | |||||||
| chr14:73067690 | G | A | 1 | a0001c0001t0031g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-15-3937G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067690 | |||||||
| chr14:73067758 | C | T | 2 | a0001c0001t0001g0265 a0001c0001t0029g0264 |
2 | NA18999.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-15-3869C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067758 | |||||||
| chr14:73067770 | A | AT | 6 | a0001c0001t0001g0263 a0001c0001t0001g0354 a0001c0001t0002g0108 others(3): Show |
6 | HG00609.hp2 HG00735.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-3843dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73067770 | ||||||
| chr14:73067812 | C | T | 1 | a0001c0002t0003g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-15-3815C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067812 | |||||||
| chr14:73067860 | A | G | 2 | a0001c0002t0003g0121 a0001c0002t0003g0199 |
2 | HG01261.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-15-3767A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067860 | |||||||
| chr14:73067949 | A | G | 1 | a0001c0001t0019g0282 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-15-3678A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73067949 | |||||||
| chr14:73068025 | G | A | 1 | a0001c0001t0013g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-15-3602G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068025 | |||||||
| chr14:73068047 | C | T | 4 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(1): Show |
4 | HG02258.hp1 HG02258.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-3580C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068047 | |||||||
| chr14:73068176 | T | C | 6 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-3451T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068176 | |||||||
| chr14:73068182 | T | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0137 others(35): Show |
39 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.-15-3445T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068182 | |||||||
| chr14:73068387 | A | AT | 216 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(213): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-15-3222dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73068387 | ||||||
| chr14:73068387 | A | ATT | 29 | a0001c0001t0001g0146 a0001c0001t0001g0194 a0001c0001t0001g0348 others(26): Show |
29 | HG00408.hp2 HG01081.hp2 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15-3223_-15-3222d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73068387 | ||||||
| chr14:73068387 | A | ATTT | 9 | a0001c0001t0001g0350 a0001c0001t0001g0352 a0001c0001t0001g0353 others(6): Show |
9 | HG00544.hp2 HG02738.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15-3224_-15-3222d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73068387 | ||||||
| chr14:73068573 | A | G | 1 | a0001c0001t0001g0353 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-15-3054A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068573 | |||||||
| chr14:73068670 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-15-2957G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068670 | |||||||
| chr14:73068681 | T | C | 1 | a0001c0001t0004g0219 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-15-2946T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068681 | |||||||
| chr14:73068692 | A | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-2935A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068692 | |||||||
| chr14:73068825 | C | T | 23 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(20): Show |
29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15-2802C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73068825 | |||||||
| chr14:73069085 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-15-2542G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069085 | |||||||
| chr14:73069104 | A | G | 13 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(10): Show |
13 | HG00323.hp1 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15-2523A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069104 | |||||||
| chr14:73069146 | C | A | 17 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(14): Show |
17 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15-2481C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069146 | |||||||
| chr14:73069264 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0203 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-15-2363C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069264 | |||||||
| chr14:73069269 | T | G | 11 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15-2358T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069269 | |||||||
| chr14:73069354 | T | C | 1 | a0001c0001t0004g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-15-2273T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069354 | |||||||
| chr14:73069417 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0203 a0001c0001t0001g0252 |
3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-15-2210C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069417 | |||||||
| chr14:73069632 | C | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0307 a0001c0001t0001g0339 others(16): Show |
20 | HG01123.hp2 HG01358.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-1995C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069632 | |||||||
| chr14:73069714 | A | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1913A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069714 | |||||||
| chr14:73069746 | T | TA | 8 | a0001c0001t0001g0136 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-1848dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAA | 5 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 others(2): Show |
6 | HG02451.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1850_-15-1848d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAA | 21 | a0001c0001t0001g0246 a0001c0001t0007g0295 a0001c0001t0011g0052 others(18): Show |
21 | HG01069.hp2 HG01071.hp1 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.-15-1853_-15-1848d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA | 16 | a0001c0001t0001g0193 a0001c0001t0001g0203 a0001c0001t0001g0252 others(13): Show |
16 | HG00735.hp2 HG01884.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15-1854_-15-1848d others(9): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(1): Show |
16 | a0001c0001t0001g0057 a0001c0001t0001g0239 a0001c0001t0001g0240 others(13): Show |
19 | HG01261.hp1 HG01346.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15-1855_-15-1848d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(2): Show |
20 | a0001c0001t0001g0185 a0001c0001t0001g0194 a0001c0001t0001g0195 others(17): Show |
20 | HG00639.hp2 HG00735.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-1856_-15-1848d others(11): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(3): Show |
25 | a0001c0001t0001g0010 a0001c0001t0001g0197 a0001c0001t0001g0230 others(22): Show |
26 | HG00408.hp2 HG00423.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.-15-1857_-15-1848d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(4): Show |
33 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0196 others(30): Show |
33 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.-15-1858_-15-1848d others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(5): Show |
19 | a0001c0001t0001g0006 a0001c0001t0001g0118 a0001c0001t0001g0126 others(16): Show |
20 | HG00408.hp1 HG01070.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-1859_-15-1848d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(6): Show |
11 | a0001c0001t0001g0181 a0001c0001t0001g0207 a0001c0001t0001g0223 others(8): Show |
11 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-1860_-15-1848d others(15): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(7): Show |
8 | a0001c0001t0001g0132 a0001c0001t0001g0205 a0001c0001t0001g0265 others(5): Show |
8 | HG02818.hp2 HG03017.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-1861_-15-1848d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(8): Show |
7 | a0001c0001t0001g0180 a0001c0001t0001g0317 a0001c0001t0001g0318 others(4): Show |
7 | HG01256.hp2 NA18942.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-1862_-15-1848d others(17): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(9): Show |
4 | a0001c0001t0001g0179 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02056.hp2 HG04204.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-1863_-15-1848d others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(10): Show |
4 | a0001c0001t0001g0269 a0001c0001t0001g0313 a0001c0001t0001g0314 others(1): Show |
4 | HG02080.hp2 HG03491.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-1864_-15-1848d others(19): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(11): Show |
2 | a0001c0001t0001g0312 a0001c0001t0014g0178 |
2 | NA18993.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-15-1865_-15-1848d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(12): Show |
6 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0349 others(3): Show |
6 | HG02602.hp1 NA18941.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1866_-15-1848d others(21): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(13): Show |
2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | NA18963.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-15-1867_-15-1848d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(14): Show |
2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02071.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-15-1868_-15-1848d others(23): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(15): Show |
3 | a0001c0001t0001g0220 a0001c0001t0001g0301 a0001c0001t0001g0348 |
3 | HG00642.hp1 NA18939.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-15-1869_-15-1848d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | T | TAAAAAAA others(25): Show |
1 | a0001c0001t0001g0175 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-15-1879_-15-1848d others(34): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | TAA | T | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0141 others(4): Show |
7 | HG00733.hp2 HG02132.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15-1849_-15-1848d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | TAAA | T | 19 | a0001c0001t0001g0142 a0001c0001t0002g0028 a0001c0001t0002g0067 others(16): Show |
20 | HG01081.hp2 HG01106.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-1850_-15-1848d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | TAAAA | T | 56 | a0001c0001t0001g0120 a0001c0001t0001g0363 a0001c0001t0002g0003 others(53): Show |
56 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-15-1851_-15-1848d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | TAAAAAAA others(2): Show |
T | 21 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(18): Show |
27 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15-1856_-15-1848d others(11): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | TAAAAAAA others(3): Show |
T | 8 | a0001c0001t0001g0251 a0001c0001t0001g0347 a0001c0001t0008g0011 others(5): Show |
8 | HG02155.hp2 HG02735.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-1857_-15-1848d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0005g0130 a0001c0001t0008g0018 a0001c0001t0031g0031 |
3 | HG00323.hp1 HG02004.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-15-1858_-15-1848d others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | TAAAAAAA others(7): Show |
T | 2 | a0001c0001t0005g0143 a0001c0002t0009g0209 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-15-1861_-15-1848d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069746 | TAAAAAAA others(8): Show |
T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0192 a0001c0001t0001g0352 others(11): Show |
15 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15-1862_-15-1848d others(17): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069746 | ||||||
| chr14:73069769 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-15-1857_-15-1846d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069769 | |||||||
| chr14:73069817 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-15-1810A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069817 | |||||||
| chr14:73069818 | T | A | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-1809T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069818 | |||||||
| chr14:73069829 | C | CT | 14 | a0001c0001t0001g0193 a0001c0001t0001g0203 a0001c0001t0001g0252 others(11): Show |
14 | HG00408.hp1 HG01074.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15-1782dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069829 | ||||||
| chr14:73069829 | CT | C | 74 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(71): Show |
75 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-15-1782delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73069829 | ||||||
| chr14:73069917 | A | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1710A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069917 | |||||||
| chr14:73069940 | G | A | 25 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(22): Show |
31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-15-1687G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069940 | |||||||
| chr14:73069974 | C | G | 1 | a0001c0001t0001g0342 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-15-1653C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73069974 | |||||||
| chr14:73070190 | G | GGC | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-1434_-15-1433d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73070190 | ||||||
| chr14:73070220 | T | G | 31 | a0001c0001t0001g0215 a0001c0001t0002g0085 a0001c0001t0002g0086 others(28): Show |
37 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15-1407T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070220 | |||||||
| chr14:73070253 | C | T | 1 | a0001c0001t0006g0039 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-15-1374C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070253 | |||||||
| chr14:73070341 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0137 others(35): Show |
39 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.-15-1286G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070341 | |||||||
| chr14:73070442 | TA | T | 371 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(368): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-15-1174delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73070442 | ||||||
| chr14:73070528 | C | G | 1 | a0001c0001t0001g0320 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-15-1099C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070528 | |||||||
| chr14:73070677 | G | A | 1 | a0001c0001t0002g0087 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-15-950G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070677 | |||||||
| chr14:73070916 | C | T | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-711C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070916 | |||||||
| chr14:73070929 | G | A | 1 | a0001c0001t0004g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15-698G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070929 | |||||||
| chr14:73070945 | C | CA | 119 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0132 others(116): Show |
120 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.-15-668dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73070945 | ||||||
| chr14:73070945 | C | CAA | 33 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0126 others(30): Show |
35 | HG00609.hp1 HG00733.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.-15-669_-15-668dup others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73070945 | ||||||
| chr14:73070980 | G | T | 23 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(20): Show |
29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15-647G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73070980 | |||||||
| chr14:73071007 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-15-620C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071007 | |||||||
| chr14:73071166 | C | T | 1 | a0001c0001t0014g0360 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-15-461C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071166 | |||||||
| chr14:73071199 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.-15-428G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071199 | |||||||
| chr14:73071240 | C | CA | 51 | a0001c0001t0001g0126 a0001c0001t0001g0175 a0001c0001t0001g0197 others(48): Show |
54 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.-15-366dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73071240 | ||||||
| chr14:73071240 | C | CAA | 7 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0002t0003g0119 others(4): Show |
7 | HG00735.hp1 HG02027.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15-367_-15-366dup others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73071240 | ||||||
| chr14:73071240 | CA | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0193 others(133): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.-15-366delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73071240 | ||||||
| chr14:73071240 | CAA | C | 33 | a0001c0001t0001g0246 a0001c0001t0002g0105 a0001c0001t0006g0032 others(30): Show |
33 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.-15-367_-15-366del others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 73071240 | ||||||
| chr14:73071263 | C | G | 11 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15-364C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071263 | |||||||
| chr14:73071369 | T | A | 1 | a0001c0001t0004g0274 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-15-258T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071369 | |||||||
| chr14:73071380 | C | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0244 a0001c0001t0001g0245 |
3 | HG02129.hp2 HG02280.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-15-247C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071380 | |||||||
| chr14:73071384 | A | G | 1 | a0001c0001t0038g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-15-243A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071384 | |||||||
| chr14:73071400 | G | A | 1 | a0001c0001t0004g0280 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-15-227G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071400 | |||||||
| chr14:73071447 | T | G | 11 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15-180T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 1/18 | chr14 | 73071447 | |||||||
| chr14:73071775 | G | A | 2 | a0001c0001t0006g0034 a0001c0001t0006g0046 |
2 | HG02056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.106+28G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73071775 | |||||||
| chr14:73071825 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.106+78A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73071825 | |||||||
| chr14:73072031 | G | A | 8 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(5): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+284G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072031 | |||||||
| chr14:73072042 | C | A | 1 | a0001c0001t0007g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.106+295C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072042 | |||||||
| chr14:73072114 | C | T | 1 | a0001c0001t0031g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.106+367C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072114 | |||||||
| chr14:73072286 | T | A | 1 | a0001c0001t0018g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.106+539T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072286 | |||||||
| chr14:73072323 | C | CA | 8 | a0001c0001t0005g0311 a0001c0001t0011g0052 a0001c0001t0011g0053 others(5): Show |
8 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.106+586dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 73072323 | ||||||
| chr14:73072507 | T | C | 1 | a0001c0001t0031g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.106+760T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072507 | |||||||
| chr14:73072586 | A | T | 1 | a0001c0001t0001g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.106+839A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072586 | |||||||
| chr14:73072618 | A | AATCC | 23 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(20): Show |
29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.106+873_106+876dup others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 73072618 | ||||||
| chr14:73072721 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.106+974G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072721 | |||||||
| chr14:73072723 | G | A | 11 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+976G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072723 | |||||||
| chr14:73072725 | G | T | 3 | a0001c0002t0003g0119 a0001c0002t0003g0155 a0001c0002t0003g0156 |
3 | HG01074.hp1 HG01099.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.106+978G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072725 | |||||||
| chr14:73072865 | G | A | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+1118G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73072865 | |||||||
| chr14:73073193 | T | G | 1 | a0001c0001t0001g0306 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.106+1446T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073193 | |||||||
| chr14:73073404 | C | G | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+1657C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073404 | |||||||
| chr14:73073430 | G | A | 25 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(22): Show |
31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.106+1683G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073430 | |||||||
| chr14:73073432 | A | G | 95 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0126 others(92): Show |
96 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.106+1685A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073432 | |||||||
| chr14:73073487 | A | C | 1 | a0001c0001t0001g0346 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.106+1740A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073487 | |||||||
| chr14:73073509 | A | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+1762A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073509 | |||||||
| chr14:73073514 | G | A | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.106+1767G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073514 | |||||||
| chr14:73073576 | T | C | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.106+1829T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073576 | |||||||
| chr14:73073669 | C | T | 1 | a0001c0001t0007g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.106+1922C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073669 | |||||||
| chr14:73073762 | A | G | 1 | a0001c0002t0003g0119 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.106+2015A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073762 | |||||||
| chr14:73073876 | G | A | 2 | a0001c0001t0018g0277 a0001c0001t0018g0278 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.106+2129G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073876 | |||||||
| chr14:73073922 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.106+2175G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073922 | |||||||
| chr14:73073985 | A | G | 1 | a0001c0002t0003g0119 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.106+2238A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073985 | |||||||
| chr14:73073990 | G | A | 39 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(36): Show |
39 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.106+2243G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73073990 | |||||||
| chr14:73074048 | G | A | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.107-2271G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074048 | |||||||
| chr14:73074203 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.107-2116T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074203 | |||||||
| chr14:73074228 | A | G | 167 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0126 others(164): Show |
169 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.107-2091A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074228 | |||||||
| chr14:73074271 | G | T | 1 | a0001c0001t0021g0293 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.107-2048G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074271 | |||||||
| chr14:73074342 | A | C | 371 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(368): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.107-1977A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074342 | |||||||
| chr14:73074358 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.107-1961T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074358 | |||||||
| chr14:73074359 | A | G | 3 | a0001c0001t0004g0255 a0001c0001t0004g0275 a0001c0001t0004g0276 |
3 | HG03688.hp1 HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.107-1960A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074359 | |||||||
| chr14:73074449 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.107-1870T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074449 | |||||||
| chr14:73074493 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.107-1826G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074493 | |||||||
| chr14:73074661 | C | T | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-1658C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074661 | |||||||
| chr14:73074702 | A | AT | 36 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0004g0001 others(33): Show |
42 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.107-1606dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 73074702 | ||||||
| chr14:73074750 | C | G | 1 | a0001c0001t0004g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.107-1569C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074750 | |||||||
| chr14:73074750 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.107-1569C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074750 | |||||||
| chr14:73074780 | A | AC | 11 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-1538dupC | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 73074780 | ||||||
| chr14:73074835 | A | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0118 others(46): Show |
50 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.107-1484A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074835 | |||||||
| chr14:73074903 | G | C | 1 | a0001c0001t0002g0088 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.107-1416G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074903 | |||||||
| chr14:73074943 | A | G | 17 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.107-1376A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074943 | |||||||
| chr14:73074971 | C | T | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.107-1348C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73074971 | |||||||
| chr14:73074991 | CT | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(17): Show |
21 | HG00733.hp1 HG00733.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.107-1313delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 73074991 | ||||||
| chr14:73075212 | A | T | 7 | a0001c0002t0003g0002 a0001c0002t0003g0152 a0001c0002t0003g0153 others(4): Show |
10 | HG00423.hp1 HG02135.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.107-1107A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075212 | |||||||
| chr14:73075277 | G | C | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-1042G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075277 | |||||||
| chr14:73075306 | G | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0185 a0001c0001t0001g0194 others(42): Show |
46 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.107-1013G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075306 | |||||||
| chr14:73075393 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107-926A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075393 | |||||||
| chr14:73075437 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.107-882G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075437 | |||||||
| chr14:73075439 | G | A | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-880G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075439 | |||||||
| chr14:73075477 | C | T | 39 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(36): Show |
39 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.107-842C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075477 | |||||||
| chr14:73075485 | C | T | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-834C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075485 | |||||||
| chr14:73075582 | A | G | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.107-737A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075582 | |||||||
| chr14:73075655 | A | C | 3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02258.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.107-664A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075655 | |||||||
| chr14:73075774 | T | C | 23 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(20): Show |
29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.107-545T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075774 | |||||||
| chr14:73075854 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107-465C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075854 | |||||||
| chr14:73075926 | G | A | 6 | a0001c0001t0001g0272 a0001c0001t0001g0308 a0001c0001t0001g0321 others(3): Show |
6 | HG00140.hp2 HG01496.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-393G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075926 | |||||||
| chr14:73075942 | A | G | 13 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(10): Show |
13 | HG00323.hp1 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.107-377A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73075942 | |||||||
| chr14:73076083 | G | C | 1 | a0001c0001t0002g0089 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.107-236G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73076083 | |||||||
| chr14:73076140 | A | G | 2 | a0001c0001t0007g0296 a0001c0001t0007g0297 |
2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.107-179A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73076140 | |||||||
| chr14:73076282 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.107-37C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 2/18 | chr14 | 73076282 | |||||||
| chr14:73076402 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.156+34T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076402 | |||||||
| chr14:73076609 | A | C | 271 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(268): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.156+241A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076609 | |||||||
| chr14:73076653 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.156+285G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076653 | |||||||
| chr14:73076661 | T | C | 2 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
2 | HG01070.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.156+293T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076661 | |||||||
| chr14:73076718 | TAAAAG | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0118 others(46): Show |
50 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.156+353_156+357del others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 73076718 | ||||||
| chr14:73076851 | G | A | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.156+483G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076851 | |||||||
| chr14:73076856 | G | T | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.156+488G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076856 | |||||||
| chr14:73076909 | G | A | 1 | a0001c0001t0011g0054 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.157-460G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73076909 | |||||||
| chr14:73077075 | C | T | 24 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(21): Show |
30 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-294C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 3/18 | chr14 | 73077075 | |||||||
| chr14:73077888 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.324+352A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73077888 | |||||||
| chr14:73077904 | G | A | 113 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(110): Show |
122 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.324+368G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73077904 | |||||||
| chr14:73077910 | C | A | 369 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(366): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.324+374C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73077910 | |||||||
| chr14:73077934 | G | A | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324+398G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73077934 | |||||||
| chr14:73078000 | C | CA | 11 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.324+470dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73078000 | ||||||
| chr14:73078022 | G | A | 1 | a0001c0001t0004g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.324+486G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078022 | |||||||
| chr14:73078186 | T | C | 7 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(4): Show |
7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+650T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078186 | |||||||
| chr14:73078273 | A | T | 1 | a0001c0001t0008g0015 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.324+737A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078273 | |||||||
| chr14:73078336 | TAAAA | T | 7 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(4): Show |
7 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+806_324+809del others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73078336 | ||||||
| chr14:73078346 | G | A | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.324+810G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078346 | |||||||
| chr14:73078365 | G | A | 1 | a0001c0001t0006g0045 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.324+829G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078365 | |||||||
| chr14:73078419 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.324+883A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078419 | |||||||
| chr14:73078486 | C | CA | 4 | a0001c0002t0003g0150 a0001c0002t0003g0163 a0001c0002t0003g0164 others(1): Show |
4 | NA18964.hp1 NA18980.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+957dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73078486 | ||||||
| chr14:73078510 | A | G | 1 | a0001c0001t0004g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.324+974A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078510 | |||||||
| chr14:73078629 | A | T | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324+1093A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078629 | |||||||
| chr14:73078800 | C | T | 8 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(5): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+1264C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078800 | |||||||
| chr14:73078956 | G | T | 3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02258.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.324+1420G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73078956 | |||||||
| chr14:73079054 | ACTTTTTT others(1151): Show |
A | 2 | a0001c0001t0008g0012 a0001c0001t0008g0016 |
2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.324+1527_324+2684d others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73079054 | ||||||
| chr14:73079056 | TTTTTTTA others(1150): Show |
T | 6 | a0001c0001t0008g0011 a0001c0001t0008g0013 a0001c0001t0008g0014 others(3): Show |
6 | HG00323.hp1 HG02735.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+1527_324+2683d others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73079056 | ||||||
| chr14:73079094 | G | A | 2 | a0001c0001t0006g0035 a0001c0001t0026g0050 |
2 | NA18948.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.324+1558G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079094 | |||||||
| chr14:73079126 | T | G | 1 | a0001c0001t0001g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.324+1590T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079126 | |||||||
| chr14:73079156 | C | T | 1 | a0001c0001t0005g0125 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.324+1620C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079156 | |||||||
| chr14:73079284 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.324+1748G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079284 | |||||||
| chr14:73079292 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.324+1756C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079292 | |||||||
| chr14:73079316 | G | A | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324+1780G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079316 | |||||||
| chr14:73079327 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.324+1791G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079327 | |||||||
| chr14:73079851 | C | T | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.324+2315C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73079851 | |||||||
| chr14:73080036 | T | C | 99 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0126 others(96): Show |
100 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.324+2500T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080036 | |||||||
| chr14:73080104 | G | A | 3 | a0001c0001t0004g0255 a0001c0001t0004g0275 a0001c0001t0004g0276 |
3 | HG03688.hp1 HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.324+2568G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080104 | |||||||
| chr14:73080155 | A | G | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.324+2619A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080155 | |||||||
| chr14:73080213 | C | CT | 78 | a0001c0001t0001g0010 a0001c0001t0001g0126 a0001c0001t0001g0175 others(75): Show |
79 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.324+2705dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | ||||||
| chr14:73080213 | C | CTT | 16 | a0001c0001t0001g0203 a0001c0001t0001g0252 a0001c0001t0001g0305 others(13): Show |
16 | HG00609.hp2 HG01123.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.324+2704_324+2705d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | ||||||
| chr14:73080213 | C | CTTTT | 24 | a0001c0001t0001g0206 a0001c0001t0007g0297 a0001c0001t0021g0293 others(21): Show |
27 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.324+2702_324+2705d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | ||||||
| chr14:73080213 | C | CTTTTT | 26 | a0001c0001t0001g0009 a0001c0001t0001g0207 a0001c0001t0001g0287 others(23): Show |
27 | HG00423.hp1 HG00735.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.324+2701_324+2705d others(7): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | ||||||
| chr14:73080213 | C | CTTTTTT | 9 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0001c0001t0001g0142 others(6): Show |
9 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.324+2700_324+2705d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | ||||||
| chr14:73080213 | C | CTTTTTTT | 8 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+2699_324+2705d others(9): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | ||||||
| chr14:73080213 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.324+2696_324+2705d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | ||||||
| chr14:73080213 | CT | C | 26 | a0001c0001t0001g0215 a0001c0001t0001g0226 a0001c0001t0001g0228 others(23): Show |
26 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.324+2705delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | ||||||
| chr14:73080213 | CTT | C | 20 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(17): Show |
26 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.324+2704_324+2705d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | ||||||
| chr14:73080213 | CTTTTT | C | 7 | a0001c0001t0001g0005 a0001c0001t0005g0004 a0001c0001t0005g0005 others(4): Show |
8 | HG01074.hp2 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+2701_324+2705d others(7): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | ||||||
| chr14:73080213 | CTTTTTT | C | 6 | a0001c0001t0005g0144 a0001c0001t0011g0052 a0001c0001t0011g0053 others(3): Show |
6 | HG02486.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+2700_324+2705d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080213 | ||||||
| chr14:73080246 | T | C | 8 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(5): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+2710T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080246 | |||||||
| chr14:73080251 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0028g0249 |
2 | HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.324+2715T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080251 | |||||||
| chr14:73080254 | T | C | 8 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(5): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+2718T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080254 | |||||||
| chr14:73080369 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.324+2833G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080369 | |||||||
| chr14:73080545 | A | G | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.325-2949A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080545 | |||||||
| chr14:73080547 | T | C | 1 | a0001c0001t0027g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.325-2947T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080547 | |||||||
| chr14:73080823 | CT | C | 58 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0118 others(55): Show |
59 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.325-2656delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080823 | ||||||
| chr14:73080837 | TTA | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0140 a0001c0001t0001g0195 others(7): Show |
11 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.325-2655_325-2654d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73080837 | ||||||
| chr14:73080838 | TA | T | 7 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.325-2655delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080838 | |||||||
| chr14:73080865 | T | C | 99 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0126 others(96): Show |
100 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.325-2629T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080865 | |||||||
| chr14:73080886 | G | A | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-2608G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080886 | |||||||
| chr14:73080903 | C | T | 1 | a0001c0001t0001g0355 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.325-2591C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080903 | |||||||
| chr14:73080905 | A | G | 3 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0102 |
3 | NA18943.hp2 NA18963.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.325-2589A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080905 | |||||||
| chr14:73080910 | G | A | 1 | a0001c0001t0004g0257 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.325-2584G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080910 | |||||||
| chr14:73080959 | G | A | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.325-2535G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080959 | |||||||
| chr14:73080965 | T | C | 1 | a0001c0001t0031g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-2529T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73080965 | |||||||
| chr14:73081170 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-2324C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081170 | |||||||
| chr14:73081225 | C | CAG | 41 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0136 others(38): Show |
43 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.325-2269_325-2268i others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081225 | |||||||
| chr14:73081239 | G | C | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.325-2255G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081239 | |||||||
| chr14:73081286 | C | T | 9 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(6): Show |
9 | HG01074.hp2 HG02486.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.325-2208C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081286 | |||||||
| chr14:73081474 | T | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-2020T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081474 | |||||||
| chr14:73081501 | AT | A | 106 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0126 others(103): Show |
107 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.325-1986delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73081501 | ||||||
| chr14:73081688 | C | CT | 3 | a0001c0001t0006g0038 a0001c0001t0006g0039 a0001c0001t0006g0042 |
3 | NA18947.hp1 NA18965.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.325-1801dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73081688 | ||||||
| chr14:73081694 | A | G | 1 | a0001c0001t0001g0363 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.325-1800A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081694 | |||||||
| chr14:73081732 | G | A | 26 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(23): Show |
26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.325-1762G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081732 | |||||||
| chr14:73081857 | A | G | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-1637A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73081857 | |||||||
| chr14:73082316 | C | G | 38 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0137 others(35): Show |
39 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.325-1178C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082316 | |||||||
| chr14:73082352 | C | T | 8 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(5): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.325-1142C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082352 | |||||||
| chr14:73082353 | A | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-1141A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082353 | |||||||
| chr14:73082424 | T | C | 1 | a0001c0001t0031g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-1070T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082424 | |||||||
| chr14:73082447 | A | C | 39 | a0001c0002t0003g0117 a0001c0002t0003g0119 a0001c0002t0003g0121 others(36): Show |
39 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.325-1047A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082447 | |||||||
| chr14:73082449 | G | A | 1 | a0001c0001t0013g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.325-1045G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082449 | |||||||
| chr14:73082500 | A | T | 1 | a0001c0001t0001g0190 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.325-994A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082500 | |||||||
| chr14:73082889 | G | A | 26 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(23): Show |
26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.325-605G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082889 | |||||||
| chr14:73082899 | A | T | 1 | a0001c0002t0003g0157 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.325-595A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082899 | |||||||
| chr14:73082907 | T | A | 2 | a0001c0001t0005g0004 a0001c0001t0005g0135 |
3 | HG02109.hp1 HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.325-587T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082907 | |||||||
| chr14:73082907 | T | TA | 35 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0002g0068 others(32): Show |
35 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.325-574dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73082907 | ||||||
| chr14:73082907 | TA | T | 27 | a0001c0001t0001g0327 a0001c0001t0001g0337 a0001c0001t0004g0001 others(24): Show |
33 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.325-574delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73082907 | ||||||
| chr14:73082941 | G | A | 1 | a0001c0001t0006g0045 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.325-553G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082941 | |||||||
| chr14:73082943 | G | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-551G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73082943 | |||||||
| chr14:73083135 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-359A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73083135 | |||||||
| chr14:73083269 | TGCAAATG others(89): Show |
T | 1 | a0001c0001t0001g0315 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.325-217_325-122del others(96): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr14 | 73083269 | ||||||
| chr14:73083343 | T | G | 3 | a0001c0001t0002g0069 a0001c0001t0030g0071 a0001c0001t0033g0070 |
3 | HG02683.hp1 HG02698.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.325-151T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73083343 | |||||||
| chr14:73083384 | T | G | 11 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-110T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73083384 | |||||||
| chr14:73083412 | A | G | 1 | a0001c0001t0002g0101 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.325-82A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73083412 | |||||||
| chr14:73083415 | A | T | 1 | a0001c0001t0006g0045 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.325-79A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 4/18 | chr14 | 73083415 | |||||||
| chr14:73083560 | TTTTTTTC others(36): Show |
T | 1 | a0001c0001t0014g0360 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.382+12_382+54delTT others(41): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73083560 | ||||||
| chr14:73083692 | A | G | 8 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(5): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+141A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73083692 | |||||||
| chr14:73083732 | GAGATC | G | 5 | a0001c0001t0010g0008 a0001c0001t0010g0283 a0001c0001t0010g0284 others(2): Show |
6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+185_382+189del others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73083732 | ||||||
| chr14:73083803 | G | T | 2 | a0001c0001t0018g0277 a0001c0001t0018g0278 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.382+252G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73083803 | |||||||
| chr14:73083821 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.382+270T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73083821 | |||||||
| chr14:73083842 | A | C | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+291A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73083842 | |||||||
| chr14:73083898 | C | CT | 15 | a0001c0001t0001g0222 a0001c0001t0001g0242 a0001c0001t0001g0316 others(12): Show |
15 | HG00741.hp1 HG00741.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.382+364dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73083898 | ||||||
| chr14:73083898 | CT | C | 7 | a0001c0001t0001g0057 a0001c0001t0001g0118 a0001c0001t0001g0239 others(4): Show |
7 | HG02015.hp2 HG02109.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+364delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73083898 | ||||||
| chr14:73084019 | T | C | 53 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0057 others(50): Show |
55 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.382+468T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084019 | |||||||
| chr14:73084028 | G | T | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+477G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084028 | |||||||
| chr14:73084059 | G | A | 30 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0121 others(27): Show |
33 | HG00423.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.382+508G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084059 | |||||||
| chr14:73084087 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.382+536G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084087 | |||||||
| chr14:73084178 | A | G | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+627A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084178 | |||||||
| chr14:73084185 | A | G | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.382+634A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084185 | |||||||
| chr14:73084201 | A | G | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.382+650A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084201 | |||||||
| chr14:73084201 | A | T | 2 | a0001c0001t0004g0260 a0001c0001t0004g0261 |
2 | HG00544.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.382+650A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084201 | |||||||
| chr14:73084410 | T | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.382+859T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084410 | |||||||
| chr14:73084537 | G | GTTTGT | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.382+999_382+1003du others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73084537 | ||||||
| chr14:73084650 | T | G | 1 | a0001c0001t0001g0308 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.382+1099T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084650 | |||||||
| chr14:73084718 | A | G | 13 | a0001c0001t0001g0005 a0001c0001t0005g0004 a0001c0001t0005g0005 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.382+1167A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084718 | |||||||
| chr14:73084767 | C | G | 34 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(31): Show |
34 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.382+1216C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084767 | |||||||
| chr14:73084811 | A | C | 2 | a0001c0001t0018g0277 a0001c0001t0018g0278 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.382+1260A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73084811 | |||||||
| chr14:73084853 | A | AT | 25 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(22): Show |
31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.382+1313dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73084853 | ||||||
| chr14:73085055 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.382+1504T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085055 | |||||||
| chr14:73085064 | G | C | 1 | a0001c0001t0001g0273 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.382+1513G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085064 | |||||||
| chr14:73085065 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.382+1514C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085065 | |||||||
| chr14:73085075 | G | A | 25 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(22): Show |
31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.382+1524G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085075 | |||||||
| chr14:73085099 | A | G | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.382+1548A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085099 | |||||||
| chr14:73085109 | C | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0046 |
2 | HG02056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.382+1558C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085109 | |||||||
| chr14:73085122 | G | T | 1 | a0001c0002t0009g0161 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.382+1571G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085122 | |||||||
| chr14:73085213 | TTCACCGT others(5): Show |
T | 2 | a0001c0001t0019g0281 a0001c0001t0019g0282 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.382+1663_382+1674d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085213 | |||||||
| chr14:73085295 | A | G | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1744A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085295 | |||||||
| chr14:73085306 | C | G | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1755C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085306 | |||||||
| chr14:73085309 | G | A | 46 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(43): Show |
49 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.382+1758G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085309 | |||||||
| chr14:73085316 | CTCATCAG others(136): Show |
C | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1766_382+1908d others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085316 | |||||||
| chr14:73085325 | A | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+1774A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085325 | |||||||
| chr14:73085418 | G | A | 1 | a0001c0001t0010g0286 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.382+1867G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085418 | |||||||
| chr14:73085460 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1909G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085460 | |||||||
| chr14:73085466 | G | T | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1915G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085466 | |||||||
| chr14:73085468 | GTT | G | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1921_382+1922d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73085468 | ||||||
| chr14:73085475 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1924G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085475 | |||||||
| chr14:73085483 | T | C | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1932T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085483 | |||||||
| chr14:73085484 | G | T | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+1933G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085484 | |||||||
| chr14:73085490 | A | G | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1939A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085490 | |||||||
| chr14:73085496 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1945G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085496 | |||||||
| chr14:73085500 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1949G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085500 | |||||||
| chr14:73085504 | G | C | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1953G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085504 | |||||||
| chr14:73085508 | C | G | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1957C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085508 | |||||||
| chr14:73085512 | T | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1961T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085512 | |||||||
| chr14:73085513 | C | T | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1962C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085513 | |||||||
| chr14:73085514 | A | G | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1963A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085514 | |||||||
| chr14:73085519 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1968G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085519 | |||||||
| chr14:73085527 | C | T | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1976C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085527 | |||||||
| chr14:73085531 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1980G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085531 | |||||||
| chr14:73085547 | T | C | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1996T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085547 | |||||||
| chr14:73085548 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1997G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085548 | |||||||
| chr14:73085549 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+1998G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085549 | |||||||
| chr14:73085555 | T | C | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.382+2004T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085555 | |||||||
| chr14:73085673 | G | A | 1 | a0001c0001t0006g0049 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.382+2122G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085673 | |||||||
| chr14:73085690 | G | A | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+2139G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085690 | |||||||
| chr14:73085793 | G | T | 34 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(31): Show |
34 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.383-2208G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085793 | |||||||
| chr14:73085815 | C | G | 5 | a0001c0001t0005g0149 a0001c0001t0005g0213 a0001c0001t0005g0214 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-2186C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085815 | |||||||
| chr14:73085861 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.383-2140G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085861 | |||||||
| chr14:73085882 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0005g0005 a0001c0001t0005g0143 others(2): Show |
5 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-2119T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73085882 | |||||||
| chr14:73086070 | T | C | 1 | a0001c0001t0015g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.383-1931T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086070 | |||||||
| chr14:73086180 | G | A | 2 | a0001c0001t0008g0017 a0001c0001t0008g0018 |
2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.383-1821G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086180 | |||||||
| chr14:73086352 | C | T | 1 | a0001c0001t0038g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.383-1649C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086352 | |||||||
| chr14:73086360 | C | T | 2 | a0001c0001t0001g0325 a0001c0001t0001g0331 |
2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.383-1641C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086360 | |||||||
| chr14:73086435 | T | TA | 7 | a0001c0001t0001g0194 a0001c0001t0001g0343 a0001c0001t0002g0102 others(4): Show |
7 | HG02055.hp2 HG02145.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.383-1551dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73086435 | ||||||
| chr14:73086435 | TA | T | 11 | a0001c0001t0001g0215 a0001c0001t0001g0345 a0001c0001t0002g0067 others(8): Show |
11 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-1551delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73086435 | ||||||
| chr14:73086446 | A | C | 12 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0002g0059 others(9): Show |
12 | HG01496.hp2 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.383-1555A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086446 | |||||||
| chr14:73086458 | G | A | 4 | a0001c0001t0005g0122 a0001c0001t0005g0125 a0001c0001t0005g0127 others(1): Show |
4 | HG01256.hp2 HG01928.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1543G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086458 | |||||||
| chr14:73086561 | T | C | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-1440T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086561 | |||||||
| chr14:73086563 | T | C | 26 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(23): Show |
26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.383-1438T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086563 | |||||||
| chr14:73086731 | G | T | 1 | a0001c0001t0001g0310 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.383-1270G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086731 | |||||||
| chr14:73086866 | A | G | 1 | a0001c0001t0001g0349 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.383-1135A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73086866 | |||||||
| chr14:73087048 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0035g0123 |
3 | HG02257.hp2 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.383-953A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087048 | |||||||
| chr14:73087058 | G | T | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-943G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087058 | |||||||
| chr14:73087081 | A | G | 1 | a0001c0001t0001g0309 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.383-920A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087081 | |||||||
| chr14:73087108 | T | C | 2 | a0001c0001t0006g0040 a0001c0001t0006g0049 |
2 | HG00408.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.383-893T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087108 | |||||||
| chr14:73087191 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.383-810T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087191 | |||||||
| chr14:73087237 | A | C | 31 | a0001c0001t0001g0120 a0001c0001t0001g0126 a0001c0001t0001g0132 others(28): Show |
31 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.383-764A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087237 | |||||||
| chr14:73087256 | G | A | 1 | a0001c0001t0001g0367 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.383-745G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087256 | |||||||
| chr14:73087333 | GTTCT | G | 68 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(65): Show |
77 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.383-662_383-659del others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73087333 | ||||||
| chr14:73087396 | C | CT | 23 | a0001c0001t0001g0215 a0001c0001t0001g0246 a0001c0001t0002g0072 others(20): Show |
24 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.383-588dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73087396 | ||||||
| chr14:73087396 | C | CTT | 18 | a0001c0001t0006g0034 a0001c0001t0006g0035 a0001c0001t0006g0036 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.383-589_383-588dup others(2): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73087396 | ||||||
| chr14:73087541 | G | A | 1 | a0001c0001t0008g0012 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.383-460G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087541 | |||||||
| chr14:73087544 | C | T | 2 | a0001c0001t0018g0277 a0001c0001t0018g0278 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.383-457C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087544 | |||||||
| chr14:73087552 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 |
4 | HG02647.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-449C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087552 | |||||||
| chr14:73087588 | G | C | 1 | a0001c0002t0003g0167 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.383-413G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087588 | |||||||
| chr14:73087617 | G | C | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.383-384G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087617 | |||||||
| chr14:73087631 | G | A | 2 | a0001c0001t0002g0068 a0001c0001t0002g0080 |
2 | HG01192.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.383-370G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087631 | |||||||
| chr14:73087656 | A | G | 1 | a0001c0002t0009g0209 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.383-345A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087656 | |||||||
| chr14:73087686 | C | T | 1 | a0001c0001t0016g0099 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.383-315C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087686 | |||||||
| chr14:73087730 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.383-271T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | chr14 | 73087730 | |||||||
| chr14:73087943 | AT | A | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-50delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 73087943 | ||||||
| chr14:73088176 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.543+15G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088176 | |||||||
| chr14:73088182 | T | C | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.543+21T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088182 | |||||||
| chr14:73088361 | T | A | 11 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+200T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088361 | |||||||
| chr14:73088463 | G | A | 13 | a0001c0001t0001g0005 a0001c0001t0005g0004 a0001c0001t0005g0005 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+302G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088463 | |||||||
| chr14:73088620 | A | T | 1 | a0001c0001t0002g0108 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.543+459A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088620 | |||||||
| chr14:73088717 | C | A | 1 | a0001c0001t0001g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.543+556C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088717 | |||||||
| chr14:73088944 | C | T | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+783C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73088944 | |||||||
| chr14:73089063 | C | A | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.543+902C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089063 | |||||||
| chr14:73089205 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.543+1044A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089205 | |||||||
| chr14:73089295 | C | A | 1 | a0001c0001t0005g0300 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.543+1134C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089295 | |||||||
| chr14:73089304 | C | G | 1 | a0001c0001t0004g0275 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.543+1143C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089304 | |||||||
| chr14:73089387 | C | T | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+1226C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089387 | |||||||
| chr14:73089394 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.543+1233G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089394 | |||||||
| chr14:73089665 | T | TTTTGTTT others(1): Show |
105 | a0001c0001t0001g0005 a0001c0001t0001g0141 a0001c0001t0001g0142 others(102): Show |
115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.543+1517_543+1524d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73089665 | ||||||
| chr14:73089665 | T | TTTTGTTT others(5): Show |
29 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(26): Show |
29 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.543+1513_543+1524d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73089665 | ||||||
| chr14:73089665 | T | TTTTGTTT others(9): Show |
3 | a0001c0001t0011g0053 a0001c0001t0022g0033 a0001c0001t0023g0051 |
3 | HG01074.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.543+1509_543+1524d others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73089665 | ||||||
| chr14:73089665 | T | TTTTGTTT others(13): Show |
1 | a0001c0001t0011g0054 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.543+1505_543+1524d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73089665 | ||||||
| chr14:73089665 | T | TTTTGTTT others(17): Show |
3 | a0001c0001t0011g0052 a0001c0001t0011g0055 a0001c0001t0011g0056 |
3 | HG02486.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.543+1524_543+1525i others(26): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73089665 | ||||||
| chr14:73089708 | C | T | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.543+1547C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089708 | |||||||
| chr14:73089894 | T | C | 7 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(4): Show |
7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+1733T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089894 | |||||||
| chr14:73089964 | C | G | 4 | a0001c0001t0013g0058 a0001c0001t0013g0061 a0001c0001t0013g0062 others(1): Show |
4 | HG01496.hp2 HG01884.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+1803C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73089964 | |||||||
| chr14:73090057 | C | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0203 a0001c0001t0001g0252 |
3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.543+1896C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090057 | |||||||
| chr14:73090075 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.543+1914C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090075 | |||||||
| chr14:73090133 | C | T | 1 | a0001c0001t0007g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.543+1972C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090133 | |||||||
| chr14:73090216 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.543+2055A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090216 | |||||||
| chr14:73090294 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.543+2133A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090294 | |||||||
| chr14:73090298 | A | C | 1 | a0001c0001t0036g0362 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.543+2137A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090298 | |||||||
| chr14:73090330 | C | T | 2 | a0001c0001t0008g0017 a0001c0001t0008g0018 |
2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.543+2169C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090330 | |||||||
| chr14:73090360 | A | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+2199A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090360 | |||||||
| chr14:73090465 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0203 a0001c0001t0001g0252 |
3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.543+2304G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090465 | |||||||
| chr14:73090677 | C | T | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.543+2516C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090677 | |||||||
| chr14:73090726 | A | T | 1 | a0001c0001t0002g0029 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.543+2565A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090726 | |||||||
| chr14:73090741 | G | A | 1 | a0001c0002t0003g0119 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+2580G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090741 | |||||||
| chr14:73090841 | G | C | 54 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0057 others(51): Show |
56 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.543+2680G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090841 | |||||||
| chr14:73090864 | A | G | 8 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(5): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+2703A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090864 | |||||||
| chr14:73090888 | ATTATATT others(4): Show |
A | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.543+2741_543+2751d others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73090888 | ||||||
| chr14:73090958 | A | G | 16 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0036 others(13): Show |
16 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.543+2797A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73090958 | |||||||
| chr14:73091089 | C | T | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.543+2928C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091089 | |||||||
| chr14:73091281 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+3120G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091281 | |||||||
| chr14:73091320 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.543+3159A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091320 | |||||||
| chr14:73091352 | C | T | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+3191C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091352 | |||||||
| chr14:73091418 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0203 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.543+3257T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091418 | |||||||
| chr14:73091424 | G | A | 1 | a0001c0001t0005g0183 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.543+3263G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091424 | |||||||
| chr14:73091709 | T | TA | 55 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0057 others(52): Show |
57 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.543+3558dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73091709 | ||||||
| chr14:73091734 | G | A | 1 | a0001c0001t0006g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.543+3573G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091734 | |||||||
| chr14:73091877 | C | CA | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+3725dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73091877 | ||||||
| chr14:73091934 | A | AATG | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+3774_543+3775i others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73091934 | ||||||
| chr14:73091937 | A | G | 14 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(11): Show |
14 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+3776A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73091937 | |||||||
| chr14:73092128 | A | T | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.543+3967A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092128 | |||||||
| chr14:73092267 | G | A | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+4106G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092267 | |||||||
| chr14:73092578 | CT | C | 21 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(18): Show |
21 | HG00408.hp2 HG00544.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.544-4324delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73092578 | ||||||
| chr14:73092591 | T | A | 2 | a0001c0001t0001g0232 a0001c0001t0028g0249 |
2 | HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.544-4324T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092591 | |||||||
| chr14:73092610 | A | C | 26 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(23): Show |
26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.544-4305A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092610 | |||||||
| chr14:73092638 | A | G | 1 | a0001c0001t0031g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.544-4277A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092638 | |||||||
| chr14:73092648 | G | A | 14 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(11): Show |
14 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-4267G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092648 | |||||||
| chr14:73092858 | T | C | 242 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0120 others(239): Show |
253 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.544-4057T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092858 | |||||||
| chr14:73092904 | A | G | 1 | a0001c0002t0009g0209 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.544-4011A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73092904 | |||||||
| chr14:73093152 | A | T | 1 | a0001c0001t0001g0222 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.544-3763A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093152 | |||||||
| chr14:73093545 | C | T | 2 | a0001c0001t0018g0277 a0001c0001t0018g0278 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.544-3370C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093545 | |||||||
| chr14:73093546 | G | A | 23 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(20): Show |
29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.544-3369G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093546 | |||||||
| chr14:73093592 | C | T | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.544-3323C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093592 | |||||||
| chr14:73093732 | C | G | 1 | a0001c0001t0001g0330 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.544-3183C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093732 | |||||||
| chr14:73093797 | G | A | 23 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(20): Show |
29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.544-3118G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093797 | |||||||
| chr14:73093823 | A | T | 5 | a0001c0001t0010g0008 a0001c0001t0010g0283 a0001c0001t0010g0284 others(2): Show |
6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-3092A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093823 | |||||||
| chr14:73093827 | G | GA | 8 | a0001c0001t0001g0306 a0001c0001t0001g0312 a0001c0001t0001g0315 others(5): Show |
8 | HG00609.hp1 HG00609.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-3081dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73093827 | ||||||
| chr14:73093852 | G | A | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.544-3063G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093852 | |||||||
| chr14:73093943 | G | GT | 11 | a0001c0001t0001g0215 a0001c0001t0004g0254 a0001c0001t0004g0255 others(8): Show |
11 | HG00741.hp2 HG01081.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-2968dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73093943 | ||||||
| chr14:73093948 | G | GT | 16 | a0001c0001t0001g0321 a0001c0001t0001g0329 a0001c0001t0002g0072 others(13): Show |
16 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.544-2949dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73093948 | ||||||
| chr14:73093948 | G | GTT | 53 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0136 others(50): Show |
55 | HG00408.hp2 HG00544.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.544-2950_544-2949d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73093948 | ||||||
| chr14:73093948 | G | T | 26 | a0001c0001t0001g0215 a0001c0001t0004g0001 a0001c0001t0004g0007 others(23): Show |
32 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.544-2967G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093948 | |||||||
| chr14:73093965 | T | G | 1 | a0001c0001t0001g0365 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.544-2950T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093965 | |||||||
| chr14:73093973 | A | T | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.544-2942A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73093973 | |||||||
| chr14:73094045 | G | A | 6 | a0001c0001t0001g0222 a0001c0001t0011g0052 a0001c0001t0011g0053 others(3): Show |
6 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-2870G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094045 | |||||||
| chr14:73094053 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.544-2862G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094053 | |||||||
| chr14:73094101 | G | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-2814G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094101 | |||||||
| chr14:73094181 | C | A | 1 | a0001c0001t0005g0122 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.544-2734C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094181 | |||||||
| chr14:73094204 | C | T | 2 | a0001c0001t0019g0281 a0001c0001t0019g0282 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.544-2711C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094204 | |||||||
| chr14:73094295 | TAGC | T | 5 | a0001c0001t0010g0008 a0001c0001t0010g0283 a0001c0001t0010g0284 others(2): Show |
6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-2618_544-2616d others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094295 | ||||||
| chr14:73094540 | C | T | 2 | a0001c0001t0019g0281 a0001c0001t0019g0282 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.544-2375C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094540 | |||||||
| chr14:73094567 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.544-2348C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094567 | |||||||
| chr14:73094616 | A | G | 2 | a0001c0001t0004g0260 a0001c0001t0004g0261 |
2 | HG00544.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.544-2299A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094616 | |||||||
| chr14:73094621 | C | T | 26 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(23): Show |
26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.544-2294C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094621 | |||||||
| chr14:73094696 | T | G | 1 | a0001c0002t0009g0212 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.544-2219T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094696 | |||||||
| chr14:73094774 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0205 |
2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.544-2141C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094774 | |||||||
| chr14:73094810 | G | GGTGTGTG others(7): Show |
1 | a0001c0002t0003g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.544-2086_544-2073d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094810 | ||||||
| chr14:73094810 | GGT | G | 116 | a0001c0001t0001g0009 a0001c0001t0001g0057 a0001c0001t0001g0118 others(113): Show |
120 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.544-2074_544-2073d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094810 | ||||||
| chr14:73094810 | GGTGT | G | 202 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0120 others(199): Show |
205 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.544-2076_544-2073d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094810 | ||||||
| chr14:73094810 | GGTGTGTG others(1): Show |
G | 24 | a0001c0001t0001g0186 a0001c0001t0004g0001 a0001c0001t0004g0007 others(21): Show |
30 | HG00099.hp2 HG00639.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.544-2080_544-2073d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094810 | ||||||
| chr14:73094823 | GTGTGTGT others(13): Show |
G | 8 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(5): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-2074_544-2055d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73094823 | ||||||
| chr14:73094833 | G | C | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.544-2082G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094833 | |||||||
| chr14:73094841 | G | C | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.544-2074G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094841 | |||||||
| chr14:73094843 | C | G | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.544-2072C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73094843 | |||||||
| chr14:73095132 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.544-1783C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095132 | |||||||
| chr14:73095268 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.544-1647G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095268 | |||||||
| chr14:73095281 | C | T | 5 | a0001c0001t0010g0008 a0001c0001t0010g0283 a0001c0001t0010g0284 others(2): Show |
6 | HG01891.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-1634C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095281 | |||||||
| chr14:73095401 | G | A | 1 | a0001c0001t0005g0127 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.544-1514G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095401 | |||||||
| chr14:73095449 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.544-1466C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095449 | |||||||
| chr14:73095474 | C | T | 26 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(23): Show |
26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.544-1441C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095474 | |||||||
| chr14:73095482 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0203 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.544-1433T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095482 | |||||||
| chr14:73095510 | G | T | 1 | a0001c0001t0001g0304 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.544-1405G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095510 | |||||||
| chr14:73095536 | G | T | 1 | a0001c0001t0019g0281 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-1379G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095536 | |||||||
| chr14:73095606 | C | CA | 110 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0126 others(107): Show |
111 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.544-1296dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73095606 | ||||||
| chr14:73095667 | C | T | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-1248C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095667 | |||||||
| chr14:73095792 | A | G | 26 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(23): Show |
26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.544-1123A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095792 | |||||||
| chr14:73095945 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.544-970C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73095945 | |||||||
| chr14:73096021 | A | G | 1 | a0001c0001t0005g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.544-894A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096021 | |||||||
| chr14:73096269 | G | A | 1 | a0001c0002t0003g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.544-646G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096269 | |||||||
| chr14:73096466 | TTTTG | T | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-437_544-434del others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 73096466 | ||||||
| chr14:73096536 | A | G | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.544-379A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096536 | |||||||
| chr14:73096572 | A | G | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0193 others(3): Show |
6 | HG01884.hp1 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-343A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096572 | |||||||
| chr14:73096645 | G | A | 1 | a0001c0002t0003g0168 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.544-270G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096645 | |||||||
| chr14:73096710 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.544-205G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096710 | |||||||
| chr14:73096724 | A | G | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.544-191A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096724 | |||||||
| chr14:73096908 | G | A | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | splice_region_variant&intron_variant | LOW | c.544-7G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 6/18 | chr14 | 73096908 | |||||||
| chr14:73097131 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.729+31T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097131 | |||||||
| chr14:73097134 | C | T | 1 | a0001c0001t0004g0001 | 6 | HG01168.hp1 HG01169.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+34C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097134 | |||||||
| chr14:73097135 | G | A | 1 | a0001c0001t0013g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.729+35G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097135 | |||||||
| chr14:73097184 | C | CTTTTTTC others(3): Show |
25 | a0001c0001t0001g0005 a0001c0001t0001g0179 a0001c0001t0001g0192 others(22): Show |
27 | HG00642.hp1 HG01123.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.729+86_729+95dupTT others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097184 | ||||||
| chr14:73097191 | C | CTTTTTTT others(4): Show |
10 | a0001c0001t0001g0302 a0001c0001t0001g0352 a0001c0001t0002g0059 others(7): Show |
10 | HG00735.hp2 HG01175.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.729+95_729+96insTT others(9): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097191 | ||||||
| chr14:73097191 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0013g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.729+95_729+96insTT others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097191 | ||||||
| chr14:73097191 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0331 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.729+95_729+96insTT others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097191 | ||||||
| chr14:73097191 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0325 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.729+95_729+96insTT others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097191 | ||||||
| chr14:73097192 | T | TTTTTTTT others(2): Show |
130 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0120 others(127): Show |
135 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.729+95_729+96insTT others(7): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097192 | ||||||
| chr14:73097192 | T | TTTTTTTT others(3): Show |
1 | a0001c0002t0003g0164 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.729+95_729+96insTT others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097192 | ||||||
| chr14:73097193 | T | TTTTTTTT others(1): Show |
113 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0118 others(110): Show |
120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.729+95_729+96insTT others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097193 | ||||||
| chr14:73097193 | TTTC | T | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.729+96_729+98delCT others(1): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097193 | ||||||
| chr14:73097194 | T | TTTTTTTC | 8 | a0001c0001t0001g0320 a0001c0001t0001g0367 a0001c0001t0005g0233 others(5): Show |
8 | HG00323.hp1 HG01346.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.729+95_729+96insTT others(5): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr14 | 73097194 | ||||||
| chr14:73097196 | C | T | 296 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(293): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.729+96C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097196 | |||||||
| chr14:73097201 | T | C | 2 | a0001c0001t0002g0029 a0001c0001t0023g0051 |
2 | HG00733.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.729+101T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097201 | |||||||
| chr14:73097203 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.729+103T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097203 | |||||||
| chr14:73097204 | T | C | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.729+104T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097204 | |||||||
| chr14:73097232 | A | C | 1 | a0001c0001t0035g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.729+132A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097232 | |||||||
| chr14:73097233 | C | G | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+133C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097233 | |||||||
| chr14:73097239 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.729+139C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097239 | |||||||
| chr14:73097358 | G | A | 2 | a0001c0002t0003g0170 a0001c0002t0003g0173 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.729+258G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097358 | |||||||
| chr14:73097518 | A | G | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.729+418A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097518 | |||||||
| chr14:73097537 | G | C | 1 | a0001c0002t0003g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.729+437G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097537 | |||||||
| chr14:73097615 | A | G | 2 | a0001c0001t0006g0035 a0001c0001t0026g0050 |
2 | NA18948.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.729+515A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097615 | |||||||
| chr14:73097656 | A | G | 1 | a0001c0001t0004g0257 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.729+556A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097656 | |||||||
| chr14:73097667 | G | T | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+567G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097667 | |||||||
| chr14:73097835 | T | G | 1 | a0001c0002t0003g0160 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.729+735T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097835 | |||||||
| chr14:73097903 | G | T | 1 | a0001c0001t0025g0041 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.729+803G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097903 | |||||||
| chr14:73097933 | A | G | 1 | a0001c0001t0038g0024 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.729+833A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097933 | |||||||
| chr14:73097977 | G | T | 7 | a0001c0001t0004g0001 a0001c0001t0004g0216 a0001c0001t0004g0218 others(4): Show |
12 | HG00099.hp2 HG00741.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.729+877G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73097977 | |||||||
| chr14:73098220 | C | A | 1 | a0001c0001t0010g0284 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.729+1120C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098220 | |||||||
| chr14:73098420 | C | A | 1 | a0001c0001t0007g0291 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.730-960C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098420 | |||||||
| chr14:73098443 | T | G | 8 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(5): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.730-937T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098443 | |||||||
| chr14:73098531 | A | G | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.730-849A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098531 | |||||||
| chr14:73098556 | T | C | 2 | a0001c0001t0001g0325 a0001c0001t0001g0331 |
2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.730-824T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098556 | |||||||
| chr14:73098654 | C | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-726C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098654 | |||||||
| chr14:73098707 | G | A | 2 | a0001c0001t0008g0017 a0001c0001t0008g0018 |
2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.730-673G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098707 | |||||||
| chr14:73098726 | C | T | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-654C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098726 | |||||||
| chr14:73098746 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.730-634C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098746 | |||||||
| chr14:73098825 | A | G | 1 | a0001c0001t0004g0219 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.730-555A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098825 | |||||||
| chr14:73098877 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.730-503C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098877 | |||||||
| chr14:73098892 | C | T | 1 | a0001c0002t0009g0131 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.730-488C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73098892 | |||||||
| chr14:73099278 | A | G | 2 | a0001c0001t0019g0281 a0001c0001t0019g0282 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.730-102A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73099278 | |||||||
| chr14:73099291 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.730-89C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73099291 | |||||||
| chr14:73099299 | A | T | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.730-81A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73099299 | |||||||
| chr14:73099332 | G | A | 2 | a0001c0001t0002g0111 a0001c0001t0002g0113 |
2 | HG01069.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.730-48G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 7/18 | chr14 | 73099332 | |||||||
| chr14:73099552 | A | G | 1 | a0001c0001t0004g0254 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.784-115A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 8/18 | chr14 | 73099552 | |||||||
| chr14:73099623 | A | G | 3 | a0001c0001t0002g0068 a0001c0001t0002g0080 a0001c0001t0002g0109 |
3 | HG01123.hp1 HG01192.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.784-44A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 8/18 | chr14 | 73099623 | |||||||
| chr14:73099962 | A | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0046 |
2 | HG02056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.867+212A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73099962 | |||||||
| chr14:73100212 | G | A | 13 | a0001c0001t0001g0005 a0001c0001t0005g0004 a0001c0001t0005g0005 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.867+462G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73100212 | |||||||
| chr14:73100512 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.867+762A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73100512 | |||||||
| chr14:73100578 | A | G | 1 | a0001c0001t0013g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.867+828A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73100578 | |||||||
| chr14:73100593 | C | T | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.867+843C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73100593 | |||||||
| chr14:73101041 | A | C | 8 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(5): Show |
8 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.867+1291A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101041 | |||||||
| chr14:73101133 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.867+1383A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101133 | |||||||
| chr14:73101474 | G | GTA | 314 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(311): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.868-1716_868-1715d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 73101474 | ||||||
| chr14:73101506 | A | ATG | 7 | a0001c0001t0001g0215 a0001c0001t0004g0256 a0001c0001t0007g0294 others(4): Show |
8 | HG01891.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.868-1680_868-1679d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 73101506 | ||||||
| chr14:73101506 | ATG | A | 26 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(23): Show |
26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.868-1680_868-1679d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 73101506 | ||||||
| chr14:73101512 | G | A | 2 | a0001c0001t0022g0033 a0001c0001t0023g0051 |
2 | HG01074.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.868-1680G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101512 | |||||||
| chr14:73101512 | G | GTA | 34 | a0001c0001t0001g0177 a0001c0001t0002g0059 a0001c0001t0002g0060 others(31): Show |
40 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.868-1660_868-1659d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 73101512 | ||||||
| chr14:73101512 | GTA | G | 40 | a0001c0001t0002g0087 a0001c0002t0003g0002 a0001c0002t0003g0117 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.868-1660_868-1659d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 73101512 | ||||||
| chr14:73101514 | A | G | 4 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG00558.hp2 NA18980.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.868-1678A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101514 | |||||||
| chr14:73101516 | A | G | 1 | a0001c0002t0003g0150 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.868-1676A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101516 | |||||||
| chr14:73101549 | C | T | 7 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(4): Show |
7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.868-1643C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101549 | |||||||
| chr14:73101826 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.868-1366A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101826 | |||||||
| chr14:73101961 | G | A | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.868-1231G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73101961 | |||||||
| chr14:73102257 | T | C | 13 | a0001c0001t0001g0005 a0001c0001t0005g0004 a0001c0001t0005g0005 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.868-935T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102257 | |||||||
| chr14:73102535 | T | G | 2 | a0001c0001t0010g0008 a0001c0001t0010g0286 |
3 | HG03209.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.868-657T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102535 | |||||||
| chr14:73102632 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.868-560T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102632 | |||||||
| chr14:73102635 | C | T | 23 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(20): Show |
29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.868-557C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102635 | |||||||
| chr14:73102655 | C | T | 1 | a0001c0001t0006g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.868-537C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102655 | |||||||
| chr14:73102767 | A | G | 39 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(36): Show |
42 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.868-425A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102767 | |||||||
| chr14:73102876 | A | C | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.868-316A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102876 | |||||||
| chr14:73102885 | C | T | 2 | a0001c0001t0019g0281 a0001c0001t0019g0282 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.868-307C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102885 | |||||||
| chr14:73102959 | T | G | 2 | a0001c0001t0002g0075 a0001c0001t0002g0114 |
2 | NA18948.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.868-233T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73102959 | |||||||
| chr14:73103058 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.868-134T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73103058 | |||||||
| chr14:73103174 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.868-18G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 9/18 | chr14 | 73103174 | |||||||
| chr14:73103781 | T | G | 7 | a0001c0001t0002g0028 a0001c0001t0002g0074 a0001c0001t0002g0075 others(4): Show |
7 | HG02015.hp1 HG02071.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154+303T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103781 | |||||||
| chr14:73103840 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1154+362C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103840 | |||||||
| chr14:73103890 | TCTGTCTG others(24): Show |
T | 1 | a0001c0001t0001g0369 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1154+413_1154+443d others(33): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103890 | |||||||
| chr14:73103897 | GTCTGTCT others(13): Show |
G | 1 | a0001c0001t0006g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1154+423_1154+442d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103897 | ||||||
| chr14:73103905 | G | C | 2 | a0001c0001t0018g0277 a0001c0001t0018g0278 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1154+427G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103905 | |||||||
| chr14:73103905 | G | GTC | 8 | a0001c0001t0002g0028 a0001c0001t0002g0082 a0001c0001t0002g0093 others(5): Show |
8 | HG01346.hp2 HG02135.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.1154+470_1154+471d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103905 | G | GTCTC | 4 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0084 others(1): Show |
4 | HG01192.hp2 HG01978.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+468_1154+471d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103905 | G | GTCTCTC | 4 | a0001c0001t0002g0083 a0001c0001t0002g0110 a0001c0001t0002g0370 others(1): Show |
4 | HG01934.hp1 HG02148.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+466_1154+471d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103905 | GTC | G | 10 | a0001c0001t0002g0102 a0001c0001t0004g0219 a0001c0001t0004g0258 others(7): Show |
10 | HG01361.hp2 HG01928.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1154+470_1154+471d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103905 | GTCTC | G | 9 | a0001c0001t0002g0066 a0001c0001t0004g0001 a0001c0001t0004g0007 others(6): Show |
10 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1154+468_1154+471d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103905 | GTCTCTC | G | 4 | a0001c0001t0004g0255 a0001c0001t0004g0275 a0001c0002t0003g0117 others(1): Show |
4 | HG03688.hp1 HG03942.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+466_1154+471d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103905 | GTCTCTCT others(1): Show |
G | 7 | a0001c0001t0006g0032 a0001c0001t0006g0038 a0001c0001t0006g0039 others(4): Show |
7 | HG00735.hp1 HG03579.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.1154+464_1154+471d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103905 | GTCTCTCT others(3): Show |
G | 10 | a0001c0001t0006g0034 a0001c0001t0006g0036 a0001c0001t0006g0046 others(7): Show |
11 | HG01975.hp1 HG02056.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1154+462_1154+471d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103905 | GTCTCTCT others(5): Show |
G | 17 | a0001c0001t0001g0194 a0001c0001t0001g0215 a0001c0001t0001g0250 others(14): Show |
17 | HG01069.hp2 HG01071.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.1154+460_1154+471d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103905 | GTCTCTCT others(7): Show |
G | 20 | a0001c0001t0006g0035 a0001c0001t0006g0043 a0001c0001t0006g0044 others(17): Show |
23 | HG00423.hp1 HG00738.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1154+458_1154+471d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103905 | GTCTCTCT others(9): Show |
G | 2 | a0001c0001t0007g0296 a0001c0002t0003g0199 |
2 | HG01243.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1154+456_1154+471d others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103905 | GTCTCTCT others(13): Show |
G | 1 | a0001c0001t0010g0283 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1154+452_1154+471d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103905 | ||||||
| chr14:73103909 | C | G | 15 | a0001c0001t0001g0187 a0001c0001t0001g0196 a0001c0001t0001g0197 others(12): Show |
15 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1154+431C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103909 | |||||||
| chr14:73103913 | C | G | 1 | a0001c0001t0004g0001 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1154+435C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103913 | |||||||
| chr14:73103923 | C | G | 2 | a0001c0002t0009g0208 a0001c0002t0009g0209 |
2 | HG00738.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1154+445C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103923 | |||||||
| chr14:73103925 | C | G | 1 | a0001c0001t0007g0296 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1154+447C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103925 | |||||||
| chr14:73103926 | TCTCTCTC others(25): Show |
T | 1 | a0001c0001t0001g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1154+450_1154+481d others(34): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103926 | ||||||
| chr14:73103928 | TCTCTCTC others(23): Show |
T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0236 |
2 | NA18939.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1154+452_1154+481d others(32): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103928 | ||||||
| chr14:73103930 | TCTCTCTC others(15): Show |
T | 3 | a0001c0001t0007g0298 a0001c0001t0007g0299 a0001c0001t0023g0051 |
3 | HG01074.hp2 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1154+454_1154+475d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103930 | ||||||
| chr14:73103930 | TCTCTCTC others(19): Show |
T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0228 a0001c0001t0001g0231 others(2): Show |
5 | HG02083.hp2 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+454_1154+479d others(28): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103930 | ||||||
| chr14:73103930 | TCTCTCTC others(23): Show |
T | 9 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0014 others(6): Show |
9 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1154+454_1154+483d others(32): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103930 | ||||||
| chr14:73103930 | TCTCTCTC others(27): Show |
T | 3 | a0001c0001t0015g0026 a0001c0001t0038g0024 a0001c0004t0015g0025 |
3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1154+454_1154+487d others(36): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103930 | ||||||
| chr14:73103932 | TCTCTCTC others(11): Show |
T | 5 | a0001c0001t0001g0273 a0001c0001t0007g0297 a0001c0001t0026g0050 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+456_1154+473d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | ||||||
| chr14:73103932 | TCTCTCTC others(13): Show |
T | 1 | a0001c0001t0019g0282 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1154+456_1154+475d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | ||||||
| chr14:73103932 | TCTCTCTC others(15): Show |
T | 2 | a0001c0001t0005g0300 a0001c0001t0019g0281 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1154+456_1154+477d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | ||||||
| chr14:73103932 | TCTCTCTC others(17): Show |
T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0128 others(12): Show |
16 | HG00323.hp1 HG00639.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1154+456_1154+479d others(26): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | ||||||
| chr14:73103932 | TCTCTCTC others(19): Show |
T | 33 | a0001c0001t0001g0006 a0001c0001t0001g0185 a0001c0001t0001g0222 others(30): Show |
34 | HG00140.hp1 HG00423.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1154+456_1154+481d others(28): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | ||||||
| chr14:73103932 | TCTCTCTC others(21): Show |
T | 3 | a0001c0001t0001g0265 a0001c0001t0008g0013 a0001c0001t0008g0015 |
3 | NA18944.hp2 NA19009.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1154+456_1154+483d others(30): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | ||||||
| chr14:73103932 | TCTCTCTC others(27): Show |
T | 1 | a0001c0001t0015g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1154+456_1154+489d others(36): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103932 | ||||||
| chr14:73103934 | TCTCTCTC others(11): Show |
T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0055 |
3 | HG02486.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1154+458_1154+475d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | ||||||
| chr14:73103934 | TCTCTCTC others(13): Show |
T | 4 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0007g0291 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154+458_1154+477d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | ||||||
| chr14:73103934 | TCTCTCTC others(15): Show |
T | 18 | a0001c0001t0001g0009 a0001c0001t0001g0139 a0001c0001t0001g0140 others(15): Show |
18 | HG00733.hp2 HG01106.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1154+458_1154+479d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | ||||||
| chr14:73103934 | TCTCTCTC others(17): Show |
T | 11 | a0001c0001t0001g0180 a0001c0001t0001g0198 a0001c0001t0001g0206 others(8): Show |
11 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1154+458_1154+481d others(26): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | ||||||
| chr14:73103934 | TCTCTCTC others(19): Show |
T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0203 a0001c0001t0029g0264 |
3 | HG03098.hp1 HG06807.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1154+458_1154+483d others(28): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | ||||||
| chr14:73103934 | TCTCTCTC others(21): Show |
T | 1 | a0001c0001t0001g0118 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1154+458_1154+485d others(30): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103934 | ||||||
| chr14:73103936 | TCTCTCTC others(7): Show |
T | 2 | a0001c0001t0006g0040 a0001c0001t0006g0049 |
2 | HG00408.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1154+460_1154+473d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103936 | ||||||
| chr14:73103936 | TCTCTCTC others(11): Show |
T | 8 | a0001c0001t0001g0138 a0001c0001t0001g0337 a0001c0001t0005g0125 others(5): Show |
8 | HG01256.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1154+460_1154+477d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103936 | ||||||
| chr14:73103936 | TCTCTCTC others(13): Show |
T | 11 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0176 others(8): Show |
11 | HG01243.hp2 HG02602.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1154+460_1154+479d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103936 | ||||||
| chr14:73103936 | TCTCTCTC others(15): Show |
T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0288 |
2 | HG02647.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1154+460_1154+481d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103936 | ||||||
| chr14:73103938 | T | A | 2 | a0001c0001t0006g0048 a0001c0002t0003g0162 |
2 | HG02738.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1154+460T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103938 | |||||||
| chr14:73103938 | TCTCTCTC others(7): Show |
T | 2 | a0001c0001t0001g0363 a0001c0001t0005g0122 |
2 | HG00609.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1154+462_1154+475d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103938 | ||||||
| chr14:73103938 | TCTCTCTC others(9): Show |
T | 12 | a0001c0001t0001g0303 a0001c0001t0001g0305 a0001c0001t0001g0315 others(9): Show |
12 | HG00609.hp2 HG01496.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1154+462_1154+477d others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103938 | ||||||
| chr14:73103938 | TCTCTCTC others(11): Show |
T | 50 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0184 others(47): Show |
51 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1154+462_1154+479d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103938 | ||||||
| chr14:73103938 | TCTCTCTC others(13): Show |
T | 12 | a0001c0001t0001g0175 a0001c0001t0001g0179 a0001c0001t0001g0186 others(9): Show |
12 | HG00642.hp1 HG00673.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1154+462_1154+481d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103938 | ||||||
| chr14:73103940 | T | A | 2 | a0001c0001t0006g0048 a0001c0002t0003g0162 |
2 | HG02738.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1154+462T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103940 | |||||||
| chr14:73103940 | TCTCTCTC others(7): Show |
T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0221 |
2 | HG02056.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1154+464_1154+477d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103940 | ||||||
| chr14:73103940 | TCTCTCTC others(11): Show |
T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0132 a0001c0001t0001g0187 |
3 | HG01952.hp1 HG03710.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1154+464_1154+481d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103940 | ||||||
| chr14:73103940 | TCTCTCTC others(13): Show |
T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0174 |
2 | HG04184.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1154+464_1154+483d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103940 | ||||||
| chr14:73103942 | T | A | 5 | a0001c0001t0006g0048 a0001c0001t0010g0286 a0001c0002t0003g0117 others(2): Show |
5 | HG02738.hp1 HG03579.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+464T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103942 | |||||||
| chr14:73103942 | TCTCTCTC others(7): Show |
T | 1 | a0001c0001t0004g0001 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1154+466_1154+479d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103942 | ||||||
| chr14:73103944 | T | A | 18 | a0001c0001t0004g0253 a0001c0001t0004g0256 a0001c0001t0004g0261 others(15): Show |
19 | HG00544.hp1 HG01361.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.1154+466T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103944 | |||||||
| chr14:73103944 | TCTCTCA | T | 3 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0371 |
3 | HG01516.hp2 HG03704.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1154+468_1154+473d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103944 | ||||||
| chr14:73103944 | TCTCTCAC others(1): Show |
T | 2 | a0001c0001t0002g0090 a0001c0001t0004g0001 |
5 | HG01168.hp1 HG01169.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+468_1154+475d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103944 | ||||||
| chr14:73103946 | T | A | 50 | a0001c0001t0001g0194 a0001c0001t0004g0007 a0001c0001t0004g0204 others(47): Show |
52 | HG00544.hp1 HG00544.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1154+468T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103946 | |||||||
| chr14:73103948 | T | A | 75 | a0001c0001t0001g0194 a0001c0001t0001g0250 a0001c0001t0002g0081 others(72): Show |
80 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1154+470T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103948 | |||||||
| chr14:73103948 | T | TCTCA | 4 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0092 others(1): Show |
4 | HG02071.hp1 NA18973.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+471_1154+472i others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | ||||||
| chr14:73103948 | T | TCTCACAC others(3): Show |
1 | a0001c0001t0002g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1154+471_1154+472i others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | ||||||
| chr14:73103948 | T | TCTCTCTC others(3): Show |
2 | a0001c0001t0002g0100 a0001c0001t0002g0111 |
2 | HG01167.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1154+471_1154+472i others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | ||||||
| chr14:73103948 | T | TCTCTCTC others(5): Show |
1 | a0001c0001t0002g0113 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1154+471_1154+472i others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | ||||||
| chr14:73103948 | T | TCTCTCTC others(3): Show |
2 | a0001c0001t0002g0085 a0001c0001t0033g0070 |
2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1154+471_1154+472i others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | ||||||
| chr14:73103948 | T | TCTCTCTC others(5): Show |
2 | a0001c0001t0002g0072 a0001c0001t0002g0112 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1154+471_1154+472i others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | ||||||
| chr14:73103948 | T | TCTCTCTC others(7): Show |
1 | a0001c0001t0002g0086 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1154+471_1154+472i others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | ||||||
| chr14:73103948 | T | TCTCTCTC others(13): Show |
1 | a0001c0001t0002g0095 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1154+471_1154+472i others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103948 | ||||||
| chr14:73103950 | A | T | 17 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0029 others(14): Show |
17 | HG00733.hp1 HG01123.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1154+472A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103950 | |||||||
| chr14:73103952 | A | T | 4 | a0001c0001t0002g0028 a0001c0001t0002g0079 a0001c0001t0002g0082 others(1): Show |
4 | NA18963.hp2 NA18990.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154+474A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103952 | |||||||
| chr14:73103982 | A | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0250 |
2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1154+504A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103982 | |||||||
| chr14:73103984 | A | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0250 a0001c0001t0010g0286 |
3 | HG02698.hp1 HG03579.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1154+506A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103984 | |||||||
| chr14:73103986 | A | T | 9 | a0001c0001t0001g0194 a0001c0001t0001g0250 a0001c0001t0006g0048 others(6): Show |
10 | HG01891.hp2 HG02145.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1154+508A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103986 | |||||||
| chr14:73103988 | A | T | 23 | a0001c0001t0001g0194 a0001c0001t0001g0250 a0001c0001t0001g0316 others(20): Show |
24 | HG01074.hp2 HG01361.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.1154+510A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103988 | |||||||
| chr14:73103988 | ACACACAC others(3): Show |
A | 1 | a0001c0001t0002g0372 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1154+512_1154+521d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103988 | ||||||
| chr14:73103990 | A | T | 109 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0182 others(106): Show |
112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1154+512A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103990 | |||||||
| chr14:73103992 | A | T | 217 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(214): Show |
227 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1154+514A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103992 | |||||||
| chr14:73103992 | ACACT | A | 3 | a0001c0001t0002g0098 a0001c0001t0002g0106 a0001c0001t0002g0115 |
3 | HG02080.hp1 NA18951.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1154+516_1154+519d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103992 | ||||||
| chr14:73103994 | A | T | 310 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(307): Show |
324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.1154+516A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103994 | |||||||
| chr14:73103994 | ACT | A | 3 | a0001c0001t0002g0097 a0001c0001t0002g0105 a0001c0001t0002g0107 |
3 | NA18975.hp1 NA18988.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1154+538_1154+539d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73103994 | ||||||
| chr14:73103996 | T | A | 27 | a0001c0001t0002g0028 a0001c0001t0002g0067 a0001c0001t0002g0068 others(24): Show |
27 | HG00558.hp2 HG01123.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.1154+518T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103996 | |||||||
| chr14:73103998 | T | A | 2 | a0001c0001t0002g0088 a0001c0001t0002g0370 |
2 | HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1154+520T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73103998 | |||||||
| chr14:73104109 | C | G | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154+631C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104109 | |||||||
| chr14:73104309 | C | CTCCTAGT others(12): Show |
1 | a0001c0001t0002g0116 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1154+833_1154+851d others(21): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73104309 | ||||||
| chr14:73104311 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0203 a0001c0001t0001g0252 |
3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1154+833C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104311 | |||||||
| chr14:73104403 | C | G | 1 | a0001c0001t0005g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1154+925C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104403 | |||||||
| chr14:73104422 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1154+944G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104422 | |||||||
| chr14:73104439 | G | T | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1154+961G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104439 | |||||||
| chr14:73104441 | T | G | 2 | a0001c0001t0019g0281 a0001c0001t0019g0282 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1154+963T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104441 | |||||||
| chr14:73104511 | A | G | 2 | a0001c0001t0012g0019 a0001c0001t0012g0022 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1154+1033A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104511 | |||||||
| chr14:73104698 | C | T | 38 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(35): Show |
38 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1155-1161C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104698 | |||||||
| chr14:73104763 | A | G | 1 | a0001c0002t0003g0121 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1155-1096A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104763 | |||||||
| chr14:73104967 | G | A | 7 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(4): Show |
7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155-892G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73104967 | |||||||
| chr14:73105038 | T | TAC | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0215 others(4): Show |
7 | HG02055.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155-795_1155-794d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACAC | 33 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0121 others(30): Show |
36 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1155-797_1155-794d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACAC | 8 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0005g0143 others(5): Show |
8 | HG02074.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1155-799_1155-794d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACACA others(1): Show |
23 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(20): Show |
28 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1155-801_1155-794d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACACA others(3): Show |
12 | a0001c0001t0001g0009 a0001c0001t0001g0057 a0001c0001t0001g0195 others(9): Show |
14 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1155-803_1155-794d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACACA others(5): Show |
9 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0231 others(6): Show |
9 | HG01074.hp2 HG01891.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1155-805_1155-794d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACACA others(7): Show |
23 | a0001c0001t0001g0247 a0001c0001t0001g0250 a0001c0001t0001g0252 others(20): Show |
23 | HG00733.hp1 HG01884.hp1 HG02148.hp2 others(20): Show |
intron_variant | MODIFIER | c.1155-807_1155-794d others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACACA others(9): Show |
57 | a0001c0001t0001g0185 a0001c0001t0001g0193 a0001c0001t0001g0203 others(54): Show |
57 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1155-809_1155-794d others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACACA others(11): Show |
22 | a0001c0001t0001g0220 a0001c0001t0001g0242 a0001c0001t0001g0265 others(19): Show |
23 | HG00323.hp2 HG01106.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.1155-811_1155-794d others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACACA others(13): Show |
26 | a0001c0001t0001g0006 a0001c0001t0001g0194 a0001c0001t0001g0223 others(23): Show |
27 | HG00558.hp2 HG01891.hp2 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.1155-813_1155-794d others(22): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACACA others(15): Show |
19 | a0001c0001t0002g0059 a0001c0001t0002g0108 a0001c0001t0002g0371 others(16): Show |
19 | HG01167.hp2 HG01169.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.1155-815_1155-794d others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACACA others(17): Show |
6 | a0001c0001t0004g0204 a0001c0001t0004g0261 a0001c0001t0008g0017 others(3): Show |
6 | HG00544.hp1 HG01257.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1155-817_1155-794d others(26): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACACA others(19): Show |
7 | a0001c0001t0001g0228 a0001c0001t0004g0007 a0001c0001t0004g0267 others(4): Show |
8 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155-819_1155-794d others(28): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | T | TACACACA others(25): Show |
2 | a0001c0001t0008g0012 a0001c0001t0008g0016 |
2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1155-794_1155-793i others(34): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | TAC | T | 22 | a0001c0001t0001g0321 a0001c0001t0001g0327 a0001c0001t0001g0334 others(19): Show |
22 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1155-795_1155-794d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105038 | TACACAC | T | 4 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0180 others(1): Show |
4 | HG02717.hp2 HG06807.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155-799_1155-794d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105038 | ||||||
| chr14:73105066 | G | C | 10 | a0001c0001t0001g0238 a0001c0001t0001g0244 a0001c0001t0001g0245 others(7): Show |
10 | HG01074.hp2 HG02129.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1155-793G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105066 | |||||||
| chr14:73105126 | C | CT | 58 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0057 others(55): Show |
60 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1155-715dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | ||||||
| chr14:73105126 | C | CTT | 34 | a0001c0001t0001g0005 a0001c0001t0001g0139 a0001c0001t0001g0140 others(31): Show |
35 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.1155-716_1155-715d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | ||||||
| chr14:73105126 | C | CTTTTTTT others(1): Show |
23 | a0001c0001t0006g0032 a0001c0001t0006g0036 a0001c0001t0006g0037 others(20): Show |
23 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.1155-722_1155-715d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | ||||||
| chr14:73105126 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0006g0034 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1155-724_1155-715d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | ||||||
| chr14:73105126 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0011g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1155-725_1155-715d others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | ||||||
| chr14:73105126 | C | CTTTTTTT others(5): Show |
4 | a0001c0001t0011g0052 a0001c0001t0011g0054 a0001c0001t0011g0055 others(1): Show |
4 | HG02486.hp1 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1155-726_1155-715d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | ||||||
| chr14:73105126 | CT | C | 96 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0126 others(93): Show |
97 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1155-715delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | ||||||
| chr14:73105126 | CTT | C | 69 | a0001c0001t0001g0369 a0001c0001t0004g0001 a0001c0001t0004g0007 others(66): Show |
78 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1155-716_1155-715d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr14 | 73105126 | ||||||
| chr14:73105151 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1155-708G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105151 | |||||||
| chr14:73105239 | G | C | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1155-620G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105239 | |||||||
| chr14:73105429 | A | G | 1 | a0001c0001t0007g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1155-430A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105429 | |||||||
| chr14:73105458 | C | A | 1 | a0001c0001t0004g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1155-401C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105458 | |||||||
| chr14:73105519 | T | G | 1 | a0001c0001t0031g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1155-340T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105519 | |||||||
| chr14:73105707 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1155-152T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105707 | |||||||
| chr14:73105720 | A | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1155-139A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 10/18 | chr14 | 73105720 | |||||||
| chr14:73106099 | C | T | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1377+18C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 11/18 | chr14 | 73106099 | |||||||
| chr14:73106117 | G | A | 46 | a0001c0001t0001g0006 a0001c0001t0001g0185 a0001c0001t0001g0194 others(43): Show |
47 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1377+36G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 11/18 | chr14 | 73106117 | |||||||
| chr14:73106471 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1467+186A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106471 | |||||||
| chr14:73106632 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0005g0004 a0001c0001t0005g0005 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1467+347C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106632 | |||||||
| chr14:73106654 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18991.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1467+369A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106654 | |||||||
| chr14:73106732 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1467+447C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106732 | |||||||
| chr14:73106824 | C | T | 5 | a0001c0001t0012g0019 a0001c0001t0012g0020 a0001c0001t0012g0021 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1467+539C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106824 | |||||||
| chr14:73106840 | C | CT | 10 | a0001c0001t0008g0012 a0001c0001t0008g0014 a0001c0001t0008g0016 others(7): Show |
11 | HG01168.hp2 HG01261.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1467+570dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr14 | 73106840 | ||||||
| chr14:73106840 | CT | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0185 a0001c0001t0001g0194 others(74): Show |
78 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1467+570delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr14 | 73106840 | ||||||
| chr14:73106848 | T | C | 2 | a0001c0001t0001g0325 a0001c0001t0001g0331 |
2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1467+563T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106848 | |||||||
| chr14:73106873 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1467+588C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73106873 | |||||||
| chr14:73107151 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1468-675G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73107151 | |||||||
| chr14:73107195 | G | A | 1 | a0001c0001t0002g0081 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1468-631G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73107195 | |||||||
| chr14:73107311 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1468-515T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73107311 | |||||||
| chr14:73107379 | CT | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(14): Show |
18 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1468-439delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr14 | 73107379 | ||||||
| chr14:73107601 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1468-225T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73107601 | |||||||
| chr14:73107704 | A | G | 7 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(4): Show |
7 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468-122A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 12/18 | chr14 | 73107704 | |||||||
| chr14:73108056 | G | A | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1541+157G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108056 | |||||||
| chr14:73108059 | G | T | 5 | a0001c0002t0009g0131 a0001c0002t0009g0161 a0001c0002t0009g0208 others(2): Show |
5 | HG00735.hp1 HG00738.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1541+160G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108059 | |||||||
| chr14:73108082 | G | A | 1 | a0001c0001t0008g0018 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1541+183G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108082 | |||||||
| chr14:73108302 | A | G | 1 | a0001c0002t0003g0168 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1541+403A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108302 | |||||||
| chr14:73108324 | A | G | 2 | a0001c0002t0003g0117 a0001c0002t0003g0159 |
2 | NA18947.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1541+425A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108324 | |||||||
| chr14:73108335 | C | T | 1 | a0001c0001t0004g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1541+436C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108335 | |||||||
| chr14:73108538 | A | G | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1541+639A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108538 | |||||||
| chr14:73108585 | T | A | 1 | a0001c0001t0002g0066 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1541+686T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108585 | |||||||
| chr14:73108755 | C | T | 7 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(4): Show |
7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1542-587C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108755 | |||||||
| chr14:73108977 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1542-365C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73108977 | |||||||
| chr14:73109015 | C | G | 11 | a0001c0001t0008g0011 a0001c0001t0008g0012 a0001c0001t0008g0013 others(8): Show |
11 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1542-327C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109015 | |||||||
| chr14:73109106 | T | C | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1542-236T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109106 | |||||||
| chr14:73109134 | A | G | 1 | a0001c0001t0002g0081 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1542-208A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109134 | |||||||
| chr14:73109190 | C | G | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1542-152C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109190 | |||||||
| chr14:73109210 | A | G | 11 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1542-132A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109210 | |||||||
| chr14:73109315 | G | T | 14 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0064 others(11): Show |
15 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-27G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 13/18 | chr14 | 73109315 | |||||||
| chr14:73109559 | C | T | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1692+67C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109559 | |||||||
| chr14:73109576 | G | A | 1 | a0001c0001t0008g0011 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1692+84G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109576 | |||||||
| chr14:73109609 | C | T | 1 | a0001c0002t0003g0159 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1692+117C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109609 | |||||||
| chr14:73109649 | C | T | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1692+157C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109649 | |||||||
| chr14:73109650 | G | T | 1 | a0001c0003t0001g0368 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1692+158G>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109650 | |||||||
| chr14:73109693 | C | T | 40 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1692+201C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109693 | |||||||
| chr14:73109742 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1692+250G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109742 | |||||||
| chr14:73109834 | C | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1692+342C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109834 | |||||||
| chr14:73109915 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1692+423C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109915 | |||||||
| chr14:73109995 | G | A | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1692+503G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73109995 | |||||||
| chr14:73110025 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1692+533C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110025 | |||||||
| chr14:73110053 | T | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0035g0123 |
3 | HG02257.hp2 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1692+561T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110053 | |||||||
| chr14:73110184 | C | CT | 19 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(16): Show |
19 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1693-635dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr14 | 73110184 | ||||||
| chr14:73110282 | G | A | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693-549G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110282 | |||||||
| chr14:73110304 | G | C | 300 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(297): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1693-527G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110304 | |||||||
| chr14:73110317 | A | G | 11 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0291 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1693-514A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110317 | |||||||
| chr14:73110346 | C | G | 69 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(66): Show |
78 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1693-485C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110346 | |||||||
| chr14:73110574 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1693-257G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110574 | |||||||
| chr14:73110652 | C | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0035g0123 |
3 | HG02257.hp2 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1693-179C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 14/18 | chr14 | 73110652 | |||||||
| chr14:73111165 | C | T | 1 | a0001c0001t0008g0012 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2017+10C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 15/18 | chr14 | 73111165 | |||||||
| chr14:73111433 | G | GAAGTATA others(4): Show |
1 | a0001c0001t0026g0050 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2018-94_2018-84dup others(11): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr14 | 73111433 | ||||||
| chr14:73111852 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2292+50G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 16/18 | chr14 | 73111852 | |||||||
| chr14:73112129 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2293-23A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 16/18 | chr14 | 73112129 | |||||||
| chr14:73112413 | G | GT | 306 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(303): Show |
320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.2391+172dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr14 | 73112413 | ||||||
| chr14:73112413 | G | GTT | 8 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(5): Show |
8 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2391+171_2391+172d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr14 | 73112413 | ||||||
| chr14:73112546 | A | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2391+296A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73112546 | |||||||
| chr14:73112568 | CT | C | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2391+319delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73112568 | |||||||
| chr14:73112673 | C | G | 136 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(133): Show |
139 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.2391+423C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73112673 | |||||||
| chr14:73112826 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2391+576C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73112826 | |||||||
| chr14:73113037 | G | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0179 |
2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2391+787G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113037 | |||||||
| chr14:73113106 | A | G | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2391+856A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113106 | |||||||
| chr14:73113140 | A | C | 5 | a0001c0001t0004g0007 a0001c0001t0004g0204 a0001c0001t0004g0267 others(2): Show |
6 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2391+890A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113140 | |||||||
| chr14:73113250 | T | C | 26 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(23): Show |
26 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.2391+1000T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113250 | |||||||
| chr14:73113368 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2392-918G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113368 | |||||||
| chr14:73113431 | C | G | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2392-855C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113431 | |||||||
| chr14:73113507 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2392-779A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113507 | |||||||
| chr14:73113517 | C | T | 1 | a0001c0001t0004g0258 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2392-769C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113517 | |||||||
| chr14:73113549 | C | G | 34 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(31): Show |
34 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.2392-737C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113549 | |||||||
| chr14:73113663 | G | A | 1 | a0001c0001t0031g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2392-623G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113663 | |||||||
| chr14:73113942 | T | A | 2 | a0001c0001t0018g0277 a0001c0001t0018g0278 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2392-344T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113942 | |||||||
| chr14:73113986 | C | T | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2392-300C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113986 | |||||||
| chr14:73113999 | G | A | 1 | a0001c0001t0022g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2392-287G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73113999 | |||||||
| chr14:73114057 | G | A | 2 | a0001c0001t0019g0281 a0001c0001t0019g0282 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2392-229G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114057 | |||||||
| chr14:73114078 | G | GTCAATTA others(23): Show |
3 | a0001c0001t0015g0026 a0001c0001t0038g0024 a0001c0004t0015g0025 |
3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2392-208_2392-207i others(32): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114078 | |||||||
| chr14:73114080 | C | A | 3 | a0001c0001t0015g0026 a0001c0001t0038g0024 a0001c0004t0015g0025 |
3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2392-206C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114080 | |||||||
| chr14:73114081 | T | A | 3 | a0001c0001t0015g0026 a0001c0001t0038g0024 a0001c0004t0015g0025 |
3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2392-205T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114081 | |||||||
| chr14:73114083 | C | T | 3 | a0001c0001t0015g0026 a0001c0001t0038g0024 a0001c0004t0015g0025 |
3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2392-203C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114083 | |||||||
| chr14:73114120 | C | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0203 a0001c0001t0001g0252 |
3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2392-166C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 17/18 | chr14 | 73114120 | |||||||
| chr14:73114366 | T | C | 54 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0057 others(51): Show |
56 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2439+33T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114366 | |||||||
| chr14:73114557 | T | C | 7 | a0001c0001t0004g0001 a0001c0001t0004g0216 a0001c0001t0004g0218 others(4): Show |
12 | HG00099.hp2 HG00741.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2439+224T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114557 | |||||||
| chr14:73114584 | C | T | 25 | a0001c0001t0004g0001 a0001c0001t0004g0007 a0001c0001t0004g0204 others(22): Show |
31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2439+251C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114584 | |||||||
| chr14:73114666 | C | T | 1 | a0001c0002t0003g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2439+333C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114666 | |||||||
| chr14:73114762 | C | T | 1 | a0001c0001t0007g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2439+429C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114762 | |||||||
| chr14:73114795 | T | C | 1 | a0001c0001t0004g0280 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2439+462T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114795 | |||||||
| chr14:73114993 | C | G | 39 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(36): Show |
42 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.2439+660C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73114993 | |||||||
| chr14:73115028 | G | A | 299 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(296): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.2439+695G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115028 | |||||||
| chr14:73115153 | C | CGT | 22 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0326 others(19): Show |
22 | HG00140.hp2 HG00408.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.2439+855_2439+856d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | ||||||
| chr14:73115153 | C | CGTGT | 70 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0126 others(67): Show |
71 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.2439+853_2439+856d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | ||||||
| chr14:73115153 | C | CGTGTGT | 30 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0138 others(27): Show |
30 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2439+851_2439+856d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | ||||||
| chr14:73115153 | C | CGTGTGTG others(1): Show |
24 | a0001c0001t0001g0005 a0001c0001t0001g0142 a0001c0001t0001g0146 others(21): Show |
25 | HG00558.hp1 HG00673.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2439+849_2439+856d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | ||||||
| chr14:73115153 | C | CGTGTGTG others(3): Show |
3 | a0001c0001t0001g0313 a0001c0001t0005g0135 a0001c0001t0005g0213 |
3 | HG02559.hp2 HG02572.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2439+847_2439+856d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | ||||||
| chr14:73115153 | CGT | C | 56 | a0001c0001t0001g0185 a0001c0001t0001g0220 a0001c0001t0001g0222 others(53): Show |
57 | HG00140.hp1 HG00423.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.2439+855_2439+856d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | ||||||
| chr14:73115153 | CGTGT | C | 42 | a0001c0001t0001g0009 a0001c0001t0001g0057 a0001c0001t0001g0118 others(39): Show |
49 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.2439+853_2439+856d others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | ||||||
| chr14:73115153 | CGTGTGT | C | 6 | a0001c0001t0001g0287 a0001c0001t0004g0217 a0001c0001t0007g0296 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2439+851_2439+856d others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | ||||||
| chr14:73115153 | CGTGTGTG others(1): Show |
C | 8 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(5): Show |
8 | HG01074.hp2 HG02165.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2439+849_2439+856d others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | ||||||
| chr14:73115153 | CGTGTGTG others(3): Show |
C | 2 | a0001c0001t0001g0365 a0001c0001t0016g0091 |
2 | HG00558.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2439+847_2439+856d others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | ||||||
| chr14:73115153 | CGTGTGTG others(5): Show |
C | 1 | a0001c0002t0003g0119 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2439+845_2439+856d others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115153 | ||||||
| chr14:73115191 | T | G | 1 | a0001c0001t0004g0254 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2439+858T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115191 | |||||||
| chr14:73115276 | G | A | 1 | a0001c0001t0001g0333 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2439+943G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115276 | |||||||
| chr14:73115318 | C | G | 4 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0005g0183 others(1): Show |
4 | HG01943.hp2 HG01975.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2439+985C>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115318 | |||||||
| chr14:73115401 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2439+1068C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115401 | |||||||
| chr14:73115425 | A | G | 9 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0064 others(6): Show |
9 | HG01496.hp2 HG01884.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2439+1092A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115425 | |||||||
| chr14:73115593 | C | T | 39 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(36): Show |
42 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.2439+1260C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115593 | |||||||
| chr14:73115644 | CTG | C | 5 | a0001c0001t0001g0308 a0001c0001t0001g0321 a0001c0001t0001g0326 others(2): Show |
5 | HG00140.hp2 HG01496.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2439+1314_2439+131 others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73115644 | ||||||
| chr14:73115726 | G | A | 39 | a0001c0002t0003g0002 a0001c0002t0003g0117 a0001c0002t0003g0119 others(36): Show |
42 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.2439+1393G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115726 | |||||||
| chr14:73115906 | T | C | 7 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(4): Show |
7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2439+1573T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73115906 | |||||||
| chr14:73116070 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 |
4 | HG02647.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2439+1737T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73116070 | |||||||
| chr14:73116072 | G | GT | 7 | a0001c0001t0001g0198 a0001c0001t0001g0309 a0001c0001t0001g0347 others(4): Show |
7 | HG01361.hp2 HG02897.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.2439+1750dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73116072 | ||||||
| chr14:73116167 | G | A | 1 | a0001c0002t0003g0165 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2439+1834G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73116167 | |||||||
| chr14:73116590 | G | C | 13 | a0001c0001t0001g0005 a0001c0001t0005g0004 a0001c0001t0005g0005 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2439+2257G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73116590 | |||||||
| chr14:73116800 | G | A | 1 | a0001c0001t0031g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2439+2467G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73116800 | |||||||
| chr14:73117041 | G | A | 2 | a0001c0001t0019g0281 a0001c0001t0019g0282 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2440-2672G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117041 | |||||||
| chr14:73117196 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0345 |
2 | NA18939.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.2440-2517T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117196 | |||||||
| chr14:73117205 | CTTTTCTT others(3): Show |
C | 1 | a0001c0001t0007g0291 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2440-2503_2440-249 others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117205 | ||||||
| chr14:73117205 | CTTTTCTT others(6): Show |
C | 2 | a0001c0001t0026g0050 a0001c0001t0036g0362 |
2 | NA18991.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.2440-2503_2440-249 others(17): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117205 | ||||||
| chr14:73117210 | C | A | 3 | a0001c0001t0007g0295 a0001c0001t0007g0297 a0001c0001t0007g0298 |
3 | HG02451.hp2 HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2440-2503C>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117210 | |||||||
| chr14:73117210 | C | CT | 7 | a0001c0001t0002g0069 a0001c0001t0002g0075 a0001c0001t0002g0085 others(4): Show |
7 | HG02698.hp2 HG02738.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.2440-2469dupT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTT | 13 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0002g0074 others(10): Show |
13 | HG01175.hp1 HG01256.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.2440-2470_2440-246 others(6): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTT | 10 | a0001c0001t0002g0067 a0001c0001t0002g0072 a0001c0001t0002g0080 others(7): Show |
10 | HG00741.hp1 HG01123.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.2440-2471_2440-246 others(7): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTTT | 6 | a0001c0001t0001g0196 a0001c0001t0002g0029 a0001c0001t0002g0068 others(3): Show |
6 | HG00733.hp1 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-2472_2440-246 others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTTTTTT others(2): Show |
4 | a0001c0001t0001g0138 a0001c0001t0004g0001 a0001c0001t0004g0253 others(1): Show |
6 | HG01168.hp1 HG01169.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-2477_2440-246 others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0005 a0001c0001t0004g0219 a0001c0001t0004g0260 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.2440-2478_2440-246 others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0004g0256 a0001c0001t0004g0261 |
2 | HG00544.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2440-2479_2440-246 others(15): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0004g0258 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2440-2482_2440-246 others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0004g0001 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2440-2483_2440-246 others(19): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0005g0149 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2440-2484_2440-246 others(20): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0004g0254 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2440-2485_2440-246 others(21): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0004g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2440-2488_2440-246 others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0004g0001 a0001c0001t0034g0259 |
2 | HG02040.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2440-2491_2440-246 others(27): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0004g0257 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2440-2495_2440-246 others(31): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | C | T | 4 | a0001c0001t0007g0289 a0001c0001t0007g0290 a0001c0001t0007g0292 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-2503C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117210 | |||||||
| chr14:73117210 | CT | C | 15 | a0001c0001t0001g0252 a0001c0001t0002g0066 a0001c0001t0002g0077 others(12): Show |
15 | HG00323.hp2 HG00558.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.2440-2469delT | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTT | C | 7 | a0001c0001t0001g0193 a0001c0001t0001g0203 a0001c0001t0011g0052 others(4): Show |
7 | HG02486.hp1 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2440-2472_2440-246 others(8): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTTTT | C | 13 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0179 others(10): Show |
14 | HG01891.hp2 HG01952.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.2440-2474_2440-246 others(10): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTTTTT | C | 34 | a0001c0001t0001g0120 a0001c0001t0001g0126 a0001c0001t0001g0132 others(31): Show |
34 | HG00140.hp2 HG00558.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.2440-2475_2440-246 others(11): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTTTTT others(1): Show |
C | 56 | a0001c0001t0001g0010 a0001c0001t0001g0180 a0001c0001t0001g0186 others(53): Show |
57 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.2440-2476_2440-246 others(12): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0001g0195 a0001c0001t0001g0313 a0001c0001t0001g0315 others(6): Show |
9 | HG01074.hp2 HG02258.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2440-2477_2440-246 others(13): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0002g0101 others(1): Show |
4 | HG00733.hp2 HG01106.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-2478_2440-246 others(14): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0273 |
2 | HG00642.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.2440-2479_2440-246 others(15): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTTTTT others(5): Show |
C | 55 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0118 others(52): Show |
56 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2440-2480_2440-246 others(16): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTTTTT others(6): Show |
C | 37 | a0001c0001t0001g0006 a0001c0001t0001g0250 a0001c0001t0002g0059 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2440-2481_2440-246 others(17): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTTTTT others(7): Show |
C | 40 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0006g0044 others(37): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2440-2482_2440-246 others(18): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0031g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2440-2483_2440-246 others(19): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117210 | CTTTTTTT others(13): Show |
C | 3 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | NA18980.hp2 NA19011.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2440-2488_2440-246 others(24): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73117210 | ||||||
| chr14:73117211 | T | A | 2 | a0001c0001t0007g0296 a0001c0001t0021g0293 |
2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2440-2502T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117211 | |||||||
| chr14:73117212 | T | A | 1 | a0001c0001t0007g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2440-2501T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117212 | |||||||
| chr14:73117215 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2440-2498T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117215 | |||||||
| chr14:73117220 | T | A | 1 | a0001c0001t0007g0291 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2440-2493T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117220 | |||||||
| chr14:73117220 | T | C | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2440-2493T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117220 | |||||||
| chr14:73117224 | T | C | 1 | a0001c0001t0026g0050 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2440-2489T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117224 | |||||||
| chr14:73117225 | T | C | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2440-2488T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117225 | |||||||
| chr14:73117336 | A | G | 1 | a0001c0001t0002g0098 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2440-2377A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117336 | |||||||
| chr14:73117385 | G | A | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG02486.hp1 HG02809.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2440-2328G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117385 | |||||||
| chr14:73117441 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0179 |
2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2440-2272G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117441 | |||||||
| chr14:73117572 | G | C | 7 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(4): Show |
7 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2440-2141G>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117572 | |||||||
| chr14:73117649 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0203 a0001c0001t0001g0252 |
3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2440-2064G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117649 | |||||||
| chr14:73117777 | T | A | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-1936T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117777 | |||||||
| chr14:73117814 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2440-1899A>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117814 | |||||||
| chr14:73117881 | C | T | 33 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(30): Show |
33 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.2440-1832C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117881 | |||||||
| chr14:73117988 | A | G | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2440-1725A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73117988 | |||||||
| chr14:73118313 | TA | T | 7 | a0001c0001t0001g0350 a0001c0001t0001g0352 a0001c0001t0001g0353 others(4): Show |
7 | NA18944.hp1 NA18971.hp2 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.2440-1395delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73118313 | ||||||
| chr14:73118407 | G | A | 4 | a0001c0002t0003g0158 a0001c0002t0003g0168 a0001c0002t0003g0169 others(1): Show |
4 | HG02165.hp1 HG02523.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-1306G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118407 | |||||||
| chr14:73118477 | CA | C | 5 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2440-1235delA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118477 | |||||||
| chr14:73118478 | A | G | 294 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(291): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.2440-1235A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118478 | |||||||
| chr14:73118479 | G | GA | 7 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(4): Show |
7 | HG02486.hp1 HG02683.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2440-1219dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73118479 | ||||||
| chr14:73118480 | A | G | 5 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2440-1233A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118480 | |||||||
| chr14:73118589 | T | C | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01074.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2440-1124T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118589 | |||||||
| chr14:73118599 | G | A | 1 | a0001c0002t0003g0150 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2440-1114G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118599 | |||||||
| chr14:73118709 | T | G | 4 | a0001c0001t0015g0026 a0001c0001t0015g0027 a0001c0001t0038g0024 others(1): Show |
4 | HG02818.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-1004T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118709 | |||||||
| chr14:73118775 | T | TTA | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2440-936_2440-935d others(4): Show |
RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73118775 | ||||||
| chr14:73118868 | A | C | 2 | a0001c0001t0001g0325 a0001c0001t0001g0331 |
2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.2440-845A>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118868 | |||||||
| chr14:73118894 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0203 a0001c0001t0001g0252 |
3 | HG01884.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2440-819G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118894 | |||||||
| chr14:73118966 | G | A | 1 | a0001c0001t0023g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2440-747G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73118966 | |||||||
| chr14:73119165 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2440-548C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119165 | |||||||
| chr14:73119180 | G | A | 37 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2440-533G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119180 | |||||||
| chr14:73119270 | T | G | 1 | a0001c0001t0018g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2440-443T>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119270 | |||||||
| chr14:73119333 | C | T | 1 | a0001c0002t0003g0166 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2440-380C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119333 | |||||||
| chr14:73119334 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2440-379G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119334 | |||||||
| chr14:73119355 | T | A | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2440-358T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119355 | |||||||
| chr14:73119368 | T | C | 314 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(311): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.2440-345T>C | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119368 | |||||||
| chr14:73119432 | G | A | 163 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0118 others(160): Show |
173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.2440-281G>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119432 | |||||||
| chr14:73119442 | T | A | 18 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0035 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2440-271T>A | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119442 | |||||||
| chr14:73119507 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2440-206C>T | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119507 | |||||||
| chr14:73119565 | A | G | 2 | a0001c0001t0018g0277 a0001c0001t0018g0278 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2440-148A>G | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | chr14 | 73119565 | |||||||
| chr14:73119626 | G | GA | 5 | a0001c0001t0012g0019 a0001c0001t0012g0020 a0001c0001t0012g0021 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2440-82dupA | RBM25 | ENSG00000119707.14 | transcript | ENST00000261973.12 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr14 | 73119626 |